We’re grateful for Sen. Kaine’s continued support of the Long COVID community. Sen. Kaine, a Long COVID patient himself, has previously advocated for and represented LCA and partners’ initiatives on…
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Watch the full panel here The long-term debilitating effects of COVID-19 on people infected with the SARS-CoV-2 virus are a serious concern for clinicians, researchers and policymakers. Four months after…
Body Politic The Body Politic Slack support group provides members with emotional support, resources, community, and opportunities for advocacy. If you have tested positive, are experiencing symptoms, or are recovering…
Dr. Klimas is an expert on multi-symptom disorders, myalgic encephalomyelitis (ME), Gulf War Illness, fibromyalgia, and other neuro-immune disorders. In the seminar, Dr. Klimas touches on the medical sexism that…
In this first webinar in a series presented by the Long COVID Alliance, learn about the latest research exploring the relationship between POTS and other forms of dysautonomia in post-acute sequelae…
From the COVID-19 Longhauler Advocacy Project: The COVID-19 Longhauler Advocacy Project has created state Facebook groups. While we have been doing a ton of advocating, we wanted to focus on…
This is a running list of recruiting studies, clinical trials, and research opportunities. If you have an opportunity to add to this list, please contact us. NIH RECOVER Studies RECOVER…
From the Pulmonary Wellness Foundation: In September 2020, Pulmonary Wellness hosted a conversation with Dr. Svetlana Blitshteyn, Director and Founder of Dysautonomia Clinic. The Pulmonary Wellness Foundation has Launched a…
From PhysiosforME: The PhysiosforME team are joined by Professor Todd Davenport and Suzan Jackson to discuss the theory and practice of HR monitoring. For more information please go to: www.physiosforme.com.
From PhysiosforME: PhysiosforME and Dr. Charles Shepherd discuss PVF, PVFS and ME. Personal experiences of supporting people with PVFS and ME, how to distinguish between PVF, PVFS and ME, exercise…