Went today to my primary care physician and talked about LDN. She had never heard of it, and initially told me no. We talked about it for a few minutes, she asked me why I was interested, and I told her what I knew and thought. The problem is that with no clinical trials there is no reason for her to prescribe something that has no connect to Multiple Sclerosis. I understand that, I don't like it, but I understand. She agreed to do a little research and get back to me, that's fair. I know life isn't fair, I guess I was just hoping for a break. I suppose I can always hold out for cyclophosphamide to come available, after it has its clinical trials? What's 5 or 10 more years?
As a side note, I just saw a piece on the tube about the mating habits of voles. It seems there are 2 types of voles, one is monogamous, the other isn't. They have been doing studies of the voles habits for years to figure out why human males stray. I was down in the dumps when I got home from the doctor today, imagine how I feel knowing a voles sex life is more important then my health!
As a side note, I just saw a piece on the tube about the mating habits of voles. It seems there are 2 types of voles, one is monogamous, the other isn't. They have been doing studies of the voles habits for years to figure out why human males stray. I was down in the dumps when I got home from the doctor today, imagine how I feel knowing a voles sex life is more important then my health!