Group Papers / Other

Papers By The 25% M.E Group Patrons, Trustees & Advisers

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Collaborative Research Strategies for Severe ME/CFS Patients

Purpose: To detail a model for enabling severely affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) patients to actively participate in research, overcoming traditional barriers and ensuring their experiences are represented. Key Points: Challenges in Participation: Severely affected ME/CFS patients are often excluded from research due to physical and cognitive limitations, sensory sensitivities, and a lack of…

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Ensuring the Voice of Very Severely Affected ME/CFS Patients in Research

Purpose: To provide a research model enabling very severely affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) patients to participate in studies, addressing their unique challenges and ensuring their voices are heard. Key Points: Challenges in Research Participation: Historically, very severely affected ME/CFS patients have been excluded from studies due to their condition being described as “hard…

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Life-Threatening Malnutrition in Very Severe ME/CFS

Purpose: To highlight the nutritional challenges faced by patients with very severe Myalgic Encephalomyelitis (ME/CFS), emphasizing the need for timely medical intervention and raising awareness among healthcare professionals. Key Points: Causes of Nutritional Challenges: Severe debilitation making eating and drinking exhausting. Dysphagia (difficulty swallowing), gastroparesis, malabsorption, and Mast Cell Activation Disorder (MCAD). Lack of recognition…

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Severe ME in Children: Challenges and Management

Purpose: To highlight the unique challenges faced by children with Severe Myalgic Encephalomyelitis (ME), emphasizing the need for accurate diagnosis, compassionate care, and tailored management strategies. Key Points: Definition and Severity: Severe ME affects children who are housebound or bedbound, functioning at 5–15% of normal capacity. Very Severe ME involves continuous debilitating symptoms, with patients…

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Work Rehabilitation and Medical Retirement for ME/CFS Patients

Purpose: To evaluate the impact of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) on work capacity, prognosis, and the effectiveness of rehabilitation and medical retirement strategies. Key Points: Overview of ME/CFS: ME/CFS is a severe neurological disease characterized by post-exertional malaise (PEM) and significant quality-of-life disruption. Common symptoms include muscle weakness, cognitive dysfunction, sleep disturbances, and chronic…

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Guidelines for Hospital Treatment of ME Patients

Purpose: To provide essential advice and best practices for treating Myalgic Encephalomyelitis (ME) patients in hospital settings, addressing their unique needs and sensitivities to improve outcomes. Key Points: Hospital Environment Challenges: Noise, light, and sensory overload worsen symptoms; private rooms and quiet spaces are necessary. Sleep disruption due to hypersensitivity requires careful consideration to avoid…

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Nimodipine Use in ME/CFS: Brief Overview

Purpose: To introduce Nimodipine, a calcium channel blocker, as a potential treatment for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (ME/CFS), highlighting its benefits, mechanisms, and usage protocols. Key Points: Potential Benefits: Improves mental clarity, alertness, energy levels, and stamina. Reduces fatigue, muscle pain, and headaches for some patients. Approximately half of users report noticeable improvement with minimal…

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Nimodipine Use in ME/CFS: A Comprehensive Guide

Purpose: To provide an in-depth exploration of the potential benefits, mechanisms, and practical considerations of using Nimodipine, a calcium channel blocker, for managing Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). Key Points: Drug Overview: Nimodipine is a second-generation L-type calcium channel blocker, primarily used to improve blood flow in the brain by relaxing blood vessel walls. It…

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Severe ME: What You Don’t Say, What You Don’t See

Purpose: To shed light on the profound challenges faced by individuals with Severe/Very Severe Myalgic Encephalomyelitis (ME), emphasizing the physical nature of the illness and the need for accurate understanding and support. Key Points: Misinterpretation of Symptoms: Severe ME symptoms are often dismissed or misinterpreted as psychological due to their invisibility and complexity. Terms like…

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ME: The Fatigue Cover-Up

Purpose: To explore the historical misrepresentation of Myalgic Encephalomyelitis (ME) as merely “fatigue,” highlighting the scientific evidence that supports its classification as a chronic neurological disease. Key Points: Origins of Misrepresentation: ME was historically dismissed as “fatigue syndrome,” overshadowing the broader neurological symptoms such as muscle pain, cognitive issues, and impaired circulation. Lack of understanding…