Why Rare Disease Month Matters to All of Us
Rare Disease Month in February and Rare Disease Day on February 28 recognizes the nearly... Continue reading »
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How to Support Those with Heart-Related Conditions
My first fainting episode happened under the fluorescent paneled lights of my biology class on... Continue reading »
Living with Rheumatic Heart Disease as an American Teen
Until I was around 12 years old, I was considered a generally healthy kid, with... Continue reading »
Legislators Heard From Us (But They Really Want to Hear From You!)
Last week, we sent our legislative priorities to more than 7,000 legislators across the country.... Continue reading »
Patients First, Progress Together: Reflecting on Our 2025 Impact
As we look at the Chronic Disease Coalition’s 2025 Impact Report, one thing is clear:... Continue reading »
Putting Patients First in 2026: The Coalition’s Policy Priorities
As we look toward 2026, the Chronic Disease Coalition (CDC) is focused on ensuring people... Continue reading »
From Patient to Policy Advocate: How My Journey With Chronic Illness Fueled My Passion for Healthcare Equity
Victoria Lopez is a high school senior from Florida and a CDC Ambassador.Hi everyone!My name... Continue reading »
Looking Ahead to 2026: Protecting Access in a Time of Change
Earlier this week the Chronic Disease Coalition board and Patient Advisory Council met to review... Continue reading »
Why SNAP Matters for People Living with Chronic Disease
For millions of Americans living with chronic disease, good nutrition isn’t just about maintaining health,... Continue reading »