How to Talk to Your Child About Mental and Emotional Health

We know that living with juvenile dermatomyositis affects the physical as well as emotional health of our children. Sometimes it is hard to distinguish “normal” behavior and feelings from more difficult ones of depression and anxiety.

This presentation aims to increase understanding and awareness of emotional health and parents’ important role in supporting and encouraging a child’s mental health habits.

Presenters address the rationale and benefits of promoting emotional health in children, impart knowledge of emotional development milestones throughout childhood, and provide practical skills and language to discuss emotional and mental health with children.

Understanding the phases of emotional development in childhood helps parents feel more equipped to manage and promote emotional health in children.

Featuring:

  • Stacey Haynes, PhD Psychologist, Seattle Children’s Hospital, Cure JM Center of Excellence
  • Megan Curran, MD, Associate Professor of Pediatrics University of Colorado Denver, Attending Physician, Pediatric Rheumatology, Colorado Children’s Hospital
  • Anna Ramsey, BA, working on MSW, Young adult living with JM since adolescence
  • Annie Mitchell, BA in Special Education, Cure JM Board of Directors and Mom to a JM child

Anita and granddaughters at walk 2024

Grandparent Giving

Supporting Cure JM: A Grandparent’s Guide to Making a Difference As grandparents, your love and support are the bedrock of your family’s strength. You provide

2027 Cure JM Family Conference

We are excited to announce that the Cure JM National Family Conference will be back in 2025! Join us for three days with world-class JM researchers, engaging sessions for all, and social time to connect with new friends. The 15th Annual Cure JM National Family Conference is taking place June 27th -June 29th, 2023, in Chicago, Illinois.

Join Cure JM

Membership is free and we’ll connect you with a network of support, encouragement, and resources.

Cure JM supports families, patients, and the juvenile myositis research community.

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