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Keagan Scott Covington

Wednesday, April 6, 2011. Another Day at Clinic. Great news: 100% O2 sat level, lungs sounded great, got the vest ordered and we will receive it tomorrow, we are stopping the albuterol before hyper-sal and if no cough arises then in 12 days we will also be stopping pulmozyme but he is satying on hyper-sal, gained 1lb 3oz so he is 22lbs 3oz.i am sooo happy! Great news: NO milk allergy! But we are doing some stool tests to try and figure out why they are still sooo loose! I am one happy momma :). In the 50...

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Keagan Scott Covington | lifeofkeagan.blogspot.com Reviews
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Wednesday, April 6, 2011. Another Day at Clinic. Great news: 100% O2 sat level, lungs sounded great, got the vest ordered and we will receive it tomorrow, we are stopping the albuterol before hyper-sal and if no cough arises then in 12 days we will also be stopping pulmozyme but he is satying on hyper-sal, gained 1lb 3oz so he is 22lbs 3oz.i am sooo happy! Great news: NO milk allergy! But we are doing some stool tests to try and figure out why they are still sooo loose! I am one happy momma :). In the 50...
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Keagan Scott Covington | lifeofkeagan.blogspot.com Reviews

https://lifeofkeagan.blogspot.com

Wednesday, April 6, 2011. Another Day at Clinic. Great news: 100% O2 sat level, lungs sounded great, got the vest ordered and we will receive it tomorrow, we are stopping the albuterol before hyper-sal and if no cough arises then in 12 days we will also be stopping pulmozyme but he is satying on hyper-sal, gained 1lb 3oz so he is 22lbs 3oz.i am sooo happy! Great news: NO milk allergy! But we are doing some stool tests to try and figure out why they are still sooo loose! I am one happy momma :). In the 50...

INTERNAL PAGES

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com
1

Keagan Scott Covington: January 2011

http://www.lifeofkeagan.blogspot.com/2011_01_01_archive.html

Wednesday, January 26, 2011. From this DAY Forward. My name is Krystal! Thursday, January 20, 2011. My Oh My.clinic days! Today was clinic day! Clinic days are exhausting! We left home at 11:30 am this morning and just got home at 8:15 pm. We drive 2.5 hours there, have clinic for 3 hours, and drive 2.5 hours home! He said if you want that then just ask your/your child's doctor for hypertonic saline! Alright so back to clinic. Lungs had some slight crackles on both sides in the upper lobes. I also learne...

2

Keagan Scott Covington: A New Year....

http://www.lifeofkeagan.blogspot.com/2011/01/new-year.html

Monday, January 3, 2011. So it's a new year! 2010 gave me one of the best gifts I could have ever asked for and that gift was Keagan! I also discovered how caring and understanding our families are of CF. They will not come around Keagan if they are sick or think they may be getting sick! The last thing I am thankful for is that my mom QUIT smoking for Keagan! My mom has smoked since she was a teenager and just put 'em down cold turkey! My name is Krystal! January 7, 2011 at 3:57 PM. Like I said youre a ...

3

Keagan Scott Covington: From this DAY Forward...

http://www.lifeofkeagan.blogspot.com/2011/01/from-this-day-forward.html

Wednesday, January 26, 2011. From this DAY Forward. My name is Krystal! January 27, 2011 at 3:26 PM. I like your new concept! Subscribe to: Post Comments (Atom). My name is Krystal! I am the mother of a fun, spunky, and happy little boy named Keagan. This blog is to share his story and journey with CF. This blog is also a place for me to share my thoughts, ideas, and opinions. Hope you enjoy! View my complete profile. Pulmozyme- once a day via nebulizer. 7% Hypertonic Saline- 2x day via nebulizer.

4

Keagan Scott Covington: November 2010

http://www.lifeofkeagan.blogspot.com/2010_11_01_archive.html

Monday, November 22, 2010. The past 7 months in the world of CF. Since we got the news of Keagan having CF, we had to adjust a lot but now it is all second nature to us! Thankfully we have not had any complications/hospitalizations with CF! He will not outgrow CF as some may think! But check for updates in the future as this is where I will be posting his CF updates rather than on Facebook! My name is Krystal! How we discovered CF. My name is Krystal! Subscribe to: Posts (Atom). My name is Krystal! Mutat...

5

Keagan Scott Covington: Another Day at Clinic...

http://www.lifeofkeagan.blogspot.com/2011/04/another-day-at-clinic.html

Wednesday, April 6, 2011. Another Day at Clinic. Great news: 100% O2 sat level, lungs sounded great, got the vest ordered and we will receive it tomorrow, we are stopping the albuterol before hyper-sal and if no cough arises then in 12 days we will also be stopping pulmozyme but he is satying on hyper-sal, gained 1lb 3oz so he is 22lbs 3oz.i am sooo happy! Great news: NO milk allergy! But we are doing some stool tests to try and figure out why they are still sooo loose! I am one happy momma :). Salt- 1/4...

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mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: CFF.org: Targeting Mutations that Cause Cystic Fibrosis

http://mycysticfibrosismutation.blogspot.com/2010/03/cfforg-targeting-mutations-that-cause.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Thursday, March 11, 2010. CFForg: Targeting Mutations that Cause Cystic Fibrosis. This article was found in the Cystic Fibrosis Foundation's Connections E-newsletter online for March 2010. Targeting Mutations that Cause Cystic Fibrosis. What Do the Mutation Classes Mean? In healthy people, CFTR is located...

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: August 2010

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

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Saturday, August 14, 2010. Delta508 is considered a Class II Mutation. Is considered a Class I Mutation. Both mutations are associated with the "Classic" or "Typical" CF, also considered "severe" in the way of how much the gene does not work properly. Subscribe to: Posts (Atom). First Day of School 2016.

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: January 2010

http://mycysticfibrosismutation.blogspot.com/2010_01_01_archive.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Friday, January 22, 2010. Severity of chest disease in cystic fibrosis patients in relation to their genotypes. Severity of chest disease in cystic fibrosis patients in relation to their genotypes. Journal of Medical Genetics. 883-887; doi:10.1136/jmg.29.12.883. Friday, January 1, 2010. Here we go again.

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: Severity of chest disease in cystic fibrosis patients in relation to their genotypes

http://mycysticfibrosismutation.blogspot.com/2010/01/severity-of-chest-disease-in-cystic.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Friday, January 22, 2010. Severity of chest disease in cystic fibrosis patients in relation to their genotypes. Severity of chest disease in cystic fibrosis patients in relation to their genotypes. Journal of Medical Genetics. 883-887; doi:10.1136/jmg.29.12.883. December 12, 2010 at 2:14 AM. Severity of c...

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: Could Kalydeco Benefit 621+1G>T?

http://mycysticfibrosismutation.blogspot.com/2014/06/6211gt-is-splicing-mutation.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Wednesday, June 25, 2014. Could Kalydeco Benefit 621 1G T? Could Kalydeco benefit 621 1G T? Some splicing mutations (621 1G- T, 1717-1G- A,1078delT, 711 1G- T, 1525-1G- A, 2751 2T- A, 296 1G- C, 1717-9T- C from. C Castellani et al. / Journal of Cystic Fibrosis 7 (2008) 179–196). First Day of School 2016.

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: Links regarding DF508 and 621+1G->T

http://mycysticfibrosismutation.blogspot.com/2010/01/links-regarding-df508-and-6211g-t.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Friday, January 1, 2010. Links regarding DF508 and 621 1G- T. Http:/ ehealthforum.com/health/mutations-g-t-and-di-t175986.html. Correlation between mutations and age in cystic fibrosis in a French Canadian population. Http:/ jmg.bmj.com/content/37/3/225.extract. Subscribe to: Post Comments (Atom).

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: Facebook Group for those with DF508 and 621+1G->T

http://mycysticfibrosismutation.blogspot.com/2012/05/facebook-group-for-those-with-df508-and.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Tuesday, May 1, 2012. Facebook Group for those with DF508 and 621 1G- T. In the world of Cystic Fibrosis, this is an exciting time! Or leave a comment with your Facebook name and we'll add you. Subscribe to: Post Comments (Atom). Blogs About Children With This CF Mutation Combination. Here we go again.

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: March 2010

http://mycysticfibrosismutation.blogspot.com/2010_03_01_archive.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Thursday, March 11, 2010. CFForg: Targeting Mutations that Cause Cystic Fibrosis. This article was found in the Cystic Fibrosis Foundation's Connections E-newsletter online for March 2010. Targeting Mutations that Cause Cystic Fibrosis. What Do the Mutation Classes Mean? In healthy people, CFTR is located...

mycysticfibrosismutation.blogspot.com mycysticfibrosismutation.blogspot.com

My Cystic Fibrosis Mutation: Class of Mutuations

http://mycysticfibrosismutation.blogspot.com/2010/08/class-of-mutuations.html

My Cystic Fibrosis Mutation. This blog is for those who have the CF mutations Delta508 and 621 1G- T. We hope this blog will keep track of research and other medical information regarding this mutation. Saturday, August 14, 2010. Delta508 is considered a Class II Mutation. Is considered a Class I Mutation. Both mutations are associated with the "Classic" or "Typical" CF, also considered "severe" in the way of how much the gene does not work properly. Subscribe to: Post Comments (Atom). Here we go again.

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Wednesday, April 6, 2011. Another Day at Clinic. Great news: 100% O2 sat level, lungs sounded great, got the vest ordered and we will receive it tomorrow, we are stopping the albuterol before hyper-sal and if no cough arises then in 12 days we will also be stopping pulmozyme but he is satying on hyper-sal, gained 1lb 3oz so he is 22lbs 3oz.i am sooo happy! Great news: NO milk allergy! But we are doing some stool tests to try and figure out why they are still sooo loose! I am one happy momma :). In the 50...

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