Kendall's Hope: Kendall's Ready for the Holidays...

Friday, December 4, 2009

Kendall's Ready for the Holidays...

4 comments:

val said...: ahhhhhhhhh! nice moves, baby!; December 4, 2009 at 1:34 PM
Heather said...: Love,love this of your little love.However HATED previous video.I will NEVER,EVER get use to see children endure these.Ever.Mine or anyone elses.Just not fair.

She is looking so beautiful.So grown up.she ahs passed through so much crap and she still manages to be filled with such joy.

You all seem to be finding your way through a new norm.You do it beautifully and my prayers continue for your gorgeous, little fighter.

*Very jealous of your Train experience ... so cool and much needed and deserved for you Jocalyn.; December 4, 2009 at 4:11 PM
Anonymous said...: Love it!! and love your sense of humor...too dang cute!!; December 5, 2009 at 9:05 AM
Anonymous said...: I love it...

Sara; December 6, 2009 at 2:27 PM

What's the Scoop?

We are very open about our journey with Kendall. We're happy to answer any questions, and welcome all your comments! The one thing we don't want is to be isolated from our friends and family. I've been that person who thinks it is easier to just ignore a child with special needs and their family. I've feared hearing their story. I've been guilty of looking through a child with special needs. I've also thought and said "how on earth do you deal everyday?" Although it certainly isn't easy, we are a normal family...celebrating all the milestones our daughter hits (and maybe cheering a little louder in the process!) Let me tell you...it's been a long road with many bumps but the love and support we receive daily is what keeps us truckin'! Click here for the full story on our precious baby girl Kendall Ann, or scroll down for the quick recap! Thanks for visiting!

About Kendall...

Kendall Ann has blessed our lives in so many ways. She is truly a gift from God and has proven herself to be a fighter from the beginning. She was born with many neurological and optical abnormalities, which we now know is due to a stroke in utero...probably due to her Factor V Leiden mutation and two copies of the MTHFR gene (1-14-09). Oh, and NOW she has Type 1 Diabetes (8-19-09) And NOW (12-16-10) she has problems with her Mitochondria ... and NOW (2-11-13) a neurogenic bladder resulting in a vesicostomy. Of course there is a possibility of a Mitochondrial Disorder, and a possibility CDLK5 caused all the problems and Mito secondary...but we will never know, because we've decided no more testing! When she was born she came right home...no NICU stay...and we had no idea anything was wrong! She has undergone numerous hospital stays and a number of surgeries, but through it all, she has maintained a smile that wins the hearts of everyone who meets her. Please join us in our journey of life with a special little girl full of spunk and personality who happens to have multiple disabilities.