Have you tested for heavy metals? I had the same problems and I have RA, lupus and Lyme disease. The doctor ordered a heavy metal tests and it turned out to be I was off the chart poisoned with many metals including uranium But after chelation with supplements and became clean from the metals, all my body temperature and cold hands and feet problems were gone. I believe Parkinson’s also has something to do with heavy metal poisoning. It’s worth having it tested with the right doctor such as environmental medicine doctor. Regular doctor doesn’t know how to test it properly. You may be in for a surprise.
@@KarlSaxell I used xymogen”s Chelex (could be chealex). It worked wonders. Xymogens also have supplements for radiations as well. While regular chelation is costly and time consuming and ineffective, Chelex took only 6 months to clean me out. It is also gentle. No die off effects. But it’s only sold by providers. The other way, much cheaper and effective is bentonite clay. They sell liquid form at Amazon. I’m taking it right now to detox mold. Make sure you study how it should be taken. To test heavy metals, don’t go to traditional doctors. They have no clue. Find an environmental medicine doctor. Blood tests will never show heavy metals, because metals lodge in your cells and brains. Not in the blood stream. If you suspect you are heavy metal poisoned, I’d start with bentonite clay. It won’t harm you, if you don’t have metals in your system. It’s cheap, and very effective. Just be aware that it will take out medicines too, so you take it away from medicines. Don’t use any metal utensils because clay will absorb the metal. Anyway, wish you the best.
It is definitely a challenge that the autonomic effects of Parkinson's can result in too much or too little sweating. Here are some resources from Stanford's Parkinson's Outreach service about sweating and temperature regulation: med.stanford.edu/parkinsons/symptoms-PD/sweating.html
Today i got out the shower which was a warm shower and once i got out and dried i felt normal but i got to my room changed and my back felt so warm as if it was burning me what could this be ? It was very uncomfortable
At first I called it Furry Forearms. It started to affect me about a year ago, Year 12 since my PD diagnosis. I experience this PD "off" symptom as chills in the cold and sometimes it feels like my upper forearms are burning up no matter the weather. A couple of female friends say what I have sounds like "hot flashes., associated with menopause. This is very uncomfortable and I know I'm going off when I feel chills, sweats, hot flashes, furry forearms whatever we call it.
Noticing the patterns as you're describing can be really helpful toward managing OFF. If you're not doing so already, you might consider keeping a record of the timing of your medication and when you start to notice the "furry forearms." This might help you and your care provider make a plan to address the issue.
@galvanizedgnome. And so many now are coming down with Parkinson's due to the spike proteins from the shots passing the blood brain barrier as so many scientists have studied and of course it's being censored. It's infuriating
