I didn't get to speak to a doctor last night after the CT as it was after midnight when we got back to the room and we were both shattered.
We did briefly speak to the doctor at the CT scan and he did say what he can see so far is ok. That was enough to get me off to sleep and just hope they didnt find anything they didn't expect to later.
We have since seen the doctors this morning and they don't know why this has happened. apparently nothing on the scan indicates an explanation and Dr Nick said its unusual in children that have tumours in the posterior fossa like Jayden to have seizures. he's booked jayden in for anEEG this afternoon to get more information.
The seizures Would have to have been one of the scariest things I have witnessed so far and I truly thought I had lost him. But now he is in my arms and i couldn't be more grateful.
It's a couple hours later and he's just finished his EEG. we are back in his room. He did really well. He cried throughout the whole process of setting up all the wires but slept during the examination.
Its another couple of hours later and I thought we would have got the results back today but we haven't. We are now on our way home and have to return tomorrow to find out results and what is going to happen next.
Dr Nick did get the results back from the urine test Jayden did yesterday though and apparently on top of everything else he has a urine infection as well. He truly doesn't seem to get a decent brake and I so wish for him that he would.