Jaymie-Lynn Robertson Memorial Fund

The Jaymie-Lynn Robertson Memorial Fund was established in memory of Jaymie-Lynn to support individuals living with or affected by epilepsy. Through this fund, we provide financial support to students pursuing post-secondary education in British Columbia.

In Memory of Jaymie-Lynn

Jaymie-Lynn Robertson

About the Memorial Fund

The Jaymie-Lynn Memorial Fund is committed to supporting the education and well-being of individuals and families affected by epilepsy. The bursary awarded through this fund helps reduce barriers and increase opportunity for students pursuing post-secondary studies while coping with the challenges epilepsy can bring.


Through this program, the Jaymie-Lynn Memorial Fund aims to reduce the financial burden on students and families affected by epilepsy, allowing them to focus on their studies and achieve their academic goals. By providing financial support, the bursary program aims to empower and encourage students to pursue their passions and make a difference in their communities.

Jaymie-Lynn’s Story

By Belinda McIsaac (Jaymie-Lynn’s Mother)

It was a shock for our family when our ray of sunshine, Jaymie-Lynn, was diagnosed with epilepsy in September 2009. The diagnosis came after she experienced a tonic-clonic seizure while living in Brooks, Alberta. Little did we know at that time the journey we were about to embark on.

Jaymie-Lynn was an amazing young woman who loved swimming, lifeguarding, dancing, music, socializing, and movies. She was an avid animal lover and pursued this passion by studying in a veterinary assistant program. Jaymie-Lynn was known as “Miss Hollywood” because she loved having her photo taken.

Despite her epilepsy diagnosis, she never allowed it to slow her down or stop her from living life on her own terms. There were challenges, including loss of independence, discrimination in the workplace, and ongoing medical appointments. Even so, she continued to embrace life fully. She enjoyed swimming, snowboarding, and spending time with the people she loved.

Prior to Jaymie-Lynn’s passing, we had not heard of SUDEP, which stands for Sudden Unexpected Death in Epilepsy. Tragically, Jaymie-Lynn passed away on October 5, 2011, at the young age of 23 due to SUDEP. Her death was devastating for her family, friends, and extended community.

Jaymie-Lynn had always wanted to be an advocate for people living with epilepsy. She lived by the motto:

“Be the change you want to see in the world.”

Her legacy began with four simple words:

“raise $ for epilepsy.”

As her family and friends, we are committed to honouring her words and continuing her legacy through awareness, advocacy, and support for others living with epilepsy.

Bursary Details

  • Amount: Two bursaries of $1,250 each
  • Eligibility: Canadian citizens living with or affected by epilepsy
  • Studies: Entering or returning to trade, college, or university studies
  • Financial need: Demonstrated financial need required
  • Essay: 300-word personal statement on how epilepsy has impacted your life
  • Note: Generative AI use on essays is discouraged

Important Dates

• Applications open: January 29, 2026
• Deadline: April 30, 2026
• Award announcement: May 28, 2026