In my opinion it would be much better to put patients in touch with support groups, either face-to-face or online, for their particular ailments. When I collapsed with ME back in 1989 and no one knew anything about it, I found details of the ME Association in the back of a book on ME that a friend gave me, who in turn put me in touch with a local support group. It saved me, no other way to put it! We all helped each other, and instead of feeling a freak with a weird freak illness, I could share with others who understood.
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