nerve damage/humira

Looking for anyone who has had nerve damage from taking Humira...I was only on it for 3 months but quit because I felt like I had the flu the whole time and it destroyed the quality of my life. Two years later after a year of being sick and ending up at the Mayo Clinic twice, finally I learned my issues are nerve damage and it's permanent. Demyelination and spinal fluid invaders that cause brain and spine inflammation. No treatment.

I have also dealt With fistulas but started drinking ionized water and they close. If I go 4-5 days with out they open up again

I hope you don't have any more issues. My neurological symptoms started after I had been off it for several months. I really hope they don;t return for you

I was on humira for about 3 months in 2014 and soon after the loading dose could barely tolerate walking on my feet. At the end of a work day, I would be in tears walking to my car. I did much research and ended up seeing all kinds of specialists, none who would say humira was the cause. I finally saw a pain management doctor who believed me and agreed. She dx me with neuropathy. She thought it was either caused by humira or it was an autoimmune response. Mine is limited to my heels and is called allodynia. I rue the day I ever agreed to change drugs. I'm so sorry this has happened to you. I found several case reports of similar side effects in patients. Have you reported it to Abbvie/humira? I did report mine although I have no idea what they do with the info.