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Hi! I’m I’m Lindah from Sweden. I’m new here so haven’t really figured out what this is all about.

I've recently got diagnosed with RRMS and I've stumbled across some information about HSCT. I was wondering if there any people here who have had the treatment, their experience with it and if you'd recommend it. I'm considering asking my specialist about it, I'm interested in the treatment if it's ...

Hi Everyone. I'm from the US looking into the cost of HSCT in different countries. How much does it cost in England?

Just an update in 2017 I had a stem cell transplant at Hammersmith hospital in London, after a resent consultation with my neurologist and MRI scan there are no new lesions to be seen. Seems to be doing the job fingers crossed it will stay like that.

Year post!!good news no new lessons and old one get smaller!Hard year….but monster it’s holds for now!!!!

Hi guys, I've just been diagnosed with RRMS last week after previously having a clinically isolated syndrome about a year prior. I feel I've got off pretty lightly so far (numb left foot and pins and needles in my fingers) but I've been reading up on treatments etc. The MS nurse is currently recom...

Hey all, Massive gratitude to the NHS and the wonderful Neurologist Prof. Gavin Giovannani. I experienced a particularly bad relapse of my MS in early September and was called into the Royal London for a consultation with Mr Giovannani the following day. (Last drug was Lematrada) Once he’d assessed...

My birthday wish has come true, I should be having HSCT this year!! although it is over the Christmas period, I am still so grateful to be having it. LETS GOOOO

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 ...

Hello just wondering if anyone had hsct and what your experience was like