- A
- A
- W
Hola, mi nombre es Xaira Miranda. Tengo un hijo de 4 años. Desde su nacimiento hemos estado luchando con una lesión que tiene en su mejilla izquierda (foto arriba). En un principio se nos dijo se trataba de un hemangioma y el mismo debería ir desapareciendo entre los 5-6 años. Luego de 3 dermatólogos y 4 años se nos informa que no debe ser un hemangioma ya que no ha desaparecido y no se ve ninguna mejoría. Es entonces cuando nos indican que debe ser una malformación vascular y que no hay centro de anomalías vasculares en Puerto Rico.
Es por esto que debemos movernos al Texas Children's Hospital en Houston, TX. Los gastos de traslado y médicos son muy altos. Te agradecemos cualquier ayuda que tu corazón nos pueda brindar para nuestro hijo.
Muchas gracias
Hi, my name is Xaira Miranda. I have a 4 year old son. Since his birth we have been fighting with a lesion in his left cheek (photo above). At first, it was supposed to be a hemangioma and disappear within 5-6 years. After 3 dermatologists and 4 years later they informed us it is not an hemangioma but it appears to be a vascular malformation since it hasn't disappear and there is no improvement. We have no vascular anomalies center in Puerto Rico to treat this condition, reason why we are going to the Texas Children's Hospital in Houston, TX. Airfare and medical expenses are high. We will thank you for any help you feel in your heart for our son.
Thank you very much.
Es por esto que debemos movernos al Texas Children's Hospital en Houston, TX. Los gastos de traslado y médicos son muy altos. Te agradecemos cualquier ayuda que tu corazón nos pueda brindar para nuestro hijo.
Muchas gracias
Hi, my name is Xaira Miranda. I have a 4 year old son. Since his birth we have been fighting with a lesion in his left cheek (photo above). At first, it was supposed to be a hemangioma and disappear within 5-6 years. After 3 dermatologists and 4 years later they informed us it is not an hemangioma but it appears to be a vascular malformation since it hasn't disappear and there is no improvement. We have no vascular anomalies center in Puerto Rico to treat this condition, reason why we are going to the Texas Children's Hospital in Houston, TX. Airfare and medical expenses are high. We will thank you for any help you feel in your heart for our son.
Thank you very much.

