THE WRITE PLACE…

to find Patti Singleton these days.


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A Writer/Caregiver Packs For A New Journey

Tokeland, WA PHALL PHOTOS 2013

Tokeland, WA
PHALL PHOTOS 2013

Tomorrow (Friday) I set off on a new journey. It may take a week, a month or maybe longer. The timeline is open and so am I. I’ve detailed my truck, except I need to vacuum it. I’ve re-potted and watered my houseplants. I stirred the compost pile and planted the lilac and rose by the fence, and a handful of mini-crocus near the pond’s edge.

I’m fairly certain that I can come home once a week. Mrs. M.’s grand daughter lives near and should be able to manage a day and night with her. It’s over 300 miles, round trip, so I hope I can break that into 2 days. I’ve got the edited hard copy of my Postcards manuscript packed and I’ll also be working on the middle book of the memoir series. I’ll take my laptop, but I will hold off on taking my printer until I have a better idea of how long I’ll be needed.

The biggest thing I will miss is my little cave/home (Maggie) and the beach. It will just be the two of us and I’ll have my own room, so I can still be a part-time cave woman:>)  I look forward to getting to know Mrs. M. better and seeing what mischief we can come up with in Portland. I’m certain to get a better schedule going and get outside more often.

Journaling is a strong habit for me, so I do plan to journal about my time with Mrs. M. I know I’ll take a lot of photos of my new surroundings. I am sure that I will be online and checking in with all of you at least a few times a week. As you can tell, until I get settled, everything is up in the air. That would frustrate many people, but I really look forward to the mystery of it. I am very adaptable and change doesn’t bother me.

The big difference with helping out this time is that I don’t know Mrs. M. I have met her maybe 3 times over the years. She has passed the main part of physical therapy and does not need a lot of assistance there. Also, there is no stress or heart break related to her care. She may be almost 91, but she is mentally sharp and physically on the mend.

These links will take you back to the posts where I talked about this new adventure and my other caregiver experiences. Here and here.

Did you notice that I changed to a static “home” page? Check it out when you get a chance and let me know what you think. I am still working on the site…

Take care,

Patti


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Someone Needs You. How Will You Answer The Call? Part 2

Bridge Along The Journey PHALL PHOTO 2013

Bridge Along The Journey
PHALL PHOTO 2013

Metaphor musings. Bridge as opportunity, to next bridge as opportunity, to next bridge as opportunity, to next bridge as opportunity…into the horizon…

Continued from Someone Needs You. How Will You Answer The Call? Part 1

An executive caregiver position came open many years later. (No phone call this time.) By then, my children were out on their own and I had divorced their step father. I was 4 years into the best relationship that I could ever have imagined. And then, my partner in life and business, was diagnosed with leukemia. I became Paul’s 24/7 caregiver. The hats I wore covered all aspects of our lives during the year of his illness, treatment, stem cell transplant, our hospital wedding and his final battle with graft vs host disease. We were fortunate to have a strong group of supporters in our family and friends. We all learned so many lessons during this time, that Paul and I began to plan a book about it. My 3-part memoir series of love, illness and loss is a work-in-progress.

I readily admit that nepotism was involved in my next caregiver position. The patient was my mother. My family (2 parents in their 70’s, and 6 siblings in their 40’s and 50’s) were still reeling from the loss of my sister in February 2012. Two months later, my mother had an accident that left her with two broken arms, 2 black eyes and a variety of pain, from head to toe. Yep, I got the call. I was back on an airplane heading north. It had only been five weeks since I returned home from Alaska after my sister’s death,

When I arrived back in Alaska, my brother picked me up and took me straight to the hospital. I stayed in my mother’s hospital room that night, and we took her home the next day.  Mom was unable to care for herself at all. I became her right-hand and left-hand person, and slept beside her at night. I would like to break off and tell you what an amazingly strong woman my mother is, but I will leave for another day.

Two of my siblings live nearby and they circled the wagons to provide support and relief. I stayed in Alaska 4 months and wore many hats while I lived with my parents. My most rewarding role was that of adult daughter to my parents, but the second best was that of caregiver to my mother. I was also able to spend some special time with 2 of my sisters and their families, as well as both of my brothers. I flew home to Washington in August, on the 3rd anniversary of my husband’s death.

A holiday bonus. The patriarch (I call him “dad”) sent Ms. Daisy (mom) and I on the vacation of a lifetime in late November 2012. I joined my Alaska family for Thanksgiving, then mom and I toured the Hawaiian Islands for weeks. We spent Christmas and New Year’s with my Arizona sister (it was her twin who we lost earlier that year) and her family. Mom flew home from Washington in January, after visiting her sister and the rest of our Washington family. [3 months later my grandson died and mom flew back to Washington to mourn with, and nurture our family here]

To make a long story short (hahaha), I received another call. It was the call from my sister that I wrote about in the first paragraph of Part 1 of this post. I’m still not perfect, but I guess I will keep on practicing this caregiver role, until I get it right. I am looking forward to this new adventure of giving care to Mrs. M. in Oregon.

I’ve taken some time this week to ponder the meaning of these calls-to-action that keep arriving in my life. They seem to be bridges to the next part of my journey, rather than minor side trips. So, now I have to wonder where this next bridge will lead me…

You can be sure that when I get the call that Mrs. M is being released, my laptop, printer and works-in-progress will be traveling with me, so please hang out for more.

How will you answer the call? Has a caregiver call been a bridge in your life? We would love to hear your thoughts and experience (in the comment section).

Here are these Helpful Links again:

http://www.caregivers.com/caregiving/ All things caregiver.

http://alzjourney.com/helpful-resources/ An incredibly helpful list of resources for dementia, Alzheimer’s, and caregivers.

Peace,

Patti