We offer a grant assistance program for home modifications, speech generating devices, power wheelchairs, or respite/home care that meets the needs of those living with ALS. This program is subject to the availability of funds.
Those living with ALS, their families, friends, caregivers, and health care professionals can speak with specialized care services staff regarding many aspects of ALS care, available community resources, and services.
This is a virtual program designed for caregivers we offer several times throughout the year. The six weekly classes provide information to caregivers to develop a wealth of self-care tools. Class participants also receive a copy of “The Caregiver Helpbook”, developed specifically for the class.
Most people diagnosed with ALS experience difficulty with speech and movement during the progression of the disease. Our Equipment Loan Program offers temporary loaner equipment.
Over the past years we’ve had many conversations and interviews with ALS caregivers, and while no two experiences are ever alike, there are often similarities and storylines throughout. In recognition of National Family Caregivers Month, we thought we would share some of these caregiver stories and advice we’ve collected along the way.
For National Family Caregivers Month, we are featuring David and Laura DuBois. David is living with ALS, and his wife Laura is his primary caregiver. As simple as it might sound, their conscious decision to truly LIVE with ALS is what has allowed them to face each challenge and each day, together.
November 1 marks the beginning of National Family Caregivers Month. There are many ways to help caregivers and families impacted by ALS. The ALS Association put together a list of ten ways to make a difference in the lives of family caregivers.
The St. Cloud VA ALS Clinic in St. Cloud, Minnesota provides focused support for people living with ALS, allowing them to receive care from specialized medical professionals during a single visit.