So, the problem with the plane still isn't resolved. They said it could be tomorrow morning, but as per usual, they can't guarantee anything. This is just so unfair to everyone. Most importantly for Dad. It is heartbreaking to see him so sick and tired, yet he can wake up to ask me if we have any info on the flight. He wants to get home so badly. It's super hard being up here now for almost two weeks with very little sleep... spending a freaking FORTUNE on hotel and food... using up sick time... esspecially when we will most likely be back here in a couple of months... How is that even possible! I will barely have enough sick time left to come up with him at all if it is before summer... uhhh!!!! Not to mention, the emotional drain of being in a hospital with a sick family member 24/7 and having little support here... I hope they have a good psyc ward because I'll be be checking in pretty soon! If having family around is such an integral part of the healing process, why would they make this so difficult?
It also must be costing the NL gov more money to have him here than at home... AND they don't have any beds left on the neuroserg floor where Dad is, so people are left down in ICU or on other floors which isn't fair to people from here and must be costing the NS gov extra money. It is just brutally unfair from all sides. ESPECIALLY when we now know that we have the equiptment and trained doctors at home, and it is just a political issue holding up the availability of the coiling procedure at home. I am much to frustrated. Please God we get home tomorrow or I may just take him in a wheelchair to the airport and take him home myself.