We are the wAIHA Warriors
We've built a vibrant community for patients diagnosed with warm Autoimmune Hemolytic Anemia (wAIHA) and their caregivers.
How We Support Patients
Education
Education
Education
wAIHA Warriors produces quarterly webinars and publishes a bi-monthly newsletter. We are also planning our first wAIHA patient conference. Watch for more information.
Research
Education
Education
Through relationships with our industry partners and other rare disease organizations, we share information about the latest clinical trials, advances in research and treatments.
Advocacy
Education
Advocacy
Educating both our state and national lawmakers and engaging federal agencies such as the Dept. of Health and Human Services, CDC and FDA are priorities.
Our Sponsors & Partners
