Our son is 25. He has been complaining of many of the CFS symptoms since 2007. He was able to graduate from college in 2008. But his symptoms rapidly worsened and he was forced to come back home to live. We have been to many doctors in town as well as flying to drs. far from home. No one has said he has CFS but based on what we've read about it, we are slowly beginning to accept that that's what he has. It's very difficult for me (his mom) to watch him go through this. Sometimes I feel most anxious about his future. Several medicines have been suggested and I am wondering what our next step should be...
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Demonstrations in San Francisco Dec 9th and Washington D.C. Dec 10th
Blog entry posted by dixielab, Jan 6, 2011.