My husband and I have been married for 7 years. Walker was 6, Avery was born the year we married, Gavin 18 months after that. When we were told of Gavin's birth defects, it was like a slap in the face. We have struggled, mentally, physically and financially for the past 5 years. Jason has been working hard while I stay home and be Mom.
I found peace in photography, Jason found peace in fishing. For the past few years we've been talking about how we can better our family, financially, yet still give back to the community. We have thrown so many ideas around but they all seem to revolve around spina bifida/special needs children.
I have finally decided to take the scary plunge into my own photography business (this is the climb, to success). I tried once and failed, but now, I have grown, I have studied, I have practiced and I have a plan (and the kids are older and will all be in school). I still wanted to give back and I have been thinking and praying on how I should or even could. I am not sure why I didn't see it before, but now, I do.
Fiddlesticks Photography will give back in a big, big way. Along with photoshoots and offering accessories Fiddlesticks wants all the special needs families to know they deserve quality, wall worthy photos too! So that is where giving back comes in. We want to offer free or low cost shoots to families with children that have special needs. We understand that is a broad description but even "invisible" disabilities are financially draining. I haven't completely decided how I will give the shoots, I want to try and do 2-4 a month. I may do something that allows people to nominate families and have my facebook fans vote. I am not sure. This is where I need your help. I need your suggestions, your input, you thoughts. How can I make this successful? How can I help these families? Would you want something like this? (I sure know I would have loved to have this when G was young).
You can visit my FB page here (I haven't said anything on there yet, but I suppose I have to let the cat out of the bag sooner rather than later)
Don't be shy, I really want to know what you think!
A random blog about my life being a Christian wife, cook and a Mother of 3 beautiful children, One with Spina Bifida, One that thinks she is a princess fairy and One that is going to be an NFL player.
Showing posts with label pictures. Show all posts
Showing posts with label pictures. Show all posts
Tuesday, July 15, 2014
The climb....
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Tuesday, May 6, 2014
FIVE and possibly a picture overload.
I am writing this early because I know I will get busy and the emotion is already there so that is when I do my best writing. On Sunday Gavin will be 5.
I read a post recently about a father of 2. He talked about how the second child's firsts weren't as amazing as the first's because he had already seen that done and he decided to make a list of lasts because these were moments he would only experience one last time.
I think Moms and Dads are wired differently, in fact, I know they are. I was just as ecstatic for Walker's first steps as I was for Avery's and of course I was elated when Gavin took his . However, my LAST baby is turning 5...FIVE as in half a decade, where did the time go, kindergarten next year, holy cow slow down, FIVE. (Walker just turned 13, don't even get me started on the 13, thirteen as in holy cow 3 years and he will drive, 5 and he's an adult, stop growing you're already taller than me, 13.)
Five. In the past five years I've lived a lot of bittersweet lasts. I will never have them again, never. Why oh why does time go so very fast.
Gavin, 'white hawk of battle'. So he was. Born a toe head and battled his wars. He's still fighting and he's winning. His name fits.
It doesn't seem as though five years has passed. May 11th 2009 I certainly didn't see today as coming as fast as it has. But it's here, I cannot stop it. As much as I want to pause, I cannot.
I read a post recently about a father of 2. He talked about how the second child's firsts weren't as amazing as the first's because he had already seen that done and he decided to make a list of lasts because these were moments he would only experience one last time.
I think Moms and Dads are wired differently, in fact, I know they are. I was just as ecstatic for Walker's first steps as I was for Avery's and of course I was elated when Gavin took his . However, my LAST baby is turning 5...FIVE as in half a decade, where did the time go, kindergarten next year, holy cow slow down, FIVE. (Walker just turned 13, don't even get me started on the 13, thirteen as in holy cow 3 years and he will drive, 5 and he's an adult, stop growing you're already taller than me, 13.)
Five. In the past five years I've lived a lot of bittersweet lasts. I will never have them again, never. Why oh why does time go so very fast.
Gavin, 'white hawk of battle'. So he was. Born a toe head and battled his wars. He's still fighting and he's winning. His name fits.
It doesn't seem as though five years has passed. May 11th 2009 I certainly didn't see today as coming as fast as it has. But it's here, I cannot stop it. As much as I want to pause, I cannot.
Gavin: Determined, strong, fighter, adorable, mischievous, flirt, happy, blue eyed, farmers tan, t-ball player, iPad guru, hard headed (wonder where he gets that), miracle, independent (I have to admit there was a lump in my throat when I typed that), five years old, FIVE.
You all know about Gavin. To sum it up without being completely redundant. Gavin was born with spina bifida, hydrocephalus and Arnold Chiari Malformation II. He spent almost 1 month in the NICU at chippenham and had 2 surgeries (on closure and one shunt placement). We were told Gavin would likely have a poor quality of life, that he probably wouldn't walk and the best option for the child was abortion.
May 2009
Finally home where he belongs!
This picture means so much to me. I don't know how many of you know this but Gavin literally cried all day (and a lot of nights) for the better part of 4-6 months. This chair he sat in I would put my foot on it and bounce him all day. It was the only way he would be happy unless he was eating. I look at this and see that smile and all those months of sobbing (he and I both) fade away. All it took was one picture, one moment to erase all of that.
boom boom fire power
I love this picture of him, however, that day I was thrust into the world of people not understanding 'special needs'. The photographer kept asking how old he was and wanted him to stand she didn't understand that he couldn't and was like I will put a block up there, lady.he.can.not.stand.yet. anyway the picture is adorable.
His first Birthday. He had serious texture issues and would not eat much of anything. I actually had to smash the cake into his face to even get a picture of him with icing on his face. He was less than thrilled.
his nemesis, the ice cream cone.
we should probably stick to a bowl and spoon.
photos he will hate me for one day.
Random photos in no particular order.
Just because this is so Gavin.
so happy birthday Gman. We love you so very much and are so VERY VERY proud of you.
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