I am pretty sure I’ve recovered from those horrible effects from the medication change. It really only took about a day for my heart rate and blood pressure to normalize after switching back to the previous medication. It took a few weeks, though, for the migraine’s vicious cycle to pause. I can say that, while I’ve had headaches, I have not had as severe a migraine since. I had told that doc that I didn’t think that medication helped with my migraines but it was fantastic on my blood pressure, and I was proven wrong after that experiment. It definitely helps more than I had previously noticed. Because I had the same reaction to Botox injections (I didn’t notice how much it had helped until it wore off), I’m going to try that again in a few months, insurance willing.
I haven’t read as much as I usually like to. I have books that I really really want to read, but find myself lacking the ability to focus on them for too long. Upcoming reviews include:
I had an appointment with my neurologist and didn’t think much of mentioning the changes she made to my meds to anyone but my husband, and I only glossed over it with him. Most chronically ill people can tell you about the every 3-6 month visits with this specialist or that, trying to find just the right combination of medications, supplements, diet adjustments, exercises, body position, hair length, etc. to significantly reduce or “cure” our pain.
So, my doctor and I decided to up the dosage of one medicine while changing my blood pressure medication. In hindsight, I should have done one change at a time. I’m not sure which caused it (probably the Bp meds), but I am still recovering from a migraine that started last Thursday. And, here in the US, it’s a holiday weekend. Even if it were just a regular weekend, this would have been a Bad Idea. I was pretty close to going to the ER, but took my Bp (not great, but okayish) and evaluated my symptoms.
This really helped calm my panic. Everything was in line with a severe migraine and I’ve survived all the other ones. I’ve even had them last this long. So I decided that the “Watch and wait” method was probably a better idea. I kept an eye on my blood pressure, which improved, and took what meds I have for the migraine. I leaned on my husband to help get medicine and cold packs and my dog, Harley, was really great with letting me rest, sticking to my side, and was a great touchstone during some of the hallucinations that came with this one. Now, it is thankfully just the headache that is left.
I am still alive after this last migraine. Without going to an ER. I know I will soon have another. I will survive that one, too, most likely without going to an ER but with the support of family and a loving dog. Thinking about the next several years worth of migraines is daunting, but I can handle just planning for how to get through the next one.
Again. Maybe? Who knows. I had moved my laptop to the office/storage/other bedroom and so didn’t bother doing anything that required doing typing for a while. I found the cord to charge my Bluetooth keyboard for the iPad, so now it’s charged and I no longer have that excuse. And of course, there’s the usual daily headaches and chronic migraines. My last migraine lasted for 5 days, so… yeah. Add to that a general depression, and I lacked motivation. While doing a blog was my own idea and it’s never been a habit, I put so much importance on starting to do this more often that it became a looming chore. Because it was a looming chore, I kept putting it off. And the cycle continued.
This happens a lot to people with mental health issues and/or chronic procrastinators. It’s a completely normal thing that millions of people probably do, but it still makes many people (including myself) extremely uncomfortable to admit. What if we were all honest that there are some things that we put so much importance on that we are even less likely to do it? Isn’t this what we do every New Year (however we measure the year, there are usually some kind of resolutions, yes?)? What if we stopped beating ourselves up for not completing our to-do lists? What if we stopped making these unattainable lists in the first place?
I finally finished my mom’s socks back in May, so this blog is obviously not the only thing being neglected. I had taken a break from the socks because I needed some simpler projects to work on. I made a garter stitch shawl and diagonal stitch scarf. Then I picked up Mom’s socks again. She still hasn’t gotten them, but they are on the “to weave in ends” pile. Right now, I’m working on two pairs of socks. I started a second attempt at a pair of Skew Socks for myself and then started a pair of simple stockinette socks so I could take something along with me to various appointments and in waiting rooms. Photos are on a different device, but I’ll try not to procrastinate too much and do a post with pics of and links to these projects.
I’ve also read several books, though only a few are on the list of neglected DRCs that I had made in November 2016. Or maybe they were. I haven’t gotten caught up on the reviews, though I do have one that I will post later today.
Yesterday, I literally slept the day away. Yes, I’m using “literally” correctly.
About 13 years ago, I worked the night shift (11:30-7:30) at a hotel in my hometown. My grandparents also live in the same town, but my grandpa never seemed to grasp that because I worked nights, I had to sleep during a large chunk of the day. He would frequently come by at 10-11 AM and, when neither my mother (who also worked nights) nor I would answer the door, he would pound on our bedroom windows until someone got up. Inevitably, he would also castigate us with “you’re sleeping the day away!” Eventually, we threatened to go over to his house at 3 AM and pound on his window until he woke up, then tell him he’s “sleeping the night away.” We all knew that because he was going deaf, it would wake my grandma up before he noticed; however, we must’ve sounded serious enough because he stopped. Mom and I still tell this story and, now that I’m a “day person” most of the time, I use “You’re sleeping the day away!” as the name for my alarm.
As a person who has both physical and mental illnesses, there are days that I can barely get out of bed. It happens. Sometimes, I am in either too much pain or just simply lack the motivation. Especially now that I am not working and on Disability. I’ve had to learn to be kinder to myself. I’ve had to learn to count small tasks like getting up, feeding the pets, feeding myself, and brushing my hair as major accomplishments. I’ve learned that, sometimes, sleeping the day away is exactly what I need so that I can do more the next day.