Wednesday, November 23, 2011
Thankful Thursday: Thanksgiving & Mckenna


Thanksgiving Visitors!!
We hit up the grocery store today to make sure we had everything we needed for the big meal on Thursday. Just off the top of my head, it looks like we'll be having: Turkey, stuffing, mashed potatoes, yams, green beans, cauliflower, cranberry sauce, corn and pumpkin pie. Think that's enough for the 4 of us (and I wouldn't be surprised if I'm forgetting a thing or two)??? I seriously can't wait as the Thanksgiving meal is one of my favorites, although I always must remember not to eat myself to death...almost literally. Have I told that story on RSBR before? The time that my Thanksgiving meal almost killed me? That's a good one.
Anyway, the whole point of this blog is to welcome my dad and Denise to Arizona and let them know I'm extremely happy they are here (as I know they'll get the message since they read this everyday). I look forward to the next 8 days and can't wait to see what trouble we get ourselves into. Thanks for the help with the yard today and please, don't hesitate to think of other projects we can knock out while ya'll are here. I mean, we can't sit around and stare at Mckenna all day every day right? Right???


Tuesday, November 22, 2011
Friday, November 18, 2011
PICC Line Dressing Change - Part Deux


Thursday, November 17, 2011
Thankful Thursday: Feedback & Caramel Brulee Decaf Soy Latte


Wednesday, November 16, 2011
I never would have thought...


Tuesday, November 15, 2011
My PFT History
05/19/14: FVC 90% FEV1 75%
05/12/14: FVC 89% FEV1 75%
04/28/14: FVC 73% FEV1 57%
12/21/13: FVC 88% FEV1 75%
12/02/13: FVC 77% FEV1 63%
06/24/13: FVC 92% FEV1 75%
05/28/13: FVC 83% FEV1 73%
05/03/13: FVC 72% FEV1 57%
01/07/13: FVC 78% FEV1 65%
10/01/12: FVC 87% FEV1 74%
11/14/11: FVC 88% FEV1 74%
3/9/09: FVC 65% FEV1 51% (last day in hospital)
2/19/09: FVC 59% FEV1 47% (in hospital)
1/27/09: FVC 42% FEV1 31% (in hospital)
Monday, November 14, 2011
Mckenna Monday: Four Week Update


Saturday, November 12, 2011
Kicking Cystic Fibrosis!!

My name's Eric, and I'm 17 years old from the Great White North's capital, Ottawa. On October 27th I officially made it 4 years that I have been blowing an FEV1 of over 100%, and I owe those numbers to exercise. At the age of 4 my parents put me in soccer, and it wasn't until I was 16 that I stopped playing. I've spent countless hours at the soccer field near my house, literally countless. I have spent summers there, the soccer field WAS my second home, and it really payed off. I managed to make a provincial team, and I played with them for three seasons. All of that time spent running around the field with a ball, practicing my shot, and whatever else I ended up doing there for hours definitely payed off for my soccer skills, but more importantly it payed off for my health.
This all started about 5 years ago, and during that time it definitely started to show that an increase in my health was being made. In about 2 years, I jumped 3 divisions and made it to a provincial level, and from 14-16 I continued to play with the same team. The practices were brutal and and honestly there were mornings I wasn't getting out of bed because my abs hurt too much, or because us scrawny soccer players can do a max of 15 pushups and our coach squeezed one more out of us. In the end it all really payed off, because once I made that provincial team my PFTs finally reached 100%. The amount of mucus I was coughing up was huge, disgusting really (ask my girlfriend), but great for me. The numbers didn't increase much for a good while after, not until I quit soccer and began running.
Running is such a simple thing (and free!) and so good for people like us with Cystic Fibrosis. I don't exactly know why running gets stuff up, maybe it's the increased and harder breathing, or maybe it's the vibration of both feet hitting the ground, but whatever it is it gets junk out of our lungs. I began running about 3-4 times a week about a year ago, and not long after that I did my first 10km run, and did it in a time of 44:37. That's when I hit my highest PFT at 114%! It's been all over the place since then, as I've dealt with minor complications, but not once did it drop below 100%.
Now I've added swimming, biking, and lifting weights to my regime, and am really looking forward to completing my first triathlon next summer! Every single Cyster and Fibro can benefit from running twice a week, even once a week! There are countless stories of CF patients increasing their lung function and living a better life because of activity, and it doesn't necesarily have to be running, go join a recreational soccer team, basketball or any of the sort! Go get a gym membership and start lifting weights, or use the cardio machines they've got there. Anything is better than nothing! If this 17 year old boy can take control of his health, then anyone can.
Bio: My name's Eric Verdon, and I'm from Ottawa, Canada. My parents put me in soccer at the age of 4, and I continued it until I was 16. When I stopped playing, I found a new passion in running. Today I swim, bike and continue to run in hopes to complete my first triathlon next summer. I absolutely love learning about the body and am planning on studying kinesiology next year in hopes to continue my studies into medical school, focusing on sports medicine.
Note from Ronnie: I just want to thank Eric for sharing his story. I think it's so important to remember something he touched on - something is better than nothing! Many of us decide that since we can't do a lot of exercise, we'd rather just do none at all. Just as Eric pointed out however, there are plenty of options available to us if we want to get active. It's all about us choosing to quit making excuses and as Nike says, "Just Do It!!". Thank you again Eric for sharing your inspirational story!


Friday, November 11, 2011
Where's Mckenna?


Thursday, November 10, 2011
Thankful Thursday - Wraps & Small Changes


Wednesday, November 9, 2011
Workout Wednesday: New Exciting Workout!


Tuesday, November 8, 2011
Extra Running Motivation


Monday, November 7, 2011
First Day Back in the Saddle



Saturday, November 5, 2011
You're Capable of More Than You Think

Guest Post by Jaime C.
My name is Jaime, I’m 26 years old, and on Monday, October 24th I ran a mile for the first time in my life. I mean EVER. Then, Tuesday I went and ran two. I know, I’m shocked also!
Those two nights were a triumph for me after five months of working out with a trainer and starting to run. I was a pretty active kid growing up, but after I graduated from high school and started college I just didn’t want to exercise any more--it got in the way of my social schedule and I didn’t want the reminder that my lungs were not cooperating with the plans I had. I was simply being lazy. This decision was quite possibly one of the worst I’ve made in my life.
Five months ago I moved to a new city with friends from college and transfered to a new office with my job. Deciding to move was a long and anxiety-filled process and taking care of myself kind of fell by the way-side. On top of that, the weekend of the actual move I caught a cold, which would. just. not. go. away. Prior to moving I had belonged to a gym but half-heartedly went a couple times a week and walked on the treadmill convinced I couldn’t really handle more than that because it was hard. My parents and new roommates (a couple of close friends from college) encouraged me to keep going to the gym and work with a trainer and really get serious about trying to get my lung function back up. I wasn’t really convinced that it would make much of a difference but decided to give it a try.
About a month into my “new” life I ended up having to do IVs which, as so many of y’all know, just takes it out of you! But one thing I did differently this time--kept working out (with a lot of prodding from my roommates). I took the full three weeks of IVs off of work and during that time got lots of rest, lots of awesome homemade meals (thanks to my church) and lots of time at the gym. After IVs my PFTs were back up to my baseline that I’ve had for the last few years, and fresh off that clean-out I hit the gym hard. The trainer I had been working out with had been doing his CF research and informed me that I was going to become a runner. I laughed in his face. And then he made me go run on the treadmill. And I did it. Very slowly at first and for very short distances, but I did it. It was really hard and I was pretty miserable for a long time. I think that much of the battle was mental for me--believing that what I was doing was, in fact, going to make a difference in my ability to breath, live longer, live better. And believing that I could actually do it.
One thing that my trainer said to me was that he thinks I am capable of more than I think I am. I was totally lame and started crying in the gym. Really cool. But it got me thinking, and I realized that there are a lot of things that I’ve decided I can’t do because of CF. I won’t go into that laundry list but the majority of it is ridiculous because I’ve done things in my life that were hard and out there and impulsive and crazy like moving to a foreign country for 10 months with a weeks notice. So why was taking care of my body and working hard, I mean really hard, to help myself so difficult? Why was I able to do things in other “areas” of my life that required a leap of faith with the absolute possibility of failure but not when it came to putting in the work to help extend my own life? I think it’s because I didn’t want to put in the work, experience the pain, deal with the emotions and the struggles and still get sick or have it make no difference. That feels so defeating and leaves me with a distinct feeling of helplessness that I’ve never experienced elsewhere.
I don’t have a good answer to my own questions or know of the best way to handle the possibility of working really really hard at something and having it go badly or not have miraculous results. But what I do know is that when I went to clinic last Thursday my PFTs were, and I quote my doctor: “the highest they’ve been in 5 years.” WHAT?! All I could do was start laughing. And almost fall off the table. I’m just not graceful. It’s ok, I’ve embraced it. But I digress. The moment after I finished my PFTs I knew they looked good, but having my doc go through my chart and really look at how high and low they’ve been in the last few years confirmed that my hard work was indeed paying off. And all of my miserable moments leading up to being able to run two whole miles were suddenly totally worth it!
Now I know that there will be times when I’ve been working hard and I might not see improvement. We all know the unpredictable nature of CF and that even when doing everything right things can still get worse; and yes that’s frustrating. I can’t in all honesty say that when I experience one of those times in the future, where, despite hard work I still get worse that I’ll have a good attitude about it. However, right now, on this side of that situation, I want to cultivate a lifestyle and disposition that reflect what I’ve learned from these last five months: when it comes to CF I am absolutely capable of more than I ever thought; that working hard through pain and burning lungs and muscles is worth it to take back my life and not feeling like CF has already claimed victory. I CAN and I WILL fight this.
Bio: I'm Jaime C. and I'm 26 years old from NC. I was diagnosed at 3 months old at Duke but have been seen at UNC by an amazing group of doctors since I was four. I work full time at a bank and have been doing that for the last two and a half years. Prior to that, I was a nanny in Italy, and before that a college student! I love my family, nail polish, exploring my city, finding new fun places to eat, cooking, the beach, baseball, fashion, traveling the world, learning about and knowing God more, and having a good beer with friends. I hope this little slice of my life helps others realize that they are stronger and capable of more than they think especially in regards to exercise.
Note from Ronnie: I can't thank Jaime enough for sharing her story. It rings so true to many of us in the CF community doesn't it? I know that when I started running, all I could do was picture failing. That fact the I decided to run was a victory in itself, but when I actually "hit the ground running" it became a battle of believing in myself. I think Jaime shows us that through some hard work, preserving and belief in oneself, anything is possible!! Thank you SO MUCH cyster!!

