Archive Page 31

Sunday rest

I was at a conference for most of last week and last night we hosted Bear’s best friend and her parents for dinner. The conference was fine and the dinner was fun, but they’ve both left me spent. Being an introvert leaves me feeling pretty drained after lots of socialization. So, we decided to take today as a day of rest. Or, really, I did. Aaron did some grocery shopping and mowed the lawn. I enjoyed the rain and watching too many episodes of Friends.

Molly seemed pretty tuckered for most of the day, too, but recently pepped up and has spent the last hour or so running in and out of the backyard. Her cheeks are rosy and her smile is large. About two minutes ago, she came running in and said to me, “Where’s Phoebe?” I pointed to the couch. She said to me, “Phoebe’s friend is outside.” Then she walked over to Phoebe and got within inches of her nose and said to her, “Phoebe, your friend is outside!” She then went to the back door, opened it, waited for Phoebe to join her and the two of them went bounding out. Maybe Bear and Phoebe will be pals after all.

Well, the 312th time is a charm

I have no idea what in the hell is going on. This morning, I got a ridiculously chipper call from Jennifer that a specialty scheduler would be calling me to schedule my tests. I asked her when she thought this special call would come. She said she imagined that it’d be today, but she couldn’t be sure. Sure. I waited. And waited. And waited.

Finally, just a few short moments ago, I steeled myself and called my doctor’s office. I said that while I didn’t know whom I should be talking to about this insanity, I’d been waiting to have tests scheduled for some time and I’d really like to get moving on it. She asked my name and date of birth and then … guess what? She transferred me to neurology and a very competent woman quickly took charge. She got two more people on the phone and within about one minute my EEG was scheduled (May 27) and my follow-up neurology appointment was scheduled, as well (June 3). I have to wait until maybe Monday to get an MRI appointment (something about something that I didn’t understand), but I have more faith in the unknown woman who said that she would call me back about it than I have had in any of these voices on the other end of the phone in sometime.

So, there you have it. Just. Keep. Calling. And calling. And calling.

UPDATE: And then, just because the story has to keep going, the Specialty Scheduler just called and offered me the May 27 appointment for the EEG. When I told her that I had already taken that one, she said, “Oh, they called you!” Uh, no. Definitely not. When she asked if I needed anything else from her, I said, “Well, I think I still need an MRI appointment.” Her response? “Someone else will be calling you about that.”

Holy Toledo

So, the last couple of weeks? Oy vey, you know what I’m saying? You probably do – because I haven’t really been able to shut up about it – but let me elaborate in writing. Thanks in advance.

On Sunday, April 26, my mom and Mollybear & Phoebe and I were heading out of Shawano (after attending my godson’s spectacular first communion party) when I slumped over in the driver’s seat (because I was driving) and became unconscious. I can’t imagine what this must have been like for my mom. I know that she, and the rest of my family, handled it beautifully, though, because when Molly talks about it she laughs and says that I got sick and that she and Steve then went to a party and ate hot dogs. I remember nothing of the event itself and even the moments after are very foggy. For example, I distinctly remember throwing up in the ambulance, but I remember neither walking to the ambulance, which I’m told I did, nor getting from the ambulance to the hospital bed. While at the hospital (or medical center, as I guess it’s more accurately called), I had a bunch of heart, brain and blood tests. Nothing looked too out of the ordinary and, after a decent amount of time with Ibuprofen and fluids inside of me, I was sent on my way with a diagnosis of having suffered a grand mal seizure and two directions: (1) no driving for three months and (2) call my primary doctor the next day to get a referral to neurology.

On Monday, April 27, I called my primary physician. I told the nurse that I was directed to ask for a referral to neurology. Instead, I was told that I would first need to be seen by an internist and the next available appointment for that wasn’t until Friday. Uh, ok. I took Monday, Tuesday and part of Wednesday off of work because I couldn’t move without significant muscular pain (for example, my jaw hurt like the dickens and moving from one position to another would have been comical if it weren’t so painful) and I was uncommonly sleepy. When Friday came, I went through the hoops of the appointment. I relayed everything that I remembered and I gave a written report of what my mom had observed. I brought all of the paperwork from Shawano, including a DVD of the CT scan of my brain. I just kept thinking, “Answer the questions and we’ll move this along.” I did all of the muscle tests that were asked of me (push here, resist here, etc). The appointment must have lasted an hour. At the end of it? I was referred to a neurologist. First, though, she asked that I do more blood tests and another EKG. I complied and the tests were all returned with mostly normal results (“Good news!” read the note to me). I was told that Neurology (I’m going to capitalize it from now on, just because) would call me, but that if I didn’t hear from them by Tuesday, I should call the office.

Tick, tock.

On Monday, May 4, I woke up with a horrible sore throat. I mean, ouch. But, I also had a bit of a cold so I thought that maybe it was related. We took Mollybear in for a dental appointment (during which she sat on my lap and cried, “I want my mommy!” – always confusing for everyone), then to school and then we went to work. My throat pain wasn’t abating and I realized I’d had chills throughout the night. Hmm. I called the doctor and made an appointment, worrying that it might be strep. I had my performance review at work at 10 and asked Aaron to take me home around maybe 11. I just wasn’t feeling right. I slept for a bit and Aaron picked me up at 2:30 to take me to my appointment. I went in, described my symptoms and was told, unequivocally, that I did not have strep throat. No swab was taken, no test performed. Although the resident said some of my lymph nodes were a little swollen, he was certain it was not strep, but was instead viral. He told me to come back if it got worse. I went home and felt kinda embarrassed. When I woke up on Tuesday, I felt no change in my condition, but I certainly felt like something was wrong. Even if this was *just* viral, it wasn’t feeling very good. I needed to stay home. As the day went on, things got worse. The pain in my throat extended up to my ear. It no longer hurt only when I swallowed, but all the time. I measured a temperature of 100.6. This just couldn’t be right. But I’d felt dismissed the day before, so I doubted myself and continued to hope that the pain would subside soon.

Tick, tock.

On Tuesday afternoon, I called my primary doctor’s office to relay that I had not yet heard from Neurology. The response? Here’s their number. Uh, ok. So, I called Neurology and explained the situation. The nice woman on the other end of the phone said, “Well, we’ve actually asked your doctor to request a couple of tests be performed before we see you and she has not yet ordered those tests. Let me transfer you back to their office, but I’ll explain to them first what we need.” So, I get transferred back and the guy to whom I’m transferred said to me – earnestly – “Ok, great, I’ll get the ball rolling on this!” Uh, ok. It’s been nine days now since I had the seizure.

Tick, tock.

On Wednesday, May 6, I woke up and felt terrible. Every time I swallowed, my body made a large jerking motion to try to offset the pain. I couldn’t talk without pain. I couldn’t breathe without pain. Whatever this was, I needed help. Ibuprofen hadn’t alleviated any discomfort since Monday evening. Enough is enough. I just couldn’t take it anymore. We dropped Molly off at school (well, AO did; I was far too reluctant to go near all of those kids) and he took me to Urgent Care. I walked in and asked to be seen. The woman at registration was so kind. The nurse who led me back to the exam room was mostly nice, but when I requested that we skip the scale – honestly, since turning 39 I feel more confident in asking to skip the scale at most appointments, but why on earth would anyone need to be weighed to determine if they have strep? Plus, I’d had it! I didn’t want to take any more time to do any of this nonsense! – she said, “Ok, I can put down that you refused.” Uh, ok, put that down. You do that. The nurse took my blood pressure and pulse and temperature (100 even) and became more sympathetic as her tasks wore on. She took a swab of my throat and left. The NP then came in and I almost started to cry immediately. She was so kind and caring and she listened so well. She looked at my throat and told me that no matter what the test results were, she was getting me medicine because things looked terrible. In about three minutes’ time, the test results came back. Positive. I had strep. I actually started to cry. I felt so validated. She sent me on my way with a prescription for penicillin, three Ibuprofen and a bottle of apple juice. Praise modern medicine and health care providers who listen.

I went home. She said that I needed to stay home for 24 hours. While I didn’t feel immediately better physically, I felt entirely different mentally. I felt listened to. I felt respected. I felt, weirdly maybe, vindicated.

This morning, Thursday, May 7, I realized that I had missed a phone call from my doctor’s office that came in yesterday after 4 p.m. The voice mail just said to return the call from someone I’ll call Jennifer. Around 8:15 a.m., on the way to take Molly to school, I returned the call. I was told that Jennifer was busy, but she would call me back. Around 11:20, Jennifer called back to tell me that Neurology had requested an EKG and an EEG. She said that I could come in anytime for an EKG, but that I’d have to wait for a call from a specialized scheduler for the EEG test. Ok, I thought, kinda puzzled. I hung up the phone, relayed the info to Aaron via text, and quickly checked MyChart. I thought, “Didn’t I have an EKG on Friday? Isn’t that what that was? And didn’t I have one in Shawano? Why would I now need a third one? And why would Neuro want yet another one?” I quickly called my doctor’s office back and – against all odds! – was actually able to speak to Jennifer during this same phone call! I said, “I think I had an EKG on Friday. I think Dr. X ordered it.” Jennifer gave me a weird answer to something that I hadn’t said, but eventually confirmed, yes, indeed, I had had an EKG on Friday and, oh wait, that’s not what Neuro had asked for at all. Turns out, Neuro had asked for an EEG and an MRI of my head, something my doctor had not previously ordered. Oops! Ok, they will get on that now (four days after Neuro had requested it) and I will, once again, wait for a specialty scheduler to call me.

Tick. Effing. Tock.

[And yet I know, despite all of this, how lucky I am to live in a time with the medicine we have, in a country in which I can access it, in a city in which it is all around me and with a job that lets me afford its privileges. Still. Holy Toledo there has to be something more efficient.]

Hometown love

I love Madison. I think I’ve made that very clear over the years. While I would not turn down the opportunity to live in Italy, and although I absolutely loved my time in Richmond, and I think it would be neat to live in Milwaukee or San Francisco or Los Angeles (hi, GAOOG!), I know that I am right where I am supposed to be. And I feel pretty strongly that Mollybear is right where she is supposed to be. I love her school, our neighborhood, her future schools, the lakes, the bike trails, the university, the Capitol, the Square, the people, the opportunities and – gasp! – the weather! At least right now.

And then, just when I think I know everything there is to know about our sweet town – afterall, I’m religiously following the public market district and the MadCity Bazaar – I stumble across other things that amazingly cool people are doing and I fall in love with Madison all over again. A couple of months ago, we stumbled upon our neighbors, Madison Circus Space. What? Why wouldn’t our fair town of 200k peeps have a space devoted to the circus arts? Corpus Christi, of similar size, had only one brand of grocery store, but in Madison you can learn how to ride the German Wheel on Sundays just a short walk from our house. And then today I stumbled upon this gift to the community, FEED Kitchens. Aaron had just been saying that he wants to start a Dude’s Stock Cooperative, but wanted a commercial kitchen space to hold the meetings. Well, voila! Fewer than two miles from our house is a space that holds five commercial kitchens available for rent. Could it get any cooler? I know that people often complain that Madison isn’t Milwaukee or Chicago or Minneapolis. And you know what? It’s not. It’s Madison. And I love it.

Say what?

As many of you know, Molly is not always the easiest child to understand. While she is very social and talkative, her speech isn’t crystal-clear. Or even always plastic-clear. While I’ve truly never obsessed over it, it’s something I’ve been monitoring. I don’t want to put on rose-colored glasses and shoo away what appears to be a small problem, only to have it blow up and become much worse than necessary if only I’d opened my eyes sooner. Make sense?

At Molly’s three-year-old pediatrician appointment last month, I took note when the doctor told us that strangers should be able to understand about 75% of what she says. Hmm. Depending on what she chose to talk about with these strangers, I was pretty sure we weren’t there. Not long after the appointment, and despite our lovely pediatrician telling us that Molly wasn’t yet old enough for the school district’s assistance, I checked out the school district’s website. Sure enough, they have a program to screen the development of children ages three to five. I figured, why not ask them and see what they say? They had us fill out a bunch of forms and give Molly some “tests” that required us to point to pictures of, say, a rabbit or a spoon and ask her to say the word. When she did, I would write down the phonetic version of what she said. She got most of them right, but she says, for example, “tar” instead of “car” and “yum” instead of “gum.” It was actually pretty interesting. On Monday, we had our appointment at Lapham with the early education specialists. While Molly played with one of the speech specialists, we talked with another one. I learned a lot. I learned that the hard C is often hard for kids, as is the hard G. R and L have their own difficulties. And then there are the combo sounds like SP and ST. Interestingly, I thought, Molly has her combo sounds down pretty well, but has more difficulty with the hard consonants. Anyway, apparently everything that Molly does is completely developmentally appropriate and the nice specialists didn’t seem to have any concerns at all. We were in and out in just over 45 minutes, sent on our way with worksheets to peruse and exercises to try.

At the end, part of me felt a little guilty for taking up their time when they probably have a million more needy people to help, but part of me feels ok about utilizing a resource available to us to make sure that our little one is getting her needs met. In the end, I learned a lot and I think I feel good about the whole thing.

I’ve also been reminded – AGAIN – that I just talk too fast. Slow. It. Down. Kate.