Simply Soares

Sunday, February 22, 2009

I love rainy days... And even more, I love the beach on rainy days!! As long as I can remember one of my all time favorite things to do on a rainy day has been to go to the beach. Now some of my friends seem to think I am weird for this, and my husband TOTALLY does not get it.. but I hope to teach my passion to my children so I will always have someone to go to the beach with on rainy days! If today was any indication, I think I might convert them yet :)

Nathaniel and Audrey on the beach walk today in Morro Bay

We even played on the swings at the park on the bay today... I love playing on swings too! My all time favorite date has always been to go play on the swings at night :)
I guess I just enjoy the simple pleasures!

Doesn't she look like she is having fun?
Such a cutie pie!

And I finally got Nathaniel to stop making funny faces long enough to get this great pic of him!

Audrey truly is my daughter.... if there was ever any doubt of it this picture proves it! Another one of my simple pleasures is writing messages on the beach... to God, to friends, to loves ones who have passes on... or just for the heck of it!

So we enjoyed this rainy day at the beach....What did you do today?

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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!)