A while back an article was brought to my attention about Mollie Tibbetts, a 20-year-old University of Iowa student who was murdered while out jogging over the summer. This wasn’t a straightforward, fact-based news story detailing the tragic death of a promising young woman, but an opinion piece by a judgemental “Christian” woman calling herself The Thinking Housewife who suggested that Mollie was at least partially responsible for her own death. Yep, she pointed an accusatory finger at the girl who was abducted, killed, and dumped in a corn field. Please tell me I’m not the only one who thinks this is ludicrous. The author of this blog post speculated that Mollie was a target for a man to murder simply due to her clothing choices and their effect on her attacker’s impressionable male brain. Here it is in her own words.
“Feminism is also to blame for her death. A society that says female modesty and restraint are oppressive does not protect young women from potential predators. No amount of feminist social engineering can change the facts of nature. A woman who jogs in skimpy clothes on country roads — or even in the city — is a serious temptation to a small criminal element. Jogging in revealing clothes – or even just jogging alone – is dangerous. Safety depends on modesty and restraint.”
The Reckless Female Jogger
This is blatant victim blaming. Heaven forbid some “ladies man” has to control not only his lustful thoughts, but his violent sexual tendencies in the presence of an attractive woman. From the news reports I’ve read, Mollie’s alleged murder got angry when she rejected his advances, and his response was to attack and kill her. First of all, females running outside (or inside, even) are not doing so for the benefit of onlookers! Believe it or not, we exercise for our own health and well-being and not as a pretense to beguile the opposite sex. Additionally, society has convinced men that they are entitled to the attention of any woman they want just for having a penis. We ladies are supposed to be flattered, bat our eyelashes, and thank our lucky stars when a member of the male species deems us worthy of their consideration. These are lessons that we all need to unlearn.
As you can see in the above photo, the members of my running group don’t wear anything remotely provocative. Some of the ladies are in great shape, but the rest of us aren’t quite so fit (including myself!). Still, even though I don’t look like a fitness model, I wear tight shorts or pants when I run (because if I didn’t I would have serious problems with chafing), and I wear fairly close-fitting shirts too (because otherwise the fabric would move against my skin and cause rashes in terrible places). No, I don’t run in short-shorts or an exposed sports bra, but my outfit still wouldn’t be considered “modest” enough for The Thinking Housewife. According to her, if some man approached me with ill intent it would be at least partially my fault for enticing him with my provocative clothing choices. How dare I wear an outfit that’s appropriate for my current activity! I have been on the receiving end of unwanted attention while running, and I’ve responded in the most rational way possible – I flipped the bird at those jerks. But I’ve been one of the lucky ones who hasn’t been physically assaulted – not because of my outfit, but because I was extremely fortunate. What a woman is wearing rarely has any impact on a man’s bad behavior, and implying otherwise does a disservice to both sexes.
“Not only do I still have twitchy legs sometimes during the day, but I’m so tired all the time. And some days I just can’t get out of bed at all. I can sleep all day, and it doesn’t feel like a choice I’m making. I just wake up in the afternoon/evening and feel depressed that I’ve lost yet another day to my poor health.”
8/10/18 webpage post
On Thursday I went back to the neurologist as a follow-up to my first appointment a little over a month ago. I’ve been taking gabapentin every night, in addition to the Requip, and that combination of drugs seems to be keeping my legs remarkably calm before I fall asleep at night. I haven’t had trouble with muscle spasms plaguing me after I get in bed, at least. (Unmedicated I’m still a huge mess. I dozed off on my couch the other evening and my legs immediately started twitching. It’s super frustrating.) It’s a major improvement over the situation I was dealing not that long ago, before I started taking any medication specifically for Restless Leg Syndrome (RLS). Unfortunately, I’m still feeling tired all the time so, while there has been definite progress, I’m not completely back to normal. When I told the doctor about my constant exhaustion he had a couple of thoughts. First of all, he theorized that the prescriptions I’ve been taking are meant for RLS, but might not be giving me the best results if I have Periodic Limb Movement Disorder (PLMD). This is what one previous doctor and the technician at my sleep study thought might be the root of my leg spasm problem. With that in mind the neurologist gave me an additional prescription for Klonopin to see if that helps me get some actual restful sleep at night. (Yep, that means I am now taking three different anti-seizure/convulsant drugs every day. Fun!) But if after a few weeks of this new protocol that doesn’t work, he suggested that I might have narcolepsy.
Narcolepsy is a condition that I knew very little about before Thursday. With my limited knowledge I thought it meant that sufferers had a tendency to simply doze off at the drop of a hat, but obviously it’s more complicated than that. From what I read, in addition to excessive daytime sleepiness (which I certainly have trouble with), narcoleptics experience abnormal REM sleep. The neurologist told me that in order to get a diagnosis I would need to do another sleep study where I would be allowed to fall asleep for several short periods of time to determine whether my brain goes through the proper progression into REM sleep. Narcolepsy apparently causes people to go directly into REM sleep without the usual hour and a half or so of NREM (non-rapid eye movement) sleep beforehand. While it sounds a little far-fetched, I wouldn’t be at all surprised if this is the cause of at least some of my medical problems. I hate to admit it, but I doze off at work sometimes. Only for very short periods of time, but it happens. Especially in meetings, and especially if I haven’t had enough caffeine. Fortunately I don’t seem to have any of the other, scarier narcolepsy symptoms – like cataplexy (periodic loss of muscle function), hallucinations, or sleep paralysis. That also means that narcolepsy might not be the right answer. We’ll see. I have another appointment with the neurologist in six weeks to discuss a path forward. I have some hope that we are zeroing in on something.
On the plus side, I’ve been able to start reading again! I’ve always loved reading, and I used to look forward to immersing myself in a good book when I crawled into bed every night. It was the way I wound down and calmed my brain after a busy day. It usually made me drowsy too. But before my days of taking any RLS drugs I started getting twitchy legs when I was stationary for more than a short period of time – either lying in bed or sitting on the couch. This really put a damper in my reading habit. Books by my favorite authors that I was dying to read piled up in my Kindle app while I was desperately trying to avoid the muscle spasms that made me want to crawl out of my skin. But now that I’m fully medicated at night I can read for a while before falling asleep without worrying about leg craziness. It’s a miracle! Even though I haven’t yet reached the end of my road to recovery (or remission), I’m still so grateful to modern medicine for improving my quality of life. Maybe one day I’ll even feel normal again!
In case you were wondering if there was any resolution to the issue in my last post, the McGaugh Elementary principal apologized in an email to school families on Thursday. From what the online article quotes, it sounded like a half-hearted apology to me. One those that basically says, “I’m sorry if I offended you,” where the inclusion of the word “if” means that the author isn’t really admitting fault. Instead, the blame is put on others for being offended. This seriously pisses me off, but it’s not up to me to forgive her. That’s for the families and the school district to decide.
As a follow-up to my previous blog post I thought I’d address a similar situation – one that involves me this time. In February 2017 I posted a statement on my Facebook wall after a shocking interaction with a friend that left me nearly speechless. In one afternoon this friend managed to make derogatory statements about blacks, transgender people, immigrants, ComicCon attendees, and the homeless. I didn’t even know it was possible to display that level of insensitivity in a single day. In general I don’t think it’s my job to try and change people’s opinions, no matter how different they are from mine, but in this instance I could only hold my tongue for so long. After she attacked homeless people for “checking out of society” I finally challenged her views. It didn’t really make a difference, but I couldn’t just passively listen to her stream of ignorance any longer. I was so upset that when I got home I posted something vague about it on Facebook. Here’s what happened next. (Note: Other than my own, the names have been changed to avoid further conflict.)
- Lauren: I’ll preface this with the fact that I’m a liberal and a feminist, but I’ve had all the intolerance I can stand. I just don’t understand how inclusiveness, sensitivity, and avoiding offense can be a bad thing.
- George: Taken from Reddit – “There’s nothing wrong with being offended by something.
There is a problem with not being able to personally deal with your own feelings of offense, and trying to regulate/control other people so that you won’t be offended. It’s selfish, bigoted, and myopic. As they say; offense is taken, not given.”
- Jane: Translation – “I want to be able to do whatever I want, and if anybody holds me accountable, I would like to pretend it is because they suck, not because I am sometimes wrong, or because being a human who has social relationships with other humans necessarily means sometimes being told I messed up and apologizing.” Seriously, George, this quote is bizarre. If you were walking down the street and someone punched you in the face, would you be wrong to say, “What the hell, man?!” Being racist, sexist, homophobic, transphobic, etc. is repulsive, hurtful and preventable, and it’s actually peak fragility to think one must never get pushback about it.
Some people don’t seem understand that there’s a difference between “offended” and “offensive.” I am not a member of any of the groups that my friend disparaged that day so I wasn’t directly offended by what she said, but her comments were undoubtedly offensive to blacks, transgender people, immigrants, ComicCon attendees (nerds like me, actually), and the homeless. Just because a person’s insulting statements don’t apply to anyone in their audience doesn’t mean that they aren’t still insults. I wasn’t to blame for objecting to my friend’s comments, but that’s what George’s response above would have you believe. I used to be married to a man who blamed me for everything so this behavior of making the opposing party the one at fault isn’t anything new. But that doesn’t mean it’s right. Never feel like you are “selfish, bigoted, or myopic,” as George said, because you call out someone for offensive things they say. We have to continue to challenge abhorrent views and behaviors or humankind will never make progress. It won’t be easy, but it will be worth it.
It’s an extraordinary day when the daily post from my least favorite blogger isn’t the thing that gets me the most riled up (although today she wrote about the “sin” of obesity so it was a close call). Nope, today it was something from my own little community that disturbed me the most. When I woke up this morning I saw a thread in the Seal Beach Facebook group regarding law enforcement and news crew activity at the local elementary school. Fortunately it wasn’t something life-threatening like a shooting or a hostage situation. Thank goodness! After reading the associated article on the Orange County Register I learned that the McGaugh Elementary School principal posted something contentious on her personal Facebook wall regarding the Nike ad featuring Colin Kaepernick. Yep, another social media scandal. We can’t seem to learn from even the very recent past when it comes to these situations. Here’s an excerpt from the OC Register article.
Along with thousands of other people around the country expressing similar viewpoints, Roni Burns-Ellis turned to Facebook Tuesday, Sept. 4, to condemn Nike for featuring controversial quarterback Colin Kaepernick in an ad. But as principal of McGaugh Elementary in Seal Beach, Burns-Ellis drew her own controversy. Above her photo of a Nike T-shirt cut into pieces, Burns-Ellis wrote on her personal Facebook page: “My newest rag! When Nike signs an anti-American thug to represent their brand, I will not support, wear, purchase or endorse their product.”
I added the bolding myself because that is the root of the problem. After reading the principal’s FB post, a Seal Beach resident went to the school administration’s office to complain about her use of a racist term to describe Kaepernick. This woman is in a position of leadership over not just adults, but also children. It’s understandable that parents would be alarmed by racist views expressed by such leadership, right? The elementary school has students of many colors and backgrounds so the principal’s FB post is not just generally offensive, but directly offensive to black students and their families. Seems straightforward to be, but unfortunately not to everyone. The main dispute in the Seal Beach FB page thread was over whether “thug” is in fact a racist term. So many people cited the bland dictionary definition to prove that race was not an implication in the principal’s use of the word. The shortsightedness of this argument is astounding. Unfortunately, there are untold numbers of words that have meanings beyond than the ones in a large, dusty, probably outdated volume. How many times have you had to consult Urban Dictionary to ascertain the current usage of a word or phrase? (I am old and out of touch so I use Urban Dictionary a lot!) We are all aware that calling a person of color an ape, baboon, or monkey is overtly racist, especially due to a few high-profile cases this year, but you won’t find words explicitly defining those terms as racist in your home dictionary. I found an NPR article that explained it better than I ever could – “One of the things that Americans have a whole lot of trouble with…is that words never keep their meanings over time. A word is a thing on the move. A word is a process. And that’s what’s so confusing about the N-word. And that’s what’s so confusing now about this word, thug. Any discussion where we pretend that it only means one thing is just going to lead to dissension and confusion.” The bottom line is that subtext is lost on folks who willfully ignore it. Luckily there was one encouraging comment from a woman in the FB thread.
A vast majority of McGaugh’s military families are minorities. Military members who take off their uniform at the end of each day and step out into the civilian world, only to face discrimination because of the color of their skin. Minorities in the military are not safe from unjust treatment by people in positions of power. I hope all of you parents/community members reading this will take a step back and remember that behind a parent’s job title, there are people and families of color, including black husbands and sons like my very own, who benefit from people like Kaepernick speaking up for them. Calling a black man a “thug” just because you don’t agree with the way he’s exercising his freedoms as an American is racist. It truly is. Please remember that every single service member past and present, signed an oath to defend the constitution and the freedoms that it grants. I don’t pretend to speak for all military families, but I do know many local military families (and thousands across the country) share my sentiments. And I hope you all will help hold those who are supposed to advocate for all of their students, students of color included, accountable for not doing so.
I couldn’t have said it better myself! In a post back in May, I stated that “Some people don’t understand that free speech means that in the United States you can’t be arrested or executed for your opinions, but it does not mean you are completely free from the consequences of what you choose to say. Hate speech can absolutely get you fired.” Freedom of speech doesn’t mean freedom from consequence! We’ll see how this plays out for the McGaugh Elementary School principal.
There was a time, not so long ago, that I wasn’t taking any prescription drugs. It was fantastic. But then 2018 came crashing onto the scene and now I am picking up one refill or another at the pharmacy just about every week. I’ve been on five different medications at one point or another since January and I’m still searching for the right one(s). In my post about my health last week I mentioned that I’ve been taking 1 mg of Requip, a Parkinson’s and Restless Leg Syndrome (RLS) treatment, to calm my legs at night so that I can fall asleep. While I believe that it has been somewhat effective, meaning I can go to sleep without leg spasms now, I am still not feeling 100% like myself again. Not only do I still have twitchy legs sometimes during the day, but I’m so tired all the time. And some days I just can’t get out of bed at all. I can sleep all day, and it doesn’t feel like a choice I’m making. I just wake up in the afternoon/evening and feel depressed that I’ve lost yet another day to my poor health. And the kicker is that I never feel rested no matter how much I sleep. For example, the other day I opened my eyes and the clock on my nightstand said 5:30 PM! I managed to drag myself out of bed, get dressed and go to my boot camp class at 8 PM, and then went back to sleep at 11:30 PM. I was only awake for 6 hours that day and I was still tired when I got up to go to work the next morning! It’s beyond ridiculous. I can’t afford for this to continue, both monetarily (I need to work to support myself!) and mentally (I am at the end of my rope!). Fortunately I had my long-awaited appointment with the neurologist yesterday afternoon. I explained all of my symptoms to him, showed him copies of my blood work from December and my sleep study in May, and told him what pharmaceuticals I have tried so far. After laying it all out on the table the doctor was a bit baffled by the whole picture. It was frustrating, but understandable. All of the other medical professionals I have seen so far have been baffled too. My symptoms don’t all fit into one nice, easy, predefined diagnosis. Of course it isn’t that simple! Some things point to RLS, but others suggest Periodic Limb Movement Disorder (PLMD), while a few could be signs of a more serious affliction. So while I don’t have any definitive answers, the neurologist did write me a prescription for another drug to try in combination with the Requip. So I will be adding Gabapentin to my nightly pill dosage to see if it makes a difference. On top of that, I have instructions to double the dose in one week if the initial amount doesn’t seem to be working at all. I also have another appointment in September to report back on the results, and perhaps conduct some further tests. (The doctor seemed concerned that I could visually see my muscles contract during the leg spasms, so he might order some electrical stimulation tests to see what’s going on in there.) I’m still encouraged by this progress, even if it is small. Finding the right combination of medications is the key to relief and the neurologist told me that it might take a while. After two and a half years of dealing with this issue I will try to be patient as we zero in on a solution!
You want to know why women don’t come forward more often when they are being abused? First of all, they might not realize are in an abusive relationship. I didn’t until after I left my marriage. I knew that my ex-husband didn’t treat me very well, but I didn’t see the whole terrible picture until I removed myself from the situation. Take a look at the above photo from December 2011. My ex-husband and I were given a huge container full of glass bulb Christmas ornaments from his grandmother when she moved to Texas. Unfortunately every year we lost two or three of them when they fell off the tree and shattered on our hardwood floor. Real Christmas trees don’t always have the strongest branches! It was never anyone’s fault if the ornaments fell, but this picture depicts what the aftermath usually looked like. (Minus the finger-pointing, generally. That was specifically for the photo.) This picture was amusing at the time, but looking back it feels like a perfect and unsettling illustration of our marriage. Me cleaning up some mess, whether or not I actually caused it, while also taking the blame for the situation.
Everything was my fault. Everything was my problem to fix. Eventually my entire life consisted of keeping my ex-husband happy. Attempting to foresee and mitigate potential issues and smoothing over ones I couldn’t prevent. I spent all of my time catering to his needs, trying to keep him from being upset with me, but it was never enough. I was always judged and found wanting. It was exhausting and soul-crushing. So why didn’t I leave earlier? Especially after he cheated on me less than three years after we got married? Because I wasn’t strong enough at the time. My self-worth had taken such a beating during our time together that I didn’t think I was worthy of better treatment. I had been groomed into such a state of submission that I couldn’t contemplate breaking free, even when he violated the vows we made on our wedding day. Honestly, I should have ended it long before I actually did. I have so many stories I could tell to back that statement up. Don’t get me wrong, I loved my husband, but I tolerated lines being crossed that should never be crossed in a relationship. It took me a long time to come to my senses, gather my strength, and save myself from my abusive marriage. It was such a difficult road to walk, but I have not regretted it for one moment. So if you’re a woman reading this, I truly hope that you do not allow your partners to take advantage of you that way I did. Do not accept poor treatment, especially from someone who claims to love you more than anyone else. You are absolutely worthy of love and respect!
P.S. I know that my blog readership is almost nonexistent, and I’m OK with that. I’ve always maintained this website (in all of its forms) for myself and not for anyone else. But I want to make sure that if any woman does happen upon this post that she reads something that empowers her to make her life better!
Another troubling topic that has been in the news lately is abuse. Specifically, the allegations that were recently made against Chris Hardwick. (Briefly I want to say that I’ve been a big fan of the Nerdist/ID10T podcast, plus a lot of his other work, so the stories I read made me immensely sad. But objectively I still stand with the accuser because charismatic people can be abusers too.) The #metoo movement that spread like wildfire last fall brought light to widespread sexual harassment and assault that is usually hushed up before it becomes public. It was eye-opening for a lot of people, but for most women this was information that we already knew. Just about every female has experienced harassment or abuse of some kind in her lifetime. It was a relief to finally talk openly about such a taboo topic and bring heightened awareness where usually we are told to keep quiet. I’ve written about this before, but reading the allegations against Chris Hardwick last week brought back bad memories of my marriage.
“I believed that, to borrow an analogy from a friend, if I kept digging I would find water. And sometimes I did. Just enough to sustain me. And when you’re dying of thirst, that water is the best water you’ll ever drink. When you’re alienated from your friends, there’s no one to tell you that there’s a drinking fountain 20 feet away. And when your self-worth reaches such depths after years of being treated like you’re worthless, you might find you think you deserve that sort of treatment, and no one else will love you.”
Rose-Colored Glasses: A Confession by Chloe Dykstra
When I read this excerpt from the article about Chris Hardwick it sounded so familiar that I went back and reviewed my post about emotional abuse from a few years ago. Isn’t this almost the same thing I wrote nearly four years ago?
“Even if you can dismiss 99% of his subtle insults, that last 1% slowly builds up, day after day, until you’re completely crushed under the weight of the chides, tsks, and sighs. Until one day you wake up and discover that you believe him. You’re not worthy of his love. You’re not worthy of having a partner who doesn’t expect you to walk one step behind him.”
9/23/14 webpage post
Emotional abuse is real, and it is often invisible outside of the relationship. You never know what someone might be going through, and the scars last long after the abuse is over. I have more to say on this subject, but this post is already getting really long. I will follow-up later this week.
I had a doctor’s appointment on Wednesday to review the results of my sleep study last month. My GP read through the report and said, “Basically you’re running a marathon every night!” This is not a surprise to me considering how much trouble I’ve had with my legs over the last couple of years, but it was a relief to have data to prove that my problems are real and not imagined. I had an astonishing 550 leg movements during the night I spent at the sleep center, and I was awakened 8 times during the night because of limb movements. Also, only 6.4% of the night was REM sleep, which is way too little. No wonder I’m tired all the time! I’ve been operating under the assumption that I’m simply lazy which is why I am always drowsy and rarely have the energy or motivation to do anything. Now I know that’s absolutely not true. Even with Ambien helping me fall asleep quickly at night, lack of restful sleep is still causing problems in every area of my life. I’m so thankful that my doctor has taken these symptoms seriously, unlike some other medical professionals I’ve seen, and is helping me map out a path forward. As a next step, she wrote me a prescription for Requip, a drug that’s used to treat not only restless legs, but Parkinson’s Disease as well. We’re not messing around with my crazy legs! Unfortunately I have to work my way up to the maximum dose so it’s going to take me over a week to get to a level that might be effective. We’ll see how that goes. I also got a referral to a neurologist so if this particular pharmaceutical doesn’t work for me I will discuss other options with him at a future appointment.
Until I am able to get some restorative sleep I am trying to honor my body’s need for more down time, but it has been difficult. I’m already a homebody so it’s not that I mind staying home more, but lacking the energy to complete my day-to-day chores means that things can start to pile up. My sink fills up with dirty dishes because I don’t always wash them in a timely manner. Cooking takes a lot of effort so I don’t always have healthy, homemade lunches to take to work. And I avoid going out shopping so I don’t always have nutritious food or other essentials in the house when I need them. It’s frustrating. Some days getting out of bed and changing out of my pajamas is about all I’m able to do. This is not beneficial to my mental health, but I am trying to cut myself some slack and let go of the guilt of resting as much as I need to. Just because I’m too tired to go to the movies or clean my house right now doesn’t mean I’ll always feel this way. I know this is a temporary state and I that I am strong enough to get through it. Life isn’t always easy, but I’m hoping that it won’t be long before I see the light at the end of this particular tunnel. Let’s hope my new prescription is just what I need.
Last Friday I did a sleep study at a clinic. My doctor ordered the sleep study after I told her about my extreme daytime exhaustion, even after sleeping 8-9 hours at night. And that was with the help of prescription sleeping pills that I got in January when I was feeling so wretched. The pills were an absolute lifesaver because they helped me fall asleep easily, but I was still inexplicably tired the next morning. Also, there was another, much harder to describe symptom that I had to take to three doctors before I felt like I was getting any recognition at all. Basically, for more than two years I’ve been experiencing muscle spasms that start as soon as I get drowsy and cause involuntary movements in my legs. Naturally the periodic twitching and jolting (about every 10 seconds) made getting to sleep nearly impossible, probably prevented me from getting much restful sleep, and made me want to crawl out of my skin. But even after describing this sensation to the best of my ability, all of the doctors I saw seemed to be at a loss. They offered little insight into my symptoms or thoughts regarding a diagnosis or treatment. I was slowly going crazy. One doctor did mention the possibility of Periodic Limb Movement Disorder (PLMD), something in the family Restless Leg Syndrome (RLS), but presenting differently and more severely. Unfortunately after some routine blood work this doctor sent me a letter (yes, a physical letter – not an email or even a phone call in this day and age) to tell me that all of my levels were normal and I should be fine. Thanks for nothing. Fortunately the next doctor I saw referred me to the sleep study clinic (for my exhaustion, not my crazy legs, but I wasn’t going to complain) where I was hopeful that answers might be more forthcoming.
So last Friday, in a very crude hostel-like room, my body was loaded up with sensors and I was told to go to sleep so that the necessary data about my slumber, or lack of it, could be compiled. I don’t think I’ve ever been more uncomfortable than I was lying on my back (not my preferred sleeping position) on the barely adequate mattress in that facility. I had wires coming off my scalp, my face, my chest, and my legs. The woman I spoke with when I made the appointment painted a much rosier picture of the sleep study than what I experienced upon arrival. I wanted to be a good patient, but even taking my usual Ambien wasn’t enough to overcome the anxiety of being in a strange place and needing to sleep on command for the purpose of science. The insomnia was strong that night. But for better or for worse, staying awake longer than usual gave my legs an opportunity to perform their little dance and provide proof to my doctor that some part of my body isn’t functioning as it should. At first I was nervous that my symptoms wouldn’t present themselves while I was at the clinic, but that fear turned out to be unfounded. That was the only bright spot of the night. I was miserable for more than an hour after lights out due to the leg spasms and even the sleep technician came in to check on me because I was moving around so much – and not all of those movements were intentional. I finally did fall asleep after much tossing and turning, but it was only for a few hours before the technician was knocking on my door at 5:45 AM to get me ready to leave. Hopefully that short amount of sleep was enough to help my doctor draw some conclusions regarding a plan of action. Heck, even the technician told me that he observed that I have a pretty serious case of PLMD. Not sure if that’s a good thing or a bad thing, but at least I’m going back to my doctor with some new information. I have an appointment to see her early next month to review the sleep study results, but I am almost certain that my next stop will be a neurologist’s office. In fact I’m so certain that I might try to make an appointment even before going back to my GP. Here’s hoping that it won’t be too much longer before I find a solution!
P.S. I did a quick search of my webpage to see if I’ve written about this topic before, but it seems that I haven’t. I find that hard to believe since I’ve been suffering with this medical condition for over two years now. We all have our inward and outward struggles, but we don’t always share them with the world. I’m going to try and be more transparent with from now on.
2018 has been teaching me a humbling lesson. We’re nearly two weeks in and I’m still not healthy. I’ve only been able to work two days so far (one of those being my birthday, but more on that in another post), and those were tough. I’ve only exercised once (I went to a boot camp class on my birthday) and that turned out to be a terrible idea because I experienced a relapse of my lingering illness the next morning. I’ve barely gone out my front door since New Year’s, and I haven’t had enough energy to do much of anything around the house either, so I’m slowly losing my mind. Suffice to say, things aren’t going well for me at the moment. If I think about everyone who’s out there living their lives to the fullest right now it makes me angry, jealous, and sad. And then there’s Facebook and Instagram showing me multitudes of pictures of smiling faces and all of their exciting experiences. It’s gut-wrenching for me. Especially seeing photos from my friends who successfully completed the Dopey Challenge last week. That was supposed to be me. I planned for it, I worked for it, and I deserved to cross the finish line with everyone else. But I’m starting to realize that I can’t live in the past anymore. I can’t compare my journey with anyone else’s. My best-laid plans didn’t come to fruition this time and I have to accept that. This wasn’t a failure, but an unavoidable obstacle that I had to navigate. The only thing I can do now is move forward. It certainly won’t be easy, but I think that once I’m healthy (whenever that is) and back to my normal routine that I can start preparing for the rest of the year. I cannot wait for that to happen.
Right now I’m sitting in a hotel room in Carlsbad. Back in October I registered for the Carlsbad Half Marathon without considering that a flu virus could knock me down so hard that I wouldn’t be in any shape to run 13.1 miles on January 14th. So last week I called the race company to ask whether it would be possible for me to switch to the 5K instead due to my extremely poor health. Luckily that wasn’t a problem at all. So tomorrow morning I’ll be attempting to complete a measly 3.1 miles and finally, finally start my 2018 running journey. Hopefully that journey will culminate in training for neat year’s Dopey Challenge (January 10-13, 2019), but I have a long road to navigate before I get there. This first step is infuriatingly small, but I have to start somewhere. I wish I wasn’t so incredibly out of shape, but there’s really no other possible outcome after three weeks of near inactivity. These next few weeks are going to be painful. So many miles, so many races, and so many more obstacles waiting for me, I’m sure. Let’s hope I’m up for it.