Dad: How to live through Alzheimer’s

I received this email and these photos on Monday which sent my feelings pouring out of me. My Dad and I rarely cry when talking to each other because we have to try to be strong but this week I sobbed to him on the phone. We are coming to the end of the road. The end of our journey and the end of our time with my mom. And to be completely honest, we don’t know what to do. Below is an update from my Dad and how he continues to live through Alzheimer’s.  

****my dad asked me to proof read this for him and fix any grammatical errors but I think there is beauty in this raw copy. Please forgive any mistakes you may find and understand that this was probably written with wet, foggy, tear filled eyes. 


Caregivers are such special people. People that have the endless compassion and the empathy to understand that we all are on the same path, and we all have the same destiny – Sadly some’s destiny reaches the end of the journey before others.

As a Caregiver I learned I needed to dig deep into my mind and heart to find the understanding, find and open the selfless patience, wrap my arms around the meaning of empathy, and most of all confirm my complete acceptance of this is what it is. Make the best of it … Why not ?

Family is so so so affected – Hardest part of this Alzheimer’s Journey is for the Family – After acceptance of that “It is What It Is” The Family must continue on trying to understand how to continue, stay one step ahead of the unknown. Who will step up to the plate and how to be in charge. The reality of deciding what is the best avenue to take for the loved one. I truly believe that the one on one care given by a Family member is the best way to go.

I learned how to try to keep 1 step in front of instead of reacting I keep thinking of how to handle what is coming in the next pages of the book. Being prepared to continue through the chapters of our journey is hardest as the thought process turns toward the time consuming task at hand of taking care of the loved one and leaving little time for the Caregiver day to day needs and cares.

Faith in good sayings have helped me tremendously – I make my own uplifting sayings about this journey that enables me to strive toward them. Gotta love – ” Smiling makes me Smile ” It is so true really I smile driving around all the time. So Blessed – And – ” It is not what happens to you – It is what You do with what happens to you ” Get out of here – That’s one saying for sure to live by.

Country music for me is still and was a great escape for my mind to wander and smile. Most of the Country songs have enjoyable lyrics about quite a few silly life’s situations and are uplifting.

In life I have been Fortunate Not Lucky – The difference is I choose my path by opening doors along the journey. Some doors lead to other doors. Most of the time I didn’t find doors just walls. These walls needed to be climbed or gone around to find the new door on the other side. I always tried to keep moving forward looking forward not in the past. And you have to find the strength and nerves to walk through doors with-out knowing what is beyond.

I am so Blessed by being able to find the resourcefulness, find the ability, let out the ideas instilled in me of keep on dreaming – Dreaming is a very strong way to for me to keep striving and moving on. And accepting that tomorrow will be another great day waiting for me to enjoy this journey.

I have had to file a lot of my memories and learned to go back when I choose to. No need to go through negative times. Uggghhh so hard to go back in the file drawers of memories. Don’t get trapped in the pity party “that these memories are now only mine” because your loved one who helped create and share so many of your life’s memories for so many years doesn’t remember. They can’t laugh, enjoy and share them with you anymore. It gets better in time but will always be there. Shut that file drawer.

Be honest with yourself – This is happening and this is real. So pull up your big boy pants and figure it out so it doesn’t figure you out first. If you get knocked down – dust yourself off and get on with living.

Attitude is self-controlled. I prefer to see the good all around – I made a decision many years ago to be positive, to be proactive and to always keep moving forward … I learned it is easier to live in the now.

You have to learn complete acceptance of “Make the Best of What you Have” and “It is what it is”. This new and always changing journey has no road map. Doctors don’t know – Nobody knows. All I know is that I did the best I could today and will do the best I can do tomorrow. That way you can feel good about yourself.

Sure things don’t always happen as expected but by moving through them with the mind set of “Whatever” you start to understand what really matters in your life. Amazing how that will let the Stress Go – As what is it that really matters in your life.

Get up every day on the right side of the bed … Do the best you can do and then enjoy you did the best you can do – So if what if you only had time to get 25% of it done. That’s 100% of 25% done. Smile and know you did the best you could.

The Responsibility shouldn’t be a burden. Turn your thoughts around and think of how well your loved one is doing. As it really is happening to them not you. Empathy leads to acceptance and acceptance leads to devotion and devotion leads to unconditional love. Unconditional love leads to a much easier journey. This journey is happening, it is real and it is now a major part of your life. Embrace your journey by knowing you would want the same care given to you if you were in this position. With time we all will need the help, empathy and compassion of a Caregiver … Special people indeed.

Caregivers have been chosen for the special job of comfortably helping others transition to the other side of the rainbow. Caregivers are instilled with the love and have found enjoyment by help others.

I have learned when I feel I have way too many things to handle I end up prioritizing and move forward with completing my highest priority items – Because I know I can’t get everything on my shrinking plate done – And then there is what pops or poops up keeping me on my toes and testing my reaction. Ahhh another saying ” Whatever ” I understand the true meaning. Situations happen that are completely out of my control. Could I have done something to change what just happened? If so then learn from it and maybe it was my fault for no thinking ahead to have been able to make it not end up this way. Not feel guilty but learn from it. Really now almost everything washes up – ( well maybe not everything – we can talk later on that ) Most things clean up.

This life journey of yours is not a dress rehearsal – So best way to go is accept, strive to enjoy the ride, look around there is beauty just gotta find it. Smile as smiling will make you smile Come on now smile … Ha see I told you …

I believe in the idea of “Find and focus on the good surrounding you”   Good mind set attracts good people. Negative mind set doesn’t attract anything good. Who wants to be around someone who projects poor me, feel bad for me. No one will ever know what you are going through until they have to face the same journey. So get over yourself, your situation. This is not a dress rehearsal. You will never get yesterday back again – So make the best of today. Always Remember:

“It’s not What Happens to You – It’s What You Do with What Happens to you”

Stay steady on the path and look at all the abundant possibilities the Lord has made available for you. I am sorry that this has happened to you. Just you don’t feel sorry it has happened to you and this long Journey will be easier.

 

John H

 

4 thoughts on “Dad: How to live through Alzheimer’s

  1. So beautifully written. Amen! Sending prayers for continued strength and endurance. Lots of love. Xo

    1. Thank you John for all the loving care you’ve been giving to my best childhood friend Pam.
      💕Debbie

  2. Your Dad has always had the best, most positive attitude ever since I met both he and your mama back at St. Mary’s – so many years ago. He truly is an example and inspiration of a man who took his marriage vows “ in good health and in bad” to heart- such a rarity these days. His reward may or may not be on this earth, but he will most certainly have a reward.
    My heart goes out to all of you …. this journey hasn’t been easy… and yet, you’ve handled it with so much love and strength. Prayers and Blessings to you guys…

  3. Cerce Hammer says:

    Natalie and John my heart reaches out to you. So funny how God picked at least two people that ask their children to proof read their post’s. As you will soon see I am the other care giver that needed her post proof read.

    This Journey your on is the hardest journey there is. I know cause my mom started the same journey when she was 60. My Dad started his when my mom finished her’s when she was 70. I knew I needed help cause at the time my mom jumped on the Alzheimer’s and Parkinson’s train. I was raising my family and I had a new born that had to share my attention with everyone going 100 miles an hour down the track. My sister was busy teaching in Riverside. My brother lives in Michigan. So you will see that I was my Mom and Dads only caregiver.

    I tried to find a doctor that might help. After 6 doctors I knew that there are no answers for this nightmare. No drugs no herbs just alot of depends. Your loved one gets used to their caregiver. There is a time when they no longer know you but they still know you emotionally. Some how if you can keep things simple and calm they match your mood and behavior. However they have behaviors that other family members and friends dont quite know how to handle. The bubble that the care giver is trying desperately to keep from poping. Pop’s then reality floods in. The air in the room becomes stale. The visitors seem to have lost any ability to have a conversation. The visits get shorter and shorter. Family become bissier and bissier. Your on your own and although it seems easier at times it gets lonely.

    There is no trainer for this 8 rounds in the ring with the heavyweight Alzheimer’s. There is no Nervana to go to. With all the years we have had trying to figure this horror out. No one and nothing has been built to take the stress off the family or the dear loved one experiencing the fears none of us can begin to think we might some day have to experience.

    I know you John. But I know the young you. The John that was madly inlove with my beautiful friend Pam. I’m so glad that you had so much fun with Pam. You made her life better than she even dreamed it would be. You had a beautiful daughter together. I know you have days when your not sure any of that life really happened. Your daughter will always be the link to your beautiful life.

    They have metals for hero’s. The metal that I have is knowing I did the best I could for my parent’s. I kept them safe, clean, well fed and as happy as possible. I know they went on to the great unknown. I thank God for giving them to my care, and gracing me with the gift of being right next to them holding their hands. They didnt know my name but they knew it was me.

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