Does anyone on here have experience of HSCT in a case of PPMS. I have PPMS, diagnosed in 2018, and have so far received 4 Ocrevus infusions. My disability and discomfort have worsened considerably of late and am thinking of any options available to help me. HSCT costs £40,000 in Mexico, about my retained share of my ex partners house, money I might potentialy raise. A huge amount of money to waste though. Any informed opinion welcome.