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06-16-2015, 12:57 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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06-16-2015, 07:26 PM | #2 | ||
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06-17-2015, 10:06 AM | #3 | ||
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One consequence of this work is that it allows clinical trials to be more effective. By taking the PD subtype into account you reduce one level of uncertainty.
The next step is to find out whether the subtypes have different causation and require different treatment. As they say in the paper, we need to understand, and this must be the PD word of the day, "clinicopathophysiologic" clustering of PD! John
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Born 1955. Diagnosed PD 2005. Meds 2010-Nov 2016: Stalevo(75 mg) x 4, ropinirole xl 16 mg, rasagiline 1 mg Current meds: Stalevo(75 mg) x 5, ropinirole xl 8 mg, rasagiline 1 mg |
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"Thanks for this!" says: | dilmar (06-19-2015) |
06-19-2015, 06:33 PM | #4 | |||
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Here is an earlier article which gives a review of other classification systems that have been developed. I wonder what system will become the standard of the future. http://www.medscape.com/viewarticle/781510
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"We don't see things as they are, we see them as we are." Anais Nin. |
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"Thanks for this!" says: | GerryW (06-19-2015) |
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