My dad has sufferd with PPMS for around 5 years but it was only confirmed in febuary 2008. just as i begin to come to tirms with the fact that he was only ever going to get worse, i find out about this new treatment. It has given me hope! But am i just going to find out that like a lot of new drugs it is only avalibe if you live in certain areas. Is it just going to be another postcode lotary?