Connect
← Return to Anyone go to a Mayo Clinic for neuropathy?
Discussion
Anyone go to a Mayo Clinic for neuropathy?
Neuropathy | Last Active: Jun 3, 2023 | Replies (43)Comment receiving replies
My experience was pretty much the same after 20+ years of living with numbness that started in my toes and finally deciding to see a Rochester Mayo neurologist for a diagnosis which was idiopathic small fiber PN. That's what brought me to Connect where I started my journey on learning as much as I can about my condition and what possible treatments are available. I wish the research focus was on healing/repairing the damaged nerves vs treating the symptoms. Just my two cents.
Replies to "My experience was pretty much the same after 20+ years of living with numbness that started..."
Connect
The drug Engensis looks extremely interesting. It is a Korean company called Helixmith. The drug is finishing up Phase III trials which is the last phase of study. Hopefully they will submit an NDA ( New Drug Application) to the FDA this year. It is an injection. This could be a real game changer if it makes it through.