US EditionUPSHER-SMITH SHOWCASES ITS COMMITMENT TO DUCHENNE MUSCULAR DYSTROPHY COMMUNITY AS A TRUSTED PARTNER IN PEDIATRIC RARE DISEASES AT THE PARENT PROJECT MUSCULAR DYSTROPHY (PPMD) 2025 ANNUAL CONFERENCE
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30 Articles
30 Articles
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UPSHER-SMITH SHOWCASES ITS COMMITMENT TO DUCHENNE MUSCULAR DYSTROPHY COMMUNITY AS A TRUSTED PARTNER IN PEDIATRIC RARE DISEASES AT THE PARENT PROJECT MUSCULAR DYSTROPHY (PPMD) 2025 ANNUAL CONFERENCE
Visit Upsher-Smith at the PPMD 2025 Annual Conference Resource Fair to Learn More About Support Services and Resources Offered for Deflazacort Tablets
·Parsons, United States
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Living in the Canik district of Samsun, Elif Acar and Mustafa Can Kayacı’s 7-year-old child Mustafa Emir Kayacı was diagnosed with Duchenne Muscular Dystrophy (DMD) at the age of 1. A governorship-approved aid campaign was launched for Emir, who cannot run and play like his peers. 2.9 million dollars (approximately 115 million TL) is required for Emir’s treatment...
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Leaning Left0Leaning Right0Center17Last UpdatedBias Distribution100% Center
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