Hi Everyone

I am in Colorado and there is a lady out here named Helen. She has arranged a meeting with a city council person and is pleading for funding and goverment reconigtion for MEDICAL RESEARCHH FOR RSD. There has been a lot of work done out here. She needs people with RSD to contact her and get on the database to show the need for this recognition. Her website is (rmrsd.org). The group is called Rocky Mountain RSD/CRPS. You can also contact Helen on this website and get information on this research that they are trying to get funded. I wait each and every day for the cure of RSD as I have full body centerlized for over 11 years now and to top it off I am pain medication intollorant. I can't even take colindine cream due to extreemly low blood pressure (80/60) on a good day. Does anyone know natural things that work and I am open to sudgestions.

Thanks everybody and don't forget to contact Helen as Goverment Recongnition would be a great start.

Goodnight