Can Neuropathy be cured?
I’ve had P. neuropathy for 30 years. Just recently I’ve better controlled my blood sugar. So, I’m wondering if Neuropathy ever goes away, Or, if once the nerves are dead they’re just dead
Interested in more discussions like this? Go to the Neuropathy Support Group.
Hi johnmacc,
I take 900mg x 3 per day. Morning, afternoon and before bed. =2700 daily. I started 300, 600, etc... per day but PN just will not go away even with the increased amounts.... I am still unable to feel feet and legs are remain numb as well. I already tried cream, gummies, etc... The PN has become extremely expensive with NO cure only Band-Aids and sad to say, I accepted its part of my life. The creams such as vicks vapor rub, icy hot, aspercreme brings temporary and very small relief to the tingling but not numbness. And I did attempt to increase to 3600+ but my feet swelled and looked like as I had elephantiasis. Michhino
Melatonin is just as bad. I wish I could help you but I don’t know if anything.
It’s not anxiety and depression. You are not alone.
I have a link to a post I made a while ago. I was in your shoes for over two years until I tried the regiment below.
https://connect.mayoclinic.org/comment/811991/
Loma linda university medical says they are having sucsess at rejuvinating nerves
Call their neuropathy clinic
Free consultation video call with MD
I was very impressed and interrested
Hi (No Name!!!)
I so hate posting with names no one understands with no address or phone or email address or what it is all about.
Like we supposed to know all about "Loma Linda University".
Where is it???
Hmmmmm.Waist of my time.
No thanks.
manny
Hi Manny,
I think using Google to look up the university's neuropathy program will give you the answers you are looking for. If not ask me, and I will send a link, not working on my phone at the moment, I am having an IVig treatment at the moment.
I will also list the litany of things I do to reduce my neuropathy symtoms.
JFN
Manny,
Did you find the links to the neuropathy program at Loma Linda University medical center neuropathy research?
Have you tried Rituximab infusions, and if so how many, was there improvement, and how long to see improvement?
I completed firsts 4 infusions, 1 per week, early this year. Now scheduled for 4 more---every 2 mths March, May, July and Sep. Haven't seen any changes, but MD said if do get improvement, it could take some time to show up. Thanks
What did they tell you. We are all looking for anything to make our lives more livable without pain