Hey everyone!
I was recently (about a week or so ago) diagnosed with Crohn's, and met with my GI today to discuss treatment. As I have a fistula developing, she is going to start me on Remicade as soon as everything goes through (health care and insurance wise)... and in the meantime has started me on Prednisone
I am beginning the first week at 40mg a day, and tapering off by 5mg each week until finished...
Ive heard and read lots of "scary stories" about prednisone, the side effects and going through tapering it off... Just looking for people's experiences with this?? I am looking forward to feeling at least a bit better, but just unsure as to what to expect!
Thanks everyone!
I was recently (about a week or so ago) diagnosed with Crohn's, and met with my GI today to discuss treatment. As I have a fistula developing, she is going to start me on Remicade as soon as everything goes through (health care and insurance wise)... and in the meantime has started me on Prednisone
I am beginning the first week at 40mg a day, and tapering off by 5mg each week until finished...
Ive heard and read lots of "scary stories" about prednisone, the side effects and going through tapering it off... Just looking for people's experiences with this?? I am looking forward to feeling at least a bit better, but just unsure as to what to expect!
Thanks everyone!