Cystic Fibrosis Apparel

I love someone with Cystic Fibrosis. A beautiful cystic fibrosis awareness gift for a proud CF mom or dad in pretty rainbow letters.

Cystic fibrosis

Cystic Fibrosis Awareness

Breathe, Just Breathe. The rest of the world takes it for granted. And for Cystic Fibrosis Warriors, it is a daily battle. Inspired by our son, warrior for over 30 years. Just breathing, when the doctor told his mother he wouldn't make it to five.

It was scary wasn't it? Scary As F@#$!!! You've been there for everything! Doctors, treatments, backslides. But you've been there for all the joys! The first Birthday! The first walk! The first run! It's a balancing act and you are the one they lean on. Spread awareness and keep the conversation going....

Cystic Fibrosis is my Superpower

The proceeds from the sales goes to Breathe Bravely’s sINgSPIRE virtual choir. A choir with singers from all over the world defying a diagnosis of cystic fibrosis through the art of singing. Join their diverse and powerful voices together in a unified chorus of strength, tenacity, and unrelenting hope. Design-cred @hannahalmerud, @foppsicle, @entapir & @elljeyLJ.

Proudly wear your El Jefe's Posse gear to show support for our little buddy and all the warriors bravely kicking Cystic Fibrosis's butt.

It's Not For The Weak

Are you a Husband with a Cystic Fibrosis Warrior? Raise awareness and show the world how Strong As F@#$ You Are!!!! You've been there for everything. In Sickness and In Health. You've done the extra drop-offs or pick-ups at school, been to the games. But you've also been to the doctor's appointments. You've held them in your arms when it was a very bad flare. You are there to help them decide to change doctors or treatments because they've had enough and it's not going anywhere. You are there for it all. You stand by them. Keep the conversation going. Spread awareness. Until there is no more.

Are you a Wife with a Cystic Fibrosis Warrior? Raise awareness and show the world how Strong As F@#$ You Are!!!! You've been there for everything. In Sickness and In Health. You've done the extra drop-offs or pick-ups at school, been to the games. But you've also been to the doctor's appointments. You've held them in your arms when it was a very bad flare. You are there to help them decide to change doctors or treatments because they've had enough and it's not going anywhere. You are there for it all. You stand by them. Keep the conversation going. Spread awareness. Until there is no more.

Other kids will never know what it is to be like a Cystic Fibrosis Kid. Whether you are the kid of A Cystic Fibrosis Warrior, watching the treatments, or seeing the ambulance pull up to the house. Or, YOU are the the CF KID!!! From that early age where the doctors are testing you trying to figure it out. They know, but they don't want to say anything to scare your parent(s). From there, it's a lifetime of doctors, breathing function tests, treatments three, four or more times a day. Vests and masks. You are taking so many pills when kids you age are chewing Flintstones vitamins. Needles. But! But! No, that's not stopping you! You fight to Breathe, and so you will fight to live!

It was scary wasn't it? Scary As F@#$!!! You've been there for everything! Doctors, treatments, backslides. But you've been there for all the joys! The first Birthday! The first walk! The first run! It's a balancing act and you are the one they lean on. Spread awareness and keep the conversation going....

Even though people with CF are living to an older age today compared to just a decade or two ago, we are still striving for a longer life expectancy and waiting for treatments that can allow for a better quality of life without several hours of treatments every day. Therefore, the proceeds from the sales will go to Riksförbundet Cystisk Fibros which is the Swedish charitable organisation for people with CF. Designcred @hannahalmerud, @foppsicle & @entapir.

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