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Anyone here dealing with peripheral neuropathy?
Neuropathy | Last Active: Oct 28 4:54pm | Replies (3050)Comment receiving replies
John, is there any way to access the protocol without Facebook? My symptoms are very simiar to yours - when they began in my forties I was screened for MS and Charcot-Marie Tooth because of the unexplained nerve damage in both legs and feet, both were negative-thankfully. Nothing progressed for over a decade, which was great - now I am experiencing some progression and am seeing a new neurologist in Chicago today. Thanks so much for sharing your success and encouragement here! I;ve used Essentrics and a rowing machine to keep up my strength for years, and after reading in this forum started introducing the Wahl protocol in to my diet a week or so ago.
Replies to "John, is there any way to access the protocol without Facebook? My symptoms are very simiar..."
John, do you have a link to the Face Book group? Or give me the name? Thanks John
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Welcome Susan @susan0514, The Facebook group for the protocol does have a website. You don't have to use Facebook but a lot of members on the protocol use Facebook for the research and sharing. Their website has gotten a lot better and they have added a lot of their background/research information along with frequently asked questions (FAQs) - https://theprotocolworks.com/. They do have a Why the Protocol answer in the FAQs but the research listed doesn't have the hyperlinks to the articles. I added those and shared the document in another post here if you want to read the research - https://connect.mayoclinic.org/comment/957496/.
It might be helpful to print out the Why the Protocol document in the above link and share it with your neurologist/doctor. Can you share an update after you see your new neurologist?