Evidence checklist
Myasthenia Gravis
Evidence strength
Mark what you already have below and your evidence strength appears here.
Specialist opinion
Highest value0 of 4 collectedSerological testing showing positive AChR binding, blocking, or modulating antibodies (positive in approximately 85% of generalized MG), or anti-MuSK antibodies in seronegative cases. Positive results confirm the autoimmune diagnosis.
Not marked
Repetitive nerve stimulation showing decremental response at 3 Hz, or single-fiber EMG showing increased jitter — the most sensitive electrodiagnostic test for myasthenia gravis.
Not marked
Medical opinion connecting MG to in-service stress, infection, medication, or toxic exposure that triggered autoimmune dysfunction during military service.
Not marked
CT of the chest documenting thymoma or thymic enlargement, which is present in 10-15% of MG patients and is surgically significant.
Not marked
Treating physician
0 of 1 collectedMyasthenia Gravis Foundation of America (MGFA) clinical classification (Class I-V) and Quantitative MG (QMG) score documenting the distribution and severity of weakness.
Not marked
Treatment records
0 of 1 collectedRecords of acetylcholinesterase inhibitor use, immunosuppressive therapy, IVIG/PLEX for crises, and thymectomy records.
Not marked
Lay statements
0 of 2 collectedA written statement from someone who can describe observable symptoms and how your condition affects daily life.
Not marked
Your own written account of how this condition affects your daily activities, work, and relationships. Describe your worst days.
Not marked
Benefits questionnaire
0 of 1 collectedVA standardized form for MG capturing muscle weakness distribution, crisis history, and functional limitations for rating under DC 8025.
Not marked
Service records
0 of 1 collectedMilitary medical records showing in-service treatment, complaints, or injuries related to this condition.
Not marked
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