New for Me and My Loved Ones
Last updated: June 2023
I was diagnosed with MS June 1st 2013.
Since then, I seem to be the only one who is doing my research. I still have a million questions. It seems I get a new symptom once a week. The dizziness, the pain, the itching, the headaches.
All I am told is from my family "suck it up". I wonder if they had MS and knew what I am going through, they would have a different attitude. I'm still trying to deal with this.
Now I am scared that I am getting depressed!!!!!
I don't know what to do.
What does advocacy mean to you as someone living with multiple sclerosis? Please select all that apply: