Cynthia Anne Greene passed away around 2:30 pm today, October 20,
2015. She was in her bed, covered with her quilts, snuggled by Kari,
Cindy, and Quincy, holding hands with Todd, Garrett at her feet, her
steady friend and caregiver Cindy by her side, and all around surrounded
with love. We shared stories and a few laughs while she gradually went
to sleep. She awoke a few times to smile but was overall peaceful and
relaxed.
Gang Greene
Another Adventure
New adventures haven't stopped since we stopped sailing.
Now my adventures are technological.
Now my adventures are technological.
Tuesday, October 20, 2015
Sailing Away
Sunday, October 18, 2015
Reaching Deep book info
Some of you have asked about my book recently.
Book Link:
http://www.amazon.com/s/ref=nb_sb_noss?url=search-alias%3Dstripbooks&field-keywords=reaching+deep%2C+cynthia+greene
Or search for "Reaching Deep, Cynthia Greene" on www.amazon.com/books
The more expensive version has color photos as the beginning of each year. The less expensive version only has photos on the front and back cover.
Book Link:
http://www.amazon.com/s/ref=nb_sb_noss?url=search-alias%3Dstripbooks&field-keywords=reaching+deep%2C+cynthia+greene
Or search for "Reaching Deep, Cynthia Greene" on www.amazon.com/books
The more expensive version has color photos as the beginning of each year. The less expensive version only has photos on the front and back cover.
Update
Dear Family and Friends,
Last January I wrote about going on hospice and the right of everyone to decline medical care. My book made me choose to delay turning off my vent. It was an exciting time to see it come together. Sharing it with others added to the pleasure. Because my health was not declining and I had no immediate plans to turn off my vent I was released from hospice. I spent a delightful summer sitting in the sun and soaking up the warmth.
Now the time has come to once again evaluate my life. I'm back on hospice and planning to turn off my vent. It has been a difficult decision, especially when looking at our grandsons. Talking with Doctor Libby, my pulmonologist, gave a certain sense of peace. He has been with me since the beginning and knew I wanted to be able to turn off the vent when the time came. He also was clear that they might not be able to get me off the vent after the gall bladder surgery, I have a lot of confidence in him.
The decision has not been easy but Todd and Kari are with me. They have seen my struggle to communicate with the eyegaze system. So on October 20th I will be turning off my venting. A memorial service will be held November 7th at 6:00 at Rose City Park Presbyterian Church in Portland.
Don't forget to live your dreams while you can.
Love to all of you,
Cynthia
Last January I wrote about going on hospice and the right of everyone to decline medical care. My book made me choose to delay turning off my vent. It was an exciting time to see it come together. Sharing it with others added to the pleasure. Because my health was not declining and I had no immediate plans to turn off my vent I was released from hospice. I spent a delightful summer sitting in the sun and soaking up the warmth.
Now the time has come to once again evaluate my life. I'm back on hospice and planning to turn off my vent. It has been a difficult decision, especially when looking at our grandsons. Talking with Doctor Libby, my pulmonologist, gave a certain sense of peace. He has been with me since the beginning and knew I wanted to be able to turn off the vent when the time came. He also was clear that they might not be able to get me off the vent after the gall bladder surgery, I have a lot of confidence in him.
The decision has not been easy but Todd and Kari are with me. They have seen my struggle to communicate with the eyegaze system. So on October 20th I will be turning off my venting. A memorial service will be held November 7th at 6:00 at Rose City Park Presbyterian Church in Portland.
Don't forget to live your dreams while you can.
Love to all of you,
Cynthia
Monday, September 14, 2015
Walk Time
Last entry I said I would focus on the Walk to Defeat ALS. It is Sunday September 27th. No matter how I'm feeling it's exhilarating to see all the people. Once started there are people spread over the entire three mile route along the Willamette river. It is exciting to look at both bridges and the far side of the River filled. Last year people were finished before some had started.
There is still time to join us or sponser me if you want.http://web.alsa.org/site/TR/Walks/?pg=team&fr_id=11029&team_id=338348
There is still time to join us or sponser me if you want.http://web.alsa.org/site/TR/Walks/?pg=team&fr_id=11029&team_id=338348
Sunday, August 30, 2015
Summer
Okay so it has been three months since I have posted.
Brief version is there have been ups and
downs .
June brought two visits from people passing through
Portland. One visit was from some long time friends from Bakersfield on their
way to visit grandchildren who recently moved to Washington. I made a good lunch
stop. It's almost time to visit again. We grandparents can't wait to long
between visits. For the same reason I don't expect them to stop by each time,
maybe just when it times right for a lunch break. Of course the best part of June was
Sam's Birthday. His other grandparents
were here too, so it was a fun day. Sam
is one of those special kids who really makes you feel special when he says
"thanks I like this".
July started hot and stayed that way. I had to laugh to
myself sometimes because I thought it felt good outside. The plants are not at all
happy. We are in a neighborhood where most people have chosen not to water the
front lawn. There are areas that have green edges where shrubs have been
watered. When the tree people plant a tree many get watering bags. These make
sure the baby trees get slow deep
watering. It also makes a green circle.
Todd was considerably nicer than me when he bought a room
air conditioner to keep my main caregiver, Cindy, comfortable. It looks like a minion and served its purpose
well. I would stay as far away as possible or go outside as my comfort level
is in the low 80's and hers, like most Oregon folks, in the low 70's. We
manage to keep a happy medium and the nights cool off so I can open all the
windows and my bedroom door. If there is
any breeze the wind chimes let me know.
Since I need a nap or two every day and time to rest my
eyes the time spent outside is good. We have been fortunate to have only one
really smoky day from all the fires. The
air I breath is filtered so I had no problem. However I am beginning to look
for rain, plants here are not accustomed to months without rain. This is one
time I can hope for a good rain. The
previous was written the two days ago. We had a real thunder storm. I don't know if
any of the fires got rain and now it is very windy.
All the yack about weather has probably bored those
facing worse. What I should be writing about that is the upcoming ALS
walk. If you don't want to know about it
or be asked to make a donation don't read the next entry.
Monday, June 15, 2015
Chemistry
It has been
a while since I have written. It is much easier to write about events than
daily living. We are in the process
of changing my anti depression medication. The one big one I had been taking
was dropped by the insurance company. At the local pharmacy it was $2237 for a
90 day supply. A bit of sticker shock. So we are in the process of easing that
one out and bringing another one.
Interesting how chemistry can have such an influence on our minds.
Saturday, May 9, 2015
Toe Signing Party
More about my
book. Several people at church had ordered my book. When they arrived my friend
and mentor, Rae passed them out. Somehow the idea of a toe signing party came
up. Sounded fun so plans were made. Caregiver Cindy got to bake several kinds
of cookies, we bought a green stamp pad, some different teas and some wine.
Let the party begin.
At the party I had two phrases that people could choose
to write in their book. After that it was stamped with a green toe. It was a
fun day.
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