Friday, April 20, 2018

BEING A LONG DISTANCE CAREGIVER


BEING A LONG DISTANCE CAREGIVER


Quite a few years ago I recall defending myself from some other caregivers. They thought I did not qualify to be mom's caregiver since I lived far away. They thought that I did not care for her in the same way that they did. Their words stung me deeply and had me momentarily question myself.

I certainly felt compassion for their situation, yet I too, had the agony of hearing and seeing my mother disappear in front of my very eyes. One moment she knew my name and the next she had no idea who I was. My heart felt equally broken as theirs and I questioned why would they judge me?

Was I any less of a daughter to my mother because I did not live near her? Unfortunately, I could not just pick up and move to another state, and my mother refused to leave her home. I am my mother's daughter and that will never change, no matter how many miles may separate us.

Before moving mom into the nursing home for years I spoke to her caregivers every single day to hear how she was doing and to help plan her day. I questioned what she ate, if she took her vitamins and if she gave them a hard time when she was being bathed. I also delighted in hearing how mom loved to sing along to the CD'S that I made for.

There were moments when mom sounded great and there were other times when I was so frightened yet unable to just jump in my car and rush over to her. I remember when they called an ambulance to take mom to the emergency room after her aides discovered she had bruises (from a fall) that she could not tell us about. Then there were the times she was hallucinating which was due to a urinary tract infection (UTI).

Once, when she was in the rehab hospital I spoke to the physical therapist who told me that my mother was not following instructions. I responded "how could mom possibly remember what you just said since she has Alzheimer's." The therapist answered, “oh I didn't know she had dementia.”

Then there was the time I received a call from a first response team who was not able to reach my brother. Mom's neighbors reported her "just sitting" outside her apartment on the curb. Her caregiver left for the day and because of confusion mom went to sit outside to wait for her. You would think that one of her neighbors would have just brought her back into her home. After all these years of knowing her how could they now just shun her like this?

The time was approaching to place mom into a nursing home my brother and I realizing she needed twenty-four hour care. Talk about feeling guilty and confused. How could we do this to mom? Her wishes were to stay in her home till she died.

Mom now has been in a nursing home for 5 ½ years and my brother and I know that it was the correct thing to do. I call often speaking to the nurses and always ask them to please go tell mom that her daughter Lisa called and send her love. I may only get to visit her every few months yet the staff knows that I take a very active interest in her well-being. Mom no longer knows where she is living yet my brother and I feel secure with the care that she is receiving.

So with deep thought my question is am I any less of a daughter than the others since I am a long distance caregiver? The answer is clear to me. I am my mother’s daughter and no matter how many miles apart we are the love and concern I have for her is as deep as the bottom of the ocean. She is my mother and I will always be her daughter, which also includes being her caregiver.



My new book "Letter To My Mom". It is the continuation of my first book "My Mom My Hero" Available Worldwide on Amazon in Paperback & Kindle.
https://www.amazon.com/s/ref=nb_sb_noss?url=search-alias%3Daps&field-keywords=lisa+hirsch&rh=i%3Aaps%2Ck%3Alisa+hirsch


Friday, April 6, 2018

THE WARMTH OF TOUCH



THE WARMTH OF TOUCH


My mom has Alzheimer's for over fourteen years and as her disease progresses so does my emotions. I often feel I am on a rollercoaster swaying back and forth as it speeds around many curves shaking up my inner feelings.

This February like the past four years, I once again spent an entire month with my mother. As a long distance caregiver having the opportunity to see her more frequently brings out a more positive responses from her.

Now on most days we find her with eyes closed and very little expression on her face. The sound of music that once delighted her seems to have disappeared. One thing that is constant is that when I take her hand, even when she seems to be sleeping, she holds on tightly as if never wanting to let go.

On several occasions with eyes wide open we also found mom speaking nonstop. Although her speech is gibberish and difficult to understand it still lifted our spirits to hear her come alive. Yet amazingly enough mom said a few profound things such as "people should be happy".

I am always grateful that my wonderful supportive husband joins me. He is so loving to mom especially when I feel a loss for words. Magically he connects with her and finds the right things to say.

The head of nursing has confirmed that mom is in the last stages of the disease. I do not know when she will finally say goodbye, yet in my heart, I do not believe that it is in the near future.

I have shared many times before that this horrific disease also fascinates me. Sometimes I question if I am now in denial or just becoming immune and accepting the situation. The once praying for mom to go to sleep has vanished and a new "space" has opened up for me.

I now feel more serene and have a calmness that is freeing. No more torturing myself of what I wish to be. I know that when mom is ready or the disease has "won", that is when I will have to say my final goodbyes. So for now, I cherish and remember how tightly our hands intertwined never wanting to let go.





My new book "Letter To My Mom". It is the continuation of my first book "My Mom My Hero" Available Worldwide on Amazon in Paperback & Kindle.
https://www.amazon.com/s/ref=nb_sb_noss?url=search-alias%3Daps&field-keywords=lisa+hirsch&rh=i%3Aaps%2Ck%3Alisa+hirsch