HSCT

Hi, new to this site so reading lots but keen to know if anyone has received this treatment. Been diagnosed 20+ yrs so a long story here, I’ll try and cut it short. Failed the new drug plegridy, then on tysabri for 5 yrs, loved this drug but failed it when my blood test came back high risk JC virus so moved to Ocrevus for 2 yrs. Bad reaction to this so went to London Bridge for HSCT last year. Still early days to see any recovery so struggling a bit atm, but the point of the treatment is to halt progression, so improvement is a bonus 🤞 Has anyone else gone down the HSCT route?