There was such a wonderful response to my posting of Jennie Spotilla's article series on Post-Exertional Malaise last week! Glad you found her articles as valuable and informative as I did.
Jennie let me know over the weekend that there was a fourth article that I missed, so here's a link to the full 4-part series on Post-Exertional Malaise.
(And, yes, please feel free to link from your own blog or share with your friends and family).
I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. Our younger son fully recovered after 10 years of mild illness. Our older son still has ME/CFS and also has Lyme disease plus two other tick infections. This blog is about how our family lives with chronic illness, with a focus on improving our conditions and enjoying our lives in spite of these challenges.
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