Participate in the BCNF survey to win!

We want to hear from you! Fill out the BCNF survey sharing your honest opinions on how we are doing. We are listening! Everyone who completes the survey will be eligible to win the grand prize of a $200 gift certificate from Future Shop or one of two $25 Future Shop gift cards. Winners will be announced on October 23, 2010 at the AGM in Vancouver. Thank you for your continued support and good luck!

Take the survey!

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Connect with the BCNF Community

It’s important to remember that you’re not alone; there are others nearby going through their own challenges with NF. Connecting with others in the NF community provides a wealth of real-world information and a chance to share your own experiences.

Connect with BCNF

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Video Gallery: Real-Life Stories

Facing a life with Neurofibromatosis may have you feeling anxious, scared and filled with questions. The most important thing to keep in mind is that you are not alone. There are nearly 10,000 Canadians who, just like you, are bravely dealing with the challenges of NF. Everybody diagnosed with Neurofibromatosis has a different story to tell. We hope you are inspired and encouraged by these courageous individuals who each face NF in their own way.

View video stories

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NF1 Symposium a huge success!

The weekend of April 10-11, 2010 saw researchers and families come together from across Canada, the United States and Europe in Richmond, BC to participate in Canada’s first national NF1 symposium. Thank you to all who attended for making this event such a success!

View the photo gallery from the event

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Get Involved!

Join the Board of Directors

Want to help chart the course for the BCNF by serving as a member of the Board of Directors? We are currently seeking people with diverse backgrounds, experience and expertise to serve on our Board of Directors. Board members need not have a direct or family connection to NF. Curious? Learn more!

New Video Stories

New Video Stories

These first-person accounts span the NF1 and NF2 spectrum. The courageous individuals you’re about to meet would like you to know that you are not alone in your journey with NF. We hope that this series of videos serve to offer you real-life solutions and hope. View the Videos

Don't Miss Out!

Events

Check out all of our upcoming events and check back often for the latest announcements. View all upcoming Events

Welcome!

Welcome to the BCNF! The British Columbia Neurofibromatosis Foundation (BCNF) is a registered, non-profit charitable organization. It was established in 1984 by Paul Ralfs to respond to the needs of individuals with Neurofibromatosis (NF), their families, related health care professionals and other interested community members. The BCNF continues its work today through the efforts of its Board of directors, part-time staff, volunteers and membership.

Upcoming Events