National PKU Alliance
Non-profit OrganizationsVirginia, United States11-50 Employees
The National PKU Alliance was formed in 2008 by parents, grandparents, and individuals to become a national voice for those with Phenylketonuria (PKU).
Strong Financial Base With a revenue range of 10 million to 25 million dollars, the National PKU Alliance demonstrates robust financial stability, providing a solid foundation for potential partnerships, sponsorships, or funding services aimed at nonprofit organizations.
Leadership Transition The recent appointment of Lisa Milberg as Executive Director and board member Homayoon Rafatijo indicates active leadership development and strategic growth, presenting opportunities for collaboration in leadership training, executive coaching, or organizational development services.
Technological Engagement Utilizing a diverse tech stack including Cloudflare, Qgiv, and Yoast SEO highlights their focus on digital presence and engagement, opening doors for digital marketing, cybersecurity, and online fundraising tools tailored for nonprofit organizations.
Market Focus As a specialized nonprofit advocating for individuals with a rare genetic disorder, there is potential for sales of medical informatics, patient engagement solutions, or health data management platforms targeted at healthcare advocacy groups.
Community & Advocacy Founded by families and individuals, the organization’s mission to serve its community offers opportunities for engagement through community outreach programs, educational content, and support management solutions that enhance nonprofit outreach efforts.
National PKU Alliance uses 8 technology products and services including jsDelivr, Cloudflare, Qgiv, and more. Explore National PKU Alliance's tech stack below.
| National PKU Alliance Email Formats | Percentage |
| First.Last@npkua.org | 41% |
| First@npkua.org | 11% |
| FLast@npkua.org | 7% |
| First.Last@npkua.org | 41% |
Non-profit OrganizationsVirginia, United States11-50 Employees
The National PKU Alliance was formed in 2008 by parents, grandparents, and individuals to become a national voice for those with Phenylketonuria (PKU).
National PKU Alliance's revenue is estimated to be in the range of $10M$25M
National PKU Alliance's revenue is estimated to be in the range of $10M$25M