Andrea Fighting for #MECFS Diagnostic Biomarkers
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mecfsnanoneedle.bsky.social
Andrea Fighting for #MECFS Diagnostic Biomarkers
@mecfsnanoneedle.bsky.social
Severe #MECFS Patient
Bedridden. No energy to speak.
#MECFSDiagnosticBiomarkers

Drug companies need a #MECFS and #LongCovid diagnostic blood test for successful clinical trials.

https://mecfsdiagnosticbiomarkers.substack.com/
Pinned
My cause is an #MECFS diagnostic blood test:

cen.acs.org/pharmaceutic...

Join me in supporting the scientists, researchers, universities, and ME/CFS organizations funding and fighting with the same goal.

#pwME #MillionsMissing #MECFSIsInTheBlood
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
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.
August 4, 2025 at 5:23 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
Isla's mother has been arrested under suspicion of causing her death from ME last year (heart failure). There was no inquest. Isla's younger sister (15), who also has ME, has been removed from the only people who understand how the disease must be managed. Imagine her fear.
#MEKills #HumanRights
July 31, 2025 at 6:45 AM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
Within a week of the plan being published, There were three petitions for people with severe ME being held against their will by the NHS. And now this mother of a child with ME being *arrested* for her death despite the harms caused by THE NHS!!!
July 31, 2025 at 1:38 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
@rthonwesstreeting.bsky.social
I can't find Ashley Dalton on here so tagging you in with total support for what you have had to do.
Hope BMA negotiations are going better.
Within a week of the plan being published, There were three petitions for people with severe ME being held against their will by the NHS. And now this mother of a child with ME being *arrested* for her death despite the harms caused by THE NHS!!!
July 31, 2025 at 1:41 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
@meactionuk.bsky.social @meactnet.bsky.social please boost on other platforms. We are scrambling for lawyers to get the sister out as the top priority. I am speaking with national print media this morning.
Isla's mother has been arrested under suspicion of causing her death from ME last year (heart failure). There was no inquest. Isla's younger sister (15), who also has ME, has been removed from the only people who understand how the disease must be managed. Imagine her fear.
#MEKills #HumanRights
July 31, 2025 at 7:11 AM
10 minute out of 65 minute interview with CEO Linda Tannenbaum on the Make Visible Podcast transcribed .

#MECFS biomarkers and the OMF BioQuest Project to find a ME/CFS Biomarker Signature/Subsets is discussed.

mecfsdiagnosticbiomarkers.substack.com/p/make-visib...
July 14, 2025 at 11:43 PM
mecfsdiagnosticbiomarkers.substack.com/p/replicated...

Replicated blood biomarkers for ME/CFS?
ME/CFS needs well-defined, quality cases stored in Biobanks

#MECFS #pwME #MillionsMissing #Biomarkers
June 26, 2025 at 12:29 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
Did you wake up with a craving for a new ME/CFS book with dozens of chapters about research methods? Well, it’s your lucky day link.springer.com/book/10.1007...
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
This book examines Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and techniques used to explore dysfunctional pathophysiology in patients.
link.springer.com
May 16, 2025 at 2:19 AM
Today is Blue Sunday for #MECFS
Support #MECFS Biomarker projects directly.
Please donate to the largest ME/CFS Biomarker study
Help make a ME/CFS diagnostic test a reality
tinyurl.com/BlueOMFBioQu...
#pwME #MillionsMissing #BlueSunday
May 18, 2025 at 8:23 AM
I have #SevereMECFS. I am bedridden. I can no longer speak.
I know that each day I am here because #Science ignores the biological and immunological underpinnings of disease in women.
Right now, I am watching a lecture series in Undergraduate Immunology by @bioprofbarker.bsky.social line by line.
February 28, 2025 at 1:32 AM
The largest #MECFS Biomarker study - BioQuest
Patient selection will be based on the Canadian Consensus Criteria (CCC) and patients will be clinically diagnosed by physicians at Harvard and Uppsala.
Read More and Donate to BioQuest #Fundraising
mecfsdiagnosticbiomarkers.substack.com
February 4, 2025 at 4:45 PM
Open Medicine Foundation BioQuest update.
OMF has raised $950,000 of the $2.4 Million dollars needed to analyze 1200 samples in the largest scale #MECFS Biomarker study
They have raised 40% of their goal.
mecfsdiagnosticbiomarkers.substack.com/p/omf-bioque...
January 30, 2025 at 8:58 PM
mecfsdiagnosticbiomarkers.substack.com/p/2025-mecfs...

Your pocket guide to potential Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) Diagnostic Blood tests
Get information on the 8 #MECFS diagnostic blood tests in development and more!

#MECFS #MyalgicEncephalomyelitis #pwME
2025: ME/CFS Diagnostic Biomarkers in Review
A ME/CFS diagnostic blood test Pocket Guide
mecfsdiagnosticbiomarkers.substack.com
January 29, 2025 at 5:30 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
Exclusive Interview by @mecfsnanoneedle.bsky.social: OMF Founder and CEO, Linda Tannenbaum, on the Large-Scale ME/CFS Biomarker Study (BioQuest)!🌟

👉 Read the interview: ow.ly/FT1i50UOFII

💙 Donate to BioQuest: ow.ly/wEHU50UOFIJ

#mecfs #mecfsbiomarker #pwME
January 28, 2025 at 3:37 PM
mecfsdiagnosticbiomarkers.substack.com/p/omf-bioque...

Open Medicine Foundation's BioQuest: Welcome to the Future

Interview with OMF's CEO Linda Tannenbaum about the largest #MECFS Biomarker Study

#MECFS #pwME #MillionsMissing #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
January 27, 2025 at 4:57 PM
67 Million people have #MECFS worldwide
#MECFS has double the disease burden of HIV with no treatments.
A diagnostic blood test would transform medicine for #MECFS patients.
Please #Donate to the largest #MECFS biomarker study
#SocialGood #Change
www.omf.ngo/me-cfs-new-b...
Announcement!!! A New Large-Scale ME/CFS Biomarker Study (BioQuest)! - Open Medicine Foundation
Learn about BioQuest, OMF's new ME/CFS biomarker study to identify a biomarker for ME/CFS that can be evaluated through a blood test.
www.omf.ngo
January 9, 2025 at 3:17 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
Worth a read
So, you may ask, why do I get so angry about the new liberal spin on RFK Jr, as in, "he gets some things right, so let's collaborate on those" or "we have to work with him because he has a huge following we need to reach"? Because I've seen this movie before. 1/
January 2, 2025 at 1:30 PM
I am excited about all the various #MECFS diagnostic blood tests in development - but my hope for 2025 is BioQuest #OMFBioQuest.
We need to focus on funding those 1200 samples!!!

www.omf.ngo/me-cfs-new-b...

@openmedf.bsky.social
Announcement!!! A New Large-Scale ME/CFS Biomarker Study (BioQuest)! - Open Medicine Foundation
Learn about BioQuest, OMF's new ME/CFS biomarker study to identify a biomarker for ME/CFS that can be evaluated through a blood test.
www.omf.ngo
December 31, 2024 at 6:27 PM
We started 2024 with 3 #MECFS diagnostic blood tests in development and we end 2024 with 7 diagnostic blood tests in various stages of development.
The most notable thing to happen is Open Medicine Foundation's BioQuest project www.omf.ngo/me-cfs-new-b.... @openmedf.bsky.social
#MECFS #pwME
December 24, 2024 at 10:02 PM
An #MECFS patient does not need professional help to move more. An #MECFS patient needs professional help to explain to friends and family that they need to move less and rest until pharmacological interventions for low ATP, T cell exhaustion and mitochondrial dysfunction are found
#MillionsMissing
December 22, 2024 at 5:31 AM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
You can have severe fatigue and cognitive dysfunction from another condition, but that doesn’t mean you have PEM. There’s way more to it and failing to acknowledge that leads to over-simplification. I can’t tell you how discouraging it is to see people get this wrong so publicly as often as they do.
December 19, 2024 at 3:29 AM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
Like, PEM isn’t a feature of other conditions. It’s something we see in ME. That’s basically it. People may *screen positive for bits and pieces* of PEM in other conditions. People may have ME *and* another condition, but it’s very important we’re clear that PEM isn’t a part of other conditions.
December 19, 2024 at 3:26 AM
The best way to help #MECFS patients right now is to donate to BioQuest.
A large-scale Biomarker study that will analyze 10,000 proteins and metabolites in 1200 samples when fully funded. It is 1/3 funded right now, let's fully fund it.

#philanthropy #fundraising

www.omf.ngo/me-cfs-new-b...
Announcement!!! A New Large-Scale ME/CFS Biomarker Study (BioQuest)! - Open Medicine Foundation
Learn about BioQuest, OMF's new ME/CFS biomarker study to identify a biomarker for ME/CFS that can be evaluated through a blood test.
www.omf.ngo
December 18, 2024 at 4:56 PM
Reposted by Andrea Fighting for #MECFS Diagnostic Biomarkers
In less than a year - Trump has gone from being a convicted felon & rapist to President Elect & Time Person of the Year

My heart is breaking for women all over the world

I think of Gisele Pelicot & everything she’s done to bring accountability to rapists. Then this happens

No wonder we’re angry
December 12, 2024 at 9:20 PM