
Elena Vogonova
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Elena Vogonova is a mother of a child with myasthenia gravis and a patient herself, advocating for the rights and needs of individuals with rare diseases in Kazakhstan. She has highlighted the significant impact of her diagnosis on daily life, emphasizing the lack of proper treatment protocols and genetic research available for patients with rare diseases in the country.
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Recent news mentions
Elena Vogonova, a mother of a child with a rare disease, shared how the diagnosis affects her life.
“Не будем молчать“: пациенты с редкими заболеваниями — о риске остаться без лекарств: 07 марта 2026, 07:02Tengri News – major Kazakh news website·
Kazakhstan· 2026-03-07



