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Blog
CMV Mom Hopes to Spread CMV Awareness at Mrs. America Pageant
Posted:
2/8/2023
Category:
Advocacy
,
Awareness
,
Community
,
Parent Perspective
CMV mom Kelsi Gagne is participating in the Mrs. America pageant in April. She plans to use this platform to increase awareness and health literacy of cCMV. Read more about her journey.
Learn More
»
2018 Early Career Research Award Recipient
Posted:
11/1/2018
Category:
Clinical
,
Fueling Our Mission
The National CMV Foundation’s mission includes supporting relevant, timely and innovative research that will assist the foundation in meeting its goals to eliminate the harmful effects of maternal and congenital cytomegalovirus (CMV) infection.
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»
Compete 4 CMV Spotlight: Jeff Rich
Posted:
10/18/2018
Category:
Community
Meet Jeff Rich. A longtime friend of founders, Kristen and John Spytek. Father of three. And, soon-to-be Compete 4 CMV - NYC Marathon finisher!
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»
Board Member Spotlight: Albert Park
Author: Dr. Albert Park
Posted:
10/11/2018
Category:
Community
Meet Dr. Albert Park. Dr. Park is Chief of Pediatric Otolaryngology at the University of Utah and principle investigator for the ValEAR study. His focus is in pediatric hearing loss, identifying a great number of babies with congenital CMV.
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»
Compete 4 CMV Spotlight: Pete Zoob
Posted:
10/8/2018
Category:
Community
Meet Pete Zoob. A longtime friend of founders, Kristen and John Spytek, and soon-to-be eight-time marathoner! We're grateful he's making #8 a Compete 4 CMV race.
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»
Raising Awareness of Congenital CMV in New Jersey
Posted:
10/4/2018
Category:
Advocacy
,
Awareness
,
Fueling Our Mission
Meet 2018 Public Health Awareness Mini Grant Recipients Allison Goldschlag-Reinking and Laurie Navin of The Central Jersey Family Health Consortium, and learn more about their project to implement a comprehensive educational program about congenital CMV in their region.
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»
What I Took Away from the CMV Public Health & Policy Conference
Author: Kristen H Spytek
Posted:
10/1/2018
Category:
Advocacy
,
Community
Our community of parents, advocates, early interventionists, state health employees, clinicians, researchers, scientists, and stakeholders, were well-represented in Burlington last week, and what was extremely encouraging to me, is that both individually and together, we all continue to operate on full cylinders at the very epicenter of what we’re each trying to ultimately do – save babies and prevent birth defects due to congenital CMV.
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»
Compete 4 CMV Spotlight: Rob Pickus
Posted:
9/14/2018
Category:
Community
Meet Rob Pickus. Rob is father to Noah, born with congenital CMV. He's an experienced runner and fundraiser. We're excited to have him as part of the inaugural Compete 4 CMV - NYC Marathon team!
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»
Board Member Spotlight: Sara Doutre
Author: Sara Doutre
Posted:
9/13/2018
Category:
Community
Meet Sara Doutre. Sara is a co-founder of National CMV Foundation and she brings real-life advocacy expertise and experience to the group. She is also a mother of three and runs her own business, Doutre Consulting, specializing in Education Policy.
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»
Raising Awareness of CMV in Arizona
Posted:
9/10/2018
Category:
Advocacy
,
Awareness
,
Fueling Our Mission
Meet 2018 Public Health Awareness Mini Grant Recipient Melissa Selbt, MPH, Executive Director of The EAR Foundation of Arizona, and learn more about her project to educate and evaluate CMV policy within her state.
Learn More
»
Football Fundraising Ideas
Posted:
9/7/2018
Category:
Awareness
,
Community
,
Fueling Our Mission
Fundraising tips and ideas just in time for football season!
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»
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