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February 2018
Resources
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Blog
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February 2018
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.
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»
Rare Disease Day
Author: Emily Walsh
Posted:
2/28/2018
Category:
Awareness
Rare Disease Day was first established by the
health organization
EURORDIS
in 2008 to bring greater awareness to conditions that typically escape widespread notice. Rare diseases are also known as orphan diseases, as they typically impact only a fraction of the population. It may not seem like a lot, but currently one in ten Americans are living with a rare disease. Congenital CMV is considered a "rare disease".
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»
A Mother's Fight: Maine's CDC CMV Recommendations
Author: Laura Sweet
Posted:
2/21/2018
Category:
Advocacy
,
Parent Perspective
LD 87 was referred to the Legislature’s Joint Standing Committee on Health and Human Services and a public hearing and work session took place in February 2017. The whole process moved much more quickly than I anticipated. We gathered other families and supportive members of Jane’s medical and early intervention teams to testify alongside us. The Committee voted not to pass the bill, but with the understanding that the Maine Center for Disease Control and Prevention (CDC-P) would convene a multi-disciplinary work group to review issues surrounding congenital CMV and make recommendations to the Committee within a year.
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»