After diagnosis last January and my neurologist not perpepared to identify my sub type although he says it more than likely PPMS. I've decided to take the bull by horns and go for HSCT in Mexico in November. EDSS currently 3.5. I know Dr Burt and NHS health experts do not recommend HSCT for PPMS as there is no evidence to show there is any benefit. I have spoken to numerous PPMS warriors that have had treatment with positive results. So now is the time. @ms.hsct. yolo on Instagram will be my treatment diary