Tag: sore throat


Unintended Consequences

11
November

Today was my D&C with hysteroscopy. I scheduled it for noon, because I didn’t want to deal with my dad ranting about having to get up at 3 or 4 in the morning for a 7 AM appointment. (You have to arrive 2 hours prior to the scheduled time.) My dad still ranted, even though his wake up call was at 8:30. (He is a strictly 10 AM kind of guy.)

Before we left, my mom had me go get her some water so that she could continue to get in her beloved ice water. (She drinks several 32 oz. cups full of water in a day.) I thought that was a little unfair, but I tried not to hold it against her. I knew that she is still a little skiddish on her feet, especially in the house.

When we got to the hospital, I didn’t have to do mountains of paperwork, since I’d had the pre-op appointment. The guy who called me to the back asked me, “Have you had a hysterectomy?” I almost laughed in his face. (How many people get hysteroscopies and D&C’s when their uterus and other female parts are gone?) Since I hadn’t, the guy made me pee in a cup. (I’m fairly certain that I was not at risk for being pregnant–heavy bleeding + my continued virginity = no pregnancy, y/n?) I did as I was told, though I hate to do the peeing in the cup thing. When I got out of the bathroom, he had me change into the pretty purple paperish gowns that keep you warm and put a blanket on my lap. I was supposed to do all of this and open the door to let the nurses know I was ready at the same time. Apparently, I’m supposed to be supergirl or Jesus or something.

When the nurses came in, they were ready to do the vitals, the remaining blood work, and the IV. I told them, fairly quickly, that I was both a hard stick and a person with hard to hear blood pressure, including with machines. They marveled at the thought, until I explained that these were common traits in my mom’s side of the family. That was interesting to them, but I think they thought at first that I was making this up. (Why would I make this shit up?) Well, the blood pressure came back fairly easily. (125 over 63, pulse of 92, O2 saturation of 99.) The blood/IV was another story. The left hand didn’t work. The left arm wasn’t having it either, though they did get enough blood to check my sugar (105) and my calcium (very low), sodium (normal), and potassium (normal) levels. The right hand also wouldn’t allow for threading the IV tube. (Apparently, they were getting the flashbacks on each, but the veins wouldn’t allow the catheter to be inserted.) So, the anesthesiologist was called in. (I suggested a Cardiac nurse if one was in the hospital, but they weren’t at Women’s & Children’s–they were all at main on the heart floor.) He used a different type of needle and went in on the bundle of veins at my wrist. He got it to work fairly easily.

During pre-op, I had to confirm my name so many times, as well as my birthday and social security number. I also had to explain what was going on and tell them who was with me. I also had to make sure that they had all of my allergies down repeatedly. It was really annoying to repeat the same things over and over. I had my 4 arm bands (ID, latex allergy, drug/food allergies, and fall risk) checked every time a new person came in the room. Once my parents came back, they reminded the CRNA that I get hyper with anesthesia and that I have the staple line left from my gastric bypass surgery. The CRNA said that hyperactivity happens a lot with kids because they have opposite reactions to sedatives, but I don’t know what that means for adults. (I do know that I tend to have the opposite of a normal reaction to a lot of drugs, though.) Because of my history of nausea with anesthesia and problems with GERD, I was given a patch of nausea medicine, a shot of some more nausea drugs, and a shot of Pepcid.

Because of all of the questioning being repeated, my dad asked the pre-op nurse what would happen if they had someone back there who couldn’t answer the question. The nurse asked if he was referring to people who were in a reduced mental capacity and my dad nodded. She said, “We get their family.” My dad said, “So, if they think they’re God–” and she said, “we defer to the next of kin.” I quietly said, “You ask Jesus?” My parents laughed, but the nurse didn’t seem to get it.

When I went to the OR, I had to go over the information one more time, after being scooted onto the table. I was also given something to “take the edge off” or, in other words, keep me calm and maybe shut me up. I felt my brain fighting the sedatives, which is a fairly normal feeling for me. I was trying to hang on to my waking state, but eventually it became too hard and I fell asleep.

I woke up in recovery with a very sore throat. (I had a similar feeling with the sinus surgery/septoplasty.) The recovery room nurse told me that I should calm down and rest, but that wasn’t going to happen. I begged for ice chips, because I was so thirsty. I couldn’t have them until they were sure I wasn’t nauseous anymore. (I had apparently complained before I realized I had come to.) The nurse got me some a few minutes later and then gave me some 7-up and graham crackers. As I ate and drank, my energy began to boost quickly and I was talking quite a bit–not as much as last time. The nurse ended up giving me some Lortab, which I was still a little too groggy to protest to taking. My stomach was cramping really bad and the nurse asked me what kind of dogs we had. Apparently, before I woken up, I had mentioned that my stomach felt like I had a basset hound on it. So, the nurse wanted to know how I knew what that felt like. We talked about dogs until she was sure I was pretty much ready to go to post-op. Before we left my recovery room, she helped me get dressed. (I don’t think they’ve ever helped me dress before leaving recovery.)

In Post-Op, the next nurse was going to hand my parents a script for Lortab. My mom threw a fit, because Lortab causes me to have chest pain. The nurse claimed that it wasn’t anywhere on my file and I hadn’t told them that anytime before. I thought that was funny since I had mentioned it prior to the surgery at the pre-admission appointment, it was in my hospital file before the appointment (I had gone to the main building of the hospital with the first reaction), and it was on the front of my chart. The nurse went out to the desk complaining, and one of the other nurses said, “Well, it is on the front of her chart.” So, she had to call the gynecologist to get his okay to prescribe something else. So I have a few doses of Ultram now. That I can take. Before the squabbling over the prescription, she had checked my BP and it was 123 over 43. I was a little worried about that, but she said it was “good”. I’m still a little skeptical about that.

I got to leave fairly quickly after that. And I am now at home, trying to get comfortable, which is really quite difficult. I still feel like my throat is dry and raw. I think that they might have used the wrong size breathing tube because I came out of surgery with a really raspy voice. (My voice may be quiet, typically, but it almost always smooth–unless I’m sick or have scratched my throat on food.)

Comment » | General, Sickness and Health

Under My Feet

6
September

I haven’t really been online a lot this weekend. That’s mainly due to heightened anxiety/stress. I think that’s due to the beginning of football season. Around the time my father woke up on Saturday morning, I started giving myself my headache medicine. It kept me asleep for around 12-13 hours. I ended up waking up during Auburn’s halftime, which meant I got to experience rants full-on. I had missed the rants about the teams that he didn’t even care about, which was good. I had wished I could make it through the Auburn ones, too, but they would have been harder to miss. Auburn ended up winning, which was good. If they had lost, then I probably would’ve started dosing myself into unconsciousness again. (I’ve often used medicines to induce sleep. It’s how I managed to sleep while I was having major sleep issues during middle and high school.)

I started crying sometime in the early morning hours on Sunday. I just felt like I was ready to scream, throw things, etc. I started composing a very long letter to my parents about how I felt like I needed to be taken more seriously. (This was what I used to do when I was a little kid–if I needed something or if I felt like I needed to apologize, I’d write a letter.) Well, the ink ran out of the pen and I got upset and threw it across the room. It barely made a sound when it hit Willow’s chair, but it was loud enough that my mom woke up. We ended up talking, and I complained about the thing on my stomach, which she checked out a little closer this time. She was surprised because it was burning up, and I told her that that was normal. (It is hot most of the time, but it gets worse in the middle of the night [around 3:30-5:00 AM] and it starts hurting worse.) I have an appointment to get it checked out with my family medicine doctor, but I have honestly lost faith in most doctors lately. Yeah, they send me for the tests, but the longer this whole saga goes on, the more dismissive they get. (Half the time, the results are never relayed to me.) And with the cardiologist refusing to even suggest anything that could help the extra beats and tachycardia, it just seems to be stupid to go through massive amounts of tests.

Speaking of tests and medical records, I think that is unfair that if I want to access my medical records, I have to pay fees. (Where is Files & Records when you need her?) If I want a copy of my blood work, I have to pay per page of the test, which can be 20-or-so pages. The doctors, who have a lot more money, don’t have to pay anything. They can get paper copies or faxes or computer access without paying anything. All that they really need is a signature from me to share the records. (If they’re in the Huntsville Hospital system and the record is on my hospital file, they don’t even need my signature.) All these people can see whatever they want about me, but I don’t get to see my own file. (At the Mental Health Center, I don’t even get the opportunity to pay for the records to see what’s been said. I can have my therapist or doctor or one of the nurses read it to me, though.)

I’m a little frustrated with the Social Security Administration. When I started on SSI and SSDI, I was told that if I started paying $200+ a month in household expenses, then my SSI check would be increased by that much. After I got the first check, I began doing just that. I’ve told the SSA about this twice. I filled out lots of paperwork the first time–nothing happened. I called again in May or June (or possibly early July)–I haven’t even gotten paperwork or anything that says that anything will happen. I get that the government doesn’t really have lots of money right now, but it seems like they could at least hold up their end of the 1/3 reduction rule.

Anyway, right now I’m dealing with an earache and headache that my mom told me was probably just TMJ. I agreed at first, but after a while, my throat began hurting. I would say it was allergies, but I know that’s not likely.

Comment » | Family, General, Mental Health, National Weirdness, Sickness and Health, So Damn Special

Gut Don’t Lie

25
July

Before I make any kind of posting, I’m going to plug Urban Sunrise again. I know that some folks who read this are under 18, so they can’t post on it yet, but if you like boards, please check it out.

On Friday, my throat started hurting and my gut instinct was that this was some kind of infection. It felt kind of like the beginning of strep. It’s been worse every day and I’ve noticed other signs of an infection of some sort. It’s still not as bad as full-on strep can be, but it’s hurting constantly and I’m trying to find ways of dealing with it. Mainly I’ve tried to eat things that coat my throat in mucus…sugars, dairy products, etc. I’m basically using anything that a choir director would’ve banned the week of a competition.

I would schedule an appointment with a family practice doctor for Monday, but I have to do the test to determine if I can work (so my rheumatologist will fill out loan discharge papers on my student loan) at the therapy center. He, my mom, and I are fairly certain of what the results are going to be. I’m not really looking forward to the test, though. I hate being in pain, and I know it will only worsen it.

My mom is going to try to explain to my dad that he gets to keep the printer that he had prior to Friday, but I get to have the one that my mom and I got at Target. My mom and I both needed one that is accessible to us. Though my dad has the printer on a desk that is, literally, right next to my chair, we have to get up, go through the kitchen, and into the old dining room to actually use the printer. It was kind of stupid to put it in such an inaccessible place, but my dad has been really irritating lately.

I’m starting to worry about my vertigo test results. I know that the blood work might have to go to a specific lab, like how some goes to the Mayo Clinic and takes 2 weeks, but the vertigo test was done in the neurologist’s office and should’ve been analyzed that day or (at least) that week.

Okay, I’m going to talk about the message board again. It’s been a while since I’ve had to plug a message board, so I was wondering if anyone had any tips. If you know of some exchanges or listings that I can join to promote it, that would be cool. There are a few things I don’t want to do, i.e. going on someone else’s board and posting an ad. I know that I’ve done that in the past, but it typically can end up causing some sort of issues. (I know that most board owners don’t like it when other boards are posted.)

BTW – Blah Blah Biddy Blah is going to be moving from the .us address to a .com later this week. This is due to .us being way too expensive to renew. Rants and opinions will probably be on a different domain that I have. I’ll announce all this again later.

Comment » | Family, FPS-Related, Message Board, Sickness and Health

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