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He thought it was arthritis. It was ALS. Dave Hall first noticed weakness in his hands after a cold front and assumed he was just getting older. What he didn’t know was that he was experiencing the
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Our goal is to accelerate drug development and grow research funding so that every person living with ALS has access to promising treatments. The ACT for ALS Reauthorization Act, led by Reps. Mike Q
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My bill to reauthorize the ACT for #ALS was just considered in an Energy & Commerce hearing! I want to thank I AM ALS Founders Brian Wallach and Sandra Abrevaya for sharing their stories with Congress
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Lauren Hamilton and Chris Conte have three things in common: 1. They lost their dads to ALS. 2. They have called Boston home at one point in their lives. 3. They are running The 130th Boston M
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Donate today! #als #alsawareness #acceleratethecure #raredisease #alscommunity
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Last week, we lost a powerful voice in the ALS community. Chris Spaulding was more than an advocate, he was a relentless fighter who stood up to insurance denials and worked to make sure people living
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It is with deep sadness that we share the passing of Chris Spaulding. Chris was a father, a husband, an advocate, and someone who gave everything he had to this community while fighting his own battl
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We wish every day could be a Walk to Defeat ALS day. ❤️ Join us at an upcoming walk near you by visiting the link in our bio. #ALS #walktodefeatals #fundraiser #alsawareness #raredisease
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A common misconception: ALS and FTD affect only a small number of people. Research tells us the lifetime risk of ALS is about 1 in 400, and FTD is the most common form of young-onset dementia. Dr.
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These are a few people who are supporting the ALS community and joining you in creating a future without ALS. Support the entire ALS community and make a donation by visiting the link in our bio. #
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ALS Matters is excited to welcome Sunny Brous! In the latest episode, Cory sits down with Sunny as she discusses the importance of community, friendship and what it means to be a woman living with A
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Thank you to our amazing volunteers and staff who went to Capitol Hill advocating for more ALS research funding and better policies for people living with ALS! They shared their personal connections
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About @als

The ALS Association is a verified Instagram micro influencer. With 60.9K followers and 1510 posts, als's account shows a follower-to-following ratio of 331.0:1. This profile demonstrates strong community engagement within its niche. View all content anonymously on Pictame - no login required.

als's engagement rate sits at 1.07%. For accounts with 10K-100K followers, the average is around 2.5%, so there's some room to grow — though every community is unique.

Out of the last 12 posts, 58% are videos and 42% are photos. Notably, photos tend to get 2.0x more engagement than videos. New posts appear roughly every 3 days — a steady, reliable rhythm. Captions lean moderate, averaging 463 characters.

1.07% engagement rate — room to grow compared to average for 10K-100K follower accounts.
58% videos, 42% photos. Photos get 2.0x more engagement here.
New content every 3 days — a steady rhythm.
331.0:1 follower-to-following ratio.

FAQs About @als

With Pictame, you can browse @als's posts, reels, and stories without logging into Instagram. The profile owner won't know you visited.

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United StatesTurkeyGermanyUnited KingdomBrazilFranceSpainItalyAll Countries (196)

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@als

The ALS Association

Public
Posts
1.5K
Top Hashtags
#alsawareness#ALS#ALSMatters#podcast#acceleratethecure#als#raredisease#alscommunity

Explore the most impactful hashtags used in recent posts. These tags highlight the core interests and trending topics that define this profile's digital influence and content strategy.

Followers
60.9K
Following
184
Avg. Likes
637
Avg. Comments
13
Engagement
1.07%

We are the world's largest private funder of ALS research, providing care services and advocating on behalf of people li...

bit.ly/m/ALS