New member to forum...old one to UC/Crohns'....

Crohn's Disease Forum

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Lisa

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new member to forum...old one to UC/Crohns'....

Just joined the forum yesterday.....

I was diagnosed wtih UC when I was @7 years old - after my Mom took me to multiple Dr's to try to figure out what was wrong with me.....been on many different treatments, azufadine, prednisone, 6MP, Asacol, etc etc etc.....each time the periods of remission would be shorter and shorter.....got to be that I would deal with pain pretty much every day, although I got pretty good at hiding it from family.....

My old GI Dr used to scold me when I would ~finally~ go see hime - because it was usually a direct trip to Hosp. admitting from his office.....well, I had a LIFE!.....I wasn't going to let something like this slow me down.....I have worked in all different kinds of jobs - from an auto parts driver (got to learn where all the CLEAN bathrooms were on my routes!).......worked on horse farms, was a Fire/Police/EMS dispatcher, and also a Volunteer firefighter.......and then some.....

Back around 2003 I started developing fistuals - omg were they PAINFUL!.....after multiple Dr visits, surgical consults etc I decided to live with them (for now).....had a flare in spring of 2004.......in the fall of 2004 I found out I was pregnant, and had a healthy baby girl March 2005.....another flare summer 2005, then started Remicade Nov 2005.....what a difference! I went from always trying to keep my weight up (to the point co-workers thought I was anorexic!) to trying to keep weight OFF due to being 'healthy'.....I am on a very low dose since then, every 7-8 weeks.....although lately I'm not sure if things are trying to flare a bit or now - have my next Remicade appt April 26th. I did just get over strep and a course of penicillian .......

I haven't really looked on line too much for support groups etc - I'm one of those people who suffers in silence mroe often than not....

Lisa
 
Hi Lisa
and welcome
Great that Remi is working for you

glad you found us tho, cos to suffer in silence isn't too good for your well being sometimes.
It's great here, if you just wanna vent or grumble, but lots of info and support too!
lotsa luv
Joan xxx
 
Welcome to the forum...glad the Remicade is working for you! Hope to see you around here :)
 
Hi Lisa - Welcome to the Forum!

Hope the Remicade continues to work for you. Is your DX still UC or did they change it to Crohn's once you developed the fistulas?

Hope you continue to feel well! - Amy
 
ameslouise said:
Hi Lisa - Welcome to the Forum!

Hope the Remicade continues to work for you. Is your DX still UC or did they change it to Crohn's once you developed the fistulas?

Hope you continue to feel well! - Amy

Well - the rx is Crohn's Colitis.....I have both large and small bowel involvement......joy oh joy.....

Thanks Amy - I am hoping this continues to work too! I can do without the skin isues I've developed - eczema/psoriasis ugh!
 
Yeah, it's amazing how many other "issues" are involved with Crohn's -skin, cankers, arthritis, etc etc. Fun, right? I have always had horrible skin on my hands - dry, cracked, rashy. Now I wonder if it is all auto-immune related.

My original Dx was UC. I had my colon removed and a j-pouch procedure. I was rediagnosed as Crohn's about 10 months ago. I think I was probably Crohn's Colitis all along but never really presented any other symptoms of Crohn's at the time.

But I am here now and just trying to get thru it like everyone else!

Good luck to you and please keep us posted on your progress! -Amy
 

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