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Our Life with Cystic Fibrosis!

Tuesday, March 31, 2009. Caleb's clinic just called and said that his last culture which was about a month ago grew B. Cepacia! They sent it to a few different places to confirm before calling me. They said out of the 5 different types this was the better of them. I would rather him not have any! I feel like I am going to puke! I thought this was something that they cultured when they were older. NOT at 7! Labels: B. Cepacia. Thursday, March 26, 2009. Sorry I really didnt fall off the face of the earth!

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Our Life with Cystic Fibrosis! | twosaltykids.blogspot.com Reviews
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Tuesday, March 31, 2009. Caleb's clinic just called and said that his last culture which was about a month ago grew B. Cepacia! They sent it to a few different places to confirm before calling me. They said out of the 5 different types this was the better of them. I would rather him not have any! I feel like I am going to puke! I thought this was something that they cultured when they were older. NOT at 7! Labels: B. Cepacia. Thursday, March 26, 2009. Sorry I really didnt fall off the face of the earth!
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Our Life with Cystic Fibrosis! | twosaltykids.blogspot.com Reviews

https://twosaltykids.blogspot.com

Tuesday, March 31, 2009. Caleb's clinic just called and said that his last culture which was about a month ago grew B. Cepacia! They sent it to a few different places to confirm before calling me. They said out of the 5 different types this was the better of them. I would rather him not have any! I feel like I am going to puke! I thought this was something that they cultured when they were older. NOT at 7! Labels: B. Cepacia. Thursday, March 26, 2009. Sorry I really didnt fall off the face of the earth!

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twosaltykids.blogspot.com twosaltykids.blogspot.com
1

Our Life with Cystic Fibrosis!: Liprotamase

http://twosaltykids.blogspot.com/2009/03/liprotamase.html

Thursday, March 26, 2009. CF Foundation Finds Collaborator to Ensure Development of Important Pancreatic Enzyme. March 25, 2009. The CF Foundation announced today it will collaborate with a pharmaceutical company to ensure development of an important porcine-free pancreatic enzyme replacement therapy. Liprotamase was previously in development with Altus Pharmaceuticals Inc. and was known as ALTU-135 and Trizytek. The Development History of Liprotamase. The Foundation selected Alnara because of its unique...

2

Our Life with Cystic Fibrosis!: Sorry!

http://twosaltykids.blogspot.com/2009/03/sorry.html

Thursday, March 26, 2009. Sorry I really didnt fall off the face of the earth! Having computer issues is no fun! That on top of sick kids and meds galore. You know that drill. Wyatt has still been having a rough time! Caleb is doing good (knock on wood). He had a cold a few weeks back but with some antibiotics and increased treatments we were able to jiggle it out of him :) Dylan is also over his cold so hopefully they are all on the mend. Its been nice around here lately its so nice to open the ...Albut...

3

Our Life with Cystic Fibrosis!: January 2009

http://twosaltykids.blogspot.com/2009_01_01_archive.html

Thursday, January 29, 2009. Caleb fell asleep half way through :). Wyatt on the other hand. Wyatts 15 month well child check! Well Wyatt had his 15 month wcc today and 3 shots :(. He was not impressed to see anyone there! He fell asleep on the way so he was out cold through the first part of the appt. He slept through me undressing him and taking him to the scale! I layed him down and everyone was laughing that he was still passed out! She said she would have thought he'd have lost a pd or more! You find...

4

Our Life with Cystic Fibrosis!: About Us........

http://twosaltykids.blogspot.com/2009/02/about-us.html

Saturday, February 21, 2009. My Name is Melissa and I have been married to jim for almost 10 yrs. We have a son dylan who is 1o and does NOT have cystic fibrosis. Our Middle son Caleb was diagnosed with Cystic fibrosis at 7 months old. 7 yrs ago today. I remember our wonderful ped. saying she just wanted to rule it out, after caleb had been sick off and on for several months. I knew in MY HEART SOMETHING WAS WRONG! I brought caleb back in and they re-assured me that I was only there due to their error!

5

Our Life with Cystic Fibrosis!: Its late........

http://twosaltykids.blogspot.com/2009/02/its-late.html

Saturday, February 21, 2009. It is too late right now so part 2 will be posted tomorrow! March 15, 2009 at 3:32 PM. Is everything okay with your family? I haven't seen you post in a while. Subscribe to: Post Comments (Atom). I am BACK with my Random loveliness. A Cure 4 Lil' Chris. 2016 CF Walk May 15th at 11am. Resep Kue Tart Spesial Enak. Happy Heart Day Miss Zoey . How Inclusion Works For Us. Confessions Of A CF Husband. Where laughter lives: The Riggs Family. Happy 5th Birthday Kayleigh.

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Our Life with Cystic Fibrosis!

Tuesday, March 31, 2009. Caleb's clinic just called and said that his last culture which was about a month ago grew B. Cepacia! They sent it to a few different places to confirm before calling me. They said out of the 5 different types this was the better of them. I would rather him not have any! I feel like I am going to puke! I thought this was something that they cultured when they were older. NOT at 7! Labels: B. Cepacia. Thursday, March 26, 2009. Sorry I really didnt fall off the face of the earth!

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