Take Action Locally
You can take action to end ALS in YOUR community.
Join a Support Group
We’re putting an end to ALS. Until that day, we’re here to help.
Give to End ALS
Can you support our work to end ALS with a donation?
I AM ALS is a community changing the story of ALS by putting people impacted by the disease at the center of one of the most successful patient advocacy movements of the 21st century.
Heroes in our advocate network.
Increase in federal funding for ALS research.
Actions taken to push forward innovative ALS policy.
Empowering the community in the fight against ALS
I AM ALS, a major ALS support organization, is committed to offering comprehensive ALS resources. Our programs are aimed at educating the public about ALS disease, pushing for policy reforms, and assisting families afflicted by the disease. We empower patients and caregivers to become advocates, fund cutting-edge research initiatives, and build compassionate communities through peer-to-peer support and storytelling.
Navigating ALS: What To Do For ALS
If you or a loved one has been diagnosed with ALS, it is critical to understand what steps to take. I AM ALS provides information about getting medical care, joining support groups, and participating in clinical trials. Our team is here to assist you every step of the way.
Supporting Families: How to Help a Family With ALS
Caring for a loved one with ALS can be difficult. We connect individuals to local advocacy groups, emotional wellness resources, and community-led initiatives that empower caregivers and families. Through collaboration and shared experiences, we help build a supportive network so no one faces ALS alone.
Understanding Lou Gehrig’s Disease
Lou Gehrig’s disease, sometimes known as ALS, impacts many people in our community. By increasing awareness, we aim to create a supportive atmosphere for those affected and help propel research efforts toward a solution.
ALS impacts every community, including yours.
“Today, I may be fighting for my life. But I know I’m not alone. I have my family of service members, I have patients and veterans living with ALS, and I now have you.”
– Guillermo “Gill” Garcia, Veteran living with ALS
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FAQs
What is Lou Gehrig’s disease, and what does I AM ALS do?
Lou Gehrig’s disease, also known as ALS (Amyotrophic Lateral Sclerosis), is a progressive neurodegenerative disease. I AM ALS is a non-profit organization that empowers people living with ALS, supports their families, and advocates for research and policy change to improve lives and find a cure.
What services does I AM ALS offer for people with ALS?
I AM ALS provides advocacy, virtual support groups, emotional and logistical guidance, and connects families to resources and clinical trials. All support is free and tailored to individual needs.
How do I know if I’ve found the best ALS disease organization?
I AM ALS is recognized for its community-driven approach, impactful advocacy, and comprehensive support. It has helped increase federal funding for ALS research and passed major legislation to improve access to treatments.
Are there affordable ALS resources near me?
Yes, I AM ALS offers free resources, support groups, and guidance for people living with ALS and their families, regardless of financial situation. There is no cost to access these services.
How can I help my family if someone is diagnosed with ALS?
I AM ALS provides expert advice, caregiver resources, and practical tips for supporting loved ones. You can join a support group or connect with a trained mentor for one-on-one guidance.
What makes I AM ALS a leading ALS organization?
I AM ALS stands out for its community-led approach, impactful advocacy, and comprehensive support for people with ALS and their families. The organization has driven major policy wins and increased federal funding for ALS research.
