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19. Subgroups of patients
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In this seminar Prof. Kenny De Meirleir answers the question: Is it possible to classify ME-patients into different groups? This web seminar is part.

19. Subgroups of patients

19. Subgroups of patients

19. Subgroups of patients

De Meirleir talks about the questions: What is LDN, how does it work and is it applicable? This web seminar is part of the project 'Wetenschap v.

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37. How is ME diagnosed? / Hoe wordt de diagnose ME gesteld? - Dr. Charles Shepherd
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37. How is ME diagnosed? / Hoe wordt de diagnose ME gesteld? - Dr. Charles Shepherd

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20. Sense and nonsense of tests
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20. Sense and nonsense of tests

20. Sense and nonsense of tests
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1. Is ME and/or CFS a isease? http://www.youtube.com/user/WetenschapvMEcvsVer?feature=watch (1 of 36)
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Chronic fatigue and blood circulation

1. Is ME and/or CFS a isease? http://www.youtube.com/user/WetenschapvMEcvsVer?feature=watch (1 of 36)

1. Is ME and/or CFS a isease? http://www.youtube.com/user/WetenschapvMEcvsVer?feature=watch (1 of 36)
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9. ME and Gastrointestinal Problems
Find this Pin and more on Myalgic Encephalomyelitis Advocacy by Elaine Boel.
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In this seminar Prof. Kenny De Meirleir talks about ME and Gastrointestinal Problems. This web seminar is part of the project 'Wetenschap voor Pati.

9. ME and Gastrointestinal Problems

9. ME and Gastrointestinal Problems
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In this video, Sophia Mirza's mother shares the story of how her daughter died. Sophia's ME/CFS was treated as a mental illness rather than as a physical disease, and the consequences for Sophia were catastrophic. Sophia's mother says insurance companies spent money trying to influence policies about ME/CFS to have it treated as a mental illness, in order to decrease their own costs.
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Sophia's mum Criona tells how her daughter Sophia unnecessarily suffered and died from the very much misunderstood diesease of ME. Sophia died because of the.

In this video, Sophia Mirza's mother shares the story of how her daughter died. Sophia's ME/CFS was treated as a mental illness rather than as a physical disease, and the consequences for Sophia were catastrophic. Sophia's mother says insurance companies spent money trying to influence policies about ME/CFS to have it treated as a mental illness, in order to decrease their own costs.

In this video, Sophia Mirza's mother shares the story of how her daughter died. Sophia's ME/CFS was treated as a mental illness rather than as a physical disease, and the consequences for Sophia were catastrophic. Sophia's mother says insurance companies spent money trying to influence policies about ME/CFS to have it treated as a mental illness, in order to decrease their own costs.
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The Last Major Disease To Be Studied? Ron Davis of Stanford Thinks So | Mendelspod
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The Last Major Disease To Be Studied? Ron Davis of Stanford Thinks So | Mendelspod

The Last Major Disease To Be Studied? Ron Davis of Stanford Thinks So | Mendelspod

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Kickstarter appeal video for Canary in a Coal Mine, a documentary film about Myalgic Encephalomyelitis ("Chronic Fatigue Syndrome")

2014 in ME/CFS and Fibromyalgia: The Biggest, Best, Least, Most and Strangest Events - Health Rising

Jennifer Brea receives ProHealth's 2013 Advocate of the Year award for her ME/CFS documentary, Canary in a Coal Mine.

2013 Advocate of the Year – Jennifer Brea

(ME/CFS) Interview: Jennifer Brea Talks About Obstacles, Adjustments, and Inspiration

28. Interview with Dr. Nigel Speight (paediatrician) - Interview met Dr. Nigel Speight (kinderarts)

Interview with Dr. Nigel Speight (about children with ME/CFS who have been mistreated by doctors and social workers)

Director of Open Medicine Institute, Linda Tannenbaum: "We have the Big Plan"

Director of Open Medicine Institute, Linda Tannenbaum: "We have the Big Plan"

Director of Open Medicine Institute, Linda Tannenbaum: We have the Big Plan

3. Is ME a hereditary condition? - WATCH VIDEO HERE -> http://arthritisremedy.info/3-is-me-a-hereditary-condition/     *** is rheumatoid arthritis hereditary ***  In this third seminar Prof. Dr. Kenny De Meirleir talks about ME and heritability. This web seminar is part of the project ‘Wetenschap voor Patiënten’ or in English ‘Science for Patients’. This project is realized through a...

In this third seminar Prof. Kenny De Meirleir talks about ME and heritability. This web seminar is part of the project 'Wetenschap voor Patiënten' or in .

Visual stress could be a symptom of Chronic Fatigue Syndrome, research suggests - ScienceDaily http://www.sciencedaily.com/releases/2015/11/151124082235.htm #mecfs

Visual stress could be a symptom of Chronic Fatigue Syndrome, research suggests

Visual stress could be a symptom of Chronic Fatigue Syndrome, research suggests - ScienceDaily http://www.sciencedaily.com/releases/2015/11/151124082235.htm #mecfs

New findings are encouraging in the fight against chronic fatigue syndrome. But the government still provides funding so minimal, one researcher is turning to crowdfunding.

With Significant Advances But Little Money, Chronic Fatigue Syndrome Research Tries Crowdfunding

Innate Immunotherapeutics Fully Enrolls Phase 2 Study of Drug Candidate to Treat SPMS April 15, 2016	Daniela Semedo, PhDby Daniela Semedo, PhD  In News.

Innate Immunotherapeutics Fully Enrolls Phase 2 Study of Drug Candidate to Treat SPMS

Innate Immunotherapeutics Fully Enrolls Phase 2 Study of Drug Candidate to Treat SPMS - Multiple Sclerosis News Today

Voices from the Shadows: Introduction - YouTube I think I need to watch this film in full to help my grieving for my old self

Nigel Speight cleared of all restrictions imposed on him after he opposes GET for ME/CFS patients.

Low bloodpressure

VIDEO: Dr. De Meirleir On Low Blood Volume, Low Blood Pressure And Chronic Fatigue Syndrome (ME/CFS)

In this seminar Prof. Kenny De Meirleir talks about ME and the blood circulation. This web seminar is part of the project 'Wetenschap voor Patiënten'.

ME/CFS Advocate Begins Hunger Strike For Ampligen Approval

ME/CFS Advocate Begins Hunger Strike For Ampligen Approval - Health Rising

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