Jenny Krshul

Co-Founder & Director

Hi! I’m Jenny Krshul. Co-founder of the Wolves of Hope Foundation! I was born and raised in Las Vegas, NV along with my husband Nick. Our son Bradley is 12 years old and was born with a rare brain abnormality, “Holoprosencephaly” (HPE) for short. He’s non verbal and non mobile, but we don’t let that define him. He has the best smile and personality, and loves to be around other kids.  I have 3 dogs (crazy animal lover), love to do anything crafty, and enjoy nothing more than spending quality time with my family. I’ve learned so much through the highs and lows of parenting a special needs child. We’ve dealt with epilepsy, cerebral palsy, hypotonia, medical equipment, g-tubes and therapies (to name a few). We are constantly researching and adapting our lives to make our world easier and more accessible for Bradley. I am beyond excited to be partnered up with Stephanie on this journey to connect with other special needs families!

Jenny@WolvesofHopeFoundation.org

Stephanie Brundage

Co-Founder & Director

I’m Stephanie, Co-Founder of Wolves of Hope Foundation! I lead a full life, balancing a career, while also being a full-time mom to two beautiful girls; sweet and sassy 8-year-old Sloan, imaginative & energetic 4-year old Layne! A recent grad from ASU with a Masters in Sociology and married for 11 years to my high school sweetheart, Jim. Sloan was diagnosed at birth with Wolf-Hirschhorn syndrome, a very rare genetic disorder, that leaves her to live a medically complex life due to multiple health impairments. While non-verbal and non-mobile, she continues to surprise us with her perseverance and fighting spirit. Throughout her years, we have experienced the trials and fails of getting her the services and assistance she needs to grow and thrive in this life. We hope with our foundation we can bring resources, advocacy and create a more inclusive community, here in Southern Nevada. I am proud and excited to be able to partner with my great friend, Jenny!

Stephanie@WolvesofHopeFoundation.org

Colleen Bye

Board of Directors

Hi! I’m Colleen Bye. I was born and raised in Minnesota and have been living in the desert for the past six years. I’m a Pediatric Occupational Therapist with a passion for helping kids reach their fullest potential. Over the years, I’ve worked with children who are medically complex or have life-limiting diagnoses, and I’ve seen firsthand how adaptive equipment and the right resources can completely change their daily lives.

I absolutely love connecting with kids and their families—whether it’s building independence, supporting communication, or finding ways to make life a little easier day to day. Outside of work, you can usually find me cheering on sports, hiking, traveling, trying new foods, or spending time with friends and family. I’m so grateful to be part of Wolves of Hope and excited to support local families on their unique journeys.

Board of Directors

I have two amazing boys, Jakob and Danyel. They both have special needs and are my greatest teachers by showing me what it means to truly live.  Being their mom on their journey has been my purpose in life.  I’m honored to use my experience to help other families navigate unique circumstances, because I know firsthand that it takes a village to thrive.

Heidi Tunea

Board of Directors

My name is Brittany Harsen. I have been working in the Clark County School District for over 10 years in the Special Education Department. I have a Bachelor’s degree  in Early Childhood and Special Education and a Master’s degree in Intellectual Disabilities and Autism.  Assisting students and their families has always been my passion. I am excited for this new journey to connect with more families throughout Las Vegas!

Brittany Harsen

We are glad you asked!! Our Foundation name “Wolves of Hope” is very sentimental and personal to our families.

• Wolves - Wolf-Hirschhorn Syndrome (Stephanie’s daughter’s diagnosis)

• Hope - Holoprosencephaly (Jenny’s son’s diagnosis). Also known as “HPE” or HoPE”

Put them together and you have a passionate “pack” spreading awareness, advocating, and creating “hope” for families with medically complex children.