Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
i have found the tingles.. sides of face, hands,
lower back running hip to hip, seat, calfs and
feet were my first symptoms. they became part
of me one area at a time and so far permanent..
the tingle is so much more fun then when they
decide pain is the plan for today..
but ...what felt like a high pressure squirt gun filled with
hot or cold water hitting the back of legs and back of
biceps either 1 of the spots or all 4 at the same time
was a very strange sensation. i put my hand on the spot
looking around fully expecting to find one of my kids thinking
it was funny to squirt mom.. only to find no one was close..
that i an happy to say, i have not had to deal with in quite awhile.
gotta grin
gotta smile
gotta laugh!!
Take care Mak!
^_^
My neuro told me that I have 'residual damage' to my feet - that is, that the MS has permanently affected my feet.
It feels like sparklers going off in my feet.
I'm used to it now and assume that until someone discovered how to repair myelin I am stuck with it.