Simply Soares: What I Love Wednesday!

Wednesday, February 9, 2011

What I Love Wednesday!

lollipops

I am going to link up with my darling friend Krystina for What I Love Wednesday today! I have been wanting to do this for a while, but life keeps getting in the way! Life will try today (and has tried if you read the earlier post from today!) but I am going to get this :)

What I Love this week.....

1. Wonderful, dear friends who mean the world to me!

2. This DARLING necklace with the BEST message on it found in a dear friends store HERE

3. The color Turquoise is IT these days to me... Love it!

4. My Family unit. Love those kids, miss seeing those girls as much!

5. The BREATH TAKING area I live in. Could a girl be more blessed when she walks down her street???

6. This super cute new headband I created today.... to be found HERE as soon as I get home from Bible study and list it :)

And my final What I Love thing is not a picture, but is heavy on my heart today....

I LOVE medical technology and the advances it is making EVERYDAY!
Thank you Lord that I live in a place we can get the care we need!

1 comments:

Unknown said...: this is absolutely gorgeous Gretchen! i love the family photo! precious!; February 9, 2011 at 8:26 PM

Subscribe to: Post Comments (Atom)

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!)