Thank you for supporting the International Alliance of ALS/MND Associations!  Our mission is a wold free of ALS/MND.  

When you support the Alliance, you are supporting our programmes and activities.  All of our programmes are aimed at increasing worldwide awareness, exchanging and disseminating information, improving quality of care, stimulating and supporting research and providing an international identity for the ALS/MND cause.

The funds we raise help us to provide travel and support grants, develop our partnership programme and defend the rights of people living with ALS/MND. Of course, our funds also allow us to grow and develop the Annual Alliance Meeting and Allied Professionals Forum and increase worldwide awareness of ALS/MND!

Thank you for your generous support of our mission.  Together, we are united in the worldwide fight against ALS/MND!


International Alliance of ALS/MND Associations

Amyotrophic lateral sclerosis (ALS), or motor neurone disease (MND), is a muscle wasting condition that affects individuals and those who care for them across the world. ALS/MND progresses rapidly; average life expectancy is estimated to be 2-5 years. Currently, there is no known cause or cure. It is estimated that over 400,000 people are living with ALS/MND worldwide!

To help people with the disease, groups of people have come together to form associations.

The International Alliance of ALS/MND Associations was founded in 1992 to provide an international community for individual ALS/MND associations from around the world.

Our vision is to engage with our members to share resources globally, advance awareness and support people with ALS/MND worldwide. Together, we're united for a world free of ALS/MND.

11 heroes fundraising today.

Our members celebrate the 2015 Annual Alliance Meeting in Orlando, FL, USA. Over 100 delegates were in attendance, representing more than 25 countries across 6 continents! 

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