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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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Reply | Forward Message #4325 of 5061 |
Re: new to group

--- In crohns_n_colitis@yahoogroups.com, "roxyander24"
<roxyander24@...> wrote:
>
> Hey, My name is Rachel and I am 22. I just got Crohns Colitis last
> thursday.. very depressing for me. My family never had it. I feel
I
> am the only one in the world who have it.. but alot of people have
> them.. and I live in Indiana..
>
> I am waitin for doctor to tell me what foods, meds, not to take
> or you can eat or take..
>
> Talk to you again next time!
>
> Rach-
>
>
> --- In crohns_n_colitis@yahoogroups.com, "Samantha" <slide_em@>
> wrote:
> >
> > Hi!
> > My name is Samantha and I'm a 17 year old female living in
> Australia.
> > About 3 weeks ago I noticed a change in my bowel movements and
> > started to bleed and experience pain. I went to the doctors and
> they
> > did blood tests and stool samples, nothing showed up. I
> continued
> > to get worse and they treated me for numerous conditions.
> > I had a colonoscopy yesterday and the bad news is that it's
> > ulcerative colitis. I've never ever been sick before in my
> life.
> > I dont feel sick, havent lost weight (i'm only very little,
always
> > have been). I dont have all the details because I have to go
> back
> > to the specialist in a week to get biopsy results etc. I'm
on
> > prednisone and sulfur tablets (cant remember the name - they are
> > yellow).
> > I was supposed to leave for the US for a 3 month holiday on
> Saturday,
> > so obviously that's on hold for a month or so. Pretty devastated
> > about that.
> > But I was told that I'm lucky I was diagnosed now, because if
I'd
> > flown I would have required colon surgery.
> > They also dont seem to know what caused it. 2 years ago my
> father
> > passed away, so I've been under a lot of stress, and also my
> father
> > had U.C. about 20 years ago, but seemed to recover pretty much.
> >
> > I have so many questions, I guess that the specialist will
answer
> > them.
> > I just hope that they can manage it, as I said I havent felt
sick
> at
> > all, just a bit of pain and feeling worn down.
> >
> > Right now, I just have to take my medication and keep an eye on
my
> > weight and nutrient levels.
> >
> > Hoping to get lots of support from people who know what it's
like
> and
> > have been confused like me at some stage but who see the light
now.
> >
> >
> > Samantha


> >



Hello, my name is Rene and I was diagnossed with chrons disease oct
2005. It has been a little weird, but as far as what you can eat or
not there are no limits. Some things bother me more than others
however. When first diagnosed stay away from black pepper and spicy
foods and tomatoe products. I can eat tomatoes now but they do often
cause diarreah? It's just part of the disease. After being diagnosed
with chrons I was so afraid to eat that I am now a diabetic. I also
have spinal stenosis and ostoperosis. The list goes on. Bottom
lineis that Life goes on with time and prayer. Remember to keep your
faith and hang in there. With faith this to shall pass. Take care
amd god bless!
>






Wed Nov 15, 2006 3:31 am

arehart1975
Online Now Online Now
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Message #4325 of 5061 |
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hi all, my name is terry, i have recently been diagnosed with colitis. don't know the specifics of what kind. i also have autoimmune vasculitis, called...
tbaradine
Offline Send Email
Jul 29, 2002
2:00 am

HI Terry Welcome to the group..You will find folks on here that care and more than willing to answer any questions that you have to the best of their...
niteowl618@...
Send Email
Jul 29, 2002
2:31 am

Hi! My name is Samantha and I'm a 17 year old female living in Australia. About 3 weeks ago I noticed a change in my bowel movements and started to bleed and...
Samantha
sammy_gal101
Offline Send Email
May 28, 2003
6:03 am

Welcome to the group, Samantha! I was just like you a year and a half ago. I never used to be sick aside from the occasional cold and maybe flu. Then all of a...
Tricia
sapho_1999
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May 28, 2003
11:26 am

Hi Samantha, Welcome to the group. My name is Amy, I am 26, and I live in Melbourne. Feel free to email me with any questions you have. I was diagnosed almost...
Amy
amyjn2000
Offline Send Email
May 29, 2003
1:30 am

Hey, My name is Rachel and I am 22. I just got Crohns Colitis last thursday.. very depressing for me. My family never had it. I feel I am the only one in the...
roxyander24
Offline Send Email
Nov 15, 2006
1:44 am

... I ... always ... on ... I'd ... answer ... sick ... my ... like ... now. ... Hello, my name is Rene and I was diagnossed with chrons disease oct 2005. It...
Rene
arehart1975
Online Now Send Email
Nov 15, 2006
3:37 am

Welcome Samantha, First of all, feel free to ask whatever you want. I'm from Brazil and I was diagnosed with Crohn's Disease three years ago, when I was 21....
Roberto Soares
rfirmeza@...
Send Email
May 28, 2003
9:55 pm

Hi, I am 36 and was diagnosed with UC about 7 months ago. I was on Asacol for the past 7 months but it didn't stop me from having 3 flare ups in seven months...
sjohnso321
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May 27, 2006
5:47 am

I do go to the health food store a lot when I am not in a flare up. I am on Asulphazine which is like prednisone but long term with no side affects. I also...
Suzanne Dorman
flydownus
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May 27, 2006
12:59 pm

Thank you Suzanne....
Sjohnso321@...
sjohnso321
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May 29, 2006
2:00 am

Hello there all. My name is Steph and I have just been diagnosed with UC in the last few months. It has been tough for me because I already have another...
Steph
vedasuess
Offline Send Email
Nov 15, 2006
12:41 am

Hey I'm Rachel.. and nice to meet you online.. ha. and I just found out I have Crohns Colitis last thursday... and sad that i have that diease not a good...
roxyander24
Offline Send Email
Nov 15, 2006
1:40 am

Hi, I saw this and just thought I would chime in. I'm 27 and had UC for 6 years, it got to the point where I decided surgery was the best option and I am very...
John Alexander
visionwind348
Offline Send Email
Nov 15, 2006
4:54 pm

Hi Steph, I'm from Indiana, too. I was diagnosed with UC in March 2003. Right now, I'm on 3 Asacols 3 times a day, doc wants to start reducing, but I freaked...
MICHAEL LANET CAREY
lanettecarey68
Offline Send Email
Nov 16, 2006
2:23 am

Lanette, Well the doc took me off the canasa because I a barely having any rectal bleeding and that is what it was for. I think I am doing ok, but today as a...
Steph
vedasuess
Offline Send Email
Nov 18, 2006
3:37 am
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