Hemophilia Foundation of Northern California
The Northern California Bleeding Disorders Foundation (NorCalBDF) is a 1958-founded nonprofit that provides free advocacy, education, outreach, and support services to individuals and families affected by hemophilia, von Willebrand disease, and other bleeding disorders throughout Northern California.
- Company typePrivate
- Founded-
- HeadquartersMorgan Hill, United States
- Headcount11–50
- GTM typeB2C
- OfferingServices
What Hemophilia Foundation of Northern California does
The Hemophilia Foundation of Northern California, operating as the Northern California Bleeding Disorders Foundation (NorCalBDF), is a 501(c)(3) nonprofit patient advocacy organization founded in 1958 and headquartered at a mailing address in Morgan Hill, California. The organization serves individuals and families affected by bleeding disorders — including hemophilia, von Willebrand disease, platelet disorders, and other rare bleeding conditions — throughout Northern California. Its mission is to provide advocacy, education, outreach, and support services free of charge to the community, with no commercial pricing model in place.
NorCalBDF's service portfolio comprises a unified set of community programs rather than a technology product platform. Core offerings include an advocacy program; culturally-specific programs for Asian Pacific (Asian Pacific Infusion), Latino (Familia de Sangre, Latino Community Bleeding Disorder Education), and women/girls (The Female Factor Retreat) populations; residential programming (Camp Hemotion, Family Camp); community events (Unite for Bleeding Disorders Walk, Springfest, WinterFest in San Jose and Fresno, Santa Rosa Fall Summit); an Emergency Assistance Program; and educational resources including a Bleeding Assessment Test, a directory of local Hemophilia Treatment Centers, crisis resources, and the quarterly INFUSIONS newsletter. The organization maintains a multi-channel presence across its website, social media (Facebook, LinkedIn, Instagram, YouTube, Twitter/X), and in-person events.
The business model is donation- and grant-funded rather than revenue-generating, with services delivered free to community members. Outreach is conducted through a 16-person staff and a board governance structure, with Ashley Gregory serving as Associate Director of Education & Advocacy. The organization does not disclose funding rounds, revenue figures, or financial metrics in the available source material.
Hemophilia Foundation of Northern California firmographics
Firmographics- Name
- Hemophilia Foundation of Northern California
- Legal name
- Northern California Bleeding Disorders Foundation
- Website
- https://hemofoundation.org
- Company type
- Private
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- The Northern California Bleeding Disorders Foundation (NorCalBDF) is a 1958-founded nonprofit that provides free advocacy, education, outreach, and support services to individuals and families affected by hemophilia, von Willebrand disease, and other bleeding disorders throughout Northern California.
- Ownership category
- akta.pro rank
Hemophilia Foundation of Northern California industry classification
Industry- Product category
- Nonprofit Patient Advocacy
- NAICS
- Voluntary Health Organizations (813212), Other Individual and Family Services (624190)
- SIC
- Services-Social Services (8300), Services-Health Services (8000)
- akta.pro primary industry
- Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS) (BPAGACAA)
- akta.pro secondary industry
- Rare Disease & Special Needs Support Organizations (BPAGACAM)
Keywords
Where Hemophilia Foundation of Northern California is headquartered
LocationHeadquarters
- HQ city
- Morgan Hill
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Hemophilia Foundation of Northern California business model
Business model- GTM type
- B2C
- Offering type
- Services
- Cost components
- Personnel, Operations, Marketing or Sales
Distribution channels1 record
Marketing channels8 records
Hemophilia Foundation of Northern California product offering
Product offeringCore offering
A nonprofit patient advocacy organization that delivers advocacy, education, outreach, and support services free of charge to individuals and families in Northern California affected by bleeding disorders, including hemophilia, von Willebrand disease, and platelet disorders. Offerings span culturally-tailored community programs (Asian Pacific Infusion, Familia de Sangre, Latino Community Bleeding Disorder Education), recreational camps (Camp Hemotion, Family Camp), community-building events (Springfest, The Female Factor Retreat, Unite for Bleeding Disorders Walk), emergency financial assistance, crisis resources, and a quarterly newsletter (INFUSIONS).
Product overview
The Northern California Bleeding Disorders Foundation operates as a non-profit organization offering a unified portfolio of community support programs and resources rather than a technology product platform. The core offerings include advocacy services, culturally-specific community programs (Asian Pacific Infusion, Familia de Sangre, Latino Community Education), recreational camps (Camp Hemotion, Family Camp), community events (Springfest, The Female Factor Retreat, Unite for Bleeding Disorders Walk), emergency assistance, educational resources (Bleeding Assessment Test, HTC Directory), and the quarterly INFUSIONS newsletter. These programs collectively serve the needs of the bleeding disorders community through advocacy, education, outreach, and support.
Differentiator
Problem solved
Functional benefit
Products and services
- Advocacy Program Advocacy services supporting individuals and families affected by bleeding disorders through education, policy support, and navigation of healthcare and patient rights resources.
- Asian Pacific Infusion Specialized program providing culturally appropriate support and education for Asian Pacific community members affected by bleeding disorders.
- Camp Hemotion Annual recreational camp program for individuals with bleeding disorders, providing community connection and outdoor experiences; Camp Hemotion 2026 is referenced as upcoming.
- Familia de Sangre Spanish-language family support program providing education and resources for Latino families affected by bleeding disorders.
- Family Camp Family-oriented camp experience designed to support families dealing with bleeding disorders through shared recreation and education.
- Latino Community Bleeding Disorder Education Educational outreach program specifically designed for the Latino community to raise awareness and provide information about bleeding disorders.
- Springfest Seasonal community event bringing together individuals and families affected by bleeding disorders.
- The Female Factor Retreat Retreat program focused on the needs of women and girls affected by bleeding disorders.
- Unite for Bleeding Disorders Walk Annual fundraising walk bringing together the bleeding disorders community, scheduled in Walnut Creek and other Northern California locations.
- Emergency Assistance Program Crisis support resource providing emergency financial assistance to individuals with bleeding disorders facing urgent needs.
- INFUSIONS Newsletter Quarterly newsletter providing updates, education, and community news for the bleeding disorders community.
- Local Hemophilia Treatment Centers (HTCs) Directory Directory of local Hemophilia Treatment Centers providing care and management resources for the bleeding disorders community.
Companies that use Hemophilia Foundation of Northern California
Customer profileSegments1 record
Ideal customer profiles2 records
Hemophilia Foundation of Northern California technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Hemophilia Foundation of Northern California partnerships and signals
Strategic signalScale indicators1 record
Recent moves6 records
Expansion highlights6 records
Hemophilia Foundation of Northern California competitors and assessment
Company assessmentEmerging players
- Factor My DNA: A bleeding disorders patient community and education platform serving patients and families with hemophilia and related conditions. Comparable target audience and educational mission to NorCalBDF, with a more digital-native delivery model.
Direct peers
- Central California Hemophilia Foundation: A California-based regional chapter serving bleeding disorders patients in Central California with education, advocacy, and family support programs. Highly comparable in scope, structure, and disease focus to NorCalBDF as a fellow state chapter.
- Hemophilia Association of San Diego County: A regional bleeding disorders nonprofit serving San Diego County with community education, advocacy, and patient support services. Another California-based chapter peer with similar operational model and constituent base.
- Bleeding Disorders Foundation of Washington: A regional chapter serving the bleeding disorders community in Washington state, providing similar programs including education, advocacy, camps, and emergency assistance. A Pacific Northwest regional peer with comparable nonprofit structure and mission.
- Hemophilia Foundation of Southern California: A regional bleeding disorders chapter serving Southern California with similar programs including camps, advocacy, and patient education. Closest direct peer given same state, same disease focus, and comparable nonprofit chapter structure.
Broad incumbents
- National Organization for Rare Disorders (NORD): A national umbrella organization representing the rare disease community, including bleeding disorders. Operates overlapping disease-specific patient support and policy advocacy with comparable nonprofit infrastructure and donor base.
- National Hemophilia Foundation: The national umbrella organization for bleeding disorders in the US, providing advocacy, education, and research funding across all states. Directly comparable mission to NorCalBDF but operates at national scale and likely funnels referrals and resources to regional chapters.
- Hemophilia Federation of America: A national patient-led organization serving the bleeding disorders community through advocacy, education, and community support programs. Operates overlapping mission and programs with NorCalBDF, particularly around community education, family programming, and policy advocacy.
- World Federation of Hemophilia: The global umbrella organization for hemophilia and bleeding disorders, focused on improving access to treatment and care worldwide. Operates the bleeding disorders community space with similar advocacy and education mission but at international scale.
Others
- American Cancer Society (California Division): A large national health nonprofit operating with regional chapters in California providing patient support, advocacy, and disease education. Comparable as a regional health nonprofit serving California communities, though focused on a different disease vertical.
Market position
Strengths4 records
Weaknesses3 records
Competitive moat5 records
Key risks5 records
Key highlights5 records
Customer concentration
Hemophilia Foundation of Northern California social profiles
Digital presenceHemophilia Foundation of Northern California financial estimates
Financial estimateRevenue estimate
Valuation estimate
Hemophilia Foundation of Northern California leadership team
Management profileNumber of profiles
Profiles1 record
Hemophilia Foundation of Northern California funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Hemophilia Foundation of Northern California 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 Hemophilia Foundation of Northern California
What does Hemophilia Foundation of Northern California do?
A nonprofit patient advocacy organization that delivers advocacy, education, outreach, and support services free of charge to individuals and families in Northern California affected by bleeding disorders, including hemophilia, von Willebrand disease, and platelet disorders. Offerings span culturally-tailored community programs (Asian Pacific Infusion, Familia de Sangre, Latino Community Bleeding Disorder Education), recreational camps (Camp Hemotion, Family Camp), community-building events (Springfest, The Female Factor Retreat, Unite for Bleeding Disorders Walk), emergency financial assistance, crisis resources, and a quarterly newsletter (INFUSIONS).
Is Hemophilia Foundation of Northern California a public or private company?
Hemophilia Foundation of Northern California is a private company. It is classified as nonprofit foundation owned and is currently operating.
When was Hemophilia Foundation of Northern California founded?
Hemophilia Foundation of Northern California was founded in -1. It employs 11 to 50 people.
Where is Hemophilia Foundation of Northern California based?
Hemophilia Foundation of Northern California is headquartered in Morgan Hill, United States, in the North America region.
Who are Hemophilia Foundation of Northern California's main competitors?
Factor My DNA is listed as an emerging player. Direct peers are Central California Hemophilia Foundation, Hemophilia Association of San Diego County, Bleeding Disorders Foundation of Washington and Hemophilia Foundation of Southern California. Broad incumbents are National Organization for Rare Disorders (NORD), National Hemophilia Foundation, Hemophilia Federation of America and World Federation of Hemophilia. American Cancer Society (California Division) is listed as an others.
Does Hemophilia Foundation of Northern California have an API?
No public API is recorded for Hemophilia Foundation of Northern California.
What industry is Hemophilia Foundation of Northern California in?
Hemophilia Foundation of Northern California's product category is Nonprofit Patient Advocacy. Its primary akta.pro industry code is BPAGACAA, Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS), with a secondary code of BPAGACAM, Rare Disease & Special Needs Support Organizations. Its NAICS code is 813212 and its SIC code is 8300.