What Exactly is Myasthenia Gravis (MG)
For many, “myasthenia gravis” is a mouthful of syllables they hope they’ll never have to hear. I first heard them while lying in a hospital bed, surrounded by doctors who were unsure why my body was failing to follow my brain’s instructions. I hoped I would never hear the term again, that this was a one-time occurrence.
But nearly a year and hours of research later, I have a much better understanding of what myasthenia gravis is; it’s a breakdown in communication. While the science behind it is complex, the lived experience is simple: the body’s “wiring” is being intercepted.
To help spread awareness, I want to walk you through the mechanics of this often debilitating invisible illness.
Attack of the Self
Myasthenia gravis is an autoimmune disorder.
Imagine your immune system as a highly trained security team meant to protect you from “contaminants” like viruses or bacteria. In an autoimmune disease, the security team gets confused. It mistakes your own healthy tissue for an intruder and begins an internal war. The attacks cause inflammation which affect many parts of the body. The areas affected depend on which autoimmune disease a person has but can result in persistent symptoms like extreme fatigue, joint pain, and digestive problems, which can come in cycles of flare-ups and remission.
In MG, the target of this confusion is the system that controls your voluntary muscles–the ones you choose to move, like your arms, eyelids, and even the muscles that help you breathe.
Anatomy & Physiology 101
To understand MG, we have to look at how a thought becomes a movement within the complicated network that is your body.
Your brain is responsible for a number of things, including converting complex thoughts into verbal language, relaying emotions through subtle body language, and simultaneously coordinating hundreds of muscle fibers while playing a sport.
The brain acts as an illustrious composer, creating a symphony of moving parts to get your muscles moving. Like a resonant bell, an electrical impulse travels from the brain, down your nerves, to the muscle. This impulse reverberates into a neuromuscular junction, let’s call it “the bridge”, a gap at which nerve signals get translated into muscle movement. This bridge is where nerve endings meet muscle fiber to trigger muscle contraction.

To cross this bridge, the nerve releases a chemical “messenger” called Acetylcholine (ACh)
- The messenger (ACh) floats across the bridge
- It lands in receptors (think of these as “landing pads”) on the muscle side
- Once enough messengers land, the muscle contracts. Your body is moving!
The Saboteurs
To recap, voluntary movement requires communication between a nerve and muscle.
For those with MG, that communication is interrupted. The immune system makes antibodies that act like saboteurs on the bridge. These antibodies block, change, or destroy the “landing pads”, so the messenger (ACh) has nowhere to go.
The result? The brain sends the signal, but the muscle never receives the message. A once harmonious melody now transformed into a disjointed and dissonant rhythm.
There are three main “saboteurs” (antibodies) that are currently recognized:
- AChR | The Common Saboteur: Found in about 85% of patients. It blocks the main landing pads throughout the body
- MuSK | The Specialized Saboteur: Found in about 10% of patients. This often affects the muscles of the face, throat, and breathing more severely
- LRP4 | A New Challenger: A rarer variant that is still being studied by modern medicine
No Saboteur Detected?
Some people have Seronegative MG (SNMG). This means they have all the symptoms but our current tests can’t detect the antibodies yet. The bridge is still broken; we just haven’t been able to catch the saboteur.
Feeling Off Key – Symptoms of MG
Because MG affects voluntary muscles, the symptoms often start where the muscles are smallest or used most often.
The Eyes (Ocular MG)
For Over 50% of people, the eyes are the first sign
- Ptosis:a sleepy, drooping of one or both eyelids
- Diplopia: double vision that may affect the horizontal or vertical vision; may improve or stop when one eye is closed
The Face & Throat (Bulbar Symptoms)
About 15% of patients’ first symptoms involve face and throat
- Speech: Voice may sound soft or nasal
- Swallowing: An increased risk for choking, with liquids sometimes going into the nose due to weakness of the throat muscles
- Chewing: Eating hard or tough foods like steak causes fatigue, making it difficult to swallow. A soft food diet is often recommended for those who experience bulbar symptoms
- Facial Expressions: Patients may lose the ability to communicate with full expressions as weakness can lead to trouble raising eyebrows or smiling
The Limbs & Neck
Generalized MG is associated with weakness of the extremities and neck. This can feel like your arms are made of lead, dragging you down with the simplest of movements. Even holding your neck up feels next to impossible, leaving you wondering if your head was replaced with a bowling ball.
The Thymus Gland
Interestingly, the root of the problem can lie in the thymus gland, which is located in your chest. It’s the training ground for your body’s immune cells, and in many MG patients the thymus grows to an irregular size and develop small tumors (thymomas). These continue to pump out the confused antibodies that cause the internal war within the body.
A Vital Note: Myasthenic Crisis
There is a point where MG moves from difficult to life-threatening. When muscles that support breathing, such as your diaphragm and chest, become too weak, you enter a myasthenic crisis.
At this point, the body is experiencing extreme weakness that does not resolve with rest. The body’s respiratory muscles are too weak to support sufficient breathing, putting you at risk for intubation.
If you find it difficult to breathe, swallow your own saliva, or hold your head up, seek emergency medical attention immediately.
An Individual Experience
Like any chronic illness, it’s important to know that MG affects everyone differently. No two cases are exactly alike. Symptoms can fluctuate on an hour to hour basis, which can make planning just one day ahead difficult. Completing the simplest tasks when fatigue hits can feel impossible. However, it’s important to remember that with treatment and support, symptoms can be managed.
As for my own journey with MG, it’s been almost a year since my first crisis; a moment full of confusion and loss. But in that time I’ve had an abundance of time to reflect on the changes MG has brought into my life. It’s forced resilience through a journey of adaptability, and through it I’ve learned to stop viewing my body as broken, and instead as one that’s simply learning to play in a new key.
Further Reading & Sources
Seronegative MG Resource Center | Myasthenia Gravis Foundation of America
Autoantibody Specificities in Myasthenia Gravis; Implications for Improved Diagnostics and Therapeutics
Myasthenia Gravis With Antibodies Against Muscle Specific Kinase: An Update on Clinical Features, Pathophysiology and Treatment
Myasthenia gravis – Symptoms and Causes | Mayo Clinic
Myasthenia Gravis | National Institute of Neurological Disorders and Stroke
Neuroanatomy, Motor Neuron – StatPearls – NCBI Bookshelf
Acetylcholine receptor antibody: MedlinePlus Medical Encyclopedia
Generalized myasthenia gravis with acetylcholine receptor antibodies: A guidance for treatment – PMC
Could You Have an Autoimmune Disease? Key Symptoms to Know
It’s been a pleasure writing this article and I sincerely hope I’ve been able to help you better understand the complex science behind myasthenia gravis. I’ve been meaning to write this one for a while, but wanted to get all the details down in a way that was easily digestible and not overwhelming. Let me know if the “bridge” analogy was helpful in visualizing things 🙂
I also have a post on instagram that illustrates this in a much more condensed manner. So if a short animation is much more your speed, feel free to check that out here: Myasthenia Gravis. Let’s talk about it
Let’s Unfold Together:
When your body’s “symphony” feels out of tune, what is one small thing (a candle, a song, a pet) that brings you back to center?
If you are a fellow spoonie, what is one term or concept you wish someone had explained to you simply when you were first diagnosed?


Share your thoughts!