Needless to say, he has not addressed any of my concerns.

I have had MS for over 30 years and I'm currently taking the immune system modulator, Avonex. This is an extremely expensive drug and my insurance covers the entire cost, except for a mere $100.00 per month.

Under Obama's plan it is likely that I and many other MS patients will no longer have access to this drug, as is the case in the U.K. where the “rationing board”, the National Institute for Health and Clinical Excellence, or NICE, determines the medical necessity of many drugs and medical procedures.

I hope the Heritage Foundation addresses this concern in its discussions with the various Congressional leaders involved in the Health “Care” Reform deliberations.

I fear that if I am unable to remain on this vital medication, the MS will progress to the point that I will be wheelchair bound for the rest of my life.