Caleb's Crusaders

Dedicated to continuing the fight until there’s a #CF cure for all | We raise awareness and fund research to cure #CysticFibrosis | #Untilitsdone | #65roses

[Caleb's Crusaders @CalebsCrusaders]

2022 @CalebsCrusaders team shirts are on sale now!

https://t.co/oa430wuJID

Every @customink shirt bought includes a donation to @CFF_Chicago & @CF_Foundation on behalf of Caleb. Please consider helping us raise awareness & fund research to cure #cysticfibrosis. #Untilitsdone!

[Caleb's Crusaders @CalebsCrusaders]

Hey @PhillipsNA, what do you think of this years #CF team shirt? Shoutout to @customink for their help.

[Caleb's Crusaders @CalebsCrusaders]

2021 @CalebsCrusaders team shirts are on sale now!

Every shirt purchased includes a donation to @CFF_Chicago and @CF_Foundation on behalf of Caleb. Please consider helping us raise awareness and fund research that will cure #cysticfibrosis

https://t.co/5NoEqOv8Yy

[Caleb's Crusaders @CalebsCrusaders]

The inspiration for this year's design. This is his chest compression therapy vest and nebulizer that he uses multiple times a day to loosen and clear any bad stuff that may be in his lungs.

[Caleb's Crusaders @CalebsCrusaders]

2021 @CalebsCrusaders team shirts are on sale now!

Every shirt purchased includes a donation to @CFF_Chicago and @CF_Foundation on behalf of Caleb. Please consider helping us raise awareness and fund research that will cure #cysticfibrosis

https://t.co/5NoEqOv8Yy

[Caleb's Crusaders @CalebsCrusaders]

#NewProfilePic

[Caleb's Crusaders @CalebsCrusaders]

We just made a $1,610 donation to @CFF_Chicago & @CF_Foundation on behalf of Caleb. This is the largest amount raised during our t-shirt fundraiser EVER! Since 2015, Caleb’s Crusaders have donated more than $22,600!

We will continue our fight until there is a #CF cure for all!

[Caleb's Crusaders @CalebsCrusaders]

TODAY IS IT!!! The final day to purchase a 2020 Caleb’s Crusaders team shirt.

Each shirt purchased includes a donation on behalf of Caleb to @CFF_Chicago and @CF_Foundation. Help us raise awareness and fund research that will cure #cysticfibrosis.

https://t.co/nnArgQ9CAl

[Caleb's Crusaders @CalebsCrusaders]

#NewProfilePic

[Caleb's Crusaders @CalebsCrusaders]

10 DAYS LEFT TO GET YOUR 2020 SHIRT!

We made updates to the design. We added an N95 mask to our crusader shield image. Also, we changed the event title to now read “VIRTUAL GREAT STRIDES 2020” since we will not be walking together in person this year.

https://t.co/nnArgQ9CAl

[Caleb's Crusaders @CalebsCrusaders]

Earlier today, thanks to the generosity, graciousness and continued support of our friends and family, we eclipsed the $20,000 mark in donations to @CFF_Chicago and @CF_Foundation since Caleb was born. Thank you all so very much! #untilitsdone #cysticfibrosis

[Caleb's Crusaders @CalebsCrusaders]

#NewProfilePic

[Caleb's Crusaders @CalebsCrusaders]

@t_sperle, thank you so much for purchasing our @customink 2020 team t-shirt to help us raise awareness and fund research that will lead to a cure for #cysticfibrosis

[Caleb's Crusaders @CalebsCrusaders]

T-Shirt sales are live!!!

Each t-shirt that is purchased includes a donation on behalf of Caleb to @CFF_Chicago and @CF_Foundation. Please help us continue to raise awareness and fund research that will lead to a cure for #cysticfibrosis

https://t.co/nnArgQ9CAl

[Caleb's Crusaders @CalebsCrusaders]

.@SenDuckworth @SenatorDurbin @repschneider, as a constituent and someone personally affected by #cysticfibrosis, I’m speaking out to call attention to the need for new antibiotics. Congress must help tackle this complex issue that impacts us all! #CFadvocacy

[Caleb's Crusaders @CalebsCrusaders]

Thank you for the hat, @CFF_Chicago. @CalebsCrusaders is registered for Northwest Suburban IL @CF_GreatStrides! More team and walk information to follow in the next few weeks. Raising awareness & funding research to cure #cysticfibrosis is #whyistride.

[Caleb's Crusaders @CalebsCrusaders]

Thank you @God_Son80 for your continuous support of #cysticfibrosis!

[Cleveland Browns @Browns]

We’re proud to announce Jarvis Landry as our Walter Payton Man of the Year nominee!

More: https://t.co/xQdzCSQIic

#WPMOYChallenge | @God_Son80 | @Nationwide

[Caleb's Crusaders @CalebsCrusaders]

Simply amazing to wake up to this news for @JenniferProstka and I.

We are making a difference in the CF world every day thanks to the continuous support from all of our family, friends, and medical team @AdvocateKids. Proof, there is always good in the world.

[Cystic Fibrosis Foundation @CF_Foundation]

With $500,000,000 in funding, the Foundation is setting out the Path to a Cure – an ambitious research agenda – and challenging industry to develop treatments for the underlying cause of disease for all people with #cysticfibrosis. https://t.co/aHip22bozY

[Cystic Fibrosis Foundation @CF_Foundation]

“This is a moment to celebrate and to reflect on how working together, and against great odds, we have effectively transformed a genetic disease in a single generation, making #cysticfibrosis the greatest story in medicine" - Dr. Michael Boyle https://t.co/X3owHnMuOv

[Caleb's Crusaders @CalebsCrusaders]

THIS.
IS.
BIG.
The work we do fundraising and raising awareness for CF is absolutely making a difference.

[Gunnar Esiason @G17Esiason]

My life changed on April 9, 2018 when I took my first dose of the ‘Triple Combo’ in a phase III clinical trial. The triple combo, named for its various components, is a drug designed to treat the underlying cause of cystic fibrosis.
1)

[Megan Walsh @megannwalsh22]

Excited to meet with @RepSchneider @RepBillFoster @CongressmanRaja @janschakowsky @SenDuckworth @SenatorDurbin tomorrow to share my story of my brother who has Cystic Fibrosis and the importance of comprehensive coverage as well as funding for NIH and the FDA #cfadvocacy