Hi,
I was wondering if any of you out there suffer with sjogrens syndrome as well as MG?

I haven't been diagnosed with it, but then I haven't been diagnosed with MG either LOL. However today I have been looking on the internet as my dry eyes are getting worse. They are burning and feel gritty. I found a website for an American Sjogrens group and was amazed at how many of the symptoms I have. But it looks like its another fun thing to diagnose as no one test is 100% positive.

The other symptoms I have is dry skin, tingling and numb hands and feet, reflux and some dryness in the downstairs lady dept! Plus the memory loss and brain fog.

Anyway as I ramble on I was wondering if anyone else suffers from it and how easy was it for you to get your diagnosis?

At the moment I dont know if I can be bothered to contact my gp about it as Im sure he thinks I spend every minute of everyday looking for an obscure new symptom. They obviously haven't heard of overlap!

Thanks in advance

Rach