As many as 30 million Americans are affected by a rare disease or condition, and many of these individuals receive unpaid care from friends, family, and neighbors. While much of the focus on caregiving has historically been on the aging population in America, policymakers are beginning to take notice of the impact of caring for rare disease patients on the volunteer friends and family who provide care, known as “family caregivers.” Many people who have rare diseases are misdiagnosed or undiagnosed, leaving their family caregivers to experience unique challenges related to access to appropriate medical care and medications, and the emotional burden associated with the uncertainty of managing the disease and its prognosis.
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- Research Opportunity: Exploring what caregivers understand about palliative care
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- Education and Support for Family Caregivers of their loved ones with Lewy Body Dementia
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Related Posts
FCSC NewsResearch Opportunity
Research Opportunity: Exploring what caregivers understand about palliative care
September 20, 2025
Research Opportunity: Exploring what caregivers understand about palliative care
FCSC News
WorkLife Law Secures Grant to Launch New Initiative to Support Family Caregivers in the Los Angeles Area (WorkLife Law)
March 17, 2025
WorkLife Law Secures Grant to Launch New Initiative to Support Family Caregivers in the Los Angeles Area (WorkLife Law)
FCSC News
Education and Support for Family Caregivers of their loved ones with Lewy Body Dementia
October 31, 2024

