Connect

Find organizations, communities, and opportunities to participate.

Explore established NF organizations, social communities and advocates, or upcoming events without treating every kind of connection as the same.

Community, support & advocacy

Nonprofit Organizations

Find NF charities, patient organizations, collaborative networks, and regional groups supporting research, care, advocacy, education, and community connection.

Filter organizationsSearch by name, service, location, or topic.
36 results
View 33 nonprofit organizations
Links
Acoustic Neuroma AssociationUnited StatesNF2-related schwannomatosisProvides education, support, provider information, and research resources about vestibular schwannomas, including concerns relevant to NF2-related schwannomatosis.View links

Provides education, support, provider information, and research resources about vestibular schwannomas, including concerns relevant to NF2-related schwannomatosis.

AMANF (Brazil)Latin America, Asia & AfricaNF1 · NF2-related schwannomatosis · Other schwannomatosesBrazilian NF association providing patient education, support, professional information, and advocacy.View links

Brazilian NF association providing patient education, support, professional information, and advocacy.

APNF (Portugal)Continental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesPortuguese NF association supporting patients and families through information, awareness, advocacy, and community activities.View links

Portuguese NF association supporting patients and families through information, awareness, advocacy, and community activities.

Association Neurofibromatoses et Recklinghausen (France)Continental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesFrench patient association offering information, support, awareness, and advocacy for people affected by NF.View links

French patient association offering information, support, awareness, and advocacy for people affected by NF.

B the DifferenceUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesSupports individuals and families affected by NF through programs that provide meaningful experiences, kindness, and practical community support.View links

Supports individuals and families affected by NF through programs that provide meaningful experiences, kindness, and practical community support.

Bundesverband Neurofibromatose (Germany)Continental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesGerman national NF organization advancing patient support, education, advocacy, and research awareness.View links

German national NF organization advancing patient support, education, advocacy, and research awareness.

Childhood Tumour TrustCanada, United Kingdom, Ireland & AustraliaNF1Supports children and young people with NF1 and their families across the United Kingdom with practical information and community connection.View links

Supports children and young people with NF1 and their families across the United Kingdom with practical information and community connection.

Children’s Tumor Foundation EuropeInternational networksNF1 · NF2-related schwannomatosis · Other schwannomatosesSupports European collaboration in NF research, clinical care, advocacy, and patient engagement.View links

Supports European collaboration in NF research, clinical care, advocacy, and patient engagement.

Children’s Tumour Foundation AustraliaCanada, United Kingdom, Ireland & AustraliaNF1 · NF2-related schwannomatosis · Other schwannomatosesAustralia’s national NF patient advocacy and support organization for children, adults, and families.View links

Australia’s national NF patient advocacy and support organization for children, adults, and families.

Cure NF2 FoundationInternational networksNF2-related schwannomatosisFunds research into potential gene, cell, and immunotherapy approaches and connects families affected by NF2-related schwannomatosis.View links

Funds research into potential gene, cell, and immunotherapy approaches and connects families affected by NF2-related schwannomatosis.

Littlest Tumor FoundationUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesSupports children with NF and their families through education, advocacy, community programs, and research-focused initiatives.View links

Supports children with NF and their families through education, advocacy, community programs, and research-focused initiatives.

Neurofibromatose Vereniging NederlandContinental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesDutch patient association providing NF information, peer connection, advocacy, and support.View links

Dutch patient association providing NF information, peer connection, advocacy, and support.

Neurofibromatosis Empowerment in Detroit (NFX)United StatesNF1Funds high-impact scientific and medical research focused on targeted treatments for NF1 and leads NF awareness and fundraising initiatives.View links

Funds high-impact scientific and medical research focused on targeted treatments for NF1 and leads NF awareness and fundraising initiatives.

Neurofibromatosis Family Association at CHOPUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesConnects families associated with Children’s Hospital of Philadelphia to NF support, education, and community resources.View links

Connects families associated with Children’s Hospital of Philadelphia to NF support, education, and community resources.

Neuroförbundet (Sweden)Continental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesSwedish neurological patient organization offering information, advocacy, and community resources that include people affected by NF.View links

Swedish neurological patient organization offering information, advocacy, and community resources that include people affected by NF.

NF CaliforniaUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesConnects Californians affected by NF with regional information, community support, events, and NF Network resources.View links

Connects Californians affected by NF with regional information, community support, events, and NF Network resources.

NF Central PlainsUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesServes individuals and families in the central Plains through NF education, support, awareness, and community connection.View links

Serves individuals and families in the central Plains through NF education, support, awareness, and community connection.

NF CollectiveInternational networksNF1 · NF2-related schwannomatosis · Other schwannomatosesConnects U.S. NF nonprofits and resource partners to strengthen collaboration, awareness, and community support.View links

Connects U.S. NF nonprofits and resource partners to strengthen collaboration, awareness, and community support.

NF Cure JapanLatin America, Asia & AfricaNF1 · NF2-related schwannomatosis · Other schwannomatosesRaises NF awareness and supports the Japanese NF community while encouraging research and better treatment options.View links

Raises NF awareness and supports the Japanese NF community while encouraging research and better treatment options.

NF DanmarkContinental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesDanish NF community organization sharing information, peer support, activities, and advocacy resources.View links

Danish NF community organization sharing information, peer support, activities, and advocacy resources.

NF Kinder (Austria)Continental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesSupports children and families affected by NF in Austria while promoting awareness, care, and research.View links

Supports children and families affected by NF in Austria while promoting awareness, care, and research.

NF MichiganUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesOffers education, NF specialist information, peer connection, events, advocacy, scholarships, and practical support through MiNF Cares for people and families across Michigan.View links

Offers education, NF specialist information, peer connection, events, advocacy, scholarships, and practical support through MiNF Cares for people and families across Michigan.

NF MidwestUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesSupports children, adults, and families through education, community programs, clinic development, and NF research.View links

Supports children, adults, and families through education, community programs, clinic development, and NF research.

NF NorgeContinental EuropeNF1 · NF2-related schwannomatosis · Other schwannomatosesNorwegian NF organization connecting patients and families through information, peer support, events, and advocacy.View links

Norwegian NF organization connecting patients and families through information, peer support, events, and advocacy.

NF North CentralUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesBuilds regional connection and shares support, education, and community information for people affected by NF.View links

Builds regional connection and shares support, education, and community information for people affected by NF.

NF NortheastUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesProvides support, education, advocacy, community programs, and research funding for people and families across the northeastern United States.View links

Provides support, education, advocacy, community programs, and research funding for people and families across the northeastern United States.

NF SimplifiedUnited StatesOther schwannomatosesMakes NF and schwannomatosis research easier to understand through clear, expert-reviewed summaries for patients, families, and caregivers.View links

Makes NF and schwannomatosis research easier to understand through clear, expert-reviewed summaries for patients, families, and caregivers.

NF TennesseeUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesProvides NF awareness, education, family support, and community opportunities for people across Tennessee.View links

Provides NF awareness, education, family support, and community opportunities for people across Tennessee.

Penny’s Flight FoundationUnited StatesNF1Funds NF1 research, expands NF awareness through school and community campaigns, and supports adaptive programs for children and teens with disabilities.View links

Funds NF1 research, expands NF awareness through school and community campaigns, and supports adaptive programs for children and teens with disabilities.

Rare Diseases South AfricaLatin America, Asia & AfricaNF1 · NF2-related schwannomatosis · Other schwannomatosesAdvocates for people with rare diseases, including improved diagnosis, access to care, policy, and patient support.View links

Advocates for people with rare diseases, including improved diagnosis, access to care, policy, and patient support.

Texas Neurofibromatosis FoundationUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesProvides education, referrals, family support, and advocacy while helping advance NF research in Texas and beyond.View links

Provides education, referrals, family support, and advocacy while helping advance NF research in Texas and beyond.

The NF TeamUnited StatesNF1 · NF2-related schwannomatosis · Other schwannomatosesBrings people together through athletic and community fundraising efforts that increase NF awareness and support research.View links

Brings people together through athletic and community fundraising efforts that increase NF awareness and support research.

Tumour Foundation of BCCanada, United Kingdom, Ireland & AustraliaNF1 · NF2-related schwannomatosis · Other schwannomatosesSupports people in British Columbia affected by NF through information, family connection, advocacy, and community programs.View links

Supports people in British Columbia affected by NF through information, family connection, advocacy, and community programs.

Progress across generations

Community Milestones Timeline

A selective, source-linked history of discoveries, care, organizations, advocacy, shared research resources, and treatment progress across the NF community.

Open any row for the concise history, why it mattered, and its verified source. “Then & Now” appears only when it adds useful context.

View 19 community milestones
  1. Clinical historyNF1 receives an early clinical description

    What happened

    Friedrich Daniel von Recklinghausen published a detailed description connecting characteristic tumors with nerves.

    Why it mattered

    The description helped establish NF as a recognizable clinical condition and shaped the language used for generations.

    THEN

    NF was understood mainly through visible signs, symptoms, and clinical observation.

    NOW

    Defined diagnostic criteria, imaging, surveillance guidance, and genetic testing can support more precise diagnosis and care.

    PubMed historical review
  2. Community organizationChildren’s Tumor Foundation is founded

    What happened

    CTF began as a grassroots organization dedicated to finding treatments for NF and supporting affected families.

    Why it mattered

    It created a major coordinated platform for NF research, clinical education, advocacy, and community participation.

    THEN

    Families and researchers had fewer coordinated NF-specific networks and shared resources.

    NOW

    CTF supports research programs, an NF Clinic Network, the NF Registry, education, and international collaboration.

    Children’s Tumor Foundation
  3. Care programThe Neurofibromatosis Institute and an NF clinic are established

    What happened

    Dr. Vincent Riccardi founded The Neurofibromatosis Institute and established a specialized clinic for patient care.

    Why it mattered

    Dedicated NF programs helped connect clinical experience, patient support, and research in a field with limited specialized care.

    NF Midwest
  4. Community organizationNF Midwest is founded

    What happened

    NF Midwest was founded to serve children, adults, and families affected by NF across the Midwestern United States.

    Why it mattered

    The organization expanded regional access to NF education, support, clinic relationships, awareness, and research advocacy.

    NF Midwest
  5. Research discoveryThe NF1 gene is mapped to chromosome 17

    What happened

    Genetic mapping narrowed the location of the NF1 gene and accelerated the work that followed.

    Why it mattered

    Mapping gave researchers a defined genomic region to investigate and helped make gene identification possible.

    THEN

    The cause of NF1 was unknown at the molecular level.

    NOW

    NF1 is understood as a tumor-suppressor gene on chromosome 17, informing testing, counseling, research, and treatment development.

    PubMed
  6. Advocacy organizationNF Network is founded

    What happened

    NF Network was founded as a national organization advocating for federal NF research funding and the development of local organizations.

    Why it mattered

    It strengthened coordinated public-policy advocacy, education, awareness, and community-building across the United States.

    NF Network
  7. Community organizationNF Northeast is incorporated

    What happened

    NF, Inc. Mass Bay Area—now NF Northeast—was incorporated and later expanded its regional identity and reach.

    Why it mattered

    The organization built continuing patient programs, education, advocacy, and an NF research-funding program that began in 1990.

    NF Northeast
  8. Research discoveryThe NF1 gene is identified

    What happened

    Independent research teams identified the NF1 gene and its role in the condition.

    Why it mattered

    Gene identification opened new paths for genetic testing, biological research, and therapies aimed at affected signaling pathways.

    THEN

    Researchers knew the chromosome region but had not identified the gene itself.

    NOW

    Researchers study neurofibromin and the RAS/MAPK pathway to understand NF1 biology and develop potential treatments.

    PubMed
  9. Research discoveryThe NF2 gene is identified

    What happened

    Researchers identified the NF2 gene on chromosome 22 and the protein now known as merlin.

    Why it mattered

    The discovery strengthened molecular diagnosis and research into tumors associated with NF2-related schwannomatosis.

    THEN

    The molecular cause associated with the condition then called NF2 was not known.

    NOW

    NF2 and merlin biology guide research, genetic testing, and the gene-based classification of NF2-related schwannomatosis.

    PubMed
  10. Clinical-care networkThe NF Clinic Network is established

    What happened

    Children’s Tumor Foundation established a network of specialized NF clinics in the United States.

    Why it mattered

    The network gave more patients a route to experienced multidisciplinary care while supporting clinical collaboration and better practices.

    THEN

    Specialized NF care was harder to identify and less formally connected across institutions.

    NOW

    The network includes more than 70 clinics across North America and serves more than 20,000 patient visits annually.

    Children’s Tumor Foundation
  11. Research collaborationREiNS collaboration is established

    What happened

    The Response Evaluation in Neurofibromatosis and Schwannomatosis collaboration formed to develop shared clinical-trial response criteria and endpoints.

    Why it mattered

    Common measurement standards help researchers compare trial results and design stronger NF studies.

    Children’s Tumor Foundation research tools
  12. Patient-powered researchThe NF Registry launches

    What happened

    Children’s Tumor Foundation established the NF Registry as a global platform for people with NF to contribute health and lived-experience information.

    Why it mattered

    Registry participation supports natural-history research, study recruitment, care planning, and therapy development.

    THEN

    Researchers had fewer scalable ways to learn directly from large numbers of people living with NF.

    NOW

    The Registry supports global participation and connects patient-reported information with research opportunities.

    Children’s Tumor Foundation
  13. Research collaborationSynodos for NF2 launches

    What happened

    CTF launched a collaborative research platform bringing multiple laboratories and medical centers together around NF2.

    Why it mattered

    The shared-work model connected tumor models, molecular data, and drug testing to accelerate research beyond isolated projects.

    Children’s Tumor Foundation
  14. Research collaborationSynodos for Schwannomatosis launches

    What happened

    An international multidisciplinary consortium launched to study schwannomatosis tumors, therapeutic targets, management, and pain.

    Why it mattered

    The project gave schwannomatosis a dedicated collaborative research effort focused on questions important to patients.

    Children’s Tumor Foundation
  15. Open research resourceThe NF Data Portal launches

    What happened

    CTF, NTAP, and Sage Bionetworks launched the NF Data Portal to make molecular and clinical data from NF studies available to researchers.

    Why it mattered

    Shared data and linked research resources make findings easier to reuse, compare, and build upon.

    Children’s Tumor Foundation research archive
  16. Treatment approvalFirst FDA-approved treatment for NF1 plexiform neurofibromas

    What happened

    The FDA approved selumetinib for certain children with NF1 and symptomatic, inoperable plexiform neurofibromas.

    Why it mattered

    This was the first FDA-approved medicine specifically for an NF condition and marked a major change in the treatment landscape.

    THEN

    For inoperable plexiform neurofibromas, options centered on monitoring, symptom management, and surgery when feasible.

    NOW

    Targeted medicines are available for certain eligible patients, although they are not cures and do not fit every person or tumor.

    U.S. Food and Drug Administration
  17. Diagnosis and terminologyInternational consensus updates schwannomatosis naming

    What happened

    Experts published revised diagnostic criteria and gene-based nomenclature, including the term NF2-related schwannomatosis.

    Why it mattered

    The update better reflects genetic causes and overlapping tumor patterns while improving precision in care and research.

    THEN

    NF2 and schwannomatosis were classified using older categories that did not consistently reflect genetic causes.

    NOW

    Gene-based terms improve precision, while older names remain useful search terms and may appear in historical records.

    PubMed
  18. Treatment approvalMirdametinib is approved for NF1 plexiform neurofibromas

    What happened

    The FDA approved mirdametinib for adults and children age two and older with NF1 and symptomatic plexiform neurofibromas not amenable to complete resection.

    Why it mattered

    The approval added another targeted option and covered certain eligible adults as well as children.

    THEN

    The first targeted approval in this setting applied to a narrower pediatric population.

    NOW

    More than one targeted option may be available for certain eligible patients, with treatment decisions made by an experienced care team.

    U.S. Food and Drug Administration
  19. Treatment approvalSelumetinib indication expands to adults

    What happened

    The FDA expanded selumetinib’s indication to adults with NF1 and symptomatic, inoperable plexiform neurofibromas.

    Why it mattered

    The expanded indication made the established treatment available to another eligible age group.

    THEN

    Selumetinib’s NF1 plexiform-neurofibroma indication was limited to pediatric patients.

    NOW

    Certain eligible adults can also be considered under the expanded indication, with individualized clinical guidance.

    U.S. Food and Drug Administration