Bill 214-The Manitoba Neurofibromatosis Awareness Month Act

Neurofibromatosis (NF) Awareness Month
The month of May in each year is to be
known throughout Manitoba as Neurofibromatosis (NF)
Awareness Month.

Earlier this summer, after a lengthy process and with the support of MLA Leanne Rowat, (new) Bill 214, declaring every May ‘Neurofibromatosis …

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Santa Picture Day at Photography by Dale

A successful Santa Picture Day took place on December 6th, 2014  in Brandon thanks to Photography by Dale!

Funds raised were over $1000. Huge holiday thanks and blessings sent to everyone who helped out!

All proceeds beNeFited our Manitoba NF Group!



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Dance 4 NF Benefit Social set for April 25th

The 3rd annual “Let’s Dance for NF” social fundraiser will take place on Saturday, April 23rd, 2015 in the Grand Salon at the Victoria Inn Brandon.

This Dance Evening showcases guest dancers from a variety of Dance Studios and is MC’d by …

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Plans to host 1st Manitoba NF Symposium, October 17th

MBNF is pleased to announce the date of our very first  NF Symposium.

It is a great pleasure to create an opportunity for individuals and families dealing with Neurofibromatosis to empower themselves at this informational event.
We aim to connect with the …

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Find Us On Facebook, YouTube and Twitter!

Social media is the way of the future and we want to be a part of it, what better way to educate others about NF. Please take the time to join our social media pages and keep yourself up to date …

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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.