Lemon8Lifestyle community
lyndsijohnson
lyndsijohnson

5617 followers

Follow
Follow
Follow
An image depicting a 'Myasthenia Gravis Starter Pack' with a woman holding a French bulldog, a bottle of Mestinon, an IV stand, and a pillow, all packaged in a blister pack style.
An infographic illustrating Myasthenia Gravis symptoms categorized by body regions: Ocular (diplopia, ptosis, ophthalmoplegia), Respiratory (breathlessness, weak breathing, respiratory failure), Bulbar (fatiguable chewing, dysarthria, dysphagia), and Limbs/Neck (dropped head, proximal > distal, arms > legs).
An infographic titled 'How Myasthenia Gravis Affects the Body,' showing a central human figure surrounded by illustrations of symptoms such as drooping eyelid, blurred vision, slurred speech, difficulty breathing, changes in facial expression, difficulty chewing or swallowing, arm and leg weakness, muscle fatigue, and trouble moving the neck.
A diagram of a human face highlighting symptoms like smoothing out of the forehead, eyebrow droop, and drooping of the corner of the mouth, alongside text describing Myasthenia Gravis symptoms including eye muscle weakness, difficulty swallowing, and slurred speech.
A table outlining the 'Main Types of Myasthenia Gravis,' including Ocular, Generalized, and Transient neonatal myasthenia gravis, with columns for definition, prevalence, and prognosis for each type.
A grid of six illustrations depicting common symptoms of Myasthenia Gravis: muscle weakness, fatigue, droopy eyelids, blurry or double vision, limited facial expressions, and trouble walking.
1/7

You may also like

No content
See more on the app
See more on the app
See more on the app
2 saved
3
10

Myasthenia Gravis Action Figure & information

I was severely gaslit and this disease left me bedridden for two years. I was then in a wheelchair and had to wait until I advocated for a treatment that worked with my body and not against it. I almost was unalived multiple times. A ton of ICU stays and hospitalizations in the process. I’m hoping this series of photos helps someone identify MG in their self (like I did when my initial doctors said I was lying when it came back I had a RARE antibody for it). This almost unalived me with delayed care, gaslighting, and lack of knowledge about this disease. If you are showing any of these signs and symptoms, please SPEAK UP and don’t let them say it’s nothing if you know it’s something. YOU KNOW YOUR BODY BETTER THAN ANYONE ELSE!! #myastheniagravis #raredisease #myastheniagravisawareness #generalmyastheniagravis #ocularmyastheniagravis #facialdrooping #nuero #hospital #rare #learnontiktok #fypシ

2025/7/11 Edited to

... Read moreMyasthenia Gravis (MG) is a chronic autoimmune disease affecting the communication between nerves and muscles. Its symptoms can vary widely, but they often include muscle weakness, fatigue, and ocular issues such as drooping eyelids or blurred vision. Patients may experience fluctuating weakness in the limbs and face, leading to very real challenges in daily activities. Awareness is key when dealing with rare diseases like MG. Often misdiagnosed or overlooked, the early signs may include difficulty in speaking (dysarthria), eating (dysphagia), and respiratory issues such as breathlessness. Despite the hardships, sharing experiences can empower others who might be struggling with their health. In dealing with MG, advocacy for proper treatment is crucial, as many individuals face gaslighting or disbelief from peers and sometimes healthcare professionals. Initiatives aimed at raising awareness and supporting those living with rare diseases are vital for better diagnosis and treatment options. By encouraging people to recognize symptoms and advocate for themselves, we can foster a more informed and supportive community around Myasthenia Gravis. The path to treatment can often be long and fraught with challenges, but understanding the disease, its signs, and the importance of voicing concerns can lead to better outcomes and a healthier life. If you experience symptoms consistent with MG, do not hesitate to seek medical advice, educate yourself, and join support groups to share your journey.