Anyone have Ms for years without disability?
I’m 18 and my symptoms are pretty bad. I wake up multiple times a night with numb limbs and get constant facial spasms and twitches. These symptoms occur every single day non stop. I’m scared on what will happen in my future. Anyone have any stories?
I was 16 when I was diagnosed, I'm 33 this year and still walking, horse riding, kayaking, gardening.... I can't hike anymore, but I'm still so much more physically able than I thought I would be by this age. It's hard sometimes, but there's still so much joy and love and happiness in my life ❤️ as much as I wish this wasn't the case for you, you'll 'get used' to your common symptoms - they just become part of your body (I can't remember what a "normal" body feels like!) and life will expand around them.
@Evie_Meldrum that sounds awesome!! I used to love hiking 💔 I know in the future it will get harder for me. It’s already getting hard now. But even still being able to walk is my goal. I want to be mobile and have sight throughout my whole life it’s been my goal since knowing I have Ms.