<div>Un día te levantas de tu cama y ya no te obedece tu lado derecho del cuerpo, le das la orden y simplemente arrastras la pierna derecha y no puedes sostener nada con la mano derecha, tienes la visión doble y borrosa, y múltiples síntomas. Te presento la enfermedad de las mil caras: ESCLEROSIS MÚLTIPLE.
</div>
<div><br />
</div>
<div>Mi nombre es Liliana Gutiérrez, madre soltera de 44 años, fui diagnosticada en Mayo del 2024, después de una ardua búsqueda con diferentes médicos especialistas, este diagnóstico llegó con este brote ( perdida de movimiento del lado derecho), que duró 6 meses. Hoy puedo caminar y moverme con normalidad, sin embargo esta es una enfermedad que no se cura, y los brotes pueden dejarte sin movimiento, o con pérdida de visión.
</div>
<div><br />
</div>
<div>Creo firmemente en que se puede vivir mejor si logro dormirla, llegar a la REMISIÓN.
</div>
<div>Actualmente vivo con muchos síntomas,pero eso no me define ni me detiene, creo en que mi cuerpo puede recuperarse, elegí un Protocolo alternativo, pues siendo un diagnóstico autoinmune, requiere de fármacos extremadamente caros que no puedo costearme y tampoco cuento con seguridad social; estos fármacos no te aseguran una mejoría y tienen muchos efectos secundarios.
</div>
<div><br />
</div>
<div>Tu apoyo contribuirá a poder costear mi Protocolo, que inicie en Enero 28 del 2025 y a estos escasos meses he tenido una gran mejoría.
</div>
<div>Mis citas con el médico que lleva mi Protocolo es cada 6 meses y se requieren análisis especiales y el pago de citas.
</div>
<div>Mi meta es la remisión antes del año y medio.
</div>
<div>Agosto 2025 tendré mi segunda consulta, tu apoyo contribuirá a mi camino de remisión.
</div>
<div>GRACIAS DE ANTEMANO ✨✨
</div>

Anonymous

Sergio Luis Pretelin Escribano

Jose Antonio Magaña Arredondo

Tu contribución apoya a pagar tratamiento de Esclerosis Múlt

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