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Just the right environment for hospice care

ust the right environment for hospice caregiving

We are pleased to share a post from you from Ira Woods, who blogs at Conscious Departures.

When it comes to going out to eat, whether it be a restaurant or someone’s home, many people find that the environment plays a big role in the enjoyment of the food. I once heard a comment attributed to a friend that when asked what he thought of the restaurants in New York City he said that it was hard to enjoy food when eating in a toilet (sorry New Yorkers, no offense meant). I never found out if he actually said this but it definitely got a laugh out of me and a nod towards the spirit of the statement. So what about the environment when we are caregiving? What about the environment when a person is going through an end-of-life process?

My mom was in the hospital during the final days of her life. There were tubes in her, the sounds of beeps, boops, people rushing up and down the hallway, people talking loudly in the room next door and so on. Her hospital room was very clinical and sterile with all the necessary equipment to keep her sustained no matter the cost. Nothing in it was familiar or cozy.

I remember one nurse coming in and cleaning the inside of my mother’s mouth. Mom was at that point where she could no longer take care of herself and was asleep or unconscious most of the time. The nurse looked like she was being a bit harsh on mom’s mouth trying to scrub out the dead skin, brush her teeth and so on. One of my family members didn’t like what they saw and decided to start a fight with the nurse. They both stood over my mother yelling at each other.

What I was experiencing prior to that altercation was mom slowing way down, getting real quiet and moving within herself. It was the first time I witnessed something like that and was feeling a lot of respect for the process and a bit in awe. So when World War III erupted it felt like someone blasted a siren in my ear while sleeping. Not only did it feel horribly wrong but my mom, although normally quite feisty and outspoken, was not going to participate in the argument. All she could do was lay there.

I begged the two belligerents to stop and respect my mother’s state. That didn’t help because it just provoked them to both gang up on me!  I finally managed to draw them out of the room without contributing to the yelling and got mom some semblance of peace again.

Let’s face it. Being taken care of and dying in a beautiful environment is a luxury. A friend of mine had a massive heart attack in a bathroom at the airport and died there.  Another had one while delivering a business presentation and died almost immediately. And then of course you have all the soldiers who die under terrible circumstances, far from home, with little or nothing to comfort them during their last moments. We can’t always choose our death spot and sometimes it’s too fast to probably ever know what happened.

One gift I have as a caregiver is the privilege to provide as beautiful an environment as I possibly can. Home seems like such a great place if that’s where the person finds comfort. When K and I talked about how we wanted to go we always came up with the same answer – at home. Even if it meant not having access to all the great life-sustaining equipment. I was so glad we were able to make that happen. Home was a place she could dictate how she wanted things to be. A place where everything was familiar and there were no distractions from the internal work she had to do. She could be quiet or stay occupied in her own way – whatever her inspiration dictated.

I made sure the environment was simple and clean, knowing that’s how K liked it. We live in a very quiet area so there was never a problem with noise. During the final nine days she was relegated to a hospital bed which I had placed in our bedroom so I could sleep there with her. There are lots of windows in the bedroom and even a sliding patio door so during the day the room was always full of light and fresh air.

In the evening I left the bedroom curtains open so that you could see out onto our patio. We had Christmas lights strung on the inside of the awning of the patio so that even with the bedroom lights out there was a nice festive glow in the room. Seeing the Christmas lights in the evening was a lot of fun and the kind of thing K liked. The overall effect of the Christmas lights was incongruous to what many would take as a sad time. Instead it felt like something very cheerful and special was taking place. And it was special.

I hope K liked what was provided. It seemed to suit her and she appeared happy and focused most of the time. I would venture to say that each one of us knows the environment we’re most comfortable with as do those we are caring for. Environment is one of those things we can discuss, be aware of and plan for.

I really like this quote by the late Dr. Timothy Leary,  “You’ve got to approach your dying the way you live your life, with curiosity, with hope, with fascination, with courage and with the help of your friends.”

2 Comments Post a comment
  1. So well put – thank you. I think for many during our lives, dying itself isn’t the struggle that bounces around in our emotions, it’s the fear of how we will die – and where – that rears its ugly head.

    February 4, 2013
  2. That’s why we re-posted Ira’s beautiful message here–it’s OK to talk about making the last place comfortable and calm, and to recognize that this IS the last place.

    February 4, 2013

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