i have rsd in the brain,the ‘master switch’ has been fooled into thinking
it is supposed to send pain signals everywhere,MY doctors, including
Stanfords best,have never told me i have dependant rsd,or
’independant’,they just told me that 0.3% of people like me do not take
thier lives. I FLAT refuse to chicken out, or feel sorry for myself,nor
allow myself to be put into a ‘coma’ by some doctor in mexico,i saw a girl
at stanford med cntr who had ALLOWED her foot to contract,because she wanted
attention by being in a wheelchair,and get medical mariuanna,what a waste.
It sounds like you need better doctors,who support you,you sound
depressed,and that is the WORST thing you can allow of yourself,you need
to fight,everyone has medical problems,i now have a spinal cord
stimulator, and am on the right meds. I have to fight the constant
contractions in my back,legs,hands, and feet…so what. You should qualify
for housing help,and medical care,and unlike me,social security,and or help
rom hospice like programs that help shut-ins. YOUR LIFE QUALITY IS NOW UP TO
YOU-
On Dec 15, 2007 4:05 PM, whitney c rsds-cpt6997@lists.careplace.com wrote: