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Ashley's Anatomy

Chronically Navigating Through Life

5 Ways MG Has Changed My Daily Routine

November 21, 2025

I live with a rare condition called Myasthenia Gravis (MG), and I wish more people understood how it touches every part of my life, from the work I do to the routines that get me through each day. Before I…

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Living with Myasthenia Gravis: My Personal MG Journey

November 18, 2025

Ever watch a movie and catch a small detail that hints at what’s coming next? A character says, “I have a bad feeling,” and then the story unfolds exactly that way. That’s foreshadowing. And honestly, it’s the best way I…

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Meet The Autoimmune Bully: Coach Anita Monique

March 31, 2025

When Coach Anita Monique was diagnosed with Multiple Sclerosis (MS) in 2016, she refused to let the condition define her life. Affectionately known as The Autoimmune Bully, she embraces this title as a declaration of strength. “MS is feared by…

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Rare But Real: Brooke H. Life with Stiff Person Syndrome

February 28, 2025

Welcome to Ashley’s Anatomy, where we aim to share real stories highlighting the experiences of those living with chronic conditions. Every year on February 28th (or 29th in leap years), we recognize Rare Disease Day, a time to shine a…

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Brain & Life Podcast Featuring Ashley B.

June 23, 2023

I had the pleasure of speaking with Dr. Correa with Brain & Life Podcast to discuss my journey with MG. To listen or read the full transcript you can visit their website: Brain & Life Podcast Episode Description: This week…

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The Benefits of Journaling With Myasthenia Gravis

May 23, 2023

Hey, everyone! I have the opportunity to share my experiences living with Myasthenia Gravis on WebMD. I wanted to ensure my subscribers and fellow MG’ers could find recent posts, so I will be posting the link to each post on…

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How I Educate Others About Myasthenia Gravis

May 8, 2023

Hey, everyone! Sorry, I’m sharing this one kind of late. If you’re new here, I have the opportunity to share my experiences living with Myasthenia Gravis on WebMD. To ensure my subscribers and fellow MG’ers can find recent posts, I…

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How I Work and Make Money With Myasthenia Gravis

March 30, 2023

Hey, everyone! I have the opportunity to share my experiences living with Myasthenia Gravis on WebMD. I wanted to ensure my subscribers and fellow MG’ers could find recent posts, so I will be posting the link to each post on…

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How a Chronic Condition Like Myasthenia Gravis Affects My Identity

February 26, 2023

Hey, everyone! I have the opportunity to share my experiences living with Myasthenia Gravis on WebMD. I wanted to ensure my subscribers and fellow MG’ers could find recent posts, so I will be posting the link to each post on…

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What I Wish People Knew About Myasthenia Gravis

August 30, 2022

This post is dedicated to all of my peeps who don’t quite understand what Myasthenia Gravis is. If I had a dollar for every time someone asked me “What is Myasthenia Gravis?”, I’d be rich. Seriously, it’s rare and I’m…

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Myasthenia Gravis Resource Guide

October 8, 2021

Well first off, welcome to Ashley’s Anatomy. My goal is to share experiences and a few helpful tips that I’ve learned along my chronic illness journey. If this is your first time stopping by feel free to take a look…

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Top 5 Must Haves for Spring Pussy Health

October 19, 2020

Hello Everyone! Spring has officially sprung. I LOVE this time of year; the April showers and May flowers, everything comes to life. If you guys are anything like me, seasonal changes cause your body to go a little Cray-Cray. Especially…

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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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  • Secrets to Growing Healthy Locs Secrets to Growing Healthy Locs $10.00 Original price was: $10.00.$3.00Current price is: $3.00.
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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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