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or Dermatomyositis: Big
My name is Diane I was on the NPF Psoriasis chat the other night
[January 23]. If you remember,
I mentioned my son Travis who is 27 and has about 65% coverage with this
stuff. It began about 10 years
ago. I think it was psoriasis
diagnosed in the beginning on his scalp, but later the docs said it was
dermatomyositis and he was losing muscle mass.
With Prednisone that condition got 98% better but his skin has
He responds to all of
this off and on because of his age I guess.
Right now he is being fairly responsive, is going to a new Doc and
is taking MTX and using Dovonex. I
guess when he is responsive I go searching for whatever help I can find,
which isn't much.
Travis and I live in
Southern Indiana and we know of no support groups here.
Travis is pretty much isolated.
He has a decent job with a great prescription plan and works on his
cutesy truck. Not much social
life beyond that.
Any conversation would
be appreciated. Thanks
in advance, -Diane U.
I looked up dermatomyositis at WebMD.com
and was appropriately horrified by the effects of this collagen disease. From
a variety of symptoms that point to the onset of the disease are fever,
loss of weight, skin lesions, and aching muscles. As the disease
progresses there may be loss of the use of the arms and legs.
lingering P seems not-so-serious in light of the awful consequences of
Travis continues to respond well to MTX; he and I are in that boat
together, for the moment.
when you feel like it, Diane, and I encourage you to continue frequenting
the NPF online chat area. Our
scheduled chat in January, about coping with P, was enjoyable.
I was delighted NPF invited me, I learned a lot.
Stay in touch. -Ed