Wyatt's Cystic Fibrosis Journey

Wyatt's Cystic Fibrosis Journey Wyatt was diagnosed with cystic fibrosis on 9/6/24 at just over a week old. Follow his journey here!
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Today is day 2 of 10 of "My Life is Good". I was nominated by Arieall Sãntorriã I am to post photos/videos that bring me...
04/15/2026

Today is day 2 of 10 of "My Life is Good". I was nominated by Arieall Sãntorriã

I am to post photos/videos that bring me joy (no explanations) because we all need a little joy right now. 10 photos 10 days.

If I choose you, please continue the happy train! Today I am choosing Phoenix Grace Creations 💕

Rainy walks with pups. 🌧

04/15/2026

👨‍🍳 Chef Wyatt is back in the kitchen! He decided on a very fulfilling dinner. Steak, mac and cheese, and some veggies! All things he will eat. Yummy!

04/14/2026

Lunch of CF warriors! 🤭 Pizza, pears, and can't forget the extra cheese! You think Wyatt could get his hand any farther in his mouth? This kid could live off cheese 🧀 What's one thing you could eat and never get tired of??

This image came across my feed from Everyday Health, and it's a very basic and easy to read explanation of how cystic fi...
04/14/2026

This image came across my feed from Everyday Health, and it's a very basic and easy to read explanation of how cystic fibrosis affects those who have it. Not all those with CF have every symptom/issue, and some have every single one. One thing not shown here is that there is also CFRD, or cystic fibrosis related diabetes, which adds a whole different thing to deal with. Something that is sort of a contradiction is the inability to tolerate exercise. Exercise and being active is crucial to help the lungs and heart stay strong, but especially the lungs of those with CF.

There is so much that comes with having cystic fibrosis. And there are many things available to help deal or treat the issues that come. But there is no cure....yet! Wyatt is our why. Wyatt is our reason. And we will be involved in finding that cure.

04/14/2026

A simple but powerful message about cystic fibrosis. It's so true. So much goes on behind the scenes to give those with cystic fibrosis any quality of life. And time becomes even more precious. With cystic fibrosis, you truly don't know how long you have. And that is why we are doing what we can to raise awareness and to one day find a cure for Wyatt and everyone else living with cystic fibrosis.

Today is day 1 of 10 of "My Life is Good". I was nominated by Arieall Sãntorriã I am to post photos/videos that bring me...
04/14/2026

Today is day 1 of 10 of "My Life is Good". I was nominated by Arieall Sãntorriã

I am to post photos/videos that bring me joy (no explanations) because we all need a little joy right now. 10 photos 10 days.

If I choose you, please continue the happy train! Today I am choosing Moose and Charlie (because she loves being given tasks, responsibilities, and homework)💕

My babies!! 🥰🙏🏽

04/14/2026

STARS CHALLENGE!!! All friends invited!!! We are giving away 200 stars on Wednesday to a lucky page! Like, comment your “why” for you page (your passion that drives you to create content), and then share. Winner to be chosen by meeting the guidelines for entry, and then random.

04/14/2026

This is how most of my videos and pictures of Wyatt go! 🤣 He has become very interested in looking in a camera. If he even slightly sees me trying to catch him doing something cute, he runs to see what's on the screen! Funny little guy!

04/14/2026

Wyatt stole his sister's slippers tonight and was walking all around! 🤭 Now it's time for pajamas and settling down! Hope everyone had a great day and has a restful night!

Alright everyone!!  It's crunch time!  The Seattle Great Strides walk for cystic fibrosis is in 5 weeks!  Cystic Fibrosi...
04/13/2026

Alright everyone!! It's crunch time! The Seattle Great Strides walk for cystic fibrosis is in 5 weeks! Cystic Fibrosis Foundation - Washington Chapter is halfway to the goal that was set. Time for us to ramp up and get things going! For those who have donated, thank you so much! For those who can't donate, we appreciate you as well! Just a share, comment, or reaction is huge! Wyatt's link is below and you can use my name (Jacquie Oka) as the participant. This picture is from last years walk and we can't wait to do it again in May. Let's find a cure!

https://fundraise.cff.org/Seattle2026/Wyattswarriors2026

04/13/2026

Wyatt was given this sweet little bear from the New Zealand Cystic Fibrosis Foundation. It was sent by a sweet lady and her family, including her oldest who has cystic fibrosis. Wyatt is now carrying this bear around calling him Blue. And I love it. It's the sweetest thing. Especially since this bear is known as Fred Bear and is given to all people with CF in New Zealand! This is a very special bear to us. 💜

Welcome to Deputy Wyatt's Wild West!  We've met some super supportive (and creative 🤭) people on Wyatt's journey!  He wa...
04/13/2026

Welcome to Deputy Wyatt's Wild West! We've met some super supportive (and creative 🤭) people on Wyatt's journey! He was even accepted into a great crew of people, known as the Chaos Crew. If you're looking for some great people and support, I'll leave their names here!

Moose and Charlie
Pitmaster Jimi's Gourmet Seasoning's and Rubs
Chuck Beyers
No Shift Coffee Company LLC
Little Native Indian Blue Bully Kennel
The GingerVeteran Productions
James Rowell
Zero Hour

It wouldn't let me tag some, so Chaos Crew do your thing and get everyone here!!! And introduce yourself! I have some other sweet moms and familes here!

Address

Anacortes, WA
98221

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