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ME/CFS San Diego
@mecfssd.bsky.social
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.
New study finds LC patients who meet ME/CFS criteria show two distinct patterns. The small cohort means these differences could reflect sex or ME/CFS subtypes. Study suggests LC+ME/CFS is not biologically uniform and future trials may need stratification. www.sciencedirect.com/science/arti...
Integrated immune, hormonal, and transcriptomic profiling reveals sex-specific dysregulation in long COVID patients with ME/CFS
Long COVID (LC) manifests with sex-specific differences, particularly in those with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Our s…
www.sciencedirect.com
November 23, 2025 at 6:49 PM
A new brain imaging study shows that chronic energy metabolism and neuroinflammatory abnormalities are detectable in GWI patients only with short echo time MRS. Future ME/CFS research may need short echo time MRS to reveal brain energy abnormalities. www.nature.com/articles/s41...
November 22, 2025 at 8:32 PM
Join the LC-REVITALIZE Long COVID Study!

Adults 18–65 with persistent Long COVID can participate in San Diego ([email protected]
| 619-324-8677) or 7 other global sites. 6 months, 8 visits, FDA-approved drugs tested. Reimbursement provided.

clinicaltrials.gov/study/NCT069...
November 21, 2025 at 8:50 PM
www.nature.com/articles/s41... maps 8 Long COVID subgroups over 15 months in 3,659 US adults (RECOVER cohort):
* 5% persistently high symptoms
* 12% relapsing/remitting
* 14% worsen after 3 months
Among those with Long COVID at 3 months: 46% stayed ill, 35% fluctuated, 19% improved.
Long COVID trajectories in the prospectively followed RECOVER-Adult US cohort - Nature Communications
Long COVID has heterogeneous presentation and clinical trajectories are not well defined. Here, the authors define trajectories using data from a prospective cohort study in the United States involvin...
www.nature.com
November 21, 2025 at 8:17 PM
Federal funding bill update:
Medicare telehealth extended until 1/31/2026
NIH & health agencies funded at last year's levels
Community Health Centers & workforce programs funded

Missing:
No permanent telehealth reform
No new ME/CFS research funding
ACA tax credits not included
November 14, 2025 at 11:53 PM
Important SNAP Update for ME/CFS – Nov 2025:
USDA ordered states to undo full SNAP payments. Partial benefits are valid; full payments may be disputed. The ME/CFS community urgently needs stable SNAP, affordable ACA coverage, and reliable telehealth. Contact legislators: www.usa.gov/elected-offi...
November 9, 2025 at 10:53 PM
ME/CFS virus study: www.medrxiv.org/content/10.1...
. Varicella-Zoster Virus (VZV) found in 6 of 17 patients, none in controls. Limitations: only plasma and DNA tested, small sample size, may miss latent/reactivating viruses.
November 9, 2025 at 10:01 PM
COVID vaccination may cut the risk of long COVID in teens by over a third.
* 36% lower risk in vaccinated 12–17 year-olds
* Severe symptoms also reduced
Even if infection occurs, recent vaccination offers protection.
www.cidrap.umn.edu/covid-19/cov...
COVID vaccination cuts risk of long-term symptoms in teens by over a third, data suggest
www.cidrap.umn.edu
November 6, 2025 at 1:27 AM
ME/CFS is awful—but our community is kind of amazing. Our researchers, clinicians & advocates work together like no other, wearing many hats & fighting fiercely to improve patients’ lives. 💙
www.facebook.com/whitneydafoe...
Whitney Dafoe
One Thing ☝️ Did you know that all the best ME/CFS researchers in the world - for example, every single researcher at Ron’s recent Working Group Meeting - every researcher there said they don’t care....
www.facebook.com
November 6, 2025 at 1:04 AM
@BatemanHorne's November Support Groups offer safe, understanding spaces for people with ME/CFS, IACCs, & loved ones.
Nov 11: Denial, Resistance & Gaslighting: batemanhornecenter.zoom.us/meeting/regi...
Nov 18: Acquainted with Grief: batemanhornecenter.zoom.us/meeting/regi...
November 6, 2025 at 12:53 AM
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
November 3, 2025 at 10:47 PM
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
October 22, 2025 at 9:08 PM
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
October 17, 2025 at 9:38 PM
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
October 16, 2025 at 12:32 AM
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
October 15, 2025 at 7:31 PM
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
October 8, 2025 at 7:59 PM
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 8, 2025 at 7:04 PM
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...
October 7, 2025 at 2:59 AM
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
October 7, 2025 at 2:45 AM
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
October 5, 2025 at 3:49 PM
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...
October 2, 2025 at 6:15 PM
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...
September 18, 2025 at 8:42 PM
Dr. Alain Moreau study, with Montreal, Uppsala & @openmedf.bsky.social computational biology team, finds haptoglobin (Hp) drops after exertion in ME/CFS, linked to worse PEM & cognitive issues. Genetic Hp variants influence symptom severity. translational-medicine.biomedcentral.com/articles/10....
Haptoglobin phenotypes and structural variants associate with post-exertional malaise and cognitive dysfunction in myalgic encephalomyelitis - Journal of Translational Medicine
Background Myalgic encephalomyelitis (ME) is a chronic, multisystem illness characterized by post-exertional malaise (PEM) and cognitive dysfunction, yet the molecular mechanisms driving these hallmar...
translational-medicine.biomedcentral.com
September 17, 2025 at 7:09 AM
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...
September 16, 2025 at 9:15 PM