tag:blogger.com,1999:blog-22576999.post116077097834769527..comments2024-03-16T10:39:00.522-04:00Comments on Live With ME/CFS: A Sense of PerspectiveSue Jacksonhttp://www.blogger.com/profile/14532098225905355332noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-22576999.post-1161592444930104072006-10-23T04:34:00.000-04:002006-10-23T04:34:00.000-04:00Yeah whenever CFIDS gets me really down (which I a...Yeah whenever CFIDS gets me really down (which I admit is far too frequently) my way of coping is to stop and list all of the things I'm grateful for. Not that it minimizes what this disease does and takes from us, but it's a nice reminder that there's good stuff too. And seeing what other people struggle with, whether it be greater disability or greater poverty, is a way to even out all the messages I see every day of people living lives I can't. I guess it's the whole yin and yang thing. ;)<BR/><BR/>Oh and glad to hear Dr. Rowe is able to work with you!Michelle https://www.blogger.com/profile/05759387306193137795noreply@blogger.comtag:blogger.com,1999:blog-22576999.post-1161146025276120472006-10-18T00:33:00.000-04:002006-10-18T00:33:00.000-04:00Sue,not everyone would come away from that experie...Sue,<BR/>not everyone would come away from that experience with a feeling of gratitude for what they do have in their life. good for you and thank you for sharing your story.Mary Annehttps://www.blogger.com/profile/15941689051872189415noreply@blogger.com