Simply Soares: Organization Queen

Saturday, May 16, 2009

Organization Queen

Have I ever mentioned that I am an Organization Queen??I am NOT a control freak, I have the certified medical diagnosis to back that up, I am NOT a control freak, instead I am an Organization Queen! And organization is a good thing :)
So, keeping in mind that I LIKE things VERY organized, you could probably imagine my EXCITEMENT when I was gifted this supper cool paper rack! (Oh, and have I mentioned that I am OBSESSED with scrapbooking???)

I was absolutely giddy Thursday night, which is my kid free night, that I could organize all of my scrapbooking paper, by color order of course, into these supper cool racks!! My friends and I met at Butterfly with a bottle of wine, good music and our stolen few hours... and I SORTED PAPER!! Silly I know, but it made me happy!

Isn't this pretty??
All color coordinated...
and waiting to be made into BEAUTIFUL creations!

Now I can't wait to organize my pics and "stuff" into the empty file cabinet in chronological order so I can get back to my FAVORITE part... creating AWESOME scrapbooks for my wonderful children!

Hope you got to do something this week that blessed you!

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Nathaniel is my darling son, the one and only boy in a gaggle of girls! He is an amazing young man with character and charisma to spare! He has a spirit that is pure and shines through to all who encounter him. But Nathaniel also has some other things that make him special too. Nathaniel was born with a sever birth defect (do you know how much I dislike that term?) called Spina Bifida. Everyday our family deals with the effects of this condition, and we all have learned to lean on the Lord to get us through the twists and turns of Spina Bifida! Nathaniel is all boy with a love for all things ball, and his new passion is surfing! Nathaniel shows wisdom and understanding beyond his years, and is such a trooper in dealing with all things Spina Bifida, and yet still living every minute of his life to the fullest in the glory of God!

Even though October and Spina Bifida Awareness Month is over, Tiffany from Growing From the Obstacles still want to continue bringing you a look at what Spina Bifida REALLY is, and the stories of our friends and family who live with it daily!!! We will feature stories of SB families and their journey every Thursday, as long as we have stories to feature! So come on over and join in!

To Tiffany and I Spina Bifida is far more than a Neural Tube Birth Defect, Spina Bifida is merely a way of live for those who live with it. (And BTW, even if that is the proper medical description of Spina Bifida, I still HATE the word defect in it, as that word implies there is something wrong with folks with Spina Bifida and we do NOT believe that! We believe these precious folks were made special for a reason.) I hope you enjoy meeting our family as much as we enjoy the honor of being able to share them with you.

(If you want to share your story with us to be featured this month please see THIS POST on how to submit it!)