Has anyone had Parsonage Turner Syndrome? What are chances of Recurrence?

[Yagswagger]

Has anyone here had Parsonage Turner Syndrome?

I had my first episode ever when I was 20 years old. I am currently 22 years old, going on 23. I'm very scared, because I heard that the genetic form affects those in their 20s.

However, when I saw my neurologist, he asked me if anyone in my family had what I had. I don't believe anyone else in my family ever got it (including aunts, uncles, grandparents, etc.).

But I'm still shocked at the age at which it occurred.

I had just recovered from the flu, and that very night, the heat broke down in my apartment, and I was left shivering all night, and my arm muscles were rigid, as I tried to contain body warmth. The following morning, I woke up with the horrible pain, which eventually was diagnosed as PTS.

[tan235]

I have no idea sorry but sounds like it was created through a trigger, so -- avoid the trigger!

[Yagswagger]

Is there anyone that possibly had this? Or known anyone who's had this?