One of my first posts! Explaining about my MS diagnosis almost 23 years ago and how it has progressed.
So, I was a normal 13 year old girl, attending school, making new friends following an across the sea move from Canada and basically just getting on with being a teenager.
When I couldn’t see the basketball hoop at school, I had no idea that this was the start of something really scary, life changing in fact. I just thought that I needed glasses – what other reason would there be for the hoop to look fuzzy? I must have mentioned this to my parents – cue LOADS of different tests, including one where I was able to miss school (yes!) and have electrode type things put all over my head whilst, I am guessing, the doctors looked to see what my brain was doing. I still remember sitting in the car on my way home from that appointment, picking away at the glue like stuff stuck in my hair…
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