Another CT scan this morning has shown he has water on the brain. So he's due in theater for neuro surgery at 8pm to have a drain inserted. They now risk damaging the healthy side of his brain with an uncomfortable high risk of death.
The doctors and nurses seem more amazed that we are holding it together and I honestly don't know how we are.
I guess we just have to keep hope that he will have something that resembles a life after all this.
I'm amazed the little guy is still going to be honest, born 35 weeks and only a week old to go through so much and still amazing the doctors.
We've been transferred back to St Mary's over the weekend as they were happy all he needs now is weaning off his drugs and ventilator. Still has the EV drain in which will be there for a fair few weeks yet until they decide it's no longer needed. Worst case with that he needs a shunt putting in for life.
We've been transferred back to St Mary's over the weekend as they were happy all he needs now is weaning off his drugs and ventilator. Still has the EV drain in which will be there for a fair few weeks yet until they decide it's no longer needed. Worst case with that he needs a shunt putting in for life.
Then it's monitoring his development to see what level of disability he gets.
They're happy at least that both his eyes respond as they should regards movement and dilation.
His legs both seem to move equally but his right arm definitely shows less movement.