Journal Entry for May 21, 2007
I stopped taking the Imuran and I feel soooo much better. The predinsone is keeping me from having flare ups now, but I know that I can't take it …
is feeling Excellent
I am a registered nurse. I have three teenage children and a wonderful husband who is very supportive. I was diagnosed with severe UC about 8 months ago. I am takings Asacol and have already been on Prednisone 3 times. My Dr. is trying to get my insurance to cover either Humira or Remicade...still waiting. I just started taking Imuran and it concerns me a little. I am looking for people to talk to that understand what I am going thru.
Reading, decorating, home improvement projects with my husband
I stopped taking the Imuran and I feel soooo much better. The predinsone is keeping me from having flare ups now, but I know that I can't take it …
I'm not so sure about this Imuran (Azasan) stuff. I wonder if it is what is causing this wierd feeling in my head....kind of dizzy and light headed. …
Still taking the prednisone and feeling the effects.....hot flashes and hungry all of the time. I ate an entire bag of snack mix on the way to work …
I had a flare up last Thursday and nearly passed out at work. My Dr. increased my Asacol and started me back on Prednisone :( He also started me on …
I hope you have a great week! love ya, Kim
Hang in there....I also have crohn's disease and I feel cruddy at times too!!
Thank you for the request. I hope all is well!
I know how you feel. I had to buy a few pairs of more comfortable pants and shirts to work in. I will be decreasing mine to 25mg on Saturday. I decrease by 5mg weekly until I get to 20 then I decrease by 2.5mg. At that rate, I'll be on it for ever it seems. Not really but I am so tired of it. I hate the shaky feeling. Which, reminds me, I haven't taken my meds yet. Gotta go and take them. Cya. mgdennis34 (have a great day)
Hi! Thanks for the friend request. I am hear if you need to talk, vent or just need a listener! Have a great week! Kim
Hospitalized with a GI bleed and diagnosed Oct. 2007 with severe UC after many years of being told I had Irritable Bowel. I am tired all of the time and my meds make me have headaches and nausea. (I think I have the "Poor pitiful me syndrome") Although I try not to feel sorry for myself because I know there are others that are worse off than I am. It's really hard to deal with a disease that people don't understand or really want to talk about, especially since it involves your bowels.