sandyscflife.blogspot.com
Sandy's CF Life: Time Flies!
http://sandyscflife.blogspot.com/2011/02/time-flies.html
Sunday, February 13. I think I'm due for a bit of an update. The last few weeks have gone well in terms of my health. I had a run-in with CMV, but after a couple of weeks of oral anti-virals, it's gone again. Otherwise, I'm keeping up with my workouts, meds, sleep, and I'm even eating better. I have probably eaten more vegetable this year than I did all. I have also officially read my first novel in over a year. It's an awesome feeling to get back to the things I enjoy! I am making all sorts of goals and...
sarahelizabethlong.wordpress.com
The Good, the Great and the Best of 2010 (so far) | Sarah and the City
https://sarahelizabethlong.wordpress.com/2010/06/13/the-good-the-great-and-the-best-of-2010-so-far
Sarah and the City. Put a little love in your heart. The Good, the Great and the Best of 2010 (so far). Dear Fans (i.e. Mom and Dad),. I know I haven’t updated this blog in the recent months. Well it’s been one heck of a whirlwind. I finished my first semester of PR at Humber College, they weren’t kidding when they said it was more like bootcamp than school. To sum it up, it was a continuous learning process and I was fortunate enough to get some really great experience. Bocci ball with Humber PR peeps.
laby-lol.blogspot.com
Lungs out Loud: 1 Year Ago
http://laby-lol.blogspot.com/2012/11/1-year-ago.html
Subscribe to RSS Feed. It's hard to believe that it has already been one year since I received the call for lungs. Last year at 1:13 am I woke up to the faintest 'beep' of my voicemail, quickly called back Toronto General and was soon well on my way to a new life. Since Nov. 23, 2011 I have. Walked around at CN Tower for my 6 month celebration. Gone zip lining. twice! Gone Hot Air Ballooning. twice. Traveled to California and surrounding states ALONE and met amazing people along the way. Be someone's hap...
laby-lol.blogspot.com
Lungs out Loud: The Last Hurrah
http://laby-lol.blogspot.com/2012/03/last-hurrah.html
Subscribe to RSS Feed. In the exercise room. End of scene, completo, fin. Can you believe it? After 10 months, I am no longer required to go to the hospital three times a week. I am now only required to return every two measly weeks for bloodwork (to measure my medication levels) and PFTs (to measure my lung function), which is the longest vacation I've had from a hospital in over a year! Bad, but man was I hungry. This isn't new news, but I am not. I got my hair done today (discovered I lost a lot of ha...
laby-lol.blogspot.com
Lungs out Loud: Merry Christmas! (The scandalous scar photoshoot)
http://laby-lol.blogspot.com/2011/12/merry-christmas-scandolous-scar.html
Subscribe to RSS Feed. The scandalous scar photoshoot). Merry Christmas from my lungs to yours. Excuse the lazy eye, the photo shoot was a bit tiring! Pictured: 26 of 53 staples removed. The remainder were removed before I left the hospital. Lower down are my 4 chest tube incisions, the sutures were removed last week. My gift to you: the rest of my documented transplant journey found here. 3 Responses so far. December 26, 2011 at 5:31 PM. December 26, 2011 at 8:11 PM. December 27, 2011 at 4:53 PM.
sandyscflife.blogspot.com
Sandy's CF Life: July 2010
http://sandyscflife.blogspot.com/2010_07_01_archive.html
Friday, July 23. It's been a pretty good week. This time leaving the hospital (two weeks ago), I didn't feel nearly as well as the previous time. I am feeling decent now as the shakiness is gone and my appetite continues to improve. I have worked my way back to my full exercise program (except for the treadmill part- only at 15 of 30 minutes). For the first time in over a year, my muscles are sore from exercising! I love saying that! I went through 30 tanks this week! It feels like Summer! Friday, July 16.
greatstridesccff.blogspot.com
Great Strides for Cystic Fibrosis: The CCFF helps me and so many others lead a longer fuller life
http://greatstridesccff.blogspot.com/2010/05/my-name-is-hattie.html
Great Strides for Cystic Fibrosis. On the last Sunday of May, each year thousands of striders come to the Toronto Zoo to walk for a cure. Last year, the Toronto great Strides Walk raised over $650,000. Nationally, the event raised $2.2 million. Join us on May 30, 2010 for a fun day in support of cystic fibrosis research and care. Wednesday, May 19, 2010. The CCFF helps me and so many others lead a longer fuller life. My name is Hattie. I. Ve Got Hattitude. (http:/ www.GotHattitude.com). Recently my battl...
sandyscflife.blogspot.com
Sandy's CF Life: July 2011
http://sandyscflife.blogspot.com/2011_07_01_archive.html
Saturday, July 23. This update is long overdue - sorry to keep you hanging. I've been busy these last five months, and my one-year transplantiversary is in two days. I have often thought about blogging. but I usually write the post in my head and that's where it ends. Let's start with the most important, I've been healthy! I love being back! The other night, a player from the opposite team said I was too. I totally thought she was talking about someone else. I was so confused! My husband and I have spent...
