Showing posts with label t-shirts. Show all posts
Showing posts with label t-shirts. Show all posts

Sunday, June 20, 2010

Update from the Godmother and Other Cool Stuff


Dear readers,

This is Joan, Piper's beloved Godmother, with a quick message about SHIRTS. We have some extras in adult S, M, L, and XL sizes. If you would like to add one of these amazing shirts to your wardrobe, please leave your email on the comments section of this site and the Godmother will get to you with details. At this point shirts will cost $10, but all proceeds go directly to the Cystic Fibrosis Foundation in support of the amazing new life my Goddaughter has received these past few days. And, as always, in honor of all of you and your amazing fights against this disease!

Got it? Good. (And don't worry, she's the wonderful, magic kind of Godmother who makes everything all better!)

In other news, who wants to see the first post-transplant pictures?! Coming to you live from the 7th floor transplant ward!

Keeping Your Shirts Warm

You've Seen the Dry Runs -- Here's the Real Thing

Columbia Pres Cough Buddy (Piper Hugs this to Cough)

Our Lady of the Greasy Hair and Big Smile

So there you have it...all the news that's fit to print! Piper is still recovering from what we'll just call a LOT of needle pricks today, so she's a little more out of it. They did reaccess the port, but it didn't help. Hopefully tomorrow will be smoother sailing in that territory, but in the meantime we're taking it in stride. On a positive note, Piper did a FULL LAP around the transplant floor on room air with minimal rest stops AND STAYED AT 96%! Um, woah.

Happy fathers day to everyone, and a very joyeous Sunday with yet more to be grateful for...as if it ever ends.

Wednesday, June 9, 2010

Special Delivery

So yesterday while I was at gyrotonics, my mother received a special delivery of new lungs!


Lots of new lungs . . .


200 pairs of them of them, to be exact.

And now we get to ship them off to you, my wonderful readers!

A few important details:

1) I hope to get all the shirts shipped off between today and tomorrow, but I have to ask for a little slack seeing as I also have transplant clinic tomorrow. When your order is packaged, addressed, and ready to go, I will send you a quick email confirmation. If you DO NOT hear from me by Friday evening and you have a shirt (or multiple shirts!) coming, please email me!

2) I will be processing and shipping orders received within the deadline first, and then overstock. Don't worry, I'm 99.9% sure I have shirts for all of you, but fair is fair. Overstock orders will be processed on a first-come, first-served basis.

3) Here's the sad part: something happened to the blog email address a couple of days ago and I know I lost 3-4 new emails. So please, if you asked for a shirt and haven't heard anything back from me at all yet, email me again! Chances are there is a shirt available for you, but I just never got your request.

4) Shirts are, as previously mentioned, free of cost. Donations are being accepted for the cost of shipping and printing via paypal at piper.beatty@gmail.com. You may also send money the old fashioned way, and please email me for my address if you'd like to take that route. Suggested donation is $10/shirt, but donation is 100% optional.

5) I've already had some people with larger requests ask about another order. Stay tuned for possible post-transplant celebratory shirts (with color options!).

Happy (stylish) breathing, beautiful people.

Friday, May 28, 2010

T-Shirt Update

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: piper.beatty@gmail.com) 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,
Piper

Wednesday, May 26, 2010

The Truth about Waiting

(Or; Why I'm Not in the Fortune-Telling Business)

First off: okay, um, wow? Can I just say that the response for t-shirts has been AMAZING? Who knew so many people were in the market for a new set of lungs (or, you know, a picture of them at least)? Anyway, here's the deal:

*The shirts are officially no cost. I know we all have enough to deal with in terms of payments and financial worries, and I don't want anyone to miss out on the opportunity to give my blog free publicity -- er, I mean to own a beautiful and timeless piece of fashion history -- because of cost. So no charge for shirts.
*If, however, you would like to make a donation toward the cost of printing and shipping, I would be thrilled to accept it. I'm working on setting up a paypal account for that purpose, or simply e-mail me and I'll send my address along for cash/check donations. Just as an FYI, the cost is about $10/shirt, so please limit your donation to that.
*Some people have asked about toddler/child sized t-shirts. As of right now I have two people interested in receiving shirts for their little guys. I'm working on finding a provider willing to print youth sizes with no minimum order, so if you're interested in showing off your kiddo in style, please let me know.
*OFFICIAL DEADLINE for shirt orders is Friday, May 28th (good catch, Jenny!). Sorry about the short notice, but I want to get these printed and sent out ASAP.

Okay, so we're cool on the shirts.

It's been about a month since my last official call, and I'm definitely starting to get restless. Don't get me wrong, there's a part of me that's grateful for the extra time to get everything in order, but you can only repack your hospital bag a certain number of times before you start just wanting to get it over with, already. It's crazy to think that headed into April (with two dry runs from March already behind me), I was absolutely certain that I would have new lungs within the month. Well, okay, so that's not entirely true -- I haven't gotten so cocky yet that I believe I can predict the future, but I was pretty sure the "real" call was coming soon. And now to suddenly find myself at the end of May and still with my CF lungs, well, let's just say I won't be setting up shop as a fortune teller anytime soon. It's humbling, when you think about it, to realize just how uncertain this whole process is. One month you're getting 1-2 calls every week, and then a whole month passes with no lungs available for you. Frustrating, for sure, and also a reminder of why it helps to be on the healthier side of the "transplant window" going into the waiting experience. Lungs don't always come when you expect them, or when you want them . . . there's more to all of this than I will ever understand, but I know I'm grateful to have time to wait, for now at least.

Anyway, after weeks of trying to stay relatively close to home and obsessively checking my phone every five seconds in case I somehow missed a call, I finally woke up and decided that's not the way this relationship is going to go down. After 4 canceled dates and now no calls for several weeks, I'm pretty sure I could do better. No, I'm not switching centers, if that's what you're thinking. I'm still happy overall with my choice and love my doctors, so that's not in the cards anytime soon. Instead, I've decided (again) that it's up to me to actually live my life as best I can during this period, despite the uncertainty of it all. I say "again" because you may remember that I already had this brilliant revelation months ago, but it's all too easy to forget your vow to keep living when the call seems imminent.

So yeah, all of this is a long way of saying that I'm now daring lungs to come and ruin my plans. I've been planning meals out with friends, trips to the Cirque du Soleil, parties at my apartment, and even a couple of day trips. On Monday my mom and I took the train out to New Haven, CT to see my wonderful friend graduate with his (second) master's degree from Yale, and then yesterday we rented a car to travel out to Woodbury Commons -- a truly amazing upscale designer outlet center -- for some shopping and a little fun outside the City. True, we brought enough O2 with us to cover if we got the call along the way, and we're still staying within a couple of hours of my center, but it's still nice to be able to actually make plans and follow through with them.

I think it all goes back to the concept of "readjustment" that I wrote about a few posts ago. For me, at least, there was this huge adjustment when I finally accepted that transplant was on the horizon for me, and then again when I actually went on the list and realized that lungs could technically come for me any day. As my father put it "we went from desperately hoping for a cure to desperately hoping for a fresh set of disease-free lungs" within the span of a couple of years (although obviously we're still hoping for a cure -- we will beat this monster even though to do so wouldn't "save" my lungs at this point). Talk about a major shift in expectations. But I still don't think it compared to the adjustment that took place after my first dry run, when we all suddenly woke up to the hard reality that this could, in fact, happen at any moment, and whether we were prepared or not wasn't going to make any difference to the lungs when they finally arrived. So we went into intense transplant mode, which continued hardcore until the "damp run," at which point we kind of shrugged our shoulders and decided that we had, in fact, seen it all and were literally as prepared as any family could possibly be. So we waited, and waited, and then the adjustments began again as it began to dawn on us all that 4 dry runs does not a transplant make. In other words, each day is a new day, with as much or as little of a chance of a matching donor as the day before it, and expectations don't mean much when the whole thing is out of your hands.

And so I decided to readjust one more time: back to life, back to being grateful for every new day with the lungs God gave me, and back to focusing my energy on the things I can control, rather than spending all my time thinking about something that is going to come when it comes regardless of what I think about it. I figure if time flies when you're having fun, the least I can do is try to speed up this waiting a little bit.

And, in the meantime, if any lungs want to come along and crash my party, that's just fine by me.

Sunday, May 23, 2010

12,500

Today was our Great Strides walk in lower Manhattan. I was SUPER proud of my team -- we raised about $12,500 (preliminary total) for a cure! That's money that will go straight to the Cystic Fibrosis Foundation, and about 90 cents of every dollar donated directly funds CF research and educational programs. And when you think about the new drugs in the pipeline and how freakin' close we are to FINALLY breaking through to target the actual defect that causes this disease, well, all I can say is wow -- Great Strides, indeed.

Thank you to all my wonderful walkers for showing up, for smiling even at 9:30 am on a Sunday morning, and for looking so amazingly HOT in my team t-shirts! I was especially proud of our two furry mascots, particularly "Tug" for rockin' the shirt like a champ. Also thanks to my CF friends Graves, Joni, and Gabby -- awesome to see you all!

And a VERY special thank you to everyone who donated to our team through this blog. You guys have no idea how amazing the response was after my post for a cure! I was truly overwhelmed with gratitude and excitement. Not that I ever for a second doubted that I had the best readers a girl could ask for, of course, but you didn't have to go to such amazing lengths to prove it! Please know that you not only made my day, you also made a HUGE difference in the lives of everyone living and breathing with CF throughout the world.

Here are a couple of pictures from the big day:

Team Piper Official Portrait

T-Shirt Front

T-Shirt Back

My Lovely Sister (and designer of the shirts!), My Father, and Me at the Walk

Okay, here's the fun part:

Are you an official "Breathhead"? Are you interested in having one of these fabulous lung t-shirts -- designed by a famous designer featured in the June issue of Vogue, no less -- for your very own? Would you like to spend the night of my transplant cruising my blog, reading updates from my talented sister, and sporting your own piece of beautiful Matter of Life and Breath apparel?

If you answered yes to any of the above questions, consider contacting a therapist for special help. Just kidding, contact me instead! That's right, we're thinking of ordering another batch of these beautiful shirts for all my wonderful supporters, and would like nothing more than to send YOU your very own. So let me know at matteroflifeandbreath(at)gmail(dot)com and please include info as to your preferred size and shipping address. All addresses will be deleted upon shipping.

Thanks guys, and thank you to everyone who donated, walked, or volunteered for the many Great Strides walks all over the country. You guys are, as ever, an inspiration.