What next? My sister had very high on hers and then found out she has ms too. Trying to figure out why I can't have any autoimmune stuff with symptoms to many things.
So sorry to hear that
Similar to my experience
So I believe my doctor until I had a procedure and under anesthesia I responded like a patient that had myasthenia
Then doctors changed their mind
My bloodwork was also negative
If there is any way change doctors
You could try letting your doctor see you taking notes or ask him if it’s ok to record section sometime you forget section
Hold on tight
I'm sorry I did see this before as I was not on the group I would reccomend you ask the headache Dr. to refer you to a neurologist, specifically to have you tested for seronegative Myasthenia gravis or an associated condition. Dr to Dr correspondence is usually taken the most seriously.
What should you do if your AChR blood test came back negative but you still have MG symptoms?
A negative AChR test doesn't rule out myasthenia gravis. About 15% of people with MG test negative for AChR antibodies, and some may have other antibodies instead.
You might want to ask your doctor about additional testing options:
I will get to see general neurologist in September. That is only doctor I can go to because their answer is no. Including primary doctor. I've tried other clinics besides UW MADISON. I can't drive to travel and obviously can't afford the tests on my own. It was my headache doctor that ordered the achr ones only because I begged him. And that was thrown back in my face when it was negative.
Wow that’s definitely not right! The last resort is to pay out of pocket but many of us can’t afford to do that. Our medical profession sucks at times.