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I think people see someone living with chronic illness for a long time and assume that eventually it just becomes easier. Like if you’ve learned how to manage it, or still function in some way, then y
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Arthritis Awarness month 💜 I was 12 when I was diagnosed with Juvenile Idiopathic Arthritis and secondary Raynaud’s. At that age, you don’t expect your life to revolve around pain, fatigue, hospital
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Let me explain… Chronically ill people are already dealing with all the normal pressures and responsibilities that come with adult life work, bills, relationships, chores, appointments, expectations,
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Dynamic disabilities shouldn’t be ignored, especially in hospital settings. I’ve been biting my tongue at these backhanded comments for 21 years. I got sick at 12, and since then it’s been constant:
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What no one really talks about when you become chronically ill is how small and lonely your world suddenly becomes. Not all at once, but slowly, in ways you don’t even realise at first. Going out sta
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Living with a chronic illness or invisible disability can be exhausting in ways people don’t always see or understand. So this is your reminder for May: you deserve support, rest, understanding and j
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When I was younger, I genuinely believed that pushing through my illness and pretending it wasn’t there made me stronger… like I was somehow proving everyone wrong. I couldn’t have been more wrong.
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I know I sound like a broken record sometimes, and maybe this page has become a bit of a diary for me, but this is something I keep coming back to. Hospital beds, chronic illness, invisible illness…
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I have so much anger and grief towards my body right now. A body that’s meant to keep me safe… but lately feels like it’s doing the opposite. No matter how hard I try, no matter how much I listen, res
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not Jesus, just your chronically ill friend briefly out of a flare suddenly you have energy, you’re making plans, replying to messages, thinking “okay maybe things are turning around” then your body
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I don’t look sick… but I am. Living with an invisible illness means constantly being seen… but not always understood. It’s hearing “you look fine” while fighting battles no one else can see. It’s pu
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212-ing with brain fog be like: you walk into a room and suddenly have no idea why you’re there… yeah, that. For a lot of people, it’s just one of those random, slightly annoying moments. But for som
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About @beanyusher

Beth Usher is a Instagram micro influencer. With 14.2K followers and 12 posts, beanyusher's account shows a follower-to-following ratio of 15.8:1. This profile demonstrates strong community engagement within its niche. View all content anonymously on Pictame - no login required.

beanyusher's engagement rate sits at 6.89%. That's 175% above what you'd typically see for accounts with 10K-100K followers (average 2.5%) — a sign of a genuinely connected audience.

Out of the last 12 posts, 75% are videos and 25% are photos. Notably, videos tend to get 2.0x more engagement than photos. Content shows up about every 4 days. Captions lean detailed, averaging 846 characters.

6.89% engagement rate — 176% above average for 10K-100K follower accounts.
75% videos, 25% photos. Videos get 2.0x more engagement here.
Posts about every 4 days.
15.8:1 follower-to-following ratio.

FAQs About @beanyusher

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beanyusher
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@beanyusher

Beth Usher

Public
Posts
12
Followers
14.2K
Top Hashtags
#chronicillness#hiddendisability#invisibleillness#spoonie#chronicillnessawareness#disability#autoimmune#autoimmunediseases

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.

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Popular Hashtags

#music#viralreels#life#ootd#motivation#friends#fun#like4like#me#makeup#selfie#foryou
Following
896
Avg. Likes
896
Avg. Comments
79
Engagement
6.89%

𝟯𝟮 | 𝒰𝒦 𝒟𝒾𝓈𝒶𝒷𝒾𝓁𝒾𝓉𝓎 𝒜𝒹𝓋𝑜𝒸𝒶𝓉𝑒 Represented by: @zebedeetalent 💌: beanysmith@hotmail.com

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