Guest Interviews Archives - Ashley's Anatomy

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Ashley's Anatomy

Chronically Navigating Through Life

Meet The Autoimmune Bully: Coach Anita Monique

Meet The Autoimmune Bully: Coach Anita Monique

March 31, 2025

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

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

February 28, 2025

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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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