My friend Keesha wrote this to me after the night I wrote about Central Pain. I thought it was so poignant.
Central Pain Syndrome.
I see your words.
I hear you.
It is true. Just as I have found there is no way to reach the deep roots of Central Pain, there are no words to describe it. The waters run too deep.
For the same reason, I sit here at 12:33 a.m. I am sorry this is the life we are in--but remember you are not alone.
See her blog at www.chiarian.blogspot.com. Learn about Arnold Chiari Malformation, Ehlers Danlos Syndrome, Tethered Cord and other related conditions. And send up a prayer for her, too!