The ALS Association

With the many questions that come with being a caregiver, there is often much to be learned from people who are or have been a caregiver for someone with ALS. As #NationalFamilyCaregiversMonth comes to a close, we encourage you to check out our From One Caregiver to Another page: https://lnkd.in/dHhCPJ5J

For people living with #ALS and their caregivers, the prospect of holiday travel may feel a little overwhelming, but with thoughtful planning and a positive outlook, it can also be deeply rewarding. Here are some tips to help with your holiday planning. https://lnkd.in/ei2QrWGa

ALS was originally identified in 1869 but didn't become widely known until 1939 when it ended the career of Lou Gehrig, one of baseball’s most beloved players. Since then, the search for a cure has never ceased. Because of your support, great progress has been made - but there’s still much more work to be done. Help us end #ALS this #GivingTuesday. https://lnkd.in/dxwiWJMR

Stacey never expected to step back into the caregiver role, but after her daughter Shelby was diagnosed with ALS at age 22, the two of them are facing their situation head on.

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