We are deeply alarmed by proposed NIH funding cuts that will devastate the fight against ALS. These cuts threaten critical research efforts that could turn ALS from fatal to livable and cure it.
Stand with us! Contact your representatives and share your ALS story. Demand they protect the funding that gives people with ALS a fighting chance.
Whether you are newly diagnosed, a military veteran, a caregiver, or someone looking to learn more about how to navigate living with ALS, we can help.
We offer a variety of local support, including programs such as equipment loans and referrals to local medical professionals. We can also help you find a local treatment center or clinic, or support group.
We expedite the discovery of treatments and a cure for ALS.
We secure policy change at federal, state, and local levels to make ALS a livable disease for everyone, everywhere until we find a cure.
The Hugh and Herbert Hoffman ALS Impact Fund is designated to advancing promising ALS therapies, developing new or strengthening existing ALS clinics, and enhancing access to ALS care for people living with ALS. It will specifically fund three programs in the areas of ALS research and care.
ALS Nexus brings together leaders in the ALS community to connect, collaborate, and change the future of ALS. This is more than a conference – it’s an opportunity to spark new ideas and accelerate progress toward our goal of making ALS a livable disease until we can cure it.
Register today to secure your spot at 2024 rates!
