MS, Peripheral Neuropathy, Trigeminal neuralgia/cluster headaches

This is my second day using the protocol. Hope I have good news to report next week. I got my B12 results back yesterday and they were good over 2,000 and next week I get my Lyme disease result back from the Mayo Clinic. My Internist fully approved of the protocol but he’s the type that if he can get answers of why he is trying to explore every avenue. He was so upset that Neurology let it go on this long. On a totally different subject I was suffering Trigeminal neuralgia/cluster headaches every day and those have disappeared. I belong to that group too so if this continues, would you like me to share this protocol with them? Keeping my fingers crossed and will report to you soon. No side effects at all.
Day 3 and no Trigeminal neuralgia/cluster headaches and my Feet are Actually Feeling a Difference for the Better! Yay! I didn’t expect it to work so fast but sure hopes it keeps up.
My only added difference and maybe it’s me because I have MS so our goal is to strengthen our myelin is that since it’s the weekend I love my sunny side up or easy over eggs cooked only in butter and get ready for this: Yes I had chicken liver cooked up in butter too as both add cholesterol and myelin to our brains. It’s not necessarily for you but for people with MS that need to increase our myelin and keeps it strong we need to add this and it does its job!
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