Mrs. Kelly Atkinson. WOO HOO! You are the winner of a Relationship Session with your wonderful husband Steve and your sweet little miracle baby Johnathan. This was a tough one. SERIOUSLY!!! I was crying my eyes out reading this as I laid in bed this morning and drank my coffee. I do know them personally as I know many of you who submitted so I am very glad I had people involved who could vote on the essays who do not know the names of those who submitted. THANK YOU…YOU KNOW WHO YOU ARE!!!
I look forward to working with you and cannot wait to document your beautiful family and your beautiful relationship.
I was so touched by all of the stories. There were 5 of us voting on the winner. 4 of the 5 placed this essay as the top vote. None of us were allowed to converse about the stories ahead of time so that we would be able to choose on our own.
Due to the fact that I was also very touched by other submissions. I feel the need to bless you all with a gift of some sort to NKP. I can tell I would love to work with each of you. I am not sure what that gift will be yet, but keep checking back as I contiue to tally the other votes and see how things fall.
Here is Steve’s essay so that you all can see why his wife was chosen:
(PLEASE COMMENT IF YOU FEEL MOVED TO. I WOULD LOVE TO HEAR YOUR FEEDBACK)
ESSAY #7:
My wife Kelly has been requesting that I look into getting some professional photos done for quite some time, but I’ve been reluctant to do so due to cost, time, and all the other typical excuses. I’m not exactly sure what a Special Relationship Session is, but maybe this is the opportunity that we’ve been looking for. Please accept this brief story as my Mother’s Day Contest entry towards that end.
As Keith and Niki may or may not know, Kelly has a rare form of Muscular Dystrophy called Central Core Disease. The doctors told us that any of our children would have a 50% chance of being born with it, so we had to do lots of soul searching and praying for direction. We decided to “roll the dice” and on December 6, 2006, we were blessed with Jonathan. He’s now 17 months old, and it’s all but been confirmed that he has the disease. We have known and suspected it for months now, and have done our best to stay on top of it and seek guidance from doctors to give him the best chance of being “normal” that we can. So far Jonathan has low muscle tone in his legs due to the disease, and has stiff hips due to the fact that he was in a cast and brace for 3 months to correct the displaced hip that he was more than likely born with. He’s now doing very well, but is delayed developmentally. Twice weekly physical therapy visits are helping him progress as fast as he can. Right now, he’s sitting up, rolling, and scooting around slowly. We’re optimistically hoping that he may crawl in a few months, and may possibly be walking at 2 years. The disease is very random, and affects each person differently, so only time will tell.
The physical effects on Kelly are that she’s a little weaker all over than most mothers. The heavier Jonathan gets, the more challenging it is for Kelly to assist him through his daily routines. She has a hard time walking up stairs, and cannot do many things that most of us take for granted such as run or ride a bike. Aside from these issues, she’s just Kelly- beautiful, glowing, and outgoing. Unless told, most people remain unaware that there is any issue at all.
The mental and emotional effects from coping with both her issues, and Jonathan’s, are just as challenging. She envies the simple physical activities that others take for granted, while participating in every other form of exercise that she possibly can. She occasionally feels guilty as she blames herself for passing the gene on to him, and in doing so has come to a greater understanding of some of the issues that her own mother faces. She worries about what Jonathan’s future may hold, and wonders daily about what our continuing family plans should be. She also struggles now knowing that because Jonathan is a carrier, he will have to go through some of the same tough life decisions.
Through it all, with both her own and his challenges, she remains persistent in her desire to be the best mom that she can. Her love for Jonathan is unwavering. She works though her limitations, and goes beyond the call of duty to see that he is cared for with love, selflessness, and enthusiasm. Her attitude is not one of negativity and self-pity resulting from what God has burdened her with, but rather one of optimism and gratefulness resulting from what God has blessed her with. She recognizes that we are luckier than most, and is the primary catalyst to the charitable and volunteer efforts in which we participate.
Because of all of this and more, I couldn’t be prouder to have her as both the mother of my wonderful child, and my wife. Having said that, I’d love to have the chance to see how Niki’s talents could reflect this on film.
Thanks for your consideration.
Steve
***CONGRATULATIONS STEVE AND KELLY…HAPPY MOTHER’S DAY!!!***











by Nichol Krupp
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