


UPDATE 9/12/23
Dear Loved Ones,
We would like to express our heartfelt gratitude for your unwavering support as we continue to navigate our daughter Cataleya's challenging journey with surfactant deficiency caused by the ABCA3 gene mutation. We wanted to provide you with an update on her recent progress.
Cataleya has shown remarkable resilience since her birth, and we remain optimistic about her future. Over the past few weeks, she has undergone significant medical interventions, including the placement and subsequent removal of seven chest tubes. We are thrilled to share that she no longer requires any chest tubes, which is a major victory for our little warrior!
Given her respiratory condition and the need for intubation, Cataleya has been paralyzed and sedated since she was only three days old. There were a few weeks when the paralytic medications were temporarily lifted to allow her some relief. However, in order to ensure the best possible quality of life for our precious baby, we made the difficult decision to proceed with a tracheotomy surgery. The procedure was a success, and it will enable her to gradually be weaned off the paralytics and sedatives for the first time.
While Cataleya is still battling her illness, we are encouraged by the progress she has been making. Despite the challenges she faces, her resilience and strength continue to inspire us every day.
Once again, we want to express our deepest gratitude for your love, support, and compassion during this challenging time. Your unwavering presence in our lives means the world to us, and we are truly grateful for each and every one of you.
With heartfelt thanks,
Nicky & Brian
Alexandra O
$25 • Recent donation
Christin Tangen
$1,000 • Top donation
Liz Grandez
$20 • First donation

Nicolette Cordova is the organizer of this fundraiser

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UPDATE 9/12/23
Dear Loved Ones,
We would like to express our heartfelt gratitude for your unwavering support as we continue to navigate our daughter Cataleya's challenging journey with surfactant deficiency caused by the ABCA3 gene mutation. We wanted to provide you with an update on her recent progress.
Cataleya has shown remarkable resilience since her birth, and we remain optimistic about her future. Over the past few weeks, she has undergone significant medical interventions, including the placement and subsequent removal of seven chest tubes. We are thrilled to share that she no longer requires any chest tubes, which is a major victory for our little warrior!
Given her respiratory condition and the need for intubation, Cataleya has been paralyzed and sedated since she was only three days old. There were a few weeks when the paralytic medications were temporarily lifted to allow her some relief. However, in order to ensure the best possible quality of life for our precious baby, we made the difficult decision to proceed with a tracheotomy surgery. The procedure was a success, and it will enable her to gradually be weaned off the paralytics and sedatives for the first time.
While Cataleya is still battling her illness, we are encouraged by the progress she has been making. Despite the challenges she faces, her resilience and strength continue to inspire us every day.
Once again, we want to express our deepest gratitude for your love, support, and compassion during this challenging time. Your unwavering presence in our lives means the world to us, and we are truly grateful for each and every one of you.
With heartfelt thanks,
Nicky & Brian

Nicolette Cordova is the organizer of this fundraiser
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