Category: Breast Cancer Radiation

Dozen inappropriate messages…sad…

Question:

I am guessing that most posters here came across the dozen or so inappropriate   posts on this group listed separately. If you would answer the poster’s question… I think I’m missing something here, what was the question?

I was thinking Kaye was referring to a multiply-posted porn spam with a rude breast-oriented subject line (that wouldn’t have shown up on all servers, probably).  But I don’t think that’s what J thinks she’s referring to . . . so I dunno. Ann T.

Response:

I think I’m missing something here, what was the question? Mary

Thakks Mary, please see "maria is asking" post Thank you, J

Response:

I was thinking Kaye was referring to a multiply-posted porn spam with a rude breast-oriented subject line (that wouldn’t have shown up on all servers, probably).  But I don’t think that’s what J thinks she’s referring to . . . so I dunno.

oh, sorry ! my isp’s server won’t let me see them . I see none of those here. Thank you, J

Response:

I think I’m missing something here, what was the question? I was thinking Kaye was referring to a multiply-posted porn spam with a rude breast-oriented subject line (that wouldn’t have shown up on all servers, probably).

If I get anything which I think will be spam (you usually can tell without the effort of opening it) I block it. But I don’t think that’s what J thinks she’s referring to . . . so I dunno.

No, it didn’t seem like that. Is J a she? Mary – Hide quoted text — Show quoted text – Ann T.

Response:

I think I’m missing something here, what was the question? Mary Thakks Mary, please see "maria is asking" post Thank you, J

Oh, I see. In that case I agree with Kaye, she had the guts to say it, I didn’t. Mary – Hide quoted text — Show quoted text –

Response:

Yes, they got past the filters on my ISP too, which are usually quite good at blocking this sort of thing.  They definitely are cross-posted (look at the headers), probably blindly to all groups with "breast" in the title.  At a guess it will link to an advertisement for a hard-core porn pay-site. I filed an abuse report with Giganews, who’s message-ID is on them. I don’t think there is any point in trying to psychoanalyse the poster, unless you want to ’shrink’ the whole porn industry.  It’s just greed and thoughtless accidental overspill. Its spam, just ignore it or file an abuse report. Tim

– Hide quoted text — Show quoted text – I am guessing that most posters here came across the dozen or so inappropriate posts on this group listed separately. I have no idea if they were only posted to this group or cross-posted, nor do I care. If the are only on this newsgrouip I assume they were written by someone who is both very angry and emotionally immature. I do hope This person has some type of medical insurance that would cover mental health services.  Then again, they could also be posted by someone who has a dx of borderline personality disorder whose condition many not be assisted by any form of ouside counseling.   They live within their  own private he*& and generally don’t have the ability to reform to most appropriate types of treatment.  If that is the case and they are trying to ruin or discredit this newsgroup,  I do hope the majority of posters realize the lack of emotional intelligence, neediness, and anxiety that this poster has and has the good sense to ignore their posts and respond to all here with ‘kindness’ and explanation, as appropriate and/or beneficial. Take care and good night…am falling asleep here again…

Response:

You are not the only one missing something since I have no idea what the question is either, nor do I care to  find out (which I probably couldn’t do anyway on aol — which is fine with me– because of the way that the messages came through).  All I saw was the title–repeated in similar, ‘offensive’ form, 12 different times, so I assumed this is some type of spam or an attempt to interrupt and discredit this group.

Response:

with a rude breast-oriented subject line (that wouldn’t have shown up on all servers, probably).  But I don’t think that’s what J thinks she’s referring to . . . so I dunno. Ann T.  <BR<BR Yep, that’s what I assumed I was doing, too!

Response:

I’ve collected as much info about radiation therapy (for breast cancer) as I could find for posters.  <BR<BR This was not what I was writing about.  I was writing about the 12 headings which appeared  in my list for this group that began: <tit fu^% although the 4 letter expletive was spelled out and then after that there was a space followed by either a 2 letter combination or or 2 symbols such as ^C or eB.  The last 2 letters were the only changes that were listed. The 12 listed posts were each a different heading starting with "tit fu*&" with my changing only the last 2 letters. As I said this had nothing to do with Maria’s radiation concerns–this was a spammer or someone else  who is purposely trying to interfere with this group.

Response:

poster, unless you want to ’shrink’ the whole…industry.  It’s just greed and thoughtless accidental overspill. <g…just responded on a whim :-)  Speaking of the above, well, um that’s another interesting story…but won’t get into that one here…lol..off to write reports for the night..until I need a break…

Response:

I think I’m missing something here, what was the question? Mary Thakks Mary, please see "maria is asking" post Thank you, J

I don’t see a "Maria is asking" thread.  Huh! Sandy L

Response:

I don’t see a "Maria is asking" thread. Huh! Sandy L It’s in the "Radiotherapy: best skincare advice" thread, I think. Susan, Su_Texas

Response:

I’m showing 30+ here as far as the posts you’re referring to, and the way you describe them as far as the way they’re posted. And you’re right very inappropriate indeed. Doesn’t it make you wonder about the person doing this….guess they’ve got nothing else to do with their time. Thanks for posting this….I was thinking the same thing, but didn’t want to reply for fear that this would just keep this an open thread or we’d gather more of the same. Take care there dear/God bless annie Ultimately…..we know deeply that the other side of every fear is a freedom. "Courage"…is *fear* that has said it’s prayers.

Response:

I filed an abuse report with Giganews, who’s message-ID is on them.

Giganews is my news provider and the messages are gone.  I was a bit surprised – they apparently responded pretty quickly  ;-) — we see things not as they are, but as we are. — Anais Nin

Response:

J wrote << They are not inappropriate IMO. I’ve collected as much info about radiation therapy (for breast cancer) as I could find for posters. I’m sorry you do not appreciate my work. Again, I am sure your work on radiation was appreciated.  I was responding to something totally different that had nothing to do with you or the radiation posts.  I am not sure how you connected my post re the 12 spam posts to your radiation posts or to Maria’s request for info re. such.

Response:

– Hide quoted text — Show quoted text – I am guessing that most posters here came across the dozen or so inappropriate posts on this group listed separately. I have no idea if they were only posted to this group or cross-posted, nor do I care. If you would answer the poster’s question… J

Response:

I am guessing that most posters here came across the dozen or so inappropriate posts on this group listed separately. I have no idea if they were only posted to this group or cross-posted, nor do I care. If you would answer the poster’s question… J

I think I’m missing something here, what was the question? Mary – Hide quoted text — Show quoted text –

Response:

I am guessing that most posters here came across the dozen or so inappropriate posts on this group listed separately.

They are not inappropriate IMO. I’ve collected as much info about radiation therapy (for breast cancer) as I could find for posters. I’m sorry you do not appreciate my work. If you have issues with what the web pages say, please do not attribute them to me ( "J wrote") Leave the source (url) and correct the information. Thank you J

Response:

I am guessing that most posters here came across the dozen or so inappropriate posts on this group listed separately. I have no idea if they were only posted to this group or cross-posted, nor do I care.

If you would answer the poster’s question… J

Response:

I am guessing that most posters here came across the dozen or so inappropriate posts on this group listed separately. I have no idea if they were only posted to this group or cross-posted, nor do I care.   If the are only on this newsgrouip I assume they were written by someone who is both very angry and emotionally immature. I do hope This person has some type of medical insurance that would cover mental health services.  Then again, they could also be posted by someone who has a dx of borderline personality disorder whose condition many not be assisted by any form of ouside counseling.   They live within their  own private he*& and generally don’t have the ability to reform to most appropriate types of treatment.  If that is the case and they are trying to ruin or discredit this newsgroup,  I do hope the majority of posters realize the lack of emotional intelligence, neediness, and anxiety that this poster has and has the good sense to ignore their posts and respond to all here with ‘kindness’ and explanation, as appropriate and/or beneficial.   Take care and good night…am falling asleep here again…

Response:

A little sun can be good

Question:

Copyright 2003 Nationwide News Pty Limited The Sunday Telegraph (Sydney, Australia) December 14, 2003 Sunday A little sun can be good GRAHAM PHILLIPS HAS the "Slip, Slop, Slap" campaign been killing people? That’s the implication of recent research on the effects of sunshine on the body. Although the Cancer Council has been urging us to stay out of the sun, a number of studies seem to be saying the body needs a little sun. If you don’t get enough UV radiation, for example, you might develop multiple sclerosis — and, ironically, even cancer. Multiple sclerosis is on the rise, but no one knows what causes this condition, in which the body is attacked by its own immune system. However, researchers have known for a long time that Tasmanians are more likely to get it than Queenslanders. A Hobart study has revealed the reason could be that Queenslanders get a lot more sun than Tasmanians. Researchers examined the backs of people’s hands for signs of sun damage, and made a remarkable discovery: those who had the most sun-affected hands where the least likely to have developed multiple sclerosis. Other studies have found that people who get less sunshine have a greater chance of developing all sorts of cancers, such as prostate and breast cancer. American researcher William Grant says sun-induced skin cancer kills thousands each year, but four times as many people die from cancers caused by not getting enough sun. These studies are preliminary, but they make you question why the anti-sun message has been so harsh for the past 20 years. The sun, after all, is natural, and we’ve been exposed to it for as long as humans have been on the planet. As well, we’ve known for years that a certain amount of sun is essential for the body’s vitamin D production. Indeed, researchers think that it could be a lack of vitamin D that’s giving some people multiple sclerosis and cancer. Health professionals say the reason for the sun-is-poison message is that, to get through to the public, you must keep the message simple and in black-and-white terms. But surely we can deal with shades of grey. After all, there’s nothing new in that wise advice: "Everything in moderation."  grah…@bigpond.com — For this and many more articles, see Paul Jones’ website at http://www.mult-sclerosis.org/

Response:

It would not in the least surprise me if the corporate sun cream industry (yep, those who sell a little bottle of cream for

mom stuff

Question:

no-space spoiler warning My mom died on July 6 :P For those of you just tuning in, or those of you who forgot (because I don’t hang around this part of the cyberverse as much as I used to) – my mother was the first perpetrator, and a pretty continuous one.  I didn’t talk to her for a little over 5 years, and shortly after we started talking, she moved a state away.  The move did much to improve our relationship, and I was very glad she was that far. I wrote here last year (I think) (I know I emailed some) about her breast cancer.  I know many of you thought nice things at me, and some said prayers.  And you know, I really think it made a difference.  To me, anyhoo.  I can feel it when people are thinking kindly of me.  So, if I didn’t appreciate you properly for it, I’m so sorry.  Do know that I am so grateful for your kindnesses. She was diagnosed just in March, I think.  She had chemo from June to December.  In January she had radiation.  She got something she called a cold in February, and her lungs never truly recovered.  They finally figured out she didn’t have ordinary pneumonia, and put her on steroids.  They said the chemo and radiation can make the lungs weak. I got to see her the last weekend in June.  I was originally going up July 4th weekend, but I got a new job [worked 3 days, and had to call in ‘bereaved’), so I was up early.  The pretense was that I was helping them clean and toss to get ready to move to the ‘home’.  She so wanted to get there before she died.  So, she kept saying ‘what do want? Take it now’  I am sure that she knew.  And we sailed the river of denial right to the end. I cried myself dehydrated – I didn’t know you could DO that.  Didn’t feel better til I got a whole bottle of water in me, much later.  She was two days away from her 64th birthday (for which my stepdad had written a most lovely parody of the beatles’ song). I needed to tell people who wouldn’t necessarily understand, but at least have some idea of the complexity it is for me.  I hated her and I loved her.  I miss her terribly.  I can’t call her to tell her about the lovely new man who has shown up in my life.  (though I had quite a crush on him, so she did get to hear alot about it when I was visiting)  I can’t call to ask how to fix the chicken or what to do for a million little things.  The sympathy people were hard.  I took a valium for the ‘gathering’ so I wouldn’t kill anyone.  I thought that was brilliant on my part.  There was a gathering for people here, and there’s going to be a buddhist service in her town next weekend. I had one aunt (second wife of uncle who is ma’s bro) ask me what she did that was so bad.  I decided not to tell her.  More for self protection than for her.  It was an interesting choice (and it was the day before the valium, I was sober) The man has been so much more than wonderful.  I’ve known him since March.  We went out when I got home from visiting mom (drinking and commiserating since both our cars had died expensive deaths).  I cooked dinner for him the night before she died.  She was in hospital, but they hadn’t called me.  I felt awful calling him (we hadn’t so much as hugged) but I really had no one else I wanted to/could be with.  He opened up his arms and I fell right in.  He’s so….appropriate. and kind.  He didn’t need to fix it, he could just BE there with me.  He makes me laugh, a lot. Weird story about coming together though.  I can’t just tell people, cuz everyone is so grieving. :P thank you thank you aar for always being there even though I’m not always here, you’re always in me and it helps tigrbunny

Response:

if it helps i empathize and sympathize with and for you.  i also know the paradox of loving and hating someone at the same time, being glad they’re gone, but grieving that loss at the same time….damned difficult place to be. good for you making your choice whether or not to answer your aunt’s question.  i’ve gotten a couple of them too…i’ve never trusted the motive behind the question…especially if it’s phrased in that particular way…my brain goes to them making a value judgement that they have not basis of comparison to make right over to them getting vicarious enjoyment of my pain…neither of which are desirable :( take special care of yourself.  i’m really glad that there’s someone special in your life to be there for you. naomi – Hide quoted text — Show quoted text – no-space spoiler warning My mom died on July 6 :P For those of you just tuning in, or those of you who forgot (because I don’t hang around this part of the cyberverse as much as I used to) – my mother was the first perpetrator, and a pretty continuous one.  I didn’t talk to her for a little over 5 years, and shortly after we started talking, she moved a state away.  The move did much to improve our relationship, and I was very glad she was that far. I wrote here last year (I think) (I know I emailed some) about her breast cancer.  I know many of you thought nice things at me, and some said prayers.  And you know, I really think it made a difference.  To me, anyhoo.  I can feel it when people are thinking kindly of me.  So, if I didn’t appreciate you properly for it, I’m so sorry.  Do know that I am so grateful for your kindnesses. She was diagnosed just in March, I think.  She had chemo from June to December.  In January she had radiation.  She got something she called a cold in February, and her lungs never truly recovered.  They finally figured out she didn’t have ordinary pneumonia, and put her on steroids.  They said the chemo and radiation can make the lungs weak. I got to see her the last weekend in June.  I was originally going up July 4th weekend, but I got a new job [worked 3 days, and had to call in ‘bereaved’), so I was up early.  The pretense was that I was helping them clean and toss to get ready to move to the ‘home’.  She so wanted to get there before she died.  So, she kept saying ‘what do want? Take it now’  I am sure that she knew.  And we sailed the river of denial right to the end. I cried myself dehydrated – I didn’t know you could DO that.  Didn’t feel better til I got a whole bottle of water in me, much later.  She was two days away from her 64th birthday (for which my stepdad had written a most lovely parody of the beatles’ song). I needed to tell people who wouldn’t necessarily understand, but at least have some idea of the complexity it is for me.  I hated her and I loved her.  I miss her terribly.  I can’t call her to tell her about the lovely new man who has shown up in my life.  (though I had quite a crush on him, so she did get to hear alot about it when I was visiting)  I can’t call to ask how to fix the chicken or what to do for a million little things.  The sympathy people were hard.  I took a valium for the ‘gathering’ so I wouldn’t kill anyone.  I thought that was brilliant on my part.  There was a gathering for people here, and there’s going to be a buddhist service in her town next weekend. I had one aunt (second wife of uncle who is ma’s bro) ask me what she did that was so bad.  I decided not to tell her.  More for self protection than for her.  It was an interesting choice (and it was the day before the valium, I was sober) The man has been so much more than wonderful.  I’ve known him since March.  We went out when I got home from visiting mom (drinking and commiserating since both our cars had died expensive deaths).  I cooked dinner for him the night before she died.  She was in hospital, but they hadn’t called me.  I felt awful calling him (we hadn’t so much as hugged) but I really had no one else I wanted to/could be with.  He opened up his arms and I fell right in.  He’s so….appropriate. and kind.  He didn’t need to fix it, he could just BE there with me.  He makes me laugh, a lot. Weird story about coming together though.  I can’t just tell people, cuz everyone is so grieving. :P thank you thank you aar for always being there even though I’m not always here, you’re always in me and it helps tigrbunny

Response:

((((((((((( tigerbunny ))))))))))) condolences …  and good to see you again. yes, it is an ambivalent situation.  and all feelings you have concerning this conundrum are valid.  all.  every single facet. azure, btdtbtts

– Hide quoted text — Show quoted text – no-space spoiler warning My mom died on July 6 :P For those of you just tuning in, or those of you who forgot (because I don’t hang around this part of the cyberverse as much as I used to) – my mother was the first perpetrator, and a pretty continuous one.  I didn’t talk to her for a little over 5 years, and shortly after we started talking, she moved a state away.  The move did much to improve our relationship, and I was very glad she was that far. I wrote here last year (I think) (I know I emailed some) about her breast cancer.  I know many of you thought nice things at me, and some said prayers.  And you know, I really think it made a difference.  To me, anyhoo.  I can feel it when people are thinking kindly of me.  So, if I didn’t appreciate you properly for it, I’m so sorry.  Do know that I am so grateful for your kindnesses. She was diagnosed just in March, I think.  She had chemo from June to December.  In January she had radiation.  She got something she called a cold in February, and her lungs never truly recovered.  They finally figured out she didn’t have ordinary pneumonia, and put her on steroids.  They said the chemo and radiation can make the lungs weak. I got to see her the last weekend in June.  I was originally going up July 4th weekend, but I got a new job [worked 3 days, and had to call in ‘bereaved’), so I was up early.  The pretense was that I was helping them clean and toss to get ready to move to the ‘home’.  She so wanted to get there before she died.  So, she kept saying ‘what do want? Take it now’  I am sure that she knew.  And we sailed the river of denial right to the end. I cried myself dehydrated – I didn’t know you could DO that.  Didn’t feel better til I got a whole bottle of water in me, much later.  She was two days away from her 64th birthday (for which my stepdad had written a most lovely parody of the beatles’ song). I needed to tell people who wouldn’t necessarily understand, but at least have some idea of the complexity it is for me.  I hated her and I loved her.  I miss her terribly.  I can’t call her to tell her about the lovely new man who has shown up in my life.  (though I had quite a crush on him, so she did get to hear alot about it when I was visiting)  I can’t call to ask how to fix the chicken or what to do for a million little things.  The sympathy people were hard.  I took a valium for the ‘gathering’ so I wouldn’t kill anyone.  I thought that was brilliant on my part.  There was a gathering for people here, and there’s going to be a buddhist service in her town next weekend. I had one aunt (second wife of uncle who is ma’s bro) ask me what she did that was so bad.  I decided not to tell her.  More for self protection than for her.  It was an interesting choice (and it was the day before the valium, I was sober) The man has been so much more than wonderful.  I’ve known him since March.  We went out when I got home from visiting mom (drinking and commiserating since both our cars had died expensive deaths).  I cooked dinner for him the night before she died.  She was in hospital, but they hadn’t called me.  I felt awful calling him (we hadn’t so much as hugged) but I really had no one else I wanted to/could be with.  He opened up his arms and I fell right in.  He’s so….appropriate. and kind.  He didn’t need to fix it, he could just BE there with me.  He makes me laugh, a lot. Weird story about coming together though.  I can’t just tell people, cuz everyone is so grieving. :P thank you thank you aar for always being there even though I’m not always here, you’re always in me and it helps tigrbunny

Response:

I am sorry about your mom. I felt kind of the same when my dad died, though I couldn’t admit it at the time. I am glad about the new man, you deserve someone who makes you happy. Take care of you… – Hide quoted text — Show quoted text – no-space spoiler warning My mom died on July 6 :P For those of you just tuning in, or those of you who forgot (because I don’t hang around this part of the cyberverse as much as I used to) – my mother was the first perpetrator, and a pretty continuous one.  I didn’t talk to her for a little over 5 years, and shortly after we started talking, she moved a state away.  The move did much to improve our relationship, and I was very glad she was that far. I wrote here last year (I think) (I know I emailed some) about her breast cancer.  I know many of you thought nice things at me, and some said prayers.  And you know, I really think it made a difference.  To me, anyhoo.  I can feel it when people are thinking kindly of me.  So, if I didn’t appreciate you properly for it, I’m so sorry.  Do know that I am so grateful for your kindnesses. She was diagnosed just in March, I think.  She had chemo from June to December.  In January she had radiation.  She got something she called a cold in February, and her lungs never truly recovered.  They finally figured out she didn’t have ordinary pneumonia, and put her on steroids.  They said the chemo and radiation can make the lungs weak. I got to see her the last weekend in June.  I was originally going up July 4th weekend, but I got a new job [worked 3 days, and had to call in ‘bereaved’), so I was up early.  The pretense was that I was helping them clean and toss to get ready to move to the ‘home’.  She so wanted to get there before she died.  So, she kept saying ‘what do want? Take it now’  I am sure that she knew.  And we sailed the river of denial right to the end. I cried myself dehydrated – I didn’t know you could DO that.  Didn’t feel better til I got a whole bottle of water in me, much later.  She was two days away from her 64th birthday (for which my stepdad had written a most lovely parody of the beatles’ song). I needed to tell people who wouldn’t necessarily understand, but at least have some idea of the complexity it is for me.  I hated her and I loved her.  I miss her terribly.  I can’t call her to tell her about the lovely new man who has shown up in my life.  (though I had quite a crush on him, so she did get to hear alot about it when I was visiting)  I can’t call to ask how to fix the chicken or what to do for a million little things.  The sympathy people were hard.  I took a valium for the ‘gathering’ so I wouldn’t kill anyone.  I thought that was brilliant on my part.  There was a gathering for people here, and there’s going to be a buddhist service in her town next weekend. I had one aunt (second wife of uncle who is ma’s bro) ask me what she did that was so bad.  I decided not to tell her.  More for self protection than for her.  It was an interesting choice (and it was the day before the valium, I was sober) The man has been so much more than wonderful.  I’ve known him since March.  We went out when I got home from visiting mom (drinking and commiserating since both our cars had died expensive deaths).  I cooked dinner for him the night before she died.  She was in hospital, but they hadn’t called me.  I felt awful calling him (we hadn’t so much as hugged) but I really had no one else I wanted to/could be with.  He opened up his arms and I fell right in.  He’s so….appropriate. and kind.  He didn’t need to fix it, he could just BE there with me.  He makes me laugh, a lot. Weird story about coming together though.  I can’t just tell people, cuz everyone is so grieving. :P thank you thank you aar for always being there even though I’m not always here, you’re always in me and it helps tigrbunny

Response:

– Hide quoted text — Show quoted text – no-space spoiler warning My mom died on July 6 :P For those of you just tuning in, or those of you who forgot (because I don’t hang around this part of the cyberverse as much as I used to) – my mother was the first perpetrator, and a pretty continuous one.  I didn’t talk to her for a little over 5 years, and shortly after we started talking, she moved a state away.  The move did much to improve our relationship, and I was very glad she was that far. I wrote here last year (I think) (I know I emailed some) about her breast cancer.  I know many of you thought nice things at me, and some said prayers.  And you know, I really think it made a difference.  To me, anyhoo.  I can feel it when people are thinking kindly of me.  So, if I didn’t appreciate you properly for it, I’m so sorry.  Do know that I am so grateful for your kindnesses. She was diagnosed just in March, I think.  She had chemo from June to December.  In January she had radiation.  She got something she called a cold in February, and her lungs never truly recovered.  They finally figured out she didn’t have ordinary pneumonia, and put her on steroids.  They said the chemo and radiation can make the lungs weak. I got to see her the last weekend in June.  I was originally going up July 4th weekend, but I got a new job [worked 3 days, and had to call in ‘bereaved’), so I was up early.  The pretense was that I was helping them clean and toss to get ready to move to the ‘home’.  She so wanted to get there before she died.  So, she kept saying ‘what do want? Take it now’  I am sure that she knew.  And we sailed the river of denial right to the end. I cried myself dehydrated – I didn’t know you could DO that.  Didn’t feel better til I got a whole bottle of water in me, much later.  She was two days away from her 64th birthday (for which my stepdad had written a most lovely parody of the beatles’ song). I needed to tell people who wouldn’t necessarily understand, but at least have some idea of the complexity it is for me.  I hated her and I loved her.  I miss her terribly.  I can’t call her to tell her about the lovely new man who has shown up in my life.  (though I had quite a crush on him, so she did get to hear alot about it when I was visiting)  I can’t call to ask how to fix the chicken or what to do for a million little things.  The sympathy people were hard.  I took a valium for the ‘gathering’ so I wouldn’t kill anyone.  I thought that was brilliant on my part.  There was a gathering for people here, and there’s going to be a buddhist service in her town next weekend. I had one aunt (second wife of uncle who is ma’s bro) ask me what she did that was so bad.  I decided not to tell her.  More for self protection than for her.  It was an interesting choice (and it was the day before the valium, I was sober) The man has been so much more than wonderful.  I’ve known him since March.  We went out when I got home from visiting mom (drinking and commiserating since both our cars had died expensive deaths).  I cooked dinner for him the night before she died.  She was in hospital, but they hadn’t called me.  I felt awful calling him (we hadn’t so much as hugged) but I really had no one else I wanted to/could be with.  He opened up his arms and I fell right in.  He’s so….appropriate. and kind.  He didn’t need to fix it, he could just BE there with me.  He makes me laugh, a lot. Weird story about coming together though.  I can’t just tell people, cuz everyone is so grieving. :P thank you thank you aar for always being there even though I’m not always here, you’re always in me and it helps tigrbunny

Hey you, I’m sorry to hear about your mom.  I always imagine I’ll feel the same ambivilance when mine goes.  I know my mother will never answer any of the questions I have but her death will mean that even that possibility is gone. I wish I had something better to say, but I hear you and hope you get through this ok. And congrats on the man  : )

Response:

rising CEA worry?

Question:

MY wife has breast cancer diagnosed 4 years ago , lumpect. and takes Tamox., had radiation and no lymph node status. Her  CEA has been under 2 for the last 4 years and is now 8 . How worried should we be?

Response:

<< Her  CEA has been under 2 for the last 4 years and is now 8 . How worried should we be?   I don’t know.  There are several other reasons that can cause elevation–not sure what they all are.  However, since she has had  breast cancer and there has been a change, it is of some concern.  What does her oncologist say?  I am guessing he is the one that ordered the test.  My best thoughts are with you both re, this.  Take care…

Response:

Dinner-plate-sized Radiation burn – was my experience common?

Question:

Thanks for reading my post.   I’m doing quite well now, but immediately after the end of my radiation treatments a huge third-degree, crusty, dinnerplate-sized radiation burn appeared on my chest.  It was seeping and pretty horrible, as well as very painful.  When my doctors saw it, their faces fell, but they didn’t tell me if it was normal, nor whether such an experience is common. It took six weeks to heal, and I was very discouraged and "down" while it was bad.  Had to demand heavy pain medication, and the withdrawal from that was also long and involved.   Are there plenty of others out there with similar stories or was my experience unusual?  Eager to know.   All the best to my fellow survivors !   signed, – Breast-Cancer-Ass-Whoppin’-Hussy "Men choose as their prophets those who tell them that their hopes are true."                                                             – Lord Dunsany 3930 Cody Road Sherman Oaks, CA   91403  USA day 818-718-1221 eve 818-784-8476

Response:

Are there plenty of others out there with similar stories or was my experience unusual?  Eager to know.

Well, mine isn’t dinner-plate-sized, but I do have a depressed, very hard, beam-shaped area on the front and back of my thigh where I had my first radiation to my femur.  When I say it’s beam-shaped I mean it’s exactly the size, shape and location of the beam of radiation.  You can feel the edges of it if you dig your fingers into my squishy thigh around it.  The docs all say it’s an artifact of radiation.  Nothing fixes it.  I just don’t wear thong bikinis anymore.  ; ) — Aloha, Catharine titubant sed non decidunt wiblia

Response:

Dear Catharine, Thanx for your reply. Hope your "squishy spot" firms up! My burn is gone and left no scar tissuebut it took six weeks. I have to tell you your latin quote at the end of your reply sent me scurrying to my Latin refs. I got the general gist of it. What is your translation? Aloha, Chick

Response:

I have to tell you your latin quote at the end of your reply sent me scurrying to my Latin refs. I got the general gist of it. What is your translation?

"Weebles wobble but they don’t fall down." — Aloha, Catharine titubant sed non decidunt wiblia

Response:

Manual Lymph Drainage , is there a How to available on net

Question:

After having surgery and radiation for Breast Cancer my Wife now has a problem with Lymphedema. I would like to perform Manual Lymph Drainage on her arm and would like to know if there is "how to" available on the web. Even better if there is a on line video available on the Internet. thanks, Ken

Response:

Ken, even if there might be a video available, it would probably be good for her to have it done first by someone who has been professionally trained.  I learned to do MLD; however, my physical therapist did it more intensely in areas that I could not possibly reach on myself.  Also, it needs to be done in a special way in terms of the amount of pressure applied or not applied. What has helped me the most–to keep it stabilized is wearing a custom sleeve during the day and a special, custom sleeve to sleep in at night.   If you have any ?’s, just ask–hoping the lymphedema can be controlled soon. Take care and all the best!

Response:

The following link gives a simplified DIY form of MLD http://www.cancerbacup.org.uk/info/lymph/lymph-12.htm There is also a host of other information about Lymphedema and cancer in general here presented in a very readable form. Tim Jackson

– Hide quoted text — Show quoted text – After having surgery and radiation for Breast Cancer my Wife now has a problem with Lymphedema. I would like to perform Manual Lymph Drainage on her arm and would like to know if there is "how to" available on the web. Even better if there is a on line video available on the Internet. thanks, Ken

Response:

I would like to say thanks to the person posting the link. This is just the type of info I was looking for. Ken – Hide quoted text — Show quoted text – The following link gives a simplified DIY form of MLD http://www.cancerbacup.org.uk/info/lymph/lymph-12.htm There is also a host of other information about Lymphedema and cancer in general here presented in a very readable form. Tim Jackson After having surgery and radiation for Breast Cancer my Wife now has a problem with Lymphedema. I would like to perform Manual Lymph Drainage on her arm and would like to know if there is "how to" available on the web. Even better if there is a on line video available on the Internet. thanks, Ken

Response:

(OT) Plastic wrap in microwaves could cause cancer

Question:

In article <1yhV9.11830$Qr4.1172…@newsread1.prod.itd.earthlink.net>, John Kakouris <tree…@earthlink.net> wrote >Hello- >I just received an email talking about how using plastic wrap to cover food >in a microwave could cause cancer.  It actually drips toxins into the food. >Also, plastic containers and fatty foods or ramen cup of soup.  I don’t know >if it is possible to attach a copy of it to this??  If not, if anyone is >interested, let me know and I can send it to your email, otherwise if I have >more energy later I could retype it.  (kind of long) >Rebecca

If you email me it, I can almost certainly extract the words and post them here, so that we can make up our minds on this matter. — Andy [Chair, N E Lupus Group] See http://www.kitzbuhel.demon.co.uk/lupus for more!

Response:

In article <1yhV9.11830$Qr4.1172…@newsread1.prod.itd.earthlink.net>, John Kakouris <tree…@earthlink.net> wrote >Hello- >I just received an email talking about how using plastic wrap to cover food >in a microwave could cause cancer.  It actually drips toxins into the food. >Also, plastic containers and fatty foods or ramen cup of soup.  I don’t know >if it is possible to attach a copy of it to this??  If not, if anyone is >interested, let me know and I can send it to your email, otherwise if I have >more energy later I could retype it.  (kind of long) >Rebecca

Here it is, for you to decide on your viewpoint. Subject: Plastic Wrap in Microwaves As a seventh grade student, Claire Nelson learned that di(ethylhexyl)adepate (DEHA), considered a carcinogen, is found in plastic wrap.  She also learned that the FDA had never studied the effect of microwave cooking on plastic-wrapped food.  Claire began to wonder: "Can cancer-causing particles seep into food covered with household plastic wrap while it is being microwaved?" Three years later, with encouragement from her high school science teacher, Claire set out to test what the FDA had not.  Although she had an idea for studying the effect of microwave radiation on plastic wrapped food, she did not have the equipment.  Eventually, Jon Wilkes at the National Center for Toxicological Research in Jefferson, Arkansas, agreed to help her. The research center, which is affiliated with the FDA, let her use its facilities to perform her experiments, which involved micro waving plastic wrap in virgin olive oil.  Claire tested four different plastic wraps and "found not just the carcinogens but also xenoestrogen was migrating [into the oil]…." Xenoestrogens are linked to low sperm counts in men and to breast cancer in women. Throughout her junior and senior years, Claire made a couple of trips each week to the research center, which was 25 miles from her home, to work on her experiment.  An article in Options reported that "her analysis found that DEHA was migrating into the oil at between 200 parts and 500 parts per million. The FDA standard is 0.05 parts per billion." Her summarized results have been published in science journals. Claire Nelson received the American Chemical Society’s top science prize for students during her junior year and fourth place at the International Science and Engineering Fair (Fort Worth, Texas) as a senior. "Carcinogens — At 10,000,000 Times FDA Limits" On Channel 2 (Huntsville, AL) this morning they had a Dr. Edward Fujimoto from Castle Hospital on the program.  He is the manager of the Wellness Program at the hospital.  He was talking about dioxins and how bad they are for us.  He said that we should not be heating our food in the microwave using plastic containers.  This applies to foods that contain fat.  He said that the combination of fat, high heat and plastics releases dioxins into the food and ultimately into the cells of the body. Dioxins are carcinogens and highly toxic to the cells of our bodies. Instead, he recommends using glass, Corning Ware, or ceramic containers for heating food.  You get the same results without the dioxins.  So such things as TV dinners, instant ramen and soups, etc., should be removed from the container and heated in something else.  Paper isn’t bad but you don’t know what is in the paper.  Just safer to use tempered glass, Corning Ware, etc. He said we might remember when some of the fast food restaurants moved away from the foam containers to paper.  The dioxin problem is one of the reasons. To add to this: Saran wrap placed over foods as they are nuked, with the high heat, actually drips poisonous toxins into the food.  Use paper towel instead. — Andy [Chair, N E Lupus Group] See http://www.kitzbuhel.demon.co.uk/lupus for more!

Response:

Hello- I just received an email talking about how using plastic wrap to cover food in a microwave could cause cancer.  It actually drips toxins into the food. Also, plastic containers and fatty foods or ramen cup of soup.  I don’t know if it is possible to attach a copy of it to this??  If not, if anyone is interested, let me know and I can send it to your email, otherwise if I have more energy later I could retype it.  (kind of long) Rebecca

Response:

Hi Rebecca http://www.aces.edu/dept/extcomm/newspaper/sept10c02.html Kind of speaks for itself, except there were some plastic wraps which I think were "imports" that did not meet the criteria of the FDA. I don’t use plastic wraps myself, I use ceramic plates/bowls to cover and/or cook foods in micro-wave.(no plastics at all with heat), but that decision was made long before the phthalate, dioxin and PVC’s discussions/reports hit the news.  The decision was based on the taste. Each to their own decision, but I have more recently seen references to kidney cancers (if I recall) in connection with PVC’s. HTH and Hugs J PS No idea what "ramen cup of soup" is, but if it’s the prepared soups in a cup, they also have a yucky "chem"and/or "paper" taste to me, so I don’t eat those either.  Home-made is best. IMO – Hide quoted text — Show quoted text -John Kakouris wrote: > Hello- > I just received an email talking about how using plastic wrap to cover food > in a microwave could cause cancer.  It actually drips toxins into the food. > Also, plastic containers and fatty foods or ramen cup of soup.  I don’t know > if it is possible to attach a copy of it to this??  If not, if anyone is > interested, let me know and I can send it to your email, otherwise if I have > more energy later I could retype it.  (kind of long) > Rebecca

Response:

Introduction

Question:

– Hide quoted text — Show quoted text – Hi My name is Susan Cartwright, known as Suze or Suzie, and I live in Brisbane , Queensland, Australia. I am a researcher and journalist and am fairly used to getting a grasp on an area of study quite quickly. Although I do not have diabetes, I find myself in a position of caring for a grandparent who has just been diagnosed. I have had a pretty good talk with the endocrinologist, have attended a diabetic training class at a local hospital, and have bought a couple of books on the subject. I find that there are discrepancies between the various sources of diabetic knowledge, particularly in the information published by Diabetes Australia and many articles in various medical research databases. Diet and the amount of acceptable carbohydrate is one of those areas. One would expect an organisation like Diabetes Australia to be very up to date, but either they disagree with many new findings, or they are an extraordinarily out of touch organisation. I am hoping to find some insight into what it is to live with, and treat diabetes, and so to that end have started monitoring several groups, alt.support.diabetes, misc.health.diabetes, and alt.support.diabetes.uk. Are there any other worthwhile groups? I have read these groups for a few days and noticed an unusually high troll and general nuisance infestation. I have selected several candidates for filtering, Chung and his puppets, Mack, %, Mu, Phildo, and one of the Bobs. Are there any others that I missed? This intro is crossposted to the three groups that I am reading, but I do not normally crosspost.

I’m sure there are some others you’d like to killfile.  I don’t see how Mack made your list though.  He’s one of the good guys.  As for the diet information, there is nothing set in stone and for a very good reason.  Each case of diabetes is different.  Some people do well by simply cutting back a little bit on what they eat and by exercising a little bit more.  Some of us have to be more strict with our diets, particularly when it comes to carbs. Still others must go the low carb route.  And then there are those who follow the glycemic index.  This works for some people and not for others. Why so much variation?  Because while diabetes tends to be lumped in a category, like type 1 or type 2, there are really many different types.  In most cases it is not necessary to delve any further to ferret out more details about the diabetes.  But for a few who do not respond to standard treatments, more tests are warranted.  People with type 1 do not produce any insulin at all.  They must use insulin or they will die.  Type 2 is a whole different thing.  People with type 2 usually produce enough insulin.  Some produce more than enough.  But they all have insulin resistance to varying degrees.  Compound these things with any other health problems we might have (like wacky thyroids) and things can get complicated. — See my webpage: http://mysite.verizon.net/juliebove/index.htm

Response:

– Hide quoted text — Show quoted text – Hi My name is Susan Cartwright, known as Suze or Suzie, and I live in Brisbane , Queensland, Australia. I am a researcher and journalist and am fairly used to getting a grasp on an area of study quite quickly. Although I do not have diabetes, I find myself in a position of caring for a grandparent who has just been diagnosed. I have had a pretty good talk with the endocrinologist, have attended a diabetic training class at a local hospital, and have bought a couple of books on the subject. I find that there are discrepancies between the various sources of diabetic knowledge, particularly in the information published by Diabetes Australia and many articles in various medical research databases. Diet and the amount of acceptable carbohydrate is one of those areas. One would expect an organisation like Diabetes Australia to be very up to date, but either they disagree with many new findings, or they are an extraordinarily out of touch organisation. I am hoping to find some insight into what it is to live with, and treat diabetes, and so to that end have started monitoring several groups, alt.support.diabetes, misc.health.diabetes, and alt.support.diabetes.uk. Are there any other worthwhile groups? I have read these groups for a few days and noticed an unusually high troll and general nuisance infestation. I have selected several candidates for filtering, Chung and his puppets, Mack, %, Mu, Phildo, and one of the Bobs. Are there any others that I missed? This intro is crossposted to the three groups that I am reading, but I do not normally crosspost. Ciao Suze

i’m new here too , as well as newly diagnoised , take this however you like , read the info , choose what you feel applies but don’t expect much , diabetes seems to be as idividual as the people in this group one will say do this , one will say no don’t , and beware of those who call you a troll , but you’ll have an avantage there , they seem to think women are less intimidating , welcome to the world of , nobody knows what works

Response:

– Hide quoted text — Show quoted text – Hi My name is Susan Cartwright, known as Suze or Suzie, and I live in Brisbane , Queensland, Australia. I am a researcher and journalist and am fairly used to getting a grasp on an area of study quite quickly. Although I do not have diabetes, I find myself in a position of caring for a grandparent who has just been diagnosed. I have had a pretty good talk with the endocrinologist, have attended a diabetic training class at a local hospital, and have bought a couple of books on the subject. I find that there are discrepancies between the various sources of diabetic knowledge, particularly in the information published by Diabetes Australia and many articles in various medical research databases. Diet and the amount of acceptable carbohydrate is one of those areas. One would expect an organisation like Diabetes Australia to be very up to date, but either they disagree with many new findings, or they are an extraordinarily out of touch organisation. I am hoping to find some insight into what it is to live with, and treat diabetes, and so to that end have started monitoring several groups, alt.support.diabetes, misc.health.diabetes, and alt.support.diabetes.uk. Are there any other worthwhile groups? I have read these groups for a few days and noticed an unusually high troll and general nuisance infestation. I have selected several candidates for filtering, Chung and his puppets, Mack, %, Mu, Phildo, and one of the Bobs. Are there any others that I missed? This intro is crossposted to the three groups that I am reading, but I do not normally crosspost. Ciao Suze

Hi Suze, Your grandparent is fortunate to have someone who will take the time to become personally involved, as you have.  I am also newly diagnosed (early june), and you are correct that sources — including those that consider themselves "specialists" — often give opposite types of information.  I am an American, and the ADA also provides information that I would consider outdated (just as you describe for Diabetes Australia).  I have found that certain carbs will send my BG spiking.  The diet that has worked best for me has been South Beach plus no flour, added sugar, pasta, or rice.  My diet is not low-carb, though — I get lots of fresh fruits and vegetables, and I can even have old-fashioned oatmeal for breakfast (but many have to avoid the oatmeal).  I suggest that you add alt.support.diabetes to your list.  Yes, there are a number of trolls, but there are also many knowledgeable and helpful people who post there — and, as you have already noted, you can filter out the worst offenders.  Of course, you will also find that many of the same people post to all of the groups you listed (and the one I added). You may have already seen these websites.  If not, I suggest that you look at these: http://www.alt-support-diabetes.org/Newly%20Diagnosed.htm http://www.geocities.com/jenny_the_bean/index.html http://www.geocities.com/lottadata4u/ MaryL

Response:

A couple of months ago, my foster mother was diagnosed as type 2. She’s been doing great with diet and meds and losing weight  and has good BGs readings as well as good a1c at 6 so soon after diagnosis.  A few weeks ago she feeling a sharp pain in her breast and mentioned it in one of doctor’s visits that she had the pain and had found a lump. The doc said it was a fibrous mass and to cut all caffeine from her diet.  Her regular mammogram was shortly after that and she brought it up.  The radiologist insisted on a specialist taking a look, who insisted on a biopsy which came back malignant.  She was scheduled for surgery and some pre surgery tests.  One of the test showed she had an aneurism in the brain, which canceled the surgery until further tests could be done to determine the exact condition of the aneurism. Surgery with that problem could easily result in death. It was found to have been old aneurism.  So much so that it had actually healed on it’s own and the image that showed in the cat scan was actually scar tissue and crystallized blood.  The specialist determined that she was okay for surgery.  Which was rescheduled for this Monday morning, Dec 6th. We’re all in town for this, even the one that was living a few thousand miles away. Breast Cancer is what killed my birth mother.  She died between Thanksgiving and Christmas on the USA calendar. So when I get off work Monday morning I’ll be heading over to the hospital.  She will already be in surgery by the time I get their. The surgery will last around 3 hours if nothing unforseen happens. She will have the cancer specialist working on the breast with the tumor and when that is done a plastic surgeon will remove the same amount / weight of material from the other breast to make sure everything matches. Unless there are complications, she will only be in the hospital 24 hours.  Recovery will be at home.  Thankfully I only work 3 days a week anyway and will have the next 4 days free to be around whenever she needs any help. The standing joke is that when the others get on her nerves enough, she’ll call me to come and bust her out of the house and take her out for some fun and relaxation. For those who are inclined to do so, prayers and positive thoughts are always appreciated. M

Breast Cancer – x-post

Question:

Ann… I still have a small area of that "orange" stuff on the skin of the breast where the mastectomy was done. I had radiation 5/99 to 7/99. Lots less of it then before obviously…but still can see a very small area of it…"pitted" as you described in your post. take care there God bless annie   Ultimately…..we know deeply that the other side of every fear is a freedom. "Courage"…is *fear* that has said it’s prayers.

Response:

"Sandy L – Hide quoted text — Show quoted text – Call me silly, but if the surgeon closes up the incision from side to side the :-) dj You’d think so, but the sutures are intermittent, with spaces between. The tissue is mostly fat, so she/he must take a fairly broad loop in order to get a hold that won’t pull out. For a mastectomy, there is such a large flap of skin that it really isn’t practical to try to sew the flap to the chest.  The drains do it all. Well if the drains do it all I all for it…..however I bet somewhere

down the line drains won’t be needed for any operations. There always finding ways. dj – Hide quoted text — Show quoted text –

Response:

Thank you I’ll meet you there. Diane….dj

– Hide quoted text — Show quoted text –   Hi Even through my Mom had breast cancer at the age of 60 in 1981.  She did pass away in 1991 but from complications of her diabetes she never had any signs of caner in her whole body for the full 10 years, which would make her a 10-year survivor of breast cancer. From the time my Mom had her mastectomy 1981 (I was 34 y/o)  I’ve had a mammogram every year and all was fine, I’m now age 55. Not this year….. The mammogram this year was showing something on my left breast, as they put it "very vague" so we went onto a ultrasound imaging. Also on the ultrasound was the word again "very vague" so an ultrasound biopsy was done on Dec. 4, 2202.  Also I was told  there is no discrete nodule or mass demonstrated on the mammogram, and no lump on the outside of my breast however, there is added density from last years mammogram. The news come back on Wednesday Dec. 11, 2002  as cancer. I went to see the breast surgeon Dr. Jan Houston on Thrus. Dec. 12, 2002 to talk.  She stated it’s in my left breast,  Stage I, Ducal, 8 something long, in England for me she said about less than a half an inch. It’s 2 cm from the nipple on the bottom part of my breast. I have decided to go with the lumpectomy.  She will remove some lymph nodes. She also stated I will be taking radiation for 6 weeks, 5 days a week. As far as chemo she stated will we see what treatments to do after the surgery which is Friday Dec. 20th. On Monday, Dec. 16th, I’m going in for per testing and on Thursday Dec.19th I’m going to Nuke…something or other… Medicine to have wires put in my left  breast? I’m scared this is all so new to me.   I, because of the ultrasound "guy" pushing hard on my breast think that the cancer is "deep" inside my breast , the biopsy "lady" also pushed hard on my breast to get a "good sample" as she stated,  however that added to the ultrasound "guy" just makes me believe is "deep" inside my breast. Which I’m thinking  it’s spread to my breast "bones". Sorry if I’m not spelling everything correct or not calling the doctors by the correct names I’m just not sure of the correct words. How does the breast surgeon (whom I do like very much) know what Stage your cancer is.  By the mammogram, ultrasound, or biopsy or is it not fare to say what Stage your cancer is until after the lumpectomy and the lymph node are checked? I do understand how she knows the size, but she can’t know how deep it is inside your breast.  Also understand how she knows where it is, in my case Ducal, but that’s all she could know until after the surgery…right. Thanks to all who took the time to read this and for any help. Hi Diane, Your best newsgroup is probably alt.support.cancer.breast they know everything over there. Click on the following and see if it takes you there. If it does, you’ll find your post and my reply there, reply on the other newsgroup, then others can reply to you, okay? J PS http://imaginis.com/breasthealth/breast_cancer.asp Also Dr. Susan Love’s book(s) on breast cancer

Response:

"Marilyn" Will I have these tube (drains) even though I going to have a

Lumpectomy? – Hide quoted text — Show quoted text – That was pretty much my situation.  I didn’t need any painkillers after the initial drug they gave me when I first woke up in the surgery. Opium? That’s what I remember, but it might have been something less fun. I was up and around slowly the next day, able to put on sweat pants and go down to the lobby for a newspaper. And the day after that I was able to wash my hair in the bathroom sink.  They made me stay in until the drain was clear, which was the morning of the fourth day.  The worst part was not being able to lift my arm for three days, because of the bandages. Yuk. But the whole thing, including chemo and rads,  was better than I had expected.  And radiation was a joy, compared to the rest of it. Marilyn Again I realize all casts are different I’m just praying all goes well

with mine. dj – Hide quoted text — Show quoted text –

Response:

"Erik If you’re having a SNB, there will likely be two pathology reports. One done immediately after node removal, and another more detailed report issued a few days later. No need to feel silly.  In the future, a great idea is to have at least one, if not two people with you, when discussing these types of procedures with your doctor/surgeon.  Between all those present, a much better recollection of the facts will be possible afterwards. And most certainly you should call her to clarify any questions you may have BEFORE the procedure(s).

That I will do. dj

Response:

"Richard Will I have these tube (drains) even though I going to have a Lumpectomy? – Hide quoted text — Show quoted text – My partner, Janet, had a lumpectomy and lymph nodes removed on 20 Novemebr, and had major worries before the op., about the op, the scars, the bandages and the drains. Now, looking back, whilst none of it is pleasant, it was nowhere near the ordeal that she expected. The drain is a thin tube which is stuck in your skin, (just under the armpit in Janets case), and it empties into a plastic bag which you carry around – not a big deal. I think it hurt a bit/lot when they took it out – my impression was like a plaster being ripped off quick. On the evening of the op., she was able to walk short distances, and I wheeled her outside for some fresh air. She came home on the 4th day, when the drain was removed, and is now moving much more freely, and can drive again. There is still some pain, and the occassional excrudiating shooting pain, but it seems to be getting better all the time. None of this has been good – it is the most devastating experience of her life, (and mine), but I can categorically state that the perception of what might be, was actually much worse than what is, so far. Fortunately, her margins were clear, and the lymph nodes were not found to be affected. She is due to have chemotherapy and radiation, probably starting in the early new year. — Richard Faulkner

Sound not to bad I’m praying that my op. goes just as well. dj

Response:

– Hide quoted text — Show quoted text – After surgery you will have a bandage over the surgery site. You may have one or more tube (drains) from the breast or underarm area to remove fluid that collects during the healing process. Most drains stay in place for a week or two. Once the flow has gone down to about one ounce a day, the drain will be removed. Will I have these tube (drains) even though I going to have a Lumpectomy? My partner, Janet, had a lumpectomy and lymph nodes removed on 20 Novemebr, and had major worries before the op., about the op, the scars, the bandages and the drains. Now, looking back, whilst none of it is pleasant, it was nowhere near the ordeal that she expected. The drain is a thin tube which is stuck in your skin, (just under the armpit in Janets case), and it empties into a plastic bag which you carry around – not a big deal. I think it hurt a bit/lot when they took it out – my impression was like a plaster being ripped off quick. On the evening of the op., she was able to walk short distances, and I wheeled her outside for some fresh air. She came home on the 4th day, when the drain was removed, and is now moving much more freely, and can drive again. There is still some pain, and the occassional excrudiating shooting pain, but it seems to be getting better all the time. None of this has been good – it is the most devastating experience of her life, (and mine), but I can categorically state that the perception of what might be, was actually much worse than what is, so far. Fortunately, her margins were clear, and the lymph nodes were not found to be affected. She is due to have chemotherapy and radiation, probably starting in the early new year. — Richard Faulkner

That was pretty much my situation.  I didn’t need any painkillers after the initial drug they gave me when I first woke up in the surgery. Opium? That’s what I remember, but it might have been something less fun. I was up and around slowly the next day, able to put on sweat pants and go down to the lobby for a newspaper. And the day after that I was able to wash my hair in the bathroom sink.  They made me stay in until the drain was clear, which was the morning of the fourth day.  The worst part was not being able to lift my arm for three days, because of the bandages. Yuk.   But the whole thing, including chemo and rads,  was better than I had expected.  And radiation was a joy, compared to the rest of it. Marilyn  

Response:

After surgery you will have a bandage over the surgery site. You may have one or more tube (drains) from the breast or underarm area to remove fluid that collects during the healing process. Most drains stay in place for a week or two. Once the flow has gone down to about one ounce a day, the drain will be removed. Will I have these tube (drains) even though I going to have a Lumpectomy?

My partner, Janet, had a lumpectomy and lymph nodes removed on 20 Novemebr, and had major worries before the op., about the op, the scars, the bandages and the drains. Now, looking back, whilst none of it is pleasant, it was nowhere near the ordeal that she expected. The drain is a thin tube which is stuck in your skin, (just under the armpit in Janets case), and it empties into a plastic bag which you carry around – not a big deal. I think it hurt a bit/lot when they took it out – my impression was like a plaster being ripped off quick. On the evening of the op., she was able to walk short distances, and I wheeled her outside for some fresh air. She came home on the 4th day, when the drain was removed, and is now moving much more freely, and can drive again. There is still some pain, and the occassional excrudiating shooting pain, but it seems to be getting better all the time. None of this has been good – it is the most devastating experience of her life, (and mine), but I can categorically state that the perception of what might be, was actually much worse than what is, so far. Fortunately, her margins were clear, and the lymph nodes were not found to be affected. She is due to have chemotherapy and radiation, probably starting in the early new year. — Richard Faulkner

Response:

"Erik That sounds like you’re having a Sentinel Node biopsy.  If your pathology comes back clear while in the operating room, and all they have to remove are this number, then this is not an axillary dissection.  Drains will be unnecessary.

I am a little confused about this, she stated I’d have to wait awhile for some tests coming back but then I remember something about the pathology department what!!!!! dj

Response:

– Hide quoted text — Show quoted text – "Sandy Wounds heal from side to side.  If the sides are not touching, they don’t heal well if at all.  The tubes are to remove serum that might accumulate in the area of the incision so that the sides will not be held apart.  Whether tubes are needed depends a bit on how large a gap there is at the site of surgery.  The tubes are a bit of a nuisance, but they are your friends and it works best to keep them in place until they stop draining, if you have them. Call me silly, but if the surgeon closes up the incision from side to side the :-) dj

You’d think so, but the sutures are intermittent, with spaces between. The tissue is mostly fat, so she/he must take a fairly broad loop in order to get a hold that won’t pull out. For a mastectomy, there is such a large flap of skin that it really isn’t practical to try to sew the flap to the chest.  The drains do it all.

Response:

"bell-lady" I had lumpectomy, as I wrote before, and had a drain in only during my 23 hour stay in the hospital. It was removed before I left, I don’t even remember it! Electron boost: During radiation, the first 5 weeks of the usual 6 week regimin is a broader, less intensive radiation. For the last usually 5 treatments, they do what is called an electron boost treatment, in addition. Zap the exact site of the lump with different ( or at least stronger) rays, to a specific depth. I found it felt no different, just took slightly longer than the usual 5 minute treatment. I did get a bit of a sunburn/suntan, nothing bad, from it, whereas the 5 minute treatments had no ill effect that I could see or feel.

Thanks good to know, I guess :-) 23 hour stay in the hospital!!!!  I must call my Doc. she never stated how long a day it would be??? – Hide quoted text — Show quoted text – Ann in PA

Response:

"A. P. Thorsen" – Hide quoted text — Show quoted text – I second that.  I was really anxious about going home with the drains in place (I had 3 due to bilateral mastectomy with axillary dissection on 1 side) . . . I live alone, and was worried about how I would handle it. It turned out not to be a huge issue. I usually wore a loose t-shirt as my inner layer of clothing, and pinned the drains to the inside of that, then wore some kind of loose overshirt on top when I went out.  I had to empty the drains several times a day, logging the amount of fluid drained.  It sounds pretty yucky, but it’s surely no more so in practice than the menstrual periods we’ve all gotten used to coping with! One of my life-lessons from all of this was that anticipating things with terror and dread was kinda dysfunctional.  Often, things I had worried about turned out to be no biggie, and I had just wasted all that good "worry time"! Wishing you the best as you continue with your treatment, Ann T.

I am with you Ann.  Kinda dysfunctional is the way I USE to live my life. Thanks be, I changed many years ago.  It’s a good thing to, for now I do have to deal with terror and nice day in the park, but I’m dealing with it and for me that’s good. dj

Response:

 The tubes are a bit of a nuisance, but they are your friends and it works best to keep them in place until they stop draining, if you have them.

I second that.  I was really anxious about going home with the drains in place (I had 3 due to bilateral mastectomy with axillary dissection on 1 side) . . . I live alone, and was worried about how I would handle it. It turned out not to be a huge issue.   I usually wore a loose t-shirt as my inner layer of clothing, and pinned the drains to the inside of that, then wore some kind of loose overshirt on top when I went out.  I had to empty the drains several times a day, logging the amount of fluid drained.  It sounds pretty yucky, but it’s surely no more so in practice than the menstrual periods we’ve all gotten used to coping with! One of my life-lessons from all of this was that anticipating things with terror and dread was kinda dysfunctional.  Often, things I had worried about turned out to be no biggie, and I had just wasted all that good "worry time"! Wishing you the best as you continue with your treatment, Ann T.

Response:

"Sandy Wounds heal from side to side.  If the sides are not touching, they don’t heal well if at all.  The tubes are to remove serum that might accumulate in the area of the incision so that the sides will not be held apart.  Whether tubes are needed depends a bit on how large a gap there is at the site of surgery.  The tubes are a bit of a nuisance, but they are your friends and it works best to keep them in place until they stop draining, if you have them.

Call me silly, but if the surgeon closes up the incision from side to side the :-) dj

Response:

Re: Drains I had lumpectomy, as I wrote before, and had a drain in only during my 23 hour stay in the hospital. It was removed before I left, I don’t even remember it! Electron boost: During radiation, the first 5 weeks of the usual 6 week regimin is a broader, less intensive radiation. For the last usually 5 treatments, they do what is called an electron boost treatment, in addition. Zap the exact site of the lump with different ( or at least stronger) rays, to a specific depth. I found it felt no different, just took slightly longer than the usual 5 minute treatment. I did get a bit of a sunburn/suntan, nothing bad, from it, whereas the 5 minute treatments had no ill effect that I could see or feel. Question for the group: I am still experiencing what the surgeon called ‘peau d’orange (skin of an orange) effect on the affected breast. Is that from radiation? Skin is sort of thickened and tough, pitted in appearance (kind of like cellulite in the cheesy newspaper ads :-) ). Anyone else? Does it ever go away? It’s only the underside of the breast, but it does get a bit heavy and tight-feeling sometimes… Ann in PA

Response:

"Erik It depends on whether you’re having an axillary dissection.  Removal of lymph nodes would mean drains.

Yes she said she would be removing 2 or 3 (maybe more, I pray not) Yes this is very scary, but I guess I don’t have to tell anyone here about that :-( No, you don’t.  But take it to heart that all will be well, and you will get through this. Yes I know the stonger power of pray.

Thanks for your time. dj

Response:

– Hide quoted text — Show quoted text – "Erik It depends on whether you’re having an axillary dissection.  Removal of lymph nodes would mean drains. Yes she said she would be removing 2 or 3 (maybe more, I pray not) Yes this is very scary, but I guess I don’t have to tell anyone here about that :-( No, you don’t.  But take it to heart that all will be well, and you will get through this. Yes I know the stonger power of pray. Thanks for your time. dj

Wounds heal from side to side.  If the sides are not touching, they don’t heal well if at all.  The tubes are to remove serum that might accumulate in the area of the incision so that the sides will not be held apart.  Whether tubes are needed depends a bit on how large a gap there is at the site of surgery.  The tubes are a bit of a nuisance, but they are your friends and it works best to keep them in place until they stop draining, if you have them.

Response:

you by name soon :-) Anyways, thanks for the websites they are very helpful and I will be asking question of my breast surgeon. Something I found on one of the websites is this: After surgery you will have a bandage over the surgery site. You may have one or more tube (drains) from the breast or underarm area to remove fluid that collects

during the healing process. Most drains stay in place for a week or two. Once the flow has gone down to about one ounce a day, the drain will be removed. Will I have these tube (drains) even though I going to have a Lumpectomy? DJ….Yes this is very scary, but I guess I don’t have to tell anyone here about that :-(

Hi DJ, it was Sandy who mentioned sentinel node.(not me)

<http://www.cancer.org/docroot/NWS/content/NWS_1_1x_Sentinel_Node_Tech… For_Breast_Cancer_Easier_On_Patient.asp <http://www.cancer.org/docroot/cri/content/cri_2_2_4x_how_is_breast_ca… reated_5.asp – Hide quoted text — Show quoted text – Sentinel lymph node biopsy: for this test, a radioactive substance or a dye is injected near the tumor. The substance is carried by the lymph system to the first (sentinel) node to receive lymph from the tumor. This lymph node is the one most likely to contain cancer cells if the cancer has spread. If the sentinel node contains cancer, more lymph nodes are removed. If it is free of cancer, further lymph node surgery might not be needed.<snip It’ll probably make more sense if you read both articles. This and other importatnt info is probably in Dr. Susan Love’s breast cancer book. I’m not spamming, really.  This is the most oft referred to book here. I’m sure it’s scarey but the folks here will help you through this.  In addition, reading the other posts will help you too. Hope this helps. J

Response:

Hi Thanks much. Please tell me what you mean by electon BOOST? Thanks again, dj

– Hide quoted text — Show quoted text – Scared? you bet!  But things really move so rapidly that there is not time for a lot of fear, as you are a little to busy to have much time for anything but action. My lumpectomy was September 30, stayed home from work for a week, then went back to a full schedule.  My drain was removed before then, but while it was in place I found that it fit nicely in a ‘fanny pack’. Started my electron BOOST yesterday and will take the final one on Friday (for this we are having to drive to a site 2 hours away, but am still going to put in half days at work before leaving for the treatment.)  YEAH!  I will be all done before Christmas and ready to celebrate the completion of treatment as well as the holidays with my family. Good luck in all that you and your medical team decides to do for your treatment.  Seems like it takes forever but it really does have an ‘end’, and life goes back to being pretty much like it was before the discovery. Me2

Response:

Scared? you bet!  But things really move so rapidly that there is not time for a lot of fear, as you are a little to busy to have much time for anything but action. My lumpectomy was September 30, stayed home from work for a week, then went back to a full schedule.  My drain was removed before then, but while it was in place I found that it fit nicely in a ‘fanny pack’. Started my electron BOOST yesterday and will take the final one on Friday (for this we are having to drive to a site 2 hours away, but am still going to put in half days at work before leaving for the treatment.)  YEAH!  I will be all done before Christmas and ready to celebrate the completion of treatment as well as the holidays with my family. Good luck in all that you and your medical team decides to do for your treatment.  Seems like it takes forever but it really does have an ‘end’, and life goes back to being pretty much like it was before the discovery. Me2

Response:

Hi DJ, it was Sandy who mentioned sentinel node.(not me) <http://www.cancer.org/docroot/NWS/content/NWS_1_1x_Sentinel_Node_Tech… <http://www.cancer.org/docroot/cri/content/cri_2_2_4x_how_is_breast_ca… Sentinel lymph node biopsy: for this test, a radioactive substance or a dye is injected near the tumor. The substance is carried by the lymph system to the first (sentinel) node to receive lymph from the tumor. This lymph node is the one most likely to contain cancer cells if the cancer has spread. If the sentinel node contains cancer, more lymph nodes are removed. If it is free of cancer, further lymph node surgery might not be needed.<snip It’ll probably make more sense if you read both articles. This and other importatnt info is probably in Dr. Susan Love’s breast cancer book. I’m not spamming, really.  This is the most oft referred to book here. I’m sure it’s scarey but the folks here will help you through this.  In addition, reading the other posts will help you too. Hope this helps. J – Hide quoted text — Show quoted text – J Thanks for the reply. Can you tell me where I can get information on this sentinel node procedure…..other then calling my Doctor. Thanks much I so very sacred dj J I’m so new to all this……I don’t see you’re reply? Diane….dj Hi Diane, Your best newsgroup is probably alt.support.cancer.breast they know everything over there. Click on the following and see if it takes you there. If it does, you’ll find your post and my reply there, reply on the other newsgroup, then others can reply to you, okay? J PS http://imaginis.com/breasthealth/breast_cancer.asp Also Dr. Susan Love’s book(s) on breast cancer Welcome aboard.  There are no replies yet.  Staging is done at and after surgery, when the pathologist measures the size of the tumor and determines whether any lymph nodes have cancer.  You may want to look into the sentinel node procedure; it is less invasive than the older methods.  Other factors go into staging, but those are the first things that will be determined. Another useful site is http://bca.ns.ca/cgi-bin/forum/index.cgi.  They have links to places where staging is defined more thoroughly.

Response:

J Thanks for the reply. Can you tell me where I can get information on this sentinel node procedure…..other then calling my Doctor. Thanks much I so very sacred dj

– Hide quoted text — Show quoted text – J I’m so new to all this……I don’t see you’re reply? Diane….dj Hi Diane, Your best newsgroup is probably alt.support.cancer.breast they know everything over there. Click on the following and see if it takes you there. If it does, you’ll find your post and my reply there, reply on the other newsgroup, then others can reply to you, okay? J PS http://imaginis.com/breasthealth/breast_cancer.asp Also Dr. Susan Love’s book(s) on breast cancer Welcome aboard.  There are no replies yet.  Staging is done at and after surgery, when the pathologist measures the size of the tumor and determines whether any lymph nodes have cancer.  You may want to look into the sentinel node procedure; it is less invasive than the older methods.  Other factors go into staging, but those are the first things that will be determined. Another useful site is http://bca.ns.ca/cgi-bin/forum/index.cgi.  They have links to places where staging is defined more thoroughly.

Response:

J I’m so new to all this……I don’t see you’re reply? Diane….dj Hi Diane, Your best newsgroup is probably alt.support.cancer.breast they know everything over there. Click on the following and see if it takes you there. If it does, you’ll find your post and my reply there, reply on the other newsgroup, then others can reply to you, okay? J PS http://imaginis.com/breasthealth/breast_cancer.asp Also Dr. Susan Love’s book(s) on breast cancer

Response:

– Hide quoted text — Show quoted text – J I’m so new to all this……I don’t see you’re reply? Diane….dj Hi Diane, Your best newsgroup is probably alt.support.cancer.breast they know everything over there. Click on the following and see if it takes you there. If it does, you’ll find your post and my reply there, reply on the other newsgroup, then others can reply to you, okay? J PS http://imaginis.com/breasthealth/breast_cancer.asp Also Dr. Susan Love’s book(s) on breast cancer

Welcome aboard.  There are no replies yet.  Staging is done at and after surgery, when the pathologist measures the size of the tumor and determines whether any lymph nodes have cancer.  You may want to look into the sentinel node procedure; it is less invasive than the older methods.  Other factors go into staging, but those are the first things that will be determined. Another useful site is http://bca.ns.ca/cgi-bin/forum/index.cgi.  They have links to places where staging is defined more thoroughly.

Response:

- Hide quoted text — Show quoted text –   Hi Even through my Mom had breast cancer at the age of 60 in 1981.  She did pass away in 1991 but from complications of her diabetes she never had any signs of caner in her whole body for the full 10 years, which would make her a 10-year survivor of breast cancer. From the time my Mom had her mastectomy 1981 (I was 34 y/o)  I’ve had a mammogram every year and all was fine, I’m now age 55. Not this year….. The mammogram this year was showing something on my left breast, as they put it "very vague" so we went onto a ultrasound imaging. Also on the ultrasound was the word again "very vague" so an ultrasound biopsy was done on Dec. 4, 2202.  Also I was told  there is no discrete nodule or mass demonstrated on the mammogram, and no lump on the outside of my breast however, there is added density from last years mammogram. The news come back on Wednesday Dec. 11, 2002  as cancer. I went to see the breast surgeon Dr. Jan Houston on Thrus. Dec. 12, 2002 to talk.  She stated it’s in my left breast,  Stage I, Ducal, 8 something long, in England for me she said about less than a half an inch. It’s 2 cm from the nipple on the bottom part of my breast. I have decided to go with the lumpectomy.  She will remove some lymph nodes. She also stated I will be taking radiation for 6 weeks, 5 days a week.  As far as chemo she stated will we see what treatments to do after the surgery which is Friday Dec. 20th. On Monday, Dec. 16th, I’m going in for per testing and on Thursday Dec.19th I’m going to Nuke…something or other… Medicine to have wires put in my left  breast? I’m scared this is all so new to me.   I, because of the ultrasound "guy" pushing hard on my breast think that the cancer is "deep" inside my breast , the biopsy "lady" also pushed hard on my breast to get a "good sample" as she stated,  however that added to the ultrasound "guy" just makes me believe is "deep" inside my breast. Which I’m thinking  it’s spread to my breast "bones". Sorry if I’m not spelling everything correct or not calling the doctors by the correct names I’m just not sure of the correct words. How does the breast surgeon (whom I do like very much) know what Stage your cancer is.  By the mammogram, ultrasound, or biopsy or is it not fare to say what Stage your cancer is until after the lumpectomy and the lymph node are checked? I do understand how she knows the size, but she can’t know how deep it is inside your breast.  Also understand how she knows where it is, in my case Ducal, but that’s all she could know until after the surgery…right. Thanks to all who took the time to read this and for any help.

Hi Diane, Your best newsgroup is probably alt.support.cancer.breast they know everything over there. Click on the following and see if it takes you there. If it does, you’ll find your post and my reply there, reply on the other newsgroup, then others can reply to you, okay? J PS http://imaginis.com/breasthealth/breast_cancer.asp Also Dr. Susan Love’s book(s) on breast cancer

Response:

Energy Etc…

Question:

    Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it. I keep thinking that with all that I know I ought to be able to do something, but I’m striking out….

You won’t like my answer. But, it will help :) ) – Hide quoted text — Show quoted text –     I mean, is it a decadron deficiency  :-o  or what??? Is that all that’s gonna get her moving or has someone found anything else not quite so drastic?     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

Response:

maybe the ulcer Cat. Hope they can get a bit more quality time for you and your dear lady. Take advantage of each good day. and God Bless, patty-anne Cat, The normal situation with advanced cancer is that the patient has no energy or appetite. Decadron will sometimes boost the appetite and make you

feel

Response:

Brian….you’ve already been told – several times – in a nice way….. message k.net…     Anyone got any idea of what causes a cancer

patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it,

what do you =do= about it. I keep thinking that with all that I know I

ought to be able to do something, but I’m striking out….

You won’t like my answer. But, it will help :) )     I mean, is it a decadron deficiency  :-o  or

what??? Is that all that’s – Hide quoted text — Show quoted text – gonna get her moving or has someone found anything else not quite so drastic?     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

Response:

Cat, I just realized I’m guilty of being one of those people who don’t know what to say, so they don’t say anything at all. (Pretty pathetic for a cancer patient, huh?) Although I’m fairly new to the group, I’ve come to really appreciate your presence here. I just wanted to let you know that you, your wife, and your children have been in my thoughts at least five times a day since you posted your wife’s recent bad turn. That may not be much comfort, but I hope it helps at least a little bit. Best wishes, Byron

Response:

Brian….you’ve already been told – several times – in a nice way…..

and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more.

Response:

- Hide quoted text — Show quoted text – Brian….you’ve already been told – several times – in a nice way….. and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more.

Brian, Obviously I had too much time on my hands today, but I did have a little fun. You keep going on about the wonders of Immunocal and how it can work to both prevent and cure cancer.  Of course, we all know this is not true, but you go on and on about clinical trials, web pages and all the rest – waving these over your head like Constantine with his banner of "In hoc signo vinces." So, for fun, I decided to perform a test, an experiment,  to see how much information is out there on the web relating to Immunocal, clinical trials and cancer.  I suggest other interested people try out the same thing to keep me honest.   Google is a wonderful search engine, but, like most, getting it to find what you are looking for can take a bit of doing.  Here’s the search string I used for Google as well as the justification for each term: Immunocal (no brainer, right?) "Clinical Trial" – we are looking for trials where Immunocal was tested "breast cancer"  - I changed breast to other cancer types during the                        search and will show the results for each type. "complete response" – this is what we are looking for, isn’t it?  All of the clinical tests I have read talk about complete response, so it’s a good thing to search for. conclusions      - Clinical trials have conclusions and they make for interesting reading if available.   I put the search objects in quotes above in quotes to Google to help limit the search results.  In order to provide a control to this experiment, I also replaced Immunocal with TAXOL and CISPLATIN – 2 chemotherapy drugs with which I am intimately familiar.  All other search strings remained the same.  In other words one string might have been: IMMUNOCAL "BREAST CANCER" "CLINICAL TRIAL" "COMPLETE RESPONSE" CONCLUSIONS and the control string would be TAXOL "BREAST CANCER" "CLINICAL TRIAL" "COMPLETE RESPONSE" CONCLUSIONS The results are listed below in tabular format:  the number represents the number of Google hits. Cancer type      IMMUNOCAL Hits     TAXOL Hits    CISPLATIN HITS Lung                    0               113             318 Breast                  0               148             377 Cervical                0                23              71 Prostate                0                58             116 Esophageal              0                23              88 Leukemia                0               109             323 Colon                   0                51             141 I quit after these 7 cancers since the results for Immunocal started to get a bit boring.  From my limited Google search, it appears that Immuncal has not been involved with ANY clinical tests (at least none published on the Web) for any of these cancers.   Just for fun, I replaced "complete response" with the commonly used CR and ran a few more searches.  I did find a clinical trial at when using breast cancer for the disease type.  The web page is located at: http://www.tivoni.com/arfiles/hms1995_1.doc This was a phase I/II study of Immunocal and the conclusion is as follows: This preliminary study indicates that this newly discovered property of whey proteins may be a promising adjunct in the nutritional management of cancer patients about to undergo chemotherapy.   Selective depletion of tumor GSH may in fact render the malignant cells more vulnerable to the action of chemotherapeutic agents.

I see several "may" in there, but no firm conclusions.  Not surprising since this is a phase I/II trial.  Interestingly, using Taxol instead of Immunocal in the same search string popped up 208 hits.   In fact, if you put Immunocal cancer "clinical trial" conclusions into Google, only a total of 19(!) hits show up!  Several of these are for health food and supplement pages, one for the patent, some where Immumocal is mentioned as being possibly a helpful NUTRITIONAL supplement and a couple from journals of alternative medicine.   Once again, I substituted Cisplatin and Taxol for Immunocal with 1370 and 587 hits respectively.   My conclusion is that Immunocal has never been submitted to serious medical testing and the disclaimer on their web page that states this is not to be used to prevent, diagnose or treat any medical conditions is true.  It’s a food supplement and nothing more. Should you wish to post any URLs to clinical trials where Immunocal is tested as a cure for cancer – any cancer – I’d sure like to see them.   Eric Unofficial C8 Homepage http://www.ngc1514.com

Response:

Here’s hoping it is something that can be fixed easily. If she has been on steroids for some time she may well have some gastric ulceration. With luck some losec and a transfusion may be all she needs

    She’s not been sick enough to get steroids yet. We saw the dr and he is having her admitted to the hospital for two bags of red cells, says it should get her numbers up. He’s unsure of the cause but he doesn’t think she has an ulcer. She’s taking Prevacid just incase. He said that all of her problems could be cancer-caused, especially without the blood causing her stools to be dark. She has normal stools and doesn’t cough up blood or anything.     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

Response:

The results are listed below in tabular format:  the number represents the number of Google hits. Cancer type      IMMUNOCAL Hits     TAXOL Hits    CISPLATIN HITS Lung      0 113 318 Breast 0 148 377 Cervical 0 23 71 Prostate 0 58 116 Esophageal 0 23 88 Leukemia 0 109 323 Colon 0 51 141 I quit after these 7 cancers since the results for Immunocal started to get a bit boring.  From my limited Google search, it appears that Immuncal has not been involved with ANY clinical tests (at least none published on the Web) for any of these cancers.     YOU DIDN’T HONESTLY EXPECT TO FIND ANYTHING, DID YOU ERIC? I MEAN, WE ALL KNOW BRIAN IS FULL OF S**T…. My conclusion is that Immunocal has never been submitted to serious medical testing and the disclaimer on their web page that states this is not to be used to prevent, diagnose or treat any medical conditions is true.  It’s a food supplement and nothing more. Should you wish to post any URLs to clinical trials where Immunocal is tested as a cure for cancer – any cancer – I’d sure like to see them.     DON’T HOLD YOUR BREATH ERIC, YOU MAY NEED IT.     CAT

Response:

Hi Cat,    YOU DIDN’T HONESTLY EXPECT TO FIND ANYTHING, DID YOU ERIC? I MEAN, WE ALL KNOW BRIAN IS FULL OF S**T….

Of course I didn’t expect to find anything.  We all know that if Immunocal did was Brian claims it to do, all our oncologists would have had us taking the stuff.  However, I was a bit surprised to find out that there are NO clinical trials (with the exception of the 1995 Phase I/II) on this stuff – absolutely zip!  Immunotec is honest in calling their product nothing but a food supplement.  I now have a nice, researched (well, as seriously as you can do in 20 minutes with Google) article that I can post behind any of Brian’s postings when he starts waxing slightly dishonest about Immunocal.  It’s good to keep the snake oil salesmen honest.    DON’T HOLD YOUR BREATH ERIC, YOU MAY NEED IT.    CAT

I’m not, but after all the ravings of Brian, I am sure he can post a pile of clinical trial URLs for all sorts of cancer.  I was just a bit surprised when they didn’t all pop out during Google searches – really.  No, I mean I was really surprised.  Heck, it has medical use patents!!!   Eric Unofficial C8 Homepage http://www.ngc1514.com

Response:

 Heck, it has medical use patents!!!     Medical use patents, bulls**t! The worst part of it all is that Brian is a true believer! He really thinks this damned crap is the Philosophers Stone or something….     CAT

Response:

– Hide quoted text — Show quoted text – Brian….you’ve already been told – several times – in a nice way….. and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more.

Brian, why does the Immunocal website state "Dietary supplements are nutritional products and are not designed for use in the treatment of disease or to substitute for a doctor’s care or for proven therapy. "? Any idea?

Response:

then go to a medical science newsgroup to peddle your product!! message

Brian….you’ve already been told – several times – in a nice way…..

and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more.

Response:

Hey Cat – I also appreciate your presence in this group.  You are incredibly brave and courageous, and you and your wife definitely have my support and prayers!  And Byron, what you said was very kind….I’m sure it does help!! Trish Cat, I just realized I’m guilty of being one of those people who don’t know what to say, so they don’t say anything at all. (Pretty pathetic for a cancer patient, huh?) Although I’m fairly new to the group, I’ve come to really appreciate your presence here. I just wanted to let you know that you, your wife, and your children have been in my thoughts at least five times a day since you posted your wife’s recent bad turn. That may not be much comfort, but I hope it helps at least a little bit. Best wishes, Byron

Response:

– Hide quoted text — Show quoted text – Brian….you’ve already been told – several times – in a nice way….. and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more.

Brian, Obviously I had too much time on my hands today, but I did have a little fun. You keep going on about the wonders of Immunocal and how it can work to both prevent and cure cancer.  Of course, we all know this is not true, but you go on and on about clinical trials, web pages and all the rest – waving these over your head like Constantine with his banner of "In hoc signo vinces." So, for fun, I decided to perform a test, an experiment,  to see how much information is out there on the web relating to Immunocal, clinical trials and cancer.  I suggest other interested people try out the same thing to keep me honest. Google is a wonderful search engine, but, like most, getting it to find what you are looking for can take a bit of doing.  Here’s the search string I used for Google as well as the justification for each term: You took the wrong route again. Google is not a medical data base. Immunocal / HMS 90 is a glutathione precursor. You cant seem to get this strainght. Go to PubMed where medical journals are archived. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=immunocal over 500 completed published medical studies check glutathione http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=glutathione over 52,000 check glutathione cancer http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=whey+protein+cancer http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=bovine+serum+albumin+cancer http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=glutathione+cancer over 6000 of those next…. Doctor Bounous about 75 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=Bounous G Immunocal double blind studies http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=(immunocal) AND ((double [WORD] AND blind* [WORD]) OR placebo [WORD]) 18 of those next…… Whey Protein Concentrate (WPC) and Glutathione Modulation in Cancer Treatment http://www.immunesystemsupport.com/wpcagmct/gmct.html next….. Oxidative Stress in Cancer, AIDS, http://www.immunesystemsupport.com/osicaand/chapt-42.html next…..  Treatment of Obstructive Airway Disease With a Cysteine Donor Protein Supplement*  A Case Report *  Bryce Lothian, MD; Vijaylaxmi Grey, PhD; R. John Kimoff, MD and Larry C. Lands, MD, PhD http://www.chestjournal.org/cgi/content/abstract/117/3/914 next….. Effect of supplementation with a cysteine donor on muscular performance (energy loss during chemo?) http://jap.physiology.org/cgi/content/full/87/4/1381 Immunocal (no brainer, right?) snip I put the search objects in quotes above in quotes to Google to help limit the go to PubMed PubMed, a service of the National Library of Medicine, provides access to over 12 million MEDLINE citations back to the mid-1960’s and additional life science journals. PubMed includes links to many sites providing full text articles and other related resources. My conclusion is that Immunocal has never been submitted to serious medical testing and the disclaimer on their web page that states this is not to be used to prevent, diagnose or treat any medical conditions is true.  It’s a food supplement and nothing more. – if you can ever grasp that is it a glutathione precursor you will be on the right road.-< Should you wish to post any URLs to clinical trials where Immunocal is tested as a cure for cancer – any cancer – I’d sure like to see them. I never said cure…..don’t misquote me. I won’t post the medical qualified cancer patents that they have again. You don’t get medical patents without clinical studies. Why don’t you phone the director of research and development? Ot talk to the doctors there? I’ll pay for your phone call.

Response:

– Hide quoted text — Show quoted text – The results are listed below in tabular format:  the number represents the number of Google hits. Cancer type      IMMUNOCAL Hits     TAXOL Hits    CISPLATIN HITS Lung      0 113 318 Breast 0 148 377 Cervical 0 23 71 Prostate 0 58 116 Esophageal 0 23 88 Leukemia 0 109 323 Colon 0 51 141 I quit after these 7 cancers since the results for Immunocal started to get a bit boring.  From my limited Google search, it appears that Immuncal has not been involved with ANY clinical tests (at least none published on the Web) for any of these cancers.     YOU DIDN’T HONESTLY EXPECT TO FIND ANYTHING, DID YOU ERIC? I MEAN, WE ALL KNOW BRIAN IS FULL OF S**T….

search the right place cat full of IT PubMed PubMed, a service of the National Library of Medicine, provides access to over 12 million MEDLINE citations back to the mid-1960’s and additional life science journals. PubMed includes links to many sites providing full text articles and other related resources. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=immunocal

Response:

Of course I didn’t expect to find anything.  We all know that if Immunocal did was Brian claims it to do, all our oncologists would have had us taking the stuff. Oncologists do prescribe it and it is covered by drug plans Medicare and Medicaid

Response:

– Hide quoted text — Show quoted text – Brian….you’ve already been told – several times – in a nice way….. and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more. Brian, why does the Immunocal website state "Dietary supplements are nutritional products and are not designed for use in the treatment of disease or to substitute for a doctor’s care or for proven therapy. "? Any idea?

Yes, as I have told you 6 thousand times. It is a glutathione precursor. by itself it does not do too much other than being a good protein source. Now if you ever figure out the cancer / glutathione relationship you get a gold star if you ever call the director of research and development and ask him I have offered to pay for the call many times phone celine dion ask her how rene is doing with his remission phone saku koivu and ask him how his cancer remission is doing http://espn.go.com/nhl/news/2002/0409/1365906.html

Response:

– Hide quoted text — Show quoted text – Brian….you’ve already been told – several times – in a nice way….. and I replied in a nice way this is a cancer support group new people may read each day high levels of cellular glutathione helps prevent cancer, reduces tumors, helps with chemotherapy and radiation treatments. this is documented science already proven. it is appropriate to inform people of this I am talking medical science from doctors nothing more. Brian, Obviously I had too much time on my hands today, but I did have a little fun. You keep going on about the wonders of Immunocal and how it can work to both prevent and cure cancer.  Of course, we all know this is not true, but you go on and on about clinical trials, web pages and all the rest – waving these over your head like Constantine with his banner of "In hoc signo vinces." So, for fun, I decided to perform a test, an experiment,  to see how much information is out there on the web relating to Immunocal, clinical trials and cancer.  I suggest other interested people try out the same thing to keep me honest. Google is a wonderful search engine, but, like most, getting it to find what you are looking for can take a bit of doing.  Here’s the search string I used for Google as well as the justification for each term: You took the wrong route again. Google is not a medical data base. Immunocal / HMS 90 is a glutathione precursor. You cant seem to get this strainght. Go to PubMed where medical journals are archived.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=immunocal over 500 completed published medical studies check glutathione

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=glutathione over 52,000 check glutathione cancer

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=whey+protein+cancer

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=bovine+serum+albumin+cancer

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=glutathione+cancer over 6000 of those next…. Doctor Bounous about 75

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… DocSum&term=Bounous G Immunocal double blind studies

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Search&db=PubMed&do… – Hide quoted text — Show quoted text – DocSum&term=(immunocal) AND ((double [WORD] AND blind* [WORD]) OR placebo [WORD]) 18 of those next…… Whey Protein Concentrate (WPC) and Glutathione Modulation in Cancer Treatment http://www.immunesystemsupport.com/wpcagmct/gmct.html next….. Oxidative Stress in Cancer, AIDS, http://www.immunesystemsupport.com/osicaand/chapt-42.html next…..  Treatment of Obstructive Airway Disease With a Cysteine Donor Protein Supplement*  A Case Report *  Bryce Lothian, MD; Vijaylaxmi Grey, PhD; R. John Kimoff, MD and Larry C. Lands, MD, PhD http://www.chestjournal.org/cgi/content/abstract/117/3/914 next….. Effect of supplementation with a cysteine donor on muscular performance (energy loss during chemo?) http://jap.physiology.org/cgi/content/full/87/4/1381 Immunocal (no brainer, right?) snip I put the search objects in quotes above in quotes to Google to help limit the go to PubMed PubMed, a service of the National Library of Medicine, provides access to over 12 million MEDLINE citations back to the mid-1960’s and additional life science journals. PubMed includes links to many sites providing full text articles and other related resources. My conclusion is that Immunocal has never been submitted to serious medical testing and the disclaimer on their web page that states this is not to be used to prevent, diagnose or treat any medical conditions is true.  It’s a food supplement and nothing more. – if you can ever grasp that is it a glutathione precursor you will be on the right road.-< Should you wish to post any URLs to clinical trials where Immunocal is tested as a cure for cancer – any cancer – I’d sure like to see them. I never said cure…..don’t misquote me. I won’t post the medical qualified cancer patents that they have again. You don’t get medical patents without clinical studies. Why don’t you phone the director of research and development? Ot talk to the doctors there? I’ll pay for your phone call.

Response:

Watching a loved one go through this must be a whole lot more traumatic than being the sufferer.

    It sure seems that way to me; I am virtually incapacitated when she is doing poorly. I am Superman when she is happy and smiles at me! All Best Wishes for you and your wife, Cat, Kim :-)

    Thanks so much, it means a lot to know others care, especially those who know what this is all about.     CAT

Response:

Dear Cat,     Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it.

I have the same thing with fibromyalgia. Yesterday I went to visit mty 16 month old grandaughter. I went by taxi and stayed only 2 hours. Today I went to the grocerystore 150 yards away and I have slept all afternoon, and still feel like a truck has hit me. Extra painkillers for me! I think I will be sleepy and wiped out tomorrow too. (my cancer gives me no symptoms and the chemo is 8 weeks ago, so the weakness has gone) — I tried sniffing Coke once, but the ice cubes got stuck in my nose. Rian

Response:

Here’s hoping it is something that can be fixed easily. If she has been on steroids for some time she may well have some gastric ulceration. With luck some losec and a transfusion may be all she needs MIKE – Hide quoted text — Show quoted text – Cat, The normal situation with advanced cancer is that the patient has no energy or appetite. Decadron will sometimes boost the appetite and make you feel better but there is a trade off (you don’t get anything for nothing). The main trade off that matters is that over time the large muscles of the arms and legs waste and ultimately cause the weaknesss you are trying to prevent. At the same time , in people taking it for longer periods, the etabolic effects cause fat and fluid retention which gives the typical ’steroid shape’ of a large round body and face with thin spindly legs i.e. the weakened legs have to carry a heavier body. This latter effect doesn’t often appear in late cancer patients because the decadron usually loses it’s effect after a while and is ceased. No your wife is not suffering the effect of a decadron deficiency. Typically when energy levels are low people will make a tremendous effort to do ’stuff’ on a good day but will pay for that (there’s that trade off again) by being wiped out for the next few days. This , to me, is at least better than not doing anything at all on any day and just existing so as not to get too tired but each person has to make up their own mind about how to spend the little energy they have.. On the days she is tired she is going to feel pain more and will need to have extra medication to cover it. Regards MIKE     Thanks Mike,     We found out today she is severely anemic, losing blood "somewhere" and so we have an appointment with a surgeon tomorrow to do a gastroscope or something like that to try to find an ulcer. She has terribly low numbers for hemoglobin and hematocrit. That explains a lot!     CAT     Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it. I keep thinking that with all that I know I ought to be able to do something, but I’m striking out….     I mean, is it a decadron deficiency  :-o  or what??? Is that all that’s gonna get her moving or has someone found anything else not quite so drastic?     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

Response:

– Hide quoted text — Show quoted text – Cat, The normal situation with advanced cancer is that the patient has no energy or appetite. Decadron will sometimes boost the appetite and make you feel better but there is a trade off (you don’t get anything for nothing). The main trade off that matters is that over time the large muscles of the arms and legs waste and ultimately cause the weaknesss you are trying to prevent. At the same time , in people taking it for longer periods, the etabolic effects cause fat and fluid retention which gives the typical ’steroid shape’ of a large round body and face with thin spindly legs i.e. the weakened legs have to carry a heavier body. This latter effect doesn’t often appear in late cancer patients because the decadron usually loses it’s effect after a while and is ceased. No your wife is not suffering the effect of a decadron deficiency. Typically when energy levels are low people will make a tremendous effort to do ’stuff’ on a good day but will pay for that (there’s that trade off again) by being wiped out for the next few days. This , to me, is at least better than not doing anything at all on any day and just existing so as not to get too tired but each person has to make up their own mind about how to spend the little energy they have.. On the days she is tired she is going to feel pain more and will need to have extra medication to cover it. Regards MIKE

    Thanks Mike,     We found out today she is severely anemic, losing blood "somewhere" and so we have an appointment with a surgeon tomorrow to do a gastroscope or something like that to try to find an ulcer. She has terribly low numbers for hemoglobin and hematocrit. That explains a lot!     CAT – Hide quoted text — Show quoted text –     Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it. I keep thinking that with all that I know I ought to be able to do something, but I’m striking out….     I mean, is it a decadron deficiency  :-o  or what??? Is that all that’s gonna get her moving or has someone found anything else not quite so drastic?     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

Response:

Dear Cat,     Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it.

No, I don’t have any answers about the cause of the yo-yo syndrome, I just observe that it exists.  The way I coped, was to plan lightly.  There were lots of things I wanted to do, like going out shopping or to the pictures or just in to town for tea with friends.  If it was a ‘good’ day I could do these things but if it was a ‘bad’ day I rang and postponed the date and settled back with an Audio book.  In effect, I gave myself ‘permission’ to feel crap.  After all, as my Oncologist says, "We are poisoning you, but for your own good!". I keep thinking that with all that I know I ought to be able to do something, but I’m striking out….

Watching a loved one go through this must be a whole lot more traumatic than being the sufferer.  Especially if the carer has a professional knowledge.  My father (who was a GP) always used to say that Medical Science was a misnomer and when it comes down to it, we are not much more advanced from the alchemists of the middle ages.  All cases are dependent on the attitude of the individual.  Best those that have to stand by and watch can do is to support a positive attitude, however that can be done.     I mean, is it a decadron deficiency  :-o  or what??? Is that all that’s gonna get her moving or has someone found anything else not quite so drastic?

I found it helped to get some gentle exercise on my ‘good’ days.  It didn’t have to be much, just a slow walk down to the river side (about half a mile round trip), with plenty of stop-and-stare moments, but lots of fresh air and evidence that there were growing things around, and proof that the World was not centering on this damned Beast! All Best Wishes for you and your wife, Cat, Kim :-)

Response:

Cat, The normal situation with advanced cancer is that the patient has no energy or appetite. Decadron will sometimes boost the appetite and make you feel better but there is a trade off (you don’t get anything for nothing). The main trade off that matters is that over time the large muscles of the arms and legs waste and ultimately cause the weaknesss you are trying to prevent. At the same time , in people taking it for longer periods, the etabolic effects cause fat and fluid retention which gives the typical ’steroid shape’ of a large round body and face with thin spindly legs i.e. the weakened legs have to carry a heavier body. This latter effect doesn’t often appear in late cancer patients because the decadron usually loses it’s effect after a while and is ceased. No your wife is not suffering the effect of a decadron deficiency. Typically when energy levels are low people will make a tremendous effort to do ’stuff’ on a good day but will pay for that (there’s that trade off again) by being wiped out for the next few days. This , to me, is at least better than not doing anything at all on any day and just existing so as not to get too tired but each person has to make up their own mind about how to spend the little energy they have.. On the days she is tired she is going to feel pain more and will need to have extra medication to cover it. Regards MIKE – Hide quoted text — Show quoted text –     Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it. I keep thinking that with all that I know I ought to be able to do something, but I’m striking out….     I mean, is it a decadron deficiency  :-o  or what??? Is that all that’s gonna get her moving or has someone found anything else not quite so drastic?     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

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    Anyone got any idea of what causes a cancer patient to feel fine and have lots of energy one day, then lay around moaning in pain the next??? Heck, I don’t care if you don’t know what causes it, what do you =do= about it. I keep thinking that with all that I know I ought to be able to do something, but I’m striking out….     I mean, is it a decadron deficiency  :-o  or what??? Is that all that’s gonna get her moving or has someone found anything else not quite so drastic?     CAT — "Love to eat them mousies, Mousies’ what I love to eat, Bite they little heads off, And nibble on they tiny feet!"  =(^-^)=

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