Unfortunately we do not get many postings to this board. I cannot imagine why, as there are a lot of Polio survivors out there. This should be a good place to share important health information. We have PPS looming over our heads and need all the information and networking skills going for us. I am no source for current information, but maybe between the two of us we can get going. There was an article on CNN about Post Polio Syndrom and you can locate it on www.CNN.com.
It has the National PPS information. I have not been able to find a local physician who will even acknowleges the problem. I was so very fortunate not to have lasting impairments from my bought with polio, but who knows what is coming now? I think you and I need to start with a good physician who is current with the PPS situation. Then we need to find a support group local to our areas. We also need to find out what if any medical trials, tests, studies for PPS ect. are available/ongoing. We are not done with this fight, unfortunately we may be entering a new phase. Good luck and good health to you. Memaa
[This message has been edited by moderator1 (edited 05-04-2003).]