One of the symptoms of MS is fatigue.
Definitely feeling that one today.
Had last date with plasma exchange. It was a bittersweet break-up but we knew it was best to discontinue.
Dad was able to come and experience some of my therapy this morning. I have been walking well with my forearm crutches, today 350 feet. These will mostly be used for around the house and short visits. I was fitted for a wheelchair and this will be used for longer distances.
I’ve received quite a few emails of hope and encouragement and stories and I thank you; I will cherish them forever! I will also respond tomorrow when possibly I’m not so tired. (:
Hope for a cure!