Featured community voice
NextGen NF
NF community account powered by the Children’s Tumor Foundation Junior Board. Highlights patient outreach, young-adult voices, community events and efforts that support patients and families.
Visit NextGen NF
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Social media can build community quickly—but personal experience, medical guidance, and research evidence are not interchangeable.
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United Kingdom · Actor, presenter and disability campaigner addressing NF1, facial difference, ableism, bullying and representation.
United Kingdom · Creates content about NF1, facial difference, confidence, bullying and self-acceptance. Nerve Tumours UK ambassador with a substantial public audience.
United Kingdom · Angel shares the realities of NF2-related schwannomatosis, self-advocacy, isolation, treatment, and community connection.
United Kingdom · Fashion and lifestyle creator who has discussed NF1, visible tumors, pain, confidence and the reasons behind her clothing choices.
United Kingdom · Rare-disease advocate and NF community creator sharing patient-centered stories, education and awareness content.
United States · A person-led podcast for people living with neurofibromatosis and the people who care for them.
Germany · A German patient-led project sharing lived experience and accessible information about NF2-related schwannomatosis and deafness.
United States · Jake writes candidly about living with NF2-related schwannomatosis and uses his story to promote awareness and research.
United States · Deaf runner, NF2-SWN advocate, CTF’s 2025 National Ambassador and 2026-2028 Junior Board Co-Chair. Shares treatment experiences, recovery, hearing loss, running and NF Endurance activities.
United States · Advocate, speaker and former CTF National Ambassador sharing experiences with tumors, treatment, deafness and disability while promoting accessibility for Deaf and hard-of-hearing communities.
United Kingdom · Michael documents life with NF2-related schwannomatosis, including brain and spinal tumors, balance, disability, and advocacy.
United Kingdom · Dr. Sheelagh Harwell is a GP, researcher, educator, and advocate sharing practical NF1 information and navigation guidance.
United Kingdom · A patient and Deaf creator sharing sign-language content and perspectives connected to NF2-related schwannomatosis.
United Kingdom · Writer, speaker and content creator discussing visible difference, discrimination, mental health, kindness and life with NF1.
United States · NF mom and artist using portraits and patient stories to educate the public, support NF awareness and show the diversity of the NF community.
United States · Longstanding advocate behind the “Just Ask” message. Addresses visible difference, public reactions, acceptance and NF awareness.
United States · Focuses on making NF visible, supporting research, sharing her lived experience and connecting the global NF community.
United States · Sonia creates English- and Spanish-language NF education and family-centered awareness content across several platforms.
United States · Tracy shares candid perspectives on living with NF1, grief, mobility, creativity, and self-expression.
India · Shares personal perspectives on visible difference, body image, difficult emotions and self-acceptance while living with NF.
United States · Whitney uses short-form education, public speaking, Capitol Hill advocacy, and FDA listening sessions to make NF1 more visible and better understood.
United Kingdom · Publicly identifies as a Neurofibromatosis advocate and creates educational content intended to make the invisible visible.
A group supported by Lucile Packard Children’s Hospital for parents, grandparents, friends, and families of children and teens with NF.
An NF2-focused community project offering connection, patient and family resources, and the NF2 and You video-podcast series.
Large peer community where people share NF experiences, questions, resources and personal stories.
A free, recurring in-person and virtual support group with peer connection, questions, and presentations from medical experts.
NF awareness, personal experiences and community-focused content.
NF communities that include general support plus dedicated spaces for teens ages 13–18 and students.
Community discussion and peer support for people and families affected by NF.
A parent-volunteer association supporting individuals and families affected by NF through CHOP.
Peer discussion, shared experiences and support related to Neurofibromatosis.
General NF peer support and community discussion.
Professional networking, advocacy, research information and NF community discussion.
A recurring virtual gathering for people and families affected by NF.
Real-time conversation and peer connection for people affected by NF.
Maintenance note: Current password: HcksqnexGx
An action-oriented group for people with direct experience of NF2-related schwannomatosis.
A private community for people affected by NF to connect with one another.
Private peer-support community for mothers and other parents of children affected by NF.
A large NF Network-hosted online support community for questions, experiences, and peer connection.
Pairs newly diagnosed patients and families with trained peers who understand NF1, NF2-SWN, or schwannomatosis.
Private support and information group for young adults with NF1 ages 18 to 30 and families of people with NF1 up to age 30.
Peer-support community for people affected by NF2-related schwannomatosis.
Independent community sharing information, lived experiences and peer support related to NF2-related schwannomatosis.
UK-based peer community specifically for people living with NF2-related schwannomatosis.
Public discussion community for NF stories, questions, research, treatment experiences and emotional support.
Peer-support community for people living with schwannomatosis and those who support them.
Featured community voice
NF community account powered by the Children’s Tumor Foundation Junior Board. Highlights patient outreach, young-adult voices, community events and efforts that support patients and families.
Visit NextGen NF ↗