Is Anyone Using Cimzia For This? | MySpondylitisTeam

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Is Anyone Using Cimzia For This?
A MySpondylitisTeam Member asked a question 💭

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?

posted February 7, 2023
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A MySpondylitisTeam Member

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…

posted February 7, 2023
A MySpondylitisTeam Member

I did cimzia for 6-9 months and found no relief. Started humira and that has helped greatly. Hope you get some relief.

posted February 7, 2023
A MySpondylitisTeam Member

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.

posted March 20, 2023
A MySpondylitisTeam Member

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.

posted February 11, 2023

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