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Ashley's Anatomy

Chronically Navigating Through Life

About

Who is Ashley B.?

Hi there! I’m Ashley of Ashley’s Anatomy. I am the writer, graphic designer, photographer, model, and editor—in—chief here. I live life with an invisible illness called Myasthenia Gravis (MG). If you’ve never heard of this disease, then don’t feel bad, some of my doctors and nurses haven’t either. MG is a rare neuromuscular autoimmune disease that affects your ability to control your voluntary muscles. You can read my blog post about MG here: What is Myasthenia Gravis. Hopefully, you will understand what MG is when you leave my site.

Featured on: VoyageATL WebMD Canvas Rebel Brain & Life Podcast Brain & Life Magazine

My Story

I was attending Georgia State University in 2017. Ironically enough I was in school studying to become a Respiratory Therapist. See, MG affects your breathing muscles tremendously! It’s a huge respiratory concern. I started having double vision, and couldn’t form a smile, or chew my food at the end of my days at school. I finally visited my primary care physician. I was officially diagnosed in my junior year of the program (April 2017). I’m happy to share that I stayed in school and graduated with a bachelor’s in respiratory therapy. Yep, that’s right it’s Ashley B., RRT. I’ve worked as a pediatric and adult therapist. I’ve even had the pleasure of treating other patients with Myasthenia Gravis.

Why do I do this?

Although I was familiar with MG from school, I still scoured the internet for support groups, chat forums, blogs, and everything under the sun when I was newly diagnosed (still do). I searched for stories and advice from other women dealing with life with an autoimmune disease. I created Ashley’s Anatomy to serve as a resource for others. I try my best to update relevant resources here: MG Resource Guide. My goal is to share my story and experiences with the hope of helping someone in a similar position. I use my unique experiences to raise awareness, educate, and support others with chronic illnesses.

What’s Ashley’s Anatomy?

Ashley’s Anatomy is a beauty and chronic illness blog. I have integrated my passion for beauty and wellness products into my mission. I am a lover of beauty products and a sucker for beautifully packaged products. I aim to provide honest product reviews. Guest bloggers are also welcome. Check out the Guest Blogger Application Here. If you have any questions or want someone to chat with, please always feel free to reach out whether via comments, email, or my contact page.

Let’s Connect

Instagram: @_AshleysAnatomy

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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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BADGES

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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