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TS-HDS Antibody and Small Fiber Neuropathy

Neuropathy | Last Active: Nov 13, 2023 | Replies (156)

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@lilotter

The Dr. Oaklander referenced in one of your articles has worked with Dr. Khosro Farhad, whom I was fortunate enough to see in New Hampshire. He was the one who diagnosed my SFN as TS-HDS mediated. Some lifestyle changes that have helped me have been giving up gluten and dairy, starting a regimen of low dose naltrexone and pool therapy. The latter is the best kind of exercise for my chronic pain. It's difficult right now with gym closures but I hope to get back this fall. Right now I am swimming in the very cold Maine ocean or my unheated pool. Not quite as therapeutic!

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Replies to "The Dr. Oaklander referenced in one of your articles has worked with Dr. Khosro Farhad, whom..."

Thank you for the information. What is the naltrexone? Also, have you ever tried IVIG?

Hi @lilotter... I have the TS-HDS with SFN as well! I noticed that you are the only one who has mentioned a diet change. Is this a diet for inflammation? Can you explain how it has helped? I am going on
Dr. Amy Myers diet for inflammatory diseases; but in doing so, I am giving up everything I enjoy eating! Are you following any particular diet? Brrrr, to that cold Maine ocean water! Thanks for your information!