This is fantastic to see PPS being acknowledged by these countries and what is being done for Polio survivors such as myself. Here in the U.S. you rarely see any mention of Polio and especially Post Polio Syndrome. The most difficult with PPS is finding a Doctor that believes it is a real problem for Polio survivors and being able to get treatment. I feel very fortunate to have a Doctor that has actually taken the time to do research and has been willing to prescribe various medications to try and find which ones provide the best relief for pain, muscle spasms, cramps, problems with sleeping and what I think is the worst thing of all is the fatigue and brain fog. For those last two symptoms the best relief is normally to get plenty of rest when it takes over.