I fasted 16hrs even though fasting and calorie restriction is very much against most of most neurologists advice for MND/ALS.
From my research they are wrong!!!
I can understand their thinking from their academic studies but they haven't a clue about anything outside of their limited knowledge on any sort of treatment for this condition. As far as they're concerned you just get diagnosed then wait to die. It's bullshit and completely wrong!!! If it's not what they call "hard science" then it has no benefits. What a load of crap!!!
I totally understand that they may be afraid to suggest much to anyone in case they get sued etc., but there are ways to word things to people that won't get you in trouble. For example, they could say: "Some people have found benefits from/by doing….. Or, "You may find it useful to look up/read… It's not rocket science and it could give people hope. Maybe save a life!!
There are numerous research studies done on the massive benefits of fasting, I've covered this already. Especially on inflammation and influencing DNA.
Anyway, my brunch today was:
Grass fed beef mince with spinach, kale (need to help keep my good gut bacteria happy), mushrooms, onions, garlic, black pepper, waaayyy too much cayenne pepper 🔥🙊Lol, curcumin and chopped tomatoes. Lovely, very filling and I'm sure it's all helping me in my fight against ALS/MND. There's leftovers for later of tomorrow's breakfast. 😉
https://www.gofundme.com/paul-s-fight-against-MND
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