Welcome to Paisley Long's page!
Thank you for visiting our fierce heart warriors page. For those of you who don't know Paisley was born 09/25/18 with a rare heart defect called "Scimitar Syndrome" (which is characterized by anomalous venous return from the right lung (to the systemic venous drainage, rather than directly to the left atrium) This anomalous pulmonary venous return can be either partial or total). This is accompanied with a a small right lung and in Paisley's case her right lung is very hypoplastic only accounting for 2% of blood flow. She also suffers from sever pulmonary hypertension (high pressures in her left lung cause her right ventricle to work to hard and start to fail. She is in a long term heart failure state. She spent nearly 7 months of her first year of life impatient with several hospital stays.
Paisley was also born with several other diagnosis'. She has bilateral colobomas (her eyes never fully developed), she had some fused ribs and vertebrate. Bronchomalacia on her left side causing her to be trach and vent dependent. She received her Tracheostomy when she was 5 months old due to aspiration, tachypnea, having trouble gaining weight.
Paisley has had multiple cardiac caths and on 11/05/2019 where a stent was placed into her left pulmonary artery in hopes to help her lung pressures. The stent did help and slightly lower her pressures and thing were going good for a while after that.
Just within the last few months Paisley was experiencing worsening symptoms. She was have oxygen desaturations, higher heart rates, not tolerating feeds, vomiting and restless. She was started on oxygen at night and changed her feeds to something more broken down for her to tolerate. Paisley had a GJ tube. She hasn't eaten in her stomach since she was 5 months old, she is fed into her intestines (jejunum) and takes very little by mouth. She is doing much better with wanting to try more and taking sips of water from a sippy cup.
She just went in for another cath on 8/14/2020 and they ballooned her stent and also tried to balloon some of her surroundings vessels to see if the overall pressures will go down but that wasn't very successful. Overall her pressures are about the same as where they were last year and they are starting to run out of options on what to try next. Her team is having conversations on surgeries or other procedures that could help. The longer we wait the more damage to her heart and ultimately her pulmonary hypertension will fail her heart. Transplants are a possible option in the future but she would require a Heart/Lung transplant.
As long as Paisley continues to thrive a home and be the happiest little girl we will always advocate and fight for her. She is walking and learning to talk above her trach while vented, learning sign language and loves her family. We are very hopeful with more funding for research they will be more options for when we need them to help give our girl the longest life possible.
Thank you for visiting her fundraising page for the Congenital Heart Walk. Raising funds for CHD research is critically important to all Heart Warriors and Heart Angels, and personally very meaningful to me.
Please help us to fund CHD research by making a donation to her personal fundraising page. Together we can make a life-saving difference!
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