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Tag: Belle and Sebastian

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.

Posted in VideoTagged 2015, Belle and Sebastian, celebrities with ME/CFS, personal accountsLeave a comment
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    AMMES needs volunteers! AMMES is actively recruiting volunteers to help AMMES grow and prosper. Fundraising coordinator –  should have experience …Read More »
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    Health outcomes one year after Omicron infection among 12,789 adults: a community-based cross-sectional study

    Summary: Background: Characterizing the paradigm and impact of long COVID is crucial for addressing this worldwide health challenge. This study …Read More »
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    Voice of the patient: people with myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS) share in their own words

    Abstract: Background: Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a serious, debilitating illness affecting millions of people worldwide. Patients with ME/CFS often …Read More »
  • Assessing fatigue in myalgic encephalomyelitis/chronic fatigue syndrome patients before and after treatment with bright light therapy: A prospective randomized controlled crossover study

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    Abstract: Objective: The aim of the current study was to test the effectiveness of treatment with bright light therapy (BLT) on …Read More »
  • Cognitive Impairments in Two Samples of Individuals with ME/CFS and Long COVID: A Comparative Analysis

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    Abstract: Cognitive impairments, including memory and concentration difficulties, are common in individuals with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and long …Read More »
  • Gulf War Illness: A Historical Review and Considerations of a Post-Viral Syndrome

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    Abstract: Gulf War Illness (GWI) is a condition that affects 30-40% of nearly 700,000 Veterans who were deployed to Operations …Read More »

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Help us continue our mission!
The American ME and CFS Society
ABOUT ME/CFS

  • What Is ME/CFS?
  • What Causes ME/CFS?
  • Symptoms of ME/CFS
  • How Many People Have ME/CFS?
  • How Is ME/CFS Diagnosed?
  • Overlapping Conditions
  • Will I Recover?
  • ME/CFS in Adolescents
  • ME/CFS in Children
  • ME/CFS: Facts & Myths
  • FAQs
  • Outbreaks
  • Anesthesia Warning
TREATMENT

  • Treatment Overview
  • Pharmaceuticals
  • Supplements
  • Alternative and Complementary Therapies
  • Experimental Treatments
  • Diet
  • Exercise
  • Coping Strategies
  • Pacing
  • Treatment Database
GET SUPPORT

  • Organizations
  • Find a Support Group
  • Work and Disability
  • Relationships
  • For Caregivers
  • AMMES Connect
  • Financial Crisis Fund
FIND A PHYSICIAN

  • How to Talk to Your Doctor
  • Physician and Clinic Database
GET INVOLVED

  • Why We Need Advocacy
  • Advocacy Groups
  • Action Alerts!
  • Volunteer
  • Donate
  • Clinical Trials
RESOURCES

  • Blogs
  • Videos and DVDs
  • Books
  • For Clinicians
  • Useful Links
  • News and Research
  • Interviews With Doctors
  • Newsletters
  • COVID-19 and ME/CFS
ABOUT US

  • What We Do
  • Who We Are
  • Policies and Disclaimer
  • AMMES By-Laws
  • Privacy Policy
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This site is not intended as a substitute for medical care. The American ME and CFS Society is not responsible or liable for actions taken as a result of the information presented on this website. Please consult a clinician before embarking on any medical treatment, therapy, or program.