I am also tired of trying to explain to my family and some friends that I cannot tolerate heat and have terrible fatigue and there is nothing I can do about it. I do not feel refreshed after my nap in the afternoon or having a good nights sleep. I am fatigued all the time and have been the entire time that I have had MS.

When I was on Avonex, everyone kept asking me if I was feeling better. I kept telling them no, the shots try to keep my MS from getting worse and do not make me feel better. I feel like crp and now have the problem with the damage to my thigh muscles and nerves to deal with.

It does get old going over this for the last 16 years but my best friends understand and know when I am fading when I am out with them. Thank heavens for best friends.