Thanks for all the welcomes.

I am from Nova Scotia and I guess I'm not sure if I have mg yet.

Here is how it works in NS you go to GP. GP refers you to another (who is not a neuro) this guy is a cardiologist. Cardiologist refers you to a neuro.

Haven't seen the neuro yet.
Waiting for ach levels had it done first week in June blood was sent to the States.
Cardiologist was going to run tenslon test. He went to do it waited 4 hrs
for him to tell me they don't make the drug anymore. They stopped 1 year ago. So Cardio guy comes and tells me... I have MG
I have a Thyomoma.
I need to have my thymus out.
Having my thymus out will make me all better.
Puts me on 30mg mestinon 3 times a day.
Tells me to come back in two days to see him.

Well I went to see him looks at and says your better. I told him Iwasn't sure
My energy had improved some what. Length of time before I become tired has increased. He saysa well you should know if it's working by now and he was going to up my amount but now he is not. I have been on vacation for the last week I'll know for sure if it's working then.

Anyway I could go on. But long story short Cardio guy doesn't seem very informed about MG. Still frustrated a bit I mean it is what it is.
He didn't even know that heat or other drugs could make it worse.
And told me mestinon wouldn't do any harm to me if I was taking it and didn't have MG.

Waiting for ach results and to see neuro not even going to think about what this guy said. Am making appointment with GP to see another doctor other than cardio guy. I hope my GP can handle it.

The overall weakness in by has improved a bit sense Mestinon I haven't even been taking it for a week yet. But my left eye still isn't open as much as I would like it.

We'll see what is down the road maybe not MG. But the heat does make things worse and so does the cold we get one extreme to the other here in NS
LOL.

Hope your all well and maybe I'm in the wrong place after all.


Cooley