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Myasthenia Gravis
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0:43
Facebook
Myasthenia Warrior
Life with Myasthenia Gravis can be difficult. Some days my symptoms come out of nowhere. Some days I can feel it coming. It is hard being a mom, a partner, working and trying
Myasthenia Warrior. Myasthenia Warrior · Original audio. Life with Myasthenia Gravis can be difficult. Some days my symptoms come out of nowhere. Some days I can feel it coming. It is hard being a mom, a partner, working and trying to run a small business. I don’t always have energy to do things. Be kind to others! You never know what people ...
2K views
9 months ago
Myasthenia gravis Symptoms
0:04
Myasthenia Gravis Symptoms can fall into 3 different categories: Ocular, Bulbar and Generalized. 👀 Ocular symptoms Droopy Eyes 👁️ Blurry/Double Vision 🫨 👄 Bulbar symptoms Weak face, throat and neck muscles Slurred/Nasal speech 🎤 Difficulty Chewing/Swallowing 🤤 Difficulty Talking 🗣️ 💪Generalized symptoms Weaks arms and legs 💪🦵 Weak diaphragm 🫁 Difficulty walking 🚶 Difficulty breathing 😮💨 Muscles tire with repetitive use. Often worse later in the day. 🫵 By raising awareness, we
Facebook
Myasthenia Warrior
6.6K views
4 months ago
Myasthenia Gravis Nursing Diagnosis & Care Plan - NurseStudy.Net
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Dec 31, 2024
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Myasthenia Gravis is rare—but the impact is huge. 💙 In this video, I break down just how rare MG is, how many people are affected in the U.S. and worldwide, and why diagnosis often takes far too long. Awareness matters. The more we talk about MG, the sooner lives can change. 👉 Watch, learn, and share to help make the rare more recognized. #myastheniawarrior #myastheniagravis #autoimmune #InvisibleIllness #raredisease
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Myasthenia Gravis is rare—but the impact is huge. 💙 In this video, I break down just how rare MG is, how many people are affected in the U.S. and worldwide, and why diagnosis often takes far too long. Awareness matters. The more we talk about MG, the sooner lives can change. 👉 Watch, learn, and share to help make the rare more recognized. #myastheniawarrior #myastheniagravis #autoimmune #InvisibleIllness #raredisease
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Living with Myasthenia Gravis (MG) means learning to listen to your body in a way most people never have to. MG isn’t just about muscle weakness — it’s about understanding that your muscles may tire quickly, symptoms can shift throughout the day, and rest isn’t optional — it’s essential because strength often returns after rest and worsens with use. Some days you might feel strong after a good night’s sleep, and other days even simple tasks can feel heavy — and that’s okay. Your body is talking
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Case Study 182 – Myasthenia Gravis 🧠💪 June is Myasthenia Gravis Awareness Month—and in this case, we’re breaking down the real-life presentation, pathophysiology, and treatment of a condition that affects about 20 out of every 100,000 people. This autoimmune neuromuscular disease often hides in plain sight—causing muscle weakness, drooping eyelids, and even trouble breathing. Knowing the signs can save a life. Watch, learn, and share. Awareness leads to earlier diagnosis—and better outcomes. �
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💙 Myasthenia Gravis (MG) is a chronic autoimmune condition that affects how nerves communicate with muscles — leading to weakness that can come and go. One of the first signs often shows up in the eyes 👀. Many people with MG experience ptosis (droopy eyelids) or diplopia (double vision), even when they’re not tired. If you notice your eyelids drooping or see double for no clear reason, don’t ignore it — 💬 get checked out by a doctor. Early diagnosis can make a big difference! #MyastheniaGravi
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An estimated 15 to 20 percent of people with myasthenia gravis will experience at least one myasthenic crisis in their lifetime. Anything from stress, infection, or surgery to an adverse reaction to medication can trigger a myasthenic crisis. Learn more about the signs and symptoms of myasthenia gravis at https://www.americanbrainfoundation.org/diseases/myasthenia-gravis/ | American Brain Foundation
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