Hello. I've been self-injecting monthly to handle my PA for about 6 years now. I still have a little bit of neuropathy in the fingers of my left hand. Has anyone had any success treating that or should I consider it to be permanent at this point? It's not that bad but a few tasks, like buttoning my right sleeve button, are difficult. Thank you.
Residual neuropathy : Hello. I've been... - Pernicious Anaemi...
Residual neuropathy


That neuropathy may well be irreversible now . I have neuropathy in my feet , which makes walking painful , but after 10 years of injecting , I have more or less given up ( but you never know . Some clever scientist may come up with a remedy . )
Best wishes .
Indeed & I was heartened to hear that scientists are looking into ways of reversing autoimmune disease by changing genes. I hope they succeed as we know B12D is a killer & type 1 diabetes even more so. autoimmuneinstitute.org/art...
I agree with Wedgewoid . I have been SI EOD for almost 3 years and still have vague peripheral neuropathy in hands and feet, not to the extent walking affected but vaguely uncomfortable especially when it’s cold. I don’t give up though and no harms done, so I would keep trying 😊
I guess the only things you can do is take DHA rich omega 3 oil, zinc and all the Bs needed for nerve myelin repair. And do lots of finger stretching exercises.
I read it was a lack of B12 which causes the neuropathy. I have a B12 shot at the surgery every 12 weeks, and my fingertips feel odd-not exactly numb, nor not really tingly, but my phone does not always respond to my touch. I like to sew, so it is very debilitating. If people are injecting every week, how much is used each time?