If you could, you would too!

 

 

 

 

 

We will eat pizza for at least a week!

When I saw the flyer earlier today, I was curious as to the authenticity of a 24″ x 24″ pizza.

Could they really sell a pizza that big?  Do they make bags that big to keep them warm?

Well…

They don’t make the bags that big, it arrived wrapped in a throw like the one we have on the couch!

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See the tiny pizza on the right?  That’s a 12″

We will eat pizza for at least a week but now I can say that I have ordered one huge pizza and it arrived in a cardboard box wrapped in a throw!

Where am I going with that?

Nowhere really except it made me think of the food Emily orders when we eat out.

When she feels for amazing breakfast and huge dessert this is what it looks like!

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Now you have it!

The bigger the better!

That’s probably why I ordered the pizza…  🙂

 

Eme’s Army: Fight for Sight

in lieu of a new post today, I am sharing this blog with you. Mommy has issues follows Oli’s journey and today is a special post about a fundraising opportunity. I encourage you to read her post and scroll back to some previous post. It’s a great blog!

mommyhasissues's avatarI'm fine, but my mommy has issues!

Oli was recently given an amazing opportunity to work with another special needs child on a campaign by a company called Paper Clouds Apparel.

Paper Clouds sells t-shirts, hats, sweatshirts, hoodies, and totes featuring the artwork of special needs children. Oli has her handprint heart on two different t-shirts and a tote that is now available for purchase. She is featured alongside another child named Logan and together they have some incredible things to choose from.

Paper Clouds Apparel employs special needs adults AND they donate 50% of the proceeds to a charity that we choose. We chose http://www.emesarmy.org. Emerie is a little girl who needs our help to get her eye sight back. Please visit http://www.papercloudsapparel.com and check it out!!

“The Cause (Sep 30 – Oct 13):

Eme’s Army
Eme is 6 years old and she is being robbed of her sight by CRB1-LCA, a very rare genetic disease…

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