For those of you that missed yesterday's No Silver Bullet speaker session by Dr. Matthew Phillips on "Fasting & Dietary Strategies as Parkinson's Therapies", it is now available on both YouTube and Spotify (and other podcast providers)
Perhaps I missed a passage of Dr Phillips' beautiful exposition and it seems to me thet there have been no questions in that regard, namely: we know that pwps are not advised to take foods rich in protein because they reduce the effectiveness of Levodopa, how then can we adopt a keto diet? Please if you have followed Dr Phillips' exposition, could you tell me what he said about it? There were probably some translation problems. Thank you very much.
I absolutely loved this information! Everything he talked about, I was very close in doing with diet and exercise, will just need to do a few tweeks. I am confused about fasting, as I was doing 18hrs daily, but then read every other day was better, but then he said daily? Unsure now which is better?
I was kind of surprised to learn that genetics is such a minor factor in parkinsons. 1%! I've been a cheerleader for the keto diet and fasting / intermittent fasting for quite a while. Can't say that it has cured me but I can say that it makes me feel better than when I eat like a regular American. Might also explain how I have managed to keep the progression down to a crawl. When I got diagnosed 10 years ago, I really thought I'd be wheelchair bound in 5 years. I'm still walking, here! And I can still play the bass guitar like a crazy demon!
I've tried a lot of things, too many to list. Cant say these will help everyone, but I would say the four things that have help[ed me the most in dealing with Parkinsons are
1. Ketogenic diet and intermittent fasting (autophagy)
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