The HemoWish Foundation is the only Hemophilia wish granting organization in the world. We are a 501(c)(3) non-profit charitable organization.
Our mission is to improve the quality of life of hemophiliacs and their families by granting a dream wish.
For those that are affected by hemophilia, the struggle is real! Life is hard enough as it is, but dealing with hurdles of a chronic, severe bleeding disorder doesn’t make things easier.
Frequent hospitalizations, trips to the ER, crutches/walkers/wheelchairs, loss of income, missed time from work, inability to keep a job, limitations from exercising and sports, spontaneous bleeds, port infections, battles with depression/fear/anxiety, etc… can all be part of the journey with hemophilia. Due to these often financially straining burdens of living with Hemophilia, many hemophiliacs have never even been on vacation in their entire life!
The HemoWish Foundation believes that every hemophiliac, whether they are 7 years old or 77 years old, deserves to experience that once in a life time, dream trip or experience that will create smiles and memories that will last a lifetime.
The granting of a dream wish can make a huge impact on the life of a hemophiliac. It can be a catalyst for change, a turning point in their battle against depression, or an emotional release from the daily grind of immune tolerance therapy for inhibitors. The value and impact of a dream wish cannot be understated.
Thank you to our donors and sponsors that are making dreams come true in the lives of those affected by hemophilia!