Team Shelby’s Wish💜 is walking in Memory of our brave Epilepsy Warrior, Shelby. We wish to spread Epilepsy Awareness and raise funds to hopefully someday find CURE!!!
- Rhonda

We are walking for our 13 yr old Daughter, sister, granddaughter, niece and friend Aaliyah. Aaliyah was diagnosed in October 2020, she has been nothing but a warrior through all of the obstacles she has faced. We are ready to walk to bring awareness to others and show support to Aaliyah and all of the Purple Warriors.

Team Shelby’s Wish💜 is also walking in Memory of another Epilepsy Warrior, Kim. We wish to spread Epilepsy Awareness and raise funds to hopefully someday find a CURE!💜

Scott is a friend to everyone he meets. This will be the 5th year that Scott and his family have joined Quinn’s Army. Scott has had epilepsy since he was a baby. He is a true epilepsy warrior and a special part of our purple family. 💜💜
Quinn’s Army 💜

We walk for our 12-year-old daughter, sister, granddaughter, niece, cousin, friend, and warrior Avary. Avary is a loving, funny, and full of life young lady. We are her team and support, we’ll always love her and have her back. We wish to spread awareness and raise funds hopefully to someday find a cure.
- Sarah

She is strong, funny and always smiling. Elise has a diagnosis of rare neurological disorder Subcortical Band Heterotopia causing unmanageable Epilepsy. Together we face this storm in hopes for a cure #purpleforelise
- Carole & Mike

Quinn was diagnosed with Infantile Spasms at an early age which later developed into Lennox-Gastaut Syndrome. She is 7 years old and has had an amazing year! After many years of medication experiments, they finally have a combination that is helping. Seizures are the most controlled that they have ever been. She has exploded developmentally. Quinn is our hero!
Quinn’s Army 💜💜

Diagnosed with Epilepsy 10 yrs ago in September 2013

We lost my sister Sarah Jackson to epilepsy. She was 23 years old. Born in 1989 and passed away in 2012.

Isla was diagnosed just this year with epilepsy and has been so strong through everything. No matter what she is faced with, she finds a way to always smile and dance through it. She is a true warrior 💜

We are walking for Sophia Rose Our daughter, grand daughter, sister, cousin, friend. Sophia is a 4-year-old loving, funny & spunky girl We are her team & we will never back down!
- Zoe

We walk in honour of our son Isaiah. The sweetest and strongest boy who continues to defy all odds. Diagnosed with KCNQ2 DEE at just 3 weeks old, he shows us everyday what having strength and faith can really do!
- Jordan & Stephanie Davis

We are walking for our son Nick who we lost to SUDEP April 14, 2018 at only 19 yrs of age. We never knew about this devastating complication from Epilepsy. He is gone too soon and just should be here. Its been 5 long years without him. We walk to raise awareness and to hopefully find a cure for SUDEP. In hopes that no other family loses a loved one. 💜
- We MISS you so much Nick!

It’s been exactly one year since our family’s life changed. What started with one seizure has turned into thousands. What started with one ambulance ride has multiplied into many, along with countless ER visits, hospital stays, and surgeries. Our son Weston had his first seizure at the beach with his family on September 18, 2022. Prior to that date he was a healthy, silly, loving 3-year-old. Everyday is a challenge, but Weston exemplifies bravery and courage and never complains despite severe injuries. He faces the worst days with a big smile. He contends with the scariest moments by laughing. We took walking for granted. Weston can no longer do something as simple as walking independently for fear of injury from seizure. We are all walking on his behalf to help find a cure to give our children their carefree lives back.
- Ashley