Alright, guys, you asked for it!
No, seriously, you totally did -- I've had over 30 messages this week alone asking for these shirts. Who knew I had such stylish friends?!
In honor of the 2012 Great Strides Walk to CURE cystic fibrosis and all 70,000 of the amazing people fighting this disease worldwide (not to mention my 2 year transplant anniversary, coming up on 6/12/2012), we here at A Matter of Life and Breath are proud to announce our second ever t-shirt sale spectacular! Featuring shirts designed by the Amazing folks at SUNO fashions (a favorite of Vogue magazine, among others), this sale is a stylish and super-cool way to say sayonara to CF! Plus, every single penny earned is going to support the work of the Cystic Fibrosis Foundation. Seriously, how cool is that?
Consider this your official sneak peek at this year's design. Even better, the award in the pictures is our FIRST PLACE trophy for best shirt at the Great Strides Manhattan/Brooklyn walk!
So here's the deal:
Adult shirts are $15 each, with all proceeds going directly to the CFF via the Great Strides fundraising system. I will send payment info to you directly upon receipt of your order.
Orders can be placed for S/M/L/XL shirts by emailing amount and size requests to Piper at firstname.lastname@example.org (note that there is no "a" in the email!). Please also include shipping address for ease of process.
Child-sized shirts will be ordered IF there is enough interest from the community, so if you want one for a kid please include that in the email as well.
All orders must be received by FRIDAY, JUNE 22.
On a personal note, I just want to say a HUGE thanks to all of you for everything you do to help us win. Each of you is already a CF Challenger in my book, and together we can say GAME OVER to CF!
Love and light beautiful people,
- I am a 33-year-old wife, sister, daughter, friend, law school graduate, CFer, lifelong student of public service, blog writer, patient, Sagittarius, reader, Top chef fan, double-lung transplant recipient (twice!), and dog owner living in Colorado's beautiful Mile High City. I love all things colorful, funny, inspiring, or needlessly sarcastic. I share my city with about 2,500,000 other remarkable people, share my disease with 70,000 other beautiful souls, share my life with some unbelievable family and friends, and share my apartment with one very handsome guy and one really fat mutt with a kick-butt personality. We make it work.
About This Blog:
This blog is about me, my life, my sometimes craziness, my disease, and my current journey as a double-lung transplant recipient. It's also a celebration of everyone out there with CF (and other chronic illnesses). It's for you, inspired by you, and dedicated to you -- the community that keeps me writing, living, and breathing.
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