Riboflavin (b2) is a complete no-brainer. 0 side effects and dirt cheap.
Especially if your second and third toes any toenails are full of fungus/athletes foot.
The Chinese believe that your second and third toe is a place where toxins leave the body. The Chinese believe PD is “stuck” in fight or flight.
My Parkinson’s is only on my right side. Coincidentally, my right foot toenails second and third toes were full of athletes foot. My left side was free from Parkinson’s and gross toenails. I started restore gold, which has many antioxidant supplements, shortly after being diagnosed. With the restore gold, I did not progress but for some dumb idea I stopped taking it for about six months after 3 or so years of taking it. In those six months I had a neurologist appointment, and my neurologist said that my Parkinson’s was moving to my left side. Coincidentally my second and third toenails on my left side were starting cloud up. I restarted the restore gold and my toenails cleared up and my neurologist said that there was no Parkinson’s in my left side anymore. Restore gold was the only difference.
About a year ago, I had a blood test showing I had almost no riboflavin in my body. I started supplementing riboflavin every 8 hrs. My toenails on my Parkinson side are now clear. They haven’t been clear for at least five years before being diagnosed. I’m back to my starting dose of levodopa. The real change other than the riboflavin is the Sauna/cold plunge/ Wim Hof/ fasting.
I copied and pasted some important information that I’ve written previously about B2 /MTHFR.
I believe a low b2 levels caused a ton of my issues. B2 help lower homocysteine that is correlated with PD. Most of all, MTHFR which is said to be a b2 deficiency. MTHFR struggles with removing toxins. They cannot convert folic acid to folate. It actually blocks the pathway. This is VITAL!!! Your folate levels will show fine but it’s not working well.Your most likely borderline anemic. Folate and B12 is vital for the production of blood. I was borderline anemic for many years. The ranges of blood test are not precise enough. (MCV 99 no anemia /MCV100 anemia) Who came up with the range?? Blood is key in most health. Long term low blood to the brain??? Diet soda, high carb, low nutrients food. MTHFR cannot process synthetic vitamins. These synthetic vitamins are harmful. In the late 90’s, the FDA decided to enrich flour with synthetic vitamins. This is causing huge problems. 30-40% of the population have a form of MTHFR. Unintended consequences.
This has pretty easy solutions. B2 is the single most important vitamin for me. 0 side effects. Everyone with Parkinson needs to supplement with this. It’s non-toxic, no side effects and dirt cheap. They actually had a study Treated PD patients with just b2 and removed red meat. They had amazing results. Modern medicine has completely discounted it for 20 years.
Modern medicine is beginning to figure out there is something related to low riboflavin and neurological degeneration.
Really you have nothing to lose. It took me a long time to notice the results, but really the only side effect was dark, yellow urine. You’re probably not gonna notice because the changes will be so gradual. Just start taking it, you’ll thank me later.
ncbi.nlm.nih.gov/pmc/articl...