((((((ANN)))))) ~
Thank you for your blessings!
Jon fell asleep about 2:30 a.m. and slept until 1:00 this afternoon. Soundly. I went to bed at 3:00, and Jim stayed up until 5:00 to keep an eye on Jon. Jon is rested and in good spirits, as if nothing happened.
We increased his seizure meds again hoping that will put the kibosh on the seizures. It's really our only alternative. We save Ativan for tonic clonic seizures.
Jim woke up with head to toe RA pain. He was feeling fine, when John was here yesterday to turn Jon. Instead of letting Jon do all of the heavy work, Jim just had to pull Jon twice to center him. John said he'd do it, but Jim insisted, even as I begged him not to do it. "I'm all right. I didn't strain."
I started on Lecture #1: "When John's here, let John do everything. If you overdo, you'll suffer the next day, and then that means you can't help me pull Jon up in bed, which I can't do on my own. So, you have a set back and that makes it harder for me, and I worry about you. Then, you have to take extra steroids, which we're trying to avoid. You always say that you're fine, but you forget that you really aren't fine. And then you pay for it."
Jim's response is: "I can't just sit/lay here all day and night and watch you work yourself into the ground. I want to help you."
My reply: "You do help me in many ways. When John is here ..."
Today, Jim caved and said "Lesson learned. I will just be a couch potato."
I'm sure that Jim would feel much better, if he got some exercise, so now I need to work on that with him. Just easy exercises, like Qigong for RA. We have a video. I need to get us started on it.
I did walk this morning, as I'd missed several days of walking due to the Toenail Team on Tuesday and going to the store on Wednesday. It's important for me to walk for a variety of reasons, primarily for my RA. When I get up in the morning, I can barely move. I have a glass of freshly squeezed orange juice, put on my walking clothes and hit the trails. No matter how severe my pain is, once I get started, it begins to abate. I get fresh air, a cardio workout, sunshine, and to meet and greet neighbors and pet their dogs. Very therapeutic.
We'll be on seizure watch again tonight, praying that the increased doses will be effective. It is always nerve wracking for us, because many times, his seizures have generalized to tonic clonic, and we've had to call paramedics, have Jon intubated, and in ICU for weeks.
Another reason to increase his meds: he's peeing like two race horses. That may be depleting his meds a little.
In addition to this, we're quite worried about John's mother, who is back in the hospital with dehydration, a UTI (very frequent for her), and possible seizures or stroke. John's sister found their mom lying in bed in urine and feces, staring at the wall yesterday. A few months ago, she had a shunt placed, and she's had multiple problems (infection, pain) since then. She's living in a retirement community, but I told John yesterday that he needs to consider one on one care. I don't think she can be left alone anymore. He said that he and his sister are looking into it. So stressful and sad.
Life ... We never know what is waiting around the bend ...
Thanks again, ANN ~
Love & Light,
Rose