Posted by Mr. Freeze on March 22, 1997 at 14:19:53:
I have read a lot on the topic as of late, and it seems that WS is not an
accepted ailment by many physicians at this time. I found an 800 number to get
a listing of referrals of nearby doctors that will help. If there aren't any doctors
in my area(NJ), I was wondering if you could share the treatment you were
prescribed. I am assuming you were given cytomel, but how did you take it?
Is Wilson's Syndrome something you must live with the rest of your life, or
is it cured after t3 treatment? Do symptoms (low body temp., excessive sweating,
cold hands) end after treatment or do they return after you finish taking
cytomel?