Very sorry about the lack of updates – in a sense, there isn’t much to update. I could not make it to the hospital until today (I had not seen Chris in about 3 weeks). There is absolutely nothing positive to be reported about his condition. We know how the visits goes: he is absolutely thrilled and excited at seeing us (which is so sad and heartbreaking), then I do the little things I normally do for him, Gabriel drives me crazy competing for attention, I take notes of things I need to follow up with staff/ carers/ therapists, and we leave – I am always emotionally crushed after these visits. More than 3 years after, I still can not believe what became of Chris and his life.
I do not have the time and energy to go visit him every weekend as we used to do before when my parents were here. I am also physically and emotionally tired. I can handle the physical tiredness but emotionally I find it increasingly difficult to go see Chris in his unchanging state. Gabriel also detests the word “hospital”, he cries, begs, implores, blackmails… but he does not want to go to the hospital… He has a very long list of things he would LOVE to do on his weekends with me, and I find it unfair for Gabriel to be forced to the hospital every weekend. I am not leaving him with a sitter on weekends as I also want to spend quality time with my son. So, put all this together and today was the first visit in three weeks.
I am trying to make sense of my life right now – it feels an endless struggle for day to day survival. It feels senseless and I am considering different options for the future. Obviously I am not equipped anymore to care for Chris with the same commitment and energy as before.
I keep in touch with his therapists and carers, despite no visible improvements, his care always requires a lot of monitoring and at any time, there is always something to be followed up on… I do not know when my next visit will be… I may try to find a solution during the week so that I do not have to force Gabriel to the hospital. The thing is… I am busy, overwhelmed and tired right now.
|
|
||||||||
Long due update...
Comments
Re: Long due update...
Hi Koo,
So sorry to hear your despair. Surely do understand the difficulty you're describing. Not in the same situation, but I can understand. I know how hard it is taking care of Samantha at home. I, of course, have no answers for you. Only you can figure out how it will all work for all of you, including Chris. I just want to encourage you to continue to seek out answers and pray for guidance. You seem to be a woman who knows how to go after the answers and what you want. Look how far and what you've been able to organize for Chris. And it's working. He's made some progress from when I first started reading about you guys. Anyways, just want to encourage you to search out ways that you can be there for him and Gabriel. Maybe it's having him closer or even at home with full time caregivers....I don't know and would not even try to suggest anything because you have earned my respect in the way you've handled things so far. I just am saddened that he doesn't get to see you or Gabriel that much, especially since he is more aware now and clearly enjoys your company. He is working so hard too. Well, Koo, I will say some extra prayers and hope for all of you. I think you are a remarkable lady. |
Recent Comments
Recent Entries
Month Archive
Recent Visitors
Roseli - Sat 21 Nov 2009 01:10 PM GMT
Guillermo - Thu 12 Nov 2009 02:38 AM GMT
yun - Tue 10 Nov 2009 07:13 AM GMT
Kristine Abrams - Sat 24 Oct 2009 03:50 AM BST
Sandra Kina - Mon 19 Oct 2009 03:32 PM BST
Login
Other Brain Injury Websites
|
|||||||