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HERWriter (reply to Anonymous)

Thanks. I appreciate it.

Fortunately things have changed in some ways since the 90s. There is more information available, at least to those of us lucky enough to be online. Most of the change is due to the sick people talking to each other, sharing information, creating websites from their beds, etc.

A sick friend and I agreed 6 yrs ago that we just needed to "paper the internet with blogs, articles and forum and facebook posts about CFS." That is what many of us proceeded to do. 

Maybe NTs of Aspie parents might be able to find some healing and connection by doing the same. There's so little out there right now, there's no direction to go but up:)

September 16, 2015 - 7:09pm


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