Frontiers in Systems Neuroscience published the study results of Cortene Inc's investigational drug CT38 in people with ME/CFS. The trial was conducted at Bateman Horne Center and Suzanne Vernon, PhD, wrote a blog post providing context about the study. Cortene Inc....
ME/CFS
September Message: Cortene Study Published
In 2018 the Food and Drug Administration approved a physician-sponsored Investigational New Drug (IND) Application, to investigate the safety, tolerability and efficacy of CT38 in the treatment of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Dr....
Finding Home
My family and I recently returned to Salt Lake City after a 22-year absence. We had missed Utah’s western landscape and snowcapped mountains and the youthful feeling of the city. Additionally, I knew there would be unique professional opportunities available to me in...
Growing Seeds through Research
Incredible people have spent time at BHC as interns, pre-med students, and clinical research coordinators as a way point in their educational journeys. As a part of our mission, we hire and train upcoming researchers and medical professionals to help be a product of...
Unexpected Impact
Incredible people have spent time at BHC as interns, pre-med students, and clinical research coordinators as a way point in their educational journeys. As a part of our mission, we hire and train upcoming researchers and medical professionals to help be a product of...
To a Loved One of Someone with a Chronic Illness
To a loved one of someone with a chronic illness: The intention behind this letter is to share the importance of believing and validating your loved one with chronic illness. This may seem simple, and perhaps even obvious, but the power behind these actions can be...
Insights Into My Chronic Illness
Introduction It is hard to know how to support others when their health becomes compromised. It can leave you feeling powerless and unsure of what to do. It is even harder when your loved one is afflicted by an “invisible illness.” An illness where there isn’t a cast...
To the ME/CFS & FM Community
My name is Lisa O’Brien, and I am a COVID Long Hauler and the founder of the Utah COVID-19 Long Haulers group, a group I started almost a year ago when no one would take me seriously after being sick for several months. I knew there would be others in my community who...
Courage
It takes courage to live with a chronic illness. It takes courage to be a prisoner in your own body. It takes courage to know that what you have isn't a cold or flu that has an expiration date. It takes courage to go to sleep at night knowing this nightmare won't end...
Share Message of Hope for Awareness Day & #MillionsMissing
Share Your Message of Hope It’s time to start preparing for ME/CFS and FM Awareness Day! This will be our 2nd annual Messages of Hope virtual event. There will be a line-up of speakers (announced soon), a poetry reading, release of Believing Your Patient and Believing...
BHC Announces Inclusion of Long COVID
COVID-19 has changed our world and at least 10% of those who become ill may have long term effects. These “long haulers” have many similar symptoms to ME/CFS and FM patients. It is critical for BHC to join the assessment, treatment, and education of these patients...
Surviving the March Madness: Tools to Balance Your Nervous System
We all have extra on our plates this year, and many coping skills, such as spending time with loved ones and being in community, are not as accessible when we are living with a chronic illness. Stress levels are rising and when stress levels rise, chronic pain and...