Medical Fund and Expensives for Milah Jade (Bean)
Donation protected
Hello evryone this wonderful beautiful baby is Milah Jade. She was born with Congenital Heart Disease. Her Pulmonary Artery is very small when she was born and had to get a breathing tube seconds after she was born and at 7 days old she had to get surgery for a right BT Shunt so that her heart can pump blood throughout her body.
When Milah was about a month old she also had to have a GI feeding tube placed on her stomach to help her eat, as her right vocal chord was also paralyzed at birth. She was also just diagnosed with Noonan syndrome.
My Milah is such a strong baby and is always laughing and smiling even when we can't. She has been through so much, what with being unable to eat on her own, and many doctors appointments and hospital stays.
We were told she would need reconstructive heart surgey to make her heart work at 100%. And even though this is such a big surgey it definelty isn't her last.
We finally got the date for surgery to May 9th at Driscoll's Children's Hospital. The only thing is we are short on funds for it. Her insurance unfortunately dosen't cover all her expensive and that's what this is for. We appreciate anything we can get because it will help in the long run. We don't know whats going to happen or how long we will be there.
We ask for everyone's love and prayers to help get us there and make sure our little Bean is good and perfect. From my family to your we say thank you and we love you all for all your help through all this.
Update: Milahs surgey has been moved to the 15th due to the surgeon going to do an emergency surgery. Now we new to wait even longer for out bean to get better. But at least we get more time with her so we are thankful for that. This also gives us more time to raise for the big day. Thank you everyone.
When Milah was about a month old she also had to have a GI feeding tube placed on her stomach to help her eat, as her right vocal chord was also paralyzed at birth. She was also just diagnosed with Noonan syndrome.
My Milah is such a strong baby and is always laughing and smiling even when we can't. She has been through so much, what with being unable to eat on her own, and many doctors appointments and hospital stays.
We were told she would need reconstructive heart surgey to make her heart work at 100%. And even though this is such a big surgey it definelty isn't her last.
We finally got the date for surgery to May 9th at Driscoll's Children's Hospital. The only thing is we are short on funds for it. Her insurance unfortunately dosen't cover all her expensive and that's what this is for. We appreciate anything we can get because it will help in the long run. We don't know whats going to happen or how long we will be there.
We ask for everyone's love and prayers to help get us there and make sure our little Bean is good and perfect. From my family to your we say thank you and we love you all for all your help through all this.
Update: Milahs surgey has been moved to the 15th due to the surgeon going to do an emergency surgery. Now we new to wait even longer for out bean to get better. But at least we get more time with her so we are thankful for that. This also gives us more time to raise for the big day. Thank you everyone.
Organizer
Samantha Torres
Organizer
Harlingen, TX