Looking forward to attending @investinmeresearch.bsky.social ME Conference in Cambridge on May 29th.
Excited to hear about all of the latest scientific research towards finding treatments.
Will be rattling the tin there to bring in some more funds for M.E
Www.justgiving.com/mikeseumarathons
04.03.2026 08:54
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Redirecting...
Starting my 11th year running marathons for @investinmeresearch.bsky.social
Update here: www.facebook.com/share/p/1By2...
14.01.2026 18:16
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Thanks mate 👍
07.10.2025 09:57
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Mike Harley - EU Marathons for ME - SKopje October 2025
Thanks to Mike Harley for another outstanding effort to raise funds to facilitate biomedical research into #MECFS
at the Skopje Marathon 2025
www.justgiving.com/fundraising/...
#philanthropy #research #CofEforME #InvestinMEresearch @mikeseumarathons.bsky.social
05.10.2025 14:52
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Dark blue background with image of DNA helix. At the top of the DecodeME ‘the results’ logo. Two spotlights shine on a speech bubble that says ‘Initial DNA results’. To the right of this is an image of a research paper. At the bottom of the graphic it says ‘Wednesday 7pm BST’.
The initial DNA results from DecodeME are coming this week! We will release them on our website on Wednesday 6th August at 7pm (approx).
We're letting you know the timing in advance so you can pace beforehand.
Thank you to our participants & supporters.
04.08.2025 17:23
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#SevereMEWeek
05.08.2025 21:10
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Severe ME - World ME Alliance
Understanding severe ME by the world ME alliance
“Severe and very severe ME/CFS represents one of the most profound states of disability found in medicine.”
– @batemanhornecenter.bsky.social , USA
worldmealliance.org/what-is-me/s...
#ME/Cfs #pwME #SevereME #SevereMEDay #ICDG93.3 #ICDG93.32
04.08.2025 18:35
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2 months until Skopje Marathon 🇲🇰
I'm very undercooked. August and September are big months, hope my stupid legs will hold out!
If you'd like to sponsor me ad edge closer to a cure for M.E
www.justgiving.com/mikeseumarathons
05.08.2025 18:38
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It’s #MEawarenesshour. I’m tweeting in the hope that if more people are aware of M.E. and the way it devastates lives, more effort and funding will be allocated to investigating and searching for answers. We need an agreed, objective diagnostic test for detailed clinical trials.
02.07.2025 19:01
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Had a 2-3 week break and now back in training.
Next one for me is Skopje Marathon, North Macedonia 🇲🇰
Marathon 38, country 34 and I'm likely to reach 10,000 miles.
It looks like a beautiful country. If anybody knows of anyone with M.E there please let me know, I'd love to meet/interview them.
27.05.2025 18:15
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Flying out to Northern Ireland today for Belfast Marathon. Looking forward to meeting Joan from the ME association there for dinner
Country 33, £51,189 raised so far @investinmeresearch.bsky.social
Weather looks good for the run, just hope my knee holds up.
www.justgiving.com/mikeseumarathons
02.05.2025 06:40
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Delighted that there's now a more accurate figure of people with ME in the UK (404,000) for the media to use.
Obviously bittersweet, as that is still a huge number of people in daily pain, ignored and with no treatments to recover.
23.04.2025 20:04
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Northern Ireland
14.04.2025
M.E in Northern Ireland
'Too many people have already suffered disastrous consequences from harmful and outdated advice. Patients in the UK have died of malnutrition as a result of inadequate care and services'
www.mikeseumarathons.eu/northern-ire...
22.04.2025 18:43
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Northern Ireland
14.04.2025
M.E in Northern Ireland
'There's no ME specialist, no ME clinics, no care pathway for severe ME... It is incomprehensible that so many patients are left without anything'
I'll be running for Richard and Aileen at Belfast Marathon on May 4th.
www.mikeseumarathons.eu/northern-ire...
15.04.2025 12:23
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Taxing UK Billionaires 1-2% more a year would bring in more than any of this proposed nonsense.
My feeling is that it will be watered down via debate and protests to the point of just sitting as a mild deterrent for people trying to cheat the system.
18.03.2025 18:52
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If the government actually committed proper funding for ME and Long Covid research they wouldn't need to target disabled people.
There'd be hundreds of thousands of people actively in the workforce.
18.03.2025 18:47
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Up to £51k for @investinmeresearch.bsky.social 🙏
Cheers all.
28.02.2025 22:49
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I've had #ME for 38 years, nothing has changed in that time, no care, treatments or funding for biomedical research
It's an appalling record for everyone who's had a responsibly to implement change for #pwME over decades
#FundThePlan @ashleydaltonmp.bsky.social &
@rthonwesstreeting.bsky.social
25.02.2025 14:24
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Translating Research into Diagnostics and Treatments image for #IIMEC17
Registration for our 17th International ME Conference is open
investinme.org/IIMEC17.shtml
#mecfs #IIMEC17 #BRMEC14 #IMECW2025 #research #CPD
25.02.2025 17:07
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Loving reminder that when you read posts from me or anyone w/ #MyalgicEncephalomyelitis:
We're among those #pwME (persons w/ M.E.) who have the strength to post.
People w/ #SevereME mostly exist in dark rooms, unable to move or to tolerate light or sound.
It's a hellish existence.
We need help
25.02.2025 18:46
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Thanks bud 👍
25.02.2025 22:35
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200 miles done, 250 to go until Belfast Marathon (May 4th).
Am creaking but ready to attack the training plan.
£50,948 raised so far for @investinmeresearch.bsky.social
www.justgiving.com/mikeseumarathons
25.02.2025 22:25
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