The National Organization for Rare Disorders is rallying support for a new bill that could change the lives of those affected by rare diseases in Vermont.
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#VT #PatientSupport #VermontRareDiseases #CitizenPortal #HealthPolicy #AdvocacyEfforts
Vermont is taking a groundbreaking step by forming a Rare Disease Advisory Council to amplify the voices of those living with rare diseases and improve healthcare access.
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#VT #PublicHealth #VermontRareDiseases #CitizenPortal #HealthcareAccess #LegislativeInitiatives
Vermont is on the brink of a groundbreaking initiative to support the one in ten residents living with rare diseases, thanks to a powerful push from the ALS Association.
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#VT #DiseaseAwareness #PublicHealth #VermontRareDiseases #CitizenPortal #PatientSupport
Vermont is racing against the clock to establish a Rare Disease Advisory Council as federal funding cuts loom, posing a dire threat to those affected by rare diseases.
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#VT #AdvocacySupport #FederalFunding #VermontRareDiseases #CitizenPortal #HealthInitiatives
A heartfelt plea from advocate Sarah Elliott urges Vermont's House Committee to support the establishment of a Rare Disease Advisory Council, aiming to transform the lives of those battling rare conditions.
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#VT #DisabilityInclusion #VermontRareDiseases #CitizenPortal