Les Turner ALS Foundation: ALS-FTD Clinicopathological Overlap ALS and frontotemporal dementia (FTD) are increasingly understood to share underlying biological connections, and some people living with ALS may also experience changes in thinking, behavior, or personality. Join Dr. David Irwin from Penn Medicine, as he explores the relationship between ALS and ALS-FTD, explaining what current research […]

A member forum focused on health literacy and improving understanding, navigation, and access to information for people affected by ALS/MND.   Registration note: Members only. To register or request more information, email alliance@als-mnd.org.

Changes with eating and swallowing are common in ALS, and can feel overwhelming, but having the right information can make planning ahead easier. Join us for a practical conversation about what to expect, ways to adapt as your needs change, and how to think through decisions about feeding tubes. You'll gain helpful tips, answers to […]

A member forum focused on health literacy and improving understanding, navigation, and access to information for people affected by ALS/MND.   Registration note: Members only. To register or request more information, email alliance@als-mnd.org.

Small tools can make a big difference in everyday life with ALS. Join us to learn about affordable products that can help with daily activities, where to find them, and which types of equipment are typically covered by insurance, and which are not. From simple over-the-counter items to practical tips for getting what you need, […]

Join us on Wednesday September 23, at 1 pm ET for "Living and Loving with Loss: A Webinar on Navigating Grief While Living with ALS." A diagnosis of ALS brings many layers of loss – both immediate and unfolding over time. Join grief therapist Andrea Warnick and ALS Canada for this compassionate webinar exploring the unique […]

In this webinar, Marie Saxon, MS, CCC-SLP will review the most commonly observed cognitive and language symptoms in individuals with ALS and FTD, as well as their functional implications. Symptoms include reduced executive functioning, attention, memory, social cognition, and communication that can impact decision making, safety, and interpersonal connection. Marie will review potential signs of […]

A member forum exploring technology solutions that can support people living with ALS/MND (PALS) in daily life, communication, and independence.   Registration note: Members only. To register or request more information, email alliance@als-mnd.org.

A member forum exploring technology solutions that can support people living with ALS/MND (PALS) in daily life, communication, and independence.   Registration note: Members only. To register or request more information, email alliance@als-mnd.org.

This webinar will provide an overview of the rapidly evolving landscape of artificial intelligence. We will look at responsible and trustworthy AI, and the importance of governance as it relates to the ALS/MND community. Join the conversation about how this growing technology can help enrich quality of life. Register now 

One of the biggest questions after an ALS diagnosis is, "What happens next?" This webinar will walk through common changes and the care decisions they may bring, helping you understand what to expect, when to start planning, and how to make informed choices that fit your priorities. Register now

As genetics becomes increasingly relevant in ALS/MND care and research, important questions are emerging around access, consent, privacy, equity, and support. This member roundtable will examine what rights should guide policy and practice in the genetics era, and how the global community can respond.   Group discussion (two options to accommodate time zones): Group 1: […]

The Access for ALL in ALS (ALL ALS) Consortium is a nationwide, NIH-funded clinical research initiative in the United States that collects and shares biological samples and clinical data to accelerate amyotrophic lateral sclerosis (ALS) research.  Aeryn Hopwood and Emma Schmidt of the Les Turner ALS Center at Northwestern Medicine will discuss the structure of the study […]

Hospice is often surrounded by fear and misconceptions, yet it can be one of the most valuable sources of support during the ALS journey. Join us for an honest discussion about what hospice care looks like in ALS, what to expect from referral through end of life, and how to make the most of the […]

In recognition of National Family Caregivers Month, join us for a special three-part webinar series exploring the family side of the ALS journey. ALS impacts not only the person living with the disease, but also the caregivers, children, and loved ones who walk alongside them. Through conversations on caregiver wellbeing, family relationships, finding joy together, […]

In recognition of National Family Caregivers Month, join us for a special three-part webinar series exploring the family side of the ALS journey. ALS impacts not only the person living with the disease, but also the caregivers, children, and loved ones who walk alongside them. Through conversations on caregiver wellbeing, family relationships, finding joy together, […]

This webinar will provide an update on ALS/MND treatments currently in Phase 3 clinical trials. Participants will learn about trial timelines, study locations, available programs, and key contacts for further information. The session will offer an overview of the current Phase 3 clinical trial landscape and the latest developments in treatment research. Register now

In recognition of National Family Caregivers Month, join us for a special three-part webinar series exploring the family side of the ALS journey. ALS impacts not only the person living with the disease, but also the caregivers, children, and loved ones who walk alongside them. Through conversations on caregiver wellbeing, family relationships, finding joy together, […]

The fourth edition of Motor Neuron Diseases brings together researchers and clinicians to share advances in understanding motor neuron diseases, including disease mechanisms and emerging therapeutic approaches. The event is organized by the Neuroscience Institute Cavalieri Ottolenghi (NICO) and the Department of Neuroscience – University of Turin in Italy. It is being offered virtually and in […]

The conSLAncio ETS Association, founded by Andrea Zicchieri, member of the International Alliance of ALS/MND Associations, EUpALS (European Organization for Professionals and People with ALS), the EU ALS Coalition, and the Italian ALS Coalition, is proud to announce the Hybrid Conference "Motor Neuron Diseases IV Edition Workshop: Understanding the Pathogenetic Mechanisms to Develop Therapies", 6-7 […]

A member forum examining how artificial intelligence may impact people living with ALS/MND, care delivery, research, and support services.   Registration note: Members only. To register or request more information, email alliance@als-mnd.org.

A member forum examining how artificial intelligence may impact people living with ALS/MND, care delivery, research, and support services.   Registration note: Members only. To register or request more information, email alliance@als-mnd.org.

Palliative Horizons is a one-day education session from the Canadian Society of Palliative Medicine (CSPM) on palliative care for people living with ALS/MND and Parkinson's disease. It is for palliative medicine physicians and other clinicians working in neuropalliative care. The session takes place in Richmond, British Columbia, and online. Recordings are available to all registrants […]

Our Annual Meeting will be taking place virtually. This meeting will provide an opportunity to reflect on achievements and discuss priorities for the coming year. Additional details will be shared closer to the date. Please mark your calendars and plan to attend.