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	Profile	Recent Articles on Subject
1	Theresa Gaffney STAT News Audio producer, health reporter. Boston audio productionhealth reporting	A STAT Investigation: Pain, loss, and coercive care - 7 days ago Morning Rounds: Inside the making of the first malaria vaccine - 4 months ago Morning Rounds: Why some doctors plan to quit their jobs - 11 months ago STAT Morning Rounds: Six health news stories you need to start your day - 12 months ago
2	Meagan Parrish Pharma Voice Senior editor @industrydive. Pharma world follower. Wisconsin, USA pharmaceuticalsjournalismparenting	A sickle cell cure exists. But patients need more than just gene therapy. - 17 days ago 2024 PharmaVoice 100s: Rare Disease Warriors - 20 days ago Behind a big-name rare disease biotech, an exec draws from personal experience - 9 months ago
3	Brittany Trang STAT News Health care business reporter. PhD. Indie rock fan. health carebusiness reporting	Morning Rounds: Newborn screenings, radiation-proof tardigrades - 24 days ago
4	Frank Vinluan MedCity News Medical innovation tracker. MedCity, USA medicalinnovation	Sanofi Drug for Rare Blood Disease Is Heading to Recordati for $825M - about 1 month ago AstraZeneca’s Rare Disease Pipeline Notches Another FDA Approval - 8 months ago
5	Ashley Gallagher, Associate Editor Pharmacy Times One of Cabra girls on GoggleboxIRL. Dublin City, Ireland televisionentertainment	FDA Grants Orphan Drug Designation to PPL-002 for the Treatment of Danon Disease - about 2 months ago FDA Grants Orphan Drug Designation to RAG-18 for Duchenne, Becker Muscular Dystrophy - 3 months ago
6	Randy Dotinga MedPage Today Indie scribbler, advocate. Board member, @ahcj. San Diego WritingAdvocacy	Gene Therapy Shows Promise in Rare Eye Disease That Causes Early Blindness - 2 months ago
7	John Pinching PharmaTimes Next-gen biopharma company. La Jolla, California biopharmadrugsdevices	World Sepsis Day 2024 highlights need for better sepsis treatments - 2 months ago
8	Jason Mast STAT News Writing about science, medicine. ScienceMedicineBusiness	STAT+: A rare disease program, portrayed as both lifeline and pharma handout, is set to expire - 2 months ago STAT+: FDA rejects Rocket Pharmaceuticals’ gene therapy for ultra-rare condition, another setback for field - 5 months ago STAT+: Avidity Biosciences says its experimental drug showed potential against form of muscular dystrophy - 5 months ago STAT+: Doudna institute hatches plan to ‘cure hundreds of diseases’ left behind by CRISPR revolution - 10 months ago STAT+: Peter Marks on creating Operation Warp Speed, but for rare diseases - about 1 year ago
9	John Wilkerson STAT News STAT Washington correspondent. Healthcare Journalism	STAT+: A rare disease program, portrayed as both lifeline and pharma handout, is set to expire - 2 months ago STAT+: ALS patients support bill that could help patients with other rare diseases - about 1 year ago
10	Kennedy Ferruggia, Assistant Editor Pharmacy Times #pharmacy news, insights. CE provider. Cranbury, New Jersey pharmacyhealthcarejournalism	FDA Grants Rare Pediatric Disease Designation to NS-050/NCNP-03 to Treat Muscle Wasting Disease - 2 months ago

Journalists covering Rare Disease Day