Does magnesium help neuropathy?
Hi All - Anyone ever receive magnesium infusions for idiopathic neuropathy?
Interested in more discussions like this? Go to the Neuropathy Support Group.
Hi All - Anyone ever receive magnesium infusions for idiopathic neuropathy?
Interested in more discussions like this? Go to the Neuropathy Support Group.
@pua0609 My neurologist told me b6 causes neuropathy. On the other hand, B12 should be supplemented if low. It may be helpful to get a blood test to guide you. Best, LL
@llmartin
Thank you so much for your feedback. My primary care doctor recommended B12, which I had taken for many months. But, recently a nurse practitioner, who mentioned that she also suffers from PN, said she takes B-Complex in addition to B12. I am particular about not overdoing any medication or vitamin. But, there's so much that is confusing. Wishing us all the best...
Thanks again.
-
Like -
Helpful -
Hug
3 Reactionsi was diagnosed with Parkinson's disease 7 years ago and found out about 2 months ago i do not have it. But i have developed neuropathy. It bothers my legs and feet. No pain but no feeling which makes it difficult to walk. I tried using a magnesium cream because it said it helped nerves.
It was like a miracle!! I could walk again. No shuffling feet. I've been using it a week now. It's made by Mama Bear and its called OASIS. It has magnesium chloride in it.
-
Like -
Helpful -
Hug
1 Reaction@besmith57 has no doctor suggested a steroid injection?
-
Like -
Helpful -
Hug
1 Reaction@pua0609 need to make sure that the B12 is the methylated form
-
Like -
Helpful -
Hug
1 Reaction@blowerk1216
I have had numerous steroid injections. I have DDD so supposedly this will rehydrate my discs.
@blowerk1216
Thanks so much. Yes, it is. All the best.
@besmith57 thank you
-
Like -
Helpful -
Hug
1 Reaction@blowerk1216
I should also mention I've had ablation, tried a stimulator, and had Viodisc injections. I don't know of anything else I could do. I'm doing PT, but that seems to make my back worse. I've had 2 medical people tell me I will always have it. Not what I want to hear.
@byhoyle hello, Dr.’s kept telling me mine was Neuropathy from Chemotherapy. Which I kept telling them it was not. Never had Neuropathy during Chemotherapy. It started almost 3.5 years later in my right toe. Long story short now CIDP!!! Waiting on my appointment at University of PA/ Penn Med 4/6/2026. They specialize in that. I am wondering if I should give that cream a try. Fingers are like pins and needles. Feet, cannot feel them half of the time. Balance is so off.