Arthritis Meggie

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Arthritis Meggie autoimmune, chronic pain & co
JA kid turned writer.advocate. wife. mom. inflamed & unwell since ‘95
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I posted this  last night on stories and it resonated with a lot of you so I wanted to give it a permanent spot on the f...
04/11/2025

I posted this last night on stories and it resonated with a lot of you so I wanted to give it a permanent spot on the feed 🤍

❄️‼️ GIVEAWAY ALERT!!! ‼️❄️I reach for my  DAILY!! For migraines, sore joints, surgery recovery, even just cooling down ...
29/08/2025

❄️‼️ GIVEAWAY ALERT!!! ‼️❄️
I reach for my DAILY!! For migraines, sore joints, surgery recovery, even just cooling down or decompressing. What sets them apart is how well they actually work: they stay cold for hours, they’re weighted so they really feel so soothing , and they were created by women who live with migraine and chronic illness🤍
I’m teaming up with ReLeafpack to give one of you a ReLeafpack + ReLeafbuddy set (you pick the style and optional scent!), plus some extra goodies.
How to enter:
1️⃣Follow and
Like this post
2️⃣Comment how you’d use the cooling relief of releaf pack
3️⃣Tag a friend
⭐️Bonus entry: Share this post to your story and tag us so we see it.
Details:
-U.S. only
-Ends September 2nd 2025 at 12pm EST!
-Winner announced in stories and contacted *only* by me or (beware of fake accounts!!)

I didn’t learn these lessons overnight. I learned them from missing out, from overdoing it, from feeling judged, from ex...
27/08/2025

I didn’t learn these lessons overnight. I learned them from missing out, from overdoing it, from feeling judged, from explaining myself a thousand times when I didn’t really need to, from crashing hard and then doing it all over again.

And if any of this feels familiar, just know I see you, and you’re not alone in it. 🤍

One of the most frustrating parts of chronic illness is how blurred all the lines become. Symptoms start to look like me...
21/08/2025

One of the most frustrating parts of chronic illness is how blurred all the lines become. Symptoms start to look like medication side effects. The things we’re told will “help” often end up triggering a flare. Even doctors don’t always know where one circle ends and the other begins.
That constant overlap is exhausting because it leaves you second-guessing yourself all the time. Is this my illness? Is it my meds? Is it just in my head? When nothing fits neatly into one category, it’s easy to feel like you’re the problem.
But here’s the truth: you’re not the problem. Chronic illness is complicated and messy.

➡️ Scroll to the last slide for a blank template you can screenshot and use to make your own!!










I can’t resist a good trend sooo I present: The Life of a Chronic Illness Girl. The an album no one asked for, made enti...
13/08/2025

I can’t resist a good trend sooo I present: The Life of a Chronic Illness Girl. The an album no one asked for, made entirely of moods we know too well 😉 plans canceled because your body said no, arguing with insurance, explaing your symptoms over and over, and somehow surviving the flares that never quit. It’s exhausting, infuriating, isolating. No perks, no awards, just life of a chronic illness girl.











What’s your vibe today slide 1-10??! I’m feeling a mix of 1, 5 and 7 🫠
12/08/2025

What’s your vibe today slide 1-10??! I’m feeling a mix of 1, 5 and 7 🫠












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