ME/CFS San Diego
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mecfssd.bsky.social
ME/CFS San Diego
@mecfssd.bsky.social
1.5K followers 41 following 240 posts
ME/CFS San Diego, a 501c3 public charity, is working locally to raise awareness of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), to help educate healthcare workers and researchers, to increase access and support for ME/CFS patients.
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Scripps Research is enrolling participants in a remote long COVID trial testing tirzepatide. Must be 18 or older, live in the US, and have medical documentation of long COVID. Info and webinar registration: longcovid.scripps.edu/locitt-t/
LoCITT-T - Long COVID Treatment Trial
The Long COVID Treatment Trial-Tirzepatide (LoCITT-T) is investigating the efficacy of repurposing this drug to treat Long COVID.
longcovid.scripps.edu
Attention #UCSD students! Enter the 2nd Annual ME/CFS Essay Contest hosted by @MECFSSanDiego! Share your ideas about a future where people with ME/CFS can truly thrive. Prizes, publication opportunities & more! Deadline: 12/31/25

Details & entry: bit.ly/mecfsSDessay
The 2025 Stanford Community Symposium on the Molecular Basis of ME/CFS is now available on YouTube.

Researchers from Stanford, Harvard, DecodeME & more share new findings on metabolism, imaging, treatment, and immunity.

📺 Watch here: www.youtube.com/playlist?lis...
Community Symposium on the Molecular Basis of ME/CFS 2025 - YouTube
Community Symposium on the Molecular Basis of ME/CFS September 5, 2025, hosted by Stanford University and Ron Davis
www.youtube.com
New from Nature: Scientists are learning to fix faulty mitochondrial DNA, offering hope for rare genetic diseases.

While not specific to #MECFS, it's a big step for understanding energy metabolism, something long suspected to play a role in ME/CFS.
🔗 www.nature.com/articles/d41...
Faulty mitochondria cause deadly diseases: fixing them is about to get a lot easier
CRISPR-based tools can’t easily access the DNA in these organelles, but researchers are finding other ways in.
www.nature.com
Two big RTHM updates that could help ME/CFS & long COVID care:

Their AI platform is now live and free: www.rthm.com

Selected for Mayo Clinic’s Platform_Accelerate, a program helping startups validate and scale AI health tools
Launch event: us06web.zoom.us/webinar/regi...
RTHM - Expert Virtual Care for Long COVID, ME/CFS, POTS, and MCAS
Get accessible, evidence-based virtual care for Long COVID, ME/CFS, POTS, and MCAS. Expert clinicians, personalized treatment plans, and free health tracking tools.
www.rthm.com
DePaul University is running a second survey to help develop a tool to assess Post-Exertional Malaise (PEM) in ME/CFS.
Open to adults 18+ globally both those with PEM AND healthy controls.
Takes ~10–15 mins. www.dsqpem2.com
Researchers at UEA & Oxford BioDynamics have developed a potential blood test for #MECFS with 96% diagnostic accuracy (92% sensitivity, 98% specificity). Early days, but could be a breakthrough. More validation needed.
www.uea.ac.uk/about/news/a...
October Support Groups @batemanhornecenter.bsky.social for ME/CFS, Long COVID, and related conditions

Oct 14 1pm MDT Navigating the Complex Healthcare Industry
batemanhornecenter.zoom.us/meeting/regi...

Oct 21 1pm MDT Parenting with Chronic Illness
batemanhornecenter.zoom.us/meeting/regi...
Coffee with a Clinician: new free series from Bateman Horne Center
Next session: Navigating Clinical Uncertainty
Oct 8, 10 AM MDT
For ME/CFS, Long COVID, IACCs
Register: batemanhornecenter.zoom.us/meeting/regi...

Will be recorded
Today’s the LAST DAY of ME/CFS San Diego’s Days of Giving 2025 💙

We fundraise once a year to power awareness, education & advocacy for ME/CFS.

Every share or dollar helps.

Give: www.mecfssandiego.com/support-mecf...

Watch: youtube.com/@mecfssd
This year has been especially hard for our ME/CFS San Diego team. Like many in our community, I’ve had worsening symptoms and limited capacity. So we’re keeping our annual fundraiser simple.
If you’re able, please support: www.mecfssandiego.com/support-mecf...
ME/CFS patients face rising barriers: ACA subsidies expire in 2025, research funding reduced, Medicaid cuts loom. Urge Congress to act now: extend subsidies, protect care access, fund research.
Find your reps: www.congress.gov/members/find...
ME/CFS Patients, families, providers, and researchers are invited to take part in a global survey on case definitions and core symptoms. Help inform research and build consensus. May take ~30 mins.
Survey: redcap.is.depaul.edu/surveys/?s=P...
TOMORROW! Join @scripps.edu Dr. Benjamin Cravatt on Sept 17 for a free online talk on turning “undruggable” disease targets into treatments. Discover how chemistry is reshaping drug discovery.
4PM PT | 7PM ET
frontrow.scripps.edu/lectures/ben...
Join the NASEM virtual workshop Oct 22-23, 11am-3pm ET, on brain-body interactions & advancing brain health. Explore how brain-immune, brain-heart, & gut-brain links impact neurological & psychiatric diseases. Details: www.nationalacademies.org/event/45148_...
Sept 25 at 3PM ET: Join the #NotJustFatigue ME/CFS livestream briefing. 30 mins of research, lived experience & policy: featuring Dr. Lipkin, Ryan Prior, Elizabeth Ansell & more. Premieres video on Dr. Maureen Hanson's work.
Register: www.notjustfatiguelivestream.org
Fall 2025 COVID-19 & Flu vaccines are here. This guide, created for the ME/CFS community, outlines current access issues: state rules, insurance basics, pharmacy limits, and key resources.
www.reddit.com/r/mecfsSD/co...
Every U.S. state has a Protection & Advocacy (P&A) agency that defends the rights of people with disabilities: free, independent, and federally authorized. Find yours: acl.gov/programs/fin...
New study: fragments of Borrelia burgdorferi (Lyme bacteria) can linger in the liver for weeks, triggering immune and metabolic issues.

May explain persistent symptoms after treatment (PTLDS).

Similar mechanisms may apply to ME/CFS and Long COVID.

www.the-scientist.com/fragments-of...
Fragments of Lyme Disease Bacteria Linked to Liver Dysfunction
Cell wall components from Borrelia burgdorferi lingered in the mouse liver for weeks, suggesting new therapeutic avenues for this chronic disease.
www.the-scientist.com
Starting Sept 30, 2025, the govt will stop mailing paper checks for Social Security, SSDI & SSI. ME/CFS patients must switch to direct deposit or Direct Express to keep benefits. Call SSA: 1-800-772-1213 or visit ssa.gov
. Please share widely!
ssa.gov
From Ron Davis: Stanford ME/CFS Collaborative Research Center Community Symposium on the Molecular Basis of ME/CFS Agenda September 5, 2025 8:00am - 2:30pm 
Register: stanford.zoom.us/webinar/regi...