Homemade Tater Tot: Tiny Dancer

Homemade Tater Tot

Our life as a family coping with Duchenne Muscular Dystrophy.

Saturday, January 7, 2012

Tiny Dancer

Posted by Katherine at 8:09 AM

Email This BlogThis!Share to Twitter Share to Facebook

2 comments:

miracle22111January 7, 2012 8:36 AM
too cute!! it's so great seeing him doing so well :)
ReplyDelete
TanyaJanuary 7, 2012 10:33 AM
Love it!!!
ReplyDelete

Newer Post Older Post Home

Subscribe to: Post Comments (Atom)

About Andrew

The Diagnosis
The Crawl
The very 1st step
The day he became a toddler
The day he began to walk

About Me

Katherine: Seeing as how I never expected it, this newest chapter of our life is definitely one to document. Ergo, Homemade Tater Tot.
Well, that's how the blog started, anyway. I am beyond happy that I started this up when I found out I was pregnant with Andrew. Now we know that he has Duchenne Muscular Dystrophy and that one day his journey here with us will end and I will have a written account of his entire life - from the moment we knew he existed. So as much as I hope this blog helps, inspires, educates, or even irritates those of you who read it, I will be equaly grateful to have something I can look back on as time goes by. I love comments, but if you want to talk to me privately, send me an e-mail at LITTLEfeedback@hotmail.com

View my complete profile

How to help Andrew

What your donation does

Thank you!!!

How to help those with muscle disorders

MDA
PPMD

Sites you might want to check out

Geronimo Gifts
Miles4Miles
10 Fitness
ErgoBaby

Followers

Popular Posts

The Diagnosis

Andrew has Duchenne Muscular Dystrophy. It's the diagnosis we've been dreading. There is no easy, no sugary way to explain the disease o...
Peyton

This is Peyton. Peyton is the son of my very good friends Tanya and James. We became friends when the Army moved Mister and I to Ft Camp...
All Aboard!

The train is leaving the station. Ignore the laundromat that is my living room floor. I was in the middle of folding the laundry when w...
We need a new goal

because we've met our "walking by his 2nd birthday" goal!!!!!!!!!!!!!!!! December 12, 2011, my baby boy took his first real steps. AND...
Building a Bridge

So as you should all know by now, there is no cure for Duchenne Muscular Dystrophy. There aren't even any treatments to slow down the pace ...

Blog Archive

▼ 2012 (22)
- ► May (3)
- ► April (3)
- ► March (4)
- ► February (5)
- ▼ January (7)

► 2011 (33)
- ► December (5)
- ► November (2)
  - Peyton
  - Ah Lawdy, Lawdy
- ► October (5)
- ► September (3)
- ► August (2)
  - Sunday, SUNday, SUNDAY!
  - A pbbbbbbbbbbbt and a yay
- ► July (5)
- ► June (4)
- ► May (1)
  - HE CRAWLED!!!!
- ► April (2)
  - "Party Dinosaur"
- ► March (2)
- ► February (2)

► 2010 (21)
- ► October (2)
- ► August (2)
- ► June (3)
- ► May (2)
- ► April (1)
- ► March (4)
- ► February (3)
- ► January (4)

► 2009 (29)
- ► December (2)
- ► November (3)
- ► October (3)
- ► September (4)
- ► August (5)
- ► July (9)
- ► June (3)

My Blog List

*The Johnson Family*
Baby and Beasts
Cheers and Jeers of A. Mears
Count your blessings instead of sheep....
Hyperbole and a Half
Mr. Mrs. and Baby
new realities
nienie
Random Thoughts
The Misadventures of Mrs. Duh
This moment is my life
Words from Dustin

Share it

Like Little on FB

Total Pageviews

Simple template. Template images by Nikada. Powered by Blogger.