In the second part of our series on congenital cytomegalovirus (CMV), we speak with two Nemours associates and mothers of children diagnosed with CMV at different stages of their journeys. They share personal stories of diagnosis, advocacy, resilience, and the everyday realities of parenting children affected by CMV.Nemours Children’s Health policy experts also join the conversation to discuss current efforts and ongoing needs at the state and federal levels, including raising awareness, improving screening and supporting families through initiatives like the STOP CMV Act and other legislative efforts.Watch the episode on YouTube.Featuring:Daniella Gratale, MA, Associate Vice President, Federal Affairs, Nemours Children's HealthCasey Osgood Landry, MPH, Senior Advisor, Legislative & Regulatory Affairs, Nemours Children's HealthCaroline Bruce, MS, RD, LDN, CDCES, NASM-CPT, mom of child with CMV, Wellness Program Manager and Peer Support Program Manager, Nemours Children’s HealthBrittany Fitts, RN, mom of child with CMV, Senior Data Analyst, Nemours Children’s HealthHost/Producer: Carol VassarViews expressed by guests do not necessarily reflect the views of the host or management. Subscribe, review or let your voice be heard at NemoursWellBeyond.org.

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“What did the council decide on item 42?” — answered with the speaker and the moment.

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