In 2018, the Arthritis Foundation launched its Live Yes! Connect pilot program for parents of children living with juvenile arthritis and other childhood rheumatic disease. In addition to providing emotional and social support, the program offers educational resources and seminars to help parents improve the quality of life for their children. Jessica Ward, whose 11-year-old daughter Mercy was diagnosed with JA at age 4, is the sole parent facilitator for the JA parent group in Columbus, Ohio. We chatted with her to hear her insights about the parent group, including benefits, future plans and the best ways to get involved. Continue reading Live Yes! Connect for JA Parents: Q&A with Jessica Ward, JA Parent Facilitator
Juvenile arthritis (JA) affects nearly 300,000 kids and families in the United States. Of all the forms of arthritis, juvenile idiopathic arthritis (JIA) is the most common type of arthritis in children. For almost seven decades, the Arthritis Foundation has upheld our unwavering promise to assist them and their caregivers. In an ongoing effort to include the patient voice in everything we do, we’re asking you – patients, parents, loved ones and others with a connection to JIA – to tell us what JIA research matters to you.
The Arthritis Foundation is excited to announce the launch of the iPeer2Peer Mentorship Program, a new initiative that aims to provide help and support for teens with juvenile arthritis and related childhood rheumatic diseases.
The iPeer2Peer Program was developed by the iOUCH (improving Outcomes in Child Health through Technology) research team at the Hospital for Sick Children in Ontario, Canada to help teens with chronic disease better manage their condition.
Continue reading Arthritis Foundation to Pilot Peer Mentorship Program