Do you care for someone rare? To study the impact of rare disease on unpaid friends and family members who provide care (known as "family caregivers"), the National Alliance for Caregiving and Global Genes, are launching a "first-of-its-kind" national snapshot of rare disease caregivers. This fall, the two groups plan to release a national survey aimed at collecting feedback from over 1,000 family caregivers of children and adults with rare diseases.
Join this national movement by sharing your story today: www.caregiving.org/rare
