Find all needed information about Als Support Web Sites. Below you can see links where you can find everything you want to know about Als Support Web Sites.
https://www.alsforums.com/
Jan 28, 2020 · The ALS forum is a support group to help people deal with the daily living issues associated with ALS. The ALS forum will connect you with people that can provide answers, support and help with ALS. We invite you to join our community. Recent news articles.
Learn how you can help The ALS Association advance scientific research to find a cure for ALS, provide resources for people with ALS and their loved ones, heighten awareness of the nature of the disease, and encourage government leaders to expand their support of research and patient care.
http://webwa.alsa.org/site/PageNavigator/WA_8_SupportGroups.html
Support Groups. The Evergreen Chapter offers monthly support group meetings in locations across the four states we serve: Washington, Idaho, Montana, & Alaska. Support groups offer a place and time for those living with ALS, their caregivers, families, friends, & loved ones to connect with each other. You are encouraged to join at any time.
http://www.alsa.org/donate/
Support ALS Research. The ALS Association has committed $90 million to find effective treatments and a cure for Lou Gehrig’s Disease. Our global research effort has helped increase the number of scientists working on ALS, advanced new discoveries and treatments, and has shed light on the complex genetic and environmental factors involved in ALS.
http://web.alsa.org/site/UserLogin
The ALS Association encourages scientific research to find a cure for ALS, heightens awareness of the nature of the disease, stimulates volunteerism and activism, and increases awareness of government leaders to encourage support of research and patient care.
http://webuny.alsa.org/site/PageNavigator/UNY_8_SupportGroups.html
The ALS Association Upstate New York Chapter. 135 Old Cove Road, Suite 213 - Liverpool, NY 13090. 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
http://webtn.alsa.org/site/PageNavigator/TN_8_SupportGroups.html
If you have a genetic form of ALS and are interested in a support group that addresses these special needs please contact: Patty Lane at (615) 331-5556 or [email protected]. If you are the caregiver of a person with both ALS and FTD (frontotemporal degeneration) and are interested in a …
Our scientists discover and develop potential treatments for ALS (also known as Lou Gehrig's disease). Led by drug development experts and people with ALS, we are 100% focused on finding effective treatments to slow and stop this disease.
http://webaz.alsa.org/site/PageNavigator/AZ_8_SupportGroups.html
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.
http://webchicago.alsa.org/site/PageNavigator/CHI_8_SupportGroups.html
Support Groups. Persons living with ALS, their family members, friends and caregivers are welcome to attend the support groups. The groups are an opportunity to meet others, learn about new information and resources, and provide or receive support and encouragement.
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