It took a long time to recognize that I have ADHD.
This is not an uncommon story for women and non-men with ADHD, Autism, and a variety of spectrum disorders. Symptoms are often excused as being a lack of discipline or an influence of their gender. Interestingly, many women who are later diagnosed or discover that they are autistic get a diagnosis for ADHD fist.
In school, one of the most common complaints heard from teachers was that I was too chatty. I liked to talk a lot, and very quickly. Sometimes people couldn’t understand me because I spoke so fast, and yet I would hear time and time again how bright I was or how articulate. I would ask endless questions, of everyone. I could never seem to learn that whole “don’t talk to strangers” lesson. In fact even now I find myself talking to strangers. When I left for university, my parents were surprised by how many people around town seemed to know me. While my frequent conversations with strangers bothered my mother endlessly, even into my adult years, so often the people I talked to would end up spilling their stories to me. There are times when one question leads to me seemingly learning a person’s entire life story.
At school, my focus would begin to wander a few months into the school year. I would start of the school year strong, then plummet towards the middle of the year, and then make back some of the marks towards the end. I followed this pattern throughout all my schooling.
Homework was difficult. If it was too easy, I wouldn’t pay complete attention and make inattentive mistakes. If it was too difficult, it was hard to stay focused and still long enough to understand. The longer it took, the more anxious I would get and the more difficult it would become to focus. I felt like I was unintelligent, and often my dad helping me with certain work would turn into screaming matches until suddenly something clicked and it all made sense. (Strange confession, I actually enjoyed those screaming matches with my father, feeling a strange sort of pride that I was the only one who could make him raise his voice. Sometimes I think he enjoyed it too.)
I found a lot of the books for school extremely tedious. I remember the teachers complaining about the fact that I mentioned that I preferred English books to French books. I was at a French school, so I can see why they had a problem with that, but no one considered that my problem might not be with the language, but rather with the fact that the French material was selected for me, while the English material I got to choose myself.
The stories I chose myself were more engaging, more enjoyable. They didn’t follow the same patterns that every “learn to read” type story did. Where the story doesn’t seem to matter so much as they were looking for excuses to use specific words. (more…)
CN/TW: Descriptions of Assault and Rape
I was at a party the other weekend, when the subject of my book came up.
I decided to tell the anecdote of the faith healer, the punch line of which was the description of his hand on my crotch and ass stroking back and forth, while I tried not to laugh in his face or look at my mother who was also struggling. I played it like I always do; for laughs at the absolute ridiculousness of the situation. But this time something was different. Maybe it was the look on the face of the person I was speaking to. Maybe it was the fact that I was already thinking about something related to assault. Whatever it was, even as I was laughing, I was suddenly face with the fact that what I was describing was sexual assault.
A man was touching my body in intimate places, in a way that made me feel uncomfortable. He was stroking my crotch because he knew he could get away with it. Despite the fact that my mother was sitting right there. I was in a position where I couldn’t object, and I couldn’t really refuse. Not without possible consequences.
It’s not as if the realization changed much. I was already an assault victim, having come to terms with what had happened to me at 18 years old with a doctor.
But the realization that I had been telling the story of my assault as a humorous story made me stop and think.
CN: Descriptions of withdrawal, hospital admission, medical symptoms and needles.
It wasn’t an accident, or even a sudden onset of something like appendicitis. No, my brush with death came about as a result of fear. Specifically, other people’s fear. Fear of addiction, fear of being wrong, and fear of being fooled.
You see, the week before I was admitted with Crohn’s. I went to an appointment with my Gastroenterologist and he sent me straight to the ER. I was admitted, and put on high doses of Dilaudid, after the usual adjusting games where they started me on 1mg every 6 hours, before finally conceding that 2 mg every 4 was what was needed. In addition to that, I had Gravol and Benadryl to control the various side effects of the opiate.
I spent the week essentially zonked out after several weeks of increasing pain and nausea, and a trip to the ER every 2 weeks since Christmas. My admission came on the heels of two weeks of being sick with a sore throat, which kept me not just from being able to take my Remicade, but my medical marijuana as well. My throat hurt too much to handle the irritation from the smoke.
My crohn’s had gone into overdrive. I wasn’t digesting, I was in pain, and I needed help.
The reason the doctors agreed to finally treat my pain properly is that I told them, that once I got home I wouldn’t be taking dilaudid anymore.
Not one doctor stopped thinking about their fear of addiction long enough to hear what I was saying and remember their training. (more…)
“We are a diverse group of student game developers from the South East. We are currently raising money to go to the Game Developers Conference.”
One of these students is a good friend of mine. If you are able and willing, help donate to send them to a Game Developer Conference.
A lot of people can’t really parse the difference between being pro-choice and supporting eugenics. If choice is choice, what does it matter if people choose to abort children with disabilities specifically? Doesn’t it make sense that not everyone is capable and able to care for a child with a disability? Aren’t we taking away a person’s right to choose by saying that making that decision on the basis of disability is wrong?
It can be confusing and difficult to deconstruct, until we realize that when we are discussing eugenics and why it is dangerous, we are not discussing whether or not a person has a right to choose to end a pregnancy, but discussing the bigoted ideas that may be the reason for the decision.
Pro-choice activists can instinctively understand for example why abortion on the basis of sex or race would be wrong, while not seeing that assertion as invalidating a person’s right to choose. So why do we have this difficulty with disability?
Because socially we see disability as a bad thing, so much so that we have a tendency to see disabled people as not being fully human. This may seem like an extreme representation of the opinion until you realize that there are still arguments over whether people with certain disabilities have consciousness, are able to experience pain, etc. That treatments considered torture against abled people such as ABA and conversion therapy (not to mention bleach enemas) are not only still allowed for treatment of certain disabilities, but outright fucking encouraged by charities that claim to speak for these disabilities. That the murder of disabled children is often excused and almost never results in jail time.
When I was a little girl, I was playing with my mother’s sewing box looking for something pretty. I found this little button or piece of a pendant or something in the shape of a small five pointed red star. At the time I loved the colour red, and I loved star shapes, so I took some thread and turned it into a necklace.
When my father saw it he froze solid. For a few moments he just stared at me, then told me with excessive calm to take it off. Shocked at seeing my father like that, the way his face paled, the way his eyes looked like someone had just stuck their hands directly into his chest and squeezed his heart, made me take it off and put the thing back in the box.
Later my mom told me that the star was a symbol of bad things that had happened to them in Poland before they came to Canada. That it brought back bad memories for them.
It was innocence only, and my father knew that. He didn’t scream, he didn’t curse or yell or threaten. He didn’t even explain. But that star disappeared.
Years later, I learned about Stalin and Soviet Russia and the Communist takeover of Poland. Over the years I learned about solidarity and bit by bit my father’s involvement with it. I learned that my father was blacklisted. I learned that my parents as newlyweds, were separated for 6 months while my father got out of the country and they worked to bring my mother down as well. (more…)
Once again I am left in a position of asking for help to cover what is an essential medication for the management of my symptoms. As many of you have doubtless figured out by now, I use medical marijuana to treat my Crohn’s disease.
The medication acts on two fronts. The first is symptoms management where it relieves the severe pain and nausea caused by my conditions. The second is by making the other medication I am on, more effective.
I’ve mentioned time and time again that it can be expensive, but for once, I am going to share specifics.
Every once in a while, someone will complain about the fact that I ask for monetary assistance. I get advice on how to “save money” which often ignores the reality of my situation.
So just how much does my medication cost?
Medical Marijuana ranges from $6 per gram to $12 per gram. Thanks to compassionate pricing, I get a 20% discount with my dispensary. I do my best to buy the cheap strains as much as possible, but often those strains are not the ones that work for my conditions.
More frequently I end up needing the strains that cost me $7.60 per gram.
My prescription is 2 grams per day.
That adds up to at least $465 in an average 30 day month. If the cheaper strains are not available, that total can go up to $600 per month. The choice literally becomes, do I buy groceries or do I buy my meds. Frequently what happens is I use the money we used to pay down our debt on the credit cards, to then purchase my medication, in effect never actually making any improvement in the debt situation. The remainder comes from the overdraft protection, which in turn can cost us up to $5 for each day that the account in overdrawn.
Some months it is a matter of deciding which is more important, my meds or groceries.
Medical Marijuana has not been covered by Trillium or ODSP since the rules surrounding prescriptions were changed by Harper’s government. It is also not covered by any other insurance, even if I wasn’t prevented from accessing other forms of insurance due to my “pre-existing conditions”. This despite the fact that it is a known treatment for chronic pain, chronic nausea, and a variety of conditions.
Every month means an overwhelming amount of anxiety as I try desperately to come up with some way to get extra money, so that maybe just this once, we don’t overdraw and can start the month without being in the red. Overdraft protection is supposed to be a failsafe, not a line of credit. The anxiety of course makes my conditions worse, increasing pain, increasing nausea, increasing blood loss, to the point where medication becomes even more of a priority.
It’s a desperate circle, and one I hope someday to be able to escape. But in the meantime, I ask for help.
Since getting involved with atheist activism, which was my first introduction to online social justice circles, I have seen people make an effort to drop racism language, cissexist language, sexist language, etc. from their vocabularies. Yes not all and not nearly enough, but still there was a visible segment of the community that made this effort.
The same cannot be said for the effort people put in to remove ableist vocabulary from their language. Sure some of the big ones like R*t*rd that many of us have known since childhood was a slur, but st*pid, Id*ot, Cr*t*n, M*r*n, l*me, Cr*zy, for those I haven’t seen as much effort, even from people who claim to care. It’s disheartening.
Every day I scroll through my newsfeed and I’m bombarded by these words from people who are my friends, who claim to care about me and people like me.
Do you really think we don’t notice?
Many of us are just too exhausted to have the same argument again and again. When many of us struggle to survive in a world that in some cases is actively trying to kill us, often through neglect (think flashing lights, they are fucking everywhere!!), it can feel like too much to tell yet another person: “Hey actually that’s ableist.”