• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • Skip to footer
  • Email
  • Facebook
  • LinkedIn
  • Twitter
  • YouTube

International Alliance of ALS/MND Associations

  • Members' Login
  • Contact
  • Join the Alliance
  • Donate
  • Understanding ALS/MND
    • What is ALS/MND
    • Genetics
    • Diagnosis
    • Glossary
    • Navigating the Community
  • Find a Member Association
  • Support for PALS & CALS
    • Fundamental Rights for People with ALS/MND and Caregivers
    • Research
      • Voice Preservation
      • Open Science
        • Open Label Extension
      • Expanded Access
      • Understanding ALS/MND Research
      • Improving Regulatory Pathways
      • Right to Try
      • US FDA Orphan Drug Designation
      • Unproven (Off-Label) Treatments
    • Advocacy
      • Advocacy Toolkit
      • Emergency Preparedness Toolkit
      • Equitable Access to Therapies
      • Recommendations for Trial Sponsors
    • Clinical Care
      • Genetic Counselling & Testing
      • Mental Health Support
      • Nursing and Symptom Management
      • Nutrition and Swallowing
      • Occupational Therapy and Activities of Daily Living
      • Physiotherapy and Mobility
      • Respiratory Care
      • Speech Therapy and Communication
      • Support for Family & Caregivers
      • Technology
      • Global Clinic Locator
    • Drugs in Development
      • Masitinib
      • NurOwn
      • CNM-Au8
      • ILB
      • AstroRx
      • Neuronata-R / Lenzumestrocel
      • PrimeC
      • NP001
      • Pridopidine
      • SOD1 Therapies and Trials
      • C9orf72 Therapies and Trials
      • SPG302
      • Regulatory T Cell Enhancing Therapies
      • Ulefnersen
    • Approved Drugs
      • Nuedexta
      • Radicava / Edaravone
      • Riluzole / Tiglutik
      • Rozebalamin / Methylcobalamin
      • Tofersen / Qalsody
    • Drugs No Longer in Development
      • AMX0035
      • Reldesemtiv
      • Arimoclomol
      • TUDCA
      • CuATSM
  • Support for Health Professionals
    • Breaking the News in ALS/MND
  • Events/Programs
    • Calendar of Events/Programs
    • Global Day Calendar
    • Alliance Meeting
    • Allied Professionals Forum
    • “Day in the Life Of” Suite
    • Alliance Webinars
    • ALS/MND Connect
    • March of Faces
    • Patient Fellows Program
    • Alliance Fellows
    • SEED Grant Program
    • International Symposium
  • About
    • Who We Are
    • ALS/MND Health Literacy Map
    • Board of Trustees
    • Councils, Forums & Committees
      • Scientific Advisory Council
      • PALS and CALS Advisory Council
      • Advocacy and Public Policy Forum
      • Research Directors Forum
      • Governance Committee
      • Finance Committee
    • Staff
    • History
    • Newsletter Archive
    • Awards
      • Forbes Norris Award
      • Humanitarian Award
      • Allied Health Professional Award
      • Student Innovation Award
  • Members
    • Member Registration
    • Forgot Password

Alliance Fellows

2026 Alliance Fellows

The Alliance Fellows program (formerly named Global Research Ambassadors) is a virtual learning and engagement program for people impacted by ALS/MND worldwide who want to deepen their understanding of ALS/MND research, treatment development, and advocacy. Using a blended learning model that combines self-directed online content with interactive live sessions, the program helps participants build the knowledge and confidence needed to engage more meaningfully in research and advocacy conversations within the global ALS/MND community.

The program is designed to improve health literacy, strengthen global connections, and ensure that lived experience remains part of the future of ALS/MND research.

2026 Program Details

  • Delivery: Fully virtual, using Zoom and an online learning platform.
  • Duration: Four-week program delivered between September 21 and October 23 (dates tentative)
  • Structure: A blended learning approach combining self-paced learning and live interactive sessions
  • Pre-session learning: Approximately 1.5 hours of individual online learning and preparation before each live session
  • Live sessions: Nine 90-minute engaging and interactive live sessions, delivered across the four-week program. Session times will vary across time zones to support global participation and inclusivity. Sessions may be scheduled at different times throughout the day to accommodate participants from multiple regions. Recordings will also be available for those unable to attend live.
  • Learning experience: Participants will engage with expert faculty and peers through discussions, practical exercises, case studies, and collaborative activities designed to build knowledge, skills, and confidence.

Who Can Apply

You are encouraged to apply if you are:

  • Living with ALS/MND
  • A current or former caregiver
  • An ALS/MND gene carrier without a diagnosis
  • A family member
  • Another member of the ALS/MND community with a strong interest in research and advocacy

Each applicant must submit a separate application.

Applications for the 2026 Alliance Fellows Program are now closed. Thank you to everyone who applied.

Why the Program Matters

The program supports people affected by ALS/MND in building a stronger understanding of ALS/MND research and treatment development, clinical trials, scientific communication, research ethics, informed consent, and the important role lived experience plays in shaping research and advocacy.

Participants leave the program with:

  • A stronger understanding of ALS/MND research and treatment development
  • Greater confidence discussing scientific developments
  • Practical tools for advocacy and community engagement
  • Connections with researchers, clinicians, and peers from around the world
  • Recognition as an Alliance Fellow

Participants who complete the program receive a certificate of completion, an Alliance Fellow social media badge, recognition through Alliance communications, and opportunities to continue engaging through the Global ALS/MND Experience Network (GAMEN).

One of the program’s greatest strengths is the global community it creates — connecting people affected by ALS/MND across countries, experiences, and perspectives.

Who Should Apply?

When people affected by ALS/MND are included in research conversations, it leads to stronger advocacy, better understanding of community priorities, and more meaningful research outcomes.

You may be a strong fit for the program if you:

  • Have a personal connection to ALS/MND
  • Want to better understand ALS/MND research and treatment development
  • Are interested in advocacy or research engagement
  • Are willing to actively participate in discussions and learning activities
  • Want to connect with others in the global ALS/MND community

To participate, you will need a device with internet access and a webcam, time to attend most live sessions or watch recordings, and a willingness to learn and contribute to discussions.

If selected, participants are expected to review materials in advance, participate actively in sessions, and share what they learn with their communities following the program.

Primary Sidebar

  • Sanjay Kumar Srivastava, India

    Sanjay Kumar Srivastava, India

  • Ian Gale, Australia

    Ian Gale, Australia

  • Mike Cels, Canada

    Mike Cels, Canada

  • Ana María Zavala, Mexico

    Ana María Zavala, Mexico

  • Dawn Morton, Scotland

    Dawn Morton, Scotland

  • Timmy, Belgium

    Timmy, Belgium

  • Andres Estevez Guersznik, Ireland

    Andres Estevez Guersznik, Ireland

  • Murat Morali, Turkey

    Murat Morali, Turkey

  • Torben Mikkelsen, Denmark

    Torben Mikkelsen, Denmark

  • Alberto Baez Murillo, Colombia

    Alberto Baez Murillo, Colombia

  • Rosie Riley, USA

    Rosie Riley, USA

  • Alex, Argentina

    Alex, Argentina

  • Gudjon Sigurdsson, Iceland

    Gudjon Sigurdsson, Iceland

  • Lin Yong Yi, Taiwan

    Lin Yong Yi, Taiwan

  • Liz Ogg, Scotland

    Liz Ogg, Scotland

  • Osiel Mendoza, USA

    Osiel Mendoza, USA

  • Laurie Petit-Jean, France

    Laurie Petit-Jean, France

  • Stephanie Christiansen Hall, Canada

    Stephanie Christiansen Hall, Canada

  • Yolanda Armendariz, Mexico

    Yolanda Armendariz, Mexico

  • Margreth Burger-Saile, Switzerland

    Margreth Burger-Saile, Switzerland

  • Dan Doctoroff, USA

    Dan Doctoroff, USA

  • Chris McCauley, Canada

    Chris McCauley, Canada

  • Norm MacIsaac, Canada

    Norm MacIsaac, Canada

  • Steve

    Steve

  • Barry de Reuver, Netherlands

    Barry de Reuver, Netherlands

  • Chun Ju Xiao, China

    Chun Ju Xiao, China

  • Lucy Lintott, Scotland

    Lucy Lintott, Scotland

  • Ching-Liang Chu, Taiwan

    Ching-Liang Chu, Taiwan

  • Willi Klein, UK

    Willi Klein, UK

  • Elisabeth Zahnd, Switzerland

    Elisabeth Zahnd, Switzerland

  • Emilienne Verhaegen, Belgium

    Emilienne Verhaegen, Belgium

  • Valdomiro Xavier Honório, Brazil

    Valdomiro Xavier Honório, Brazil

  • Mauril Belanger, Canada

    Mauril Belanger, Canada

  • Michael Lee, Australia

    Michael Lee, Australia

  • Phil Rossall, UK

    Phil Rossall, UK

  • Danny Reviers, Belgium

    Danny Reviers, Belgium

  • Chen Yin Xue, Taiwan

    Chen Yin Xue, Taiwan

  • Gudjon Sigurdsson, Iceland

    Gudjon Sigurdsson, Iceland

  • Steven Spencer, New Zealand

    Steven Spencer, New Zealand

  • Colm Francis Davis, Ireland

    Colm Francis Davis, Ireland

  • Rudiger Hanemann, Germany

    Rudiger Hanemann, Germany

  • João Marcos Andrietta, Brazil

    João Marcos Andrietta, Brazil

  • Yessenia Hernandez Mendoza, Mexico

    Yessenia Hernandez Mendoza, Mexico

  • Daniela Maria Daverio, Argentina

    Daniela Maria Daverio, Argentina

  • Marcelo Farinelli, Brazil

    Marcelo Farinelli, Brazil

  • Denis Blais, Canada

    Denis Blais, Canada

  • Chen Chun-Chin, Malaysia

    Chen Chun-Chin, Malaysia

  • Den Haag, Netherlands

    Den Haag, Netherlands

  • Eric Von Schaumburg, USA

    Eric Von Schaumburg, USA

  • Sharon Corosanite, USA

    Sharon Corosanite, USA

Learn more about the March of Faces

Footer

Stay connected to the global ALS/MND community.

Subscribe to receive our newsletter and updates on how to get involved across the Alliance network.

 
This field is for validation purposes and should be left unchanged.
  • Email
  • Facebook
  • LinkedIn
  • Twitter
  • YouTube
Return to top of page

Contact | Disclaimer | Privacy Notice & Cookies | Sitemap

Copyright © 2026 The International Alliance of ALS/MND Associations. All rights reserved.


Registered in England: Charity Number 1079504 · Site built by graphics.coop · Powered by WordPress · Members' login