The Little Miss Hannah Foundations’s mission is to help enhance the quality of life for young children diagnosed with rare, life-limiting. and complex medical conditions, as well as children who have been placed in hospice or palliative care.
Our foundation also gives parents the necessary tools and financial assistance to empower them to meet their child’s unique medical and lifestyle needs, as well as provide support resources and special attention for their other children.
By working hands-on with families that are faced with the financial and psychosocial challenges of caring for a child with a complex medical condition, the Little Miss Hannah Foundation will strive to empower, educate and support families during the most emotionally-charged times of their lives.
We are a Las Vegas based, family-run nonprofit organization that was started in memory of our daughter, Hannah. During Hannah’s life, there were many things that our family needed to help us manage Hannah’s care and enhance her quality of life. Because her disease was so rare, there were very few services available to us.
After she passed away at the age of 3 years 4 months in December 2011, our family decided that we would create an organization that would directly help other local rare and medically complex families by supplying the equipment and services we were so desperately in need of during Hannah’s life.
Our organization staff is completely volunteer-based and made up of some amazing family and friends who loved Hannah and believe that children like her deserve so much love and support.
This organization is not only dedicated to Hannah’s memory and legacy, but it was created in honor of our two other children (Ethan and Abigail) who were Hannah’s best friends, junior nurses, and the ones who were able to get Hannah to smile the biggest.