The US Action Working Group - a powerful group of ME/CFS advocates that recently came together to build a strong voice for change - send a list of question to the NIH regarding the Clinical Center study. It's a list that demonstrates the commitment and expertise found in this group. I am part of the group but did not put together the list. Looking at it I'm astonished at its breadth!
It's attached to this post.
It's attached to this post.