Simply Soares

Sunday, May 5, 2013

Right as the storm clouds threaten to close in and take over, that is the moment God meets you in and reminds you why it is all worth it!

God used so many people to bless our life today, remind us how loved we are, and most of all remind us how much HE loves us!

I am ever humbled as I start into this week, the first of our new journey.

To my Rock Harbor family, your love and prayers fuel us in those dark moments. Words can not express my gratitude.

To the Joyful Voices Choir that we had the privledge of listening to and watching today.... inspirational, humbling and uplifting! Thanks Cindy Crowley Price for the invite!

To the Rock Harbor Worship team, just what this broken heart needed tonight. Thank you for providing such a spirit filled platform where He was able to meet us right where we are. You folks are such a blessing!

And to the prayer warriors that rallied around my little man tonight... there are not words! John M Pallanes, Brandie Bledsaw, Randy Ponder and MeLisa Neal Dicus... thank you for showering my boy in the love that comes from God!

I feel strengthened to start this week!

0 comments:

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!)