New and 16 in 11 days, decided to tell my story to see if anyone had the same problem

Crohn's Disease Forum

Help Support Crohn's Disease Forum:

Joined
Feb 13, 2012
Messages
2
Location
manchester
new and 16 in 11 days, decided to tell my story to see if anyone had the same problem

i was diagnosed with crohns in september after 2 years of symtoms , was in hospital for 2 weeks after bad flare up, one flare up in august nearly ment i couldnt fly to america as it happened in the hotel near heathrow lol i had no idea what was wrong

i was so thankful after many doctors had said there was nothing wrong with me even though CRP was 54 i was screaming in pain and being sick, the childrens hospital believed me that i was ill and addmitted me, it took a while to find and had many many tests, i was loosing weight very fast i had an ng tube in

i was told i had it in the terminal illuem and was put on pred, they never saw in the terminal illeum as they couldnt get to it, i left hospital and had many check ups i was then put on azathioprine as a long term durg it was fine for a week but i got a bad infection and was took off, they put me back on aza a month later but it made me sick as anything flu symtoms within hours of taking it and vomiting they admitted for a week and abit thinking it was my crohns but was still on 20mg of pred, they said it was a bug i knew it was aza , they gave it me again i was sick in front of them but somehow it was a bug , but they took me off it as they thought it was making me get the bugs, so while i was in there they decided to tell me that my crohns should hardly cause me any pain it is so mild this was by a random consult i have never seen as mine was off i was always in so much pain how can this be while i was in hospital i missed my school trip to barcelona all paid for:(

ohh yeah and tryed to pin me with ANOREXIA OR ANY EATING DISORDER

saw a psychologist and they said no its not its disordered eating a completely different thing so releved and she helped me about my dad and nan, NG tube feeds all day and night, so i went home and came off my steriods and was left with no meds and then had ng tube out, this takes me up to the middle of nov i felt so ill over nov and december had an appointtment and told them had bloos RP wasnt high,

had my dads wedding on the 31st of december luckely made it though that but was feeling ill , the next day so new year i was took in to hospital as i had major flare up , CRP wasnt high why:( so i spent another week on my usual ward 7 NG tube back in lost weight alot! i had a video capsual test as they have never had a look inside proberly, i left after a week an a few days by me begging hehe still no meds just feeds, however i got a call back they were shocked when they found it in the jejuem , terminal illeum and distanal illeum there was alot of inflimation ulcers that were bleeding and puss coming from them , they said it was bad they were considering surgry but as an important year at school and how treament has come along they put me on encort which has done nothing,and aza however same again made me so sick but they made me take it 3 times and made me sick to prove i was allergic, now its in my notes intolerent to aza so glad!!!!!

so back to hospital so now its remicade infusions i had my first on the 7th of march and next 21st of march , hasnt really worked so far hoping it will on the next one:) NG tube in since new year hoping for that out on the 21st for my birthday on the 24th , come to think of it i have only had a months break from the NG since september part of me now i call it timmy tube :)

i only really used to eat a pack of crisps or two at a push or abit of mash!!! eating has got better now, i havent really come to terms with the fact i have crohns i dont get upset ever, i dont think of myself as ill , i more think about my dad and nan because while i was being diagnosed my dad got told he had CML and my nan had motor neurone disease. all in all i dont cry but people think i should after all thats happened to me but i dont feel the need there are worse things , but its just fustrating, hoping remicade works so thats my story , and has it worked for anyone else and has encort not worked for anyone while waiting for remicade? xxx

----------------
meds used:
pred- worked so good
aza- allergic

On:
encort- not working
remicade: not fully working yet praying it does
NG tube: all day and night

"dont take life so seriously you will never escape it alive anyway"
 
Last edited by a moderator:
Welcome livinglife16:)!

Thank you for sharing your story with us. I am sorry to read about all the trouble you have had since September! You seem like a veteran Crohn's Disease sufferer the way that you are cycling through many of the medications like many of us also have had to!

Hopefully Remicade will start to work better after the second infusion. In case you did not know we have a dedicated Remicade support and information forum that you might want to check out.

Good luck until the next infusion and happy early birthday!
 
Hello and welcome to the forum :bigwave: Sorry to see you have had such a tough time of it :( I will keep fingers crossed that the Remi kicks in soon for you, pls do have a look at the above mentioned forum as there will be a lot of advice and support here.

Wishing you well soon

xxx
 
Greetings and welcome to the forum :)

That they found active disease all the way into your jejunum makes me think that you're finally on the right track with those Remicade infusions. You may want to research enteral nutrition as you may be able to tolerate that and it can help calm your system down. With disease that widespread and them talking surgery has me a little concerned that they would remove a SIGNIFICANT amount of intestines. I think surgery like that should be a final option and not this early in the game.

Again, welcome to the forum. Please keep us updated as to your progress.
 
awww thankyou all glad i got in to this now, hopefully it will, and yeah they said that surgery would be last option but because the illem was so bad they were considering it , hopefully remicade will work i will keep everyone updated how it goes:)
 

Latest posts

Back
Top