Mayse SMA fund

Our daughter is two months old and all of a sudden she started not eating right and having different issues. The doctors knew I was a carrier of SMA (spinal muscular atrophy) there is only a very small chance she would have it. They ran a bunch of different tests and confirmed she has SMA and for an infant this is not very good at all. We have a very long road ahead of us but there is some hope they have a test trial in New York for a medicine that may be able to help her. We need as much help as we can get to be able to help our daughter. I also have a 4 year old son and step son that love her more than words can describe. All I ever wanted is for my children to be happy and healthy. Now one of my kids health is not good and I wish it was me instead of her. She is my gift from God. I am praying everyday for her to be healthy again. We are good people and I never ask anyone for anything. For my kids I will make sure I do my best to keep them safe and healthy. Please donate anything you can it will be greatly appreciated I assure you. Thank you everyone and keep our princess Mayse in your prayers!!
www.cureSMA.org