Donate to the Bateman Horne Center Capacity Campaign – Wings to Fly!

Share on facebook
Share on twitter
Share on email

Wings-FBArt.jpgOur Destination: We want to bring ME/CFS and Fibromyalgia into the mainstream, ensuring ready diagnosis, effective treatments, and wide reaching empathy and understanding.

Our Pathway: Biomarkers will improve diagnosis and treatment and put us on the pathway to a cure. Biomarkers are a critical first step and their discovery will dramatically increase the rate of progress overall. 
The Bateman Horne Center is a unique example of an independent non-profit integrative health center where medical care informs research, and research informs medical care; we are uniquely positioned to create collaborations between amazing, well-qualified patients and stellar research partners – an important component to progress. We have an urgent need to increase our capacity to see patients and grow our research program.
As exciting and innovative research takes flight, investigators are seeking access to our Research Ready Army more and more. Yet due to physical and personnel capacity restrictions, too many patients are on waiting list and even more turned away. Medical assistants and research associates are doubled up in offices; there is no more room for the equipment needed to expand our research efforts.
We have secured a new, larger facility but require the funding needed to expand our critical work. Every gift, of any size, is an investment in:

  • allowing us to see more patients and give life-altering support and care
  • enrolling more patients and healthy controls in the expanding pool of cutting edge, innovative research – especially those efforts targeting critical biomarker discovery
  • expanded educational efforts for both patients and medical providers

Learn more about the Bateman Horne Center here.
You can give BHC wings to fly and fund real progress. Your monthly donation or one-time gift is an investment in help and hope to millions in dire need. Please donate today!
DonateSquare.jpg

Share on facebook
Facebook
Share on twitter
Twitter
Share on whatsapp
WhatsApp
Share on email
Email

Leave a Comment

Your email address will not be published. Required fields are marked *

Latest News

In Memory of Dr. Ronald G. Tompkins MD, ScD

Mourning the loss of Dr. Ron Tompkins

Today #MEAction joins the community in mourning the loss of Dr. Ronald G. Tompkins, MD, ScD, who passed away this week. Ron Tompkins was a clinician, clinical researcher, and friend and ally to people with ME. He was the Sumner M. Redstone Professor of Surgery at Harvard Medical School, Founding Director of the Center for

Read More »
National Institutes of Health campus buildings from above

NIH Long COVID research lacks clear plan to identify and track ME/CFS

MEAction has written to the National Institutes of Health (NIH) expressing our deep concern that the RECOVER Initiative research agenda lacks a clear plan for how to accurately identify or consistently track the onset of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) cases among patients with Long COVID. This is of particular importance because a sizable fraction

Read More »

The Last Two Years Changed the World…

What a year 2021 was! People with ME have always faced formidable challenges: every day combatting stigma, lack of understanding from clinicians, NIH’s and CDC’s low budgetary commitments, and a world of challenges navigating disability on top of symptoms.  It’s no exaggeration to say that 2020 and 2021 changed the world – and the world of chronic,

Read More »

Help keep our work going

We rely on donations from people like you to keep fighting for equality for people with ME.

Donate

Get actions alerts and news direct to your inbox

You can choose what you want to be kept up to date on.

Subscribe
Scroll to Top