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Kaden's Battle with Leigh SyndromeThis is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome.
http://kadethebattler.blogspot.com/
This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome.
http://kadethebattler.blogspot.com/
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Kaden's Battle with Leigh Syndrome | kadethebattler.blogspot.com Reviews
https://kadethebattler.blogspot.com
This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome.
kadethebattler.blogspot.com
Kaden's Battle with Leigh Syndrome: February 2011
http://kadethebattler.blogspot.com/2011_02_01_archive.html
Kaden's Battle with Leigh Syndrome. This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome. Wednesday, February 23, 2011. Kaden turned six yesterday. We had a party with Miki's family on Sunday and Keden really enjoyed all the attention. He always loves seeing his cousins and the chaos of all of them together with he and his siblings. Overall he's doing well. We see his neurologist next week and I will post an update after that appointment.
Kaden's Battle with Leigh Syndrome: September 2011
http://kadethebattler.blogspot.com/2011_09_01_archive.html
Kaden's Battle with Leigh Syndrome. This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome. Wednesday, September 28, 2011. The Scariest Eight Minutes. It was a typical Monday morning in the Stark household. Miki, Maddie and Jacob were up at about 5:30am. I decided to stay in bed instead of going for my morning walk, due to the rain (lazy ass! Then it happens. he answers. I have kept asking him to talk to me, asking if he's okay, telling him how much I love...I fou...
Kaden's Battle with Leigh Syndrome: November 2010
http://kadethebattler.blogspot.com/2010_11_01_archive.html
Kaden's Battle with Leigh Syndrome. This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome. Saturday, November 27, 2010. Kaden is not much for laying down when he is awake. He always wants to see what's going on. The neurosurgery physicians assistant told us it could take several more weeks for that to heal. We see the actual neurosurgeon in a couple weeks and it will be interesting to see what he has to say. Friday, November 19, 2010. So what is it? We decide to ...
Kaden's Battle with Leigh Syndrome: July 2011
http://kadethebattler.blogspot.com/2011_07_01_archive.html
Kaden's Battle with Leigh Syndrome. This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome. Sunday, July 10, 2011. Kaden also had Make a Wish come to see him and the whole family two weeks ago. He has been granted a wish! We all had a great 4th of July! Very busy. Fireworks, parade, pool party. I swear the kids could have slept for a couple days straight. I know Miki and I could have. Camp is right around the corner for Kaden and Kylie. This is the 1st year Ka...
Kaden's Battle with Leigh Syndrome: January 2011
http://kadethebattler.blogspot.com/2011_01_01_archive.html
Kaden's Battle with Leigh Syndrome. This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome. Wednesday, January 12, 2011. Hope everyone had a great holiday season! We had a very nice Christmas and got a chance to spend time with both Miki's family and mine. The kids of course are all spoiled rotten from the holidays. Overall though, the kids were good. Hope everyone has a great start to 2011! Subscribe to: Posts (Atom). Dystonia Medical Research Foundation.
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Kaden's Battle with Leigh Syndrome
Kaden's Battle with Leigh Syndrome. This is the story of my son Kaden. He is fighting a Mitochondrial disease called Leigh syndrome. Monday, October 8, 2012. First Annual Kaden's Wish Fundraiser. 2012 we will hold the first annual Kaden’s Wish Fundraiser at Champps Americana inBrookfield, WI. There will be a silent auction and a watch party for the Wisconsin vs Indiana football game. Come join us for some Badger fun and support the Make-A-Wish Foundation. Check out our Kaden's Wish facebook page. Our exp...
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