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  • Over 15 sessions that will offer NF families the opportunity to listen to and speak with the best NF physicians and researchers
  • Specialized tracks will be created for NF1, NF2 and Schwannomatosis
  • Special presentations on the Children’s Tumor Foundation’s National Programs
  • Inspirational keynote speech and special video presentations
  • Kids and Teen Activities
  • Chapters Council, the national volunteers’ meeting and workshops
  • NF Walk through historic New Orleans
  • NF Moms and Dads Rock group
  • One-On-One, a specific day filled with personal medical reviews for selected participants
  • Meals and time to build friendships
     

If you have any questions, concerns or need further assistance please email Traceann Adams at This e-mail address is being protected from spambots. You need JavaScript enabled to view it .
 

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