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most of them know about the disease just from hearing me talk about it, but they cant relate to it in terms of they think "tummy ache" when in reality its more like "please shoot me"

i was on prednisone and flagyl the first couple weeks after the hospital, but the latest theory is my meds arnt working as well because im fighting off anemia...

i see my doc every month and i used to be in the nursing field so im not 100% lost, only about 90% lol. i think one of my bigger problems with coping is then fact that almost everyone i associate with cant relate and i just come off as a big baby with a tummy ache to them...

im on apriso and entocort and a few others. right now its alot of back and stomach pain, pressure and nausea, LOTS of fatigue.....and a bit down feeling so trapped and helpless for such a long time this time around

not too sure about the meds yet, i almost always feel sick or hurting, lots of ups and downs, but things could be worse. Im still playing the what can i eat game and still adjusting to the lifestyle changes, theyre alot more stressful than i ever imagined and im sure that isnt making things any...

its really hard, i havent even figured it out yet, so i try the denial method, i watch alot of movies and tv to TRY take my mind off of it....

So i was just diagnosed with Crohns 6 months ago, and i am completely lost. Ive had LOTS of GI trouble on and off for a good chunk of my life, but i was always told it was probably just IBS or that i was lactose intolerant. Then a doctor told me, "hey, youre probably not getting enough fiber in...