So I finally got a doctors appointment for a week tomorrow 👌

It seems so far away and im so miserable. I dont know what the hell is wrong with me. Im going to have a blood test and be tested for coeliacs disease.

At this point im just ready to get a diagnosis on whatever this is and try and fix it.

Im actually miserable and in pain all the time. Im starving myself 3 days at a time or longer if I can stand it just so I dont have to go through the horrendous pain that happends after.

Has anyone been diagnosed with coeliac disease, chrones disease or any IBD.

I could really use some advice and just someone to vent to be honest. Im so sick of everyone thinking im exaggerating

Can't wait for remicade!

I’ve not made a post a about my ibd before, however right now I feel like I’ve been hit by a truck! I’m in my third flair up since June 2014 (when I was diagnosed). My belly and joints are suuuuuuper painful and keep me awake at night. My GI doctor wants me to start remicade this week, and I’m super nervous, but at the same time I’m looking forward to feeling better! Any advice for starting remicade?


I found out a few hours ago my grandfather, my only grandfather I ever knew has prostate cancer. They don’t know how bad it is yet but he is going to fly in to the states to get more treatment ( he lives in Ghana). First my great grandmother dies of either breast cancer or cervical cancer, few years later my mother is diagnosed with colon cancer and chrones lupus and now this. I just don’t know anymore.


Theyve been just playing it off as bad ibs for weeks but I think after I eneded up in a and e on Thursday night hopefully im finally gonna get tested for coeliac and chrones. At this point I dont care what it is i just wanna be diagnosed and get better. I think its chrons, ive been on gluten free since Thursday amd nothing has got any better.xxxx