The MonSter abroad

January 2016

Now I knew of HSCT as something new and exciting in the MS world but what I didn’t know was how good it was and how achievable it was to get.

Joining all the HSCT groups I could asking all the questions I could researching. I thought to myself, no I won’t be able to have this, no one will say yes to me. I saw that ordinary people with MS just like me were standing up and saying hold on this isn’t a cure but its near as close to it and I want a piece of that pie, and I thought yes me too I want my life back. I’ve forgotten what it was like to be normal, having a night out with my friends and not cancelling at the last minute because I wasn’t well enough. I want to see and do things like everyone else.

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