Happy New Year

I'm approaching the 2 year mark since my life was jeopardized by a series of Synvisc injections. If ALL of the information to make a true "informed consent" had been mandated by the FDA then my life would have been far healthier and more productive during this time. Every human being considering Synvisc should be aware that permissible levels of formaldehyde
[a known neurotoxin and carcinogen with a Health Rating: 3 - Severe (Poison)and cannot be made nonpoisonous] and Divinyl Sulfone
[the blistering agent of mustard gas] are allowed and not disclosed.


This injection poisoned me and burned through my entire nervous system. As it stands, I've come a long way thanks to the incredible dedication and extensive IV and detox treatments from my NMD. He has never wavered in seeing me through this ordeal. But I am still plagued with brain tremors and debilitating fatigue since these injection. And I am not alone. Many others have suffered and were blatantly dismissed by their injecting physicians as well.

It's a sad state of health affairs when pharmaceutical companies are so powerful that the welfare and lives of individuals mean absolutely NOTHING. On Feb 20, 2008 the US Supreme court voted 8:1
to protect the manufacturers of medical devices from ANY liability if the FDA deems the device "safe". Yet Synvisc and other viscosupplementations break 2 of the 4 criteria for Medical Device classification. 1) it metabolizes and 2) it causes a chemical change. This classification also means that the metabolic by-product is NOT KNOWN. This classification allows Synvisc on the market without a REMEDY when it goes systemic and causes problems like poisoning and pharma injury. How does this happen? MONEY...follow the money.

Read through the extensive information on this blog BEFORE you consent. The least I can do is warn others so they don't SUFFER hardships like too many of us have. I wish someone would've INFORMED me.