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FTD is a devastating disease that impacts thousands of families—but too few people know about it. 🧠 It’s the most common dementia for people under 60. ⏳ The average time to diagnosis is 3.6 years. �
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Frontotemporal degeneration (FTD) is the most common dementia for people under 60, yet it’s frequently misdiagnosed. It can affect personality, behavior, language, and movement—impacting families, wor
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Bruce Willis has been diagnosed with FTD, the actor’s family said in a statement released today. In March 2022, Willis announced his retirement from acting due to a diagnosis of aphasia. However, th
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This #NationalVolunteerWeek, we’re honoring the people who help keep AFTD’s mission rooted in service and growing together! ❤️ Across the country, volunteers show up for families facing FTD by leadi
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FTD research is moving forward — and you can be part of it! From joining the FTD Disorders Registry to sharing your lived experiences, there are many ways to contribute to research. Your participati
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Communicating about frontotemporal degeneration with professionals outside your care team can sometimes feel challenging. AFTD’s Provider Letter is a resource that persons diagnosed and care partners
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#FlashbackFriday to moments of connection and learning at last year’s AFTD Education Conference. We’re looking forward to bringing together people diagnosed, care partners, families, friends, healthc
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AFTD recently held a Congressional briefing on Capitol Hill to underscore the impact of #FTD, educate legislators on what families need to navigate it, and highlight the support scientists need to #en
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Standing in our nation’s capital this week felt exciting and deeply personal. Since becoming an FTD and caregiver advocate, I’ve always dreamed of bringing this work to Washington, to help ensure that
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Finding the right information and support after a diagnosis of frontotemporal degeneration can make a meaningful difference. AFTD offers resources for people diagnosed and their care partners, includ
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Our runners are fueled and ready. ❤️ Big thank you to @drinklmnt for gifting our team with electrolytes to keep them going on race day. We're grateful for partners who show up for the AFTD community
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Wendy Cogan and her husband, Jeff, who lived with corticobasal degeneration, a form of FTD, faced a long and challenging journey to find answers. Today, Wendy is sharing her family’s story in hopes
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About @theaftd

theaftd is a verified Instagram micro influencer in the Nonprofit organization category. With 14.4K followers and 2796 posts, theaftd's account shows a follower-to-following ratio of 11.4:1. This profile demonstrates strong community engagement within its niche. View all content anonymously on Pictame - no login required.

theaftd's engagement rate sits at 2.28%. This is right in line with the 2.5% average for accounts with 10K-100K followers — a healthy, steady performance.

Out of the last 12 posts, 17% are videos and 83% are photos. Notably, photos tend to get 14.4x more engagement than videos. Content shows up about every 105 days. Captions lean moderate, averaging 468 characters.

2.28% engagement rate — right on track for 10K-100K follower accounts.
17% videos, 83% photos. Photos get 14.4x more engagement here.
Posts about every 105 days.
11.4:1 follower-to-following ratio.

FAQs About @theaftd

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Popular Hashtags

#streetstyle#blogger#influencer#photographer#naturephotography#landscape#travelphotography#architecture#portrait#wanderlust#adventure#vacation#trip#weekend#morning
theaftd
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@theaftd

theaftd

PublicNonprofit organization
Posts
2.8K
Top Hashtags
#endFTD#BrainAwarenessWeek2025#NationalVolunteerWeek#FlashbackFriday#FTD#frontotemporaldementia#caregiversupport

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
14.4K
Following
1.3K
Avg. Likes
299
Avg. Comments
31
Engagement
2.28%

AFTD envisions a world with compassionate care, effective support, and a future free of Frontotemporal Degeneration (FTD...