There’s nothing like starting the new year with a new possibility. Following failures by scores of other researchers, Ian Lipkin and his new Serochip technology recently fingered the culprit behind the acute flaccid myeltis (AFM) outbreak that’s been...
The fact that ME/CFS is a mystery doesn’t daunt the leader of the NIH’s big intramural study on ME/CFS at all. Just a couple of years ago Avindra Nath and his compatriots cracked a mysterious neurodegenerative disease in East Africa that researchers had...
It’s always hard to lose a loved one, but the deaths in ME/CFS seem particularly hard. They tend to be quite painful, they often take place in the midst of a non-supportive medical system, and they’re a complete mystery. With no seeming way out it’s...
The Solve ME/CFS Initiative’s Ramsay Awards are small grants (@$50K – only in the medical field is 50K small) but potentially mighty grants. They are designed to give researchers the funding to produce pilot data needed to get really big grants – the...
As we know, grant applications in chronic fatigue syndrome (ME/CFS) are hard to come by. Freedom of Information Requests indicate that the NIH received the lowest number of ME/CFS grant applications in memory last year – just 15. Since the NIH spends MUCH more...
“The bottom line is that we should rethink this whole area and encourage proper clinical trials.” Dr. Nancy Klimas This article is the last of a three-part series on IVIG which came out of my attending the 2018 Dysautonomia Conference in Nashville, Tennessee. An IVIG...
