2014 AGM Meeting

2014 AGM Meeting

The next MBNF  meeting will be held on Saturday, October 25th at the Dakota Lawn Bowling  Centre in Winnipeg. (1212 Dakota Street). The meeting will take place from 2-4 PM. Anyone connected to NF may attend our meetings. Membership is not required. Please RSVP tracy@mbnf.ca to confirm your attendance. You can also…

2nd Annual Dance 4 NF on Proclaimed Awareness Day in Brandon

2nd Annual Dance 4 NF on Proclaimed Awareness Day in Brandon

The 2nd annual “Let’s Dance for NF” social fundraiser took place on Saturday, May 3rd, 2014 in the Grand Salon at the Victoria Inn Brandon. We were very pleased to have the City of Brandon proclaim May 3rd 2014 to be NF Awareness Day in Brandon and have representation from City Council attend…

Find Us On Facebook, YouTube and Twitter!

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 on our current events. These pages are fully interactive and we encourage…

Summer Picnic date is set

Summer Picnic date is set

Mark your calendar for this year’s summer picnic gathering. We will be meeting at Kildonan Park in Winnipeg on Sunday, August 24th from 1-4 PM. We will be in the North Shelter, Site 2B. KildonanPark Map. Can’t wait to see everyone again!!!

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.