Stuck

I feel like someone pressed the pause button on my life.

I’ve been working on the skatepark for over three years now, and multiple times have been close to signing a lease. Each time something has gone wrong.

I walked for so long with Oregon City landlords, trusting they would get things figured out. I pointed out all the problems from the beginning and was consistently dismissed by an old white man who reminded me of my grandfather. He had assumed he knew what he was doing becuase he’d done it before.

“The laws have changed” I repeated, “they are going to require surveys, and fire inspections, you will have to make these changes, it will take a lot of time and money.” He reassured me it would be fine and and I would be in the space soon.

Eventually it became clear I was correct, it was going to take several months of work and a lot of money. I walked away and told them to call me when the building was cleared for occupancy. I haven’t heard back.

I’m not sure the first time I went to the Milwakie space, but it was several months ago. This one is better. It is one big room, right about 5000 square feet. Its between a very similar family focused sports entertainment business, and a bottle drop facility. Neither will care that we are loud and both places attract lots of families. There is a coffee and ice cream shop in the parking lot. There is a pizza place in the same building. And best of all, its close to home.

But again, I’m being left hanging by the landlords who are dragging their feet. We’ve negotiated the lease, we got to a point we are all happy with. But we have yet to sign it. Its been weeks of hearing nothing.

This waiting is killing me. This lease is everything right now. Its so hard to know how much to work on the skatepark. I don’t want to put my time into this building only for them to drop us. I don’t want to start paying for things specific to this space until I’m sure its ours.

I’ve pushed my broker multiple times, she’s just as frustrated as I am. Or so she thinks.

For her this is just one deal, just one pay day. For me this is my life. My life on hold, my life with no income, my life just waiting. I want to do something. I can’t pick up anything new until I know how this chapter ends.

Its like I’m reading a book but the last chapter hasn’t been published yet, the author is just not sure how to end it. Except maybe I’m not reading it. I’m the protagonist, and they’ve left me at a climax with no resolution.

I’m not sure how to cope with this. Its like waiting to know if you’ve been accepted to the school with your dream program. Except there is a hard deadline for things like that. For this they can drag me along as long as they want. And they hold all the cards, while I’m here just waiting, hoping, dreaming, and stressing.

Again last night I was up for much of the night with this problem in my head. Should I be doing more? Should I be assuming  I will get this lease? Moving forward with plans and permits?

No. I did that before. It didn’t get us ahead enough to make any difference and wasted time and money in the process.

I have done some work, some big stuff. Reworked the business plan for our new financial situation and specific to this space.  I also talked to a prospective employee and she’s totally on board.

She’s an incredible person who I met pretty quickly after moving to Portland, at one of the only indoor skateparks around. She introduced me to Skate Like a Girl where we volunteered together and over the years we’ve gotten to know each other better.

Knowing she’s willing and excited not just to work for me, but take on a managerial role literally helps me sleep at night. Becuase I can’t do this alone. I need a team, and building that team is going to be one of the most crucial parts of this endeavor.

A few things are moving forward, but the biggest most important peice is just on hold and my whole life is on hold with it.

My Complicated Relationship with Autism

Today I was sent a message by a woman I don’t know claiming we were both “Autism Momma Bears.” This is a label I’ve never once claimed or identified with. I’ve never thought seriously about my son being autistic.

I’ve only thought seriously about me being autistic.

Many months ago, I took the “Aspie Quiz” and scored pretty high. I was in a period of deep self-discovery via research about the brain. I laughed it off.

I might be smart, and I might be anxious. I probably have ADHD, but not Aspergers I thought. I laughed and moved on with my life.

Months later an article came though  my life outlining how autism looked different in girls and woman. It was like someone was reading my mind.

I was freaked out by how accurately it described both my inner and external life.

It set of weeks of frantic research that have now turned into months.

I’m still researching. There is so much to know. I’ve read many books written about autism and written from the perspective of someone diagnosed.

I’ve learned that getting a good diagnosis as an adult woman can range from difficult to impossible.

I once worked up the courage to email someone who specializes in psychological testing, including autism, in adults. She first emailed me back to say she would be happy to help me though the whole process including getting as much covered by insurance as possible. But then she wrote me again to say she was too busy to take me on at the time.

I felt defeated and have not tried again to be tested.

Now I don’t have insurance and I’m waiting to hear if I will be covered by the State Medicaid, OHP. I have no idea what testing might be covered for an adult.

At this point, most days, I believe that there is a place on the spectrum for me. The things that make me think this include my sensory issues.

I get overwhelmed and often don’t realize it until I’m already panicking. Heat, light, small spaces, loud sounds, people touching me. I often don’t consciously realize how these things are affecting me until I feel like I need to move to another space or until I’m snapping at someone for something small. Its not them, its the overwhelming sensory input.

Sensory issues alone do not equal autism. The bigger issues are what really convince me.

When in an intense conflict with someone I love (primarily my partner) some weird things can happen. First, I lose my ability to talk. I can become completely non-verbal at times, and often semi-verbal. Sometimes I have words I want to say, but I can’t get them out, other times my mind goes totally blank. It shuts off. This has a name in autism, autistic shutdown, its a coping mechanism for times of extreme stress.

I remember this happening as a child as well. It would make me angry, both at myself, but also at the people putting me in the position. It usually happened when I was sent to see therapists. It was way too out of the ordinary and way too much pressure. I would close up completely and not talk.

When I’m stressed out in conflict I can sometimes move from shutdown to meltdown, where I want to hit myself (and sometimes do), and often sob or even scream uncontrollably.

These episodes are exceedingly rare these days, though a few do stand out in recent memory and I feel deep shame when I think about them.

There was a period in my life when I was under a lot of stress and had yet to learn any of the coping strategies I have now and would sometimes have these meltdowns very regularly. When I get too deep into a meltdown I become suicidal. I see the only way out as death.

These experiences of meltdowns with suicidal ideation (I’ve never made an attempt) are part of what drove me to seek therapy. Those moments as well as with anxiety.

In that same period of life where I was having meltdowns regularly I also started experiencing intense panic attacks. More than once in a short period I thought I was dying right there on the spot and that no one could save me.

These are among the worst experinces of my life. Anxiety alone does not make one autistic, but it is a hallmark of autism in girls and woman.

Often for autistic women a long road of misdiagnoses starts with a diagnoses of an anxiety disorder.

For the record, I have no official diagnoses from a psychologist. I’ve only seen a therapist. But I’m a smart person who’s done my research, I could fit under several diagnoses, SPD, ADHD, Generalized Anxiety…. ASD?

Intelligence, I hate talking about this one, because it makes you seem like you are just trying to sound better than other people. I don’t think anyone is valuable based on their capabilities or skills. But intelligence plays into all this.

“Giftedness” is another term I hate, but its the one we have. Its a term for people with high IQs, which granted, is a hard thing to measure and controversial way of measuring intelligence. Giftedness is another “diagnosis” that comes with its own flurry of traits. I have zero doubts that all three of us, myself, my son, and my husband, fall into this category. As do many in our immediate and extended families. In my mother’s family, its probably just about everybody. I don’t talk about it much becuase there is no point in talking about it.

Giftedness tends to come with heightened sensory awareness, sensitivity to justice issues, an ease of being able to learn new things, an ability to focus deeply on an area of interest, high levels of creativity, independent thinking, and in the case of a coexisting diagnosis, the ability to create coping mechanisms.

I remember the day I brought up ADHD with my therapist and she said, “I can see you do sometimes struggle to listen carefully to what people are saying, but you are smart and are able to make up for those challenges in other ways.”

I had never heard something so profound about my life before. Looking back on my childhood that could sum up just about everything. Some things, such as language, logic, and the natural sciences, came extremely easily to me. Other things; math, social skills, coordination, and paying attention, were extremely difficult, but I found ways on my own to scrape by.

I could pass classes with no understanding of the material becuase I knew the best ways to game the system, I also knew I wouldn’t actually ever need that skill, so why bother.

Other classes I had mastered before I walked in the door.

At the time I saw myself as average, becuase it all averaged it out. But when I got to college I excelled. It came as a slap in the face when I realized I was actually pretty smart, but no one had noticed or told me. Or if they had told me I wrote it off as something all kids were told.

Last week when my Mom told me I was smart, I believed her. Like everything else, I had to learn it for myself before I could believe someone else.

People who are gifted, autistic, and female often do not look a typical autistic person. There are autistic stereotypes and we don’t fall into those. You have to look closely to see us “stimming”, which I’ve now noticed I do almost constantly with my teeth. Its hard for me to sit completely still, sometimes painfully hard, my body needs to move, pretty much constantly. Its not as obvious as hand-flapping, but its always there.

Growing up I was called wiggly more times than I care to remember. That was the one way I was constantly compared to my cousin who was diagnosed with aspergers. We were both wiggly. They put us in the same bed on vacations so we could wiggle and kick each other all night and our younger sisters would be undisturbed.

I feel like this is getting long. I could go on. I’ve been thinking about this for months and months and watching myself, looking back on my day and the places that were hard and the way I reacted to things, noticing, taking notes, and most days I come to the conclusion that yes I do fit on the spectrum. But I have fears and reservations about coming out and saying it. The biggest being that I’m worried others will look at me and call me “too able.”

I’m verbal, in fact I consider language one of my strengths. I’m often self-employed (which is actually extremely common among autistic woman). I don’t have a lot of the visible struggles that so many autistic people do. This is the trouble with autism being a spectrum, and with that spectrum being wider than ever before. With each new DSM more people are included.

I’m worried because everyone diagnosed in my extended family is male. I’m worried my own family will dismiss me or worse.

But its time I wrote this becuase people are wondering why I post about autism on facebook so much. So here it is, am I autistic? Its complicated, but probably.