“A burden shared is always lightened. There is no limit to compassion." - Sarah, Rare Mother
The Histiocytosis Association is a global nonprofit dedicated to raising awareness about histiocytic disorders, providing educational and emotional support, and funding research leading to better treatments and a cure. ANGEL AID understands the unique role of caregivers, particularly Rare Mothers and Rare Fathers. We support histiocytosis patients (both children and adults).
Our Histio Caregiver Community provides a safe forum to offer and receive emotional support from other Histio Caregivers who truly understand.
Let’s put the self back into care, together.
join ANGEL AID weekly workshops
Join Our Caregiver Community on Mighty Networks.
There is a group just for you ~ the Histiocytosis Caregiver Community on Mighty Networks. This group is part of the larger ANGEL AID Rare Mother Community. The purpose is to build relationships and share experiences with other Rare Caregivers. You can chat privately or in groups, as well as post into the wider community.