Saturday, June 16, 2012

Yes, I'm alive!!


It's true, I'm alive! Yes, I know it's been over a year since I last posted, but life has been....super crazy and continues to be crazy...however, I really want to start posting again since this blog is our family journal and I want to keep it updated.  It may be another week or so before I get around to making an actual post, but I just had to let you know I'm still around, life is wonderful, and I have sooooo much to tell you all!!! For now, enjoy just a few pictures to hold you over until I post next :)

                                       Tried out having brown hair for the first time ever...it was fun! I only kept it for a couple of months though.  I also did tried out straight-across bangs, which I really loved! 
 Daddy and Conner
 Big family trip to Disney Land in March 2012...so much fun! 
 Family Pictures done at Foto Fly/March 2012 




8 comments:

BECKY said...

I'm excited to hear updates! Can't wait to hear your birth story!

Mike & Rebecca said...

yeah, you are back!

KaShan said...

You left out pics of your girls!!!

Jessica said...

I was so happy to see this post! Can't wait to hear an update! (From the other comments, I'm assuming your family grew. Did you have twins??)

Sydney said...

I just wanted to let you know that I saw your comment and was just totally touched by it. You're the sweetest! And congrats on your new little additions! Your family is beautiful!

Smilen Champ said...

Hi Conner

My name is Jenna. You are a brave courageous fighter. you are a special miracle from god, a gift from above, earthly angel,and you are a smilen hero. You are full of happiness, life, smiles, joy, fun,love, and spunk.


I was born with a rare life threatening disease, and have 14 other medical conditions, and developmental delays.

I wrote this poem
Each of us are Special
Each of us different,
No one is the same
Each of are us are unique in our own way,
Those of us who have challenges, we smile through our day.
Those who of us who have challenges, we smile through our day.
It doesn't matter what others say
we are special anyway.
What is forty feet and sings? the school chior
http://www.miraclechamp.webs.com

Holli said...

Annie, My son, Ethan, also has Digeorge syndrome and we are working with Amy. She gave me your blog and I wanted to contact you. Your family is just beautiful!
Holli Glover
pixy_oak@hotmail.com

Heather said...

Hi I'm Heather! Please email me when you get a chance, I have a question about your blog! LifesABanquet1(at)gmail.com