HI~~~I was so thrilled to see something from PPS. I have it and am just amazed
at how our symptoms are identical. Please email me and tell me more about Dr.
Bruno's book and where I can get it. My symptoms were intensified during and
since chemo and radiation. The dr. said it was because my"Neurons" didn't
repair themselves as quickly as someone's who didn't have polio. Made sense!

I know we are fighters...and I now am forced to take life easier. I take care
of myself more than ever since learning our need to be like everyone else
doesn't matter anymore. Love you guys and want to share emails with you and
learn more. Marianne
mariannerichards@...<mailto:mariannerichards@...>
----- Original Message -----
From: Patti Gross<mailto:cobaltt72@...>
To:
bluerollersppssupport@yahoogroups.com<mailto:bluerollersppssupport@...\
om>
Sent: Thursday, September 16, 2004 11:06 AM
Subject: RE: [BlueRoller's PPS Support] new member


dear PG, wow - you are so young............ i thought polio was
erradicated (sp) by the 70's.
Dr Bruno is great. He and Dr Zimmerman are who i went to see. Please see
someone soon the pain in your leg could be anything - not nesscarily PPS.
My PPS is pain all over my body - kind of like bad case of the flu and
severe fatigue and joint and muscle pains. It pretty much makes me feel
crummy most of the time but us polios have learned how to fight thru the
pain and thats what has gotten our motor neurons all worn out. we need to "
preserve to conserve" what we have left.
get Dr brunos book - Polio Paradox and read it - it is very informative.
Do you have a appt yet? are you working? where did the polio affect you?
how did you get it in the 70s? from the vaccine?
have a apin free day,patti


>From: "pgmhpers" <pgmhpers@...<mailto:pgmhpers@...>>
>Reply-To:
bluerollersppssupport@yahoogroups.com<mailto:bluerollersppssupport@...\
om>
>To:
bluerollersppssupport@yahoogroups.com<mailto:bluerollersppssupport@...\
om>
>Subject: [BlueRoller's PPS Support] new member
>Date: Sun, 12 Sep 2004 00:21:19 -0000
>
>Hi, I am 28, had polio at 5, residing in CA. Of late, I am having
>unbearable pain in my left leg. I plan to visit Dr. Bruno and Dr.
>Julie Silver for PPS diagnosis/thearaphy. Please share any
>suggestions/thoughts, experiences you had dealing with PPS, and
>leading normal life.
>Thanks,
>-pg
>

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