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Cargando...
23 de abril de 2024
Un grito de ayuda
IAPOS no autoriza su tratamiento: "Los responsabilizo por lo que me pueda suceder" domingo 10 de julio de 2022 18:29 Savina tiene 29 años y vive en Casilda. Padece una enfermedad genética que si no se trata puede tener efectos irreversibles. La obra social IAPOS, a pesar de pedidos judiciales, se niega a comprar el medicamento que evita daños en las neuronas motoras de la joven.
En comunicación con CasildaPlus Savina Barbagallo explica:"Tengo Atrofia Muscular Espinal, una enfermedad progresiva. El medicamento que detiene la patología es SPINRAZA. En junio de este año la justicia me otorgó la cautelar pero IAPOS sigue sin cumplir" .
La joven oriunda Arroyo Seco, cursa sus estudios en la Facultad de Ciencias Veterinarias, por esa razón se rafico en nuestra ciudad. "Hace algunos años salió este tratamiento que frena la patología. La obra social nos dio miles de vueltas. Es por eso que, con documentación requerida, nos presentamos a la justicia y dictaminó a mi favor " . Continúa contando Savina.
Y describe angustiada: "La sentencia fue el 10 de junio, IAPOS nos pidió un plazo de 5 días para poder realizar la compra de SPINRAZA, pasado ese plazo no cumplió, mis abogados pidieron que se aplique una multa por incumplimiento y el juzgado le dio 2 días más para luego comenzar a aplicarle una multa por una suma de dinero TOTALMENTE BAJA. Recurrimos ese decreto expresando que se pida una multa más alta ya que a IAPOS le conviene más pagar la multa que comprar la medicación y lamentablemente en el día de ayer 8 de julio la justicia nos rechazo el recurso".
La enfermedad no sabe de esperas burocráticas, Savina necesita respuestas urgentes. "Tristemente a IAPOS y a la justicia parece no importarles nada, y los responsabilizo de todo lo que siga perdiendo o me pueda llegar a suceder" . Cierra Savina con la espera que desespera.
Aqui el link para firmar la petición: https://chng.it/7frLgQMtHN