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@...>
>Reply-To: bluerollersppssupport@yahoogroups.com
>To: bluerollersppssupport@yahoogroups.com
>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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