MS representation is really important
Roxy Murray from London was diagnosed with MS in 2014. She appeared in the Hope Reborn film alongside other people living with MS. Roxy shares her story and why it’s important to raise awareness of MS.
I was diagnosed with relapsing remitting MS in 2014 after having double vision and blindness in my left eye.
When I was first diagnosed I had migraines and vision problems, but now I get more weakness in my left side, fatigue and drop foot. I need to plan my days accordingly. If I do something amazing one day I’ll need a day after to rest.
Opening up about MS
It can take a long time in your MS journey to want to open up to the world – but MS representation is really important.
Lots of people don’t know what MS is, so taking part in this film was an opportunity to let people know how it can affect us day to day. It gets the message out to the wider community and society. Helping them to help us create change.
We need people to see what the face of MS really is. There’s a misconception that it’s one mould or model, but actually MS doesn’t discriminate and anyone can be affected.
Being part of the film
Working on this film was really exciting. I think Fabio’s work is incredible and it was a pleasure to be a part of this.
It was nice to be around other MSers on set and to share our stories, speak about MS and have a common ground. Bringing greater awareness of MS together, as a community, is something I love to do. It’s something I take a lot of pride in.
