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cfsteph.blogspot.com

CF Steph

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family.

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CF Steph | cfsteph.blogspot.com Reviews
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This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family.
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CF Steph | cfsteph.blogspot.com Reviews

https://cfsteph.blogspot.com

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family.

INTERNAL PAGES

cfsteph.blogspot.com cfsteph.blogspot.com
1

CF Steph: November 2010

http://cfsteph.blogspot.com/2010_11_01_archive.html

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family. Saturday, November 27, 2010. I have so many things to be thankful for this year and not a minute went by on Thanksgiving that I did not think of my number one thing: my donor. Or vest treatme...

2

CF Steph: March already

http://cfsteph.blogspot.com/2011/03/march-already.html

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family. Tuesday, March 1, 2011. Yes, I am a very bad blogger. It is not that I don't want to but finding the time is difficult. Tomorrow, I go to Brigham and Woman's for my almost one year anniversar...

3

CF Steph: December

http://cfsteph.blogspot.com/2010/12/december.html

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family. Wednesday, December 29, 2010. My Nana and I. I cannot believe it is already December 29th. Two more days and 2010 will be over. What a year it was! Lots have or will happen this month:. I am ...

4

CF Steph: June 2010

http://cfsteph.blogspot.com/2010_06_01_archive.html

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family. Monday, June 28, 2010. I am excited I got tickets for Maine Day at the Redsox on July 18th. This will be the first game I have been able to go to in a few years. Last year, I just did...I am ...

5

CF Steph: March 2011

http://cfsteph.blogspot.com/2011_03_01_archive.html

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family. Tuesday, March 1, 2011. Yes, I am a very bad blogger. It is not that I don't want to but finding the time is difficult. Tomorrow, I go to Brigham and Woman's for my almost one year anniversar...

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LINKS TO THIS WEBSITE

sandyscflife.blogspot.com 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...

sandyscflife.blogspot.com sandyscflife.blogspot.com

Sandy's CF Life: Merry Christmas

http://sandyscflife.blogspot.com/2010/12/merry-christmas.html

Saturday, December 25. It's been a while since I posted, but things have been going so well and I've been busy with other stuff! To be honest, I have a harder time sitting at the computer and focusing, so I haven't been on it nearly as much. So many people complain about hitting the big 3-0, but I see it as an accomplishment. Sure, we're all getting older but it's an achievement to pass a milestone. I have gotten back into one of my hobbies- scrapbooking. I am about two and a half years behind, but t...

pegsoninthepresent.wordpress.com pegsoninthepresent.wordpress.com

Bleed just hit me. Updated « Pegson In The Present . Com

https://pegsoninthepresent.wordpress.com/2011/05/12/bleed-just-hit-ne

Pegson In The Present . Com. Living in the Present…Aware of the Future…. You have CF when? Bleed just hit me. Updated. Was just getting to lay down and go to bed and my lungs started bleeding. First time of considerable volume in about 2 years. If you remember previous blogs I had very bad bleeds between 2002 and 2008 until I had my lungs embolised* combined with starting a continued use of nebulised antibiotics. Colistin and Tobi alternated month to month. May 12, 2011. Leave a Reply Cancel reply. Enter...

pegsoninthepresent.wordpress.com pegsoninthepresent.wordpress.com

pegson123 « Pegson In The Present . Com

https://pegsoninthepresent.wordpress.com/author/pegson123

Pegson In The Present . Com. Living in the Present…Aware of the Future…. You have CF when? Bowl of mucus…….I mean 2 year old cream corn. May 25, 2011. About 2 years ago my jack Russell, zaphyr was his name. Died in the space of two weeks from a quick growing massive abdominal Tuma. The household was devastated. Especially my dad since zaphyr was like his third son. Anyone so that didn’t work. So as a Christmas present I decided to get another jack Russell puppy and surprise the family. May 14, 2011.

pegsoninthepresent.wordpress.com pegsoninthepresent.wordpress.com

Films & TV « Pegson In The Present . Com

https://pegsoninthepresent.wordpress.com/films-tv

Pegson In The Present . Com. Living in the Present…Aware of the Future…. You have CF when? Ok so this is a page for favourite films and TV series of mine. It’s a work I progress and I intend to add to it whenever a new films or TV series comes to mind. List are in no particular order. 8211; I truely love this film, I even bought it on bluray though I already own it on dvd. 8211; An amazing independent film written and directed by Zach Braff, your also treated to an amazing performance by Natalie Portman.

sandyscflife.blogspot.com sandyscflife.blogspot.com

Sandy's CF Life: Ready to Run!

http://sandyscflife.blogspot.com/2010/10/ready-to-run.html

Wednesday, October 27. I ran on the treadmill today in the gym! I only ran for one minute at a time, but it felt great. My legs even remembered how to do it! It was a pretty cool experience. As I increased the speed on the treadmill and started to increase my pace to a jog, everybody in the gym stopped to watch and cheer me on. I think I impressed a few people, including myself! October 29, 2010 at 8:17 PM. Last time I tried to jog my legs felt like jelly! You have some goals, girl. CF - Cystic Fibrosis.

sandyscflife.blogspot.com 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.

pegsoninthepresent.wordpress.com pegsoninthepresent.wordpress.com

My dog Boady « Pegson In The Present . Com

https://pegsoninthepresent.wordpress.com/2011/05/14/my-dog-boady

Pegson In The Present . Com. Living in the Present…Aware of the Future…. You have CF when? About 2 years ago my jack Russell, zaphyr was his name. Died in the space of two weeks from a quick growing massive abdominal Tuma. The household was devastated. Especially my dad since zaphyr was like his third son. Anyone so that didn’t work. So as a Christmas present I decided to get another jack Russell puppy and surprise the family. So below are some of my fav photos. May 14, 2011. Leave a Reply Cancel reply.

pegsoninthepresent.wordpress.com pegsoninthepresent.wordpress.com

You have CF when? « Pegson In The Present . Com

https://pegsoninthepresent.wordpress.com/you-know-you-have-cf-when

Pegson In The Present . Com. Living in the Present…Aware of the Future…. You have CF when? You have CF when? You know you have CF when. Please leave your additions to this list no matter how serious, funny or just plain stupid, in the comment section or alternatively email them to me at pegson1986@hotmail.com. You wish more people would be open to stem cell research as it would help others. You can instruct the nurses how to work the IV machine at the hospital. The sound of your Pari pumps calms you.

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CF Steph

This blog discusses cystic fibrosis, organ donation and life as I know it. My name is Stephanie. I have cystic fibrosis and received a double lung transplant on March 17, 2010. I would not be where I am today without the support of my husband, my family, my friends and last but not least my donor and his/her family. Monday, March 16, 2015. Where has time gone? After these few posts, I am not sure where my blog will take me but I look forward to the journey. Tuesday, March 1, 2011. I have been enjoying ti...

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