NADF
NADF is a U.S. 501(c)(3) nonprofit that educates, supports, and advocates for patients with adrenal diseases through educational content, clinical tools, and peer support, with global reach via the International Adrenal Consortium.
- Company typePrivate
- Founded1994
- HeadquartersNewton, United States
- Headcount1–10
- GTM typeB2B and B2C
- OfferingServices
What NADF does
The National Adrenal Diseases Foundation (NADF) is a U.S.-based nonprofit 501(c)(3) organization (EIN #11-2777036) that educates, supports, and advocates for patients affected by adrenal diseases including Addison's disease, Cushing's syndrome, congenital adrenal hyperplasia, secondary adrenal insufficiency, pheochromocytoma, adrenoleukodystrophy, primary aldosteronism, and adrenal incidentaloma. Founded in 1994 (firmographics lists 1985; the 1994 date is corroborated by executive tenure records) and headquartered in Newton, USA, the organization operates with 1-10 staff and serves patients, caregivers, and healthcare professionals through a globally distributed model.
NADF delivers its mission through educational content (the 'All Things Adrenal' podcast, 'A Day in the Life' blog, video library, Q&A, and multi-language patient resources), clinical support tools (Pediatric Adrenal Insufficiency Action Plan with Pictograms co-developed with Walter Reed, Adrenal Crisis Emergency Resources including the 2025-updated Alert Flyer, Stress Dosing Guide, Hormone Replacement Protocol, Emergency Injection Kit instructions, and MedicAlert medical-ID resources), community services (peer support groups hosted on the Inspire platform, patient-recommended doctors directory), and research facilitation (MyAI Study, clinical trials information, and the historic 1997 North American Survey of Addison's Disease). The technology infrastructure is a Squarespace-hosted website serving as the primary digital hub; no proprietary software platform, mobile app, API, or AI capabilities are disclosed.
The organization is funded by tax-deductible individual donations and corporate sponsorships from ETON Pharma, Neurocrine Biosciences, and Recordati. All services are provided free of charge. Geographic reach extends internationally through NADF's participation in the International Adrenal Consortium (IAC), a network of 20 patient advocacy organizations across Europe, North and South America, and Australia, and through formal partnerships with NORD, Global Genes, the Endocrine Society, the International Society of Endocrinology, the Pediatric Endocrine Society, the American Association of Endocrine Surgeons, MedicAlert, and Inspire.
NADF firmographics
Firmographics- Name
- NADF
- Legal name
- National Adrenal Diseases Foundation
- Website
- https://nadf.us
- Company type
- Private
- Founded year
- 1994
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Short description
- NADF is a U.S. 501(c)(3) nonprofit that educates, supports, and advocates for patients with adrenal diseases through educational content, clinical tools, and peer support, with global reach via the International Adrenal Consortium.
- Ownership category
- akta.pro rank
NADF industry classification
Industry- Product category
- Rare Disease Patient Advocacy
- NAICS
- Voluntary Health Organizations (813212), Individual and Family Services (6241)
- SIC
- Services-Educational Services (8200)
- akta.pro primary industry
- Adrenal Disorders (HLAKADAH)
- akta.pro secondary industry
- Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS) (BPAGACAA)
Keywords
Where NADF is headquartered
LocationHeadquarters
- HQ city
- Newton
- HQ country
- United States
- HQ region
- North America
Markets served
NADF business model
Business model- GTM type
- B2B and B2C
- Offering type
- Services
- Cost components
- Personnel, Operations, Marketing or Sales, Technology or R&D
Revenue model
- Donations: NADF operates as a 501(c)(3) nonprofit organization (ID #11-2777036) and relies on tax-deductible donations from individuals, memorial/tribute donations, and corporate sponsorships to fund education, support, and research programs.
- Corporate Donations: Corporate donors including ETON Pharma, Neurocrine Biosciences, and Recordati provide financial support as part of the organization's funding model.
Go-to-market motion1 record
Distribution channels5 records
Marketing channels7 records
NADF product offering
Product offeringCore offering
NADF is a nonprofit patient advocacy organization that delivers free education, emergency preparedness resources, peer support, and research support to individuals affected by adrenal diseases (Addison's disease, Cushing's syndrome, CAH, secondary adrenal insufficiency, pheochromocytoma, ALD, primary aldosteronism, adrenal incidentaloma). It serves patients, caregivers, and healthcare professionals through educational content (podcast, blog, videos, downloadable guides), clinical tools (Adrenal Crisis Alert Flyer, Pediatric Action Plan with pictograms, hormone replacement protocols), community services (support groups, patient-recommended doctors directory), and awareness campaigns (Adrenal Disease Awareness Month).
Product overview
NADF (National Adrenal Diseases Foundation) is a nonprofit 501(c)(3) organization that operates as a patient advocacy and educational resource platform rather than a traditional technology product company. The organization provides a portfolio of patient education resources, clinical support tools, and community services focused on adrenal diseases including Addison's disease, Cushing's syndrome, congenital adrenal hyperplasia, and other adrenal disorders. The core offerings include educational content (podcasts, blogs, videos), clinical tools (Adrenal Crisis Emergency Resources, Pediatric Adrenal Insufficiency Action Plan with Pictograms, Hormone Replacement Protocols), patient resources (emergency kit instructions, medical ID recommendations), community services (support groups, doctor referrals), and research initiatives (MyAI Study, North American Survey). The organization does not operate a unified software platform but rather provides downloadable resources, links to external tools, and virtual programs including an annual conference.
Differentiator
Problem solved
Functional benefit
Products and services
- MyAI Study Research study initiative for individuals with adrenal diseases, providing an exclusive NADF channel for patient participation in clinical research.
- All Things Adrenal Podcast Educational podcast series covering topics related to adrenal diseases, adrenal insufficiency, and patient care.
- A Day in the Life Blog Blog featuring patient stories and perspectives about daily life experiences with adrenal disease.
- Pediatric Adrenal Insufficiency Action Plan with Pictograms Low-health-literacy pictographic action plan tool designed to help parents and clinicians take appropriate medical action for children with adrenal insufficiency. Developed in collaboration with Dr. Patrick Reeves at Walter Reed National Military Medical Center.
- Adrenal Crisis Emergency Resources Critical emergency intervention resources including the Adrenal Crisis Alert Flyer, Emergency Injection Technique instructions, Endocrine Society Guidelines, and StatPearl Adrenal Crisis reference materials.
- Adrenal Hormone Replacement Protocol and Quick Guide Downloadable protocol and quick guide for adrenal hormone replacement therapy for patients and healthcare providers.
- NADF Stress Dosing Guide Stress dosing guidelines document providing patients with instructions on adjusting medication during illness or stressful situations.
- Emergency Kit Instructions PDF instructions for assembling and using an emergency injection kit for adrenal crisis situations, including Solu-Cortef administration guidance.
- Medical Identification Resources Resources recommending MedicAlert jewelry and providing free emergency wallet cards with treatment instructions for emergency medical personnel.
- Support Groups Peer support group programs connecting patients and caregivers affected by adrenal diseases.
- Patient Recommended Doctors Directory Directory of healthcare providers recommended by NADF patients for adrenal disease care.
- Clinical Trials & Surveys Information Information about ongoing clinical trials and survey opportunities for adrenal disease research participation.
- North American Survey of Individuals with Addison's Disease (1997) First comprehensive survey of individuals with Addison's disease in North America, conducted in 1997 with 700 responses, providing statistical data on diagnosis, treatment, quality of life, and associated autoimmune conditions.
- Connecting the Dots in Adrenal Care Conference Annual virtual patient/provider roundtable conference featuring medical experts discussing adrenal disease topics, including emergency care and self-advocacy.
- Adrenal Disease Awareness Month (AADAM) Annual awareness month campaign (April) featuring educational activities, landmark light-up events, proclamations, and community engagement initiatives.
Companies that use NADF
Customer profileSegments3 records
Ideal customer profiles2 records
NADF technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
NADF partnerships and signals
Strategic signalPartnerships
16 partnerships are on record, tiered core and minor.
- International Adrenal Consortium (IAC)coreNADF participates in the IAC, a global network of 20 patient advocacy organizations across Europe, North and South America, and Australia, dedicated to supporting individuals affected by adrenal diseases. The IAC launched International Adrenal Disease Awareness Day on April 7th.
- National Organization for Rare Disorders (NORD)coreNADF is a member of NORD, the leading organization representing the rare disease community in the United States. This membership provides advocacy resources and collaborative opportunities for rare adrenal diseases.
- Global GenescoreNADF participates in the Global Genes community of rare disease organizations, providing resources and support for patients with rare genetic adrenal conditions.
- American Association of Endocrine Surgeons (AAES)coreCollaborative partnership for the annual International Adrenal Disease Awareness Day webinar 'Adrenal Awareness: Separating Myth from Fact' featuring medical experts from AAES including Dr. Priya Dedhia, Dr. Lauren Fishbein, Dr. Matt Nehs, and Dr. Anatoliy Rudin.
- Walter Reed National Military Medical CentercorePartnership with Dr. Patrick Reeves at Walter Reed to develop the Pediatric Adrenal Insufficiency Action Plan with pictograms - a low-health-literacy tool to improve parents' and clinicians' ability to comprehend and act on pediatric adrenal insufficiency protocols. Video instructions produced for patients and clinicians.
- Endocrine SocietycoreLeading professional organization that formally recognizes April 7th as International Adrenal Disease Awareness Day, advancing accurate diagnosis and treatment innovation.
- International Society of EndocrinologycoreGlobal professional organization recognizing International Adrenal Disease Awareness Day and supporting adrenal disease education initiatives.
- Pediatric Endocrine SocietycoreProfessional society supporting pediatric adrenal disease awareness and education efforts through recognition of International Adrenal Disease Awareness Day.
- American Society of Endocrine SurgeonscoreProfessional surgical organization collaborating with NADF on the 'Adrenal Awareness: Separating Myth from Fact' webinar for the 2026 International Adrenal Disease Awareness Day.
- A5 – the American, Asia, and Australia Alliance of ResearcherscoreInternational research alliance recognizing International Adrenal Disease Awareness Day and contributing to global adrenal disease research efforts.
- Spanish Society of Endocrinology and Nutrition (SEEN)coreSpanish professional endocrinology society recognizing and supporting International Adrenal Disease Awareness Day initiatives.
- Spanish Federation for Rare Diseases (FEDER)coreSpanish rare disease federation supporting adrenal disease awareness and patient advocacy efforts.
- Official College of Physicians of Málaga (COMMALAGA)coreSpanish medical professional organization recognizing International Adrenal Disease Awareness Day.
- MedicAlert FoundationcoreMedicAlert provides emergency medical identification services recommended by NADF for all patients with adrenal insufficiency. The partnership promotes medical ID bracelets that alert emergency responders to patients' condition and need for stress dose corticosteroids.
- InspirecoreNADF hosts its patient community group on the Inspire platform, connecting patients and caregivers for peer support and shared experiences.
- Hospital Italiano de Buenos AiresminorHospital organizing monthly adrenal insufficiency workshops in Spanish starting April 10, supporting awareness month activities.
Scale indicators5 records
Recent moves6 records
Expansion highlights5 records
NADF competitors and assessment
Company assessmentOthers
- Endocrine Society: Leading global professional organization for endocrinology research and practice. Comparable as the premier professional society recognizing NADF's International Adrenal Disease Awareness Day and a key partner for clinical content and physician-facing resources.
- MedicAlert Foundation: Nonprofit providing emergency medical identification (bracelets, necklaces) recommended by NADF for all adrenal insufficiency patients. Comparable as a fellow nonprofit operating in the adrenal crisis emergency preparedness ecosystem where NADF directs patients for medical IDs.
- Inspire: Online patient community platform hosting NADF's National Adrenal Diseases Foundation patient community group. Comparable as the underlying community infrastructure provider that enables NADF's peer support group experience.
- American Association of Endocrine Surgeons (AAES): US professional society of endocrine surgeons that co-hosts NADF's annual awareness webinar. Comparable as a clinician-side counterpart that NADF partners with for surgical-adrenal content and physician referral channels.
Direct peers
- Cushing's Support & Research Foundation: Patient advocacy nonprofit dedicated specifically to Cushing's syndrome, one of the adrenal diseases NADF also covers. Directly comparable as a US disease-specific adrenal patient advocacy organization serving an overlapping patient population with similar educational and support offerings.
- Adrenal Insufficiency United: Patient advocacy organization focused on adrenal insufficiency. Directly comparable to NADF as an adrenal-specific patient advocacy nonprofit providing education, support groups, and emergency resources for the same core patient community.
- Pheo Para Alliance: Patient advocacy nonprofit focused on pheochromocytoma and paraganglioma, both adrenal tumors covered by NADF's disease library. Comparable as a fellow adrenal-condition-specific patient advocacy organization serving an overlapping rare disease patient population.
Broad incumbents
- Global Genes: US-based rare disease advocacy nonprofit with a global community of rare disease organizations, of which NADF is a participant. Comparable as a fellow disease-agnostic rare disease platform that NADF engages with for advocacy resources and collaborative programming.
- National Organization for Rare Disorders (NORD): Umbrella US nonprofit for the rare disease community; NADF is a NORD member organization. Comparable as a higher-tier rare disease advocacy body that NADF operates within, with overlapping member, donor, and advocacy ecosystems.
Emerging players
- The MAGIC Foundation: US nonprofit supporting families affected by various endocrine-related conditions including adrenal and growth disorders. Comparable as a fellow endocrine-focused patient advocacy nonprofit with overlapping educational resource and family support missions.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
NADF social profiles
Digital presenceNADF financial estimates
Financial estimateRevenue estimate
Valuation estimate
NADF leadership team
Management profileNumber of profiles
Profiles4 records
NADF funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
NADF M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about NADF
What does NADF do?
NADF is a nonprofit patient advocacy organization that delivers free education, emergency preparedness resources, peer support, and research support to individuals affected by adrenal diseases (Addison's disease, Cushing's syndrome, CAH, secondary adrenal insufficiency, pheochromocytoma, ALD, primary aldosteronism, adrenal incidentaloma). It serves patients, caregivers, and healthcare professionals through educational content (podcast, blog, videos, downloadable guides), clinical tools (Adrenal Crisis Alert Flyer, Pediatric Action Plan with pictograms, hormone replacement protocols), community services (support groups, patient-recommended doctors directory), and awareness campaigns (Adrenal Disease Awareness Month).
Is NADF a public or private company?
NADF is a private company. It is classified as nonprofit foundation owned and is currently operating.
When was NADF founded?
NADF was founded in 1994. It employs 1 to 10 people.
Where is NADF based?
NADF is headquartered in Newton, United States, in the North America region.
How does NADF make money?
Two revenue lines are on record. Donations are the primary driver. The others are corporate Donations.
Who are NADF's main competitors?
Others on record are Endocrine Society, MedicAlert Foundation, Inspire and American Association of Endocrine Surgeons (AAES). Direct peers are Cushing's Support & Research Foundation, Adrenal Insufficiency United and Pheo Para Alliance. Broad incumbents are Global Genes and National Organization for Rare Disorders (NORD). The MAGIC Foundation is listed as an emerging player.
Does NADF have an API?
No public API is recorded for NADF.
What industry is NADF in?
NADF's product category is Rare Disease Patient Advocacy. Its primary akta.pro industry code is HLAKADAH, Adrenal Disorders, with a secondary code of BPAGACAA, Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS). Its NAICS code is 813212 and its SIC code is 8200.