@kateee experienced MS Energy 4 years after being diagnosed with ms
What was the tipping-point that made you realise it was time to take control?
When I needed a wheelchair all the time
What adjustments did you make?
I have SPMS and so only use Sativex.I had to leave my teaching job which I miss. I am however keen to do as much as I ca
What advice would you give to someone struggling to find their MS Energy?
To not give up and think what they enjoyed before MS and there will be a way of still doing something similar