Sara Hope's Medical Fund

Sara was diagnosed with Trisomy 21 and an AV canal defect in uetero. She was born Novenber 27th, and spent 6 long weeks in the NICU.  We were finally able to bring our bundle of joy home, January 8th.  Sara came home with a nose feeding tube, after being home for a month and many episodes of projectile vomiting her doctors decided to place g-tube, which she still is fed through.  Right now Sara is gaining weight and doing great.  We are wating on a date for her heart surgery which will be by the middle of October.  

With all the specialist we see, the therapist we visit, and 3 hospital stays we have had in 9 short months, the bills are adding up.  Our insurance covers some of the cost but we will need to come up money for Sara's heart surgery.  With all the time we have taken off for appointments, surgery,and hospital stays, we do not have much vacation time to take for Sara's surgery.  While we are caring for her at the hospital we will still have all of our monthly bills to pay.  We are starting to worry about how we will continue to make ends meet.  

We started this page to help get us started with what we can. Any little bit can help, if you can't help we understand but please share this with anyone you can.  We thank you in advance.

Sara, Belinda, and Jeff Walker

Please follow our journey and like Sara's page. https://www.facebook.com/sarashopewalker