
Martha Vera Soledispa
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Martha Vera Soledispa is the president of the National Foundation for Myasthenia Gravis, a condition that severely impacts her ability to breathe and perform daily activities. She has been vocal about the struggles faced by patients with rare diseases in accessing vital medications and healthcare.
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Martha Vera Soledispa is a patient and president of the National Foundation for Myasthenia Gravis, who shared her struggles with the disease.
‘Todos los días estamos luchando por vivir’: pacientes con enfermedades raras reclaman por medicinas y fallas en la atención hospitalaria | Comunidad | GuayaquilEl Universo – major Ecuadorian daily, est. 1921·
Ecuador· 2026-02-03






