-image-When doctors go on vacay
So I went for the EEG on Friday, the one to determine whether I actually do have epilepsy. My biggest concern is that if it’s not epilepsy, I’d like to know just what *is* causing my episodes, because they get freakier and freakier by the day. My second biggest concern is that I’ve been on anticonvulsants for over two years, and I’d like to not take unnecessary meds for a second longer.
I called the doc on Monday, because waiting is not the forte in the brain of the SarahK. I was informed that the doctor only reads the EEGs and EEG reports on Fridays, and since I’d had my EEG on Friday, my report wouldn’t be available until this coming Friday (tomorrow). Okay, I can wait until then. Oh, but the doctor went on vacation Tuesday for ten days. When he gets back, he’ll have to wait until the following Friday to read the results, because, again, he only reads his results on Fridays. So basically his assistant told me I would be waiting three weeks for my results. Awesome.
I get that he’s the epileptologist, and since he’s the big freaky brain-waves expert, he wants to make sure he’s the one to read everything, I do get that. But I’m also thinking that since my report was available to him on Friday, the same day I took the test, he could have done one of two things: read the report Friday afternoon or Monday, or coordinate with another neuro to read his patients’ test results in case they call in his absence. As someone waiting on pins and needles (and feeling pins and needles all over my body), I don’t think it’s too much to hope for. If he read the results differently when he returned, he could call and tell me that he disagrees and all that.
Oh, then his assistant told me that he’ll go over my results with me at my follow-up appointment. That’s great, but my follow-up isn’t until September, and considering that the good doctor made it clear that he thinks there is .0000001% chance that I have a seizure disorder, I don’t want to be on meds for another month or six weeks while I’m waiting for him to tell me that, yes, I should get off the unnecessary meds.
Bah.
I’ve started researching again, because he’s pretty much got me convinced that it’s something else. Also because of the freakish ramping up of symptoms this week. I sometimes get these electrical pops (harsh ones) in my right thigh while walking. Only occasionally, but it freaks me out when it happens, because my tingly symptoms are at their worst then. So yesterday evening, I was walking to the kitchen at work to grab something off the printer, and I felt the electrical pop. Ow, fine, nothing new. A few steps later, I felt the same type of shock from mid-calf all the way down to my ankle. And every time I moved my foot yesterday evening, I felt the same shock. It finally went away after Bible study, but it was back today. That stuff? That makes me lose my mind a little.
Anyway, the research has turned up some good possibilities. Bad ones, too, of course. MS, but an MRI two years ago came up empty in that respect, and I’m so grateful for that. It’s also possible that it was there and the radiologist missed it. The other thing that keeps coming up is a calcium deficiency. Makes sense. Things seem to have gotten worse with the tinglies since I quit dairy again in March. And then since we thought these were seizures, Dr. Wonderful upped my dose and told me to get my butt to a new neuro STAT. And they’ve gotten worse since the increased dose of seizure meds, and as it turns out, calcium deficiency can be exacerbated by anticonvulsants. Vicious circle I’ve got myself in, no? Calcium deficiency also makes sense, because it could be caused by another autoimmune. Hypoparathyroidism can be an underlying cause of calcium deficiency, and considering I’ve got a thyroid issue and celiac (diagnosed, undiagnosed, either way my intolerance of gluten is autoimmune), it could follow that my parathyroid glands could be compromised by autoimmune issues. When a person has one autoimmune disease, there is a 40% chance of developing a second autoimmune. GI/celiac = 1. Thyroid could be #2. Parathyroid #3? Wouldn’t surprise me. Not to mention that four years of malabsorption has seriously compromised the balance of minerals and vitamins in my body.
And honestly, it would be the best news. Calcium supplements for the rest of my life would be likely, but it’s so much better than the prospect of MS or living with epilepsy.
I have an appointment with a family practitioner Monday. One, I need a referral to an endocrinologist. Two, I’m not waiting three weeks to jump on this. I’ve already started cutting down my anticonvulsant dose; no, I didn’t consult a doctor, because he’s on vacation. I cut my nighttime dose in half and am still taking the same morning dose. I’ll do that for a few weeks, and maybe by then I’ll have found out about the epilepsy. Anyway, I normally avoid family practices like the plague (namely because with all the little snot-nosed kids running around, it’s likely I’ll actually contract the plague on a routine doctor visit). I actually decided to see this one because a girl at church recommended her. She (the doctor) has a daughter who was recently diagnosed with celiac, and she’s apparently researched the crap out of it, just like me. So I’m thinking when I suggest calcium deficiency, she won’t balk and wave me off; she’ll probably think it’s likely and send me for the serum tests to confirm.
So that’s the update.













