Caregiver: a person who provides direct care (as for children, elderly people, or the chronically ill) Void: an empty space; emptiness My father passed away peacefully in his sleep on January 8th, 2012 as a direct result of Alzheimer’s Disease. For the 6 months leading up to his death, we took him into our home …
For the past 6 months, I, along with my loving husband and 3 wonderful children, had the honor of caring for my father, Sherman Marcus on the final leg of his life journey. Alzheimer’s Disease is difficult, but we all made the best of it each and every day, spending quality time with him, smiling …
We are all going to die – how, where, why and when are the unknown we live with from day to day. Dying naturally does not have to be depressing, sad maybe (if you choose to see it that way)…but not depressing. This is why we are reminded over and over throughout our life to …
This is Dad’s new addition to his face, compliments of his Houdini abilities! Alzheimer’s Disease is by far the most unpredictable thing I have ever encountered (besides my mood off my hormones LOL). I look at all the stages that have been studied and seem to have created some new classifications via Dad – Zaydeh …
My Dad, known as Zeydeh to everyone (Jewish Grandfather for you slow kids), has happily entered in his Alzheimer’s Disease, what we now refer to as the “Zaydeh Zone.” In a previous post I wrote about his end of life “working.” The “working” post was referring to him overriding all his sleep medications and staying …
Yep, we are in full-swing with the “H” word and things are running as smoothly as possible. My previous post on hospice (a damn good post if I must say so myself – so go read it!) talked about how I would embrace it and not fear it when it came. Dad turned 83 on …
Dad is sinking more and more into his happy world and away from us. I view Alzheimer’s Disease as a process of unlearning and unpredictable firing of the brain. As time goes on, his brain may have unlearned many of the things we take for granted, such as chewing food or putting on glasses, while …
Rounding up just ten things I have learned about Alzheimer’s Disease and being a caregiver for my father with it, was quite difficult. I knew absolutely nada, zip, zero zilch about the disease when my father came to live with my family 5 months ago. I took a crash course and still learn every day. …
Continue reading “10 Things I Have Learned About Alzheimer’s”
Not the “H” word, Hospice! Well…chillax folks, it is not necessarily a bad thing and actually something I will welcome with open arms. Oh no…you may think that positive and upbeat Greta is going to get all depressing on you. Who wants to talk about “end of life” stuff? Well…back to the book, All I …
I want to preface this post with the warning that my writing here draws from my personal experiences only. I’m certainly not an expert in Alzheimer’s Disease or Dementia, so please take what is written here with a grain of salt. My Grandfather has dementia and has lived in a Veterans Hospital for many years …
Continue reading “Alzheimer’s, Dementia: Holiday Calls and Visits”
From the Rolling Stones song, “Sympathy For the Devil” comes a line that always makes me think of Dad, “Pleased to meet you, Hope you guess my name.” Heeeelllllloooo has become a standard greeting at our house, because frankly, dad does not recall who he is actually looking for but wants someone’s attention. Jokingly, it …
A couple of months ago, I noticed dad talking to himself in the mirror. Sometimes he slips into his happy little world of talking to himself and he goes on and on with conversations. I used to try and draw him out, but realized he is most happy and comforted with this state of mind. …
I have quickly learned that there are great tools out there as far as medical equipment and assistive devices to help dad. Medicare pays for some and the rest needs to be purchased new, used or borrowed. Since he has only been here 5 weeks, we seem to finally have our act together! Thanks to …
Continue reading “Alzheimer’s: Medical Equipment & Assistive Devices”
“I love everyone. I really do. My life has been beautiful. If I can help anyone I will.” ~My Dad talking in his sleep August 1, 2011~ What can I say – but when the sun goes down, things change with Dad. The medical staff has been using the word “Sundowner” frequently since my dad …
It has been 3 weeks since dad came to stay with us now. I have been reading a lot about Alzheimer’s and music is mentioned just about everywhere for therapeutic uses. Dad is doing amazingly well and I have found, when he has a down moment, music can change his mood miraculously. He may not …