COVID vaccines and neuropathy
I am 85 with small fiber neuropathy that is getting worse. My neurologist thought it would be a good idea for me to wait with the covid vaccine and not be first in line to see how it affected other people with neuropathy. Probably because it is a new technology. Has anyone had a problem with neuropathy after receiving the vaccine? If so, which vaccine?
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Thank you for sharing your experience, sounds VERY SIMILAR to my story, and seems you have had same thoughts that I do.
I guess all these symptoms are post covid?
I'm 2 1/2months post covid, I too had, and have, the bruising and nerve issues, including DDD in spine and neck, tingling, numbness, in hands, arms and legs (seems to come and go, changing intensity. As you said, difficult to explain precisely. Im on Mobic too, (I know Cymbalta well, Gabapenton too.) I was precovid diagnosed with Fibromyalgia. I also had head pressure and Vertigo seeing ENT first time today.
Hard to keep calm and patient when you're dealing with chronic pain and anxiety and the stress with these symptoms.
BTW, I had Moderna vaccine. No one wants to points blame of my symptoms POST-COVID to the vaccine but the virus itself. I was sick day 21 AFTER SECOND vaccine.
Keeping fingers crossed for answers.
Today marks 5 months since my 2nd Moderna shot. Neuropathy that began right after has not gotten any better with time, but the opposite. Have been to the neurologist 3 times now, had all the testing and labs. All negative, no nerve damage. Doctors still refuses to blame vaccine or prior Covid for any of this. I am 53 with no prior health issues. The burning and numbness in feet and toes has slowly progressed up my ankles and calves. I now have same in wrists and starting in my fingers. I have constant feeling of stepping on rocks under balls of my feet when I walk. Also a feeling of tingling in my left ear and nostril. Constant sneezing. Sometimes feeling of something crawling on my right arm and leg, always in the same area. Doctor now says he thinks I have restless leg syndrome????? Put me on meds for that. Makes my legs heavy at night, but burning doesn’t go away. I don’t think this is RLS. Anyway, 5 months and not getting any better. My hope is dwindling as my quality of life slowing diminishing. Doctor makes me feel like I’m crazy. My husband is a neuro radiologist, thank God he sees me everyday and sees what I have been experiencing and let’s me know it’s not all in my head. Thinking I want to get tested for MS. Wish I lived in an area with better healthcare resources. I’m very pro vaccine, but will not be getting any boosters.
Mine lasted 3 months . Every week that went by was a little bit better but it was still scary . My doctor suggested I stay away from alcohol and any other foods/drink that cause inflation .
I developed peripheral nerve issues after my first Moderna shot. My doctor refuses to believe that the shot is to blame. He is testing me for auto immune issues. I was feeling all alone too! Not getting the second shot, at least for now.
How are you now?
Much better. Over the months it has slowly gone back to normal!
I have three autoimmune diseases, I have autoimmune disease caused neuropathy. When I got the vaccines my neuropathy increased significantly. My neurologist said that it was probably an autoimmune reaction to the vaccine.
My son, 34 years, had the 2nd Pfizer injection in May. In July, he complained of tingling in both hands, both legs from the knees to toes. No pain, but sometimes feels weakness and fatigue in these affected areas. MRIs of head, cervical and lumbar are negative as was the EMG/NCV of his legs. Lab work was all negative. The neurologist cannot explain the symptoms, but states he wouldn’t rule out that it may be related to injection. It is now Oct and he says the symptoms are unchanged. I’m greatful that they have not worsened. Any recommendations are appreciated. Has anyone recovered from the symptoms?
You are experiencing the similar symptoms as my 34 year old son. He is 4 months post 2nd Pfizer injection and had had no changes in the tingling of both hands and feet to knees. Are you better? If so, what treatment worked? God bless you
@dag10 your son’s symptoms sound quite similar to mine. I am now almost 9 months out from 2nd Pfizer and am experiencing very slight improvement. I have tried so many things such as dietary changes without any real effect. I do take a few supplements and vitamins but I think more than anything the passage of time is the biggest thing giving me slow improvement. I am just so grateful it isn’t worse and doesn’t really keep me from doing what I want and need to do. But it has been an extremely frustrating and at times frightening experience. Best wishes for your son!