National Cancer Survivors Day – A Community Recharged

On June 1st, Cancer Fatigue Services (CFS) proudly took part in the 3rd Annual National Cancer Survivors Day Expo in Brantford, Ontario. The day was nothing short of extraordinary.

Representing CFS was our founder, Dr. Scott Adams and exercise therapist, Matthew Dhanushan. This dynamic duo was on-site at our dedicated booth, engaging with attendees and fielding thoughtful questions about cancer-related fatigue. Their approachable style and in-depth knowledge contributed to remarkable connections and almost 100% of the survivors in attendance registering with CFS before the expo concluded.

As emcee for the day, I had the distinct pleasure of guiding the audience through a packed schedule filled with heartfelt stories, a powerful caregiver panel discussion, and emotional tributes from life experience. Many attendees, vendors and fellow speakers shared overwhelmingly positive feedback – not only about the quality of this year’s expo but specifically about the energy and professionalism brought to the stage. Balancing crowd control with comedic moments and emotional authenticity, I aimed to create an atmosphere that felt as cathartic as it was celebratory.

The day was more than an event – it was a testament to the resilience and humour of our community. We also capitalized on valuable networking opportunities, strengthening bonds with local health professionals, advocacy groups, and fellow survivor-led organizations.

To read more about the event and it’s impact, check out Brant Beacon’s coverage here: https://
www.brantbeacon.ca/honouring-cancer-survivors-with-stories-and-support/


Pride in Partnership – Princess Margaret’s 2025 SGDc Pride Event

On June 12th, I was invited to participate in the Princess Margaret Hospital’s Sexual and Gender Diversity in Cancer Care 2025 Pride Event as their emcee, hosted by their remarkable Chosen Family Team. Held in celebration of the 2SLGBTQIA+ survivors and supporters, the event seamlessly wove joy, visibility, and inclusion into every corner of the space.
You can view the event recap here: Instagram Reel and visit the official post from @PMChosenFamily on my role as a Patient Partner here.

Following the event, being asked as a Patient Partner what it means to me was both a highlight and so touching to be able to contribute:

What Does Being A Patient Partner Mean To Me?

“I don’t just want a seat at the table. I want to feel like my chair matters.”
“I want people to know that the moment you include survivors in decisions, the outcomes feel more human and more honest.”

These words encapsulate the purpose behind every conversation we had that day.

From the CFS perspective, the event was another powerful platform for visibility and dialogue. We had meaningful one-on-one discussions with survivors who were curious about cancer-related fatigue and it’s lingering effects. I was so pleased to be able to share information about our services and the allyship that CFS stands for. I was incredibly honoured to receive an open invitation to return as the official emcee for future SGDc events.

Looking Ahead

With summer in full swing, Cancer Fatigue Services continues to move forward with a simple mission: to reduce the burden of cancer related fatigue so survivors can reclaim their energy and thrive. Whether it’s standing behind a podium, beside a booth, or alongside another survivor – I remain committed to showing up, speaking up, and amplifying the voices of our community.

If you’re reading this and wondering where to start your own fatigue recovery, know that our doors are always open.

Stay connected, stay proud, and stay energized.

Peter Laneas
Advocacy & Outreach Communications Manager
Cancer Fatigue Services