Experiences with

Adipine

Adipine which was like going through chemotherapy. Rampril, confusion, flu symptoms, Losartan, caused huge anxiety, blood pressure rise.

I just found this on YouTube, thought I'd share. https://youtu.be/e2dPS8cx0Kc

It has been 5 years since my Diagnosis and now 7 years living with PD or from my first symptoms thhat were a little tremor R/H, dry eye, loss of smell. I am now 73 and have posted and joined in others discussions here over the years and have great faith in what I read on many of your posts. Not to re-hash

 There have been very many studies published on the effects of exercise, especially of endurance/aerobic exercise, in restoring the number, the quality and the activity of mitochondria, both in the skeletal muscles, the heart and in the brain neurons. As these are our highest energy demanding tissues

If I was smarter, I might not be so excited about Niacin. I am pretty excited. Niacin in the Central Nervous System: An Update of Biological Aspects and Clinical Applications 2019 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412771/ "Parkinson’s disease (PD) is a progressive disorder characterized

I've been doing a little reading on these two supplements as treatments for Chronic Fatigue. Just a few articles I found through a google search. Seems like this might be promising approach but I also don't know anyone that's tried it. I'm hoping someone here could chime in... In addition to chronic

*** I ended up with High Blood Pressure taking TTFD. I no longer take TTFD. Based on my experience, I would not recommend TTFD. *** Someone asked, if I ever heard of NADH? I believe when a cure is found for PD, it will a combination of factors. I take NMN which supposedly increases NAD which is the

Diagnosed with PD two years ago at the age of 48, I guess I’m one of the lucky few to be selected for Roche’s Prasinezumab trial, due to begin this fall. Since my diagnosis, I don’t feel that my symptoms have gotten worse and I’m still able to keep the diagnosis to my inner circle (symptoms: slower

Explanation: I would like to share this chapter with all of you. Because of a worsening in my mother's health, I don't know when I will be able to resume the English translation of my book on curing Parkinson's. I will be sharing some chapters in this extraordinary forum. I have to stop my investigation

This is the information that gave us hope while my father was alive and has given hope to many since then (March 2012). 1. News that worried us. In the coming decades the number of Parkinson's disease patients is feared to increase very worryingly, to double by 2030 (Dorsey 2007) and even to triple

NADH might be better than our other options. Emphasis on might. Please share any knowledge on this! https://www.enada.com/

Dehydroascorbic acid is the oxidised and reversible form of ascorbic acid or vitamin C. It can protect the brain and reduce stroke mortality, due to its ability to cross the blood-brain barrier, whereas vitamin C or ascorbic acid cannot easily do so. In one study it was proposed as a possible treatment

I’m working on understanding the process by which niacin ultimately increases NAD and if supplementing with NMN, a more immediate precursor is more advantageous or perhaps NADH is better?

So... I speculate a lot. I started the Circadian Diet based on the knowledge that PWP have weak circadian rhythms. I should add that my RBD is getting worse, so either nothing is working, or some of the things I do are working against me. But I digress. This study is about how if you restrict a mouse's

Saw this one on a dental summit. Used to detox and other things. Has a lot of familiar ingredients! Has anyone used it? https://oradix.com/product/stemdetox-detoxification-anti-germ-and-weight-loss/ How to Use StemDetox™ Take 1 capsule 2X daily for the 1st 5 days, 3 capsules 2X daily for the next 5

This coming Monday (if everything goes as planned) I will publish on my blog "Parkinson's here and now" the link to a free book of about 250-300 pages and in printable pdf format, which collects the most interesting of the book I published in 2015 (now translated into English) as a tribute to my father

This is chapter 17 of a book I published in 2015, "A Different Way of Looking at Parkinson's. Almost 20 years of experience with my father's disease (1994-2012)" (only in Spanish). Although we have learned a lot more since that year, I think it can still be useful to most sufferers and family members

NADH, Does anyone with or close to someone with Parkinson's have any information and or experience or success with taking NADH?

(Excerpt from the book I am writing now. I hope you find it useful). Is Parkinson's disease a lifestyle disease? 3. Antiparkinsonian lifestyle. What took my father and I the longest to understand was that not only were there lifestyles that increased or decreased risk, but that it was possible to

I started taking NADH about a week ago. Instead of feeling better, I notice extreme fatigue, nausea and sleepiness but at the same time I have trouble sleeping. Has anyone else experienced these side effects?