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crohns_n_colitis · This list is intended for those who suffer from the chronic illnesses, Crohn's Disease and Ulcerative Colitis. I hope to be abl
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Would appreciate advice on Remicaid   Message List  
Reply | Forward Message #4355 of 5061 |
Re: [crohns_n_colitis] Re: Would appreciate advice on Remicaid

HI Len B,
 
I have been on remicade 6 months now, and have y life back...had severe crohn's UC, bit tired after infusion, but side affects minimal.

soklueles2002 <soklueles2002@...> wrote:
--- In crohns_n_colitis@yahoogroups.com, "Len B" <thelenshow@...> wrote:
>
> My 13 year old son has not responded well to traditional treatments
> for his UC...azacol, pentassa, etc. His colon remains severely
> inflamed.
>
> His Gastroenterolgoist has proposed the use of Remicaid through bi-
> weekly IV drips for six weeks followed by monthly treatments. When
> I read Remicaid descriptions on the internet, it said that treatment
> with Remicaid may increase the risk of lymphoma and other cancers.
> This stopped be dead in my tracks as my father passed away from
> Lymphoma.
>
> The other option is a J-Pouch which I guess I view as a severe
> solution in its own right.
>
> My question is whether anyone has been treated with Remicaid and have
> they heard anything different than what I have heard? Is the
> lymphoma connection something that they have to put in disclaimers to
> cover themselves aginst lawsuits? What is the real risk?
>
> Alternatively, what are the risks with the J-Pouch procedure.
>
> Thank you in advance for any words of wisdaom you may offer.
>
>
> Len B
>
hi len, im sorry about your son and being diagnosed with crohns disease.
first of all, have you talked to your doctor about your family medical
history? I do know that people have tried to sue the makers of
remicade in the past because it is known to cause blood diseases. I,
and a few friends of mine have crohns disease and remicade is a
blessing for us.
When i had my second round of remicade, i could feel a huge difference
in my body. I didnt hurt, and i had a new lease on life
I would definately talk to my doctor about the risks about crohns
disease and remicade and the side effects and find out what the
percentage of people is who get the blood disorders etc from it
I have one friend with the j pouch. She has no colon. I do know that
she has had some problems with the pouch crimping up and she gets
consitpated.
good luck with whatever you choose.




Elisa
 (647-287-3748)


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Thu Feb 1, 2007 7:40 pm

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Message #4355 of 5061 |
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My 13 year old son has not responded well to traditional treatments for his UC...azacol, pentassa, etc. His colon remains severely inflamed. His...
Len B
thelenshow
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Jan 30, 2007
10:12 pm

Len B.....I am 19 years old. I was diagnosed with UC when I was 13 myself. I struggled and I leterally mean struggle with UC for all of these years. I never...
tamara crotts
bikinigirl2005
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Jan 31, 2007
2:43 am

... hi len, im sorry about your son and being diagnosed with crohns disease. first of all, have you talked to your doctor about your family medical history? I...
soklueles2002
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Jan 31, 2007
6:06 pm

HI Len B, I have been on remicade 6 months now, and have y life back...had severe crohn's UC, bit tired after infusion, but side affects minimal. ... hi len,...
Elisa
jewish_diplo...
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Feb 1, 2007
7:41 pm

Hello everyone - I'm new to the group. I'm 24 and was diagnosed with UC in the fall of 2004. I've been battling with it ever since. I've been on and off...
Kristen Altobello
kmaltobello
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Feb 1, 2007
9:21 pm
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