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Tag: myalgic encephalomyelitis

Rep. Ilhan Omar to Introduce Major Long Covid Bill

On Friday, Minnesota Rep. Ilhan Omar (D-Minn.) will introduce a potentially groundbreaking piece of federal legislation in the House of Representatives—one allocating $10 billion in funding to fight Long Covid, the increasingly widespread, chronic condition that follows many Covid infections. The Long Covid Research Moonshot Act is a companion bill to one that Sen. Bernie Sanders (I-Vt.) introduced in the Senate in August.

“Long Covid is a silent health crisis impacting over twenty-three million Americans, including one million children,” Omar said in a statement to Mother Jones. (Rep. Ayanna Pressley, D-Mass., is the co-lead on the legislation.) “I’m proud to lead this effort in the House to recognize Long Covid as the public health emergency that it is and invest in countering the effects of this terrible disease.”

Long Covid symptoms often include debilitating fatigue, and many people found to have it have also been diagnosed with conditions like myalgic encephalomyelitis/chronic fatigue syndrome and postural orthostatic tachycardia syndrome. ME/CFS, which is characterized by post-exertional malaise, is known to be associated with other infectious diseases—the CDC states that about 1 in 10 people infected by the Epstein-Barr virus (which 95 percent of adults get) experience ME/CFS-like symptoms. And research shows that repeated Covid infections increase people’s risk of developing Long Covid.

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As COVID Surges, the High Price of Viral Denial

COVID is surging once again and, if you live in British Columbia, you probably already know someone sick with fever, chills and a sore throat.

As of mid-August, about one in every 19 British Columbians were enduring an infection, with or without symptoms.

Although the media routinely dismisses all COVID infections as an inconsequential nuisance, that’s not what the science says. The virus remains deadlier than the flu and repeated infections can radically change your health.

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Vancouver’s Opera Mariposa presents month-long programme benefitting the ME | FM Society of BC

This May, Opera Mariposa is rallying the community to support people with chronic and post-viral illnesses. From May 1 to June 1, 2024, the disability-led indie arts company is presenting their 2024 Benefit + Awareness Month: an all-digital charity extravaganza featuring music, art, prizes, and special events benefiting the ME | FM Society of BC.

The initiative honours the International Awareness Month for chronic neuro-immune diseases, and it showcases disabled and chronically ill artists from around the world. Proceeds aid people and families affected by myalgic encephalomyelitis (ME or ME/CFS), fibromyalgia, and long COVID – a group of complex chronic illnesses that are surging due to long-term health impacts from COVID-19.

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Long COVID still has no cure — so these patients are turning to research

When Lisa McCorkell got COVID-19 in March 2020, her symptoms were mild. Her physicians told her to isolate from others and that she would recover in a few weeks. But the weeks stretched into months and McCorkell, who was working on a master’s degree in public policy at the University of California, Berkeley, started having debilitating and bewildering symptoms: fatigue, dizziness and shortness of breath. Previously an avid runner, McCorkell found her heart racing from simple efforts.

She struggled to find an explanation, and soon realized that her physicians didn’t know any more about her condition than she did. To complicate matters, the limited availability of high-quality testing for the coronavirus SARS-CoV-2 in the early days of the pandemic left many of her doctors wondering whether her symptoms were really due to COVID-19 at all. “I didn’t have health-care providers that took me seriously,” McCorkell says. “That largely pushed me out of the health-care system.”

McCorkell turned instead to those who were experiencing the same puzzling symptoms and frustrations, joining a support group for people with what would eventually be called long COVID. As they compared notes, McCorkell and a handful of others — many of whom had research experience — realized that the information they were sharing might be helpful not only for those with long COVID, but also for those looking to study the condition. So, they founded a non-profit organization, called the Patient-Led Research Collaborative (PLRC), to design, provide advice on and even fund basic and clinical research into long COVID and other chronic illnesses.

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