LOL - that sounds scary, I won't ask!
The first doctor was worried and took heaps of blood tests.
The second doctor was good at noses, but knew nothing about epilepsy/ADHD. It drives me crazy that all the different doctors deal with their piece of the puzzle (autism/ADHD/epilepsy/nose bleed) but there is no communication between them.
I'm trying to get on to the psychiatrist, to ask whether the nose bleed could be a side effect. He'll probably say no.
I was calm when it all was going on, and so was my son. He was quite heroic!
I'm rattled now - it was scary, and for a while I thought his liver was failing because of the meds . (when he was examined his liver was tender). It's as if every time they check him for something, he's got it, so I seriously started thinking what now? How do we get round this one.
My son has started talking about how unfair it is that he "always" has to go to hospitals, why he got another "sickness" and generally about dying, so he must have been quite scared, too. It makes me sad he had to go through this, too.
I know it was just a nose bleed, I guess I just wanted to tell someone...