This site is designed to record the progress of living with, dealing with, and trying to understand the Invisible Disease. I hope to have post from myself, my husband, and my children on what its like as a family to live and deal with Fibromyalgia.
Friday, March 27, 2009
OK, I am back now. I took a nap then we went to see Jeff, Leatrice and family and we gave them some love. I am still feeling drained and my legs are about a 7 on a scale of 1 -10 but my brain is still clear. Going to bed
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