The contributions of volunteers are essential to the chapter achieving its mission. Each year, our Chapter participates in numerous fundraising and information-based opportunities throughout our area.
Regulation 38 CFR 3.318 provides that the development of ALS at any time after discharge or release from active military, naval or air service is sufficient to establish service connection for that disease. Learn more.
Steve realized he needed to turn to his faith to help him live with ALS. Steve assembled a team and got to work developing ALS Family of Faith, a new ministry designed to meet the needs of those looking for prayer and spiritual counseling during their journey with ALS.
In recognition of Rare Disease Day, Kristina Woody shares more about what it’s like to be a caregiver for her husband, Lamar, and her unique perspective on the rarity of ALS.
Learning that you should consider a feeding tube can be overwhelming. It is a lot to take in, particularly in combination with the many medical issues that come with an ALS diagnosis. It is common for patients to be hesitant about it, but often, once they see the benefits of tube feeding, they often regret not making the decision sooner.
ALS Focus™ is administered by the ALS Association with direct input and guidance from members of the ALS Focus Steering Committee and the Patient and Caregiver Advisory Committee (PCAC).
Like many family caregivers, Linda juggles caregiving and her career. According to the National Alliance for Caregiving, 61 percent of family caregivers continue to work.
By establishing what is known as a life-income gift with The ALS Association, you can have a substantial impact on our life-saving mission and receive income for life with notable tax benefits.