Hello! Thank you for your reply! I also have costochronditis! For me, the joint pain seems to accompany the UC symptoms but also increase when I'm able to decrease my steroid dose. Thank you both!...
Me again....I don't know if this helps or means anything but when I did the at home Methotrexate injections it was used as my concomitant immune suppressant for Remicade. I never tolerated Azo well...
Thank you!!...
I'm being treated with Tacrolimus and no one in the US or the UK has ever uttered a word about PML. When I was treated with Cyclosporin in the UK I was told it was only possible to be on it for a...
Indycat23: unfortunately in the UK Remicade is usually not offered for UC on the NHS which is why many people must choose from Cyclosprorine, Tacrolimus or Methotrxate.......
Hello I'd like to chime in. I'm also in the UK and have been on all three drugs plus Remicade at one time or another. First I'm really sorry but Tacrolimus has absolutely nothing to do with PML. I...
Hello I'm due to start Vedolizumab soon and everyone has already been so helpful on this site in addressing some of my general concerns. I'm just curious whether anyone has received info from their...
Hello, I'm wondering whether it's "normal" to experience joint pain in fingers and feet as a UC flare comes on?...
Thank you everyone for the great advice. The Vedolizumab sounds like it will be much better than the Remicade experience who obviously took all day and frequently left me exhausted and dizzy. Katmom:...
Thank you so much for the great advice! So - I should ask to be tested for the JS virus before my first dose? Is it something that can be in your body without your knowing it and then the Vedolizumab...
Hi, I'm soon starting Enyvio / Vedolizumab for Ulcerative Colitis. I'm extremely nervous about it. Does anyone have any advice or experience they can share? Some things I'm wondering specifically...