Forgotten Plague

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
Jump to: navigation, search
Forgotten Plague.jpeg

Forgotten Plague is a documentary film about Ryan Prior, an ME/CFS patient and journalist and his journey to understand the disease.

Plot[edit | edit source]

Ryan Prior’s life imploded October 22, 2006, when he was struck down by a disease that dozens of doctors were powerless to diagnose, let alone treat. Against great odds, he becomes a reporter and ventures to tell the story of his suffering and improbable recovery. He is shocked that millions globally remain sidelined by the same disease, many bedridden for decades.

Forgotten Plague is a journey into the hidden world of myalgic encephalomyelitis (chronic fatigue syndrome). It is a chilling tale of our medical system’s failures in addressing many chronic, complex diseases. Yet it is also a riveting story of science’s remarkable ability to transform medicine and improve human life itself.[1]

IMDB Page: An afflicted journalist embarks on a quest to find out why the CDC and medical system have neglected his disease and left millions sidelined from life. [2]

Interviews in documentary[edit | edit source]

Available DVD and Streaming[edit | edit source]

  • Music From The Documentary "Forgotten Plague" By: David Conley available free on Spotify.

Reviews[edit | edit source]

HuffPost Health "Forgotten Plague: A Must See Documentary" By: Bill Johnson II, Psychologist, Author[3]

ME-gids - Dutch Translation of HuffPost Health Article "Forgotten Plague: Een documentaire die je gezien moet hebben" By: Bill Johnson II, Psycholoog, Auteur[4]

Featured in media reporting[edit | edit source]

Chronic Fatigue: Missing Millions (Carte Blanche DSTV)

The Blue Ribbon Foundation[edit | edit source]

In the spirit of a true grassroots organization, The Blue Ribbon Foundation started as an idea, which manifested into a documentary (Forgotten Plague), and eventually shaped a movement.

The Blue Ribbon Foundation’s mission is to foster a national public dialogue that can lead to finding the cause, cure, and prevention of neuro-immune diseases.[5]

The Blue Ribbon Fellowship[edit | edit source]

The summer between the first and second years of medical school is sometimes described as the last “free time” medical students have. However, most driven medical students will pursue research fellowships to set themselves up for success in competitive residency programs. We have launched a highly competitive fellowship in neuro-immune medicine for students from across the nation or the world to study with leaders in the field. The goal of The Blue Ribbon Fellowship is to foster a new generation of physicians devoted to solving complex neuro-immune diseases.[6]

Learn more[edit | edit source]

Online Presence[edit | edit source]

See also[edit | edit source]

References[edit | edit source]


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