Confessional

I have a confession to make. I love my son, like more than I could ever possibly describe. He is my everything, but… Right now…I do not want to Mom, like, at all. And that my dear friends, is causing me to feel like a massive piece of shit human.

Here’s the deal, my recent life circumstances made it impossible for me to care for him in the way that I normally would. Thank everything holy, his dad was able to step in and fill the role that is and has been since my son’s birth, mine. The role of primary parent.

The part of me that feels like a massive piece of shit human wants to tell you that I got used to having less responsibility and I don’t want to give it up. The part of me that loves to beat myself up for everything, even the things out of my control, wants to hang it’s (my…our?) head and wallow in shame, calling myself selfish, self centered, lazy, uncaring, heartless, bad bad bad… Bad mom. The truth, I think, is more complicated.

I have, since my son was born, as is my tendency, given too much of myself. I, mostly on my own and chronically ill, attachment/gentle parent an autistic, PDA child. If you don’t understand what that means, I took the hard road without near enough support, in a broken body, with a child who is “extra”.

Looking back, I would not change the decisions that I made in my choices of how to parent but…I was burnt the fuck out before life just knocked me on my ass. *Sigh*. On top of that, the ass kicking that the universe just bestowed upon me, made a couple of things very clear to me. If I want to heal, I have to put myself first. I have to engage in the activities that bring me joy, peace, and help me to process. I have to invest time in my healing. I don’t get to just half ass try and fit healing tools in on the sly when I steal a moment alone. I HAVE TO. If not, my son won’t have a mom at all.

I wrote recently about how I healed the first time that I had a run in with chronic illness. On my own, in a safe space for the first time in my life, I spent my time learning what I needed (that’s key, what I actually needed) and immersing myself in those routines/activities. This is how I became regulated. This is how I healed.

I’m in a tough spot right now. My son’s father will be returning to work soon. I will have to go back to full time primary parent. And this is where I feel like a selfish asshole. I don’t want to. I feel resentful about it. I think that that actually makes sense though and it definitely doesn’t mean that I am a horrible person or mom. It means that I need to focus on healing and I an unsure of how to navigate this. How is it possible to find balance? It means that I’m scared, terrified really. What if I lose the gains that I’ve made? What if I’m unable to heal I’m this circumstance? What if, and I think this is my biggest fear, what if I don’t make it? And by that, I mean, I either become fully incapacitated or I lose my life and… The part of that that kicks me in the teeth, rips my guts out, stabs me straight through the fucking heart..my son doesn’t have his mom.

I feel like I need to be selfish temporarily,in order to ever truly be what he needs. Pray for me. Send me love. All the good things that might help me to figure out this balance. Or advice? Leave a comment below.

But Everyone Feels this Way

I was thinking about writers and how it’s easier to publish a book if you already have an audience, and the need to support those that you enjoy and that brought me to the realization that I totally forgot to do a review for Paige Layle’s book, But Everyone Feels this Way. I read it quite awhile ago, so I don’t really remember the specifics but I do remember what I wanted to say.

If you are unfamiliar with Paige, she makes content on social media speaking about autism. I like Paige. I have from the first video of her’s that I came across. She does , however, have a way of sometimes coming across as if her opinion is THE truth. I find that irksome at times but…. I like her. I find her content relatable and entertaining.

That said, after reading her book, I like her even more. Reading her story helped me to reframe some of what I found off-putting. This is definitely one of my favorite memoirs about autism.

Autism presents in such a wide variety of ways… If you’ve met one autistic person, you’ve met one autistic person, so it’s hard to say whether or not anyone else would feel the same way that I do. I think the memoirs people tend to like best are the ones they most relate to but… Other than Drama Queen… This is my favorite.

So, here’s me showing support for Paige. I highly recommend it.

One Step at a Time

I have something interesting (read strange) going on.

When I sleep, upon waking, in that space between consciousness and unconsciousness, I find myself writing. That is, I find my mind filled with lines as if they are being set to page. The tone is clear, voice strong. Only problem is that the stories are not stories that I have lived. I’m currently reading, Mary Karr’s The Art of Memoir. I appear to writing a memoir but it is not mine.

Sometimes, if I read a lot, right before bed, I have something similar happen. I will wake up reading. I continue reading the book, in the style of the writer, (making it up as go, apparently) in my sleep. This only happens when I’ve been reading for a long time before going to sleep. My assumption is then, that reading The Art of Memoir has my brain working overtime thinking about writing my memoir.

I have thought about writing a memoir (or three… I’ve lived many lives) for years. I’ve been told by countless people that I need to write one. I’ve assumed that some day I would write one but… Every time that I’ve thought about it I’ve become so overwhelmed that I just put that thought right away…some day.

The prospect of writing a book is intimidating, for anyone, I assume, but my overwhelm has been paralyzing. Where would I start? How would I know what parts of my life to include? Would I be able to remember enough detail? Should I reread all of my journals? And on and on. There is another reason though (or reasons, kinda).

I saw this on Facebook recently…

This trips me up… The other people part. A memoir is about the writer, your stories, what you’ve learned but… We do not live in a vacuum and those stories often include others.

There are many others throughout my life that would not come off the best. There are many ways that I wouldn’t either but that’s fine. I own my past fully but… Those others. I have a tendency to avoid talking about people in my past, other then with those closest to me, because it’s complicated. Things are never black and white and I don’t want anyone to come off as a villain. There are no villains in this story, only wounded people. I feel the need to protect those people, though they did not feel that same need towards me. *sigh*

There’s also the issue of my mother. I’ve always felt terrified at the prospect of my mom reading any book that I might write. She is one of those that I feel the need to protect and, well, even though I live with her, she really knows nothing about my life. I think I’d prefer to keep it that way. I don’t want to hurt her and I’m not a fan of drama. My guess is that she wouldn’t even read it and if she did happen to, she would just sweep the whole thing under the rug. Never happened. That is her go to.

When I was in my early twenties, I had her come to a therapy session with me. I had gotten a tattoo and had been hiding it from her….

The session did not go well. There was no drama, but there was no honesty on her part either(other than her telling me, directly after said appointment, that my therapist was not to be trusted because… She was gay… You have got to be kidding me). The anger I felt over the dishonesty prompted a conversation (more just me crying and rambling and admitting all of what I thought would have been my failings in her eyes). You see, up until that point, I believed that my mom didn’t love me, or that any love that she had for me was dependant upon me living up to the image that she held of me. The actual me could not be further from her held image. What I learned was that my mom loves me to the best of her ability. That ability does not include changing that image. She can hear it and continue to love me but she can’t hold it. Denial is her survival. It’s the only thing she knows and she is not self aware enough to know more.

I am though. I am self aware enough to see that all of this, while valid, is also an excuse so that I can self sabotage. I am called to write a book. Maybe several. I have been for basically my entire life. I think I’m finally finding my footing. Maybe I can finally do what’s right for me, regardless of my desire to protect those around me. Maybe I can finally put myself first. Admittedly, even writing that, put myself first, feels icky. I’m getting there though. One foot in front of the other. One step at a time.

Realization…unmasking as the key to healing

I’ve just had a realization.

I’ve been sick for almost 12 years but this is not my first run in with chronic illness. I was sick first, when I was about 19. I was only sick for a year or two and while debilitating, I was not as sick as I have been this time.

The causes of chronic illness, in general, are complex. My situation is no different and I’m not going to go into all of that in this post. What I do want to talk about is my “recovery”.

At the time, I attributed my healing to diet changes. Other than rest forced by the illness and a few supplements (I can’t remember any specifics other than a prenatal multivitamin. That was my doctor’s advice. Rest, take a prenatal and, you know, don’t be stressed). If you’ve read any of my recent posts, you know that I am doing Primal Trust, and that I believe nervous system regulation to be key to healing. Not that I think the diet changes and supplements had nothing to do with my healing, I am positive that they contributed but… What I just realized, is that it was nervous system regulation that was the key.

This… This all comes back to me being undiagnosed autistic. At the time of my healing, I was no longer in school and had just moved into my own house. My ex husband and I were in the best place, relationship wise that we ever were. And I… I had a lot of space to experiment with just being myself. I, my dear readers, was unmasked for the first and dare I say, only time in my life.

My days were spent doing as I pleased with no fear of repercussion. I got up, took a bath, exercised (as I became able), sang (I’ve recently realized that this is my biggest stim), danced… I spent all of my time with my animals or with my then husband, who, at the time, I trusted. At night, we watched movies and I engaged in my special interests.

This is not a life that is supported by the society that we live in but it is a life ideally suited to me. Add in abundant time in nature (which hey, guess what? I had my own home with a pool, I was out in the back yard a lot in the summer) and I’m in heaven. Of course I was regulated. Of course this was the only time in my life that I’ve ever felt truly healthy.

My task then, (and this really is THE task of all neurodivergent folks (and honestly, of all people, it’s just that it comes glaringly into focus for those of us whose needs are further outside of the societal norms), isn’t it?) is to find a way to build a life that suits me within the confines of this oppressive society (all the while, attempting to effect change in any was possible). A life that prizes space and creativity and regulating movement/sound and nature and deep deep dives into the topics that feed my soul…

This is no small task. All the more reason to keep talking about our needs as autistic humans. This is integral to our health, to our very existence. This is essential to a healthy society as a whole.

Have you the courage to change?

I was listening to music on YouTube Music. Just a random playlist that is supposed to include all of my tastes (YouTube Music does a pretty good job diversifying my playlists, that’s why I use it, but it definitely does not include all of my tastes. I find I have to actively find something and listen to it before the genre is included, as opposed to just including all of my liked music), and the song Courage to Change by Sia played. I found myself annoyed.

If you aren’t aware, Sia received a lot of backlash, from the autistic community in particular, over her movie Music. Criticism includes her decision to use a non autistic actress for the role of Music (who is an autistic character), the portrayal of said character being inaccurate and coming across as a caricature, Music’s character being used as a prop to support other characters stories, rather than having a story of her own, and the depiction of prone restraint (which is dangerous and can result in death) used as the way to handle Music’s autistic meltdowns.

I agree, the movie is highly problematic. And if you, or anyone feels the need to stop listening to Sia’s music on that basis, I get it. I, however, do not. Personally, I’ve found many of Sia’s songs emotionally cathartic and therefore helpful, for me…. But now I can’t listen to this song without feeling annoyed. I mean, I didn’t know Sia, have you the courage to change?

From an interview that I recently saw in a video from Meg, of I’m Autistic, Now What?, it appears that Sia may have deluded herself into believing that the criticism was not real. That it stemmed from crazy conspiracy theories šŸ¤· If that is the case, it doesn’t seem an apology or promised changes to the movie (such as a warning or removal of the restraint scenes) is forthcoming.

I am annoyed with my annoyance. What do you think? Is it possible to remove the artist from the art? Or should we distance ourselves from the art itself when the artist is problematic in some way? Please comment, let me know your opinion.

Those Parts Lost Along the Way

I’m watching the documentary Strip Down, Rise Up on Netflix. I’ve only just started it, so I don’t really have an opinion on the documentary itself as of yet. It’s about a woman who teaches pole dance. She teaches women to pole dance in order to bring them back into their bodies, back to themselves. Reconnecting with their bodies, opening themselves to vulnerability, processing trauma and reawakening their feminine essence.

Oh, it’s bringing up feelings of longing in me. I miss dancing. I miss moving my body, like at all (I currently have almost zero exercise tolerance and it’s been this way for over a decade), but in this moment, especially that way. The slow, sensual, in touch with yourself way.

I’m thinking about it and back in my stripping days, I don’t think I was ever really dancing for the customers. If, by chance I did happen to try, I’m guessing it wasn’t my best work. I started dancing for myself at home. I would put on my boots (yep, the kind with the statuesque heels) and dance in front of a mirror, in my undies, for myself.

This remained my method, even in a club full of people. Internal. Connecting with myself. My sensuality. My sexuality. Me. And, in my opinion, that’s hot as fuckšŸ¤· I miss that. I’m looking forward to getting it back. This, among other parts of myself that have gone missing in the duration of this illness. I’m healing. I believe that. No matter the extent of my physical healing, I will find a way to reclaim those parts of me lost along the way.

Autistic… Just a traumatized INFJ?…No

Last night, while watching videos on YouTube, I watched a video by Irene at The Thought Spot. Irene shared a comment that she received. The comment read “Hey just wondering how autism shows up for you? You seem very articulate and self aware and have deep empathy. I’m wondering if you perhaps have the INFJ HSP CPTSD COMBO that can look and feel a bit like autism and or ADHD but when we get our nervous system regulated AND our attachment traumas healed we would not qualify for an autism diagnosis ā¤ļø”

Ok, so Irene does a full assessment of the comment, line by line, in her video. You can watch that here. Since she does such a thorough job, I’m not even going to get into the implication that if you are autistic, you can’t be articulate, self aware or have deep empathy (šŸ™„). I only want to touch on my reaction, my internal response to hearing this comment.

I’ve written before that I no longer question whether or not I am autistic. I know that I am. I’ve done enough research, I’ve had my autismness validated by an autistic therapist and I just know, man… My life finally makes sense. I am autistic.

At first, for a long time, I experienced an almost panicky sense of imposter syndrome. Even though I knew…I needed outside validation. What if I was wrong? I can’t claim something this huge and be wrong. That is why I am on a two year waiting list to have an official assessment. Even though I no longer question it and I no longer feel like I need that outside validation, I intend on going through with the assessment so that I will (hopefully…) come up against less backlash from the outside.

Even though I KNOW, and I do know, this comment threw me for a bit of a loop. Imposter syndrome and fear of being wrong struck me hard, briefly. I am an INFJ. Once upon a time, I identified as an HSP, and Lord knows I am highly sensitive. C- PTSD…check. I also know that my nervous system is dysregulated, that is why I’m doing Primal Trust (I do think that most, if not all autistic people would benefit from nervous system regulation work. We the in and process so much information, it serves that better regulation of our nervous systems would help with “symptoms” of autism but autism is not the “symptoms” it is a difference in brain structure). Attachment traumas….again…. check.

After breathing through a bit of panic, I started thinking about it. Irene mentions, in her video, that she was actually at her healthiest when she was diagnosed with autism. Thinking about myself…same. I am most definitely not at my physically healthiest but mental health wise, yeah, I am. I may still have work to do on my attachment wounds (and yes, definitely my nervous system) but I’ve already done a lot of work. Irene says that she believes that if she had sought an autism diagnosis when she was less mentally healthy, she would have been misdiagnosed with OCD and BPD. That is what happened to me. My official diagnosis, back in the day, back when I was very unstable, was Borderline Personality Disorder with Avoidant and Obsessive Compulsive Personality Disorder traits. Healthier does not equal no autism.

The more I thought, the more irritated I felt. My personality type and my trauma has nothing to do with autism traits that have present since my childhood. Especially, if they were present before enough trauma to cause C- PTSD, like the fact that I started speaking abnormally early (first word four months, sentences before one year). My personality type and trauma also has nothing to do with my father (my dad is an INTP) or the much of his family that, now that I know what I’m looking for, seem clearly autistic to me.

Then there is my son. My personality type and trauma does not account for his hand flapping and other very obvious physical stims that have been present his whole life. It does not account for his damn near all encompassing demand avoidance, or his use of echolalia, his food sensitivities, his tendency to hit himself when frustrated, or constant vocal stimming…

It’s funny, this comment, which was meant to be invalidating of Irene’s experience, diagnosis…life, actually ended up reinforcing what I already know that I know. Which is that I an autistic, as is my son. It also highlights just how important autism awareness is, like awareness spread by those who are actually autistic. The misinformation is…*sigh*…it just is….

I will continue to do my part and speak about my experiences. If you are able, I ask I that you do the same.

Art, like beauty, is in the eye of the beholder

The other day, I wrote of feeling creatively stifled. I wrote about how a situation in my life feels too sensitive to speak about publicly at this point, too raw, too vulnerable (which, by the way, I’ve decided that that situation will go in my book. I’ve planned on writing a memoir for like ever but I get too overwhelmed whenever I think about it. Ideas are coalescing. It will happen.) Anyway, this got me thinking about another way that I feel stifled in the creativity department.

I used to make, what I can only call, selfie art. I would edit selfies in a way that transmuted emotion. In the same way that I use drawing to process and purge myself of emotion, I edited my photos in way that enhanced the emotional experience of said photo.

Like any public art form, I had my fans and of course, my haters. I received criticism for using selfies as an art form. Apparently they can’t be art (bitch, anything can be art. Art, like beauty, is in the eye of the beholder). For posing provocatively (it’s my body, I’ll do with it as I please. Don’t like it, don’t look), and, among other things, being too thin (why people think it’s ok to comment on other bodies is beyond me).

Along with the criticisms of my weight came one comment from a woman who was in her words “fat”. Her claim was that I only shared my photos for attention. That I was only able to do so because of the shape of my body and that I would not do it if I were overweight.

Like all criticism that comes from a place of complete misunderstanding of my intentions, the comment irritated me. My photos, for me, encompassed a wide range of emotion. Some were joyous , and some sensual but the overwhelming majority were expressing the so called “negative” emotions…anger, sadness, abject despair.

Did I feel good about myself in some of my photos? Hell yes, and I don’t see anything wrong with that. I spent years hating myself, that self love was hard fought and well earned (and why is it so horrible for someone to like the way that look? Again, I don’t get it). Again, though, most were a purge of the darkness inside of me. Most were edited in a way that highlighted my flaws. They were intended to make me look “ugly”. The insinuation that I was only sharing for the sake of vanity felt so completely off the mark and I felt, like most of my life, wholly misunderstood.

Here’s the thing, she wasn’t completely wrong. I do not make selfie art anymore. The reason is because I am not currently a fan of my body. Pregnancy + mold toxicity has equalled a lot of weight gain. That said, I didn’t stop making them because I can no longer solicit a response that appeals to my vanity (there is shame around my weight but that’s a whole nother issue). I stopped making selfie art because, for me, “fat” doesn’t translate into the emotions that I need to process and express. What does? Bones. I was very thin at the time I made those photos (underweight actually. Again, illness related. I don’t choose which way it throws me.. under…over…. It’s all illness), and my body was my perfect canvas.

I miss creating selfie art. I am a huge fan of emotional photography. I often see images in life around me and wish I could capture what my eyes see, but nothing works for me in the way that my body did. It just doesn’t.

That said, I did create a few photos of my son the other day. I don’t usually share him in a public forum but I’m making an exception.

Creative Energy

I hadn’t drawn in 5 years. I was drawing frequently, almost daily, when I got pregnant with my son. Shortly after I found out that I was pregnant, I got really sick. I wasn’t physically able to draw… And then I had an infant and then a toddler…What I was drawing at the time never got finished.

I’ve felt the need to process some emotions recently and because I’ve had a bit of space, I decided to get myself some drawing pencils and get back into it.

Yesterday, I mentioned that I’ve been doing Primal Trust. Dr. Cat makes it clear that when starting the program, you may feel worse before you feel better. You may have an increase in symptoms, more anxiety, insomnia… While I am already feeling somewhat better, I’m definitely experiencing some of that.

I’ve had a slight increase in energy. When I say slight, I mean that I still have virtually no energy. I can not do much but I can feel the difference. What I do have though, is an abundance of creative energy…. But not enough physical energy to express it all. It’s uncomfortable to say the least, but as I understand it, a good thing. Healing is happening. Things are moving.

Anyway, I guess all of that was just to say, I may be sharing more…more posts, more drawings, more who knows what … We shall seešŸ¤·