I’d like to thank everyone for all the support though the years of my PD. I have come quite a aways. Your kindness and support helped me get through the hardest years of my life. I will check back from time to time if I come up with something that can help others. I have chosen to let go of my Parkinson’s obsession, and live. One main ways is to cut out these boards. I believe my PD is more of a mental disorder. My PD, maybe yours too?? Maybe not? My symptoms were the same for years until I figured it out what the symptoms were, then I fell of a cliff.
The number 1 thing I would do suggest to do is WIM HOF method. It’s changed my life more than anything else. I’m driving home, my extended family was amazed on how well I’m doing. They haven’t seen me in about a year. It’s not meds. It’s the method. It so simple and effective, most will discount it . I will soon be off levodopa. My mao-b inhibitor may take longer to get off. Please read this book with an open mind. I’m not saying I’m cured. I just don’t need the c/l anymore. I’m back to my starting dose, 5.5 years ago.
My extremities were cold my whole life. The cold exercises your vascular system. My hands and feet are now always warm. More blood flow. Also more blood flow to the brain.
Vitamin B2, especially if your 2nd and third toenails are infected with athletes foot. MTHFR is key. B2 can overcome MTHFR genes. Look at my previous post. No side effects, no brainer.
amazon.com/Wim-Hof-Method-A...
Also, look into GylNAC. Read my previous posts about it.
Stay away from Sugar as much as possible. It’s terrible for the brain.
Look into fasting. It’s more of a path to your brain. Autophagy is crucial for fighting PD, fasting is a great way to induce it.
Nicotine is my substitute for c/l. Less is more. Try the gum. I believe the patch trial failed because it’s too much nicotine all the time. Like too much c/l can do the opposite. Read my previous posts.
Of coarse exercise. It’s a no brainer.
If anyone who reads this, wants to talk. My email is cameronhermansen@gmail.com
Maybe it’s all placebo. Maybe not. My PD never responded that great to c/l.
The best advice I’ve ever had with PD is act like you don’t have it. Live!