Just ran into this video of a lady with agressive PD who was able to improve her symptoms to a great extent. Anyone here tried this diet and would mind sharing their experience?
Link below
Just ran into this video of a lady with agressive PD who was able to improve her symptoms to a great extent. Anyone here tried this diet and would mind sharing their experience?
Link below
Video not working
Thanks for the headsup. Let's try it again. youtu.be/Ty5l5ZF10qY?si=VDk...
If we believe this lady (and no reason not to) this is a life changing turn around in her health.
The more I read the more overwhelming are the choices.
More medication - less medication -
keto diet - carnivore diet - fasting - intermittent fasting - exercise - fast walking - supplements - dairy - gloves - light therapy - blah blah blah.
Save me lol
everybody is different: for someone keto diet works, for some others not, but light therapy works... and so on....
Parkinson' symptoms are different in everyone. We have to work to find our best therapy.
There actually is a reason to be a bit skeptical since the video is also a commercial for the interviewer's business. Sorry but I tend to be a bit cynical when there's money involved. That said, I've heard others who have PD also tout the carnivore diet. I've not heard a reputable doctor / neurologist recommend it though. They all emphasize the MIND / Mediterranean diet.
Interesting
I have been on the Carnivore diet over 4 months now. Diagnosed in 2018, I followed a no sugar, low inflammatory diet for 6 years , keto for 6 months then switched to Carnivore. I had DBS surgery in 1/2023. I have begun to see changes in the last few months. Pain from neuropathy in my legs and restless leg syndrome have gone away. I am able to fall asleep at night. My finger and toenails have gone from chipped and easily broken to solid and hard. My body has begun slimming down. My brain is less foggy. I don’t get cold as easily. My mood is improved. My energy is more sustained. Everyone’s body is unique. My system has been sensitive to sugar and refined carbs all my life. I think I would most certainly have been an alcoholic if I ever started drinking. I don’t smoke or drink.
Boston Scientifics is the brand I had implanted. The battery lasts 20 years. I charge the battery weekly. The surgery is intrusive in the fact that it’s brain surgery but after healing it is not noticeable to others. I have a small bulge on my left front chest area where the battery is placed. I can trace the leads from there up my neck to the side of my head where they end at the two pins on top. None of this is visible to others. There’s no discomfort after the healing is complete. I did notice a few tingling effects in my skull while nerves were healing from the surgery. The most uncomfortable time for me was between surgery and the first programming. My tremors and rigidity had been debilitating but since programming I basically had my life back again. Drove my car for the first time in 5 years.
Thank you a bunch for your detailed experience description. Did you have issues with off-time or freezing prior to the DBS? If so, did DBS helped?
I had off time but no freezing before surgery. After surgery I quit taking Amantadine entirely (which I had been on for 3 years) and started taking extended release C/L. That eliminated dry mouth, low blood pressure and the “marbled veins” look on my arms and legs. I also wanted to reduce the anti-cholergenic effect by reducing this medication. My off time now is minimal. I think the ER C/L helps. I take one every 5-6 hours. Less needed evenings and while sleeping.
Been on for 5 months. My worst symptom anxiety and depression almost completely resolved. I think very soon. I’ll be able to come off c/l (didn’t work all that great for me) I’ve been ramping up my nicotine to replace it. Nicotine works better for me. I will be eating this way the rest of my life.
How much nicotine are you using, and how much do you think you might go up to?
I am slowly increasing my dose, but it makes me feel nauseous every time I do, so I have to take things slowly.
Thank you so much for sharing your story. Do you know of a good youtube channel or any online place you follow for recipes? So on carnivore there is no carbs allowed from what i read, so not even fruit?
I dunno about recipes. I eat mainly beef that I have got from a local rancher. What’s weird is that it taste good when I’m hungry and then when I have enough it doesn’t taste as good. Look up Dr Berry and Dr Chaffee. They are some genuine fellas that make a ton of sense. Make sure u eating plenty of fat, especially animal fat. Good luck.
Been on it 4 months (less than 20g carbs) . All non motor symptoms 75% better. Tremors a slight improvement. Everything moving in the right direction. The closer I am to 0 carb the better. Im never going back.
Thank you kindly for sharing your story. Did you have freezing/off-time before? Did the carnivore diet help?
i didnt have freezing. im currently not on meds, came off them a month ago.
Its been very subtly slowly improving for everything but mainly non motor symptoms seem to improve fastest. Motor symptoms seem to be the most resistant to change but i think it is very very slowly improving too. I think stress, sports, socialising also all make a slight difference but for me the main culprit is food specifically carbs and sugar. Only more time will tell but i feel better which is positive!!!!