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Ashley's Anatomy

Chronically Navigating Through Life

Doin’ What I Want: A 2026 Check-In

March 13, 2026

Growth, Fear, and Living Authentically

This year I started with a clear intention: “Doin what I want.”

Truth be told, I lost the plot for a little while. I wasn’t satisfied with the way I was living. I found myself sitting at home feeling unchallenged and unfulfilled because I had started playing small.

I stopped sharing my real-life, watered down my truths, and slowly pulled back from showing up the way I once did. I turned down opportunities of a lifetime because I was fearful. I forgot that I create my own reality.

Well… if you don’t like something, change that shit.

That’s exactly why this year I’ve been “Doin what I want.” I’m protecting my energy and saying yes to meaningful opportunities. I’m talking my shit, and taking it back to the basics and sharing what started Ashley’s Anatomy… the writing.

So I’m sharing again. Through writing.

I’m No Worker Bee

If you know anything about me, you know I hate working for other people. It’s always a struggle going from being your own boss to cosplaying as a worker in a traditional 9–5. I usually take contract positions because they offer more flexibility, perfect for people with questionable attendance like me.

Maintaining a conventional job has always been hard for two reasons: I hate anyone telling me what my schedule is, and working a job can seriously stifle my creative energy. It’s hard to create when you’re tired as hell.

That’s exactly what I’ve been experiencing lately. Between work and the chronic fatigue that comes with living with Myasthenia Gravis, I’ve been worn down. And on top of that, Ashley’s Anatomy is a whole ass business in itself: meetings, brand emails, and the constant work of creating and maintaining content.

If you’ve noticed, I haven’t been as active in my Ashtrology Shop either. New products are in the making, I promise.

By the end of the week, I’m exhausted. Most weekends are spent recovering, only for me to realize I didn’t record or post last month’s newsletter because I was too tired to write.

I have been working as a contractor for a hospital remotely since September and was recently offered a full-time position (YAYYYYYYY!). Is it weird to say I wasn’t super ecstatic? It meant starting the whole process of requesting workplace accommodations. Necessary for job security with MG, but definitely a headache.

I’ll keep y’all posted on how the process goes, but your girl has a full-time job with benefits now.

Stabbing Myself in the Thighs Every Day

After eight years of receiving IV infusion treatments, I recently switched to a self-injection medication. It wasn’t a decision I made lightly. In fact, I wrote about the experience for WebMD; you can read it here: How Changes in My MG Meds Affect Me.

One thing I consistently noticed with my IV treatments was that the effects would start to wear off a few weeks before my next infusion. That gap made a real difference in my schedule and in how many “usable” days I had each month.

So my neurologist started asking me: what if there was a medication with a similar mechanism to the one I’m already on, but without that drop-off between treatments? It sounded ideal, so I decided to give Zilbrysq a try.

I won’t lie, the idea of stabbing myself in the stomach or thighs every day made me nervous. I’ve had surgeries, countless IVs, and I’ve even helped save a few lives in my time in healthcare, but the thought of putting a needle into my own body gave me pause.

I’m only on day three (3/12/2026) of the injections (currently going with the thighs), but I’ll be sharing a more detailed update soon. One thing I can tell you already, though: I’m definitely not a fan of stomach shots.

What’s to Come for AA

I have a few upcoming interviews and opportunities focused on community building for my fellow MG’ers, and I’m really excited about sharing some loc and makeup product reviews. One thing I’ve learned on this journey is that none of us is meant to navigate chronic illness alone. I want to continue sharing stories, resources, and real conversations.

I invite you to follow along and keep up with updates over on Instagram at _ashleysanatomy. There’s more writing, more conversations, and more community coming soon, and I’m grateful you’re here for it.

Let’s Stay Connected 💫

Loved this post? There’s more where that came from!
Follow me on social media for inspiration, behind-the-scenes content, and real talk about beauty, chronic illness, and everything in between.

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Read More
  • Doin’ What I Want: A 2026 Check-In
  • Taliah Waajid Love My Locs Leave-In Conditioner Review
  • THE ATL MG BRUNCH & LEARN: RECAP
  • 5 Ways MG Has Changed My Daily Routine
  • Living with Myasthenia Gravis: My Personal MG Journey

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MEET ASHLEY B.

About Me
Living with a rare neuromuscular autoimmune disease, I’m a published blogger, founder, and passionate chronic illness advocate. A loc’d beauty with a love for scents, skincare, and all things self-care. Let’s connect—find me on my socials below!

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Doin’ What I Want: A 2026 Check-In

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Chronic Illness Bloggers
🌸 My My Hero 360 interview is officially LIVE! We 🌸 My My Hero 360 interview is officially LIVE!
We talked about my journey with myasthenia gravis, patient advocacy, and finding purpose through life’s challenges.
I’d love for you to give it a watch and let me know what resonates with you. 💕
🎥 Link in bio!
🌸 Thank you @myhero.360 for the opportunity to share. 
#MyHero360 #MyastheniaGravis #RareDisease #PatientAdvocate #AshleysAnatomy ChronicIllness
Taking a break from the MG content to give you all Taking a break from the MG content to give you all a loc product review 💜(it’s been a while). When I’m not feeling like myself, self care always does the trick ☺️. 
Today I am trying Loc Hoopz for the first time on my locs! ✨ 
This is Part 1️⃣ of the process, stay tuned for the final results and my full review.
💜 Using 2 packs of the long Loc Hoopz curlers 
💜 If you want to try them for yourself, use my code ASHLEYSANATOMY10 for 10% off your order.
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#LocHoopz #LocStyles #loccurls #LocJourney #NaturalHairCare
❄️ June is Myasthenia Gravis Awareness Month! 🎀 M ❄️ June is Myasthenia Gravis Awareness Month! 🎀

Myasthenia Gravis (MG) is a rare autoimmune neuromuscular disease that causes muscle weakness and fatigue by disrupting communication between the nerves and muscles.

Symptoms can include:
✨ Drooping eyelids
✨ Double vision
✨ Difficulty speaking or swallowing
✨ Weakness in the arms and legs
✨ Shortness of breath
✨ Extreme fatigue

MG is often invisible, unpredictable, and misunderstood, but for those of us living with it, the impact is very real.
This month, I’m helping spread awareness, sharing my journey, and amplifying the voices of others in the MG community 🩷
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#MyastheniaGravis #MGAwarenessMonth #RareDiseaseAwareness #ChronicIllnessWarrior #MGStrong
💗 June is Myasthenia Gravis Awareness Month, and i 💗 June is Myasthenia Gravis Awareness Month, and it only feels right to share what I’ve been navigating behind the scenes.

What started as the flu quickly spiraled into one of the most severe MG exacerbations I’ve experienced. Within days, I found myself in the ICU fighting to regain strength to breathe & walk comfortably. 

✨This carousel walks through my timeline, treatments, and what recovery has looked like so far. ℹ️I’m unable to get IVIG for MG emergencies ✨

🩸 PLEX is a procedure that removes blood from the body, separates out the plasma containing harmful antibodies, and returns the blood with replacement fluids. For MG’ers it can help remove the antibodies that attack communication between nerves and muscles.

💕If Ashley’s Anatomy has ever educated, encouraged, or helped you feel less alone, I would be grateful if you would:
✨Like & interact with my post
✨ Share my mutual aid request
✨ Donate if you’re able
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#MGAwarenessMonth #MyastheniaGravis #MGWarrior #RareDisease #rarediseaseawareness
🌸🎀🌸 #locs #locgoddess #naturalhair #loccommunity 🌸🎀🌸
#locs #locgoddess #naturalhair #loccommunity
Got questions about life with MG? This is your spa Got questions about life with MG? This is your space 🩷
I’ve partnered with @myastheniagravisnews a few days to answer your questions. 

✨ Ask me anything 
✨ Read and learn from others
✨ Be part of a community that truly gets it

🗓 March 23–27
Come join the conversation, I’d love to hear from you 💬
Drop your questions in the forum or just come read and connect.

🔗Sign up at the link in my bio 
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#ad #bionews #rarediseasecommunity #myastheniagravis

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