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Hakuna Matata for Alexander

Hakuna Matata for Alexander. Living Up Life With SMA. Friday, May 18, 2012. Ohio Walk N Roll. A couple of weekends ago, we went over to Ohio for a FSMA Walk N Roll! Alexander and Daddy on the SMA stage! Alexander and Roman with their balloons! Alexander and MJ. she sent him his B4SMA blanket! Friday, May 18, 2012. Wednesday, April 11, 2012. Alexander's version of We Are Young! This video is definitely Alexander's motto! Hakuna Matata for Alexander. Cure SMA! Wednesday, April 11, 2012. Alexander was so ex...

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Hakuna Matata for Alexander | thedavisfamilythree.blogspot.com Reviews
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Hakuna Matata for Alexander. Living Up Life With SMA. Friday, May 18, 2012. Ohio Walk N Roll. A couple of weekends ago, we went over to Ohio for a FSMA Walk N Roll! Alexander and Daddy on the SMA stage! Alexander and Roman with their balloons! Alexander and MJ. she sent him his B4SMA blanket! Friday, May 18, 2012. Wednesday, April 11, 2012. Alexander's version of We Are Young! This video is definitely Alexander's motto! Hakuna Matata for Alexander. Cure SMA! Wednesday, April 11, 2012. Alexander was so ex...
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5 one busy boy
6 alexander's 3rd birthday
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8 new bath chair
9 alexander's ipad
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Hakuna Matata for Alexander | thedavisfamilythree.blogspot.com Reviews

https://thedavisfamilythree.blogspot.com

Hakuna Matata for Alexander. Living Up Life With SMA. Friday, May 18, 2012. Ohio Walk N Roll. A couple of weekends ago, we went over to Ohio for a FSMA Walk N Roll! Alexander and Daddy on the SMA stage! Alexander and Roman with their balloons! Alexander and MJ. she sent him his B4SMA blanket! Friday, May 18, 2012. Wednesday, April 11, 2012. Alexander's version of We Are Young! This video is definitely Alexander's motto! Hakuna Matata for Alexander. Cure SMA! Wednesday, April 11, 2012. Alexander was so ex...

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thedavisfamilythree.blogspot.com thedavisfamilythree.blogspot.com
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Hakuna Matata for Alexander: May 2012

http://thedavisfamilythree.blogspot.com/2012_05_01_archive.html

Hakuna Matata for Alexander. Living Up Life With SMA. Friday, May 18, 2012. Ohio Walk N Roll. A couple of weekends ago, we went over to Ohio for a FSMA Walk N Roll! Alexander and Daddy on the SMA stage! Alexander and Roman with their balloons! Alexander and MJ. she sent him his B4SMA blanket! Friday, May 18, 2012. Subscribe to: Posts (Atom). Our Lil Man's Master Plan. View my complete profile. Multiply Life By the Power of Four. 3rd Annual Give4Gav Fundrasier. Ohio Walk N Roll.

2

Hakuna Matata for Alexander: Alexander's iPad

http://thedavisfamilythree.blogspot.com/2011/01/alexanders-ipad.html

Hakuna Matata for Alexander. Living Up Life With SMA. Thursday, January 6, 2011. Alexander with his iPad Christmas Day! Alexander playing his "Animals" game! Alexander and Daddy playing with the iPad! Thursday, January 06, 2011. January 23, 2011. I am so glad he likes it! Nicholas got one for Christmas too and it has been so fun for him! He loves his fish app.he sings the ABC song and its adorable! Glad you had such a nice Christmas! Subscribe to: Post Comments (Atom). Our Lil Man's Master Plan.

3

Hakuna Matata for Alexander: July 2011

http://thedavisfamilythree.blogspot.com/2011_07_01_archive.html

Hakuna Matata for Alexander. Living Up Life With SMA. Monday, July 18, 2011. Florida. Magic Kingdom and Animal Kingdom! We continued our Florida trip with a visit to the Magic Kingdom! Alexander was so excited to ride some rides and see all his favorite characters walking around. He was on the look out for Captain Hook, and we were all a little afraid he would not see him. Sure enough when we got there Captain Hook was at the castle doing a show with Mickey Mouse! It was the greatest start to the day!

4

Hakuna Matata for Alexander: April 2011

http://thedavisfamilythree.blogspot.com/2011_04_01_archive.html

Hakuna Matata for Alexander. Living Up Life With SMA. Wednesday, April 13, 2011. Alexander turned 3 on March 31! HAPPY BIRTHDAY to our sweet lil man! Alexander got to go see his new preschool on his birthday, and then we spent the afternoon at Chuck E Cheese! Chuck E Cheese is one of his favorite places to go. He loves to play the all the games and NEVER wants to leave once we are there. I really think he enjoyed spending the day with Momma and Dadda at his favorite place! Wednesday, April 13, 2011.

5

Hakuna Matata for Alexander: Ohio Walk N Roll

http://thedavisfamilythree.blogspot.com/2012/05/ohio-walk-n-roll.html

Hakuna Matata for Alexander. Living Up Life With SMA. Friday, May 18, 2012. Ohio Walk N Roll. A couple of weekends ago, we went over to Ohio for a FSMA Walk N Roll! Alexander and Daddy on the SMA stage! Alexander and Roman with their balloons! Alexander and MJ. she sent him his B4SMA blanket! Friday, May 18, 2012. May 23, 2012. Subscribe to: Post Comments (Atom). Our Lil Man's Master Plan. View my complete profile. Multiply Life By the Power of Four. 3rd Annual Give4Gav Fundrasier. Ohio Walk N Roll.

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give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: April 2011

http://give4gav.blogspot.com/2011_04_01_archive.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Thursday, April 7, 2011. 2nd Annual Give4Gav Motorcycle Ride Sponsored by "That Place". There w...

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: May 2010

http://give4gav.blogspot.com/2010_05_01_archive.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Monday, May 10, 2010. Gavin in his new stroller. We are ready for the Give4Gav fundraiser!

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: 2nd Annual Give4Gav Motorcycle Ride Sponsored by "That Place"

http://give4gav.blogspot.com/2011/04/2nd-annual-give4gav-motorcycle-ride.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Thursday, April 7, 2011. 2nd Annual Give4Gav Motorcycle Ride Sponsored by "That Place". For dir...

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: 3rd Annual Give4Gav Fundrasier

http://give4gav.blogspot.com/2012/08/3rd-annual-give4gav-fundrasier.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Thursday, August 2, 2012. 3rd Annual Give4Gav Fundrasier. Subscribe to: Post Comments (Atom).

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: Showing Improvement

http://give4gav.blogspot.com/2010/04/showing-improvement.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Tuesday, April 27, 2010. Now, we just need to get him off the oxygen during the day :). My daug...

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: April 2010

http://give4gav.blogspot.com/2010_04_01_archive.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Tuesday, April 27, 2010. Now, we just need to get him off the oxygen during the day :). Excitin...

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: Gavin's New Stroller

http://give4gav.blogspot.com/2010/05/gavins-new-stroller.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Monday, May 10, 2010. Gavin in his new stroller. We are ready for the Give4Gav fundraiser!

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: Gavin's Wagon Ride

http://give4gav.blogspot.com/2010/05/gavins-wagon-ride.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Thursday, May 6, 2010. Check out his sunglasses! May 7, 2010 at 7:55 PM. Exciting news for the ...

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: 2nd Annual Give4Gav Fundraiser

http://give4gav.blogspot.com/2011/04/2nd-annual-give4gav.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Thursday, April 7, 2011. 2nd Annual Give4Gav Fundraiser. Every little bit helps! Thank you for ...

give4gav.blogspot.com give4gav.blogspot.com

Give4Gav: Exciting news for the Huffman Family!!!

http://give4gav.blogspot.com/p/exciting-news-for-huffman-family.html

Give4Gav is an organization designed to help children affected by Spinal Muscular Atrophy ("SMA"). SMA is a genetic disease that has no current treatment or cure. SMA causes respiratory failure due to low muscle tone and is the leading genetic killer in infants. Give4Gav was founded in 2010 by Brad and Crystal Huffman and Amber Norton. Brad and Crystal lost their son Gavin to this tragic disease June 22, 2010. Exciting news for the Huffman Family! Subscribe to: Posts (Atom). Garage Sale and Bake Sale.

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Saturday, November 16, 2013. First of all, I want to say we are all okay and doing great! Y'all are so sweet to email and check on us since I haven't posted in months. I have a lot of reasons for not posting but nothing really earth shattering. Ha! The main reason is that Reagan pulled my camera off the counter back in September so I haven't had a camera (besides my phone) since then. I haven't done one thing to my house. I didn't even decorate for fall! The wonderful Amber Dickey. Here is the before:.

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The Davis Family – All Davis - All Day!

All Davis - All Day! Are you one of us? June 17, 2014. Calling all members of the Davis Family! If you are one of our super awesome gang you can now join the website! Joining the website for the low low cost of FREE. Gets you all these great perks:. Access to the family directory. Ability to add yourself to the family directory. And other cool stuff I have yet to think of 😉. SO – hit the big blue button to the right and get yourself signed up! Filed Under: Family News. June 11, 2014. I am a Davis!

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Davis Family Reunion

You are trying to access. This site has expired as of . If it is your site and you wish to reactivate it by purchasing it you can do so by logging into your control panel and clicking on the ORDER tab at the top of the page. To log into your control panel, click here. Powered by MyEvent.com. Click Here 7 Day Free Trial.

thedavisfamilyshenanigans.blogspot.com thedavisfamilyshenanigans.blogspot.com

Davis Family Shenanigans

Te valde amo ac semper amabo. Tuesday, August 3, 2010. Adam and I just got back from a weekend filled with awesome diving. Adam was getting his Open Water cert, and I ended up getting my Advanced cert. The weather was beautiful, the water was clear, and the friends we went with were amazing! Can't wait for our next dive trip! Kaylee got to spend a few days with Adams parents, and she was thrilled! So excited, that when we called to talk to her she wanted nothing to do with us. Stinker. See, I'm trying.

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Davis Family Site

160;                               Cromartie • Davis • Kemp • McKoy • Monroe. Welcome to the Davis Family Site. The Davis family reunion for 2014 has been cancelled. Due to lack of response. The next reunion will be held in 2016 in Wilimington NC. 2014 is our year. We will celebrate it in Tinton Falls, New Jersey! View the Family Tree. Talk about it in our Family Forum. Find the Family on Facebook. Message to the Family. Dear Family and Friends,. Remember, the family circle never ends.

thedavisfamilythree.blogspot.com thedavisfamilythree.blogspot.com

Hakuna Matata for Alexander

Hakuna Matata for Alexander. Living Up Life With SMA. Friday, May 18, 2012. Ohio Walk N Roll. A couple of weekends ago, we went over to Ohio for a FSMA Walk N Roll! Alexander and Daddy on the SMA stage! Alexander and Roman with their balloons! Alexander and MJ. she sent him his B4SMA blanket! Friday, May 18, 2012. Wednesday, April 11, 2012. Alexander's version of We Are Young! This video is definitely Alexander's motto! Hakuna Matata for Alexander. Cure SMA! Wednesday, April 11, 2012. Alexander was so ex...

thedavisfamilytimes.blogspot.com thedavisfamilytimes.blogspot.com

The Times

Monday, August 3, 2015. Nora Katherine was born July 13th at 12:01 pm weighing 6 pounds, 10.5 ounces and 20.5 inches long. It's surreal to think this day ever happened- it feels like a dream that happened in my heart. We are loving every minute with this beauty. Nora's first days in the hospital, in photos. Hospital photographs courtesy Lindsay McGowan Photography:. She's mine. She's really mine. Sunday, June 14, 2015. Second Year of Marriage: The Top 10. In no particular order. Despite all our personal ...

thedavisfamilyupdate.blogspot.com thedavisfamilyupdate.blogspot.com

Sooooo......yeah...

In the Davis house, nothing stays the same and every day is an adventure.buckle your seatbelts, you're in for a ride! Monday, May 13, 2013. Friday, May 10, 2013. EAR PIERCING SIREN ENTER HERE. Stand there mortified, with your dirty bare foot three year old and his brother with their hands over their ears. The workers are like roaches running over to the exit to silence the alarm. Head down. Walk away quick. I can't even blame this craziness on taking all of them with me. Saturday, April 20, 2013.

thedavisfamilywillbethree.blogspot.com thedavisfamilywillbethree.blogspot.com

THE DAVIS DAYS

Sons are a heritage from the Lord, children a reward from him. Psalm 127:3. Wednesday, July 6, 2011. Happy 4th of July. We had a GREAT Independence day.We hope you did too! We started the day watching the 4th of July parade in downtown Prattville. See the picture above of Evan watching for the parade to come! He enjoyed it and caught lots of candy. We then ate lunch at Mellow Mushroom because Jason and I didn't get our act together to cook. Evan sleep through lunch.so we came home for him to eat. You are...

thedavisfirm.blogspot.com thedavisfirm.blogspot.com

The Davis Firm

America's Premier Source for Humor, Repartee, and Industrial Grade Manganese. Thursday, March 10, 2011. What's almost worse then the stuff you need is the stuff THE MAN tries to convince you that you need. Yeah, Fisher-Price, Playskool, and Mattel are all part of the evil establishment. The only truly pure soul in the children's industry is Raffi. And he's a bloody weirdo. For her to play in. But what came up in our search for a perfectly reasonable toy? And I thought they smelled bad on the outside!

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The Davis Firm

Under Construction Check Back Soon! 800 So. McDonough Street, Ste. 104. Montgomery, Alabama 36104. Direct Dial: (334) 215-4430.