MBNF is Charity Partner with Manitoba Marathon

RUN 4 NF at the Manitoba Marathon. #run4NF
Run for an NF HERO:)
http://www.active.com/donate/mbnf15
YOU can run, volunteer or support this event.

 

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Bill 214-The Manitoba Neurofibromatosis Awareness Month Act

The month of May each year will be acknowledged as Neurofibromatosis (NF) Awareness Month!

This past year and with the support of MLA Leanne Rowat, (new) Bill 214, declaring every May ‘Neurofibromatosis Awareness Month’ was successfully passed!
Individuals from MBNF were present in legislature …

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Dance 4 NF Benefit Social POSTPONED until 2016!

The 3rd annual “Let’s Dance for NF” social fundraiser has been postponed until Saturday, May 14th, 2016
This will still take place in the Grand Salon at the Victoria Inn Brandon.

This Dance Evening showcases guest dancers from a variety of Dance Studios …

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Manitoba NF Symposium to take place October 17th, 2015

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

This is an opportunity for individuals and families dealing with Neurofibromatosis to empower themselves.
We aim to connect with the greater NF community, learn from NF Specialists and stay …

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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.