Bay Area NF Support Group at Stanford

Saturday, March 7, 2020, 9:30 am

Come join us for a discussion about NF and how it has affected your family. With the support of the Lucile Packard Children’s Hospital, this group brings together parents, grandparents, friends and family of children and teens who have been diagnosed with Neurofibromatosis. Our goal is to:

·      Share experiences, information and ideas that have made a difference

·      Be listeners and supporters of families who are coping with NF

·      Learn from each other how to maximize the home and educational environment for families and children

·      Hear guest speakers with perspectives and expertise on NF

We meet quarterly on the first Saturday in March, June, September, and December.  

Location of our next meeting TBA.

Our support group is not intended to be a source of expert advice or information nor can it substitute for the medical supervision of your physician.  We expect to get together quarterly to provide mutual support and encouragement and to give parents and family members an opportunity to speak openly in a safe, confidential and supportive environment 
about their day-to-day issues in living with NF.

Parents and grandparents of children who have been diagnosed with Neurofibromatosis are welcome to participate, wherever your child is being treated. Please send us an email if you plan to attend.

To RSVP for the meeting or to get on our mailing list, please contact:

Nat and Marcia Sterling
(650) 494-1498