I cannot believe this, but I actually forgot to write here Sunday! There was so much preparation for our girls- afternoon- movie- plan, and I only had so much energy and time before everyone arrived.
Actually Sis and MissS arrived earlier, around noon, so we could watch the DVD MissS had brought, which contained a few minutes of our Gramma on film. ( I apparently took the ancient video camera to FL with me back in '94 when I visited her, and filmed some of the things we did, and her. Then there was another visit a few years later--'98? But that one must have been when I flew down there to help Dorothy with packing Gramma up to move to Spokane.... I don't remember any of this, but little bits of memories came back when we watched the video.)
Anyway, seeing Gramma, alive and well, speaking in that soft voice, clearing her throat in that well-remembered way-- well, it made both me and Sis get teary. How lucky we were to have her for so long! How much we both miss her...
And by the time we were done with that emotional bath, then it was time for the real reason for the get-together: we settled in to watch LOTR, the Fellowship of the Ring, the first one in the trilogy. I have the 4-hour extended version on DVD, so that was an utter joy, watching it with my sister, daughter, and shortly after we started it, BIL's daughter joined us too. It was wonderful.
Yesterday I was very tired, and yet found the energy to try two different recipes for gluten-free bread. So I did those in the morning, sat down for a rest, and suddenly it was time for my appt with my PCP.
I love my visits with her. She spent the vast majority of the 50 minute visit reviewing meds and the conditions/ reasons for each med, dosing, etc. I have so many meds, and she looked up whether each had interactions with the other, and wrote it all down. She planned out a new medication schedule, and added two new meds; so mornings are now taking meds at waking time, 2 meds 90 minutes later, 1 an hour after that, and one more at 10am, then 1 at noon, and one at 2pm, then 2 more at 5, 2 at 6:30, and 2 at 9pm. Not including the supplements: Vit D, E, calcium, and the probiotics and fiber capsules. All of those get taken in the morning.
Then she did the physical exam, reassured me about some interesting skin issues, and put in the order for my tetanus shot to be given in October, and ordered the pneumonia vaccine. In a couple of months I will also get the flu vaccine. Today as a result of the pneumonia injection my left arm is quite sore, but nowhere near as bad as when I had the second Covid booster.
I got good news too: my repeat labs done last week showed marked improvement in both the elevated triglycerides and the bad cholesterol. Both of those improved solely because I stopped eating cheese. Sigh. Damn it! I love cheese. I hated giving it up...but those levels were quite high, and can certainly be improved with diet.
Last week: Tuesday was J's appt with his GI, to learn the results of the labs he had done. I've never been to any of his GI appts (or any of his PCP or heart doc appts either for that matter, because of my work schedule, but now that I am not working I can accompany him). His appt was at 11:15, and it was a 35-40 minute drive, so he insisted on leaving at 10:15. Naturally we arrived quite a bit early, and after he was checked in, we sat. And sat, and sat. At 12:25, we were brought back and put in an exam room, where we waited another 15 minutes.
I had overheard several conversations in the waiting room about the waiting time, and the reasons for it. If we hadn't needed those results, we would have rescheduled...as it was we did choose to wait. Although I told J that if this were my doc's office, I would be looking for another GI. However, he likes this doc, so I shut my mouth.
The doc basically ran into the exam room, and immediately sat down and asked how things were. J slowly started to recount the past month on the new GF/wheat-free plan, and the effect it was having on his system. I caught the doc's eye at one point, and he immediately broke in and said to me, "Now, what was it you wanted me to know?" I said, "Yes, J is somewhat better, but nowhere near what he is reporting, and he sleeps a lot, he has no energy." I liked that the doc was so sensitive to the patient's partner's comments.
So the results show pancreatitis. We were both surprised. (And both extremely grateful it was not the big C.) This can be caused by age, smoking, drinking, or "other reasons". J's pancreas is operating at only 20% of its ability; the remedy is a ridiculously expensive enzyme prescription he is to eat with every meal, to aid the pancreas in producing the enzymes needed to digest his food. Without it he would slowly be starving to death, because his body isn't able to absorb the nutrients.
Oh, okay, we said, sitting in stunned silence and shock...
Now, the medication, Creon, is $9000 every three months. We just about fell over. Obviously we cannot afford that, but this doc's office has a specialty pharmacy which deals directly with J's insurance company to force them to pay for it (because it is considered life-threatening). So what we actually pay is still ridiculously expensive for us at $120 month. He was given samples to use at home until the first shipment arrives, which it did Monday.
And two days later he was remarkably improved. I was so amazed. He has his energy back, and can eat, and is spending far less time in the bathroom. While he is to continue on the wheat/gluten-free meals, the doc is pretty sure this won't be necessary for a life-time. In other words, when he goes back in a month, he might be able to return to regular food. In the meantime, we are both pretty much following this plan.
Tuesday was also our 14th wedding anniversary. We decided to splurge on a take-out meal from RedRobin, one of the few restaurants that has GF foods. That too was ridiculously expensive, reminding us why we don't normally eat out. But it was a special occasion, and we really loved the meal.
Tuesday I also received the best news: Springsteen is touring next year both in the US and overseas. We I have been waiting anxiously for announcements of tour dates and on-sale dates, and prices. All of this was announced Tuesday: you have to go to TicketMaster's website to become a "verified fan", (which I did promptly), and then you will hear from them as to whether you have been given an "access code". If you have won this lottery, you can try to buy tickets the next day at 10am when they go on sale. Otherwise, you have to wait until 3pm that day...by which time the tickets will be all gone, of course.
So, tonight is the night I hear whether I've won an access code. I am so anxious about this. I also have my Sponsee, and my daughter both helping: they registered also, and if either of them gets an access code and I don't, they will buy the tickets. My Sponsee is a huge BossFan also, and the three of us will be going together. Hopefully to both Tampa and Orlando.
Currently it is raining so hard, with thunder. We desperately need it, so we are very happy to see it. I love being inside and watching the rain. It won't last long, but it's always welcome.
Well, Dad was the one today who inquired about my blog entry, and why it hadn't happened on Sunday. I can't believe I actually forgot, but that's my poor brain these days. I'm so glad he reminded me!!
This coming Saturday is J's 84th birthday. Sis and BIL, and MissS, and Shannon and Chris are all invited to help celebrate. Bro and SIL are leaving for Vermont Friday after work so they can't make it. They'll be gone for a month this time, to be with Dad for his surgeries, and maybe even the CTscan he will be having. I am so glad and grateful they will be with him.
That about brings this up to date.
TYG