ALS Association raises awareness and supports patients with innovative technology solutions

Hope is a strong emotion that can propel us through any challenge that confronts us. A group of people who radiate hope are members of the Amyotrophic lateral sclerosis (ALS) community. ALS is a neurodegenerative disease that, unfortunately, doesn’t have a cure. According to the ALS Association, people who are diagnosed with ALS usually have two to five years to live. Even with that grim circumstance, people with ALS Exude hope and still enjoy life while they have it. The ALS association seeks to support people with ALS and their caregivers. With empathy and enthusiasm, this organization desires to give those with this disease a chance to live and experience the world before the end of their journey. “ALS is a devastating disease Physically, emotionally, and financially. This needs more awareness because we should care about people’s opportunity to live, love, and engage with a world in ways that are meaningful to them,” said Dean Feener, Chief Information Officer of the ALS Association. The ALS Association has several projects underway to raise awareness of the disease. The #ShareYourALSStory campaign began on May 1. This initiative highlights people living with ALS and reveals their daily realities. ALS is such a crushing...