
Aubrey Whelan
Health Reporter at The Philadelphia Inquirer
Reporter at Philly Health Insider
Reporter covering addiction and public health for @PhillyInquirer. Contact me at [email protected]! Pronouns: she/her.
Articles
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2 days ago |
inquirer.com | Aubrey Whelan |Kayla Yup |Stephen Stirling |Lizzie Mulvey
President Donald Trump’s administration says it has cut tens of millions of dollars in research funding from universities and research centers in Philadelphia. The Inquirer has been tracking these cuts for months, analyzing the impact to research in the region from the grant terminations playing out nationally.
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2 weeks ago |
inquirer.com | Aubrey Whelan
Philadelphians who want to eat healthier don’t have to sacrifice taste or money to do so. Demonstrating how to prepare familiar dishes that pack in flavor with less fat and salt are the focus of regular “lunch and learn” events by the Frazier Family Coalition for Stroke Prevention and Education, a North Philadelphia-based stroke prevention organization.
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3 weeks ago |
gazettextra.com | Aubrey Whelan
PHILADELPHIA - KJ Muldoon, an infant with a life-threatening metabolic disorder who received a pioneering gene-editing therapy at Children's Hospital of Philadelphia, went home Tuesday after 307 days at the hospital, CHOP announced. KJ risked irreparable brain damage from his condition, called severe carbamoyl phosphate synthetase 1 (CPS1) deficiency, in which his liver could not process protein. CPS1 deficiency is deadly in more than half of cases. Copyright 2025 Tribune Content Agency.
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3 weeks ago |
thederrick.com | Aubrey Whelan
PHILADELPHIA — KJ Muldoon, an infant with a life-threatening metabolic disorder who received a pioneering gene-editing therapy at Children’s Hospital of Philadelphia, went home Tuesday after 307 days at the hospital, CHOP announced. KJ risked irreparable brain damage from his condition, called severe carbamoyl phosphate synthetase 1 (CPS1) deficiency, in which his liver could not process protein. CPS1 deficiency is deadly in more than half of cases.
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3 weeks ago |
miamiherald.com | Aubrey Whelan
PHILADELPHIA - KJ Muldoon, an infant with a life-threatening metabolic disorder who received a pioneering gene-editing therapy at Children's Hospital of Philadelphia, went home Tuesday after 307 days at the hospital, CHOP announced. KJ risked irreparable brain damage from his condition, called severe carbamoyl phosphate synthetase 1 (CPS1) deficiency, in which his liver could not process protein. CPS1 deficiency is deadly in more than half of cases.
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