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Do you do tai chi in addition to meds ?  

Sent from my iPhone

> On Oct 6, 2013, at 2:11 PM, Sharon <[log in to unmask]> wrote:
> 
> i have been doing tai chi and it really does make a big difference in balance.  if you try just be careful to get a class for beginners or you will be lost and lose interest.  my class is at YWCA
> ----- Original Message ----- From: "Rayilyn Brown" <[log in to unmask]>
> To: <[log in to unmask]>
> Sent: Tuesday, October 01, 2013 2:18 PM
> Subject: Re: So many questions
> 
> 
>> welcome Michael, you should be able to find some answers here
>> 
>> -----Original Message----- From: Michael Tentis
>> Sent: Monday, September 30, 2013 3:56 PM
>> To: [log in to unmask]
>> Subject: So many questions
>> 
>> Hi
>> I'm newly diagnosed. New to group. Has anyone tried acupuncture? Tai Chi? Qigong? Marijuana?
>> Is moderate alcohol use ok? I'd appreciate all feedback.
>> 
>> Michael
>> Sent from my iphone.
>> 
>>> On Sep 30, 2013, at 4:38 AM, Rayilyn Brown <[log in to unmask]> wrote:
>>> 
>>> no hallucinations? it seems that when meds help t hey poop  out over time or have  bad sides
>>> 
>>> -----Original Message----- From: Nic Marais
>>> Sent: Monday, September 30, 2013 2:20 AM
>>> To: [log in to unmask]
>>> Subject: Re: MJ fOX meds
>>> 
>>> I'm not sure, but I think MJF also started taking Amantadine lately.
>>> 
>>> Three years ago I could hardly walk in a shopping mall WITH a walking
>>> frame, and a wheelchair was glowing in the very near future.
>>> 
>>> Then I started taking 2 X 100mg Amantadine daily, and we stored the
>>> wheelchair AND the walking frame!
>>> 
>>> All my symptoms improved significantly for at least two years, and is only
>>> lately becoming a big burden again.
>>> 
>>> Nic 61/19
>>> 
>>> 
>>> 
>>> 
>>>> On 30 September 2013 05:35, Rayilyn Brown <[log in to unmask]> wrote:
>>>> 
>>>> Does anyone know what meds Fox is taking that allow him to return to TV
>>>> after 20+ years with PD?
>>>> 
>>>> The articles I’ve found don’t say.
>>>> 
>>>> I haven’t seen his new show but my PD friend in Flagstaff tells me he is
>>>> seen running up stairs.
>>>> 
>>>> I think this and Mt. Everest climbs give the public a false impression of
>>>> the reality of PD for those of us over 10  years into PD.  The public likes
>>>> the  “positive” view, but I don’t see happy endings in our future.
>>>> 
>>>> What do you  think?
>>>> 
>>>> Ray
>>>> Rayilyn Brown
>>>> Past Director AZNPF
>>>> Arizona Chapter National Parkinson Foundation
>>>> 
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