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This trend, but for the chronically ch✨ill✨ babes. Drop a 🩡 if you share the same vibe! Literally me 🀝🏼 you. Yes, we have each others’ back! If you’re new here, hi πŸ‘‹πŸΌ I’m Ashleigh and I was diag
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It’s #MsAwarenessMonth + #MsMonday! Time to get to sharing, educating, and spreading awareness! Flood the comments with 🧑🧑🧑 to let the world know we’re ready for it! πŸ’ͺ🏼 This will be my 5th MS Aw
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Backstory:: last year we learned my MS had relapsed. There were new lesions, activity, inflammation, progression… it was scary. I ended up switching medication + I’ve been on that treatment for a year
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If your doctor has never asked you to complete this hieroglyphs puzzle or walk as fast as you can down the office while being timed I don’t wanna hear it from you πŸ™‚β€β†”οΈβœ¨ If you can relate to this, I
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And that’s on living with chronic illness β€οΈβ€πŸ©Ή if you heard this 5 second audio and felt it in your soul, then you already know. These are words I’ve told myself over and over again- β€œI’ll be good” β€œ
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Mother’s Day can hold so many emotions at once. Whether you’re celebrating, grieving, waiting, healing, hoping, or a mixture of it all HONOR yourself + your emotions. Let this video serve as a reminde
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Sometimes I catch myself daydreaming about a life where I don’t have to constantly think of ways to adapt, ways to get insurance to approve xyz, ways to teach loved ones to be considerate, ways to not
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To those who stick by our side, who silently and loudly support, who show up day after day. Thank you β€οΈβ€πŸ©Ή we love you. Send this to your gem of a person (or several gems) πŸ«‚ and may this serve as
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Autoimmune babes waiting for their infusions to take the edge off like πŸš¬β€οΈβ€πŸ©Ή if you can relate, you can relate. May your fatigue eff off and may your treatments be helpful xx Tag/share with a frie
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It’s MS Awareness Week in the UK (April 20-26th) 🧑 + with that I have a little psa to share: 🚨STOP disregarding people’s disability just because it doesn’t fit into your definition of disability. IN
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"Displaying the quiet parts out loud 🧑 it’s natural to talk about the more obvious realities of MS, but what about the quiet parts? The parts that we might not even notice are related to MS, like the
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πŸ—£οΈ just because we did a thing yesterday doesn’t mean we can do it again today. Living with chronic illness 🀝 living in a body that changes without warning πŸ₯΄ so your empathy and understanding is be
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About @arose

Ashleigh Rose | chronic illness + ms advocate is a verified Instagram micro influencer. With 36.4K followers and 12 posts, arose's account shows a follower-to-following ratio of 74.6:1. This profile demonstrates strong community engagement within its niche. View all content anonymously on Pictame - no login required.

arose's engagement rate sits at 2.06%. For accounts with 10K-100K followers, the average is around 2.5%, so there's some room to grow β€” though every community is unique.

Out of the last 12 posts, 92% are videos and 8% are photos. Notably, videos tend to get 11.8x more engagement than photos. Content shows up about every 73 days. Captions lean detailed, averaging 1190 characters.

2.06% engagement rate β€” room to grow compared to average for 10K-100K follower accounts.
92% videos, 8% photos. Videos get 11.8x more engagement here.
Posts about every 73 days.
74.6:1 follower-to-following ratio.

FAQs About @arose

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arose
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@arose

Ashleigh Rose | chronic illness + ms advocate

Public
Posts
12
Top Hashtags
#MultipleSclerosis#ChronicIllnessSupport#Ms#ChronicallyChILLClub#ChronicIllness#ChronicIllnessAwareness#MsSupport#ChronicallyChILL

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
36.4K
Following
488
Avg. Likes
617
Avg. Comments
134
Engagement
2.06%

🌱 just a girl held together by spite + ice packs πŸ’« ur chronic illness bestie with a podcastπŸŽ™οΈ πŸͺ© founder of Chronical...

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