HELP US:
Support us in our fight against ALS
Key Themes
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Information for patients
Here you can find all the services offered by the ALS League. From personal support from our Liaison or Case Manager, to information sessions on various topics, to more practical help we can offer. For more information on ALS, the care landscape, government services,… please refer to the bar at…
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Our mission and vision
Mission As a non-subsidised national ALS organisation, our mission is to represent the interests of pALS ‘persons with ALS’ at both national and international levels. Nationally, we do this by offering free of charge expert care and support physically (ALS Mobility & Digitalk), mentally and socially (Mamuze) to pALS, their…
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Information for donors
The ALS League is fully committed to the fight against ALS every day. Help in the fight against ALS in various ways: donate and receive a tax certificate, consider a gift in your will or organise a campaign. Together we make a difference! Help out: Strong together against ALS At…
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Axoltis Pharma announces topline Phase 2 results for NX210c in Amyotrophic Lateral Sclerosis
15 September 2026 Post-hoc analysis shows substantial reduction in ALSFRS-R decline rate versus placebo at week 6; sustained at month 4 follow-up Axoltis Pharma, a biotech company dedicated to developing novel therapeutic solutions for neurodegenerative diseases, announced the topline results of SEALS, its Phase 2 clinical trial evaluating the effect of NX210c in patients with […]
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Revamped plan aims to hasten US approval of treatment for ALS
2 September 2026 Neurosense is fast-tracking PrimeC, its experimental oral therapy for ALS, to secure faster approval. The revamped plan features a head-to-head trial against Radicava and a restructured Phase 3 study. It also includes analyses of existing data using artificial intelligence. Neurosense Therapeutics is revamping its development plan for PrimeC, the company’s experimental […]
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Stanford team wins $13M grant to find genetic causes of ALS
10 June 2026 Researchers will use AI to study cells, identify potential therapy targets A team at Stanford University has received a $13 million grant to uncover previously unknown genetic causes of amyotrophic lateral sclerosis (ALS), with the goal of identifying targets for future treatments. The grant, awarded by the California Institute for Regenerative Medicine (CIRM) to a team […]
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2025 Campaign – Roberta Flack – Killing me softly- World ALS Day
Together we make a difference: Discover our new campaign Killing Me Softly, a powerful call against ALS From 16 to…
Stand up for ALS
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ALS Actions
From now on, taking action is very easy and transparent. Would you like to help raise awareness of ALS and raise money for ALS? Then create an action page directly via ALSacties.be. This way, you can easily start an action to help in the fight against ALS. The ALS League’s current…
Activities
Info sessions
Along several channels, we hear the need for information. So this is where we started!
We are starting a new project, namely organizing free monthly information sessions.
Activities by us
At the ALS League, we are actively committed to organizing events and initiatives that not only bring people together, but also contribute to awareness and support for pALS and their loved ones. From informative meetings and sporting challenges to fundraising events, all of these activities are set up by us with one goal: to strengthen the fight against ALS. Discover here which activities we organize and how you can participate.
Activities for us
Many people are committed to supporting the ALS League by setting up events or actions themselves. Whether it is a benefit concert, a sponsored walk or a creative collection campaign, every effort helps us to support research and provide pALS with the necessary help. On this page you will find an overview of initiatives that are organized for the benefit of the ALS League.
Together we make the difference!