Nice idea on the Facebook page of Dr Ron Davis's new CFS Research Center:
He's just posted an answer to the first one.
https://www.facebook.com/cfsresearchcenter
Remember, he's a top-flight geneticist and not (I think) a clinician so questions should be related to research, especially genetics research.
Here's his foundation's website:
http://cfsresearchcenter.org/
His son has severe ME and is a member of this forum.
We're very lucky to have a scientist of Dr. Davis's calibre on board.
Another very worthy target for donations...
We are excited to announce that we will be starting a weekly "Ask Dr. Davis" where you can submit questions on here and we will pick one every week to have him answer! So start posting your questions! We will be posting an answer to one next week!
He's just posted an answer to the first one.
https://www.facebook.com/cfsresearchcenter
Remember, he's a top-flight geneticist and not (I think) a clinician so questions should be related to research, especially genetics research.
Here's his foundation's website:
http://cfsresearchcenter.org/
His son has severe ME and is a member of this forum.
We're very lucky to have a scientist of Dr. Davis's calibre on board.
Another very worthy target for donations...