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.

The world needs more moms like Melissa 💙 Read Melissa's story, and join us as we continue to spread awareness and fight ...
05/28/2026

The world needs more moms like Melissa 💙

Read Melissa's story, and join us as we continue to spread awareness and fight for a future without ALS.

ALS Is Stealing Their Bodies. These Moms and Dads Are Fighting to Keep Parenthood on.today.com/4uDGcET

This Memorial Day, we honor the courageous service members who gave their lives in defense of our country. We also recog...
05/25/2026

This Memorial Day, we honor the courageous service members who gave their lives in defense of our country. We also recognize the veterans and military families impacted by ALS — a disease that is known to affect veterans at a significantly higher rate than the general population.

Today, we pause in gratitude for their courage, service, and sacrifice. 🇺🇸

A key House panel has unanimously approved the ACT for ALS Reauthorization Act. This bipartisan legislation would help c...
05/22/2026

A key House panel has unanimously approved the ACT for ALS Reauthorization Act.

This bipartisan legislation would help continue programs that are accelerating ALS research, supporting expanded access to investigational therapies, and strengthening the shared infrastructure needed to move promising therapies forward.

is working. Congress must keep it going before the current law expires this September.

Ask your Member of Congress to support ACT for ALS reauthorization. Copy the link below or click in our story to take action now.

https://app.oneclickpolitics.com/campaign-page?cid=D9ywLshuaKgGZbKAWUKOI

✨ Shop for a cause with us at Kendra Scott! ✨Join ALS United of Georgia for a special Kendra Gives Back event TOMORROW, ...
05/22/2026

✨ Shop for a cause with us at Kendra Scott! ✨

Join ALS United of Georgia for a special Kendra Gives Back event TOMORROW, May 23 from 12–2 PM at the East Cobb Kendra Scott location. Whether you shop in-store or online, 20% of your purchase will support ALS families across Georgia through local care services, support programs, and advocacy efforts. 💙

🛍️ In-store: May 23 | 12–2 PM - Kendra Scott
💻 Online: May 23–24
🏷️ Use code: GIVEBACK-LYMKC at checkout online

Bring a friend, treat yourself, and shop for a meaningful cause. Every purchase helps make a difference for Georgians living with ALS.

You are invited to join us for ALS United of Georgia's Educational Webinar Series, happening this Wednesday, May 20th, a...
05/17/2026

You are invited to join us for ALS United of Georgia's Educational Webinar Series, happening this Wednesday, May 20th, at 7:00 pm.

Topic: Knowing When Hospice or Palliative Care is the Right Choice
Presented by: Bridget Kurt of Agape Hospice

To secure your place, please register in advance for this meeting:
https://us02web.zoom.us/meeting/register/ApXRrL9EQ0KnT1Ix_QN-Gw

Don’t forget to Grab your tickets for Lou Gehrig’s Day at Truist Park – June 2nd! ❤️⚾️Cheer on the Atlanta Braves vs. To...
05/14/2026

Don’t forget to Grab your tickets for Lou Gehrig’s Day at Truist Park – June 2nd! ❤️⚾️

Cheer on the Atlanta Braves vs. Toronto Blue Jays at 7:15 PM while supporting ALS United of Georgia.

⚾️ Join us for a pre-game social at ASW at The Battery at 5 PM—RSVP: [email protected]

Click the link in our bio to grab your tickets before Monday, May 18th!

https://www.gofevo.com/event/Alsunited2026

🎟 A portion of every ticket purchased benefits families living with ALS.

One week, ALS wasn’t part of David’s story. The next week, it was.After his ALS diagnosis, David left the clinic with a ...
05/13/2026

One week, ALS wasn’t part of David’s story. The next week, it was.

After his ALS diagnosis, David left the clinic with a folder full of resources from ALS United of Georgia. He set it on a shelf. He wasn’t ready.

Months later, when he opened it, he found more than information - he found practical help, guidance, and a community ready to walk alongside him.

Because of supporters like you, every service and resource we provide is free to Georgians living with ALS.

The folder will be waiting. The community will be here.

💙 alsgeorgia.org/donate

Have you downloaded the new WalkALS Fundraising App? Now, everything you need for the Walk is all in one place - so you ...
05/12/2026

Have you downloaded the new WalkALS Fundraising App? Now, everything you need for the Walk is all in one place - so you can fundraise from wherever you are.

We want to hear from our captains and teams prepping for WalkALS on September 19th. Drop an emoji in the comments that describes your walk team energy this year 👇

💙 Strong & steady
🔥 Fired up
🎉 Team hype squad
👟 Walking with purpose
📣 Here to spread the word

See you there!

This May, ALS United brought ALS Awareness right to where the world is watching, Times Square in New York City. But awar...
05/11/2026

This May, ALS United brought ALS Awareness right to where the world is watching, Times Square in New York City. But awareness alone isn’t enough. We need action.

Congress must pass the ACT for ALS Reauthorization Act before it expires on September 30th.

This is momentum. Real, hard-won, life-changing momentum.

Ask Congress to pass this bill today. Visit the link in our story.

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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