Read more blogs from our MS community
I was 15 years old when I was diagnosed with MS, though in hindsight my problems started even before that, when I had optic neuritis aged 13.
My work life has changed immeasurably over the past couple of years as my MS has changed from relapsing to secondary progressive.
Us MSers often know what it is like to miss out on social occasions. But to suddenly be told we have to stay in thanks to COVID-19 is a whole other ball game.
Multiple Sclerosis Society. Registered charity nos 1139257 / SC041990. Registered as a limited company in England and Wales 07451571
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