Does Anyone With Close Relative With Ms Successfully Take Enbrel Or Humira?
My Mom has ms and I have psoriatic arthritis (not much psoriasis) Since 2011 or 12 different rheumatologists have wanted me to take enbrel or humira but I am afraid of ms/nervous system side effects. Took methotrexate, otezla, sulfasalazine, now stelara for almost year. Stelara helps but could be better. Dr still recommends enbrel. Any insights? Thanks very much. My dads mom died of als which of course is also neurological.
Hey summergirl. That's ok. I am taking the risk as the drug works so well for me. If something goes sideways I will deal with it then!
I've been taking Enbrel & Methotrexate for 22yr now. It has kept my skin clear & the only way I'm able to function with my joints. I recently relocated to a much warmer climate for the first time. I'm still adjusting, have had some flares, & increased joint pain. This is very unusual, & I'm attributing it to the stress & family issues.
The pharmacist tells me chances are 1 in 1000 when taking enbrel or humira or other tnf inhibitors of getting ms. From what I read with some people that develop ms it goes away when drug is stopped but sometimes doesn't. Some doctors and studies I've read say people with first degree relatives with ms shouldn't take the tnf a's but all the doctors and pharmacists I've talked to say the benefits outweigh the small risk. Sorry, didn't mean to scare you. Thanks for your reply.
WOW _- did not realize there was a correlation between PsA and MS! I have been on Enbrel for about 3 years and I feel good.
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