FUNdraiser Success at Santa Picture Day!

Photography by Dale graciously helps our group each year with a SANTA PICTURE DAY in support of our group.
This year’s 4th Annual Photo Day was held on SATURDAY, DECEMBER, 5th.

Thanks to Photography by Dale in
Brandon, Manitoba

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NF Empowerment Symposium

The 2015 NF Empowerment symposium was held in Winnipeg on October 17th at the Victoria Inn. SEE OUR PICTURES in the GALLERIES dropdown bar. We are thrilled with the responses we have had. Comments like, “I wish I had had …

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New Run for NF

This fall MBNF had a new location for a running event! Lockport was a beautiful, well organized and supportive run. The success of this event was obvious by the number of participants, smiles on everyone’s faces and the comments to …

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MBNF Summer Picnic is great place to connect!

Each summer our support group meets for our annual picnic. The summer of 2015 was the first picnic in 10 years to have been totally rained out. It will be a long wait, but we are already looking forward to the 2016 get-together for …

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NF Happy Campers

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. Four teens attended this summer: Tyler, Seth, Isaak and Kiara. 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.