Wishing you all a joyous Christmas.

Blessings to you and your loved ones, this glorious day!

Today, I headed over to visit my mother in the hospital earlier than planned, as we have predictions for “snow showers” this evening. I stayed until she was served her lunch – she got her turkey, mashed potatoes and gravy that she likes so much. When I was a kid, we never did turkey, unless we happened to raised some ourselves that year, so this is a preference she picked up (or finally got to indulge) some time after all us kids were grown and gone.

My mother is looking so much better. Yes, she is still struggling with pain and mobility, but her overall appearance and even mood are great. She honestly looks happier now that she’s in the hospital than I think I’ve seen her in years!

She has commented more than a few times on how good the hospital food is. She doesn’t have any dietary restrictions, and the meals I’ve seen look awesome. What I’m also appreciating is that she is no longer saying things like she needs to stop eating, she eats too much, because she’s too fat (I don’t remember my mother ever being thin). She has also stopped blaming her food, especially meat, for any problems she has had, like the mystery pain in her sternum (not related to her heartburn), or not being able to breathe at night, or headaches or [insert malady of the day here]/ In fact, now that she’s sleeping in a hospital bed that is set at an incline, I haven’t heard her complaining about her breathing, either. From what I’m seeing, she is getting an excellent ratio of protein in her meals; far more than she ate on her own, and the meals themselves are larger than what Meals on Wheels had, which she would say were soooo much food.

They are weighing her regularly, as a way to monitor how much fluids they’ve drained from her edema. She told me what she weighted today, and comments on how it was too much. I told her, this is how they keep track of how much fluids they’ve drained from her with her treatment, so she has probably lost quite a bit of weight, just in the time she’s been in the hospital. Plus, she’s 94 years old. Who cares? Seriously. If all the scare mongers were right when it comes to being fat, she should have died decades ago. Instead, she’s ridiculously healthy, as far as her vitals show. So much so, it’s almost a problem, because then the doctors just want to send her home, when she has mobility and the beginnings of cognitive issues that really should prevent that.

Thankfully, that does not seem to be the plan now. We have yet to see or talk to a doctor, and my mother says she’s seen a doctor only twice since she’s been admitted, and none of the nursing staff we talk to know anything. All they can tell us is, she’s staying for now. There are no discharge plans that they can see. I know I’ve stressed, every time I call and ask about it, that she cannot live independently anymore. I’ve even added that none of us can take her in; I have a disabled husband, and my siblings do not live in accessible housing. Plus, my sister (the oldest of us) is almost 70, so we’re not exactly spring chickens ourselves! Ha! When talking to one of the nurses one time and I mentioned that my sister (who has the closest thing to accessible housing, for at least part of her home) is almost 70, the nurse admitted she was shocked. She said she thought my mother was in her 70’s, so how could she have a daughter that was almost 70?

I told her I have plans to go to her place soon (probably tomorrow, if the roads are good) to empty our her fridge. There are a few things she asked me to bring to her as well. She told me they haven’t been giving her the special vitamin for her wet macular degeneration, so on the way out I talked to today’s nurse about it. I couldn’t remember the name of it – it’s not normally a prescription, but something you can buy off the shelf. My mother got a prescription for it specifically so they could be included in her bubble packs. He said he would look into it.

He phoned me at home some time later and asked more questions about it. Since I was at my computer, we were able to confirm the name of it. He asked me to bring her bubble packs so they could use what she has while they got authorization from their pharmacy to include it with her other meds. They should have had it on their med list for her, but I think the fact that it’s a supplement, not a prescription medication, it fell through the cracks.

My mother also admired the hat I crocheted for myself using the blanket yarn my daughter got me. She asked if I could make one for her, too! Something she can wear at night, because she gets so cold. My brother and SIL had brought her an extra blanket and slipper socks, but her head still gets cold.

So that is a project for me tonight. A simple hat worked up quickly, and I have enough of the blanket yarn left to make one.

Meanwhile, as I write this, my daughters are taking care of roasting the turkey and making our Christmas supper. Since I headed out when I did, everything got shifted around.

All in all, it’s been a very quiet Christmas, which we are quite happy with. When we lived in this province before, and my MIL was still with us, we would do Réveillon on Christmas Eve at my in-laws, Christmas day at my parents, then another big feast on Boxing day with my BIL’s family. As great as it was, we’re more than content to have our quiet Christmases at home. Or course, my husband can’t handle the trip to the city to see his family for any celebrations, anymore, either. Perhaps, one of these year’s, we’ll be up to hosting such a celebration, but my FIL isn’t very mobile, either, and probably wouldn’t be able to make it out here anymore.

The good thing is, with modern technology, we can still be “with” our family members on this happy day.