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PANDORA
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
PANDORA or Patient Alliance for Neuroendocrineimmune Disorders Organization for Research & Advocacy is a patient advocacy and lobbying group founded on May 1, 1988.
Mission[edit | edit source]
PANDORA's mission is to advocate and restore quality of life for individuals with NeuroEndocrineImmune diseases (NEIDs) chronic fatigue syndrome (CFS), myalgic encephalomyelitis (ME), fibromyalgia (FMS), Lyme disease (LD), multiple chemical sensitivity-Environmental Illness (MCS-EI), & Gulf War Illness via educational patient-medical programs, community support, and grass roots initiatives.[1]
Services[edit | edit source]
Notable people[edit | edit source]
- Rebecca Artman
- Lori Chapo-Kroger, RN
Patrons[edit | edit source]
Medical advisors[edit | edit source]
Research/Notable studies[edit | edit source]
History[edit | edit source]
Funding[edit | edit source]
Interviews and articles[edit | edit source]
Online presence[edit | edit source]
- Website
- Facebook page
- YouTube channel
See also[edit | edit source]
Learn more[edit | edit source]
- Wikipedia
