AGM will be at Winakwa Community Centre on October 23rd

AGM will be at Winakwa Community Centre on October 23rd

Looking forward to seeing many new and treasured friends and this year’s AGM.
We will be meeting at the Winakwa Community Centre from 2-4PM. (980 Winakwa Rd, Winnipeg, MB)
Contact tracy@mbnf.ca for more details.

 

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Third Party NF FUNdraiser coming October 15th at Cowboys- CD Realease PARTY!

Come join the fun at Cowboys!
Nicole Rayy is having a CD Release Party and helping our cause at the same time! This is a bud, spud and chicken dinner for $20. Or $10 for admission and no supper.  The NF Party …

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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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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 …

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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.