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UK Grant applications accepted by the Medical Research Council Projects live from 1993-94 to June 2008 All grant applications that were accepted by the Medical Research Council before the 2011 set of funding had primary investigators that were either psychiatrists or psychologists

UK Grant applications not accepted by the Medical Research Council

Research update: The relation between ME/CFS disease burden and research funding in the USA https://pubmed.ncbi.nlm.nih.gov/32568148/ Updated ME/CFS prevalence estimates reflecting post-COVID increases and associated economic costs and funding implications...

Arguably the most important time for a total is when the target is close to being reached: one doesn’t want to put in too much effort that is not required (i.e. if a target has been reached). At the moment, we are clearly a long way from reaching the target so everyone should be trying their...

Just released: The Final episode of M.E, Myself and I Episode 6: Love This is a low-budget dramatisation of the (fictional) life of a young person with ME

Good to see that they are not messing around with open-label trials as they have sometimes done in the past. This looks more useful e.g.

I saw this post on Tumblr. Despite the tags that the poster uses my guess is that the character doesn't have ME/CFS. But other people have posted chronic illness characters in this thread so I thought I might also. ----- The Strange Case of Starship Iris (@iriscasefiles) is the most wonderful...

Seems a bit odd to me that this paper only has one author and the author doesn't even live in the Netherlands.

Thursday April 20 #MEACTION GEORGIA SUPPORT CALL https://www.meaction.net/event/meaction-georgia/2023-04-20/ This free support online call is open to people around the world. 1PM EDT/6 PM in Great Britain & Ireland Find the time in your time zone here...

Executive Summary Page for MPs A summary of the work of UK charity Invest in ME Research and researchers in Norwich Research Park in developing a UK/European Centre of Excellence for Myalgic Encephalomyelitis (ME or ME/CFS 1) by facilitating and initiating world class research...

ME/CFS and post-exertional-malaise among patients with Long COVID. https://faculti.net/me-cfs-and-post-exertional-malaise-among-patients-with-long-covid/ Recording of a talk by Prof Jason. Looks like requires free registration.

I haven't listened myself. Fresh RB Podcast: Everyday People, Talking Health. Episode 43 **TW: Mentions Attempting Suicide** ME Association 651 subscribers 41 views 4 Apr 2023 #PVFS #MECFS #COVID19 Fresh RB Podcast: Everyday People Talking Health: Getting To Know ME - Accepting &...

Do we know the current service has biomedical doctors or indeed many hours allocated for any sort of qualified doctors? This relates to the past: I think last time I heard it was headed by a psychologist?

I think I’m right in saying she has had ME.

#Raspberries4MECFS Social Challenge to support the work of Dr. Alain Moreau's RAman SPectroscopy BiomarkER-Based DiscoverY (RASPBERRY) & Dr Morten...

Turns out it is also to fund Dr Morten's research. I will adjust the heading.

Here's information from the account. Well done and thanks to them for trying: Severe ME/CFS patient. Cannot speak. Bedridden. Stranger things have worked. I remember there was the chilli challenge for ME which raised quite a lot.

Saturday, April 15 ME CAREGIVER SUPPORT CALL https://www.meaction.net/event/me-caregiver-support-call/2023-04-15/ 3:30 PM EDT (US)/8:30 PM in Great Britain & Ireland Find the time in your time zone here: https://www.meaction.net/event/me-caregiver-support-call/2023-04-15/ ======= Please join...

#Raspberries4MECFS Social Challenge to support the work of Dr. Alain Moreau's RAman SPectroscopy BiomarkER-Based DiscoverY (RASPBERRY) & Dr Morten...