Below are links to helpful and informative websites for patients, their families and caregivers.
ALS Therapy Development Institute is a non-profit biotechnology organization devoted entirely to the development of treatments that slow and stop Lou Gehrig’s disease. ALS TDI provides free, web-based informational programs designed to keep patients, caregivers and their families up-to-date on ALS research, including the ALS Forum (www.als.net/forum), Monthly Webinars (www.als.net/webinar) and Quarterly Research Webcasts (www.als.net/researchconcall) as well
as an annual Leadership Summit (www.als.net/summit).
CaringBridge provides FREE, personalized websites that support and connect loved ones during critical illness, treatment and recovery. Click here to find out more.
Patientslikeme is a community of patients, doctors, and organizations that inspires, informs, and empowers individuals with life-changing conditions, click here to learn more. For documents that make great support group meeting handouts, community postings and event presentations click here then choose "ALS" under the "Select a Community" drop down menu .
ALS Worldwide, created by Stephen and Barbara Byer, is a not for profit organization for ALS patients and their families to obtain information, advice, direction, support, guidance and, perhaps, most importantly, hope. Click here to visit this site.