This is to assure Mum and Dad can be there full time for Esme with no need to worry financially.
Auckland
Esme Joy is 10 weeks old & has spent 8 weeks of her life in hospital due to a Congenital heart defect. She is the 2nd child & first daughter of David & Shanka. She was born with an Absent right pulmonary artery, which means that the heart isn’t able to pump blood to the right lung only to the left lung. She also has a mild-moderate ASD (hole in her heart). She was postnatally diagnosed at 2 weeks of age.
She underwent her first open-heart surgery to place a shunt to allow blood flow to her right lung at just 4 weeks old. She seemed as if she was recovering quite well up until 1-2 weeks ago where she deteriorated greatly and was not managing without breathing support and the doctors saw no change in terms of her getting any better.
She has been also diagnosed Pulmonary hypertension, which is high blood pressure in her left lung due to her CHD and is quite unstable at the moment.
Mum and Dad have been told that Esme will need a second open-heart surgery to save her life as her condition has now become life threatening. This is because the pressure causes her to have episodes that don’t allow any blood into her left lung as it stiffens up and causes low oxygen & her to stop breathing quite suddenly- over time pulmonary hypertension can also cause right sided heart failure.
This is set to happen in the next 2-3 weeks depending on her condition as if she continues to deteriorate they will need to operate sooner.
She is currently in starship PICU & will be their until her surgery & afterwards. She is still her happy self and loves attention, her parents adore her and are staying as strong as they can for her & her older brother Corinthian who is 2. They travel to and from the hospital to also try and juggle some time to spend with their Son.
As you may know this is quite a stressful time for Esme’s parents and anyone who may be in a similar situation & they had unfortunately not had the time to prepare mentally, physically and financially for what they are going through & this page is to share Esme’s story and also to hopefully raise money to help her parents get through this hard time without having to worry about David returning to work while his daughter is in ICU & to help ease the load with their bills, transport costs and just anything worrying them at this point as the road ahead looks like a long journey and recovery for Esme.
Esme is my granddaughter, I am Shanka’s mum & David is my son in-law.
Transport costs, living costs and necessities for the family incl. bills etc.
One day at a time for Esme❤️ 21 January 2021
Firstly, we as a family would love to thank everyone who has donated & shared little Esme’s story. Also, thank you greatly for keeping her in your prayers❤️ An update: She is currently on CPAP (a breathing support) and will stay in PICU until her surgery. She has 2-5 minute breaks off of the CPAP while she has her “mask cares” & she absolutely loves being mask free! Drs have told us to take each day as a milestone itself (as her body will really determine when her surgery will be), aslong as she is happy & gaining weight- when her surgery comes she will be as ready as she can be. She continues to have minor hypertension episodes (to about the 70’s in oxygen readings) when she gets upset, but nothing our little PHighter can’t handle with God always by her side! Thank you for your support and kindness, we will continue to update about Esme’s Journey. God bless❤️
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