In Michigan we are currently getting a ton of snow. I hope those that are local are ready for it, cause winter is here. It looks like we will have a white Christmas.
Speaking of Christmas, have you ever done an advent calendar at this time of the year? I never did one when we were kids, but Hunter’s ‘Regular Grandma’ got her one when she was 5, I think.
Note: Hunter has 4 Grandmas and 1 Great Grandma so we have names for them all :). Phyllis is of course just Grandma, my Mom is Harmony (할머니 Korean for Grandma), and Regular Grandma (Sometimes Grandma Sarah) is John’s mom. Hunter came up with the names, so they have stuck after 11 years.
Now, with the advent calendars, the one Hunter got the first time was a little piece of chocolate in every day. As a momma who tries to monitor the sweets (yes, I am that momma), having chocolate every morning before breakfast wasn’t going so well with me. However, Hunter loved it and I kept up with the tradition every year, but I changed it up a bit. I found these Lego advent calendars a few years ago. So we have the Lego calendars now and do this along with the Avon advent tree Phyllis got me in 96. So every morning, Hunter has fun with the little surprises waiting for her when she wakes up. This year she got the Star Wars Lego advent calendar. I did mention I am a nerd/geek and Hunter is following in my footsteps, we are a little excited for the Rogue One movie next Friday.
The advent calendar got me thinking. With the changes we are seeing with Phyllis. It reminded me that every day is a gift, like the advent calendar. I know that sounds corny but it is true while dealing with her ALS. Except, some of the ‘surprises’ we are getting each day are pretty hard to deal with. But, I try to think about the positives in each day. Like, being able to ask her how she is over messenger. Getting her to smile and laugh when I ask if she wants me to slap my dad for joking and aggravating her. Or getting a call from my dad and it is just a general question on how my day is and not one in panic because something is wrong. It is the little positives I look for each day. Because as my dad said this week, ‘we are taking it day by day now.’
Update on Phyllis’s ALS for this week: This was a rough week. We had some scares on Wednesday and we spent some time in the ER. I have to say that U of M is pretty awesome. I had calls from the nurse, the social worker (we were assigned one from the ALS clinic), and her neurologist. Each of them asked how she was, how we were, and while being honest with what we were dealing with, they were all very compassionate and caring. She was very dehydrated and after she got IV fluids into her she was doing better. All her tests with the CT scans and blood work came back good so she was able to get the green light to get the feeding tube on Friday. For the rest of the week, between John Covel and Bryan and I, we rotated to try to give my dad a break. On top of what is going on, I am worried about his health and well-being. All of us are pitching in to take turns spending the night, and being there during the day to let him get some rest or get things done.
The feeding tube procedure went well on Friday. John Covel and my dad went to get her Saturday and she is home now. John, Hunter and I went down on Saturday to visit and welcome her home, clean the house and make her some soup.
This week we are planning our annual Family Christmas party on Saturday. So I will be making the journey down on Friday. We are also working with Great Lakes Home and Hospice to get my dad some help and they will be calling on Monday to set things up. He finally agreed with me to get some help after a lot of arguing on my part.
Dad:’You don’t think I can take care of her?I can handle it’.
Me:’No Dad, I know you can but you need help’
Dad: ‘No I don’t need any help. I can do it’
Me: ‘You are getting help, and you are getting it now, I don’t care if you like it or not dammit’
Stubborn Hillbilly :). However, I am just as persistent and stubborn as he is (I am a Russell and therefore it is in my DNA) and I won.
We have been blessed with many offering prayers and help from family and friends in the area. With me being an hour away, it kills me that I can’t just stop by daily to help or see if they need anything. John Covel and Bryan do this and I would love to be able to, but having others do it too just is amazing. My Dad and Phyllis are the ones that would typically do anything for you and now that’s coming back from all of you. So for those that have helped or sent messages. Thank you from the bottom of my heart and bless you.
I saw this message by a friend a few weeks back and it hit home. I am a Christian and firmly believe in the power of prayer and have been praying for strength during all this, but I am beginning to believe that God does think I am a Bad Ass 🙂
In closing, as we are getting ready for the holiday festivities, take a moment to appreciate your own ‘advent calendar’. Think of the simple beautiful gifts around you that you have every day. It will really help with the negatives that come around with the stress of the holidays.
One thought on “Every day is a gift.”
I stopped by today with my Dad and Sister. I was wondering how Butch is doing, I see it often when loved ones health declines because they are so focused on caring for their spouse. They are lucky to have you and the boys. My Dad gave Butch his number he lives a mile down the road and can call him anytime of He needs something. I also told him he Could call me, I will do whatever I can to help. I’m not far either. Phyllis has my number I texted her today to confirm. Taking it day by day is all that everyone can do. I hope you guys have a great time Saturday celebrating Christmas. Let me know if there is anything I can do.
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