New for me and my loved ones
I was diganosed 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 sympthm 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 know what i am going though they would a different attitude. Im still trying to deal with this.
Now i am scared that i am getting depressed!!!!!
I don't know what to do.
Do you live with any comorbidities aside from MS?