This short animation was created by Alexandra Hohner using interviews with a young man who developed ME/CFS following a giardia infection. She says ” The experiment is based on the idea to create a simulation of Olly’s photophobia (sensitivity to light)”
Category: Video
VIDEO: Ron Davis Talks About the New NIH Grant
In this brief video, Dr. Davis talks about his newly funded NIH grant. This grant will fund research for 5 years at $500,000 a year and will involve 15 collaborators, 9 of which have never worked in the ME/CFS field before. The project is designed to shed new light on the immunology of ME/CFS.
VIDEO: Advancements in ME/CFS Research, David M. Systrom, MD; Brigham and Women’s Hospital | ME/CFSAlert 98
Dr. Systrom covers how an interest in exercise intolerance led him to MyalgicEncephalomyelitis. He talks about his work, a new research incubator he has assembled, the testing of an old medicine, Pyridostigmine, on ME patients and the importance for researchers to talk to each other.
VIDEO: Interview with Lisa Hall and Rivka Solomon
Lisa Hall, a Registered Nurse at Northampton Integrative Medicine, and chronic fatigue syndrome patient Rivka Solomon join Carrie Saldo to shed light on the symptoms of Myalgic Encephalomyelitis, its treatment, and what it’s like living with the condition.
VIDEO: M.E. and me | BBC Newsbeat
ME sufferer Emma Donohoe investigates how young people cope with the debilitating illness, of which symptoms can include devastating fatigue, digestion issues and brain fog. It comes as current treatments for the condition are being reviewed, after years of controversy.
VIDEO: Dr. Bateman’s Summary of Clinicians’ Summit March 2-3, 2018
Bateman Horne Center hosted the first annual ME/CFS Clinicians’ Summit at the BHC Education Center on March 2-3, 2018. Clinicians from all over the country joined us to discuss treatment options and what research they would like to see to combat this devastating disease.
VIDEO: Stuart Murdoch of Belle and Sebastian ME/CFS Interview in L.A.
Stuart Murdoch, lead singer of the indie band Belle and Sebastian, talks to the Solve ME/CFS Initiative about his experience with the disease Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Stuart was in town for the FYF Fest on Aug. 22-23, 2015.
VIDEO: Chronic Fatigue Syndrome: Scientific Discoveries and Future Targeted Treatments
In this video, Dr. Montoya discusses clinical implications of recent scientific reports that are pinning down the development of this disease. Treatment implications and future avenues for research are also discussed.
https://www.youtube.com/watch?time_continue=3532&v=ADVQvzXwDUg
VIDEO: Science for ME Q&A with Dr José G. Montoya, 16th January 2018
Science for ME’s vision is to identify biomarkers associated with chronic unexplained illnesses, including ME/CFS, with the aim of translating that knowledge into early diagnoses and effective treatments.
Discovery Forum 2017: An Interview with Dr. Maureen Hanson
Solve ME/CFS Initiative’s 2nd Annual Discovery Forum, held on October 14th in Washington DC, brought together leaders from across industry, academia, federal agencies, and biotech companies to tackle the most pressing issues confronting ME/CFS. In this interview, Dr. Zaher Nahle discusses ME/CFS science and policy with Dr. Maureen Hanson, founder and director of the Center for Enervating Neuroimmune Disease at Cornell University and member of the Solve ME/CFS Initiative’s Research Advisory Council.