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	Profile	Recent Articles on Subject
1	Meagan Parrish Pharma Voice Senior editor @industrydive. Pharma world follower. Wisconsin, USA pharmaceuticalsjournalismparenting	Musk’s rare disease torpedo, hospitals’ pharma fix and other policies leaders are tracking - 5 days ago The Dodgers’ World Series run brought attention to a rare disease. Annexon is stepping up to the plate. - 2 months ago A sickle cell cure exists. But patients need more than just gene therapy. - 3 months ago 2024 PharmaVoice 100s: Rare Disease Warriors - 3 months ago Behind a big-name rare disease biotech, an exec draws from personal experience - 11 months ago
2	Isabella Cueto STAT News Journalist on chronic disease. healthjournalism	2025’s looking like the year of chronic disease. Here are three issues to watch - about 1 month ago With a rare immunodeficiency disease, a performer and patient advocate learned lessons the hard way - over 1 year ago
3	The Conversation Science Alert Science news. Official account. Australia science news	Mysterious Fatal 'Disease X' Outbreak in Congo Still Can't Be Explained - about 1 month ago
4	Jonathan Wosen STAT News West Coast Biotech Reporter. Formerly @sdut. Stanford PhD. UCSC alum. San Diego, California BiotechLife SciencesImmunology	Sanofi advances a drug for a rare, platelet-destroying disease - about 2 months ago
5	Adam Feuerstein STAT News Reporter at STATnews. Dog lover. Polk Award winner. Boston, Massachusetts biotech reporting	Sanofi advances a drug for a rare, platelet-destroying disease - about 2 months ago Listen: The long journey to make malaria vaccines, and Sarepta’s ties with patient advocates - 6 months ago
6	Jason Mast STAT News Writing about science, medicine. ScienceMedicineBusiness	STAT+: Sarepta, Arrowhead Pharmaceuticals partner to advance RNA-based drugs in rare diseases - about 2 months ago STAT+: A rare disease program, portrayed as both lifeline and pharma handout, is set to expire - 4 months ago STAT+: FDA rejects Rocket Pharmaceuticals’ gene therapy for ultra-rare condition, another setback for field - 7 months ago STAT+: Avidity Biosciences says its experimental drug showed potential against form of muscular dystrophy - 7 months ago STAT+: Doudna institute hatches plan to ‘cure hundreds of diseases’ left behind by CRISPR revolution - about 1 year ago STAT+: Peter Marks on creating Operation Warp Speed, but for rare diseases - over 1 year ago
7	Ashley Gallagher, Associate Editor Pharmacy Times One of Cabra girls on GoggleboxIRL. Dublin City, Ireland televisionentertainment	FDA Grants Rare Pediatric Disease Designation for Treatment of Neonatal SP-B Deficiency - 2 months ago FDA Grants Orphan Drug Designation to PPL-002 for the Treatment of Danon Disease - 4 months ago FDA Grants Orphan Drug Designation to RAG-18 for Duchenne, Becker Muscular Dystrophy - 5 months ago
8	Theresa Gaffney STAT News Audio producer, health reporter. Boston audio productionhealth reporting	A STAT Investigation: Pain, loss, and coercive care - 2 months ago Morning Rounds: Why some doctors plan to quit their jobs - about 1 year ago STAT Morning Rounds: Six health news stories you need to start your day - about 1 year ago
9	Brittany Trang STAT News Health care business reporter. PhD. Indie rock fan. health carebusiness reporting	Morning Rounds: Newborn screenings, radiation-proof tardigrades - 3 months ago
10	Frank Vinluan MedCity News Medical innovation tracker. MedCity, USA medicalinnovation	Sanofi Drug for Rare Blood Disease Is Heading to Recordati for $825M - 4 months ago AstraZeneca’s Rare Disease Pipeline Notches Another FDA Approval - 10 months ago

Journalists covering Rare Disease Day