For many, a world without bleeding disorders is simply a dream. Thousands of kids and adults affected face internal bleeding, costly treatments and lifelong infusions.
My son, Keaton, was born with an extremely rare bleeding disorder called Factor 13 deficiency. It was quite a shock because there is no history of hemophilia in either my family or my husband's family. Keaton was 5 years old when we finally got his diagnosis and had answers for all the bruises and poor wound healing. Factor 13 deficiency affects men and women equally and occurs in 1 in 2-5 million people.
I’m all in to help end bleeding disorders. My personal goal is to raise as much as possible for this worthy cause. Will you help me reach my fundraising goal? It’s easy — just click “donate” to make a secure donation.
Every dollar stays within our community and supports critical initiatives such as funding research to find better treatments, educating medical providers on the latest innovations and care, ensuring families have access to quality healthcare and providing access to the best educational resources available.
Will you help me reach my fundraising goal? Please make a donation today.
Thank you in advance for your support and united, we will make a difference.
La Fundación Nacional de Hemofilia (NHF) se dedica a buscar mejores tratamientos y curas para los trastornos hemorrágicos hereditarios, y a prevenir las complicaciones que dichos trastornos generan mediante la educación, el apoyo y la investigación. "Unirse es un principio. Permanecer juntos es progresar. Trabajar juntos es alcanzar el éxito".