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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Wednesday, May 27, 2009
Isolation and CFS
Just wanted to share this wonderful essay on isolation and CFS:
Yes, thank you so much! Great article and great website.
I have completed my page for my website, but I haven't linked it in yet. You can preview it at www.chronic-fatigue-community.com/chronic-fatigue-syndrome-activist.html . Please let me know if you would like me to make any changes or corrections before it goes "live!" Thank you for allowing me to include this wonderful information!
Gosh, her site is really worth a visit. Thanks for this.
ReplyDeleteYes, thank you so much! Great article and great website.
ReplyDeleteI have completed my page for my website, but I haven't linked it in yet. You can preview it at www.chronic-fatigue-community.com/chronic-fatigue-syndrome-activist.html . Please let me know if you would like me to make any changes or corrections before it goes "live!" Thank you for allowing me to include this wonderful information!
This is a great article and I like her website too. Looks like some good info is out there for us.
ReplyDeleteThanks for sharing it with us.
This was very moving. Thanks for posting the link.
ReplyDelete