Hi all, I am from Serbia, and living with a diagnosis of APS 8 months.
Whatever it is difficult to reach a diagnosis, I had the good fortune to meet a great neurologist.
I had a facial paresis with poor reflexes of the right arm and leg.
During two weeks of treatment and subsequent tests, we came to this diagnosis.
So far I have only joint pain, dry mouth, and sometimes poor concentration
Aspirin 100mg treat me and honestly I'm not sure whether it was good.
I try to accept this without panic and fear, but since little is known about this dont nou what awaits me in the future.
But I am always positive and smiling and I hope only nice things.
I know that I must be strong because I have 36 years and two children and life is still ahead.
This summer we had a wonderful holiday in Halkidiki, Greece.
I try to be informed, to get to the good doctor and to eat healthy and move.
What tomorrow brings, we'll see.
I love you all and wish you the best.