@dagamundo 

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dagamundo

1 year post HSCT tomorrow

Tomorrow is my one year post HSCT transplant. Full remission, a lesion smaller, so many improvements, working again, no more fatigue, no more DMTs! I don't come on here much, but if you want to read more about HSCT, Im on Facebook. My name is Anna Mosca....Im the one from Maine.
@Alexr76

Hi it’s great to read your story and know there maybe light at the end of the tunnel here in the UK stem cell treatments are only available if you pay(£25k ++).or free on the NHS if your case is deemed serious enough and your ms is active ,most people would really like to feel as good as you but pharmaceutical company’s won’t make money from that great to hear your doing well keep us all informed ps I don’t do fbook

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@dagamundo

@Alexr76 can you get referred to the Star MS trial? It is best available DMT vs. HSCT. Many of my friends in the UK have fundraised to go overseas for HSCT with the help of the AIMS charity. I had to fundraise to do it, as I didn't have the funds and my insurance refused as I was rejected from the BEAT MS trial here.

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