Hi,

I'm new to this group. I've had ME/CFS (this seems to be the new
acronym) for about 16 years. I've lived in SF for 14 years.

I was wondering if anyone knew of a primary care doc at Kaiser who
was actually interested in CFS. I'm assuming that they don't exist or
won't admit to it, but Sharon (who told me about this group) suggested
I ask. I've got a non Kaiser CFS doc, Eric Gordon, but he's not nearby
and it would help to have someone at Kaiser who actually cared.

Also, I'm in the Stanford Valcyte trial if anyone is curious
about it. I have a hunch I'm on the placebo, but it's a blinded study
so I can't be absolutely certain.

michael