The Dysautonomia Project
The Dysautonomia Project is a 501(c)(3) nonprofit that educates dysautonomia patients, clinicians, and medical residents through an award-winning book, a free online video library (Autonomic Education), CME-accredited training, and the annual Residents Course mini-fellowship. Founded in 2014 and headquartered in Clearwater, Florida.
- Company typePrivate
- Founded2014
- HeadquartersClearwater, United States
- Headcount1–10
- GTM typeB2B and B2C
- OfferingServices
What The Dysautonomia Project does
The Dysautonomia Project, Inc. (TDP) is a 501(c)(3) nonprofit organization founded in 2014 and headquartered in Clearwater, Florida, that operates as the self-described global leader in dysautonomia education. The organization produces educational content and programming targeted at two primary constituencies: dysautonomia patients (undiagnosed, recently diagnosed, experienced, and pediatric) and clinicians/medical residents seeking training in autonomic medicine. TDP's product portfolio centers on a foundational book authored by founder Kelly Freeman with Dr. Randy Thompson and Dr. David Goldstein, the Autonomic Education online video library (a free, self-serve platform hosted at autonomiceducation.com), a Patient Assessment Tool for symptom screening and tracking, and structured training programs including The Residents Course (a three-day mini-fellowship for 36 medical residents per year presented with the American Autonomic Society), The Clinician Program (CME-accredited via joint providership with the Florida Medical Association), and DysCourse (a five-session virtual patient and caregiver education series).
TDP is governed by a board led by Carlton Ward (President) and advised by a medical advisory committee drawing from Mayo Clinic, Harvard/Mass General Brigham, UT Southwestern, Johns Hopkins All Children's, the Uniformed Services University, and Wellstar. Operationally, the staff is small, with an Executive Director (Angela Devlen), Director of Education (Cheryl Faber), and Development and Events Manager (Ashleigh Goforth) identified by name. TDP's distribution is digital-first and global, with free patient-facing resources distributed via the website, social media (Facebook, Instagram, YouTube), and email, while the Residents Course requires in-person attendance in Florida. There are no AI/ML products, APIs, or mobile applications in the portfolio.
The business model is donation- and event-driven rather than commercial. Revenue streams include individual and corporate donations, book sales, corporate event sponsorships with tiered pricing ($1,500 Friend to $15,000 Presenting for DysCourse), and proceeds from the annual Under the Umbrella Gala and Pi Day Give Day. Core patient resources are provided at no cost, and the Residents Course is fully funded by TDP; only the Clinician Program charges registration fees for CME credits. The organization relies on sponsors including CAC-HFF, Network People, Pinellas Community Foundation, JVK Foundation, Adtalem, Raymond James, AdventHealth, and Johns Hopkins All Children's, among others.
The Dysautonomia Project firmographics
Firmographics- Name
- The Dysautonomia Project
- Legal name
- The Dysautonomia Project, Inc.
- Website
- https://thedysautonomiaproject.org
- Company type
- Private
- Founded year
- 2014
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Short description
- The Dysautonomia Project is a 501(c)(3) nonprofit that educates dysautonomia patients, clinicians, and medical residents through an award-winning book, a free online video library (Autonomic Education), CME-accredited training, and the annual Residents Course mini-fellowship. Founded in 2014 and headquartered in Clearwater, Florida.
- Ownership category
- akta.pro rank
The Dysautonomia Project industry classification
Industry- Product category
- Patient and Clinician Health Education
- NAICS
- Voluntary Health Organizations (813212), Individual and Family Services (6241)
- SIC
- Services-Misc Health & Allied Services, Nec (8090), Services-Health Services (8000)
- akta.pro primary industry
- Autonomic Disorders (Dysautonomia) (HLAKAIAN)
- akta.pro secondary industry
- Movement Disorders (Parkinson’s, Tremor, Dystonia) (HLAKAIAC)
Keywords
Where The Dysautonomia Project is headquartered
LocationHeadquarters
- HQ city
- Clearwater
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
The Dysautonomia Project business model
Business model- GTM type
- B2B and B2C
- Offering type
- Services
- Cost components
- Personnel, Operations, Marketing or Sales, Technology or R&D, Others
Revenue model
- Donations and Fundraising: The organization relies on donations from individuals and corporate sponsors to fund its educational programs and initiatives.
- Book Sales: Sale of The Dysautonomia Project book, a cornerstone educational resource for providers and patients.
- Event Sponsorships: Corporate sponsorship tiers for DysCourse event ranging from $1,500 (Friend) to $15,000 (Presenting), providing marketing exposure and brand association.
- Gala and Annual Events: Under the Umbrella Gala serves as the premier annual fundraiser with sponsorship packages and auction items.
Go-to-market motion2 records
Distribution channels2 records
Marketing channels4 records
The Dysautonomia Project product offering
Product offeringCore offering
The Dysautonomia Project is a non-profit organization that educates patients, healthcare providers, and communities about dysautonomia and autonomic nervous system disorders. It delivers this through an award-winning educational book, a free online video library (Autonomic Education), CME-accredited clinician training programs, a resident mini-fellowship (The Residents Course), virtual patient education events (DysCourse), and a free online patient symptom assessment tool.
Product overview
The Dysautonomia Project is a non-profit organization offering a portfolio of educational products and programs centered on dysautonomia awareness and training. The core offerings include an award-winning book (The Dysautonomia Project Book) that serves as the foundational educational resource, DysCourse as a virtual patient and caregiver education event, The Clinician Program as a CME-accredited training program, and The Residents Course as a mini fellowship for medical residents. Supporting these are Autonomic Education (a free online video library) and a free Patient Assessment Tool for symptom screening. The organization also hosts the annual Under the Umbrella Gala and Pi Day Give Day fundraising events.
Differentiator
Problem solved
Functional benefit
Products and services
- The Dysautonomia Project Book
Quantifiable outcome
- Reduced average diagnosis time from 6 years to several months
Companies that use The Dysautonomia Project
Customer profileSegments2 records
Ideal customer profiles2 records
The Dysautonomia Project technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
The Dysautonomia Project partnerships and signals
Strategic signalPartnerships
Four partnerships are on record, tiered core, major and minor.
- American Autonomic Society (AAS)coreJoint partnership presenting The Residents Course mini-fellowship program for medical residents. AAS provides faculty and evidence-based content while TDP provides funding and administration.
- Florida Medical AssociationcoreJoint providership of CME-accredited medical training for the Clinician Program. FMA is accredited by ACCME to provide continuing medical education for physicians.
- JVK FoundationmajorSponsor and grantor supporting The Residents Course and other TDP programs.
- Clearwater Beach Marriott Resort on Sand KeyminorVenue partner for The Residents Course (February 2027) and Under the Umbrella Gala events.
Scale indicators3 records
Recent moves6 records
Expansion highlights5 records
The Dysautonomia Project competitors and assessment
Company assessmentDirect peers
- The EDS Society (Ehlers-Danlos Society): Disease-specific nonprofit providing patient and clinician education, CME programs and research grants for Ehlers-Danlos syndromes, which are frequently comorbid with dysautonomia. Closely comparable model: education-first nonprofit with CME, conferences, and clinical community building.
- Dysautonomia Support Network: Patient-centered nonprofit providing resources, advocacy and education across the dysautonomia spectrum. Direct peer with overlapping patient education, support directory and awareness missions.
- Dysautonomia International: Patient advocacy and education nonprofit focused on autonomic disorders, including POTS. Most directly comparable peer — same disease category, similar patient/clinician education mission, and competes for the same donor and awareness pool as TDP.
- Standing Up to POTS: Nonprofit focused on POTS (Postural Orthostatic Tachycardia Syndrome), a core dysautonomia subtype. Comparable mission of accelerating diagnosis, funding education, and supporting patients and clinicians in the same autonomic disorder space.
Emerging players
- Inspire: Digital health community platform connecting patients and caregivers across conditions, including autonomic disorders. Comparable online patient-education and peer-support mission delivered through a technology platform model rather than nonprofit events.
Broad incumbents
- National Organization for Rare Disorders (NORD): Large US umbrella nonprofit for rare diseases including dysautonomia subtypes. Comparable in nonprofit patient/physician education model but operates at much broader scope across 7,000+ rare diseases rather than a single condition.
- American Autoimmune Related Diseases Association (AARDA): National nonprofit advocating for and educating across autoimmune-related diseases, which often overlap with autonomic dysfunction. Comparable education, advocacy and clinician engagement model at a broader disease category.
Regional players
- POTS UK: UK-based charity dedicated to POTS and dysautonomia awareness, education and patient support. Mirrors TDP's disease focus and education-first nonprofit model but serves a primarily UK patient and clinician base.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
The Dysautonomia Project social profiles
Digital presenceThe Dysautonomia Project financial estimates
Financial estimateRevenue estimate
Valuation estimate
The Dysautonomia Project leadership team
Management profileNumber of profiles
Profiles15 records
The Dysautonomia Project funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
The Dysautonomia Project 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 The Dysautonomia Project
What does The Dysautonomia Project do?
The Dysautonomia Project is a non-profit organization that educates patients, healthcare providers, and communities about dysautonomia and autonomic nervous system disorders. It delivers this through an award-winning educational book, a free online video library (Autonomic Education), CME-accredited clinician training programs, a resident mini-fellowship (The Residents Course), virtual patient education events (DysCourse), and a free online patient symptom assessment tool.
Is The Dysautonomia Project a public or private company?
The Dysautonomia Project is a private company. It is classified as nonprofit foundation owned and is currently operating.
When was The Dysautonomia Project founded?
The Dysautonomia Project was founded in 2014. It employs 1 to 10 people.
Where is The Dysautonomia Project based?
The Dysautonomia Project is headquartered in Clearwater, United States, in the North America region.
How does The Dysautonomia Project make money?
Four revenue lines are on record. Donations and Fundraising is the primary driver. The others are book Sales, event Sponsorships and gala and Annual Events.
Who are The Dysautonomia Project's main competitors?
Direct peers on record are The EDS Society (Ehlers-Danlos Society), Dysautonomia Support Network, Dysautonomia International and Standing Up to POTS. Inspire is listed as an emerging player. Broad incumbents are National Organization for Rare Disorders (NORD) and American Autoimmune Related Diseases Association (AARDA). POTS UK is listed as a regional player.
Does The Dysautonomia Project have an API?
No public API is recorded for The Dysautonomia Project.
What industry is The Dysautonomia Project in?
The Dysautonomia Project's product category is Patient and Clinician Health Education. Its primary akta.pro industry code is HLAKAIAN, Autonomic Disorders (Dysautonomia), with a secondary code of HLAKAIAC, Movement Disorders (Parkinson’s, Tremor, Dystonia). Its NAICS code is 813212 and its SIC code is 8090.