The ALS Association

Caregiving for a loved one with ALS can feel very overwhelming. Join us for our upcoming webinar where we will discuss how to meet the needs of your loved ones while maintaining your sense of self. Register TODAY: https://lnkd.in/eDRst233

Stacey Kinsey thought she was done with the day-to-day caregiving part of being a mom. Her daughter Shelby had just graduated from college, after all. But when Shelby was diagnosed with a rare genetic form of ALS, all that changed. Still, both mom and daughter have faced their new situation with grace, and humor. https://lnkd.in/dBjXkfMZ #NationalFamilyCaregiversMonth

During the giving season we come together to shine a light on people living with ALS. People like Shelby, who was diagnosed at just 22 years old. Even as she faces the challenges of living with the disease, Shelby is finding ways to advocate for change, not just for herself, but the entire #ALS community. Support people like Shelby by making a contribution today: https://lnkd.in/dxwiWJMR #GivingTuesday

We did it! The House passed the Senator Elizabeth Dole 21st Century Veterans Healthcare and Benefits Improvement Act (H.R. 8371)! Tell the Senate to pass the bill TODAY: https://lnkd.in/dG2s77Fi #ALSAdvocacy #ALSVeterans

"I have to say, I feel people with ALS are often perceived as less than others. People tend to overlook us, focusing on the assistive equipment and physical limitations that accompany our condition. Despite the alterations in our physical abilities, our minds remain resilient." Chanel is a vibrant 54-year-old living in Virginia. Despite her ALS diagnosis she remains determined to share her family's personal journey. Read her story: https://lnkd.in/efPwJwsD

ALS caregivers are often forced to juggle a seemingly endless list of tasks each day, all while somehow trying to manage the everyday responsibilities like cooking, lawn care, and running the kids here and there. It can be hard to know when and how to ask family members, friends, and neighbors for help, but using tools like ALS Care Connection can make life as a caregiver a little bit easier. https://lnkd.in/efhgrhGt #NationalFamilyCaregiversMonth

Casey and his sister Breanna started ballet dancing when they were young, and both pursued dancing professionally, at least for a while. But when Breanna learned she had ALS they decided they needed one last dance, together. https://lnkd.in/e-KmSAp6 Support people like Breanna and the #ALS community by making a contribution this #GivingTuesday: https://lnkd.in/dxwiWJMR

Young caregivers like Addison and Riley embody an incredible spirit of resilience, compassion, and hope as they balance their childhood with the responsibilities that ALS has brought into their lives.

Caring for someone living with #ALS can be a challenge, and caregivers often feel unprepared for changes due to the nature of the disease. But help is out there through our FREE online caregiver education course. Learn more: https://lnkd.in/er2C8k-Q #NationalFamilyCaregiversMonth

Join us for this special caregiver virtual event in recognition of #NationalFamilyCaregiversMonth as we host a panel of caregivers who will help shine a light on both diversity and the universal role of caregiving. This event will offer practical insights on personal growth, honoring cultural traditions, and addressing unique needs in caregiving. Don’t miss this opportunity to learn and grow together! Register Now! https://lnkd.in/e2jK_PgQ