Rare disease news

FDA approvals, research breakthroughs, clinical trials, and advocacy updates

Curated and summarized by AI for patients and caregivers

🔍
AllDrug approvalsClinical trialsResearchGrants & fundingAdvocacy & policyPipeline
Show:All newsBreaking onlyImportant & breaking
Date:7 days30 days90 daysAll time

3 articles from the last 90 days matching "living with rare disease"

NewsRSS6 days ago

Flying High With AATD: Finding Inspiration From a Movie

A patient with AATD (Alpha-1 Antitrypsin Deficiency) found personal inspiration by watching the movie Top Gun: Maverick, discovering parallels between the fighter pilot's perseverance and their own journey managing a chronic lung disease. The article explores how popular culture can provide emotional support and motivation for people living with rare diseases. This is a personal reflection piece rather than medical news.

WHY IT MATTERSFor AATD patients, finding relatable stories and sources of inspiration in everyday media can help combat the isolation and emotional burden of managing a progressive genetic lung disease.
Good to knowAlpha-1 Antitrypsin DeficiencyRead →
NewsRSS6 days ago

The gift of a song reminds me that my son is more than his challenges

A parent shares a personal story about receiving a song recording from their son with hemophilia, reflecting on how their child's talents and abilities extend far beyond his medical condition. The article emphasizes that people living with rare diseases like hemophilia are whole individuals with gifts and passions that deserve recognition. This piece appears in Hemophilia News Today and focuses on the emotional and human side of living with a chronic blood disorder.

WHY IT MATTERSFor parents and caregivers of children with hemophilia, this story validates the importance of seeing their child as a complete person with abilities and dreams, not just defined by their bleeding disorder diagnosis.
Good to knowhemophiliaRead →
ResearchUNITERAREApr 3

New Recruiting Trial: Stakeholders of Rare Diseases Informing Values In Neuroethics

This is a research study looking for patients and families affected by rare diseases to share their thoughts and values about brain and nerve-related medical decisions. Researchers at St. Jude Children's Research Hospital want to understand what matters most to people living with rare diseases so they can make better ethical decisions in medical research and treatment. The study is now accepting participants and will start in April 2026.

WHY IT MATTERSThis study gives rare disease patients and caregivers a direct voice in shaping how medical ethics and brain-related research decisions are made — your input could influence future treatment guidelines and research practices.
Good to knowRead →

Get personalized rare disease news

Follow your conditions to see news about the diseases that matter to you — FDA approvals, trial openings, and research breakthroughs.

Create free account →Browse diseases