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The Tale of Olivia's 65 Roses.

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, July 1, 2015. Olivia had her quarterly CF Clinic today. It was not bad but it was tiring as it always is. Here are her numbers from the last 2 clinics. Normally I post a percentile for her FEV1, but it was explained to me today that her liter number is a more important and accurate thing to watch. So from now on I will be posting those numbers instead. Monday, February 23, 2015. We're ge...

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The Tale of Olivia's 65 Roses. | taleofolivia.blogspot.com Reviews
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The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, July 1, 2015. Olivia had her quarterly CF Clinic today. It was not bad but it was tiring as it always is. Here are her numbers from the last 2 clinics. Normally I post a percentile for her FEV1, but it was explained to me today that her liter number is a more important and accurate thing to watch. So from now on I will be posting those numbers instead. Monday, February 23, 2015. We're ge...
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6 january clinic
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The Tale of Olivia's 65 Roses. | taleofolivia.blogspot.com Reviews

https://taleofolivia.blogspot.com

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, July 1, 2015. Olivia had her quarterly CF Clinic today. It was not bad but it was tiring as it always is. Here are her numbers from the last 2 clinics. Normally I post a percentile for her FEV1, but it was explained to me today that her liter number is a more important and accurate thing to watch. So from now on I will be posting those numbers instead. Monday, February 23, 2015. We're ge...

INTERNAL PAGES

taleofolivia.blogspot.com taleofolivia.blogspot.com
1

The Tale of Olivia's 65 Roses.: April 2013

http://taleofolivia.blogspot.com/2013_04_01_archive.html

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Tuesday, April 9, 2013. Playing on the swingset. I love being outside! Eewww, is that a bug? Why are you not climbing with me? What do you mean "You're tired? Dirty feet are a sign that fun has been had. The grass has turned to lava! I feel a song coming. Its exhausting to be me. Its exhausting to be your dad. I think she's doing The Platypus Walk here. It wasn't me.it was the one-armed man! Mirala...

2

The Tale of Olivia's 65 Roses.: August 2014

http://taleofolivia.blogspot.com/2014_08_01_archive.html

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, August 20, 2014. Week and a half ago, Olivia asked how she got CF. It caught me COMPLETELY off guard so I proceeded to draw a Punnett Square and explain dominant and recessive genes. The whooshing sound of my explanation going over her head was almost audible. A few days later, she asked me again and I explained it in more understandable terms. Thursday, August 14, 2014. O2 Sat 96% (98%).

3

The Tale of Olivia's 65 Roses.: April 2014

http://taleofolivia.blogspot.com/2014_04_01_archive.html

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, April 2, 2014. Olivia had clinic today. I have been dreading clinic because she's been sick so many times lately and I knew her weight was going to be an issue. So here are her numbers for this clinic-I'll put last clinic's numbers in parentheses so you see what the changes are. Height-46 inches (44.25 inches). Weight-43.3 lbs (42.7 lbs). I'm ready for a nap now! CF is an inherited chron...

4

The Tale of Olivia's 65 Roses.: July 2015

http://taleofolivia.blogspot.com/2015_07_01_archive.html

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, July 1, 2015. Olivia had her quarterly CF Clinic today. It was not bad but it was tiring as it always is. Here are her numbers from the last 2 clinics. Normally I post a percentile for her FEV1, but it was explained to me today that her liter number is a more important and accurate thing to watch. So from now on I will be posting those numbers instead. Subscribe to: Posts (Atom). CF is a...

5

The Tale of Olivia's 65 Roses.: February 2015

http://taleofolivia.blogspot.com/2015_02_01_archive.html

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Monday, February 23, 2015. It is THAT time of year again.It is time for our yearly Great Strides walk! If you want to donate! If you want to join Olivia's Outlaws! Our daughter, Olivia, has Cystic Fibrosis, a life shortening disease. It is our daily battle and greatest intention to keep her strong and healthy and her lungs disease free. What is Cystic Fibrosis? Real progress has been made in the se...

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Sherman Family: March/April

http://shermfamily.blogspot.com/2011/05/marchapril.html

God gives the Mama's He trusts the most, His most delicate babies." - Unknown. Thursday, May 26, 2011. March and April were busy months but at our house it seems every month is busy. Olivia mastered crawling and standing up to everything! Addison has sure become quite the big sister! Olivia loves playing in the stools. She just can't figure out how to get out! We caught Addison mimicking her father. Olivia was in the hospital for a weekend with the Rotavirus. We all had never been so sick. CF is an inher...

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Sherman Family: September 2010

http://shermfamily.blogspot.com/2010_09_01_archive.html

God gives the Mama's He trusts the most, His most delicate babies." - Unknown. Thursday, September 23, 2010. Please Vote This Week! Monday, September 20, 2010. Look at that beautiful face! Both girls did very well all day! Olivia's first outing was at Peru State College's annual kickoff to begin the school year and the first home game. There were kids games, snow cones, a band, everything Addison loves. Olivia pretty much slept but it was a great day to get out of the house! A quick call to the hospital ...

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Sherman Family: Bank!

http://shermfamily.blogspot.com/2011/06/bank.html

God gives the Mama's He trusts the most, His most delicate babies." - Unknown. Thursday, June 2, 2011. I found Olivia this way one morning. She is sure a climber! Then I realized maybe it's time we take the piggy bank to the bank! Addison enjoyed helping dad estimate how much was in the piggy bank that we haven't dumped in over a year! 500 to their saving account! Addison wanted to know why we take it to the bank. "They don't have a piggy bank mom! Subscribe to: Post Comments (Atom). Andrew and Maya "Ang...

shermfamily.blogspot.com shermfamily.blogspot.com

Sherman Family: Standing

http://shermfamily.blogspot.com/2011/06/standing.html

God gives the Mama's He trusts the most, His most delicate babies." - Unknown. Thursday, June 2, 2011. Subscribe to: Post Comments (Atom). Cystic Fibrosis and MSPI Sites. Http:/ www.mspimama.com. Http:/ taleofolivia.blogspot.com/. What is Cystic Fibrosis (CF)? Olivia's Meds and Treatments. Delta F508, Delta F508. The Tale of Olivia's 65 Roses. THE OLESON DAILY TIMES! 2010 Palisade Pioneer Days. Peyton and Sawyer's Place. Andrew and Maya "Angel Baby Project".

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Making Strides To Cure Found: Diagnosis Day

http://stridestocurefound.blogspot.com/2014/03/diagnosis-day.html

Making Strides To Cure Found. Cystic Fibrosis Awareness, Fundraising, and Hope. Tuesday, March 25, 2014. The title of this post is a little bit of a misnomer. The fact is that it was about 36 hours or so before we were told everything about Samantha’s situation. Most of that process was due to the need to do PFTs (Pulmonary Function Test), something that Alicia will talk about in the next post. In short, that night stunk. I won’t revisit it for you. You can read about it HERE. If you haven’t already.

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Making Strides To Cure Found: Subaru Fall Classic Half Marathon Report

http://stridestocurefound.blogspot.com/2014/12/subaru-fall-classic-half-marathon-report.html

Making Strides To Cure Found. Cystic Fibrosis Awareness, Fundraising, and Hope. Subaru Fall Classic Half Marathon Report. Tuesday, December 2, 2014. A side goal was to finish in under 2 hours. Unfortunately, I made just about every rookie mistake out there. It was like I had never run a half marathon before! I ate the wrong food before the race, I stopped training consistently a few weeks before the race, I started out too fast, I didn't manage water intake very well, and a whole host of others! My name ...

stridestocurefound.blogspot.com stridestocurefound.blogspot.com

Making Strides To Cure Found: Sleepless in Milwaukee, PT II

http://stridestocurefound.blogspot.com/2014/03/sleepless-in-milwaukee-pt-ii.html

Making Strides To Cure Found. Cystic Fibrosis Awareness, Fundraising, and Hope. Sleepless in Milwaukee, PT II. Monday, March 24, 2014. I realize that I'm writing now not so much to report to the greater CF community about what's going on as I am to make sure I report everything that happens to Alicia without (a) calling her in the middle of the night and (b) not forgetting anything. It's been a long night. Posted by Belly Surfer. Subscribe to: Post Comments (Atom). A Cure 4 Lil' Chris. My CF Journey W/God.

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Making Strides To Cure Found: Diagnosis Day PT II: PFTs

http://stridestocurefound.blogspot.com/2014/03/diagnosis-day-pt-ii-pfts.html

Making Strides To Cure Found. Cystic Fibrosis Awareness, Fundraising, and Hope. Diagnosis Day PT II: PFTs. Wednesday, March 26, 2014. Hopefully we’ll know more tomorrow. Posted by Belly Surfer. Subscribe to: Post Comments (Atom). A Cure 4 Lil' Chris. Tale of Olivia's 65 Roses. Cure CF for Reilly. My CF Journey W/God. Why we do this. My name is Samantha, and I have a disease called Cystic Fibrosis. It creates sticky mucus in my pancreas and lungs which makes it hard for me to gain weight and breathe!

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Making Strides To Cure Found: Adjusting to a new Climate

http://stridestocurefound.blogspot.com/2014/09/adjusting-to-new-climate.html

Making Strides To Cure Found. Cystic Fibrosis Awareness, Fundraising, and Hope. Adjusting to a new Climate. Monday, September 1, 2014. Alicia and I were talking this morning about what success would look like this week. Alicia mused that, "I'd be happy if we could just keep both kids in school and not home sick this week! Clearly our standards aren't too high! But seriously, our kids are obviously still trying to adjust to the different climate in Florida. How do you deal with moves and cystic fibrosis?

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The Tale of Olivia's 65 Roses.

The Tale of Olivia's 65 Roses. This is the story of our amazing daughter and her life with Cystic Fibrosis. Wednesday, July 1, 2015. Olivia had her quarterly CF Clinic today. It was not bad but it was tiring as it always is. Here are her numbers from the last 2 clinics. Normally I post a percentile for her FEV1, but it was explained to me today that her liter number is a more important and accurate thing to watch. So from now on I will be posting those numbers instead. Monday, February 23, 2015. We're ge...

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