• We support research programs that aim at improving treatment options, and finding the cure
  • We provide information to the medical community, teachers, the media, the public and newly diagnosed patients, their families and friends
  • We have a provincial toll free number
  • We work with volunteers throughout Ontario to develop and maintain support groups such as the Mother's Meeting in the greater Toronto area and the Brantford Support Group
  • We have recently established a member registry where we connect people wanting support in their vicinity
  • We provide opportunities for children and youth with NF to get together to have fun and meet others facing similar health concerns
  • We have bi-annual meetings with guest speakers, panels and informal discussions
  • We have an annual family picnic
  • We walk in the Queen's Birthday Parade each year to increase global awareness about NF
  • We have an array of fundraising events including annual events such as the May Tea Party, Silent Auction, Hat Day, and an annual raffle
  • We publish a quarterly newsletter
  • We have a variety of booklets and pamphlets dealing with NF available upon request
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