Hello, I usually hang out on the crohn's forum but have a couple of questions. My medication, Pentasa does not work at all for my crohn's. My Dr wants to put me on the big guns as he calls them Remicade or Humaria. While having a CT scan for TMJ they noticed something and I had to go back in for an MRI of the brain. They saw Dawson's Fingers but did not say it was MS. After reading about these meds and so many people getting MS, FM or Lupas from these I am afraid if I start them it will bring out MS due to the Dawson's Fingers. What could the Dawson's Fingers be if not MS? Should I be concerned? I live in the Pacific Northwest and I understand we have a higher MS rate here then the average.
Thank You in advanced for your reply.
RIP my beloved Chihuahua: Roxy
DX with CD of the TI in 2004 by colonoscpy biopsy, with partical obstructions x 3. Anemic, constant elevated ESR & WBC. Constant abd. pain and fatique.
Meds: Vit B-12 shots monthly, zinc, multi vit, Vit E, Pentasa.