Having been proved right, or rather not proved wrong, the neurologist had proceeded with treating me exactly as he had said he would. The quantity of drugs were to increase week by week until I hit the magic quantity, and then I’d continue at that level for the rest of my days. Providing I didn’t fit, he saw no reason to scale the medication back down, as it’d only increase the chances of me fitting again and therefore losing my licence for another year. I’d also be tested (and tested and tested) for side-effects, abnormalities and anything else anyone could think of on a regular basis.
Once I’d got the hang of getting hold of repeat prescriptions, it was all fairly straightforward. For some reason, the taxpayer foots the entire bill for those of us taking treatment for epilepsy, so it’s not even costing me the standard prescription charge. All I do is renew with the pharmacist every month (it seems dumb that I can’t get larger quantities less frequently, but I’m not complaining), take a bunch of tablets twice a day, drop in at the local surgery every six months for blood tests, and that’s basically it.
Just as he said he would, the neurologist also factored in my bipolar disorder when prescribing the medication. Curiously, quite a number of anticonvulsants also have mood-stabilising properties, so there were a good few drugs from which he could choose that would tackle both at once, providing he got the dose right. So I followed all the instructions, and the months began to roll by.
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