My feet have been feeling as if they are on fire, does anyone else have this issue and if so what do you do about it.
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Recently I've had to start using catheter at home because I've been diagnosed with a neurogenic bladder due to my advancing MS. Does anyone else have this problem? Looking for a friend.
Just read this article and so can relate. MS is a robber grabber! If I go out I have to deal with getting tired or if it's hot - forget it! It's just easier to stay home, turn on the AC, and lie down in bed - REPEAT... Such is the story of my life!