cfmama1105.blogspot.com

A CF Journey

Thursday, December 16, 2010. Wow, It's been awhile. It has been awhile since I have been on here so basically Emmie is getting bigger and stronger and thriving! Love to hear that! She is up to the 95th percentile in weight! Why do our children have to suffer because the FDA doesn't want to deal with it? Melissa, Jason and Emmie too! Saturday, September 25, 2010. Emmie is cheering you on thats for sure! For tonight that is all, tired yet still excited about our win! Tuesday, August 3, 2010. Em previously ...

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A CF Journey | cfmama1105.blogspot.com Reviews

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Thursday, December 16, 2010. Wow, It's been awhile. It has been awhile since I have been on here so basically Emmie is getting bigger and stronger and thriving! Love to hear that! She is up to the 95th percentile in weight! Why do our children have to suffer because the FDA doesn't want to deal with it? Melissa, Jason and Emmie too! Saturday, September 25, 2010. Emmie is cheering you on thats for sure! For tonight that is all, tired yet still excited about our win! Tuesday, August 3, 2010. Em previously ...

<META> KEYWORDS

1 a cf journey

2 so hi all

3 love ya

4 posted by

5 no comments

6 labels venting

7 hockey is back

8 great job boys

9 keep it up

10 love

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A CF Journey | cfmama1105.blogspot.com Reviews

https://cfmama1105.blogspot.com

Thursday, December 16, 2010. Wow, It's been awhile. It has been awhile since I have been on here so basically Emmie is getting bigger and stronger and thriving! Love to hear that! She is up to the 95th percentile in weight! Why do our children have to suffer because the FDA doesn't want to deal with it? Melissa, Jason and Emmie too! Saturday, September 25, 2010. Emmie is cheering you on thats for sure! For tonight that is all, tired yet still excited about our win! Tuesday, August 3, 2010. Em previously ...

INTERNAL PAGES

cfmama1105.blogspot.com

1

A CF Journey: Wow, that's all I can say.

http://cfmama1105.blogspot.com/2010/06/wow-thats-all-i-can-say.html

Monday, June 28, 2010. Wow, that's all I can say. Then on Tuesday my pain in my teeth and cheek came back, quite severly may I add. So I went to the local walk in clinic to be told I have an ear infection. Seriously? So they change my pain meds and send me on my merry little way. They did say if it swells up or the pain gets worse come back. Ok, fine. They order a CT scan of my head with contrast of course it costs more. Of course with contrast means that they have to start an IV right? Whatever. So ...

2

A CF Journey

http://cfmama1105.blogspot.com/2010/06/good-morning-and-happy-fathers-day-to.html

Sunday, June 20, 2010. Good Morning, and Happy Fathers Day to all the wonderful daddys out there! We are still fighting this "stucky" nose, we are going to the ENT tomorrow so hopefully he can figure somethin g out to help munchkin feel better. On a GI note we are doing additional prevacid to attempt to combat belly troubles. We will see! I am blessed to have him and do not think he understands how much we all love him. Subscribe to: Post Comments (Atom). CF Clinic: February 4, 2011. Allegra 5ml x2 daily.

3

A CF Journey: September 2010

http://cfmama1105.blogspot.com/2010_09_01_archive.html

Saturday, September 25, 2010. So, I know it has been awhile and I apologize. Em has been doing ok since my last blog. The only main issue has been her allergies going haywire! On another note hockey is for sure back in full swing. Miss Princess made her debut with the "new" Delta College Hockey team, (and by new I mean at least 15 incoming freshman)! Emmie is cheering you on thats for sure! For tonight that is all, tired yet still excited about our win! Subscribe to: Posts (Atom). Allegra 5ml x2 daily.

4

A CF Journey: Another day, another appointment!

http://cfmama1105.blogspot.com/2010/06/another-day-another-appointment.html

Monday, June 21, 2010. Another day, another appointment! Ok enough complaining. More updates to come as they happen! June 21, 2010 at 8:37 PM. Subscribe to: Post Comments (Atom). CF Clinic: February 4, 2011. Prevacid solutabs 15 mg x2 daily. Allegra 5ml x2 daily. Allergies (gotta love Michigan). Zenpep 10,000 2 caps with every feed. Enzyme to break down food. Albuterol Sulfate: 0.083% 2.5mg/3ml x2 daily up to x4 daily. Opens up the airways. Pulmozyme: 1 mg x1 daily. Disolves mucus like a mad man!

5

A CF Journey: August 2010

http://cfmama1105.blogspot.com/2010_08_01_archive.html

Tuesday, August 3, 2010. Lots of new stuff. Sorry this has been a long time coming, been a bit busy. There has been SO much going on here in the Ruple household, kinda crazy actually. So Emmies surgery went well. Labial adhesions taken care of. We had clinic this past week and am (somewhat) happy to report that Miss emilie has been put on a diet! That is actually one amazing feat for a CF baby! They have also changed her nasal spray b/c she was complaining of burning, have not picked that one up yet.

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cfmama1105.blogspot.com

A CF Journey

Thursday, December 16, 2010. Wow, It's been awhile. It has been awhile since I have been on here so basically Emmie is getting bigger and stronger and thriving! Love to hear that! She is up to the 95th percentile in weight! Why do our children have to suffer because the FDA doesn't want to deal with it? Melissa, Jason and Emmie too! Saturday, September 25, 2010. Emmie is cheering you on thats for sure! For tonight that is all, tired yet still excited about our win! Tuesday, August 3, 2010. Em previously ...

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