I’m newly diagnosed. They have me on lovely steroids and Cimzia shots. Is anyone using Cimzia, any side effects, long term effects or relief?
So far I am finding some relief, however it has completely destroyed / suppressed my immune system. That scares me, especially with winter months (everyone being sick). And I am not great with giving myself the shots, I have a serious phobia and anxiety of needles. Good times…
Your Dr. is correct about the 3 months. I did not have any side effects when I was on this medication. My body eventually built up a tolerance and I had to be switched to another medication.
Hi Angie! I’ve been on Cimzia for about 3 months. I don’t feel any different. When I tell my Rheumatologist, she just says it could take 6 months for it start working. Well this is my 5th type of medicine, so that means 6x5=30 months of waiting for the medication to start working. I’m in great pain in my lower back, and all throughout my back, up to my neck! Both hips are on fire. If we go anywhere that requires a long walk, or standing for very long, we bring my wheelchair. I’m sorry, Cimzia hasn’t started working yet.