ALS United of Georgia

ALS United of Georgia Enhancing the lives of people living with ALS, every day until we find a cure. Community Guidelines

Thank you for connecting with us on Facebook!

The purpose of this page is to establish an online community where people with ALS, family members, caregivers and friends can interact amongst themselves and with our organization in a positive environment. The ALS Association strives to be the best resource for all people who are facing Lou Gehrig’s Disease. We value comments and feedback from everyone and want our presence on Facebook to inspir

e thoughtful conversations. We want our page to be an open forum and kindly ask that you review our community guidelines, below. Should posts or comments fall into any of these categories, we reserve the right to remove them.

1. Solicitation or advertising of products or services. Please refrain from advertising products, services or other such information on our page, particularly if they refer to non-FDA approved treatments or devices.

2. Offers or solicitations for used or unused durable medical equipment (DME) (hoyer lifts, shower stands, walkers, etc.) or unused prescription medication due to potential liability or sanitation-related issues.

3. External fundraisers not approved or vetted by The Association as we cannot verify whether funds collected will go toward stated charity or cause.

4. Posts containing profanity. Profane or offensive language will be omitted from posts and comments.

5. Posts requesting we endorse a survey. Surveys will remain on our page only if we have officially approved, vetted and confirmed the methodology for a particular survey. We wouldn’t want you to think we have endorsed a survey that we know nothing about.

6. Posts requesting support for a petition. Unless the petition has been officially vetted, we cannot endorse third party requests to endorse a particular cause.

7. Personnel-related issues. If you have concerns regarding staff or volunteers of The ALS Association, please submit information via email to [email protected].

8. Patient privacy issues. We serve thousands of people living with ALS through our chapters, Certified Centers and clinics. Information gathered from these people will not be shared on Facebook and is considered a violation of The Association’s confidentiality policy.

9. Comments that are factually inaccurate, misleading, or defamatory. We will always do our best to respond to and correct factually inaccurate information that is posted to our page and dispel any misinformation. Personal attacks, accusations, or misleading/defamatory content does not create an atmosphere conducive to healthy dialogue.

10. Comments or content that violates The Association or another company’s trademark or intellectual property or legally privileged information. Please post in accordance to Facebook’s “Statement of Rights and Responsibilities,” which states that users may not add content that infringes upon another party’s intellectual property rights. Intellectual property refers to symbols, names, images, and designs used in business. Similarly, a trademark refers to words, symbols or designs (such as a brand name or a logo) that identify and distinguish the products or services offered by one organization from those offered by others. In addition, please do not disclose proprietary, confidential, or legally privileged information. Thank you for reviewing our community guidelines. Please note that we reserve the right to block individuals who repeatedly violate these community guidelines or who continually foster a negative and unproductive environment for our followers. Questions or comments about our page can be sent to [email protected]. We will do our best to follow up with individuals who have specific concerns via email or phone.

06/18/2026

“It’s my future. It’s my kids future. It never stops until we have a cure.”

For Liz and her dad, walkALS Georgia began in 2006 as a way to honor loved ones lost to familial ALS. Twenty years later, Team Travis has become so much more.

Every year, Liz keeps walking—honoring her family, remembering her dad, and fighting for a future without ALS.

We’ve hit a huge milestone this week—$128,000 raised toward our $625,000 goal for walkALS Georgia 2026!Every dollar rais...
06/17/2026

We’ve hit a huge milestone this week—$128,000 raised toward our $625,000 goal for walkALS Georgia 2026!

Every dollar raised goes toward our mission and to aid in the fight to . Join us in reaching our goal for the 25th Anniversary Celebration of walkALS.

Every step. Every story. Together, we keep walking because Together, We End ALS.

Have you downloaded the walkALS Georgia app yet?📱The new ALS Fundraising app puts your fundraising page, team updates, a...
06/16/2026

Have you downloaded the walkALS Georgia app yet?📱

The new ALS Fundraising app puts your fundraising page, team updates, and progress all in one place—right in your pocket.

✔️ Track your progress
✔️ Connect with your team
✔️ Share your story
✔️ Fundraise from anywhere

Download today and start making every step count.

Already using the app? Tell us your favorite feature below! ⬇️💙

June is full of opportunities to connect, learn, and find support. Whether you’re living with ALS, caring for a loved on...
06/09/2026

June is full of opportunities to connect, learn, and find support. Whether you’re living with ALS, caring for a loved one, or navigating loss, our monthly support groups are here for you.

Join us this month and remember—you never have to face ALS alone.

📅 View the schedule below and learn more at alsgeorgia.org.

What does your support do? Your dollars are put to work every day across Georgia—helping families affected by ALS throug...
06/08/2026

What does your support do?

Your dollars are put to work every day across Georgia—helping families affected by ALS through support groups, transportation assistance, educational programs, and communication devices that help people living with ALS stay connected.

These services are provided at no cost to the families who rely on them, and they’re only possible because of generous supporters like you.

Swipe through to see the impact your gift can make. 💙

Lou Gehrig Day 2026! ⚾️💙 Thank you to everyone who joined us at the Braves game and our pregame social to honor Lou Gehr...
06/04/2026

Lou Gehrig Day 2026! ⚾️💙

Thank you to everyone who joined us at the Braves game and our pregame social to honor Lou Gehrig’s legacy and support the ALS community.

Lou Gehrig’s legacy continues to inspire hope, awareness, and action in the fight against ALS. We are grateful to every person who showed up, shared their story, honored a loved one, or stood alongside those living with ALS.

Thank you to the Atlanta Braves, our supporters, families, volunteers, and advocates for helping make this special day possible.

Today, we remember Lou Gehrig and honor the legacy he left behind.Nearly a century after his diagnosis, his name remains...
06/02/2026

Today, we remember Lou Gehrig and honor the legacy he left behind.

Nearly a century after his diagnosis, his name remains forever connected to the fight against ALS—and to the hope that one day no one will have to hear those words again.

As we celebrate Lou Gehrig Day, we stand with every person living with ALS, every caregiver, every family, and every advocate working toward a future without ALS.

We’ll see you tonight at the Braves game! 💙⚾

Who’s coming? Let us know in the comments!

https://www.mlb.com/braves/ballpark/disability-access-guide

ALS United of Georgia encourages members of the ALS community to apply for the Paula Kovarick Segalman Family Scholarshi...
06/01/2026

ALS United of Georgia encourages members of the ALS community to apply for the Paula Kovarick Segalman Family Scholarship, part of the EveryLife Foundation’s Community Scholarship Program. This renewable scholarship supports U.S. students age 17+ living with ALS, or with an immediate family member with ALS, enrolling full-time in college, university, or technical/vocational school for the 2026–2027 school year.

Learn more and apply at everylifefoundation.org/segalman. Applications accepted through June 18.

Address

227 Sandy Springs Place, Suite D, Box #304
Sandy Springs, GA
30328

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+14046369909

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