I have the crud.
The Friday before Christmas, we tried to get together with a friend to celebrate her birthday. Jim had the crud, so he stayed home. The Friday before New Years, we tried to get together to celebrate Jim’s birthday and my friend got the crud and couldn’t make it. This week, we tried to get together for lunch, but I have the crud. We’ll try again next Friday.
Crud sucks. The federal regulations for pseudo-ephedrine are absurd, ineffective, and a flaming nuisance. Claritin-D used to come in 750 mg strength. It was great. Now with the current regulations, I can only get Claritin-D in 270 mg dose. These are 24 hour pills and there are 15 in the box. They cost $20 if I buy the Walgreens version (which I did). I have to take at least two of them to get any relief. I can only buy 3.6 grams per day and only 9 grams in a 30-day period. Jim bought a box shortly before Christmas. I bought a box today. If I need any more, I may have to have the cat go buy them. And what does all this do to stop the production and use of methamphetamine? Not a darned thing. Why? As a client explained, it’s too difficult to extract the pseudo-ephedrine from Claritin-D. As for the number of meth addicts? I don’t see any progress there. I’m basing that on drug cases I’ve handled.
I’ve been dealing with slamming into both depressed and manic states. After the last trip to the neurology clinic at the medical school in El Paso, I had blood drawn. Lots and lots of blood. The good news: the ANA test is negative and I don’t have an auto-immune disease. The expected news: My A1C is in the pre-diabetes range. The glucose monitor will arrive this week. I’ll be monitoring my glucose, keeping a food diary, and hoping to have a better A1C result in a few months. The unexpected news: I got a call asking if I wanted financial aid to pay for a blood text that got sent out of network. How much is the blood test? $4,000. Nope – no financial aid and don’t run the test. Next, I got a letter telling me the out-of-network lab can’t use the blood that was sent because it was drawn at a hospital rather than in my doctor’s office.
I recovered from that, and called my HMO to see if the prior authorization request that was submitted early December for my appointment at the neurology clinic at the medical school in Albuquerque had been authorized. No, because the paperwork from my doctor’s office was wrong. I called the doctor’s office and asked for a call back or I would camp out in the office until I got a satisfactory answer. Turned out I had to camp out in the office. The doctor’s office sent in corrected paperwork late December. My appointment is for January 18. I get to call later this week to see what progress has been made. If I have to cancel this appointment, I won’t get another appointment for about 4 months – if I’m lucky.
I’ve decided I don’t want to go back to the medical school in El Paso. I had been wondering most visits if I were the only one in the room who had ever taken cell biology. I had a nerve conduction series that left me furious. First, I had to deal with a resident who is clearly hearing impaired and clearly too arrogant to do anything about it. He’s going to kill someone eventually. The neurologist supervising the test, after I asked in frustration how she would feel if someone told her she would be in pain for the rest of her life, said, “You’re not managing your pain well enough.” THIS ISN’T MY FAULT YOU TWIT. I didn’t say that. I asked her who was doing research on peripheral neuropathy. “No one here.” When I got home, I did a google search and found 496 clinical tests. There’s a pretty nice one in France, but I doubt the cheapskates at the HMO will authorize trips to France. There is a clinical test in Salt Lake City and in Albuquerque. That they might be willing to authorize.
The next appointment, I was in severe pain. When the pain hit a 5, I took a double dose of gabapentin and sat hooked up to a TENS unit for an hour or so. That’s when the pain hit a 7. I took another double dose of gabapentin. That meant I had taken a full day’s dosage in a span of 2 hours.The pain dropped back to a 5. I was walking into walls, stoned out of my mind, in pain, and pissed off. The neurologist said he could raise the dose. “No you can’t, because I won’t take it.” The gabapentin works sometimes, but not always. There’s no pattern that I’ve been able to spot.
After being told the nerve conduction series showed damage to the axion, I started asking microbiology type questions. Turns out, I really was the only one in the room who had taken cell biology. It was clear that the neurologist had no idea what I was asking about. I told him that I thought I figured out the problem. He’s used to dealing with big things and I’m used to microbiology. He told me neurology wasn’t rocket science. I strongly suspect the $4,000 blood test was retaliation. The test if for a genetic abnormality. No one asked me if anyone else in the family has neuropathy. And if this were genetic, it would have shown up 40 years earlier.
All of this excitement caused an outbreak of hives. It took me a couple days to figure out the redness and swelling was hives. Usually, stress hives start on the insides of my arms. This time, it was on the outsides of both arms. One antihistamine cleared up the hives.
I’ve been working, now and again, on designing the perfect purse. I know what I want…zippered pockets on the outside, the top with a recessed zipper, and a flap with a zippered pocket. I also need a pocket on the end that will hold a water bottle. I need a purse large enough to hold my 12.9” iPad Pro. I was trying to work out a pattern yesterday when Tinker decided to help by insisting on sitting on the drawing paper. He wants to be by his humans and he likes the sunbeams in the sewing room.
One odd thing has been happening. I’ve been having flashbacks of crap that happened to me when I was growing up. My psychologist, when I asked him if flashbacks ever end said it was finite. Got news for you. PTSD is for life. It’s been more than 45 years since I lived in an insane asylum run by a violent drunk and a violent narcissist. I’m still having flashbacks. Years ago, I stumbled upon a way to deal with the flashbacks – look at the memory, acknowledge that what happened was horrible. Since then, the flashbacks haven’t been debilitating. They seem to have less power. They also seem to show no signs of ever stopping.
I’m linking with Nina Marie here. See what some other artists have been doing.
Please stop by my web store, Deb Thuman Art here.