RSD 'N ME
Hello all,
You can also go to www.rsdhope.org and find out alot more information about this rare,not well known but most painful Neurological condition. Please find out more, if not for me, then for yourself, for your own knowledge. Thank you so much...
I am a "Mentor" for RSD people who are new with the disease. I try to help them through the hard times when things are new and confusing. Also, I have been doing a support group on facebook called "invisible diseases especially chronic pain and RSD/CRPS" . You can just put that in the search box on facebook and my group will show up. You can join if you would like to. You do not have to have RSD/CRPS to join the support group because it is also for the : education, awareness and support of this painful rare Neurological disease. Thank you so much for watching...suzannne
This is the Ribbon explaining How RSD Feels to those Who Suffer
****These are some of the pictures of the places where my RSD "flares up" most of the days....Just FYI













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