Recently on the news, we heard that the medical profession and the MS Society turned down the "liberation" treatment that is now available to patients with multiple sclerosis. They will not even consider trials, which tells me there is no interest in helping MS people have a better quality of life. How sick is that?

In one breath they say more testing is needed. In the next, it's "No, we won't try Dr. Paolo Zamboni's findings."

We took our granddaughter to Costa Rica and she had marvellous results. Each week, she seems to be more excited because she's getting her life back.

She's walking now, seeing better, etc.

I would like to know if the medical community and MS Society have followed any of these patients around with a new life.

Maybe they should get off their butts and do this kind of research because what they are doing is ignoring the help that is there. We don't know if this is a cure but we do know there are blockages in the veins that, when opened, all are in way better health than before.