In a couple of months, I will have been on the Protocol for three years.
When I found this group my feet were becoming so numb I feared I would have to give up driving.
13 Dec 2015, the toxicity of Levaquin and prednisone altered my life forever tearing my left shoulder,
Holy Shazam..am I dreaming or what…? Seems my PN is gone…feeling good in toes…
I was diagnosed with MGUS but did not experience PN until diagnosed with myeloma and after treatment with velcade.
I have had nonstop ringing in both my ears for so many years I cannot remember when it started.
In May I started getting small signs of PN and then it progressed quickly in June and a July…feet,
I wanted to share my story! Seems like a lot of people are hesitant to start the Protocol for some reason!?
I also had Follicular Non-Hodgkin’s, 18 years ago. Neuropathy is much better on the protocol.
Yes. The Protocol helps. My neuropathy began after RCHOP to treat Lymphoma. I had numbness,