Robert Saunders (aka McMullen)
banner
roberthmcmullen.bsky.social
Robert Saunders (aka McMullen)
@roberthmcmullen.bsky.social
Author of "stranger and stranger”, letter writer, advocate and fundraiser for biomedical ME/CFS research.
Reposted by Robert Saunders (aka McMullen)
Interested in ME/CFS research?
Want to do a PhD with @aryback.bsky.social, @avakhamseh.bsky.social, @sjoerdvbeentjes.bsky.social & @cgatist.bsky.social?
Then apply for a *funded* Future Medicine PhD Fellowship.
See: www.findaphd.com/phds/project...
Please contact us to discuss before applying.
Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh on FindAPhD.com
PhD Project - Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh, listed on FindAPhD.com
www.findaphd.com
October 28, 2025 at 8:27 PM
Refreshingly progressive letter in today’s Times: www.thetimes.com/comment/lett...
November 6, 2025 at 1:19 PM
Reposted by Robert Saunders (aka McMullen)
New Trial By Error Interview--with Irish psychologist Brian Hughes @bmhughes.bsky.social --

Links:
crowdfund.berkeley.edu/project/47768
&
www.youtube.com/watch?v=0K75...

Screenshot is latest update David Tuller @davetuller1.bsky.social has sent out by email to previous donors.

#MEcfs #LongCovid
November 4, 2025 at 8:12 PM
Reposted by Robert Saunders (aka McMullen)
"Graded exercise" is neither supported by evidence nor recommended for people with an illness defined by worsening with exercise. #mecfs #longcovid www.medscape.com/viewarticle/...
No Evidence Supports Using Graded Exercise for ME/CFS
Studies examining the effects of activity-based interventions haven’t required post-exertional malaise as a core criterion for the now-termed ‘myalgic encephalomyelitis/chronic fatigue syndrome.’
www.medscape.com
October 31, 2025 at 1:18 PM
Reposted by Robert Saunders (aka McMullen)
Want to join our amazing team for a PhD in ME/CFS research as part of a funded Future Medicine PhD Fellowship?
See: www.findaphd.com/phds/project...
We offer: Exciting and rigorous science, PPI, truly interdisciplinary and fantastic research culture!

Please contact us to discuss before applying!
Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh on FindAPhD.com
PhD Project - Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh, listed on FindAPhD.com
www.findaphd.com
October 28, 2025 at 11:23 PM
Reposted by Robert Saunders (aka McMullen)
🧵
Thanks very much to my good friend, Orla Ní Chomhraí, for bravely giving a 6-minute talk about my #MECFS story & work to a crowd of 470 people at the Belvedere College (past pupils’) Union dinner on Friday where I was presented with the Social Justice award.

#PwME @irishmecfsassoc.bsky.social
1/
October 24, 2025 at 7:53 PM
“Grief sits heavily indeed when it must be stared full in the face, day after day. But joy, conversely, soars high in a life stripped bare. How intense is the beauty of the sky or a spring flower when days are bleak.”

Another beautifully written blog by @naomiwhitt.bsky.social
On Gratitude and Grief
Through many years living with severe illness, I’ve come to know a lot about emotions.  From the sorrow and regret of a life lived so differently to anything that might have been chosen; to th…
alifehidden.com
October 25, 2025 at 12:12 PM
@georgemonbiot.bsky.social I’m sure you will be delighted to learn that Dame Clare Gerada, Lady Wessley, has been appointed to the House of Lords. Judging by the responses to the congratulatory RCGP post on X she appears to be nearly as unpopular with drs as she is with ME/CFS patients.
October 24, 2025 at 2:38 PM
Reposted by Robert Saunders (aka McMullen)
For the first time, Berkeley's Trial By Error crowdfunding campaign has reached 50% of the goal right at the 15-day half-way point. Most times, it's at about a third at this point. If you'd like to donate, here's the link:
crowdfund.berkeley.edu/project/47768
David Tuller's Trial by Error Fall 2025
Help UC Berkeley raise $68,000 for the project: David Tuller's Trial by Error Fall 2025. Your gift will make a difference!
crowdfund.berkeley.edu
October 23, 2025 at 10:45 AM
Poignant sequel to Rilke’s poem The Panther by Veronica Ashenhurst who has severe ME/CFS: www.westtrestlereview.com/wtr_septembe...
Rilke's Panther Befriends Me by Veronica Ashenhurst
Now, the cat soars through rooms of sky, roars at stars, and recalls old years of midnight hunts. He springs his unbound will, and comes to condole with me. I can see his paws, claws withdrawn like sw...
www.westtrestlereview.com
October 17, 2025 at 1:39 PM
October 15, 2025 at 5:35 PM
Reposted by Robert Saunders (aka McMullen)
1) We’ve just published our second instalment on the DecodeME results, this timing zooming in on the genes associated with ME/CFS.
October 13, 2025 at 8:58 AM
Reposted by Robert Saunders (aka McMullen)
1) Another interesting interview of Prof Chris Ponting by David Tuller.

They talked about PRIME, a new 4-year project that will provide an infrastructure to accelerate ME/CFS research. It received 0.8 million in funding from the Medical Research Council (MRC).
October 14, 2025 at 8:37 AM
Reposted by Robert Saunders (aka McMullen)
Our 2025 Big Survey is now open! 🎉

For more information, our FAQs, and to take part, head to our web page: www.actionforme.org.uk/research-campaigns/our-research-work/big-survey/

Thank you for supporting our research💙

🤝in collaboration with
@durhamimh.bsky.social @kacheston.bsky.social
October 13, 2025 at 10:19 AM
A rare October wheelchair outing yesterday. Wakehust was magical in the autumn sunshine.
October 10, 2025 at 12:40 PM
Reposted by Robert Saunders (aka McMullen)
The research used to claim reliability of a ME/CFS blood test has important limitations, shown here.

www.theguardian.com/society/2025...
October 8, 2025 at 6:39 AM
Reposted by Robert Saunders (aka McMullen)
7) Here’s the link to our article:
DecodeME: the biggest ME/CFS study ever - ME/CFS Science
The first results of DecodeME are in, the largest research project ever undertaken on myalgicContinue readingDecodeME: the biggest ME/CFS study ever
mecfsscience.org
October 4, 2025 at 8:28 AM
Reposted by Robert Saunders (aka McMullen)
1) We’ve written an article about the DecodeME results: what the study measured, what the results show, and why its findings are important.
October 4, 2025 at 8:27 AM
The big issue of the day: fewer or less than half of children? www.thetimes.com/comment/colu...

@susiedent.com please can you adjudicate?
September 13, 2025 at 3:08 PM
Reposted by Robert Saunders (aka McMullen)
ME Research UK and the ME Association are excited to announce funding to Dr Fatima Labeed and Dr Jackie Cliff to develop a diagnostic test for ME/CFS, expanding on their initial study showing electrical differences in blood cells from people with ME/CFS. 

https://meassociation.org.uk/wohx

#MECFS
Research: Second-Phase Funding to Advance the Development of a Diagnostic Test for ME/CFS - The ME Association
The ME Association and ME Research UK are excited to […]
meassociation.org.uk
September 10, 2025 at 1:04 PM
In 2023 I unsuccessful nominated Tom for an honorary degree at Trinity College Dublin with the support of numerous scientists, organisations and others. (Details here: www.s4me.info/threads/tom-...)

Delighted that Tom has now been honoured by the Belvedere Union. Hugely well-deserved 💪 🥳
September 3, 2025 at 12:55 PM
Reposted by Robert Saunders (aka McMullen)
Prof Chris Ponting, lead author of DecodeME: “It is clear that ME is not a research priority for this UK government ... We have to asked the question of them: Why is ME not a priority when all these other diseases have been and are?“

Why is that @rthonwesstreeting.bsky.social?
August 15, 2025 at 12:53 AM
Prof Chris Ponting, lead author of DecodeME: “It is clear that ME is not a research priority for this UK government ... We have to asked the question of them: Why is ME not a priority when all these other diseases have been and are?“

Why is that @rthonwesstreeting.bsky.social?
August 15, 2025 at 12:53 AM
Reposted by Robert Saunders (aka McMullen)
Sometimes the historical dictionary offers solace through the existence of an obsolete word that is sorely needed now. One of them is ‘respair’, recorded just once, in the 15th century. It means fresh hope, and a recovery from despair.
July 26, 2025 at 8:59 AM
Reposted by Robert Saunders (aka McMullen)
"DecodeME is now calling on researchers worldwide to join us in accelerating ME/CFS research.” - Prof Chris Ponting (DecodeME Investigator).

We encourage researchers to explore and build on our findings. Apply for access to our rich dataset now shorturl.at/F8aOM
August 12, 2025 at 10:11 AM