
Ditch the negative talk to yourself and others. Speak kindly to all.
Rather than closing the door on our chapter of caring for Mom, it’s time to expand it a bit. Not for the purpose of reliving the experiences, but our growth from them.
I think we’ll begin with a bit of nurturing again. Posting something positive a couple of times a week – whether it will benefit others I don’t know, but I do know it helps me get through each and every day more easily. So here goes:
Make some “magic” happen today.

May 22nd – Mom suffered a devastating intracerebral hemorrhagic stroke. She was awake and lucid when the EMTs transported her to the ER. The doctor explained what had happened and that there were two options, transport to another hospital for care in a neuro ICU or hospice. Mom chose hospice and we knew that would be what she would have wanted us to choose if she hadn’t been able to convey that message to the medical staff in charge of her care. She was so happy when the EMTs brought her home again and placed her back in her room and comfy bed.
We celebrated each and every day after that. And on June 3rd at 4:32 am, Mom’s journey was complete. She passed away peacefully. I was grateful to be there when she took that last breath.
We are forever grateful for the Intermountain Homecare & Hospice team that helped us in Mom’s final days. Their support was wonderful and while Mom surprised us all by ‘extending’ her stay nearly a week beyond what anyone thought. We admire what you do and the compassionate care you provided not only Mom but our family and continue to do for other families in similar circumstances.
While this part of our journey with Mom is now complete… we’re looking at how we can help others in similar circumstances navigate their journey with Alzheimer’s – or as caregivers and know that they aren’t alone.
Our hearts and lives have been forever altered through this experience.
Yesterday didn’t quite follow the “plan” of the day. Mom had a stroke and it’s a bad one. She’s resting comfortably at home under hospice care. We imagine that the time left is pretty short. And as always, she surprised everyone! Doctors, nurses, techs and more. She shouldn’t even be awake, but she is. She shouldn’t be able to smile, but she can.
She’ll fade a lot faster now. I’m sure we only have a few days left as the bleed continues in her brain.
We’ve thoroughly enjoyed the last several months — the laughter, smiles and quirky things she’s shared with us. We’ve listened to music until we know every song and intro by heart. Every performer’s actions and maybe even a background story or two. Watched her favorite movies, wearing out a few DVDs and even having to replace a DVD player. 🙂
Shared more good than bad. Learned lots of new ways to reframe things to get around her stubborn streak at times. Dealt with more intense sundowning moments… Late nights and early mornings, when all we would like to do is catch up on a couple of hours of sleep.
Yesterday threw a real ringer in the works. I’m not ready for her to leave, but I do know there are those on the other side of the veil anxious to greet her and she’s growing more anxious to be there with them. Last night’s pucker up of the lips and reaching out for a hug was a demonstration that the veil is very thin.
We love you Mom — We cherish the last 5 years of being able to care for you and have you in our home. To be around your sweet spirit every day, rain or shine. There are so many things I’ll miss — and a few I miss already.
I love you unconditionally. With all my heart!
