Fda and amalgam

[17Hillview]

parkinsonsnewstoday.com/202...

[Jennyjenny2]

Good news! At last the FDA is finally on board!

Dr Boyd Haley, world class biochemist, has been trying for years to make the FDA aware of the dangers of mercury fillings, but instead they stopped the funding of his extensive research.

I’d love to post the link but I’m afraid I’m not computer savvy. Can someone help me out please? It’s a long one, goes for nearly an hour. His research uncovers more than the effects of mercury poisoning for PD, MS and Alzheimers.

It’s on YouTube...’Ora Wellness, Dr Boyd Haley, How to effectively remove mercury from your body’. Scroll down to see video.

[jujulini in reply to Jennyjenny2]

Unfortunately the FDA doesn’t say they are unsafe for everyone. And the ADA still insists they are safe. Too many potential lawsuits.

[17Hillview in reply to jujulini]

My thoughts exactly. They have to ease into it having covered the lie for so long. Only a matter of time before they admit to it being unsafe for everyone.

[MarionP in reply to jujulini]

A few days ago I had to decide how to replace a filling that has aged out, with amalgam or something without metal, only the choice was not described like that, the alternative was stated as something of a different color only. I asked about the difference, "one has metal and the other doesn't," so I asked "does the metal include mercury?" "Oh, well, umm, yes." It was like pulling teeth.

[17Hillview in reply to jujulini]

Hi Jujulini

I just read that you have been doing the ACC protocol. I just completed round 9.

Can you share briefly how your experience is going? What round are you on and have you noticed a sustained improvement?

Thanks in advance.

[jujulini in reply to 17Hillview]

17Hillview--

If ACC is Andrew Cutlers protocol, then yes, I did that. But that was 15 yrs ago. After having the amalgams removed (properly), I chelated for a year. I did notice improvement at the time, but I had been experiencing symptoms for 3 years prior, so I think alot of damage was already done. I still had symptoms (mostly bradydyskenesia), just not as severe. After chelating, I was diagnosed with pd and started on carbidopa/levodopa. That was in 2006.

[17Hillview in reply to jujulini]

Yes I was referring the Andy Cutler Chelation. 15 years is a long time. They have evolved the protocol significantly since then. I only came across it a few months ago. There is a Facebook group that offers support for persons wanting to have a go at this. They now have it clearly defined and documented. Which includes many years of the experiences of persons that have been helped with it. I will post any progress here. Thanks for sharing.