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Vince's Life!!!

Standing in my toybox =). Wednesday, April 17, 2013. It's been a long time since i updated here.vince was doing REALLY well for a long time! Lung wise he went from i believe april-october with no antibiotics reguarding his lungs or sinus (he had a few skin infections this summer).on september 21,2012 we had our 2nd baby boy Trevor (who does not have CF).vince was up to 34 pounds,taking all of his medications! In november he started preschool-going 4 days a week from 1-415pm! Wednesday, September 19, 2012.

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Vince's Life!!! | vinceslifestory.blogspot.com Reviews
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Standing in my toybox =). Wednesday, April 17, 2013. It's been a long time since i updated here.vince was doing REALLY well for a long time! Lung wise he went from i believe april-october with no antibiotics reguarding his lungs or sinus (he had a few skin infections this summer).on september 21,2012 we had our 2nd baby boy Trevor (who does not have CF).vince was up to 34 pounds,taking all of his medications! In november he started preschool-going 4 days a week from 1-415pm! Wednesday, September 19, 2012.
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Vince's Life!!! | vinceslifestory.blogspot.com Reviews

https://vinceslifestory.blogspot.com

Standing in my toybox =). Wednesday, April 17, 2013. It's been a long time since i updated here.vince was doing REALLY well for a long time! Lung wise he went from i believe april-october with no antibiotics reguarding his lungs or sinus (he had a few skin infections this summer).on september 21,2012 we had our 2nd baby boy Trevor (who does not have CF).vince was up to 34 pounds,taking all of his medications! In november he started preschool-going 4 days a week from 1-415pm! Wednesday, September 19, 2012.

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vinceslifestory.blogspot.com vinceslifestory.blogspot.com
1

Vince's Life!!!: December 2011

http://www.vinceslifestory.blogspot.com/2011_12_01_archive.html

Standing in my toybox =). Thursday, December 15, 2011. CF showing its ugly side. Vince's med list also changed. He gets ventolin-4 puffs 2x daily. Albuterol-if run out of ventolin. Pulmicort 1mg (2 .5mg viles) 2x daily-when sick. Zenpep-2-3 per meal w/fat. Zantac 1.5ml 3x daily. Miralax 1/2 cap up to 4x daily. Subscribe to: Posts (Atom). CF showing its ugly side. View my complete profile. TOBI-every 28 days on/off. Plum or prune juice - 1/2 cup daily as needed. Salt- 1/4tsp. 1x a day. Zantac- 1mL 2x a day.

2

Vince's Life!!!: upcoming plans :)

http://www.vinceslifestory.blogspot.com/2012/07/upcoming-plans.html

Standing in my toybox =). Tuesday, July 24, 2012. As everyone knows i am getting closer to my due date.and having a young child with special needs and no babysitter has had me thinking on what to do with him while i'm in the hospital.sam and i have come up with the perfect solution for US! We will allow those 2 people to stay for a while and after that we will give the new baby his 1st bath and have our 1st family of 4 time! Subscribe to: Post Comments (Atom). This will become private! I am 20 years old,...

3

Vince's Life!!!: April 2011

http://www.vinceslifestory.blogspot.com/2011_04_01_archive.html

Standing in my toybox =). Friday, April 29, 2011. Too much in one day! Hes still my 100% perfect BEAUTIFUL and HEALTHY little man! The only thing is we will learn through Occupational therapy how to discipline him for hurting us (pulling hair,biting) for now we are to just redirect his attention.and it helps but not all the time.i will also not try making him try any food.its all up to him.he needs to have trust in us and the therapist. Tuesday, April 19, 2011. We're home for easter :). Vince had his wor...

4

Vince's Life!!!: February 2012

http://www.vinceslifestory.blogspot.com/2012_02_01_archive.html

Standing in my toybox =). Wednesday, February 29, 2012. Zenpep 5,000-2-3 per meal. Zantac 1.5ml 3x daily. CF vitmain 2ml daily. Plus abx and steroids when needed. Because he does not take his enzymes he does not abosrb most of the fat or nutrients in the foods he takes in.so therefore both his body and brain will grow at a slower rate.here is what happened yesterday! Soooafter all that he did not look at the blisters on vinces butt/mention the 95% o2/or even say when he wanted to see vince again! He is v...

5

Vince's Life!!!: biggg update!

http://www.vinceslifestory.blogspot.com/2013/04/biggg-update.html

Standing in my toybox =). Wednesday, April 17, 2013. It's been a long time since i updated here.vince was doing REALLY well for a long time! Lung wise he went from i believe april-october with no antibiotics reguarding his lungs or sinus (he had a few skin infections this summer).on september 21,2012 we had our 2nd baby boy Trevor (who does not have CF).vince was up to 34 pounds,taking all of his medications! In november he started preschool-going 4 days a week from 1-415pm! I am 20 years old,and I stay ...

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lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: CF and its Drugs

http://lifeofkeagan.blogspot.com/2011/02/cf-and-its-drugs.html

Wednesday, February 23, 2011. CF and its Drugs. So news juat broke that a new medicine is going for FDA approval! Thank you to everyone who already supports the CFF! If you would like to help Keagan's Great Strides team then you may do one of the following:. 1) go to www.cff.org/great strides/krystalcovington. 2) order a team shirt $15 for adults and $10 for youth/toddler e-mail me kscott0305@gmail.com. 3) my mom is selling CF bracelets and keychains e-mail he kitty19705@gmail.com. My name is Krystal!

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: November 2010

http://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...

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: A little Peek into Keagan's daily LIFE....

http://lifeofkeagan.blogspot.com/2011/01/little-peek-into-keagans-daily-life.html

Monday, January 10, 2011. A little Peek into Keagan's daily LIFE. Just wanted to post Keagan's current feeding and treatment schedule. You may look at Keagan's treatment and think.WOW! That's a lot. But really his treatments are not a lot compared to other CF babies and as he gets older the list will more than likely only grow! 9 am: wake up and eats. 1 1/2 enzymes in applesauce before meal. 2 teaspoons of Omeprazole (reflux med compounded into liquid). 1 mL of Aquadeks (multivitamin: A, D, K, and E).

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: April 2011

http://lifeofkeagan.blogspot.com/2011_04_01_archive.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...

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: My Oh My....clinic days!

http://lifeofkeagan.blogspot.com/2011/01/my-oh-myclinic-days.html

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. Ears are slightly red and irritated. Has gained 1lb 10oz in a month. The nutritionist...

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: Another Day at Clinic...

http://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...

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: Another Day spent Driving and Waiting....

http://lifeofkeagan.blogspot.com/2011/02/another-day-spent-driving-and-waiting.html

Thursday, February 24, 2011. Another Day spent Driving and Waiting. And unfortunately, we did not get to see the allergist today to figure out whether or not he has a milk allergy but we will see her when we go back on March 16th! Even with a runny nose and cough (I know it can turn into something for you negative thinkers). 28 7/8" long.almost an inch in a month. This is a 2.5 lb weight gain in a month! Continue getting him FAT lol. In the 50th-75th percentile for weight for length ratio! I am the mothe...

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: January 2011

http://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...

lifeofkeagan.blogspot.com lifeofkeagan.blogspot.com

Keagan Scott Covington: From this DAY Forward...

http://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.

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From This Point Forward

From This Point Forward. Thursday, March 13, 2014. Redeemed" (Big Daddy Weave). Seems like all I could see was the struggle. Haunted by ghosts that lived in my past. Bound up in shackles of all my failures. Wondering how long is this gonna last. Then You look at this prisoner and say to me "son. Stop fighting a fight it's already been won". I am redeemed, You set me free. So I'll shake off these heavy chains. Wipe away every stain, now I'm not who I used to be. I am redeemed, I'm redeemed. I took a step ...

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Vince's Life!!!

Standing in my toybox =). Wednesday, April 17, 2013. It's been a long time since i updated here.vince was doing REALLY well for a long time! Lung wise he went from i believe april-october with no antibiotics reguarding his lungs or sinus (he had a few skin infections this summer).on september 21,2012 we had our 2nd baby boy Trevor (who does not have CF).vince was up to 34 pounds,taking all of his medications! In november he started preschool-going 4 days a week from 1-415pm! Wednesday, September 19, 2012.

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Vince's Travels

Thursday, September 22, 2011. Today we are heading back to Seattle but our plane doesn't leave until 3:45 so we are going to Brooklyn to see Lianna and Billy (now married) and my Aunt Jane and Uncle John. We've never been to Brooklyn so it'll be great to see but I'm bummed to not have time to go back to Central Park playground. Hope they have a nice park over there somewhere! Here's the view of the Brooklyn Bridge and Manhattan:. After lunch we got a car ride to the airport and headed home. This is a pic...