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...
Long COVID
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 โinvisible illness.โ An illness where there isnโt a cast...
To the ME/CFS & FM Community
My name is Lisa OโBrien, 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...
The Crushing Aftermath of COVID-19
Being a Long COVID Warrior myself, I wanted to tell my story as well as millions around the world who have never felt well after contracting COVID-19. Many are being diagnosed with ME/CFS, dysautonomia, fibromyalgia and other post-viral illnesses. The weight we feel...
Share Message of Hope for Awareness Day & #MillionsMissing
Share Your Message of Hope Itโs 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 โlong haulersโ 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...
ME/CFS Organizations Urge Congress to Fund Collaborative Long COVID Work
On February 2nd, Bateman Horne Center joined 10 other ME/CFS organizations in a letter to the US Congress urging them to prioritize investments that will address the impending surge of people experiencing Long COVID. In this letter we ask congress to: fund three...