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Social media

Share responsibly. Verify before you amplify.

Social media can build community quickly—but personal experience, medical guidance, and research evidence are not interchangeable.

Review misinformation guidance ↗

Before you post or repost

  • ✓Can you trace the claim to an original, credible source?
  • ✓Is the evidence human, animal, laboratory, or opinion?
  • ✓Does the post separate personal experience from medical advice?
  • ✓Are limitations, uncertainty, and conflicts of interest visible?
  • ✓Could the wording pressure someone to change treatment without a clinician?

Community voices & places to connect

Explore NF social media

Search people and communities while keeping iNFluencers and Social Media Groups in their own clearly labeled tables.

Search and filter social mediaShowing 46 listings
Search and filter iNFluencers22 of 22 voices
iNFluencers (22)+
Platforms
Adam PearsonNF1Patient / AdvocateSocial media, television, film and speakingView links ⌄

United Kingdom · Actor, presenter and disability campaigner addressing NF1, facial difference, ableism, bullying and representation.

Find Adam PearsonVisit profile ↗
Amit GhoseNF1Patient / AdvocateInstagram, TikTok, podcasts and public speakingView links ⌄

United Kingdom · Creates content about NF1, facial difference, confidence, bullying and self-acceptance. Nerve Tumours UK ambassador with a substantial public audience.

Find Amit GhoseVisit profile ↗
An NF Point of ViewNF2-SWNPatient / CreatorLived experience and rare-disease advocacyView links ⌄

United Kingdom · Angel shares the realities of NF2-related schwannomatosis, self-advocacy, isolation, treatment, and community connection.

Find An NF Point of ViewInstagram ↗Essay ↗
Arooj Aftab - Vogue WondersNF1Patient / AdvocateInstagram, fashion content and bloggingView links ⌄

United Kingdom · Fashion and lifestyle creator who has discussed NF1, visible tumors, pain, confidence and the reasons behind her clothing choices.

Find Arooj Aftab - Vogue WondersVisit profile ↗
Beth - Beth’s Bumpy JourneyNF1Patient / AdvocateYouTube, blogging and social mediaView links ⌄

United Kingdom · Rare-disease advocate and NF community creator sharing patient-centered stories, education and awareness content.

Find Beth - Beth’s Bumpy JourneyVisit profile ↗
Decoding NFAll NF conditionsPodcaster / Community educatorInterviews, research, and living with NFView links ⌄

United States · A person-led podcast for people living with neurofibromatosis and the people who care for them.

Find Decoding NFWebsite ↗
Greta Brenken & Larissa Kaefer / SomehowdeafNF2-SWNPatients / AdvocatesDeafness, ABI, and NF2 educationView links ⌄

Germany · A German patient-led project sharing lived experience and accessible information about NF2-related schwannomatosis and deafness.

Find Greta Brenken & Larissa Kaefer / SomehowdeafWebsite ↗
Jake LipeNF2-SWNPatient / Blogger / AdvocateLived experience, awareness, and research advocacyView links ⌄

United States · Jake writes candidly about living with NF2-related schwannomatosis and uses his story to promote awareness and research.

Find Jake LipeWebsite ↗NF Fighter Blog ↗Instagram ↗
Leanna Scaglione - Running NF2NF2-related schwannomatosisPatient / AdvocateInstagram, TikTok, Facebook, endurance events and public speakingView links ⌄

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.

Find Leanna Scaglione - Running NF2Visit profile ↗
McKinnon GallowayNF2-related schwannomatosisPatient / AdvocateWebsite, social media, Deaf District and public speakingView links ⌄

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.

Find McKinnon GallowayVisit profile ↗
Michael Archer / NF2.archNF2-SWNPatient / AdvocateTumors, balance, disability, and awarenessView links ⌄

United Kingdom · Michael documents life with NF2-related schwannomatosis, including brain and spinal tumors, balance, disability, and advocacy.

Find Michael Archer / NF2.archInstagram ↗
NF1 NavigatorNF1Clinician / AdvocateEducation and care navigationView links ⌄

United Kingdom · Dr. Sheelagh Harwell is a GP, researcher, educator, and advocate sharing practical NF1 information and navigation guidance.

Find NF1 NavigatorInstagram ↗
Nicola / Sign With NicNF2-SWNPatient / Deaf creatorSign language, deafness, and lived experienceView links ⌄

United Kingdom · A patient and Deaf creator sharing sign-language content and perspectives connected to NF2-related schwannomatosis.

Find Nicola / Sign With NicInstagram ↗YouTube ↗
Oliver BromleyNF1Patient / AdvocateInstagram, blogging, podcasts and public speakingView links ⌄

United Kingdom · Writer, speaker and content creator discussing visible difference, discrimination, mental health, kindness and life with NF1.

Find Oliver BromleyVisit profile ↗
Rachel Mindrup - Many Faces of NFNF mom and parent advocateParent advocate / ArtistVisual art, Instagram and storytellingView links ⌄

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.

Find Rachel Mindrup - Many Faces of NFVisit profile ↗
Reggie BibbsNFPatient / AdvocateSocial media, public appearances and traditional mediaView links ⌄

United States · Longstanding advocate behind the “Just Ask” message. Addresses visible difference, public reactions, acceptance and NF awareness.

Find Reggie BibbsVisit profile ↗
Sarah PowlisonNF1Patient / AdvocateInstagram, LinkedIn and bloggingView links ⌄

United States · Focuses on making NF visible, supporting research, sharing her lived experience and connecting the global NF community.

Find Sarah PowlisonVisit profile ↗
Sonia Melendez / Book NeurofibromatosisAll NF conditionsFamily / Education advocateBilingual family education and awarenessView links ⌄

United States · Sonia creates English- and Spanish-language NF education and family-centered awareness content across several platforms.

Find Sonia Melendez / Book NeurofibromatosisAll links ↗
Tracy / Styling With NFNF1Patient / CreatorLived experience, writing, and styleView links ⌄

United States · Tracy shares candid perspectives on living with NF1, grief, mobility, creativity, and self-expression.

Find Tracy / Styling With NFInstagram ↗CTF profile ↗
Varshika Agarwal - Scarz and StoriesNFPatient / AdvocateInstagram and personal storytellingView links ⌄

India · Shares personal perspectives on visible difference, body image, difficult emotions and self-acceptance while living with NF.

Find Varshika Agarwal - Scarz and StoriesVisit profile ↗
Whitney ScheibelNF1Patient / Research advocateEducation, policy, and research advocacyView links ⌄

United States · Whitney uses short-form education, public speaking, Capitol Hill advocacy, and FDA listening sessions to make NF1 more visible and better understood.

Find Whitney ScheibelNF Network profile ↗CTF recognition ↗
Zoe - Chronically ZoeNF1Patient / AdvocateInstagramView links ⌄

United Kingdom · Publicly identifies as a Neurofibromatosis advocate and creates educational content intended to make the invisible visible.

Find Zoe - Chronically ZoeVisit profile ↗
Search and filter Social Media Groups24 of 24 groups
Social Media Groups (24)+
Links
Bay Area NF Support Group at StanfordAll NF conditionsFamilies of children and teensClinic-supported family groupUnited States — Bay AreaWebsiteView links ⌄

A group supported by Lucile Packard Children’s Hospital for parents, grandparents, friends, and families of children and teens with NF.

Connect or followGroup information ↗
Can You Hear Us? / NF2 and YouNF2-related schwannomatosisPatients, families, and caregiversPatient-led community and mediaUnited Kingdom / GlobalYouTubeView links ⌄

An NF2-focused community project offering connection, patient and family resources, and the NF2 and You video-podcast series.

Connect or followYouTube ↗
Faces of NeurofibromatosisAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Large peer community where people share NF experiences, questions, resources and personal stories.

Connect or followFacebook ↗
Henry Ford Neurofibromatosis Support GroupNF1 and NF2-related schwannomatosisPatients and care partnersHybrid support groupUnited States — Michigan / VirtualWebsiteView links ⌄

A free, recurring in-person and virtual support group with peer connection, questions, and presentations from medical experts.

Connect or followSupport group ↗
Living with NeurofibromatosisAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

NF awareness, personal experiences and community-focused content.

Connect or followFacebook ↗
Nerve Tumours UK CommunityAll NF conditionsPatients, families, teens, and studentsOrganization-run communitiesUnited KingdomWebsiteView links ⌄

NF communities that include general support plus dedicated spaces for teens ages 13–18 and students.

Connect or followCommunity options ↗
Neurofibromatosis CommunityAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Community discussion and peer support for people and families affected by NF.

Connect or followFacebook ↗
Neurofibromatosis Family Association (NFFA)All NF conditionsCHOP patients and familiesClinic-affiliated family associationUnited States — PhiladelphiaWebsiteView links ⌄

A parent-volunteer association supporting individuals and families affected by NF through CHOP.

Connect or followCHOP program ↗
Neurofibromatosis Support CommunityAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Peer discussion, shared experiences and support related to Neurofibromatosis.

Connect or followFacebook ↗
Neurofibromatosis Support GroupAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

General NF peer support and community discussion.

Connect or followFacebook ↗
NF (Neurofibromatosis) Professionals NetworkAll NF conditionsProfessionals and advocatesPeer support / communityGlobal / OnlineLinkedInView links ⌄

Professional networking, advocacy, research information and NF community discussion.

Connect or followLinkedIn ↗
NF California Virtual Meet-UpAll NF conditionsPatients, families, and caregiversVirtual peer meet-upUnited States / VirtualWebsiteView links ⌄

A recurring virtual gathering for people and families affected by NF.

Connect or followUpcoming meet-ups ↗
NF Community DiscordAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineDiscordView links ⌄

Real-time conversation and peer connection for people affected by NF.

Maintenance note: Current password: HcksqnexGx

Connect or followDiscord ↗
NF Midwest NF2ACTNF2-related schwannomatosisPeople with direct NF2-SWN experienceAction and community groupUnited States / GlobalWebsiteView links ⌄

An action-oriented group for people with direct experience of NF2-related schwannomatosis.

Connect or followNF Midwest community ↗
NF Midwest Private CommunityAll NF conditionsPatients, families, and caregiversPrivate peer communityUnited States — MidwestWebsiteView links ⌄

A private community for people affected by NF to connect with one another.

Connect or followJoin information ↗
NF Moms Rock!!!!!All NF conditionsParents and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Private peer-support community for mothers and other parents of children affected by NF.

Connect or followFacebook ↗
NF Network Inspire Support CommunityAll NF conditionsPatients, families, and caregiversOnline peer communityUnited States / GlobalWebsiteView links ⌄

A large NF Network-hosted online support community for questions, experiences, and peer connection.

Connect or followInspire community ↗
NF Northeast — Matched for HopeAll NF conditionsNewly diagnosed patients and familiesOne-to-one peer supportUnited States — NortheastWebsiteView links ⌄

Pairs newly diagnosed patients and families with trained peers who understand NF1, NF2-SWN, or schwannomatosis.

Connect or followPeer-support program ↗
NF1 Support & InformationNF1Patients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Private support and information group for young adults with NF1 ages 18 to 30 and families of people with NF1 up to age 30.

Connect or followFacebook ↗
NF2 CrewNF2-related schwannomatosisPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Peer-support community for people affected by NF2-related schwannomatosis.

Connect or followFacebook ↗
NF2 IS - NF Type 2 Information & ServicesNF2-related schwannomatosisPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Independent community sharing information, lived experiences and peer support related to NF2-related schwannomatosis.

Connect or followFacebook ↗
NF2-SWN Patient UK NetworkNF2-related schwannomatosisPatients, families, and caregiversPeer support / communityUnited KingdomFacebookView links ⌄

UK-based peer community specifically for people living with NF2-related schwannomatosis.

Connect or followFacebook ↗
r/neurofibromatosisAll NF conditionsPatients, families, and caregiversPeer support / communityGlobal / OnlineRedditView links ⌄

Public discussion community for NF stories, questions, research, treatment experiences and emotional support.

Connect or followReddit ↗
Surviving Schwannomatosis Support GroupSchwannomatosisPatients, families, and caregiversPeer support / communityGlobal / OnlineFacebookView links ⌄

Peer-support community for people living with schwannomatosis and those who support them.

Connect or followFacebook ↗

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 ↗

Keep exploring

Related resources

ON THIS SITENF creators and advocatesBrowse people sharing NF experiences and education.↗ON THIS SITEFind NF organizationsExplore established charities, networks, and resources.↗ON THIS SITETips for sharing your storyReview purpose, privacy, consent, and accuracy before posting.↗
Lasting Impressions Coffee NF Research & Advocacy Hub

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Patient-Led Independent Resource Disclaimer: This website is independently created, operated, and managed by a person living with Neurofibromatosis (NF) for educational and advocacy purposes.

External Resources and Independence Disclaimer: Links and listings are provided for convenience and informational purposes. Inclusion does not constitute endorsement, certification, referral, or a guarantee of services, qualifications, availability, accuracy, safety, or outcomes. Lasting Impressions LLC is not affiliated with or responsible for external organizations, clinics, companies, websites, AI tools, or their content unless a relationship is specifically disclosed.

Medical Disclaimer: This website provides general educational and informational resources only. It is not a substitute for professional medical advice, diagnosis, or treatment and does not establish a healthcare provider-patient relationship. Always consult a qualified healthcare professional regarding medical concerns or treatment decisions. Never disregard or delay seeking professional advice because of information found on this or any website. If you may be experiencing a medical emergency, call 911 or your local emergency services.