Meet Artist Alumni

Artist Alumni

Meet the incredible artists from FairPlay's previous Holiday Card Fundraisers!

FairPlay artists are our youngest volunteers, helping raise important funds and creating awareness for accessible play programs. We are inspired by their and their family's creativity and drive to make a difference in their communities. Learn more about FairPlay's artists through their biographies below, written by their families. We always welcome new artists to join the team!

Aries

“Aries Reign Williams is six years old as well as an eight-time brain surgery survivor and NICU alumnus. Beloved by everyone he meets, he inspires those around him with his signature resilience and “million dollar smile” as he continues to thrive through his diagnoses of hydrocephalus, cerebral palsy, and autism spectrum disorder. Recognized in the medical world as a pioneer for his participation in the clinical trial of the revolutionary CTOT device, Aries has been featured in several news media outlets over the years including ABC’s Localish and The Houston Chronicle. In his free time, Aries loves singing, making music on his keyboard, and playing with his friends.” - Aries’s Family

Bradley

“This is Bradley’s third year participating in FairPlay’s holiday card fundraiser! We cut out a snowflake and used bleeding tissue paper and a spray bottle for the tie dye effect. Bradley is a fun, hardworking and very opinionated seven year old. He loves spending time with his friends and family and is very much looking forward to the holidays!”
- Bradley's Family

Briella

"Briella is 5 years old with Spastic Diplegia Cerebral Palsy. But that does not define her or stop her from doing amazing things!! Briella loves to go to school, play with her puppy, swim and read books. Briella loves painting and making crafts! She is one happy, smiley, and determined little girl." - Briella's Family

Caroline

"Caroline is a 2-year-old little girl who lives with cerebral palsy. While she faces many obstacles in her daily life, she continues to persevere and finds her own way to do things!" - Caroline's Family

Conner

"Hi! I'm Conner. I was born at 24 weeks weighing 1lb 6oz. I've been beating the odds ever since. I love music - especially the guitar and piano. My favorite thing about Christmas is seeing Christmas trees everywhere!" - Conner's Family

Eli

"Eli is 6 years old and during his first year of life he had several surgeries including open heart. He also has a magical extra 21st chromosome - Down syndrome. His favorite things are French fries and dinosaurs. He is in first grade and fully included at his amazing school! His mom wrote a book all about him being included in school called "Eli, Included." Eli has three older sisters who are fierce advocates for him. Eli is funny, loving and so sweet."
- Eli's Family

Exton

"Exton is just like any other toddler, wild and super mischievous, but in a lot of ways he has an old soul. He has a calmness to him that makes him seem like he is years older than he should be! We constantly call him Extra Exton. He's got it all - the extra chromosome, the extra equipment, and the extra sass! He is our light!" - Exton's Family

Grace

“Grace, 4 years old, loved to make art with her friends at school, getting a smooch from her dog, Bella, and holding hands with her little brother Leo. Grace passed away earlier this year; her light shines on through the love she shared with so many, including each of you during the holiday season.” - Grace’s Family

Hannah

"Hannah is a sweet 5 year old who has significant hypotonia from a unique genetic code that makes it challenging for her brain to communicate with her muscles. She is the happiest kiddo who loves to do art projects, listen to music, do yoga and take care of her dolls and stuffed animals. Hannah is fast in her purple walker- but she loves to stop for dance breaks or to give out hugs to her big sister Talia! Hannah’s family is so proud of all of her hard work. " - Hannah's Family

Harris

"Harris Doctor is a 5 year old that entered the world, prematurely, just two days before Christmas. The best Christmas gift was being discharged from the NICU on Christmas Day. Harris loves listening to music, singing, swinging his beads, and looking at books. He has Down Syndrome and is a CHD heart warrior. Even open heart surgery couldn't keep that infectious smile off of his face!"

-Harris's Family

Malachi

"Malachi approaches his art as he does life: with natural ease, sparkling eyes and an effortless laugh. His playful charm and daring charisma bring a smile to the face of everyone he meets. Born with Spina Bifida and congenital heart defects, Malachi lives with his parents and fur-siblings in the Seattle area." - Malachi's Family

Malakai

“Malakai is a happy, funny, and smart, six year old boy with the best smile. He loves WWE wrestling, hulk, ninja turtles, music and playing with his two sisters. His favourite colour is green. Malakai has Cerebral Palsy but he doesn’t let that stop his determination. This is Malakai’s 5th year participating in the holiday card fundraiser!” - Malakai's Family

Mateo

"This is the artist Mighty Mateo. He is 4 years old add loves books, music, dancing, climbing, and anything with wheels. Mateo also loves to make art. Mateo was born 2 months early weighing only 1 lb 2 oz. "Chiquito pero picosso"...tiny but strong is the best way to describe Mighty Mateo." - Mateo's Family

Max

"My name is Maxwell, but my friends call me Max. I am a triplet with Maggie and Miller and we were born at 24 weeks. I have Cerebral Palsy and it affects how my brain communicates to my muscles. I might have a disability that makes it harder for me to get around, but it doesn't stop me from having fun! What I want people to know is that my disability doesn't define me! I'm doing the same things as you, just taking a different path to get there." - Max & Max's Family

Nettie & Lottie

"Lottie is a true artist; she is always taking time to truly see the people and beauty around her. Nettie is a lot like her artwork: bold." -Nettie & Lottie's Family

Ozzie

The FairPlay team is grateful for Ozzie's participation in FairPlay's projects over the years.

Penelope

“Hi, I’m Penelope! This is my 3rd year participating in the holiday card fundraiser for FairPlay! I love arts and crafts and all things that sparkle. I’m 4 years old and have an ultra-rare genetic condition that comes with a lot of medical complexities. Accessibility and inclusion are important to me so that it’s possible for me to experience the world. I love going on a new adventures with my family! Hope you have a wonderful holiday!”

Love, Penelope

Riley

Riley is 3 years old and was diagnosed with Spina Bifida, Myelomeningocele, Hydrocephauls, and Chiarimalformation II, but she doesn't let her diagnosis define her. Riley is full of life, love, and happiness. She loves to make those around her smile & laugh. Riley enjoys dancing, singing, and playing outdoors. This princess doesn't let anything stop her!" - Riley's Family

Ryken

"Ryken is a 3 year old boy, born at 24 weeks gestation, weighing 1lb 9oz. He has a lengthy list of complex medical diagnoses, none of which define him! He loves to be outside in his swing, look at lights, float in the pool, snuggle, and have people chat with him. Ryken is a warrior boy who brings his family an indescribable amount of joy!" -Ryken's Family

Savannah

"Savannah is a sweet girl who lives in Salem, Massachusetts. She is beautiful and uniqe in every way. She loves music and adaptive sports. She has a rare genetic mutation known as NAA10. In addition, she has a vision impairment known as cortical/cerebral visual impairment, epilepsy, hydrocephalus, and an esophagus disease. Despite all her challenges, she is so happy, funny, and so loved." - Savannah's Family

Sebastian

"Sebastian is 6 years old with a rare genetic disorder called Pontocerebellar Hypoplasia type 1b. He loves music/dancing, being outside and most of all- creating art!" - Sebastian's Family

Silas & Atlas

"Meet Silas and his best friend Atlas! Silas is a 12 year old boy who loves funny noises, switch toys, and hanging with his Dada! Atlas is his best buddy who always includes Silas in his adventures and helps him along the way. These boys created this one-of-a-kind piece together using switch adapted scissors and other mixed media." - Silas's Family

Spiro

“At 6 years old, Super Spiro is an LGS, Infantile Spasms, VNS, and Corpus Callosotomy Survivor. Spiro also has CVI and we dedicate a lot of his learning at a Vision School. Spiro works on his adaptive play, CVI art and walking in his Trexo Machine the most. This year Spiro went on many new adventures for the first time: a waterpark, rides, arcades, an aquarium, and a movie theater thanks to Make-A-Wish. We hope his smile continues to shine bright with those who follow his journey at @CVI.Mom.” - Spiro’s Family

Stella

"Stella is turning six years old just two days after Christmas. She has cerebral palsy and a condition known as HIE due to a birth injury that stopped her heart for 18 minutes, so we are so fortunate every day to have Stella with us. Stella loves Cocomelon, music, and her cat named KitKat. She loves playing in the pool and has an infectious laugh." - Stella's Family

Yaroslav

"Yaroslav is a 4-year old cheeky boy who loves to seek adventures and sensory experiences. He is very bubbly, social and loves to sing away. He doesn’t let his diagnosis to define him." -Yaroslav's Family