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After experiencing muscle weakness for several months last year, the doctor ordered the AchR blood test in July 2025, which came back negative. A second AchR blood test in August came back 0.07, and a third test in October was 0.1. That was followed by a visit to see a neuromuscular neurologist. She did an EMG and separate nerve conduction test, which I had in December 2025. The results were negative for having Myastenia Gravis, and the doctor gave no other diagnosis for a muscle disease
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March 12
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A MGteam Member

I don't think so, but am not sure. All the doctors do is focus on the fact that I have narrowed nerve canals in my spine and no doctor ever wants to look "outside the box." Thanks for your suggestion, Carol. I'll mention it to my doctors at my next appointments and hope they will listen to me.

March 29
A MGteam Member

Have you been tested for rheumatoid arthritis ?

March 29
MGteam

How can you confirm a myasthenia gravis diagnosis when test results are conflicting?

Your situation is challenging because your AChR antibody levels are rising (from negative to 0.16) but remain just above the normal range of less than 0.05, while your EMG came back negative. This creates uncertainty.

Here are some Show Full Answer

How can you confirm a myasthenia gravis diagnosis when test results are conflicting?

Your situation is challenging because your AChR antibody levels are rising (from negative to 0.16) but remain just above the normal range of less than 0.05, while your EMG came back negative. This creates uncertainty.

Here are some important points to consider:

About 1 in 5 people with MG don't have AChR antibodies, and EMG tests are accurate only 75-80% of the time. Some MGTeam members have shared similar experiences - one noted, "My diagnosis was not confirmed until I had an EMG. My neurologist was convinced at the first visit that I had MG, but the blood work did not confirm this."

Your rising antibody levels are noteworthy, even if they're borderline. The progression from negative to 0.16 suggests something is changing in your immune system. Since your symptoms primarily affect your lower extremities rather than the typical eye, face, or throat muscles, you might want to discuss additional testing with your neurologist:

* MuSK antibody testing - about 30-40% of people without AChR antibodies have MuSK antibodies instead
* LRP4 antibody testing - found in about 1% of seronegative MG cases
* Single-fiber electromyography (SFEMG) - a more sensitive type of EMG that may catch what standard EMG missed
* Repeat testing as symptoms evolve

Your pattern of lower extremity weakness with morning difficulty is less typical for MG, which often affects eye muscles first. However, MG can present differently in different people.

Given your rising antibody levels and ongoing symptoms, it's worth having another conversation with your neuromuscular neurologist about whether additional testing or monitoring might help clarify your diagnosis.

March 12

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