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Cystic Fibrosis Canada depends on volunteers to help raise awareness and funds in support of cystic fibrosis research, advocacy and clinical care. Whether you or someone you love has CF or you just want to help advance the cause for Canadians living with CF, there are volunteer opportunities for you. Our volunteers make a huge difference in the fight against this disease.
Volunteers are the backbone of Cystic Fibrosis Canada. Hundreds of volunteers from across the country work together every day to drive progress and change the lives of people with CF and their families. Please see below for a list of current volunteer opportunities. If you have certain skills you would like to offer that are not listed below, please specify them in the volunteer contact form.
Remain informed on CF Canada’s upcoming initiatives and connect with volunteers across the country in our monthly Volunteer Virtual Meetings! Join us the second Tuesday of every month at 7:00 pm EST to hear from CF Canada staff members and fellow volunteers about topics of interest to the cystic fibrosis community.
Click here to attend the next Volunteer Virtual Meeting - all volunteers are welcome!
From helping at the registration table to chairing fundraising events, CF Canada event volunteers play a key role in guaranteeing the success of the organization’s fundraising activities. The volunteer roles in this area are divided into two categories:
Chapter leadership volunteers offer strategic and tactical guidance as they contribute with their professional and past volunteer experience to the development and growth of the local Chapter. Responsibilities may include recruiting other volunteers, assisting with the communications of the Chapter, fundraising, and securing sponsorships.
CF Canada has built a thriving network of more than 250 advocacy volunteers in every province across Canada. Through our National Advocacy Network, CF Canada’s advocacy team provides training, mentoring and support, to help advocates build relationships with elected and non-elected officials to increase support for programs, services, and policies that improve access to medicines and quality CF care. Joining CF Canada’s advocacy network is a meaningful way to make your voice heard and to positively impact the lives and livelihoods of people with cystic fibrosis and their caregivers. For more information about CF Canada’s advocacy program, please click here.
Many CF Canada volunteers have a personal connection to cystic fibrosis. Whether you are a patient, parent, sibling, grandparent or caregiver of someone who has CF, sharing your story is a powerful tool in creating awareness and driving change. Speakers may share their stories about living with cystic fibrosis formally at events or informally through online platforms or peer-to-peer conversations.
Third-party volunteers are a key part of expanding CF Canada’s reach in the broader cystic fibrosis and non-cystic fibrosis communities. From Shinerama, to Lawn Summer Nights, and Kin Canada, third-party volunteers carry out the important role of raising funds through their own events, or supporting other CF Canada volunteer initiatives.
CF Canada is committed to the highest quality standards of volunteer involvement and it has been awarded with Imagine Canada’s Standards Program accreditation.
With this achievement, CF Canada joined a select group of approximately 200 organizations dedicated to operational excellence. The Standards Program is a Canada-wide set of shared standards for charities and non-profits designed to strengthen practices in five fundamental areas, including volunteer involvement.
Though there won't be a physical Maritime Time for a Cure event this year, our community has already started to come together through generous donations of items for a silent auction. We're inviting you to participate in the auction as it goes live in the coming weeks and, in the spirit of Maritime Time, to help us go further once again for cystic fibrosis research and care.
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My name is Kelly Ann Quinlan and I am 19 years old. I was diagnosed with cystic fibrosis at birth. My 24-year-old brother Michael also has cystic fibrosis, which is a challenge, as we both live in the same home but must live separately to a degree. We are very close to our parents and sometimes they struggle with the extra duties and constant cleaning that comes with raising two CF children.
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