Nicknamed welders disease.
Same symptoms as PD.
His manganese is way high in hair analysis.
Has anyone got experience about this ?
Nicknamed welders disease.
Same symptoms as PD.
His manganese is way high in hair analysis.
Has anyone got experience about this ?
The world has known about Welders PD for a long time now. Your father should contact the government to see what compensation he can get . Example he would be contacting Workman's Compensation in Canada. Most companies that had welding operations drastically changed the equipment several years ago, forced air masks etc. If the company he worked for did not , well they are responsible. Hopefully you wont come back and tell me he was self employed. The ground work for all of this is done. You maybe should talk to other welders.
thehartlawfirm.com/blog/wha...
I put the above link to a lawyer firm not because i recommend them or any lawyer , but just so you get an idea what is out there.
I had high Mn levels in my hair analysis and urine analysis. I was exposed to molten metal fumes and ore for years. First indication was limping and no arm swing on left side. That was seven years ago. Tried a number of standard PD medications that didn’t work but had negative side effects. Not on any medication now.
Currently using a combination of diet, supplements ( especially amino acids), EDTA chelation, IR Sauna , glutathione IV ,exercise as my main protocol.
Thankyou Dragon. The meds were of very little help with my dad.Your plan reads sound. I'm really interested in what aminos and how much.
After watching that U tube video on IV glutathione. We are looking.
Any info you care to share I'm very greatful. Wishing you the best dragon.
I had been telling dad about PAS for ages.Have you had this dragon? We got a small health shop here. Nac. Acetyl l carnitine r-. Ala , tyrosine, tryptophan.glutamine,
How much how often. What other supplements have you found helped dragon? Did you have live blood analysis?
Has your heavy metals been coming down? Is your arm swinging now. Are your symptoms refreshing?
Did you or do you have trouble walking backwards? That IV glutathione U tube is David PEARLMUTTER.
Any guidance that you have been given and or learnt through experience would be priceless.
I wonder about my dad and saunas. He's 78. ? Thanks for sharing.
Every case reacts differently of course, so whatever I take is just my own personal protocol. Although my condition has not gone away by any means, I hope that I’ve slowed down the progression while avoiding drug related side effects like dyskinesia, hallucinations, and cognitive decline among many others. I still have many mobility issues, especially freezing and slow movements. I take all those amino acids you mentioned. I also take a multi supplement (Mitocore), Mucuna , CBD, taurine, etc.
Detoxification by chelation, an IR sauna , dietary choices , glutathione and removal of amalgam fillings are measures that I believe are important as a starting point. I’m still a little high in lead and Mercury but haven’t got a recent update on Mn levels.
What took years to develop may take years to recover from.
Thankyou dragon. This info on high dose thiamine is interesting.Dad has some freezing and slow movements as well. Nd has him drinking charcoal now. Liquid b. C. Liquid mag. Aloe vera powder. Silica.
Trying hdt. Will let you know if he starts Improving.
Dragon. Do you take full spectrum macuna or extract. Empty stomach or with food? With lemon juice or green tea extract. ? How much? How often?
Thanks. This community is priceless.
I read that vitamin E helps detox manganese. Thanks Dragon
Wishing you all the best