• Identifying and establishing trial sites.
• Collecting and monitoring patient data in sickle cell disease registries, across disparate geographies.
• Enhancing patient support and education during trials.
• Addressing ethical regulations and patient safety when conducting clinical research among pregnant persons with Sickle Cell Disease.

Early ML, Eke AC, Gemmill A, Lanzkron S, Pecker LH. Severe Maternal Morbidity and Mortality in Sickle Cell Disease in the National Inpatient Sample, 2012-2018. JAMA Netw Open. 2023 Feb 1;6(2):e2254552. doi: 10.1001/jamanetworkopen.2022.54552. PMID: 36729452; PMCID: PMC9896307.

...Bringing Reproductive Justice To The Forefront Of