Talking to Your Child About NF1 (English)
Talking to Your Child About NF1 is a comprehensive guide that helps caregivers decide what and how to share a diagnosis of neurofibromatosis type 1 (NF1) with their child. It can be used on its own or together with the children's resource, Super Emerson, designed to complement it.
Talking to Your Child About NF1 is a comprehensive guide...
Talking to Your Child About NF1 is a comprehensive guide that helps caregivers decide what and how to share a diagnosis of neurofibromatosis type 1 (NF1) with their child. It...
Talking to Your Child About NF1 (French)
Talking to Your Child About NF1 (French translation) is a comprehensive guide that helps caregivers decide what and how to share a diagnosis of neurofibromatosis type 1 (NF1) with their child. It can be used on its own or together with the children's resource, Super Emerson, designed to complement it.
Talking to Your Child About NF1 (French translation) is a...
Talking to Your Child About NF1 (French translation) is a comprehensive guide that helps caregivers decide what and how to share a diagnosis of neurofibromatosis type 1 (NF1) with their...
Talking to Your Child About NF1 (Spanish)
Talking to Your Child About NF1 (Spanish translation) is a comprehensive guide that helps caregivers decide what and how to share a diagnosis of neurofibromatosis type 1 (NF1) with their child. It can be used on its own or together with the children's resource, Super Emerson, designed to complement it.
Talking to Your Child About NF1 (Spanish translation) is a...
Talking to Your Child About NF1 (Spanish translation) is a comprehensive guide that helps caregivers decide what and how to share a diagnosis of neurofibromatosis type 1 (NF1) with their...
Understanding NF2-SWN Comic
Understanding NF2-SWN is an eight-page educational comic book that tells the true story of Billy Nguyen, who was diagnosed with NF2-related schwannomatosis at the age of six. The story tracks Billy’s childhood struggle to understand his diagnosis and navigate tumors and progressive hearing loss.
Understanding NF2-SWN is an eight-page educational comic book that tells...
Understanding NF2-SWN is an eight-page educational comic book that tells the true story of Billy Nguyen, who was diagnosed with NF2-related schwannomatosis at the age of six. The story tracks...
Understanding NF2-SWN Comic (Spanish)
Understanding NF2-SWN is an eight-page educational comic book that tells the true story of Billy who was diagnosed with NF2-related schwannomatosis at the age of six. The story tracks Billy’s childhood struggle to understand his diagnosis and navigate this difficult condition. This version has been translated into Spanish.
Understanding NF2-SWN is an eight-page educational comic book that tells...
Understanding NF2-SWN is an eight-page educational comic book that tells the true story of Billy who was diagnosed with NF2-related schwannomatosis at the age of six. The story tracks Billy’s...
Archie Comics’ Sounds Like Music
Meet Grace, the first member of the Archie Comics universe living with NF2-related schwannomatosis (NF2-SWN), formerly called neurofibromatosis type 2.
Meet Grace, the first member of the Archie Comics universe...
Meet Grace, the first member of the Archie Comics universe living with NF2-related schwannomatosis (NF2-SWN), formerly called neurofibromatosis type 2.
Café Au Lait – Children’s Picture Book
Available for purchase at the CTF Store, this 36-page picture book tells the story of Enzo and his story about café au lait spots.
Available for purchase at the CTF Store, this 36-page picture...
Available for purchase at the CTF Store, this 36-page picture book tells the story of Enzo and his story about café au lait spots.
Moxie and Sparx Explain NF1
A short comic book for kids explaining NF1 with CTF mascots Moxie and Sparx.
A short comic book for kids explaining NF1 with CTF...
A short comic book for kids explaining NF1 with CTF mascots Moxie and Sparx.
Moxie and Sparx Explain NF1 (Spanish)
The Spanish translation of CTF's short comic book for kids explaining NF1 with CTF mascots Moxie and Sparx.
The Spanish translation of CTF's short comic book for kids...
The Spanish translation of CTF's short comic book for kids explaining NF1 with CTF mascots Moxie and Sparx.
NF Parent Guidebook
A 160-page guidebook for parents of children living with NF1 from the Children's Tumor Foundation. Read more about the parent guidebook HERE.
A 160-page guidebook for parents of children living with NF1...
A 160-page guidebook for parents of children living with NF1 from the Children's Tumor Foundation. Read more about the parent guidebook HERE.
