It surprises how little effort is put into raising funds for CFS research and awareness campaigns.
It seems to me that our time would be used more efficiently if we spent it trying to raise funds to pay professional medical researchers to figure this out rather than reading medical journals and trying to become researchers ourselves.
I've only seen two fundraisers, that I can remember, in the past 5 years or so: Lipkin's microbiome study, and Bhupesh Prusty's "Something in the blood" study. Both were successful.
Why don't we see more of this?
It seems to me that our time would be used more efficiently if we spent it trying to raise funds to pay professional medical researchers to figure this out rather than reading medical journals and trying to become researchers ourselves.
I've only seen two fundraisers, that I can remember, in the past 5 years or so: Lipkin's microbiome study, and Bhupesh Prusty's "Something in the blood" study. Both were successful.
Why don't we see more of this?