Fighting Lou Gehrig's Disease on Every Front!

Our Mission: To lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.

Thursday, November 15, 2012

Saluting Caregivers



The ALS Association Michigan Chapter again salutes those special people who serve as family caregivers during National Family Caregivers Month. The theme for this year’s campaign is “Family Caregivers Matter!” And indeed they do as they put forth much time, energy and effort to care for spouses, children, parents and other loved ones who require daily assistance in living with Lou Gehrig’s Disease.
Please help us honor these individuals this month and throughout the rest of the year. If you know someone living with ALS who has served in the military, please ask them to submit their information to the Wall of Honor. Also, remember to send a note of encouragement and thanks via an e-card to show your support to that special family caregiver.

Thank you for your support and commitment to the fight against this disease.

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