Home / Care Tools / Video / Care Tools Video

Care Tools Video

Community members discuss daily living strategies for motivating their adult children living with juvenile-onset DM1.

Community members Penni Warford, Sarah Clarke and Ann Spaulding discuss best practices for planning and implementing your child's Individualized Education Plan.

Dr. Craig Campbell, MD, of Western University in Ontario, Canada, has a discussion with audience members about congenital DM.

Community-led session led by Sarah Berman, Erica Kelly, and Catherine Wycoff, DPT, GCFP, ABMCP. Parents of children living with DM and a hippotherapy specialist discuss the benefit that this type of therapy can often have.

Community-led session presented by Diane Bade, Chuck Hunt, and Larry Lord. Parents of adults living with juvenile-onset DM discuss the challenges specific to this group.

This webinar is presented by a group of mothers offering their knowledge and experience raising children with congenital DM. This webinar includes informed, practical suggestions from alleviating gastro-intestinal challenges with proper diet and natural supplements to advocating for your child's Individualized Education Program (IEP).

An MDF community member and mother describes the medical team she has assembled for her daughter, Kate.

Jacinda Sampson, M.D., Ph.D., University of Utah School of Medicine

Jacinda Sampson answers questions from the audience.

Shannon Lord, Founding Chairman, Board of Directors, MDF, Family

Lisa M. Harvey, Former Executive Director, MDF, Family

Partners

© Myotonic Dystrophy Foundation. All rights reserved.