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I have been in email communication with someone in Australia who has  
been on their therapy for 5 weeks and this is her progress so far.
see email at end.

  I have started the therapy with my husband for a week now, and he   
has stopped feeling depresssed has more energy and has now today only  
woke up once in the night. His balance and walking is the same, has  
not gotten worse and he has been on a hour walk each day where as  
before he was only able to walk for 15 minutes..

I spoke to a practictioner in NYC yesterday who said she was
working with one person who has not gotten an worse since she started
the therapy.

There are many people on their web site whose case studies they report
This is the email I got from the women in Australia last week.
> I have been on the FSR treatment now for only five weeks and I feel  
> so much better and family and friends (most of whom were pressuring  
> me to go on  the medication rather than see me suffer) have  
> commented on how very much improved I am.
> But it is imperative that your husband stop taking the drug now and  
> that you or  a practitioner commence the FSR.  I felt better from  
> the very first treatment.
> I  did have 4 sessions of acupuncture the month before I started  
> and that helped.  The reason I did that is because I could not find  
> anyone in Australia (where I live) to perform  the FSR for me,  
> until one of my friends said she would give it a  try.  I live  
> alone so I was very grateful for her offer.  We were both amazed  
> at  the difference after just one treatment and she had no experience.
> However, if anyone has been taking the drugs for  more than four  
> weeks the patient will have to stay on the medication for ever as I  
> understand it.


Nancy cg of Leigh 81 diag  pd 80 ( 1 month ago).
On Oct 2, 2005, at 2:31 AM, M.Schild wrote:

>> Parkinson's research, what if they are going down the wrong alley  
>> as the
>> pdrecovery.org thinks? They finance their own research and are  
>> getting
>> recoveries.
>>
>
>
> so they claim but do you know anyone who has recovered from PD  
> through their
> scheme?  Claiming results is easy but why donīt we hear about them?
>
> In the same department, you can go to:
> http://www.parkinsons-success.com
>
> If PD doesnīt attracct money for real research it certainly attracts
> charlatans
> Maryse cg John 76,16
>
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