Fabulously Fun Family of Four – Montgomery County, PA – Child and Family Photographer

I’m fairly sure my title describes this family and our session perfectly – we had a blast! This was true lifestyle, a fun day at the park – it’s exactly how I would imagine them even when I’m not there (maybe minus the awesomely coordinated outfits!) There was dancing, singing, races, cuddling, “bear hunting”, so many laughs, and even a really cool praying mantis that decided to join the fun. 

I found an awesome tip that Fab-Four-Momma left on my YELP page – thank you SO much for your kind words!

“If you have kids with no patience for stiff studio portraits, Kel’s your girl. She has great energy. The kids loved her. Never laughed so much getting our pics taken!”

Gorgeous family of four outside in the fall with yellow goldenrods lifestyleYoung brother and sister sitting outside little girl's head resting on brother's shoulderFamily of four sitting outside in grass laughingLittle girl smelling goldenrod weed plant outside in the fallLittle boy laughing outside in goldenrod plants and photo of praying mantisGorgeous family of four sitting outside in the fall with yellow goldenrodsCute brother and sister outside in the fallYoung brother and sister laying down on stomach outside laughingBrother and sister walking down pathway with rainbow sunflarebrother and sister holding hands, smiling and serious posesfamily of four parents swinging children near pond refection

Spring Mini Sessions are still available but spots are VERY limited!
Book yours now – kel@kelmurphyphotography.com



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Ava and Jake – Cystic Fibrosis Awareness – Montgomery County, PA – Child Photographer

Ava and Jake are the typical (ridiculously adorable!) siblings. They are both at the age where sitting still is just-not-so-fun and their parents really wanted an image with the two of them together. Can all parents of young children relate to this or what? :)

In addition to being spunky and gorgeous, Ava has Cystic Fibrosis. Her parents say that she’s doing great, and they’re hoping it stays that way! Unfortunately, there are a lot of other children and adults with CF who aren’t so lucky. Ava and her family are helping to raise money and awareness for the Cystic Fibrosis Foundation – to help fund research for a cure. Ava’s parents share more of her story below.

“Ava was diagnosed with Cystic Fibrosis at 2 months, and us being new parents, we were scared – we had never even heard of CF before.”


Ava’s story.

“Ava was diagnosed with Cystic Fibrosis at 2 months, and us being new parents, we were scared – we had never even heard of CF before. It was a quick learning curve though, and the three of us now have our new normal. Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that clogs the lungs, leads to life-threatening lung infections, obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food. To combat these effects, Ava has to take pancreatic enzymes before every meal so that she can gain the nutritional value from the food. She also does a treatment everyday, where she wears a vest that vibrates her chest to break up the mucous inside her – along with taking various daily medications. To help the CF Foundation raise money & awareness to find a cure, in 2011 we started a fundraising team called G-Crew. We walk every year at the Doylestown Great Strides event in May, and have started to fundraise year round.” – Chris and Christine Gardyasz

Register for the walk or donate to Ava’s team here – www.gcrew.org

Help raise awareness for Cystic Fibrosis!
Please share Ava’s story & leave a comment for her and her family. 



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