Our AGM was held on October 23rd

Thanks to everyone who attended this year’s AGM!
It was great meeting a new family and welcoming 2 new directors and executives to the board.
We also acknowledged this year’s Volunteer Award winner, congratulations to Corinne Thompson Bobrowich!

 

Read More


Cowboys- CD Realease PARTY and NF FUNdraiser big success!

Thanks to everyone who came to Nicole Rayy’s CD Release Party! This event was a third party fundraiser for our group.
We are so appreciative to Nicole and Janice Starodub for sharing their time and talents with us.
It was such a …

Read More


2016 Charity Partnership with Manitoba Marathon !

We did it!!! On June 19th our NF group had 51 participants running on the course at the 2016 Manitoba Marathon! We love being a Charity Partner with this amazing run event! Thank you so much to our Runners, Expo Volunteers …

Read More


Great Turnout for Lockport River’s Edge – Run for NF

We would like to thank everyone who attended the Lockport River’s Edge run on September 17th! This event was a huge success with over 200 participants running the variety of distances offered.  (30 km run, 1/2 marathon, 10km and 5 km …

Read More


NF Campers return eager for next summer!

MBNF sends our younger members to a specialized NF Camp each summer, this camp is organized by the Children’s Tumor Foundation and happens annually at Camp Kostopulos in Emigration Canyon, Utah. Three teens attended this summer:  Kiara, Seth and Isaak. Campers …

Read More


Find Us On Facebook and Twitter!

Social media is a great way to educate others about NF.
Please take the time to join our social media pages and keep yourself up to date on our current events.
Twitter @mbnfsupport and Facebook at MBNF are the most active sites.
These pages …

Read More

The Manitoba Neurofibromatosis Support Group is committed to improving the lives of individuals and families affected by NF. MBNF provides support, promotes awareness by educating the public and aids in funding research to improve treatment and ultimately find a cure.

MBNF envisions lives freed of physical and emotional pain caused by Neurofibromatosis.

MBNF provides confidential support and distributes information about NF to members, families, health care professionals, and various organizations. We publish an annual newsletter and hold two Support Group Meetings each year. We host an up-to-date website and a discussion forum on Facebook. We host a variety of fundraising events and get-togethers in support of those living with neurofibromatosis and we continually look for ways to advance the awareness of NF.