Posted by Rita on 4/21/04

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Hi fellow MCS sufferers.

I tell you what gets me, over and above the fact that I
have been totally disabled by MCS,is that the medical
community: Doctors offices, labs and hospitals have no
awareness of the needs of MCS Patients' for an accomodated
environment. I find it impossible to overcome the hurdles
of perfume filled waiting rooms, offices on high floors,
no windows,cold air and in addtion medical personnel
wearing hairsprays, perfumes etc. to access much needed
medical services. What use is all this talk about ADA,
recognizing Environmental Illness as a deficit requiring
accomodation, when no one pays any attention to it?
Especially medical personnel?

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