This is the story of Buzz. My Dad, my hero and my absolute closest friend. This is our journey as we struggle to say goodbye while Alzheimers takes over our lives and robs us of our last years together.



Buzz is more than my Dad. Growing up he was a big brother. He really understood, loved and accepted me more than any other person I know. He loved me and stood by me… warts and all.



Because he stood by me when others said I was lost...because he was always open and honest and accepting of me...because he encouraged me to do things when others said I shouldn't or couldn't, I will stand by him and hold his hand, look in his eyes and tell him I love him every day until the day he dies. Which, unfortuately, will be sooner than later.



Friday the 25th of June 2010 we were informed that Buzz's congnative abilities will probably be gone in 6 months. By Christmas he will forget us completely, forget how to eat, be put on IV and die of pneumonia within a year.



I am compelled to tell the story of my journey with my Dad. I hope it will help me get past the loss of the one man who means more to me than any other person in my life. I hope people will see, through the tragedy of Alzheimers, an amazing, charming, gentle, fun loving man who deserves to be remembered.







How do you say goodbye when you don’t want to.


1969 Flin Flon Me, Dad and Candy the Boxer

I have had a lifetime full of compromises over the past 6 months.  Compromise and move on.  Compromise and move on.  Understand that your Dad will never go home again, cry, work through it and move on.  Understand that your Dad’s brain will be Swiss cheese in 6 months, cry, work through it and move on.  Understand that your Dad can’t feed himself, cry, work through it and move on.  Understand that your Dad will never be able to tell you he loves you again, cry, work through it and move on.  Every day it’s a new compromise, a new set of tears, new things to have to work through. 
The problem is that Alzheimer’s disease doesn’t care about compromise.  It doesn’t care that it rips you apart every single day. There is no compromise with Alzheimer.  The only compromise you have is with yourself and just how much more you are going to cave in today.  There is no peace.  Alzheimer does not play by the rules.  It doesn’t care that you have to change tack every day because every day presents a new set of challenges.  That once you’ve dealt with a new set of problems another tragedy is handed to you.  
Two weeks ago my Mom and I had to have the conversation about how we are going to let Dad die.  Another horrible compromise.  We sorted through it, understanding that once his mind was gone we would not allow feeding tubes and we would not allow resuscitation. When we spoke we put all our sentences in the form of questions.  This is the right thing to do for Dad, right?  We don’t want him wasting away, right?  This isn’t what Buzz would want, right? Compromise.  Tears.  Work through it. Move on.  I thought we did the right thing.  I thought we came to a proper dignified resolution to end my Dad’s life.   Choosing how my Dad is to die is not what I want to do.  Compromise, cry and move on….right?  Well…no.  You are not allowed to move on.  Alzheimer doesn’t care that you are wrecked because you had to decide how you were going to let your Dad die.  Instead it lets you know that it is in control and it will decide for you just how your Dad is going to die. 
A few days after my Mom and I came to terms with how we were going to let my Dad die I came to a sort of realization that, although I hate what is happening , death is really the best thing for him because he will never come back from this disease.  Once he is gone, he is gone.
 Compromise. Work through it.
 I had a week to cry and work through it and I had reached a place where I thought I could live with my decision regarding the whole end of life situation.  It’s not what I wanted for my family but it is here and it is terrible but soon, once my Dad’s brain is gone, we will help him move on and he will be free and whole  again.  Compromise. Work through it.
Three days ago I got “the call”.  My Dad’s sodium levels spiked again. His organs are beginning to fail.  A new twist. A new compromise.  The people in charge are telling me I have to fly out to say good bye.  Now instead of being able to be at peace with the terrible decisions we have had to make, a new devastation.  My father is still in there….he still smiles when he gets my phone calls, he still kisses my Mom.  His brain is not gone yet.  We made that deal already.  We compromised. And now everything is being taken away again. 
Christamas 2008
I have to fly out to say goodbye to my Dad.  I know that when I get back on that plane to come back to Winnipeg I will probably never see him again.  I will never be able to hold his hand or look into his beautiful grey eyes again.  How am I supposed to say good bye when I don’t want to.  How am I supposed to compromise when we've compromised enough already?  Honestly.  I just want my Dad back.

3 comments:

shari said...

reading your story has brought back many feelings of losing my mom to Alzheimers, and I know how difficult this time is for you.

Unknown said...

Frazier I know how difficult this has been for you but know your dad would not want to suffer anymore. It is never easy saying goodbye but he will no longer be suffering. I can completely understand what you are going through as I am watching my dad go through it every day myself.
He is not at the stage your day is and hopefully, won't be for a long time, but it tears my heart out every time I leave him knowing he will never come home again.
You have lots of support at the Alzheimer Society and we are here if you need us.

Unknown said...

Frazier...I sit here reading your blogs on the anniversary of 1 year after my mother's passing. She had cancer of the voicebox and it was removed. The last thing I heard my Mother say was"I'm Sorry".It was a lifetime of hardships with her and I have had days of trying to remember any good times.I always envied people that had close relationship with their parents but I would never take away the love and happiness that you shared in memories.The memories that you have shared with us in your blogs are priceless.My heart goes out to you. I did volunteer at the "Alzheimer's Society" for 5 years on the Help line and understand of what you speak.
Take time for yourself. Stay in touch with the Society and let them be there for you as you have been here for others in your blogs.
I was with my Mother the last few days of her life and we still had a big gap to fill but giving her hugs and holding her hands started the healing for both of us in a sort of a way that I never thought could happen.
I wish I could say that it gets alot easier but it doesn't....at least for me.
I just know that she is now in a better place and that fills my heart with a little more happiness every day.Not that she is gone but that she is at rest with no pain...if that makes any sense.
Sorry to have rambled on but you really are an awesome person and I am sure that your Father is sending his love...whereever he is.

Hugs and Prayers
Thanks again for the blogs..you have touched and will touch alot of people with your kind words and memories.