Loved this family session. Little man was far too adorable. Even though he didn't want to do anything we wanted him to do...hahaha. Thus is life will all children 1-4 years old. :) We had a fabulous time!
I love these two chillens. They were just much too adorable. I photographed Helene about a year ago...she liked me MUCH more this year. It's amazing what time will do. We're friends now. :) A few from their session...
If you missed the sneak peek of the coleman's family session you must go and see. It has lots of information about little Jonas and Maggie who have SMA Type I is a terminal genetic disease that results in loss of nerves in the spinal cord and weakness of the muscles connected with those nerves. And how you can help.
Can't you just feel the love they have for each other?
I loved this family. They are just awesome people. And their little guy...oh my gosh, so CUTE!! I could have kept shooting all night if hadn't have gotten so dark on us! :)
If you would like to feel grateful, and let your heart grow few sizes bigger...meet the Coleman family. This family is simply inspiring. I couldn't edit their session with out crying. Not out of sadness, but out love. Love over the connection this amazing family has for each other. Love that I know God has for them. Love that I had for those sweet children after only laying eyes on them. Love that I had for these parents, knowing what a struggle everyday must be. Not only physically, but emotionally. And gratitude. Lots and lots of gratitude. It really puts life into perspective when you meet such a solid family, who seem to be weathering the storms of life with calmness in their hearts.
At six weeks old Jonas was diagnosed with a genetic disorder called SMA (spinal muscular atrophy). SMA Type I is a terminal genetic disease that results in loss of nerves in the spinal cord and weakness of the muscles connected with those nerves. He's now almost 3. They just had their 2nd baby, little Maggie. They had a very small chance that she would have SMA, however Maggie was also born with this disease. Because of the weighing costs that come from taking care of 2 children with SMA friends and family have put together a carnival to raise money for the Colemans.
Kieli is ultra photogenic. We did her engagement pictures downtown salt lake just a while back and had a blast. Now it's time for her bridals...there are a ton. I'll post them a bit later...here's a few for now that don't give away her entire dress. Just in case a certain someone tries to peek. :) By the way, has anyone else noticed I've been spelling peek wrong for months??? Hello, why didn't someone TELL ME! hahahaha
Photographed the sweetest brother and sister this week. Just one for today....
I met Kathy almost 3 years ago when little Sophie was born. We sat at my house a chatted for many an hour while we waited for Sophie to fall asleep so I could do her newborn pictures. Kathy is an amazing mother, wife and friend...and I must mention that the woman can RUN. :) I'm so thankful for a job (even calling it that sounds like work) that lets me meet so just fabulous people. Many who I can now call friends. Anyway, enough cheese box...a few thousand photos from their family session in Salt Lake.
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