Chilli ME Challenge

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The Chilli ME Challenge was an innovative project for ME/CFS awareness and biomedical research funding started by four young women with ME/CFS who call themselves, the 4 Chillis in a Pod Girls. The are Nicola Lavin, living in The Republic of Ireland, Catherine Schofield living in England, Lindsey Michelle and Brenda Hankins, both living in the United States.[1]

According to Nicola, they started the project because they "wanted to use social media for positive use and try to emulate the success of last years ice bucket challenge for ALS. We decided to heat things up so to speak and because Flea from the Red Hot Chili Peppers has ME (we thought this might help with celebrities endorsing it, it hasn’t ME isn’t a sexy or cool illness to have)...we came up with the Chilli ME Challenge where healthy participants take a bite of a hot chilli to show support for those suffering with ME. They film their funny reaction upload it nominate five others and donate."[2]

Fundraising[edit | edit source]

For the UK division, donations went to Invest in ME for biomedical research.

For the US division, donations went to The Center for Infection and Immunity at Columbia University’s Mailman School of Public Health, especially for the work being done for Mady Hornig, MD.

Sampling of videos by ME doctors/researchers/advocates[edit | edit source]

Online presence[edit | edit source]

References[edit | edit source]

myalgic encephalomyelitis (ME) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.