This is hard to share but I feel like sharing...not ready to share with friends and extended family yet. In May we had a Nuchal Translucency Scan and our baby's neck measured large. After a CVS procedure his chromosomes looked normal. We were very hopeful that things were fine. Unfortunately we got the bad news that we had been praying against. We went on Thursday for the Fetal EKG. The doctors took a long look at his heart and then shared the bad news. Travis has what is called Hypoplastic Left Heart Syndrome with a common atrium. His Left Ventricle never fully developed properly and will not be able to function without intervention. Additionally, his atriums are not separate into two chambers....it is one by itself. This syndrome happens spontaneously in 1 out of ever 10,000 births. Years ago, it was a death sentence. Fortunately, there is now a well defined surgical approach to his condition...it is a series of three complex open heart surgeries spread out over the first year of his life. The first surgery would need to be immediately performed after birth. The surgeries (in essence) will jerry rig his two chamber heart to function as a regular four chamber heart. Since these procedures (called Norwood/Fontan) have only been around for 20 years or so they only know the possible life expectancy of 20 yrs. However, the 20 yr patient is still doing well. We will not know the severity of Travis' heart until later. They are planning to do a full study on August 18th and then we will need to meet with the surgeons at Children's Hospital in LA to discuss delivery (probably will be via a scheduled c-section) and what will happen afterwards. Travis will likely be in the NICU for the first few months of his life and he will need one on one care for the first year of his life. My husband and I have so much to figure out. Our heads and our hearts feel so heavy. As you can imagine we are beyond scared and full of grief. What is supposed to be the happiest time in our life is now so uncertain. It hurts that God has picked Travis to have to go through all this. We just keep thinking how unfair it all is. We could definitely use some prayers. Send them our way!
Re: Baby Diagnosed with HLHS (long)
God Bless early testing. I am so glad you have time to plan and make all of these decisions. It is so amazing what they can do.
I will keep you in our prayers. I hope you still check in with us.
I'm so sorry for what you're going through.
If it's any help, my FIL was born with a hole in his heart in 1955. He was the first baby to have open heart surgery. The docs told his parents he would be sickly all his life and die before he reached 15. He would never do anything athletic and may not be as bright as other kids.
Today he is alive and well. He broke his school track long-distance record twice. He is a certified genius on IQ tests. He has high BP, but no other problems.
Just goes to show Drs don't know everything. Though there will be difficult times, there is no reason your sons illness should ness. limit his dreams or potential. He can definitely beat the odds and defy every negative diagnosis. God will carry you and your son through.
You are all in my prayers. I know god handed you this challenge because He knows you can handle it - as tough as it sounds. I'll be thinking of you - what a scary set of events, but thank God there's steps to help Travis.
I am keeping you in my thoughts and prayers. I am a special Ed teacher and thought maybe... just maybe... this might help ease your mind a little bit.
Welcome to Holland
I am often asked to describe the experience of raising a child with a disability, to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this?
When you're going to have a baby, it's like planning a fabulous vacation trip---to Italy. You buy a bunch of guidebooks and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may even learn some handy phrases in Italian. It's all very exciting.
After months of eager anticipation, the day finally arrives. You pace your bags and off you go. Several hours later, the plane lands, and the stewardess remarks to you, "Welcome to Holland." "Holland??" you ask. "What do you mean Holland? I signed up for Italy! I'm supposed to be in Italy. All my life I dreamed of going to Italy."
But there's been a change in the flight plan. They've landed in Holland and there you must stay. The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.
So you must go out and buy new guidebooks. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.
It's just a different place. It's slower-paced than Italy, and less flashy than Italy.But after you've been there for a while, and you catch your breath, you look around, and even begin to notice that Holland has windmills. Holland has tulips. Holland even has Rembrandts.
But everyone you know is busy coming and going from Italy, and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say, "Yes, that's where I was supposed to go. That's what I had planned."
And the pain of that will never, ever, ever go completely away, because the loss of that dream is a very significant loss.
But if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things about Holland.
Taken from Orange County MOP's
March 2001 Newsletter
Written by Emily Perl Kingsly
Heartline, December 1989
Ethan Michael - 12/21/09
Norah Jewel - 2/26/14
Be strong, your baby will need that from you. You will be in my thoughts and preayers.
I just wanted to say good luck and you'll be in my t&p's.
A little side note to pass along. Dr. Norwood (which the prodedure your baby needs is named after) completed my heart surgery in 1980, I was 3 months old. My parents and I for that matter were very lucky that he was practicing at Boston Childrens at the time or else I probably wouldn't be here today. This man was a pioneer in cardiac surgery and defects. While I realize he isn't the one performing the surgery, I'm sure those that are will be well equipped and I wish you the best!!! Keep us posted
I am sorry you are dealing with something so tough right now. My thoughts and prayers are with you.
I am so sorry to hear that. I pray for you and your SO for the strenth and courage to make it through this difficult time and through the surgeries. I also pray for your Little One to be strong and pull through all of this. It is amazing what doctors can do these days, so I have no doubt they will be able to help little Travis.
P.S. I'm just "down the road" from you in Escondido...My DH and I got married in Temecula.
Sounds like something similar to what baby T will need. Thank you all for the kind messages!! And the prayers!!
www.teamtravis.info