Posts Tagged ‘ME/CFS treatment’
Ongoing Developments at the Bateman Horne Center
BHC as a ME/CFS Center of Excellence A Center of Excellence is a program assembled to supply an exceptionally high concentration of expertise and resources in an area of medicine. The Fatigue Consultation Clinic and OFFER joined forces to establish the Bateman Horne Center, a ME/CFS and Fibromyalgia Center of Excellence. The objective is to…
Read MoreNIH Announces Precision Medicine Initiative
Research tends to neglect ME/CFS and FM – until right now. Precision medicine is the emerging scientific idea that medical treatment can and should be maximally efficient by tailoring medicine and healthcare to individual circumstances. Current research studies, however, do not have the size and diversity necessary to produce enough statistical power for individualized treatments.…
Read MoreME/CFS and Related Illness: Putting It All Together
Understanding how ME/CFS and Fibromyalgia are related to and affected by other illnesses is key in helping patients find relief from symptoms. At the BHC Education Meeting in October, Dr. Nathan Holladay gave a broad view of the key aspects of the various problems that can cause these diseases or make them worse, including infections, immune system issues, and mitochondrial, metabolic, and endocrine dysfunction. Making the connections between these illnesses can help doctors and patients decide on customized treatment methods rather than “one-size-fits-all” treatments.
Read MoreBuilding the Ranks of Skillful and Informed Medical Providers
BHC Strategies for Bringing Doctors up to Speed on ME/CFS and FM presented by Lucinda Bateman, MD, BHC Founder and Medical Director Improving the way medical providers understand, diagnose, and treat ME/CFS and Fibromyalgia is critical to progress and a primary focus of the Bateman Horne Center. At the August 2nd BHC Education Meeting, Dr. Bateman shared her…
Read MoreDr. Bateman Determined to Power-Up in 2017
Dr. Bateman, BHC founder and medical director, reflects on the progress in 2016 and plans to power-up her dedication to patients. __________ The “wear wild socks” year was amazing, marked by the quick-paced steps of the turtle-carrying-hares toward illness recognition and biomarker discovery. (Read how it all began HERE.) The recipe for this success has been…
Read MoreRedefining POTS so that Everybody Understands
“Redefining POTS so that everybody understands: a primary care pediatric sports medicine perspective and review” Presented by Dr. Craig Colebey Postural Orthostatic Tachycardia Syndrome or POTS is a disabling disorder, representing “a common pathway” for multiple different causes. The heterogenous nature of its pathophysiology presents a challenge in its diagnosis and treatment. I present…
Read MoreA Report of Clinical Progress in 2016
Improved objective diagnosis and the ability to assess treatment outcomes, has made many aspects of MECFS and FM appear before my eyes. I am committed to infusing the medical community with this information to dramatically improve patient diagnosis and treatment. Careful observation of 10 minute NASA Lean test results as part of the CDC multisite…
Read MoreKeeping It Clean: Clean and Dirty Suffering
presented by Timothy Weymann, LCSW Life – and chronic illness – has an inherent level of difficulty (i.e., “Clean Suffering”). The natural difficulties of life often trigger conscious and subconscious responses from us; responses we believe will help us solve our concerns. If we fail to critically identify, evaluate and intentionally select our responses to…
Read MoreGlobal Report of Progress with Lucinda Bateman, M.D.
An ME/CS Progress Report Lucinda Bateman, MD, BHC Founder and Medical Director, is actively engaged in ME/CFS and FM thought leadership across the globe. In October she was on the road to take part in and advance the discussions that lead to progress. In a few short weeks she participated in: October 8th – SMCI Scientific…
Read MoreOvercome Fear After Diagnosis
Being diagnosed with a chronic illness such as ME/CFS or Fibromyalgia can be quite a blow. Being afraid is one of the most common reactions to forced changes, but it isn’t something you should let consume your life. It’s normal to experience a range of emotions in the wake of such a diagnosis. However, you…
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