Hi Georgia, MG can be as frustrating as doctors, I was diagnosed by one neurologist as having OMG and when he was not available for my next appointment I was seen by another neurologist who doubted the findings of the first and has instructed me to have more tests. It is like one doctor wanting to be better than the other - frustrating like MG. Remember every day is a good day but some are better than others 😉

My ER doctor took about 15 min. It just takes someone familiar with the disease, and not everyone is. Georgia, I would advise you getting another provider.

I knew last 4 years something is wrong… after 4 years of mri and tests my neurologist reffered me to a neuromuscular specialist, she recomended to do new emg RNS not just in elbow , but also in arms, and that was it, it was positive only there, also my symptoms and then dit CT scan and found enlarged thymus and here I am taking imuran
problem is I didnt have any ocular symptoms , mostly my limbs, so nobody thought it will be MG

Thank you so very much for that information. It is a great help. Now if I can only find a doctor to treat me!

Georgia Erickson 🌟💕

Georgia wow I don’t know what to say . I feel for you and what you’re going through. Maybe someone on here can recommend where you can go as I’m not familiar with Tucson. There’s a list of neurologists on this site by state - maybe you can find a doctor on that list????