The ALS Association is at the forefront of public policy working to improve the lives of people living with ALS and their caregivers. Our federal advocacy work focuses on educating and mobilizing all members of Congress in a nonpartisan fashion to achieve the mission of The ALS Association: to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
The more you learn about ALS, the better prepared you'll be. Remember, in addition to doing your own research, speaking regularly with your healthcare provider(s) will help you make the most informed decisions moving forward.
At the Healey Center for ALS, we are on a quest to discover life-saving therapies for approximately 500,000 people worldwide who are affected by amyotrophic lateral sclerosis (ALS).
Berkshire County ALS is strictly a support and informational website based on our ALS journeys. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
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