ALS treatment and care is changing at a pace never seen before. To maximize the benefit of these advances, we are striving to optimize existing therapies, reduce complications and ensure the best standard of care is available to everyone, everywhere through our Quality of Care Research Awards.
Through our Assistive Technology Grants, we provide up to $400,000 over 2 years to support the development of a diverse array of devices and other technologies that make it easier for people with ALS to communicate, move, breathe and perform daily activities.
No two cases of ALS are the same, nor are any two ALS caregiver experiences. While there is no one-size-fits-all answer to every caregiver question, there is often much to be learned from people who are, or who have been, a caregiver for someone with ALS. As National Family Caregivers Month comes to a close, we wanted to take a moment to highlight some of the advice, resources, and support available for ALS caregivers all year long.
The ALS Association offers a variety of ways to support caregivers. We have programs to help cover the costs associated with in home care as well as targeted trainings for caregivers to ensure they have the information they need to take care of themselves and their loved one.
The ALS Association offers a variety of ways to support caregivers. We have programs to help cover the costs associated with in home care as well as targeted trainings for caregivers to ensure they have the information they need to take care of themselves and their loved one.
The Senator Tomassoni Caregiver Support Program provides financial support to help cover some of the costs associated with in-home care, as well as education for personal (non-paid) and professional (paid) caregivers in Minnesota.
The Jack Norton Caregiver Respite Program is dedicated to serving family caregivers North Dakota and South Dakota. Eligible caregivers must live with the person with ALS.
The Jack Norton Caregiver Respite Program is dedicated to serving family caregivers North Dakota and South Dakota. Eligible caregivers must live with the person with ALS.
The grant program provides financial assistance to individuals diagnosed with ALS and their families. This support covers costs associated with their diagnosis, including communication devices, medical expenses, home modifications, home care, and transportation needs.