1/30/2013

When time is ticking away,

you can't help but wish it would slow down. He was told yesterday three months, maybe up to six. I've known this for a while in my heart and after speaking with the doctor the other day. In my gut I don't think he will make it to April, but he has surprised us so many times he will probably prove me wrong. :) He was pretty calm telling me this while I visited him last night. I already knew so I was able not to become a blubbering mess. I mean we are all going to die, it is just a fact of life, but now all of  a sudden I feel like there is this gigantic clock ticking away over our heads. He is ready even though he is scared. He wants to be with my mom and to feel better. I am spending as much time as I can with him without neglecting my family, although I can't say the same for my house. The house is the least of my worries right now and if anyone has an issue they can kiss my ass. No one can ever understand what I am dealing with unless they too have dealt with it and even then we all have different circumstances.

I am so thankful for my in laws who have been able to care for the kids at a moment's notice even though they are dealing with an ailing family member. I am thankful for my "computer" friends who have been an continuous source of support, for my real life friends who always ask if I am ok, how he is, or just being the person on the other end of the phone I can vent to. I am thankful for my amazing husband who held me up when I was losing my mom and is doing the same while I deal with this. He understands when sometimes I just don't want to talk because I am all talked out. Also for my family who help as much as they can. You really find out who your true friends are when you deal with something like this.

Today would have been my parent's 48th anniversary. They only have one picture of their wedding, thankfully it turned out good. ;)

1/26/2013

My dad is dying.

There, I said it even though it is hard to utter those words out loud. It is amazing that I started this blog because of a shocking pregnancy and I needed an outlet to talk, then the death of my Mom, my own health issues and now my dad.

 He was diagnosed with Esophageal cancer in 2001, but after chemo and radiation he was doing well and was considered in remission for many years, until this past July.  It started with him having a hard time eating and throwing up. I brought him to the doctor to see if it was a recurrence which was what I thought. At first glance there was no tumor, but the doctor did a biopsy around the previous area to see. It came back positive. We also found out that he has a very small aneurysm in his aorta starting which can't be fixed because of where the cancer is. He opted not to do treatments this time around. He lost his will to live the day my Mom died. He ended up having a stent put in his lower esophagus because the cancer was closing his esophagus making it hard for him to eat or swallow.  In the meantime, we had to move him out of his house to a retirement type place because he just was not able to live by himself and he couldn't afford someone to live with him 24/7 to care for him. He seemed to be doing well, he made friends and was even going on some of the outings. However, his health started to nose dive again, he developed pneumonia and his congestive heart failure was irritated. We got that cleared up and he started having problems swallowing again which meant another stent had to be placed.  We did that and I ended up having to take him to the hospital for extreme weakness, he couldn't even sit up unassisted for more than a couple of minutes before he fell back. They found he was dehydrated and kept him to pump his fluids back up. He was doing better and was supposed to go home today, but the doctor called to tell me he got worse overnight and he was sending him for a ct scan of his head and back since he was unable to sit up again.

There is nothing I can do but be there for him. He is so tired of living in his body that is giving out on him. He cries and tells me he just wants to go to sleep and never wake up. What do you say to that? He is debating between hospice and something called palliative care which is basically the step before hospice. I want him to choose palliative care, but in the end it is his choice.

My dad and I had our differences when I was growing up, Hell you can even say I hated him, but I have learned long ago  to let go of that. He raised us the way he was raised, he didn't know any better. I am not saying I don't still suffer the scars from his hurtful words, but I am moving on. The thing that strikes me funny is how so many people including the doctors and nurses tell me what a great thing it is that I am taking care of him. I find this unbelievable. I am doing what needs to be done. I am fulfilling my promise I made to my Mom to take care of him and I will keep doing it until he dies. So I am asking all of you to please pray for him, that he finds the peace he deserves.

1/24/2013

When it is time for me to die

I hope it is quick. As much as my Mom's death was quick and almost unexpected I have come to learn that it was for the best. Watching a love one die a slow agonizing death and not being able to do anything is horrible. I lose a little piece of myself everyday that I have to see him in pain.