The Bateman Horne Center is a medical center of excellence for people with ME/CFS, Long COVID, fibromyalgia, post-viral illness, and comorbid conditions.
Bateman Horne Center
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☕ Join us Wed, June 10 at 10:00 am MDT
Section 4.7 Management of PEM
This session will explore pacing, energy conservation, symptom tracking, supportive interventions, and individualized routines that may help support symptom stability and reduce PEM crashes.
Register: https://bit.ly/3JCHAFq
Education begins with listening.
Created by @pillowwriters.bsky.social, “What Is Myalgic Encephalomyelitis Like?” shares firsthand patient and caregiver experiences living with ME/CFS. Bateman Horne Center was honored to write the book and chapter forewords.
Available now on Amazon.
Living with chronic illness can bring anxiety, uncertainty, and fear. 💙
Join us June 2 at 1 PM MDT for our virtual support group:
Coping with Anxiety Amidst Chronic Disease
Participants can engage however feels comfortable. Loved ones welcome.
Register here: https://batemanhornecenter.org/events/
Our most-viewed YouTube video last month is worth another look.
"What is ME/CFS?" breaks down the core symptoms of ME/CFS, including PEM, cognitive impairment, unrefreshing sleep, and orthostatic intolerance.
Watch now: bit.ly/4fNwHhG
Been told your orthostatic testing was "normal," but standing still makes you feel worse?
Orthostatic intolerance is broader than POTS. Our latest blog explores emerging research, diagnostic gaps, and why "no POTS" doesn't always mean "no dysautonomia."
Read blog: https://bit.ly/4egSlcU
June Events 💙
Coffee with a Clinician
June 10: Section 4.7 Management of PEM
Support Groups
June 2: Coping with Anxiety Amidst Chronic Disease
June 16: My Illness is Real and So Am I-Successfully Facing Invalidation, Prejudice and Discrimination
https://batemanhornecenter.org/events/
Medical Terms, Explained
Biomarkers are measurable signs in the body that can help diagnose, monitor, or understand disease.
Researchers are actively studying potential biomarkers for ME/CFS and Long COVID, but no single biomarker is currently used to confirm ME/CFS.
https://bit.ly/4jScKFu
After developing Long COVID in 2020, Christy was later diagnosed with ME/CFS and other complex chronic conditions. Her story is a reminder that adapting to illness doesn't mean losing who you are, it means discovering new ways to move forward. 💙
#LongCOVID #MECFS
New research estimates nearly 4 million U.S. adults are living with Long COVID that significantly limits daily activity.
The study found Long COVID’s disability burden is comparable to Alzheimer’s disease and asthma.
Read study: https://www.nature.com/articles/s43856-026-01516-7
