Clara Ray's Heart Journey

As many of you know our daughter Clara Ray Morton has been diagnosed with CHD's and Heterotaxy Syndrome . With her Full heart block and her AV Canal defect, being two of the CHD's.  she will need a pace maker once born. As well as  needing open heart surgery later in the months to come.  Now she has a possible Valve not growing that will mostly likely lead her to a 3-4 stage open heart surgeries.  She is a miracle from God. We were told she would not make it past 18 weeks. Then once she did we were told she she most likely would be born still not long after 20 weeks. We never gave it a second thought. We knew our daughter had a fighting chance. Doctors are shocked to see her come this far. She has deafeated so many odds against her! We are now out here in Boston. Away from our NY home.  Awaiting the arrival of our princess. 

      We will be going to many doctor appointments along the way to monitor Clara's heart. Our insurance, covering most of the expenses, does not cover it all. As you can imagine, it starts to add up after a while. Also with the mutiple heart surgerys on the way, I feel I should try and prepare the best I can. With saving as much as we can along the way, as much as we wish we didnt have to ask... any help to pay Clara's expenses will be greatly appreciated. With everything going on this is the last thing we want to think about. We know we will make it through this no matter what with God as our guidence, therefore we do not wish to beg, but if you'd like to help us during this time, in anyway, we thank you.


Claras Bible verse, 

"I can do all things, through Christ who strengthens me" -Philippians 4:13

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"And though she be but little, she is FIERCE"
-Shakespeare