
Re: A question for the the Prostatitis Foundation
From my "Boss Man:" (Just kidding, the guys who run this are some great folks!)
To the forum.
At this time we are not aware of any other organized group doing coordinated research like the MAPP Research Network is doing. That does not mean there are not any, We need any country that may have such a system to report it to the forum. We have read the reports here about the interest in a possible East London advocacy group forming. We hope that happens. Every country needs an advocacy group to promote research for the cause and cure for prostatitis.
There are plenty of individual doctors and Universities pursuing their own ideas and research around the world.
We have information about a Dr. Saada Patrick in Paris who is now working at the Society Guevalt who says he has had success with massage.
We have some information from Karl Monahan in London who maintains a guide to Physical therapists around the world. Always under review and construction he says.
www.thepelvicpainclinic.co.ukWE have an abstract about: Organism Causing Urinary Tract Infection with Special reference to Saphylococcus saprophyticus. Lead author is Amar C. Sajjan. They close by saying that “ The study showed predominance of Saphylococcus saprophyticus in sexually active young women.
WE will be investigating all these things to see if we can get any of their published articles and permission to print them.