MICHAEL H started this petition to Collaborative Medicinal
Development and 1 other
IMMEDIATE MEDICAL BREAKTHROUGH ALERT:
“ALS” (aka Amytrophic Lateral Sclerosis, aka “Lou Gherig’s Disease”) is a terminal, progressive, and utterly devastating disease that eventually causes death in 100% of diagnosed cases, occurring on average between 3 to 5 years after diagnosis. About 6 in every 100,000 people contract the disease across the world.
ALS causes the motor neurons in the human body to fail completely, thus leaving sufferers 100% paralyzed, unable to care for themselves, and immobile until death. For the first time in history, a compound exists that has shown “remarkable” progress in halting progression of this evil, insidious disease.
In 2014, a currently available drug that has already been proven to be safe in humans, and which is already FDA approved and used as a “contrast dye” in PET scans called “CuATSM” was theorized for use as a treatment in ALS by amateur biologist Dr. Joseph Beckman from the Linus Pauling Institue (LPI).
The reason that CuATSM works so well to treat ALS is because it has the unique ability to pass the “blood brain barrier” in several minutes, which heretofore had been the major obstacle in treating ALS and other neurological disorders. “CuATSM” delivers a missing copper molecule directly to misfolded proteins right where the help is needed- in the spinal canal and the brain.
More recently, and after further investigations over the last 3 years, a company in Australia just completed a traditional, devastatingly slow “double blind placebo” Phase one “safety study” on CuATSM as a treatment for ALS in humans, and to determine appropriate dosing levels. Needless to say, these results were labeled as a “remarkable breakthrough” by everybody involved with the compound.
In fact, the compound CuATSM worked so well in this first study that it was able to demonstrate a remarkable 70% reduction in the speed of progression of ALS symptoms. Needless to say, this potential result is BEYOND incredible, and represents the first time in history that any drug or treatment for ALS has shown such promise.
We the people afflicted with ALS hereby request immediate access to the currently available drug “CuATSM”, within the guidelines of current FDA “compassionate use” laws. We the people who are suffering from ALS will not stand idly by and die quietly for two more years while irreplaceable time is wasted by more unethical, cruel, “placebo”based trials that employ human beings like test animals – when a drug exists right now that could literally change the world!
There is simply no time to waste. We must force people with access to the drug to do the right thing. People currently afflicted with ALS are already “terminal” in nature, have nothing to lose, are in VAST agreement in this effort, and the fact that a currently FDA approved drug that IS ALREADY AVAILABLE IN THE USA means that people in dire need of help could slow down the progression of their disease- TODAY.
PLEASE JOIN ME IN THIS CRUCIAL FIGHT. For the very first time in history, a drug exists that has shown a REMARKABLE ability to slow ALS. It also holds great promise for Parkinson’s, Alzheimers, and other “incurable” neurological conditions.
WE DEMAND THE RIGHT TO TRY THIS DRUG IMMEDIATELY, WITHOUT DELAY.