Hello to all my fellow and beloved breathheads (ps: loving the new nickname)!
So here's a quick update on the shirt situation:
*Today (Friday the 28th) is the official deadline. I will be placing the order at 4:00 pm EST, so please have your order in by then. I will probably be getting a limited number of extra shirts, but those will only be available on a first-come/first-served basis.
*Youth sizes update: they will be available! However, the youth sizes will be simply xs/s/m/l (no special toddler sizes available, sorry!). If you have a little one and asked about a shirt for him/her, you'll be receiving an email from me confirming that you still want one and the right size for your child.
*I will send a confirmation to each of you with your order "invoice" (i.e., number of shirts and size breakdown). If there is a problem, or if you don't receive your confirmation by noon Friday, please contact me!
*Once you have received your confirmation, then feel free to donate toward the cost of the printing/shipping either by paypal (email: firstname.lastname@example.org) or by snail mail. I'll send a mailing address to those who requested it along with the confirmation. Remember, no official cost for t-shirts, and donation is NOT required for your shirt.
On a personal note, I have been incredibly touched (and my sister is flattered) by the response to the t-shirts. Thank you all for your support, your readership, and your general awesomeness. I hope you enjoy the shirts and wear them with pride -- these lungs are for all of you!
xoxo 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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