At 17, Hollie Amadio began a nine-year search for answers before being diagnosed with hereditary angioedema. Now, she’s an advocate, fighting for faster diagnoses and greater awareness.
Living Rare, Speaking Loud - a Column by Hollie Amadio
Recent Posts
- Rare genetic variant may help explain recurring angioedema attacks
- I’m grateful for my family of caregivers as we support one another
- Case study links blood pressure drug to woman’s stomach pain
- Being a caregiver means learning it’s OK to ask for help
- Blood pressure medicine tied to man’s severe tongue swelling