Born

Last Friday, the prompt for Five Minute Friday was “born”. I assume many writers, being Christian, will have written about the moment of their salvation. Even though or maybe because I consider myself a progressive believer, I didn’t have such a moment. I was saved 2000 years ago. Rather, something else came to mind. Here goes.

I am still not done reading the book Preemie Voices by Saroj Saigal. It is a collection of letters from people born very prematurely between 1977 and 1982, which was published in 2014. One of the letters I did read, however, spoke to me.

In it, the woman said she was born three times. Once, when she was actually born. Then, when she was supposed to be born, so her due date. For me, this would be September 29, 1986. I was actually born on June 27.

Then there was her moment of rebirth in a spiritual kind of way, but dit didn’t have to do with any organized religion. Rather, she considered the day she was diagnosed as autistic to be her day of rebirth.

I am also autistic. For me, the day of my diagnosis was March 16, 2007. It wasn’t some type of epiphany moment though. My support coordinator at the time called the physician who’d assessed me because she hadn’t heard anything about the results of my diagnosis after my assessment was complete. Neither had I. She was told I had been diagnosed with autism and the report had been sent to my GP. How blunt!

I didn’t even dare write about it on my blog till some days later. It was so weird. Because I was diagnosed three or four more times, I never quite considered this day to be of any significance. Sometimes I wish I had such a moment of rebirth.

A Twelfth Grade Memory

Last Monday, I already shared some memories from the year 2003. Today, one of the prompts over at Mama’s Losin’ It’s Writer’s Workshop is to share a twelfth grade memory.

My senior year of high school was the year I was supposedly planning on going to university after graduation. I knew this was going to be hard, but my aversion to going to college straight out of high school, didn’t really form. Besides, I had no idea what else I was going to do. I remember one day, August 31, 2004, one of the first few days of the school year. I had already come out as dissociative (multiple personality) on my blog in March, but had only been aware of three alters at the time. That day, Carol, who was up to that moment my assertive helper part, gave up and a new one, who called herself Clarissa, emerged.

I wasn’t aware at the time that what I was experiencing was an actual mental health diagnosis, mind you. A friend of mine had told me about dissociative identity disorder after I first came out in March of 2004, but I was still in denial. Part of the reason is that one criterion of DID is amnesia, which we rarely experience.

In March of 2005, my high school tutor had arranged for me to see a blindness rehabilitation center psychologist. The high school tutor, I must say, read my blog, so he knew about the parts, including Clarissa. He had told the psychologist, who obviously immediately thought of DID. She started to ask me all sorts of questions, all of which I either circumvened or answered negatively to. I knew, after all, that, if I’d gotten the psychologist to think I had DID, I wouldn’t be accepted into the rehabilitation program.

In hindsight, of course, I wish I would’ve been more honest. I knew I didn’t have amnesia or time loss, but I did have most other symptoms of DID, some of which I hadn’t become aware of being abnormal. It took over five more years before I was diagnosed with DID.

In the end, I was accepted into the rehabilitation program. I started on August 22, 2005.

Full disclosure: after being diagnosed with DID in 2010, I lost my diagnosis again in 2013. I am pretty sure I don’t have full-blown DID, but probably do have some dissociative disorder.

Mama’s Losin’ It

Reflecting on My Life: 2003

Last night, I couldn’t sleep. I was looking for some link-up parties to join in and came across the Life This Week linky. In this week’s edition, host Denyse shares her memories of the year 2003. As this is my first time participating in the linky, I should really start my story from the beginning on, but for some reason, I can’t.

I may have shared this before, but in secondary school, I always had this superstition that life ran in circles. There’d be a year of struggle and crisis, a year of renewed hope and finally a year of disillusionment, after which I’d spiral back to struggle and crisis. The year 2003 was a year of disillusionment.

In 2003, I was sixteen. I turned seventeen at the end of June. I was in the tenth grade for the first half of the year and in the eleventh for the last half.

In the summer of 2002, I had barely moved up a year. My grades weren’t that good and I only moved up because I worked very hard the last few weeks of the year. I had been struggling with feeling like an outcast due to my blindness the entire 2001/2002 school year. That was to change by late 2002, or so I believed. My high school tutor promised me he’d help me feel better.

What he did was come up with a social skills assessment for blind students and have the teachers fill it out. That was no good for my self-esteem, as I showed considerable weaknesses. No-one knew at the time that I was also autistic, even though I suspected it.

The year 2003 was the year I started to learn about myself from a possibly autistic point of view. Even though I had started suspecting I was on the spectrum in mid-2002, I didn’t feel comfortable joining online support groups for it till 2003.

This was also the year I expanded my horizons where it came to using the Internet in general. I had gotten an Internet connection in May of 2002. By April of 2003, I started keeping an online diary on DiaryLand, which several years later morphed into my first WordPress blog.

In the summer of 2003, I attended the International Computer Camp for blind students in Switzerland. I had attended it the year before, when it was held in England, too. This year, I felt a bit disappointed in the end, because it didn’t provide me with the cathartic experience I’d felt the year before.

In 2003, I also explored fictional storytelling as a way of expressing myself. I was experiencing some significant selective mutism at the time, which I could circumvent by pretending I wasn’t talking about myself. This is how my “mirror image”, Kirsten, came to be. She is one of my main alters to this day.

Finally, this was the year I was first starting to explore future planning. Here in the Netherlands, students with disabilities attending mainstream education didn’t get any type of special transition planning at the time. I was expected to just get by and go to university straight out of high school in 2005. In 2003, I started to doubt this would be a success, but I didn’t voice my doubts yet. As it is, I didn’t actually make it clear that I wasn’t going to university right out of high school until April of 2005.

Where were you on the path of life in 2003?

Looking Forward To…

Today’s Five Minute Friday prompt is “forward”. Let me share what I look forward to.

I look forward to seeing my husband tomorrow. The visiting rules for nursing homes were relaxed in prime minister Rutte’s latest speech on Tuesday. The new regulations wouldn’t take effect till next Monday, but my care facility decided to allow visitors from this Thursday, the day of Christ’s ascension and hence a bank holiday, on.

There are still strict guidelines. Visitors cannot touch clients or even be within five feet distance. We’re not allowed to travel in the car with our visitors or go to public places such as shops or snack vendors.

My husband was a little disappointed at the strict guidelines, and I wholeheartedly agree. Of course, I want to hug him too. After all, we haven’t seen each other in real life in over two months. Too bad we can’t at this point. However, it’s better than nothing.

I look forward to hopefully spending some good time with him. Hopefully, of course, the rules will be relaxed even more soon. That’s still unknown though. As far as I know, our care facility is already less strict than what Rutte said, as he said only one person per client can visit. Our facility allows two at a time. Not that I need that, as my parents or in-laws are a long way from visiting me, but oh well.

Wow, I actually finished writing this in five minutes flat. Thanks so much for reading.

Coffee and Tea: My Favorite Hot Beverages

I’ve had a post by this title in my Drafts folder for over a month. I originally started to write it for my letter C post in the #AtoZChallenge, because I didn’t feel like writing a self-care themed post. I ultimately did anyway and this post sat in Drafts forever. I didn’t actually end up writing about coffee or tea in the draft. The post was, or so I believe, inspired by a fellow blogger’s question of the day or something. Anyway, today let’s discuss hot beverages.

I should really ask my parents whether they still have this photograph of me drinking one of my first cups of coffee and, if so, whether they can digitally send it to me. You see, I was about six when I first started drinking coffee and I hated the taste. I truly had a disgusted look on my face!

I at the time drank coffee with lots of milk and sugar in it. The milk was supposedly to lessen the impact of caffeine. I always left the sugar sitting at the bottom of the mug and spooned it up after finishing my coffee. I hardly ever drank tea as a child. When I drank it, I had milk and sugar in it as well.

When I was around fourteen, I had a weird nightmare about someone having switched the sugar with some type of poison. After that, I acutely decided to leave the sugar out of my coffee. Then some years later I left out the milk. Now I drink the pure stuff, but I still get the same disgusted look on my face that I got as a six-year-old. Guess I’m addicted.

With respect to tea, it took me a long time to figure out what I liked. When I was around nineteen, I somehow convinced myself that I liked strong, black tea. Well, I don’t. Then followed rooibos, which my fellow patients and I at the psych hospital referred to as stress tea for its supposed calming effect. I went through a phase of particularly liking rooibos with strawberry-whipped cream flavor.

Then followed Earl Grey tea, because my now husband was into it. I tried a lot of different tea flavors with him when he visited me at the psych hospital.

I don’t even remember when or how I got into the green tea phase. In any case, I now drink pure green tea only. Some years ago, I tried green tea with pink pepper and pineapple flavor because my mother-in-law had bought a package, but I really didn’t like it. I, by the way, drink my tea without sugar too.

Are you a coffee or a tea person? How do you like your coffee or tea?

Normal

This past Friday, the prompt for Five Minute Friday was “normal”. I didn’t have anything to write on the topic then, but I do now. Here goes.

Today I listened to a meditation on Insight Timer. The teacher said your observing self is like the sky (or heavens), while your thoughts, feelings etc. are like the weather. No matter how bad the weather gets, the sky remains the same. It can withstand even the darkest thunderclouds.

This is maybe how we need to look at ourselves in this time of COVID-19. We are told to adjust to the “new normal”. Even though our “intelligent” lockdown or stay at home order ended last week, I still cannot have visitors at the care facility and just found out the day center won’t reopen till October. I’m not sure how I feel about this. Well, about the day center. I know how I feel about the no-visitors policy, but that one might change this week.

Like Kate, the FMF hostess, I somehow settled in. I actually love being at the home for day activities and don’t mind not seeing people from other homes that much. I miss my husband, but I’m adjusting to that too.

This is where the meditation comes in again. I mean, no matter how hard life gets, I’ll manage. My thoughts may be dark, my feelings bleak, but I will ultimately be able to keep going.

#AtoZChallenge 2020 Reflections

Oh boy, it’s already May 10. Can you believe May is already one-third over? I think time flies. Today, I am rather late joining in with the #AtoZChallenge reflections. April seems so far behind me, but it’s good to look back on the challenge.

The good part is I actually completed the challenge this year. As you may know, I signed up each year since 2015, first on my old blog and last year here. In 2015 and 2016, I completed the challenge. I had the topic of autism awareness/acceptance as my theme for 2015 and the alphabet of mental health in 2016. In 2017, I made it myself rather hard by picking autism again even though I was in the midst of being re-assessed for it. I only published one post. I can’t remember how I did in 2018, but last year, I was fooled by the letter X. I had had a word in mind that I thought meant something different than it turned out to mean (xenial) and couldn’t think of any other word once I found out I couldn’t use that word.

Then this year, I had the letter X already figured out before I even wrote a post. I know, I cheated a little, but well. I ended up unconsciously choosing the theme of self-care. I actually stuck to this theme rather well to be honest. I know I also cheated by using The More or Less Definitive Guide to Self-Care for inspiration. However, I mostly wrote down my own thoughts and gave credit to Anna Borges, the author, where needed.

The more challenging part was reading an dcommenting on other bloggers’ posts. I still must say I find the Google spreadsheet a harder to use format than the linky the challenge used until 2017. However, I was able to work it somehow. Then, still, it took quite a bit of time to visit a satisfactory (to me) number of other bloggers. I had only a few bloggers I followed in my feed reader, so most I visited only occasionally. I liked the new connections though.

The absolute best part of the challenge though was that it kept me motivated to write. Or maybe my motivation to write helped me complete the challenge. I’m not sure. In any case, I loved being active on my blog and look forward to staying in this zone for a long time to come.

#IWSG: Keep on Writing!

IWSG

Today is the first Wednesday of May and this means it’s another Insecure Writer’s Support Group (#IWSG) day. I didn’t really understand the optional question for this month, but I have enough to share without answering it.

You see, I finally did pretty well in the writing department! Firstly, I finally completed the #AtoZChallenge for the first time in four years. I loved it actually. Of course, occasionally it got a little boring and difficult at the same time, but overall it was quite a cool experience. I got to know a few bloggers I hadn’t known before or only four or five years ago when I did the #AtoZChallenge on my old blog. It’s so cool to see bloggers actually keep blogging year after year.

Secondly, I wrote a few poems. I actually had some more in my head that I haven’t written down yet and I may’ve forgotten. I find it pretty easy to come up with particularly syllabic poetry. Not wanting to brag, of course, since I honestly don’t want to claim my poems are any good. However, the words flow quite naturally.

Next time it’s open at dVerse, I might try my hand at a quadrille. I had no idea what one was and thought it had a lot of rules. Apparently not.

I also wrote my very first piece of flash fiction. Looking back, I should have explained a little more, as my piece left a lot to be filled in by the reader. That was on purpose, but it did make it a little weird maybe.

I look forward to keeping up the writing mojo in May. Of course, I know I’ll face writer’s block, lack of motivation or both someday, but I hope I’ll continue to be inspired and motivated for a long time to come.

When I Was Five

This week it’s 29 years ago that I spent a week in the children’s hospital with a collapsed trachea. It closed up on the night of April 28, 1991, the night after we’d celebrated my mother’s birthday, two months before my own fifth birthday. I was unquiet all night or so I’m told, getting up to go to the bathroom a dozen times. Eventually, my parents discovered what was going on and I was rushed to the hospital.

Thankfully, my trachea opened again within a day or two. I don’t know whether I had to be on a ventilator. In fact, I remember very little of these first few days. Then, on May 3, I had surgery to take out my tonsils and adenoids. That surgery had been scheduled for May 21 at another hospital anyway, but the children’s hospital could fit me in earlier now that I was there anyway.

After surgery, I had to stay in the hospital for another few days because I had a breathing tube inserted. That is, I’m not 100% sure the breathing tube was before or after surgery. I remember trying to talk through my tube, which was pretty much impossible.

This was probably also the time in hospital that my parents brought me their supermarket’s brand of peanut butter to eat, as I wouldn’t eat the premium brand the hospital had. Can you tell I was spoiled or autistic or both?

Finally, I got home on May 7. I was already a calendar freak, so I actually remember this without having been told.

As I write this, my inner five-year-old is trying to speak up, but she can’t. I don’t know whether this hospital stay was particularly traumatic for me, even though the going to the bathroom compulsively became a habit of mine in my teens. I may have made Lisel (that’s my inner five-year-old) up, because after all I remember this particular hospital stay so well.

I do think falling ill in early 1992, was more of an adverse childhood experience for Lisel (or me, if you think Lisel is made up). I remember I had some form of the flu, but in my own memory, it wasn’t entirely medically explained. My parents will probably say I’m trying to find clues that aren’t there so am making them up. I mean, they never talked about this experience when, in my teens, I was trying to remember when my negative mood started. They claim, as did I at the time, that it started when I was seven and having to learn Braille. In other words, I was going blind and I knew it but refused to accept it, so was becoming defiant to show a middle finger to the world. It’s easy to say it doesn’t matter. In a way, it doesn’t, but too often, I feel my parents are hiding the truth from me as a way of denying that I had significant mental health issues before the all-important age of seven. I mean, if my problems started at seven, I cannot possibly be autistic or have a dissociative disorder or anything originating in early childhood, right? Besides, I could have been old enough to be manipulative.

Am I being manipulative indeed? Or am I an early childhood trauma survivor? I don’t know and I’m not sure Lisel knows the answer.

Joining in with V.J.’s Weekly Challenge.

How COVID-19 Changed My Outlook on 2020

Yes, I’ve said it before, but can you believe it’s May already? Four months have passed since the beginning of 2020. Time flies when you’re having fun, they say. Well, time also flies (and drags at the same time) when in a pandemic. Today I’m joining in with Finish the Sentence Friday (which is open all week), for which the question this week is how the pandemic changed your word of the year.

In January, I chose the word Wellbeing as my word of the year for 2020. I was at the time already a bit angsty about it, as I was in a bit of a hypochondriac phase and thought that if I chose this word, I’d die this year or something. Some kind of reverse law of attraction.

Still, so far, my word is still pretty true. I am taking preventative measures to hopefully keep the coronavirus out of my body. Just yesterday, my staff started taking everyone’s temp twice daily with a no-contact thermometer. Since the virus hit the home below mine, I have been a little more scared. At the same time, I still often avoid thinking about the pandemic too much. Actually, I realize that, as the month of April continued, I included fewer and fewer references to the pandemic in my posts.

I had a few hopes for 2020 too. The first one was to keep my marriage strong. I felt I needed to learn to travel to my husband for this, as I thought ultimately living apart wouldn’t be very good for our marriage otherwise. While I still feel I need to learn to travel to him independently once the crisis is over, I have learned that our marriage can survive a time of not seeing each other. It’s hard, but it’s doable.

Honestly, I must say the pandemic has given me a clearer focus on what matters most. I try to appreciate my husband more. After all, he isn’t a given. One day one of us might catch the virus. Besides, we can’t see each other now and it isn’t altogether logical that a marriage survives this.

On my other goals, I did pretty well so far. I’m actually loving it. I don’t know whether the crisis is the reason I’m doing so well, but I’m pretty sure it’s one of the factors.