Job Opportunity as Managing Director

We are looking for a Managing Director to join our Manitoba Neurofibromatosis Support Group Team! 
Application Deadline: January 31st, 2017.
Download the Managing Director_Job Posting.


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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!


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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 …

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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 …

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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 …

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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 …

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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.