Parkinson's Disease Tulip


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Old 07-10-2007, 02:16 PM #1
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Default tested all three links and they all opened fine

Quote:
Originally Posted by made it up View Post
I totally agree regarding the value of exercise.
It definitely helps me feel less symptomatic and I wish I'd started it sooner.
Couldn't access the websites you mentioned though.
Like to know what EECP and blood modulation therapy is if you have time to reply.
Thanks,
Lee
tested all three links and they all opened fine.

As regards the other options mentioned:

oogle)eecp = enhanced external counterpulsation, a cardiac therapy which proved to improve pd symptoms:



(Google)Acceleration therapeutics = back and forth moving bed

(Google)Blood modulation therapy -BPM- = See-saw moving bed
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Old 08-25-2007, 11:49 AM #2
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http://www.scielo.br/scielo.php?scri...lng=en&nrm=iso

High doses of riboflavin and the elimination of dietary red meat promote the recovery of some motor functions in Parkinson's disease patient

Abstract
Introduction
Patients and Methods
Results
Discussion
References
Acknowledgments
Correspondence and Footnotes

Abstract

Abnormal riboflavin status in the absence of a dietary deficiency was detected in 31 consecutive outpatients with Parkinson's disease (PD), while the classical determinants of homocysteine levels (B6, folic acid, and B12) were usually within normal limits. In contrast, only 3 of 10 consecutive outpatients with dementia without previous stroke had abnormal riboflavin status. The data for 12 patients who did not complete 6 months of therapy or did not comply with the proposed treatment paradigm were excluded from analysis. Nineteen PD patients (8 males and 11 females, mean age ± SD = 66.2 ± 8.6 years; 3, 3, 2, 5, and 6 patients in Hoehn and Yahr stages I to V) received riboflavin orally (30 mg every 8 h) plus their usual symptomatic medications and all red meat was eliminated from their diet. After 1 month the riboflavin status of the patients was normalized from 106.4 ± 34.9 to 179.2 ± 23 ng/ml (N = 9). Motor capacity was measured by a modification of the scoring system of Hoehn and Yahr, which reports motor capacity as percent. All 19 patients who completed 6 months of treatment showed improved motor capacity during the first three months and most reached a plateau while 5/19 continued to improve in the 3- to 6-month interval. Their average motor capacity increased from 44 to 71% after 6 months, increasing significantly every month compared with their own pretreatment status (P < 0.001, Wilcoxon signed rank test). Discontinuation of riboflavin for several days did not impair motor capacity and yellowish urine was the only side effect observed. The data show that the proposed treatment improves the clinical condition of PD patients. Riboflavin-sensitive mechanisms involved in PD may include glutathione depletion, cumulative mitochondrial DNA mutations, disturbed mitochondrial protein complexes, and abnormal iron metabolism. More studies are required to identify the mechanisms involved.
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Old 08-16-2008, 03:18 PM #3
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Default stem cell treatments

I'm new here and I dont know if you talked about it in the past - stem cell treatment.
what about treat PD with stem cells?
I just start to read about it, and I find this success stories at the frc-family research council.


what you think ?
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Old 07-14-2014, 10:28 AM #4
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Thumbs up Stem cell tx

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Originally Posted by cris View Post
I'm new here and I dont know if you talked about it in the past - stem cell treatment.
what about treat PD with stem cells?
I just start to read about it, and I find this success stories at the frc-family research council.


what you think ?
Hi Chris, I just received stem cell treatment for pd. they say it takes 2months to really kick in. It's only been 6 days, but at least I'm no worse. See Facebook group called "adult stem cell therapy not embryonic," and stemcellpioneers.com and linked in group called "adult stem cell advocates."
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Old 07-28-2014, 08:54 PM #5
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Hi Owlish, this is my first post on this forum. I'm very interested in more information on your stem cell treatment. First of all how are you doing since the treatment? Under what circumstances did you receive these stem cells, clinical trial or other circumstance. Where did you travel to for treatment and what was. e cost?
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Old 07-28-2014, 08:59 PM #6
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I wasn't done posting and something happened but anyway I'd like to know the cost and where these cells were injected, I'm assuming your brain. Any details you'd like to share I'd appreciate. Do you feel any results? I know it's probably too early. Thank you.
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Old 04-09-2015, 06:49 PM #7
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Hello, I received a fetal stem cell tx a few years ago and saw very little improvement. I am going to try adult stem cell tx in a few months, and will post shortly after. As a side not, be careful dealing with a Dr Paneri, all he did was take my money and sent no products. Take care
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Old 04-09-2015, 08:16 PM #8
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Originally Posted by drtom80 View Post
Hello, I received a fetal stem cell tx a few years ago and saw very little improvement. I am going to try adult stem cell tx in a few months, and will post shortly after. As a side not, be careful dealing with a Dr Paneri, all he did was take my money and sent no products. Take care
Hello Dr Tom and welcome to Neurotalk...
May I ask if your fetel stem cell tx was human cells or animal?
I did an adult stem cell tx in Oct 2013, derived from adipose. I received 500 million cells. It didn't help my movement problems, (or maybe it did? perhaps I'd be worse?) but it definitely helped improve my energy levels. Best of luck to you!
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Betsy859 (04-20-2015)
Old 04-20-2015, 12:49 AM #9
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Quote:
Originally Posted by drtom80 View Post
Hello, I received a fetal stem cell tx a few years ago and saw very little improvement. I am going to try adult stem cell tx in a few months, and will post shortly after. As a side not, be careful dealing with a Dr Paneri, all he did was take my money and sent no products. Take care
Drtom, thank you for your input I'll be interested in the stem cell treatment you are getting. Where is this being done and by whom? Cost?
Best of luck wishing you the best.
Betsy
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Old 03-28-2009, 09:39 AM #10
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Default Parkinson ear implants

Hi
Any experiences in using dr Werth¨s ear implant acupuncture
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