Piper’s nominator writes: “Hello Heather, I found your site on Facebook and love what you are doing. I have the perfect little girl to nominate for your Princess Photo Shoot, Piper Kay Nolan. Piper is 3 years old (almost 4) and is just about the most darling little girl you have ever met. Piper loves […]

Schuyler is a princess with severe cerebral palsy. Schuyler and her twin brother Sean were born at 26 weeks on June 3, 2007, Sean weighing 1 pound 13 ounces, and Schuyler weighing in at 1 pound 10 ounces. After 16 hours Sean was not able to hold on anymore and Schuyler had a grade IV […]

Marianna’s nominator writes: My name is Amber Smith. I am a kindergarten teacher in Marietta City. I would like to nominate one of my former students for the fairy photo shoot. Marianna is a beautiful 6 year old little girl who loves all things princess, fairy, and Frozen! Marianna LOVES the movie Frozen. Last year, […]

Arden’s first nominator Tori writes “Hi, I saw your post on a friends page and if it’s not to late I would like to nominate a special little girl whose was born with a rare heart disease, and continues to shine through everything even on her darkest days! She has a smile that lights up […]

Hannah’s nominator Laura writes “Hannah is known around ESP as a beautiful smile, a sweet hand to hold & a social butterfly. Hannah is a friend to all and never meets a stranger and for a good reason. Not only does Hannah have the personality to light up a room, but Hannah has grown up […]

Arya’s nominator writes “Arya Skye was just like any other little girl until one day a slightly swelled joint turned into a huge change in her entire life. Arya was diagnosed with juvenile rheumatoid arthritis 6 days before Christmas 2012 since then she has gone through numerous changes in her life. Arthritis in children is […]

Faith’s nominator Laura Whitaker writes “ESP has had a recent addition to our family. She is blond beauty and a little ball of joy that lives up to her name: Faith. Faith was born with a deletion of the 4th chromosome a very rare condition that doesn’t have a full lifespan and there is no […]

Her nominator writes: “Gabby has a mitochondrial disorder. She is non verbal, has difficulty with mobility (walks, but has irregular gait pattern), and has numerous health issues. Lately she has been battling gastrointestinal issues and has made many trips to Children’s Hospital. Gabby is a rider in our therapeutic riding program. She loves riding and […]

Her nominator writes “Hi Heather, My name is Ilona and I would like to nominate my grandaughter Illyra for your memorial princess session.Illyra has Williams Syndrome or WS, (also called “Pixie-ism”) a chromosome deletion which includes developmental delays, cortical visual impairment, heart and vascular issues, and the inability to make the protein elastin. (This is […]

Katie was actually nominated three different times by three separate people! Her first nominator writes “Katie is a little girl that I met in 2010 when she was our Heart Hero for our Heart Walk. Katie was only three, but she had already gone through more in her three years than most people face in […]