steroids
hey guys. im 19 and have crohns and i have a long story as im sure you all do, but i dont have much time to post this becuase i need assistance asap. basically my main concern is with a medicine im taking now called entocort. ive been on it for about 8 days now(9mg), and i really havent noticed any improvement at all.
i went into the hospital becuase of extreme pain, seems it was from a bad fistula forming. when i was in the hospital for 11 days they put me on bowel rest and i was taking my two probiotic tabs daily(vsl3). i was also taking my daily dose of asacol(3.2grams, but im not sure if these things do anything for me to this day or if theyre just a waste of money). i was also on flaygl becuase i had a raging c.diff infection but i switched to vancomycin because the flaygl raised my lfts way to much. and they started me on 40mg of iv prednisone. after about 5-7 days i noticed a big improvement from the steroid, and althought it was still hell, i went home on the 11th day. i kept taking my prednisone asacol probiotics vanomycin, went through hell, noticed TONS of side effects, but i eventually went into remission.
now i am back into a flareup once again, and im still taking my asacol and probitoics and up until now i have been fine with this. at first i thought it was a c.diff infection so i got tested. came back negative got tested again, and again but still negative. i was hoping the c.diff was caused me to go into a flareup within a matter of a couple days and use the bathroom 10+ times a day, have urgency to run to the bathroom, have abdominal pain and bleeding with every stool, but i guess not.
so here is the real question. what the doctor put me on was entocort(9mg) and ive been on it for about 8 days. i havent noticed any real improvement at all. i thought this stuff would work fast like the prednisone. how long does this stuff take to start working? could the prednisone also have worked much quicker becuase of the bowel rest, and taking the prednsione through iv rather than orally? and why does entocort work for only some but not all, but prendisone will work for all? arent they essentially the same substance, corticosteroids?
also, all over the website i keep reading "ENTOCORT EC is approved to treat mild to moderate Crohn’s disease affecting part of the small intestine called the ileum and/or part of the large intestine called the ascending colon." in every paragraph. does this mean that if my disease is elsewhere (such as the descending colon) that entocort wont work for me?
i havent gone for a colonoscopy in awhile, but im planning to do an mri very soon. please help me becuase i want to go into remission before winter break is over so i can start school back up and not fall even further behind! i had to quit my part time job and dropout of a live away school and take lots of time off becuase of this stupid disease and i dont want to now have to take a medical leave from a community college! thank you so much
hey guys. im 19 and have crohns and i have a long story as im sure you all do, but i dont have much time to post this becuase i need assistance asap. basically my main concern is with a medicine im taking now called entocort. ive been on it for about 8 days now(9mg), and i really havent noticed any improvement at all.
i went into the hospital becuase of extreme pain, seems it was from a bad fistula forming. when i was in the hospital for 11 days they put me on bowel rest and i was taking my two probiotic tabs daily(vsl3). i was also taking my daily dose of asacol(3.2grams, but im not sure if these things do anything for me to this day or if theyre just a waste of money). i was also on flaygl becuase i had a raging c.diff infection but i switched to vancomycin because the flaygl raised my lfts way to much. and they started me on 40mg of iv prednisone. after about 5-7 days i noticed a big improvement from the steroid, and althought it was still hell, i went home on the 11th day. i kept taking my prednisone asacol probiotics vanomycin, went through hell, noticed TONS of side effects, but i eventually went into remission.
now i am back into a flareup once again, and im still taking my asacol and probitoics and up until now i have been fine with this. at first i thought it was a c.diff infection so i got tested. came back negative got tested again, and again but still negative. i was hoping the c.diff was caused me to go into a flareup within a matter of a couple days and use the bathroom 10+ times a day, have urgency to run to the bathroom, have abdominal pain and bleeding with every stool, but i guess not.
so here is the real question. what the doctor put me on was entocort(9mg) and ive been on it for about 8 days. i havent noticed any real improvement at all. i thought this stuff would work fast like the prednisone. how long does this stuff take to start working? could the prednisone also have worked much quicker becuase of the bowel rest, and taking the prednsione through iv rather than orally? and why does entocort work for only some but not all, but prendisone will work for all? arent they essentially the same substance, corticosteroids?
also, all over the website i keep reading "ENTOCORT EC is approved to treat mild to moderate Crohn’s disease affecting part of the small intestine called the ileum and/or part of the large intestine called the ascending colon." in every paragraph. does this mean that if my disease is elsewhere (such as the descending colon) that entocort wont work for me?
i havent gone for a colonoscopy in awhile, but im planning to do an mri very soon. please help me becuase i want to go into remission before winter break is over so i can start school back up and not fall even further behind! i had to quit my part time job and dropout of a live away school and take lots of time off becuase of this stupid disease and i dont want to now have to take a medical leave from a community college! thank you so much
Last edited: