Potential Targets for ME/CFS Clinical Trials This week showcased Bateman Horne Center’s strategic plan in action. The new research published in two separate papers in the prestigious journal, Cell Host & Microbe, provided further evidence that the microbiome and...
BHC News
News Release: Microbiome Disturbances in ME/CFS
Signature microbiome disturbances in ME/CFS may point to biomarker and treatment trials New research reveals differences in the gut microbiomes of people with myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS) compared to those of healthy controls. ME/CFS is...
22 Years of Illness: A Perspective on Gratitude
If you are reading this, congratulations! You have survived another day. And that’s something when you’re living with or supporting someone with diseases like myalgic encephalomyelitis, fibromyalgia, long Covid, POTS, mast cell activation syndrome, and similarly complicated fatiguing illnesses. (Even listing them is exhausting!)
Dr. Bateman on Biomarkers and Wild Socks
In January 2016, I cut my hair and started wearing wild socks, vowing to do so until we had a biomarker. It must have worked [!] because in 2017 BHC was included in two of the three National Institutes of Health (NIH)-funded ME/CFS Collaborative Centers grants...
The Germiest Place on Earth
The fatigue began at the top of my head and rolled down my body, as if I’d been standing under a cold shower. I felt flushed, chilled, achy, and unsteady on my feet. I had to lean against the display case of the cupcake shop, hoping my son wouldn’t notice. We were on...
Everyone Deserves Informed Medical Care
Season’s Greetings to all Our Friends of the Bateman Horne Center (BHC). As you may know, our fundraising theme this year is, “Everyone deserves informed medical care.” This is BHC’s message of inspiration that started with Dr. Bateman and has been adopted by every...
Research Participant Data Integration
Over the past 5 years, 285 of you have participated in an NIH-funded research study at Bateman Horne Center! This study was led by The Jackson Laboratory (JAX), one of the three ME/CFS Collaborative Research Centers funded by the NIH. BHC was the Clinical Core for JAX...
Community Helps Me Live Better with Fibromyalgia
I felt like a normal mom. I had three girls, so I was busy, but I still liked to hike, bike, run and go for walks. I had finished my bachelor’s degree and considered getting a master’s when my youngest started school. I kept up my teaching certificate in the meantime....
From My Dream Medical Job to Life with ME/CFS
Before I got ME/CFS I was a women's health nurse practitioner working in a busy practice. I had spent years of education preparing for this dream job: two bachelor's degrees in biology and nursing and two master's degrees in philosophy of science and nursing. I loved...
Josie’s Story
I was only 11 years old when I got ME/CFS and my life changed forever. Before ME, I was a normal, happy kid. I loved going to school and got straight A’s. I was that crazy kid who couldn’t wait for school to restart after a break. I also loved music. I played the...
My 36-Year Journey with ME/CFS and FM
Prior to becoming sick, I worked a variety of jobs including an orthodontic receptionist, dental assistant, massage therapist, yoga instructor, answering service operator, waitress, cleaner, and costume jewelry designer and maker. I loved riding my ten-speed bicycle...
The Day My Life Changed
After high school, I attended and graduated from a class in machinist training through NASA. I worked for multiple machine shops throughout the years and ultimately became a journeyman machinist, CNC milling/CNC lathe programmer. In the late 1990s/early 2000s I...