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Hunters Day of Hope for Children on Saturday, February 12, 2011 from 1:00pm - 4:00pm at the Buffalo Bills Field House in Orchard Park, New York. Each February, Hunters Hope invites children of all ages and their families throughout Western New York to come together for a day of family fun including food & beverage, entertainment, activities and more all at no cost. This FREE event is organized by the Foundation to recognize the local community for helping children suffering all over the country and to encourage families to s... read more
21 Princeton Pl Suite 12, 21 Princeton Place Suite 12, Orchard Park, NY, 14127, United States
Get directionsWeekday | Schedule | Status |
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Mon | 9:00 a.m. to 6:00 p.m. | |
Tue | 9:00 a.m. to 6:00 p.m. | |
Wed | 9:00 a.m. to 6:00 p.m. | |
Thu | 9:00 a.m. to 6:00 p.m. | |
Fri | 9:00 a.m. to 6:00 p.m. | |
Sat | Closed | |
Sun | Closed |
We had lost our son to Krabbes Disease at 20 months old in 2001. Late diagnosis is a death sentence for our babies with this terrible disease. Our second child was born in 2002 and was diagnosed in vitro and had a transplant at birth. She is now a heathy happy 12 year old. So thankful for Hunters Hope and the dedication to this terrible disease and their pursuit to making every state add this to their newborn screening. Now if only Michigan had been one of them, I would have a fun loving 16 year old boy today in my life.
All we have to do is take the time to care and not stare at someone's happenings, just be kind all the time and thankful for anything and everything.
My sister lost her two little girls from this disease. Her first child Felicity they never really new what truly happened the doctors jus made up what they thought. When Riley was born and getting sick is when we found out what kind of disease it was and what really happened to Felicity too.Thankfully my nephew got checked when he was still in the belly and gets testing done every year and is healthy as can be.
My son was diagnosed with Adrbnoleuko dyrophy Friday praying for little Jacob Cory is our page my son is 6yrs old . I seen Kelley story on Espn a few days ago and it gives me hope . Keep the fight for the boys .
Simply inspiring foundation founded by simply inspiring human beings.
I just want to say, I heard your story today on ESPN and made me cry, you and your family are truly inspirational. I came to the Facebook page because my son has an undiagnosed type of Leukodystrophy he has been through so many tests and they can't figure out which one he has yet. The doctors told me he wouldn't live to be four then they said seven, he is fourteen now. He has a rough time and he has been through so much and I love him and he is my hero. Your family doing so much to offer support to families is wonderful. It ... read more
Hunter's Hope Foundation has a 4.7 star rating with 103 reviews.
Hunter's Hope Foundation is closed now. It will open tomorrow at 9:00 a.m.
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