Families and ALS Resource Guide
This resource guide is the result of many years of clinical social work practice and research with families, children, and youths affected by neurological illness. While much attention is paid to the person with ALS and their adult family member/caregivers, children and youths are often voiceless, despite experiencing much of the same shock, sadness, caregiving, and grief as their adult counterparts.
The resource guide was created primarily for families living with ALS, including parents, grandparents, siblings, and other family members. However, it was also created to support the many school-based and health care professionals who work with families affected by ALS. The goal of this guide is to help families start answering many of the questions that will be asked, as well as to offer support and suggestions for professionals assisting with families affected by ALS. A key theme throughout this guide is communication—how to do it, maintain it, and include it in everyday life.
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Resource Guides designed to inform and educate people about ALS in a comprehensive and easily understood format
These materials have been developed as communication and educational tools to help inform medical providers as well as provide pertinent insurance and family information.
Many children may have experienced temporary illness or even disability issues within the family, what makes a discussion about ALS particularly challenging is the progressive nature of the symptoms.