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"Invisible" symptoms of MS 🧡 Do they look invisible? Sometimes. Do they feel invisible? Never. Quite often, the invisible symptoms are the ones that are hardest to deal with. Do you have any sy
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Part 2: The invisible symptoms of MS that are hardest to explain. Just because you can’t see it, doesn’t mean it isn’t real. 🙃 Continue the conversation 💬 . . . #Awareness #MultipleSclerosis #Invi
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Part 3: The invisible symptoms of MS people don’t always see. ✨ Tremors. Muscle stiffness. The “MS hug.” Balance issues. Trouble swallowing. Constant, invisible pain. Not everything shows on the out
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TGIF✨ This is your reminder that happiness is a journey and not a destination. 🙏🏼 Living with chronic illness means learning how to carry both hope and uncertainty at the same time. It teaches you
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I’ve just received all of my MRI images from diagnosis 13 years ago up to now, and it’s such a surreal thing to look through. 🫪 MRI scans are fascinating, but also a little freaky. Especially when y
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MS still doesn’t have a cure, but that doesn’t mean nothing can be done. 🧡 The reality is, treatment has come a long way. Many people with MS are now able to reduce relapses, slow progression, and k
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Nobody is telling you this, but living with a chronic illness means constantly thinking about things other people never have to- energy, pain, pacing yourself, recovery, and whether your body will cop
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Motivation is unreliable. Tiny steps are repeatable. Some days “success” is just putting both feet on the floor, and that still counts. 💪🏼 How are we all feeling today? 🧡 #multiplesclerosis #livi
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Reflection time ✨ How has living with a chronic illness affected you? 💬 #multiplesclerosis #invisibleillness #strength #journey #awareness
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I had such a lovely time on our annual trip to Butlin's last year, but this year has felt even more special. The pain still showed up (of course it did… day one 🙃), but the difference is how I handl
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Being 35 is supposed to be about building, growing, planning ahead. Throw MS into the mix, and suddenly there are questions you never expected to carry. Some of these fears are loud. Some sit quietly
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MS fatigue isn't just tiredness. It's losing spoons you didn't even know you had. Which one hits you hardest? 🧡 #multiplesclerosis #spoonielife #spoonie #fatigue #invisibleillness
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About @ms.and.me

Ami 🧡 | Living with MS | 🧡 is a verified Instagram nano influencer in the Personal blog category. With 3.8K followers and 12 posts, ms.and.me's account shows a follower-to-following ratio of 1.5:1. View all content anonymously on Pictame - no login required.

ms.and.me's engagement rate sits at 9.87%. That's 97% above what you'd typically see for accounts with 1K-10K followers (average 5%) — a sign of a genuinely connected audience.

Out of the last 12 posts, 67% are videos and 33% are photos. Notably, videos tend to get 2.1x more engagement than photos. Content shows up about every 6 days. Captions lean moderate, averaging 465 characters.

9.87% engagement rate — 97% above average for 1K-10K follower accounts.
67% videos, 33% photos. Videos get 2.1x more engagement here.
Posts about every 6 days.
1.5:1 follower-to-following ratio.

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@ms.and.me

Ami 🧡 | Living with MS | 🧡

PublicPersonal blog
Posts
12
Top Hashtags
#multiplesclerosis#invisibleillness#awareness#spoonielife#comment#journey#life#spoonie

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

#wedding#foodporn#drawing#likeforlike#beach#insta#cat#memes#nofilter#flowers#amazing#hair
Followers
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2.5K
Avg. Likes
345
Avg. Comments
31
Engagement
9.85%

Real talk about invisible illness, surviving one day at a time 🙌 RRMS 2013 🧡 | Bronchiectasis 2023 🫁 👇 Follow for re...

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