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01-23-2014, 12:28 PM | #1 | |||
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Born 1948. Diagnosed 2011. DBS ON 7/17. Taking cd/ld 200 MG at 6 am, 9 am, 12 pm, 3 pm, 6 pm and 9 pm. Finasteride 5 mg, Life Extension Mix and Once-Daily Health Booster, Mitochondrial Energy Optimizer with BioPQQ, Optimized Curcumin (longvida), Triple Action Cruciferous Vegetable Extract with Resveratrol, Vectomega-3, Vit D3 5000U,Lithium orotate 5 mg, AMPK Activator, Kefiran, N-Acetyl-L- Cysteine (NAC), Tri-Magnesium, Advanced NeuroPro, Duozyme, Palmitoylethanolamide (PEA) Updated 9/21/17. |
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01-23-2014, 01:48 PM | #2 | ||
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Quote:
Your research looks very promising. As it did in 2009. As it did in 2011. And here we are in 2014. What has been happening with this line of research in the past 5 years? Shortage of volunteers? I think Parkies would fall over each other to sign up for a drug-free treatment. Shortage of money? Well, did you try all the usual suspects and then make a public appeal? Electrical stimulation would not be patentable or profitable to the existing drug empire? From the year 2009: http://neurotalk.psychcentral.com/sh...guel+Nicolelis From the year 2011 http://neurotalk.psychcentral.com/sh...guel+Nicolelis Will we hear about this again in another 5 years? If you are facing roadblocks, alert the Parkinson Archipelago, so at least they will know what they are missing. |
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01-23-2014, 08:56 PM | #3 | |||
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Junior Member
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Bob Dawson, what you say is so sad, but true. I have friends who are depending on research for their recovery. How can this ever happen if people profit more from research than from cures? I don't put much faith in research results ever reaching us in this lifetime. But that won't stop me from recovering!
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