Does anyone have a form letter they have sent doctors (locally) to seek treatment for CCSVI? I am going to try to spread word around western/central Pennsylvania more than I have been to get others the help they need (MS prevalence is pretty high here). I have a letter I wrote - that I think is pretty good ... but want to know what others have sent so I can compare what I said.
Also is there a way we could link all the relevant research to show doctors here (research and presentations and protocols)?
Could we make this a sticky ... so that it doesn't get lost in the shuffle of the hundreds of posts daily? I tried finding them, but I'm just not good at this website.