Developer docs
API playgroundTry for free, no card

Search company profiles

National Down Syndrome Congress

Full company profile

uuid02lga1j

Namestring
National Down Syndrome Congress
Legal namestring
National Down Syndrome Congress
Websiteurl
ndsccenter.org
Company typeenum
Private
Founded yearint
1973
Descriptiontext

The National Down Syndrome Congress (NDSC) is a 501(c)(3) nonprofit organization founded in 1973 and headquartered at a Cincinnati, Ohio mailing address (3825 Edwards Road), operating as the leading national resource organization dedicated solely to Down syndrome. Its mission centers on educating through awareness, advocating for civil rights protections, empowering self-advocates, and inspiring inclusive understanding of Down syndrome. The organization serves a multi-stakeholder audience including families of individuals with Down syndrome (parents, siblings, grandparents, caregivers), self-advocates ages 15 through 70+, K–12 educators and special education professionals, healthcare providers, and a network of local and state Down syndrome affiliates.

NDSC's core product is the annual NDSC Convention, which in 2026 will be held as the 54th Annual Convention at the Hilton Signia at Bonnet Creek in Orlando, Florida, and aggregates 3,000–3,500 attendees. The convention bundles multiple specialized tracks — a general conference, the Youth & Adult Conference, Siblings Conference (grades 7–12), Educators Conference, DSAIA Leadership Pre-Conference, Advocacy Training Boot Camp, Kids Camp (ages 6 months to 14 years), Deep Dive 3-hour workshops, and an NDSC College Fair — supported by a digital portfolio of English and Spanish webinars, a Policy Action Center, and the NDSC Down Syndrome Policy Summit. The underlying platform is a relatively standard nonprofit digital stack (website, email newsletter, social channels, action-alert tool) rather than proprietary technology.

The revenue model is diversified across four streams: individual donations (annual campaigns, monthly giving, memorial giving, NDSC Champions legacy program), convention registration fees (e.g., $200 Kids Camp, $150 Educators Conference, $75 Deep Dive, $75 College Fair booth), corporate sponsorship (Microsoft, Comfees, Daymark, Global, Dr Noze Best for 2025), and planned/stock gifts including donor-advised funds and charitable IRA rollovers. The go-to-market motion is event-driven and community-led: the annual convention anchors acquisition and engagement, supplemented by the DSAIA affiliate network, NDAC coalition, Self-Advocate Council, and 900+ convention volunteers. Revenue is not publicly disclosed, and the organization has no parent company, subsidiaries, or external funding rounds.

Short descriptiontext

The National Down Syndrome Congress (NDSC) is a Cincinnati-based 501(c)(3) nonprofit founded in 1973 that serves individuals with Down syndrome, their families, educators, and healthcare providers through an annual convention, advocacy training, policy engagement, and an affiliate network of state and local Down syndrome organizations.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersCincinnati, United States
HQ citystring
Cincinnati
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
disability advocacy services, nonprofit support programs, annual convention events, community education resources, special needs advocacy
Industry3 codes
1Down Syndrome & Intellectual/Developmental Disabilities (IDD) Childcare
CodeHSAAAIACPrimaryYes
2Assistive Technology (AT) & AAC Services
CodeEDAJAKAFPrimaryNo
3Assistive Technology & AAC for Young Children
CodeEDACAFALPrimaryNo
NAICS code3 codes
  • Voluntary Health Organizations813212
  • Human Rights Organizations813311
  • Services for the Elderly and Persons with Disabilities62412
SIC code3 codes
  • Services-Social Services8300
  • Services-Membership Organizations8600
  • Services-Educational Services8200
Product category
Disability Advocacy and Support Services
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1Donations and Annual Campaigns
TypeGrants Donations
Description

Individual donations through annual campaigns, monthly giving programs, and memorial giving. Major gift program and NDSC Champions legacy giving.

ndsccenter.org
2Convention Revenue
TypeProfessional Services
Description

Registration fees for the annual convention including general conference, youth & adult conference, siblings conference, educators conference, kids camp, and deep-dive sessions.

ndsccenter.org
3Corporate Sponsorship
TypeAffiliate Referral
Description

Convention sponsorship from corporations including Comfees, Microsoft, Daymark, Global, Dr Noze Best, and others at various sponsorship tiers.

ndsccenter.org
4Stock and Planned Gifts
TypeGrants Donations
Description

Stock gifts, donor advised funds, charitable IRA rollover gifts, and legacy giving programs.

ndsccenter.org
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Personnel, Operations, Marketing or Sales, Others
Pricing details5 tiers
1Kids Camp full weekend registration
ModelUnit PricingBilling cadenceOne time
Notes

$200 per child for the entire weekend (ages 6 months to 14 years)

ndsccenter.org
2College Fair exhibitor booth
ModelUnit PricingBilling cadenceOne time
Notes

$75 per booth

ndsccenter.org
3Educators Conference registration
ModelUnit PricingBilling cadenceOne time
Notes

$150 per registrant includes certificate of attendance (7 professional hours), breakfast and lunch. Optional 0.6 CEUs for $30 additional.

ndsccenter.org
4Deep Dive sessions
ModelUnit PricingBilling cadenceOne time
Notes

$75 per deep-dive session (3-hour intensive workshops)

ndsccenter.org
5General Conference registration
ModelSubscriptionBilling cadenceMulti-year contract
Notes

Multi-day convention registration with various add-ons including deep dives, meal plans, and Saturday evening celebration tickets

ndsccenter.org
GTM typeB2C
B2C
Offering typeServices
Services
Core offering1 text field

The National Down Syndrome Congress (NDSC) is a 501(c)(3) nonprofit advocacy and support organization that operates a national annual convention (the 54th in 2026) and surrounding program portfolio for the Down syndrome community. It provides advocacy training, policy engagement, professional development for educators, scholarships, webinars, and a national affiliate network (DSAIA), all centered on educating, advocating for, empowering, and inspiring people with Down syndrome and their families.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • 50+ years of annual conventions bringing together thousands of families and professionals
+1 more record
Product overview1 text field

The National Down Syndrome Congress operates as a comprehensive advocacy and support organization offering a portfolio of interconnected programs and events. The core offering is the annual NDSC Convention, which serves as the central hub integrating multiple specialized conference tracks (Youth & Adult Conference, Educators Conference, Siblings Conference, Kids Camp) and professional development opportunities (DSAIA Leadership Conference, Advocacy Training Boot Camp, Deep Dive Sessions). Supporting programs include webinars, policy and advocacy resources, scholarships, and signature fundraising events (Big Game Ball, Golf Classic). The organization also operates the NDSC College Fair to connect individuals with Down syndrome to postsecondary educational opportunities. This integrated program structure provides the Down syndrome community with year-round education, advocacy training, and fellowship opportunities centered around the annual convention.

Product and service12 records
1NDSC Annual Convention
CategoryAnnual Convention Program
Description

Flagship multi-day annual event bringing together thousands of people with Down syndrome, their families, and professionals for workshops, networking, advocacy training, and community support. Includes general conference, youth & adult conference, siblings conference, kids camp, and deep-dive sessions.

2Youth & Adult Conference
CategoryConference Program
Description

Dedicated conference track for individuals with Down syndrome ages 15 and older, focused on self-advocacy, independence, and personal development through interactive workshops and social activities.

3Educators Conference
CategoryProfessional Development Program
Description

One-day conference designed for educators working with students with Down syndrome and intellectual disabilities, offering hands-on, research-based strategies for K-12 classrooms. Registration is $150 per registrant and includes 7 professional hours of training.

4Siblings Conference
CategorySupport Program
Description

Program for siblings (rising 7th through 12th grade) to learn about Down syndrome, disability issues, and how to be effective advocates for their siblings.

5Kids Camp
CategoryChildcare Program
Description

Supervised camp for children ages 6 months to 14 years (with and without Down syndrome) during the annual convention, featuring educational and therapeutic play, arts and crafts, and physical activities.

6Advocacy Training Boot Camp
CategoryAdvocacy Program
Description

Free training program at the annual convention that helps parents, professionals, and self-advocates build advocacy skills and learn how to engage effectively with legislators.

7DSAIA Leadership Conference
CategoryProfessional Development Program
Description

Pre-conference event bringing together leaders from local, state, regional, and national Down syndrome organizations for best practices and professional development.

8NDSC College Fair
CategoryEducational Program
Description

Event showcasing inclusive postsecondary programs for individuals with intellectual disabilities, held during the annual convention.

9Deep Dive Sessions
CategoryWorkshop Program
Description

Intensive 3-hour workshops offered at the annual convention providing in-depth learning experiences with expert presenters on various Down syndrome topics.

10Webinars
CategoryEducational Resource
Description

Online educational presentations covering topics related to Down syndrome, available in English and Spanish for parents, professionals, and self-advocates.

11Policy & Advocacy Resources
CategoryAdvocacy Resource
Description

Tools and resources to help advocates engage with policymakers, including action alerts, policy briefs, and the NDSC Policy Summit.

12NDAC Town Hall
Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierMinorTypeGTM or Marketing Partner
Description

Convention sponsor for 2025 NDSC Convention. Comfees appears as a sponsor logo on the convention sponsors page.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Convention sponsor for 2025 NDSC Convention. Microsoft appears as a sponsor logo on the convention sponsors page.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Convention sponsor for 2025 NDSC Convention. Daymark appears as a sponsor logo on the convention sponsors page.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Convention sponsor for 2025 NDSC Convention. Global appears as a sponsor logo on the convention sponsors page.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Convention sponsor for 2025 NDSC Convention. Dr Noze Best appears as a sponsor logo on the convention sponsors page.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

DSAIA is a membership organization dedicated to creating a powerful network of local, state, and national Down syndrome organizations. NDSC hosts the DSAIA Leadership Pre-Conference at its annual convention and collaborates on programming.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global nonprofit providing year-round sports training and competition for people with intellectual disabilities. Shares a similar event-driven GTM, corporate sponsorship model, and self-advocate movement, though at much larger scale and broader IDD scope.

TypeBroad incumbent
Description

Federation of disability rights protection and advocacy organizations funded by federal grants. Operates a parallel policy and member-services model focused on legal advocacy rather than direct community programming.

TypeBroad incumbent
Description

Long-established maternal and infant health nonprofit historically connected to Down syndrome. Operates a similar advocacy, research-funding, and maternal-health programming model at national scale.

TypeDirect peer
Description

A network of Down syndrome achievement centers offering free educational, therapeutic, and career development programs. Operates a brick-and-mortar delivery model distinct from NDSC's convention-centric approach but serves the same community.

TypeDirect peer
Description

Denver-based Down syndrome research and medical care foundation. Competes for healthcare-research funding, corporate sponsorships, and family engagement, with a stronger medical-research orientation than NDSC.

TypeDirect peer
Description

The largest US Down syndrome advocacy organization, founded 1979. NDSS operates the National Buddy Walk, advocacy, and public awareness programming, directly competing with NDSC for donors, sponsors, and self-advocate engagement.

TypeBroad incumbent
Description

National cross-disability advocacy organization. Operates a parallel model of policy advocacy, coalition-building, and member engagement at broader (cross-disability) scope, occasionally competing for the same corporate disability-inclusion sponsors.

TypeBroad incumbent
Description

National disability advocacy organization with a comparable operational structure (national office, affiliate network, annual conference, advocacy, family support). Serves a different disability community but follows the same nonprofit disability-advocacy playbook.

TypeDirect peer
Description

A peer Down syndrome organization focused on supporting new and expectant parents at diagnosis. Overlaps with NDSC's New Parents resources and competes for early-stage family donor dollars.

TypeDirect peer
Description

Down syndrome research foundation funding medical and cognitive research. Competes for research-aligned donors and corporate sponsors, particularly in life sciences and pharmaceutical categories.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment5 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile5 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

National Down Syndrome Congress

Disability Advocacy and Support Servicesndsccenter.org

The National Down Syndrome Congress (NDSC) is a Cincinnati-based 501(c)(3) nonprofit founded in 1973 that serves individuals with Down syndrome, their families, educators, and healthcare providers through an annual convention, advocacy training, policy engagement, and an affiliate network of state and local Down syndrome organizations.

What National Down Syndrome Congress does

The National Down Syndrome Congress (NDSC) is a 501(c)(3) nonprofit organization founded in 1973 and headquartered at a Cincinnati, Ohio mailing address (3825 Edwards Road), operating as the leading national resource organization dedicated solely to Down syndrome. Its mission centers on educating through awareness, advocating for civil rights protections, empowering self-advocates, and inspiring inclusive understanding of Down syndrome. The organization serves a multi-stakeholder audience including families of individuals with Down syndrome (parents, siblings, grandparents, caregivers), self-advocates ages 15 through 70+, K–12 educators and special education professionals, healthcare providers, and a network of local and state Down syndrome affiliates.

NDSC's core product is the annual NDSC Convention, which in 2026 will be held as the 54th Annual Convention at the Hilton Signia at Bonnet Creek in Orlando, Florida, and aggregates 3,000–3,500 attendees. The convention bundles multiple specialized tracks — a general conference, the Youth & Adult Conference, Siblings Conference (grades 7–12), Educators Conference, DSAIA Leadership Pre-Conference, Advocacy Training Boot Camp, Kids Camp (ages 6 months to 14 years), Deep Dive 3-hour workshops, and an NDSC College Fair — supported by a digital portfolio of English and Spanish webinars, a Policy Action Center, and the NDSC Down Syndrome Policy Summit. The underlying platform is a relatively standard nonprofit digital stack (website, email newsletter, social channels, action-alert tool) rather than proprietary technology.

The revenue model is diversified across four streams: individual donations (annual campaigns, monthly giving, memorial giving, NDSC Champions legacy program), convention registration fees (e.g., $200 Kids Camp, $150 Educators Conference, $75 Deep Dive, $75 College Fair booth), corporate sponsorship (Microsoft, Comfees, Daymark, Global, Dr Noze Best for 2025), and planned/stock gifts including donor-advised funds and charitable IRA rollovers. The go-to-market motion is event-driven and community-led: the annual convention anchors acquisition and engagement, supplemented by the DSAIA affiliate network, NDAC coalition, Self-Advocate Council, and 900+ convention volunteers. Revenue is not publicly disclosed, and the organization has no parent company, subsidiaries, or external funding rounds.

National Down Syndrome Congress firmographics

Firmographics
Name
National Down Syndrome Congress
Legal name
National Down Syndrome Congress
Website
https://ndsccenter.org
Company type
Private
Founded year
1973
Operating status
Operating
Headcount range
11–50 employees
Short description
The National Down Syndrome Congress (NDSC) is a Cincinnati-based 501(c)(3) nonprofit founded in 1973 that serves individuals with Down syndrome, their families, educators, and healthcare providers through an annual convention, advocacy training, policy engagement, and an affiliate network of state and local Down syndrome organizations.
Ownership category
akta.pro rank

National Down Syndrome Congress industry classification

Industry
Product category
Disability Advocacy and Support Services
NAICS
Voluntary Health Organizations (813212), Human Rights Organizations (813311), Services for the Elderly and Persons with Disabilities (62412)
SIC
Services-Social Services (8300), Services-Membership Organizations (8600), Services-Educational Services (8200)
akta.pro primary industry
Down Syndrome & Intellectual/Developmental Disabilities (IDD) Childcare (HSAAAIAC)
akta.pro secondary industries
Assistive Technology (AT) & AAC Services (EDAJAKAF), Assistive Technology & AAC for Young Children (EDACAFAL)

Keywords

  • Disability advocacy services
  • Nonprofit support programs
  • Annual convention events
  • Community education resources
  • Special needs advocacy

Where National Down Syndrome Congress is headquartered

Location

Headquarters

HQ city
Cincinnati
HQ country
United States
HQ region
North America

Offices1 record

Markets served

National Down Syndrome Congress business model

Business model
GTM type
B2C
Offering type
Services
Cost components
Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. Donations and Annual Campaigns: Individual donations through annual campaigns, monthly giving programs, and memorial giving. Major gift program and NDSC Champions legacy giving.
  2. Convention Revenue: Registration fees for the annual convention including general conference, youth & adult conference, siblings conference, educators conference, kids camp, and deep-dive sessions.
  3. Corporate Sponsorship: Convention sponsorship from corporations including Comfees, Microsoft, Daymark, Global, Dr Noze Best, and others at various sponsorship tiers.
  4. Stock and Planned Gifts: Stock gifts, donor advised funds, charitable IRA rollover gifts, and legacy giving programs.

Pricing tiers

ModelBillingPrice
Unit PricingOne timeKids Camp full weekend registration
Unit PricingOne timeCollege Fair exhibitor booth
Unit PricingOne timeEducators Conference registration
Unit PricingOne timeDeep Dive sessions
SubscriptionMulti-year contractGeneral Conference registration

Go-to-market motion2 records

Distribution channels4 records

Marketing channels7 records

National Down Syndrome Congress product offering

Product offering

Core offering

The National Down Syndrome Congress (NDSC) is a 501(c)(3) nonprofit advocacy and support organization that operates a national annual convention (the 54th in 2026) and surrounding program portfolio for the Down syndrome community. It provides advocacy training, policy engagement, professional development for educators, scholarships, webinars, and a national affiliate network (DSAIA), all centered on educating, advocating for, empowering, and inspiring people with Down syndrome and their families.

Product overview

The National Down Syndrome Congress operates as a comprehensive advocacy and support organization offering a portfolio of interconnected programs and events. The core offering is the annual NDSC Convention, which serves as the central hub integrating multiple specialized conference tracks (Youth & Adult Conference, Educators Conference, Siblings Conference, Kids Camp) and professional development opportunities (DSAIA Leadership Conference, Advocacy Training Boot Camp, Deep Dive Sessions). Supporting programs include webinars, policy and advocacy resources, scholarships, and signature fundraising events (Big Game Ball, Golf Classic). The organization also operates the NDSC College Fair to connect individuals with Down syndrome to postsecondary educational opportunities. This integrated program structure provides the Down syndrome community with year-round education, advocacy training, and fellowship opportunities centered around the annual convention.

Differentiator

Problem solved

Functional benefit

Products and services

  • NDSC Annual Convention Flagship multi-day annual event bringing together thousands of people with Down syndrome, their families, and professionals for workshops, networking, advocacy training, and community support. Includes general conference, youth & adult conference, siblings conference, kids camp, and deep-dive sessions.
  • Youth & Adult Conference Dedicated conference track for individuals with Down syndrome ages 15 and older, focused on self-advocacy, independence, and personal development through interactive workshops and social activities.
  • Educators Conference One-day conference designed for educators working with students with Down syndrome and intellectual disabilities, offering hands-on, research-based strategies for K-12 classrooms. Registration is $150 per registrant and includes 7 professional hours of training.
  • Siblings Conference Program for siblings (rising 7th through 12th grade) to learn about Down syndrome, disability issues, and how to be effective advocates for their siblings.
  • Kids Camp Supervised camp for children ages 6 months to 14 years (with and without Down syndrome) during the annual convention, featuring educational and therapeutic play, arts and crafts, and physical activities.
  • Advocacy Training Boot Camp Free training program at the annual convention that helps parents, professionals, and self-advocates build advocacy skills and learn how to engage effectively with legislators.
  • DSAIA Leadership Conference Pre-conference event bringing together leaders from local, state, regional, and national Down syndrome organizations for best practices and professional development.
  • NDSC College Fair Event showcasing inclusive postsecondary programs for individuals with intellectual disabilities, held during the annual convention.
  • Deep Dive Sessions Intensive 3-hour workshops offered at the annual convention providing in-depth learning experiences with expert presenters on various Down syndrome topics.
  • Webinars Online educational presentations covering topics related to Down syndrome, available in English and Spanish for parents, professionals, and self-advocates.
  • Policy & Advocacy Resources Tools and resources to help advocates engage with policymakers, including action alerts, policy briefs, and the NDSC Policy Summit.
  • NDAC Town Hall

Quantifiable outcome

  • 50+ years of annual conventions bringing together thousands of families and professionals
  • +1 more outcomes

Companies that use National Down Syndrome Congress

Customer profile

Named customers3 records

Segments5 records

Ideal customer profiles5 records

National Down Syndrome Congress technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

National Down Syndrome Congress partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered minor and core.

  • ComfeesminorGTM or Marketing PartnerConvention sponsor for 2025 NDSC Convention. Comfees appears as a sponsor logo on the convention sponsors page.
  • MicrosoftminorGTM or Marketing PartnerConvention sponsor for 2025 NDSC Convention. Microsoft appears as a sponsor logo on the convention sponsors page.
  • DaymarkminorGTM or Marketing PartnerConvention sponsor for 2025 NDSC Convention. Daymark appears as a sponsor logo on the convention sponsors page.
  • GlobalminorGTM or Marketing PartnerConvention sponsor for 2025 NDSC Convention. Global appears as a sponsor logo on the convention sponsors page.
  • Dr Noze BestminorGTM or Marketing PartnerConvention sponsor for 2025 NDSC Convention. Dr Noze Best appears as a sponsor logo on the convention sponsors page.
  • DSAIA (Down Syndrome Affiliates in Action)coreStrategic or Co-development PartnerDSAIA is a membership organization dedicated to creating a powerful network of local, state, and national Down syndrome organizations. NDSC hosts the DSAIA Leadership Pre-Conference at its annual convention and collaborates on programming.

Scale indicators5 records

Recent moves6 records

Expansion highlights5 records

National Down Syndrome Congress competitors and assessment

Company assessment

Broad incumbents

  • Special Olympics: Global nonprofit providing year-round sports training and competition for people with intellectual disabilities. Shares a similar event-driven GTM, corporate sponsorship model, and self-advocate movement, though at much larger scale and broader IDD scope.
  • National Disability Rights Network: Federation of disability rights protection and advocacy organizations funded by federal grants. Operates a parallel policy and member-services model focused on legal advocacy rather than direct community programming.
  • March of Dimes: Long-established maternal and infant health nonprofit historically connected to Down syndrome. Operates a similar advocacy, research-funding, and maternal-health programming model at national scale.
  • American Association of People with Disabilities: National cross-disability advocacy organization. Operates a parallel model of policy advocacy, coalition-building, and member engagement at broader (cross-disability) scope, occasionally competing for the same corporate disability-inclusion sponsors.
  • Autism Society of America: National disability advocacy organization with a comparable operational structure (national office, affiliate network, annual conference, advocacy, family support). Serves a different disability community but follows the same nonprofit disability-advocacy playbook.

Direct peers

  • GiGi's Playhouse: A network of Down syndrome achievement centers offering free educational, therapeutic, and career development programs. Operates a brick-and-mortar delivery model distinct from NDSC's convention-centric approach but serves the same community.
  • Global Down Syndrome Foundation: Denver-based Down syndrome research and medical care foundation. Competes for healthcare-research funding, corporate sponsorships, and family engagement, with a stronger medical-research orientation than NDSC.
  • National Down Syndrome Society: The largest US Down syndrome advocacy organization, founded 1979. NDSS operates the National Buddy Walk, advocacy, and public awareness programming, directly competing with NDSC for donors, sponsors, and self-advocate engagement.
  • Down Syndrome Diagnosis Network: A peer Down syndrome organization focused on supporting new and expectant parents at diagnosis. Overlaps with NDSC's New Parents resources and competes for early-stage family donor dollars.
  • LuMind IDSC Foundation: Down syndrome research foundation funding medical and cognitive research. Competes for research-aligned donors and corporate sponsors, particularly in life sciences and pharmaceutical categories.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat5 records

Key risks5 records

Key highlights6 records

Customer concentration

National Down Syndrome Congress social profiles

Digital presence

National Down Syndrome Congress financial estimates

Financial estimate

Revenue estimate

Valuation estimate

National Down Syndrome Congress leadership team

Management profile

Number of profiles

Profiles2 records

National Down Syndrome Congress funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

National Down Syndrome Congress M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about National Down Syndrome Congress

What does National Down Syndrome Congress do?

The National Down Syndrome Congress (NDSC) is a 501(c)(3) nonprofit advocacy and support organization that operates a national annual convention (the 54th in 2026) and surrounding program portfolio for the Down syndrome community. It provides advocacy training, policy engagement, professional development for educators, scholarships, webinars, and a national affiliate network (DSAIA), all centered on educating, advocating for, empowering, and inspiring people with Down syndrome and their families.

Is National Down Syndrome Congress a public or private company?

National Down Syndrome Congress is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was National Down Syndrome Congress founded?

National Down Syndrome Congress was founded in 1973. It employs 11 to 50 people.

Where is National Down Syndrome Congress based?

National Down Syndrome Congress is headquartered in Cincinnati, United States, in the North America region.

How does National Down Syndrome Congress make money?

Four revenue lines are on record. Donations and Annual Campaigns are the primary driver. The others are convention Revenue, corporate Sponsorship and stock and Planned Gifts.

Who are National Down Syndrome Congress's main competitors?

Broad incumbents on record are Special Olympics, National Disability Rights Network, March of Dimes, American Association of People with Disabilities and Autism Society of America. Direct peers are GiGi's Playhouse, Global Down Syndrome Foundation, National Down Syndrome Society, Down Syndrome Diagnosis Network and LuMind IDSC Foundation.

Does National Down Syndrome Congress have an API?

No public API is recorded for National Down Syndrome Congress.

What industry is National Down Syndrome Congress in?

National Down Syndrome Congress's product category is Disability Advocacy and Support Services. Its primary akta.pro industry code is HSAAAIAC, Down Syndrome & Intellectual/Developmental Disabilities (IDD) Childcare, with a secondary code of EDAJAKAF, Assistive Technology (AT) & AAC Services. Its NAICS code is 813212 and its SIC code is 8300.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
EIN PresswireNDSC and Nation-wide Coalition Call on Administration & Congress to Protect Children with Disabilities & Reverse LayoffsThe National Down Syndrome Congress (NDSC) joined over 800 national, state, and local organizations from all 50 states in urging the Administration to reverse layoffs that have gutted key U.S. Department of Education offices serving students with disabilities. Massive layoffs have decimated offices including OSEP, RSA, OCR, OESE, and OPE, which are responsible for protecting disability rights under IDEA and holding states accountable. The advocacy effort, timed during the 50th anniversary year of the Individuals with Disabilities Education Act, calls on Congress to restore staffing and protect educational access for children and adults with disabilities.GlobeNewswireFifteen Years of Hard Work Recognized with Exceptional Meritorious Service Award and Standing Ovation at the NDSC Annual Convention in Orlando FloridaMichelle Sie Whitten, president and CEO of Global Down Syndrome Foundation, received the Exceptional Meritorious Service Award from the National Down Syndrome Congress at its annual convention in Orlando, Florida. The award recognizes her work establishing the first Down syndrome research institute in the U.S. fifteen years ago and her advocacy that increased NIH funding from $16 million in 2004 to $130 million in 2023.GlobeNewswireGlobal Down Syndrome Foundation, the National Down Syndrome Congress, and the National Down Syndrome Society Highlight the FDA’s Public Warning About Risks Associated with Non-Invasive Prenatal ScreenThe FDA warned the public of false results and inappropriate use of non-invasive prenatal screening tests (NIPS). Three Down syndrome advocacy organizations—GLOBAL, NDSC, and NDSS—highlighted the warning and plan to release an updated pamphlet this summer. They urge accurate information for parents and physicians.GlobeNewswireAN UPDATED PRENATAL TESTING PAMPHLET ABOUT DOWN SYNDROME FOR PREGNANT WOMEN AND NEW PARENTSGlobal Down Syndrome Foundation, National Down Syndrome Congress, and National Down Syndrome Society announced a strategic collaboration to co-publish a free prenatal testing pamphlet. The resource, created in 2012, covers definitive versus non-definitive tests, expectations, milestones, and resources, and is available in English, Spanish, and Icelandic.PR NewswireNational Organizations Join Forces To Publish New COVID-19 & Down Syndrome ResourceA consortium of six national Down syndrome organizations published a new COVID-19 and Down Syndrome Resource on March 2, 2021, providing updated guidance on testing, vaccines, mental health, safety, and hospital advocacy for individuals with Down syndrome. The resource was developed following the CDC's December 2020 decision to add Down syndrome to its list of high-risk medical conditions for severe COVID-19 illness, based on studies showing adults with Down syndrome are four to five times more likely to be hospitalized and ten times more likely to die from COVID-19 complications. The resource is available in English and Spanish and is intended to help families and healthcare professionals navigate vaccine prioritization and appropriate care.PR NewswireGlobal Down Syndrome Foundation, National Down Syndrome Congress, & International Mosaic Down Syndrome Association Expand CollaborationsThe Global Down Syndrome Foundation, National Down Syndrome Congress, and International Mosaic Down Syndrome Association announced they are expanding existing collaborations to consolidate and create Down syndrome resources across the lifespan for families. The collaboration covers prenatal testing pamphlets, annual conventions, research conferences, and the Global Medical Care Guidelines for Adults with Down Syndrome, with plans to expand resources into additional languages and add virtual components to reach more attendees.PR NewswireLocal Family Takes Extra Steps to Raise Awareness About Research For Down SyndromeTJ Angus and his family are participating in the Miles for Breakthroughs 5K in Dallas to raise awareness and funds for Down syndrome research. The event, held during the National Down Syndrome Congress Convention, supports projects by the LuMind Research Down Syndrome Foundation aimed at developing therapies and improving quality of life for individuals with Down syndrome.