I haven't gotten an official diagnosis yet but have had improvements but not total resolution of symptoms since starting pyridostigmine. My doctor is using my response to medication as a potential indication of MG but i dont follow up until september. Im just not sure what I should be expecting for this process and if partial response is even good enough for a diagnosis. Thanks!
Mestinon does not work for everyone with MG, it really depends on type of MG and personal response. I have Musk GMG and it did not work for me but I do remember the first neuro-opthomologist wouldn’t treat me because I did not have acetacholine antibodies. So if certain drugs work they can diagnose by symptom management. I hope you get full management of your symptoms.
My symptoms have not fully disappeared, even after being on pyridostigmine for 6 years now. They may go away for a day or two (or more), but always come back, and I think that's probably common with mg. The meds help to control symptoms but even when they're invisible to others, they're still present to some degree, at least for me. I was diagnosed on the basis of symptoms and response to Mestinon (I'm seronegative), so just as stated in the AI response, even an improvement is signifant. Best Wishes to you on this challenging health journey!
What a great question — and honestly, the waiting game before a diagnosis is one of the hardest parts. A partial response to pyridostigmine is actually quite meaningful and commonly seen. It's often used as a first-line treatment specifically because it helps improve nerve-to-muscle communication, and not everyone Show Full Answer