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The European Polio Union group gathered informally and began to unite all the European country Post Polio group leaders and advocates at a conference in Italy in 2007.They have become stronger and…Continue
Started this discussion. Last reply by L1z H1ncks Mar 4, 2012.
Here is the link to an article about the Rotary and Bill Gates efforts to eradicate polio through vaccines being unreachable. …Continue
Started this discussion. Last reply by Janice Cootey Mar 18, 2011.
I found a WATSU message therapst several years ago or I should say she found me through a referral from PPSers that take a specia-needs aquatic therapy class every week at a local County swimming…Continue
Started this discussion. Last reply by Barbara Angelica Crowe Nov 22, 2010.
Yesterday, our Miami Post Polio Support group (Post Polio Assn. of South Florida) met at the University of Miami Miller School of Medicine and enjoyed the second of four seminars that the new…Continue
Started this discussion. Last reply by Stella Newall Feb 19, 2010.
L1z H1ncks replied to Barbara Gratzke's discussion Anyone want abstracts of what speakers at the European Polio Union conference covered?
Helen Brown replied to Barbara Gratzke's discussion Anyone want abstracts of what speakers at the European Polio Union conference covered?
Barbara Gratzke posted a discussion
John Noble left a comment for Barbara Gratzke
Barbara Gratzke replied to JAMES E DAVIS JR's discussion An email I sent to a well known polio support organization.
Barbara Gratzke left a comment for John Noble
Barbara Gratzke left a comment for Barb O
Barbara Gratzke replied to Vee S's discussion Polio and normal growth
Barbara Gratzke replied to L1z H1ncks's discussion Congrats to Lisa Zion!!
Michele Marsh joined Barbara Gratzke's group
Vee S replied to Barbara Gratzke's discussion Dr. Bruno's post on Rotary Eradication Effort versus monies needed to find cure for polio and PPS
Barbara Gratzke posted a discussion
John Noble said… Hi Barb
Thanks for the warm welcome. Not sure if we know each other? I was just diagnosed last week. I had surgery and woke up with all the PPS anesthesia symptoms. 2 and a half weeks of hell. Lower leg spasms in the middle of the night with extreme pain. Doctors couldn't stop them or the pain. Finally found a Neurologist that gave me Baclofen that worked. I need surgery asap. I'm walking around with a stent in my ureter and stones in my kidney. Need to get the stone blasted. I think I may have found some PPS Doctors in Albany NY. Hope they can do surgery w/o the side effects. Found some info about PPS Dr Bruno and a great youtube video about the PPS. Never knew I had polio til just a couple months ago when talking to y brother about remembering being real sick and wearing braces on my legs. He said I had polio. WOW The more I find out about the PPS the more the puzzle unfolds.
sheila bayard said… Hi Barbara,
Since the streets in NY have become treacherous, I'm spending more time
on the computer, and learned how to navigate a little better, and found your
message. Strongly thinking about coming to Florida now, despite protests from my children who live near me here. My husband also still works, soooooo,
we will see. Sorry about the debackle ( or whatever you would call it) with
the chats on iipso, just when I had learned of them. Can't anyone else do them?
I don't think Professor Mike is anyone who will ever change his mind.
Anyway, hope you are well. I am continuing my downward slide, but not too
bad. Getting around with a walker.
YVONNE ELLANOR ISAACSON said…
Liliana Marasco Garrido said…
Liliana Marasco Garrido said… 
Cilla Webster said…
Susan Clay said… 2 members
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