What is MG?
gMG is a rare, chronic autoimmune neuromuscular disease Rare autoimmune disease of the NMJ that may result in chronic impaired muscle function1
What are the symptoms of gMG?

- Droopy eyelids
- Double vision

- Difficulty speaking
- Jaw fatigue

- Weakness in the arms, hands, fingers, and legs

- Poor cheek puff
- Drooling

- Weakness in the neck

- Fast breathing
- Respiratory failure
Prevalence and incidence of MG
The worldwide prevalence of MG is estimated to be between 80 and 278 per million1-7

Manifestation of MG


- Jaw fatigue/difficulty chewing
- Difficulty swallowing (dysphagia)
- Nasal speech (dysarthria)
- Hoarseness (dysphonia)
- Diaphragm weakness/difficulty breathing
- Respiratory failure

Characterized by fluctuating and fatigable muscle weakness,often in the ocular muscles

In 80%of patients, the disease generalizes
(gMG)to affect other muscles
Unpredictable gMG symptom fluctuations lead to a profound burden
96% experienced symptom fluctuations In concept elicitation interviews conducted in 28 adult patients with gMG.




Vision problems in gMG are common and may impact QoL
These issues can have a negative impact on activities of daily living, such as working or driving
Patients rate vision problems as one of the top 2 most burdensome gMG symptoms
~85% of patients with gMG experience ocular muscle weakness, which can be progressive
- Resultant double vision and ptosis can impact quality of life
- 54%-79% of patients with gMG (n=22/28, n=245/452, respectively) report double vision
gMG exacerbation and myasthenic crisis
- Generally defined as significant worsening of gMG symptoms
- Typically requires inpatient treatmentv
- The most severe type of gMG exacerbation is myasthenic crisis
- Severe weakness in respiratory muscles, leading to respiratory failure and requiring
- Intubation and mechanical ventilation
Certain factors are associated with worsening of symptoms and with a high risk of exacerbations2

Late onset of disease

Late onset of disease

Late onset of disease

Late onset of disease

Late onset of disease

Late onset of disease
gMG crises
- Are more common on the first 2 years following disease onset
- Can cause acute symptoms that impact daily life
- Can lead to hospitalization, mechanical ventilation, tube feeding, and death

of patients may experience MG-related hospitalizations, moststriking within the first 2-3 years of disease onset
This retrospective longitudinal cohort study evaluated 1149 adult patients with gMG living in England using data recorded from 1997 to 2016

of hospital stays were followed by discharge to a skilled nursing or longterm acute-care facility.
Hospitalized and treated between 2010 and 2019 in USA
Burden of gMG impact multiple aspects of individuals' livesa

Emotional impact
- Anxiety (82%)
- Depression/sadness (75%)
- Frustration (64%)
- Fear (57%)
- Embarrassment (54%)

Social impact
- Dating/partner (57%)
- Feeling misunderstood (46%)

Physical impact
- Gross motor impairment (93%)
- Hobbies and sports (89%)
- IADLsb (82%)
- ADLsc (57%)
- Fine motor impairment (46%)

Other life domains
- Impact on work/career (100%)
- Need for increased planning (89%)
- Sleep disturbances (89%)
- Needing assistance (64%)

