miniaturestump.blogspot.com

Miniature Stump

Wednesday, October 2, 2013. All for Kylie and the love from her Papa. Feel free to click on her picture on the blog to the right, or you can click the link here. To see her page, and read about so much of the progress Kylie has made. Saturday, August 3, 2013. This is the first time my dad held her. He wanted so badly to hug her and hold her tight, but those sensory issues of hers wouldn't allow it. I love this picture so much! My hub's with my dad and Kylie.and Abbie. Kylie wasn't really into holding han...

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Miniature Stump | miniaturestump.blogspot.com Reviews

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Wednesday, October 2, 2013. All for Kylie and the love from her Papa. Feel free to click on her picture on the blog to the right, or you can click the link here. To see her page, and read about so much of the progress Kylie has made. Saturday, August 3, 2013. This is the first time my dad held her. He wanted so badly to hug her and hold her tight, but those sensory issues of hers wouldn't allow it. I love this picture so much! My hub's with my dad and Kylie.and Abbie. Kylie wasn't really into holding han...

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6 forever her papa

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Miniature Stump | miniaturestump.blogspot.com Reviews

https://miniaturestump.blogspot.com

Wednesday, October 2, 2013. All for Kylie and the love from her Papa. Feel free to click on her picture on the blog to the right, or you can click the link here. To see her page, and read about so much of the progress Kylie has made. Saturday, August 3, 2013. This is the first time my dad held her. He wanted so badly to hug her and hold her tight, but those sensory issues of hers wouldn't allow it. I love this picture so much! My hub's with my dad and Kylie.and Abbie. Kylie wasn't really into holding han...

INTERNAL PAGES

miniaturestump.blogspot.com

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Miniature Stump: July 2012

http://miniaturestump.blogspot.com/2012_07_01_archive.html

Tuesday, July 31, 2012. Swinging into fun times (Ohio Trip). Just when I think I am getting caught up on the blog, I fall behind :) So let's get back into it and start with our trip to Ohio. I can never say enough how Awesome Kylie does when we are on the road. I think she only asked to stop twice in our 15 hour drive. Here is a cheese smile part way through the drive. I will let you all know that we picked up a new camera lens on our drive, so I was able to use the nice camera for our trip.yay! Kylie fo...

2

Miniature Stump: March 2013

http://miniaturestump.blogspot.com/2013_03_01_archive.html

Wednesday, March 20, 2013. Who do you wear Purple for? We wear purple for Kylie.how about you? Every year we try to see how many people we can get to wear purple for Kylie and all of her friends with Epilepsy, especially those that have shared the IS (Infantile Spasms) diagnosis. Purple Day is coming up (Tuesday, March 26th), so start digging through your closets for something purple to wear for our girl! Please wear your purple for Kylie and send me your pics so I we can have a Purple Party on the blog!

3

Miniature Stump: All for Kylie and the love from her Papa

http://miniaturestump.blogspot.com/2013/10/all-for-kylie-and-love-from-her-papa.html

Wednesday, October 2, 2013. All for Kylie and the love from her Papa. Feel free to click on her picture on the blog to the right, or you can click the link here. To see her page, and read about so much of the progress Kylie has made. Subscribe to: Post Comments (Atom). Click on the link above to donate to Team Kylie - an annual fundraiser for the LeAnn Britain Infant Development Center at Shawnee Mission Medical Center. Last year, Team Kylie raised $615. Click to visit Mae Blossoms.

4

Miniature Stump: June 2012

http://miniaturestump.blogspot.com/2012_06_01_archive.html

Tuesday, June 12, 2012. Rainbows and happy hearts. Kylie loves to color pictures, and she has learned how to make a smiley face, but then I thought hmm.what about a rainbow? It just took one time to show her what to do, and now we are filling up the place with rainbows! Hey, look at my rainbow.cheese! Hahashe knows the cheese face was silly, so she just had to laugh about it. Kylie walking back with Matt. I love the little feet next to her dadda's :). She's in the blue vest). Kinda funny, how she was jus...

5

Miniature Stump: January 2013

http://miniaturestump.blogspot.com/2013_01_01_archive.html

Thursday, January 31, 2013. Christmas Dream Come True! Once again, forever behind on blogging.buuut, I have a great excuse :) Apparently, I have reached my limit on pics posted on the blog. Google says I can change that buy paying to upgrade.umm, no. So I got around that, but posting pics to Matt's Google account, and then I have to upload them here. A total pain, but it beats paying Google. Kylie is a ROCKSTAR! Kylie's OT was even assigned to attend, just to be there for support if Kylie needed it. ...

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oursweetsophie.blogspot.com

Our Sweet Sophie: December 2011

http://oursweetsophie.blogspot.com/2011_12_01_archive.html

Saturday, December 17, 2011. We are home. We actually got home late Thursday night. Sorry for the lack of timely updates. Sophie is doing well. She is getting stronger by the day. Sophie's Story by Elaine. Labels: Surgery.Take 2. Tuesday, December 13, 2011. She is doing Ah-May-Zing. What a difference a couple of days have made. Here's a picture just a few hours after surgery on Friday. Then she slept for the next 3 days. Looking so awake and alert after therapy. After therapy, these clowns came by. Now i...

oursweetsophie.blogspot.com

Our Sweet Sophie: Against All Odds

http://oursweetsophie.blogspot.com/2013/12/i-have-most-ridiculous-smile-on-my-face.html

Monday, December 09, 2013. I have the most ridiculous smile on my face. My world seems a bit lighter. I can now let go of the anticipation of this day, as it is now here. A day that did not seem possible. Today marks 2 years since Sophie's second round of brain surgeries. Two years. It's hard to believe. But to fully appreciate today, that. Day and so many other pivotal moments along this journey that lead us to today must be remembered. Then a few days after mailing the CD, I received a call saying they...

oursweetsophie.blogspot.com

Our Sweet Sophie: Home Sweet Home

http://oursweetsophie.blogspot.com/2011/12/home-sweet-home.html

Saturday, December 17, 2011. We are home. We actually got home late Thursday night. Sorry for the lack of timely updates. Sophie is doing well. She is getting stronger by the day. Sophie's Story by Elaine. Labels: Surgery.Take 2. Love the picture. Happy holidays! Hope by the time the New year rolls around everyone feels like their old self again. Sun Dec 18, 08:05:00 AM CST. Oh, Elaine. It puts special meaning to home for the holidays, doesnt it? Sun Dec 18, 06:55:00 PM CST. Mon Dec 19, 06:04:00 AM CST.

oursweetsophie.blogspot.com

Our Sweet Sophie: October 2010

http://oursweetsophie.blogspot.com/2010_10_01_archive.html

Monday, October 25, 2010. I was decompressing somewhere in the house. Brandon was giving all the little kids a bath. Sophie was screaming her head off. Which is very UNusual for her. She loves bath time. She is constantly trying to find a way to take a bath or shower several times a day. But things have been off lately.ever since we started weaning the Dilantin. She immediately calmed down and smiled at me. So I asked her. Why were you crying. It was at the front door. It was at the front door. We met wi...

oursweetsophie.blogspot.com

Our Sweet Sophie: December 2013

http://oursweetsophie.blogspot.com/2013_12_01_archive.html

Monday, December 09, 2013. I have the most ridiculous smile on my face. My world seems a bit lighter. I can now let go of the anticipation of this day, as it is now here. A day that did not seem possible. Today marks 2 years since Sophie's second round of brain surgeries. Two years. It's hard to believe. But to fully appreciate today, that. Day and so many other pivotal moments along this journey that lead us to today must be remembered. Then a few days after mailing the CD, I received a call saying they...

oursweetsophie.blogspot.com

Our Sweet Sophie: She is doing GREAT!!!

http://oursweetsophie.blogspot.com/2012/01/she-is-doing-great.html

Friday, January 27, 2012. She is doing GREAT! But this time is different. It just has to be. I am once again filled with so much hope. Seizure-freedom seems so real. So permanent. Why not? Sophie's Story by Elaine. Fri Jan 27, 09:02:00 AM CST. Elaine, This is such wonderful news! I hope and pray this miracle of seizure freedom is yours to proclaim forever more. I know it is absolutely amazing to have that weight and heartache lifted from your shoulders. Rejoicing with you here in NC! Hugs, prayers and ch...

oursweetsophie.blogspot.com

Our Sweet Sophie: A whole new ballgame...

http://oursweetsophie.blogspot.com/2012/03/whole-new-ballgame.html

Monday, March 12, 2012. A whole new ballgame. Sophie has been through a LONG list of anti-seizure medications. I can name off a dozen without even blinking an eye. Somehow, I have gained comfort in the knowledge that I have built up over the years when it comes to anti-seizure medications. But now that she is seizure-free, I am changing my focus to ADHD medications. I meant to do a whole post on Friday, March 9th.her 3 month seizure-free anniversary. I can't believe it.3 months already! For the posting t...

oursweetsophie.blogspot.com

Our Sweet Sophie: Surgery is over!!!

http://oursweetsophie.blogspot.com/2011/12/surgery-is-over.html

Friday, December 09, 2011. Now it is a "wait and see" game to see how much weakness she has and how much therapy she needs. Just like we wanted Sophie to have lots of seizures to be captured during the grid monitoring, we are also wanting to see weakness immediately after surgery. But we are hoping it will only be temporary and she should regain her strength within two weeks. Thank you for all your prayers, support and love. Sophie's Story by Elaine. Labels: Surgery.Take 2. Fri Dec 09, 01:00:00 PM CST.

oursweetsophie.blogspot.com

Our Sweet Sophie: January 2012

http://oursweetsophie.blogspot.com/2012_01_01_archive.html

Friday, January 27, 2012. She is doing GREAT! But this time is different. It just has to be. I am once again filled with so much hope. Seizure-freedom seems so real. So permanent. Why not? Sophie's Story by Elaine. Subscribe to: Posts (Atom). Sophie's 1st Year Montage October 2006. Best of Sophie Video October 2008. Find out more about Infantile Spasms. NINDS Infantile Spasms Information Page. Life with the Lundgrens. Maddie's Marathon Against Leukemia and IS. Our journey with infantile spasms.

oursweetsophie.blogspot.com

Our Sweet Sophie: September 2011

http://oursweetsophie.blogspot.com/2011_09_01_archive.html

Tuesday, September 06, 2011. She rode the Special Education bus. It's not the bus I had ever envisioned her riding to her first day of kindergarten. Well, at least not before she was born.when all my hopes and dreams for her were of those of typical. Parents. And then there was a time in my life that I didn't even know if she would go to school. So, riding the Special Education bus is.in fact.a huge milestone for her. But she was making tremendous gains. Social. One of the reasons I loved preschool s...

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Wednesday, October 2, 2013. All for Kylie and the love from her Papa. Feel free to click on her picture on the blog to the right, or you can click the link here. To see her page, and read about so much of the progress Kylie has made. Saturday, August 3, 2013. This is the first time my dad held her. He wanted so badly to hug her and hold her tight, but those sensory issues of hers wouldn't allow it. I love this picture so much! My hub's with my dad and Kylie.and Abbie. Kylie wasn't really into holding han...

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