Princess M turned the big 1-oh this month! And they came out the way from CA just so I could take her picture (okay, so her family actually lives out here and maybe, just maybe, they came out to with celebrate them) but she was just as sweet and cute as can be!
Archive for August, 2008
New in my inbox just this week:
“Oh my gosh!!!! This will be such a hard decision!!!! They are wonderful! WONDERFUL! I almost started crying! I have to go look at them again…. Thank you!!!!!!!!!!!!!!!!!!!!!!!” -Mindy
“My son hates having his picture taken and he actually wants me to order some for him to hang of himself in his room!” -Robin
“Thank you so much. The pictures are wonderful and I can not wait for Kevin to receive his album. He is going to be so surprised and I know that he will absolutely love it.” -Lisa H.
“Thanks for being so patient through feeding and fussiness!” -Lisa E.
In 2006 I had the honor of photographing a little boy named Reece.
Reece is an adorable little boy with an infectious smile. Reece is also living with SMA (or Spinal Muscular Atrophy).
Spinal muscular Atrophy is a motor neuron disease affecting the voluntary muscles that are used for activities such as holding your head up, crawling, walking swallowing, neck control and even BREATHING. Though it is a rare genetic disorder, 1 in 40 people are genetic carriers. This condition is the #1 genetic killer of babies under the age of 2 years old. SMA CAN QUICKLY PARALYZE A CHILD FROM HEAD TO TOE. There is no CURE!
Reece has been very sick lately and future is unknown at this point. The Rubinos are an amazing family with amazing faith. I continue to pray for them everyday and invite you to learn more about them:
So yes, I am behind on posting teasers and I’m behind on getting photos done, but today it is not about the photographs, today I sit in silent reflection and prayer for a family that needs it.