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]

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]

See also[edit | edit source]

Learn more[edit | edit source]

  • Wikipedia

References[edit | edit source]