websc.alsa.orgThe ALS Association South Carolina Chapter

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websc.alsa.org

Maindomain:alsa.org

Title:The ALS Association South Carolina Chapter

Description:Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support.

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Website / Domain: websc.alsa.org
HomePage size:70.243 KB
Page Load Time:0.086343 Seconds
Website IP Address: 74.123.153.33
Isp Server: WhippleHill Communications Inc.

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Ip Country: United States
City Name: Bedford
Latitude: 42.94421005249
Longitude: -71.519409179688

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ALS Ice Bucket Challenge Progress Sign up | Login | Find local services | Search Close | Menu Close South Carolina Chapter Find local services Certified Centers & Clinics Support Groups Calendar of Events View Ice Bucket Progress Donate Certified Centers & Clinics Support Groups Calendar of Events About ALS About Us Our Research Local Care Services Advocate Get Involved Donate Your tax-deductible donation is the key to unlocking ALS Please give today! Donate Your tax-deductible donation is the key to unlocking ALS Please give today! Donate Coronavirus Statement With the developing news regarding COVID-19, we want to take a moment to share how The ALS Association is addressing the concern about our programs and events. Please be assured that the work of the ALS Association will continue. Our first priority is the safety and well-being of people with ALS, their families and caregivers, and our staff. Chapter staff will be working remotely and still available to our constituents daily. We anticipate that some activities may need to be cancelled, modified or rescheduled; we will communicate with you directly regarding changes to upcoming plans, so please watch your email. You can find the latest updates about our activities on our Facebook and Twitter pages. For the most recent information about the coronavirus (COVID-19), The ALS Association recommends that you reference the websites for the Centers for Disease Control (CDC) , the World Health Organization (WHO) , and state and local health authorities. For specific information about symptoms you may be experiencing or questions about personal exposure as someone living with ALS or as a caregiver, please contact your physician directly. Thank you for your patience as we manage this rapidly shifting situation. The South Carolina Chapter supports people living with ALS and their loved ones through services and education. We leave no stone unturned in search for the cure of this progressive neurodegenerative disease. Our Mission 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. Find Services Take Action Raise Awareness Latest Research Find Services Take Action Raise Awareness Latest Research Get Involved With Us Help create a world without ALS by getting involved in the way that best suits YOU! When you fundraise with friends and family you take us closer to discovering a cure. Walk to Defeat ALS More than 180 walks take place in communities across the country February through November. Walk to Defeat ALS draws people of all ages and athletic abilities coming together to honor a loved one with the disease, to remember those who’ve passed and to show their support for the cause. Find A Walk Near You Host your own event to support our Chapter Hold a golf tournament, run a marathon, or donate your birthday to raise funds that will help create a world without ALS. Get Started Celebrate a Loved One with ALS Pay tribute to a friend or loved one affected by ALS. Each tribute is a personalized online fund designed to honor or memorialize someone special. Your Community of Hope fund creates a lasting legacy. Learn More Discover More Ways to Help Fight ALS November is National Family Caregivers Month Learn More About Caregiver Resources Resources Whether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you. Let us help you and your family cope with the day-to-day challenges of living with ALS. For People with ALS Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate. For Researchers Caring for someone with ALS is hard work. We offer resources and support to help you. For Caregivers In The News How The ALS Association’s is Pursuing 2020 Public Policy Priorities During the COVID-19 Pandemic March 26, 2020 The ALS Association Furthers Commitment to Develop Technologies to Help People with ALS Live Better March 25, 2020 The Jane Calmes ALS Scholarship Fund Kicks Off Year Two March 24, 2020 Questions and Answers about COVID-19 and Its Impact on People with ALS March 23, 2020 Read More News Here Stay Connected With Us Sign up to receive the latest news in ALS and learn how you can continue making a difference in the search to treat and cure this disease. Join Us You Can Help Create A World Without ALS Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS. Give Now Give Now Give Monthly Give In Honor Or Memory End Hide -- Learn About Other Ways to Give Privacy Policy | Link Policy | Important Information | Contact Us | Manage Your Profile 7499 Parklane Road, Suite 144 Columbia, SC 29223 803-851-3233 All content and works posted on this website are owned and copyrighted by The ALS Association. ©2020 Lou Gehrig® used with permission of the Rip Van Winkle Foundation / www.LouGehrig.com...

websc.alsa.org Whois

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