Discussion in 'General ME/CFS News' started by Sasha, Jul 4, 2015.
Just stumbled across this while looking for OFFER:
Anyone know who "Horne" is?
From the site:
"It is estimated that 5 million people in the US are affected by Fibromyalgia and ME/CFS—more than those with MS, lupus or many forms of cancer—yet only $15 million in combined federal dollars is dedicated to researching both diseases. The result is a wide research and medical literature gap that has left no standard diagnostic tests and fueled misinformation. Bateman Horne Center takes aim at filling these gaps through integrated research, clinical care and education."
Respectful, personalized, science-based health care that emphasizes patient engagement and education and results in practical and accessible solutions to all regardless of their demographic and socioeconomic background.
Health care teams that are knowledgeable, empathetic, committed to professional and personal advancement, and trained as good listeners and teachers.
Research that is based in science, cutting-edge knowledge, creativity and ingenuity.
Clinic practices that promote safety, technology, 360-degree communication and training opportunities.
Advocacy that fuels informed and positive health care change."
That sounds great!
Interesting, the board of directors includes a disability attorney, people with financial and investment management experience, research experience, healthcare resource experience, an EdD, a mind body health psychologist, a living with pain and fatigue counselor, and a student from the U of Utah.
They also have research and education sections.
Go, Dr. Bateman!
You can also try a Google Site Search
Separate names with a comma.