“Love bears all things, believes all
things, hopes all things, and endures all things.”
1 Corinthians 13:7
Our story
begins with our first ultrasound we had with our daughter, Alba. We were
excited, scared, everything an expectant parent would be. With just 15 minutes
into the ultrasound, we heard the words "Cystic Hygroma" for the
first time in our lives. We were devastated. Our baby was sick. We
knew at that point our baby either had Noonan syndrome or Turner syndrome. A
few months later we had a Amnio and that's the day we found out our Alba was a
little girl...with Turner syndrome.
As the
pregnancy progressed, other issues began to show up. Five days before Alba was
born we found out she had Hypoplasitic, also known as Left Heart syndrome. We
heard another suggestion for the first time…"Heart Transplant".
On September
22nd, 2010 our little miracle was born. Alba was very puffy, but so full of
life. Doctors immediately placed her on life support and within 9 days old she
was flown to St. Louis Children's Hospital for transplant
evaluation. After many issues in St. Louis, the doctor decided to list her
for a new heart.
On November
27th, 2010 Alba got her new perfect heart after she had coded twice, endured 30
surgeries, and beat everything that has ever been thrown at her. She is now an
active 3 year old and even though she shows a lot of the characteristics that
go along with Turner syndrome, Turner syndrome will never define her.
God has shown
us that nothing can hold anyone back if you love and believe. We never lost
hope that we would have our little Alba home someday because all things are
possible through God.
Jason Carter,
Alba’s Daddy
Together we change lives and create awareness for Turner Syndrome, CHD, and Organ Donation.
Together we change lives and create awareness for Turner Syndrome, CHD, and Organ Donation.
Little Alba and their foundation blankets.
Your Alba is an amazing little girl! My granddaughter, Hannah, who has TS is due in July, so I was very moved and encouraged by your post.
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