Andrea Fighting for #MECFS Diagnostic Biomarkers
banner
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/
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
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/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
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
What's interesting is that #MECFS blood is banned in 5 countries. The psychologization of #MECFS has deep origins in the UK - yet the NHS has taken care to ban blood donation from "every single name of ME/CFS in use". But isn't funding a blood screen to screen the blood supply.
November 27, 2024 at 6:52 AM
Renaming #MECFS either through new viral or bacterial outbreaks or because of regulatory capture has been a long tradition. Before it was M.E. It was Icelandic disease. It's Tapanui flu in New Zealand. Now it's LongCovid.
Divide the patients with new name and definitions.
Hide the dataset.
November 27, 2024 at 6:45 AM
Are your donor dollars supporting #MECFS orgs that prioritize your priorities?
CEO Linda Tannenbaum started
Open Medicine Foundation in order to find a diagnostic blood test for ME/CFS so that patients could be diagnosed earlier and with accuracy.
www.omf.ngo?form=TGN2024
#MECFS #MillionsMissing
November 18, 2024 at 4:34 AM
#MECFS Self-care
Setting up scheduled e-cards to myself on particularly bad grief anniversaries with positive messaging
(ie. last time I saw my Dad in person, remembrances for family members we've lost that I never got to grieve properly, last time I was outside, last time I took a shower)
November 12, 2024 at 11:40 AM
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
October 27, 2024 at 11:02 AM
tinyurl.com/PleaseInterv...

"Right now, on the heels of the Maeve Boothby O'Neill Inquest, Karen Gordon and Carla Naoum are being psychologized and mistreated in UK hospitals because of prejudice against #MECFS and prejudice against women in medicine. "
#SaveCarlasLife #SaveKarenGordon #pwME
October 23, 2024 at 12:02 PM