ALS United of Georgia

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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 inspire 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.

With severe weather expected across Georgia and surrounding areas in the coming days, we are sharing our ALS Emergency P...
10/09/2026

With severe weather expected across Georgia and surrounding areas in the coming days, we are sharing our ALS Emergency Preparedness Guide to help you plan ahead and stay safe. This guide was created by ALS United of Georgia to support people living with and their families before, during, and after an emergency — helping you prepare, access help quickly, and navigate recovery.

Link to guide in comments!

Connection matters—especially when navigating ALS. Our monthly support groups offer a space to come together, share expe...
10/08/2026

Connection matters—especially when navigating ALS.

Our monthly support groups offer a space to come together, share experiences, ask questions, and find support along the way. 💙

Visit our website for more information about our support groups: https://alsgeorgia.org/navigating-als/support-groups/

WE CAN’T STOP THINKING ABOUT WALK DAY!More than 3,500 people. 25 years of stories. Over $648,000 raised (wow!) — and cou...
10/07/2026

WE CAN’T STOP THINKING ABOUT WALK DAY!

More than 3,500 people. 25 years of stories. Over $648,000 raised (wow!) — and counting. What a day! 💙

We’re still smiling about the energy from that day, the stories shared, and everyone who made the 25th walkALS anniversary celebration so special.

If you’re still working toward your team fundraising goal, or waiting for some gifts to come in, there’s still time. Fundraising pages remain open through the end of the year, and every gift helps carry the legacy of walkALS Georgia forward for families impacted by ALS across Georgia.

Every Step. Every Story. Together We Keep Walking. Together, We End ALS.®

We are heartbroken by the loss of Brooke Eby, a remarkable voice in the ALS community.Brooke invited hundreds of thousan...
10/02/2026

We are heartbroken by the loss of Brooke Eby, a remarkable voice in the ALS community.

Brooke invited hundreds of thousands of people into the reality of living with ALS with honesty, vulnerability and a sense of humor that was entirely her own. She made people laugh, she made people listen, and she helped so many understand the realities of living with ALS.

Her voice reached far beyond her own community, and her impact will continue to be felt by people living with ALS, their families, and all of us working toward a future without this disease.

Our hearts are with Brooke’s family, friends and everyone who loved her. 💙

Brooke Eby

photo by Gesi Schilling for nytimes

A great day on the course and a special round of golf. 💙Monday’s George Klisures Charity Golf Tournament raised an incre...
10/01/2026

A great day on the course and a special round of golf. 💙

Monday’s George Klisures Charity Golf Tournament raised an incredible $10,000 for ALS United of Georgia!

We’re so grateful to everyone who came out to honor George’s memory and continue the fight against ALS. ⛳️💙

We did it.The Senate has passed the ACT for ALS Reauthorization Act, completing congressional action and sending the leg...
09/29/2026

We did it.

The Senate has passed the ACT for ALS Reauthorization Act, completing congressional action and sending the legislation to the President for signature.

This moment belongs to the ALS community. People living with ALS, families, caregivers, advocates, researchers, clinicians, and ALS United member organizations worked for years to help make reauthorization possible.

ALS United of Georgia was proud to be part of this effort. ALS United members brought more than 50 advocates to Capitol Hill for Hill Day and met with lawmakers in their home districts, while ALS United organized a congressional briefing and met with House and Senate committees throughout the reauthorization process.

Thank you to everyone who shared their experiences, contacted lawmakers, joined advocacy efforts, and helped carry this effort forward.

Together, we got ACT for ALS across the finish line.

09/24/2026
Over 3,500 people. 219 teams. $638,097 raised — and counting. 💙This is what it looks like when Georgia shows up for fami...
09/23/2026

Over 3,500 people. 219 teams. $638,097 raised — and counting. 💙

This is what it looks like when Georgia shows up for families facing ALS.

Every Step. Every Story.

For 25 years, thousands of people have walked, remembered, celebrated, supported, and shown up for one another — and this year was no different.

Together, we keep walking. Together, We End ALS.®️

We did it! 🎉 $625,000 raised! ❤️💙What an incredible way to celebrate 25 years of walkALS Georgia.25 years. Every step. E...
09/21/2026

We did it! 🎉 $625,000 raised! ❤️💙

What an incredible way to celebrate 25 years of walkALS Georgia.

25 years. Every step. Every story.

We are so grateful to every walker, team, donor, volunteer and supporter who made this day possible.

TAG US IN YOUR PHOTOS! We love to see them!

Tomorrow’s the day! 25 years in the making. Every step has led us here. Every story inspires us to keep walking. Togethe...
09/18/2026

Tomorrow’s the day! 25 years in the making. Every step has led us here. Every story inspires us to keep walking.

Together, we have raised more than $550,000 toward our $625,000 goal. It’s not too late to join us! Your support brings us closer to a world without ALS.

Register. Donate. Learn more.
➡️ alsgeorgia.org/walk

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

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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