Les Turner ALS Foundation

The International Alliance of ALS/MND Associations

The International Alliance of ALS/MND Associations was founded in 1992 to provide support to patient-driven associations through networking and exchanging information about ALS. The Les Turner ALS Foundation and the Motor Neuron Disease Association of England, Wales and Northern Ireland (MNDA), along with several others, were founding Alliance members. Today, more than 40 organizations representing 30 countries worldwide have joined forces to combat ALS and Motor Neuron Disease (MND).

The Les Turner ALS Foundation is one of the founding members of the International Alliance of ALS/MND Assocations

The key objectives of the Alliance are: to increase awareness of ALS/MND worldwide, to exchange and disseminate information, to improve quality of care for people with ALS/MND everywhere, to stimulate and support research and to establish an international identity.

The International Alliance of ALS/MND Associations partners with MNDA, one of the largest Alliance Members, on the coordination of an annual International Symposium of ALS/MND. The Foundation hosted these international meetings in 1996 and 2012 in Chicago.

Members of the Foundation’s Home and Community Team as well as members of the Les Turner ALS Research and Patient Center regularly present at these annual meetings, sharing their knowledge and experience with other ALS professionals from around the world.

To learn more about the Alliance and its annual meetings and symposium, visit http://www.alsmndalliance.org/

Read the latest newsletter from the Alliance to learn about updates from its members here.

Share this Page

International Symposium on ALS/MND

Seven representatives were in Ireland at the 27th International Symposium on ALS/MND. These representatives include six members of the Les Turner ALS Research and Patient Center at Northwestern Medicine, Senda Ajroud-Driss, MD, Lisa F. Wolfe, MD, P. Hande Ozdinler, PhD,  Javier Jara, PhD, Nailah Siddique, RN, Teepu Siddique, MD as well as Les Turner ALS Foundation Executive Director, Andrea Pauls Backman. Learn about the Symposium here.

Watch a recording of the Ask the Experts panel here: http://asktheexpert.webcastlive.co.uk/

The Foundation’s mission supports:

Support Services

Patient Services

The Les Turner ALS Foundation patient services programs help patients and their loved ones cope with the day-to-day difficulties of living with a chronic disease.

Learn More

Research & Patient Center

Research & Patient Center

The Center brings together all ALS disciplines under one umbrella, enabling enhanced collaborations between researchers and clinicians to provide a full spectrum of treatment to ALS patients while facilitating the development of new therapies for ALS.

Learn More

Events, Education & Awareness

Events, Education & Awareness

Local focus—Global reach. Events in various neighborhoods support ALS families in Chicago and beyond.

Learn More

Hope and help for people with ALS.

Your contribution helps support the vast majority of the Chicagoland ALS population.