When you live in total squalor—cookies in your pants drawer, pants in your cookies drawer, and nickels, dresses, old New Yorkers, and apple seeds in your bed—it’s hard to know where to look when you lose your keys. The other day, after two weeks of fruitless searching, I found my keys in the refrigerator on top of the roasted garlic hummus. I can’t say I was surprised. I was surprised when my psychiatrist diagnosed me with ADHD two years ago, when I was a junior at Yale.
In editorials and in waiting rooms, concerns of too-liberal diagnoses and over-medication dominate our discussions of Attention Deficit Hyperactivity Disorder, or ADHD. The New York Times recently reported, with great alarm, the findings of a new Center for Disease Control and Prevention study: 11 percent of school-age children have received an ADHD diagnosis, a 16 percent increase since 2007. And rising diagnoses mean rising treatments—drugs like Adderall and Ritalin are more accessible than ever, whether prescribed by a physician or purchased in a library. The consequences of misuse and abuse of these drugs are dangerous, sometimes fatal.
Yet also harmful are the consequences of ADHD untreated, an all-too-common story for women like me, who not only develop symptoms later in life, but also have symptoms—disorganization and forgetfulness, for instance—that look different than those typically expressed in males. While the New York Times’ Op-Ed columnist Roger Cohen may claim that Adderall and other “smart” drugs “have become to college what steroids are to baseball,” these drugs have given me, a relatively unambitious young adult who does not need to cram for tests or club until 6 a.m., a more normal, settled life.
The idea that young adults, particularly women, actually have ADHD routinely evokes skepticism. As a fairly driven adult female who had found the strength to sit through biology lectures and avoid major academic or social failures, I, too, was initially perplexed by my diagnosis. My peers were also confused, and rather certain my psychiatrist was misguided. “Of course you don’t have ADHD. You’re smart,” a friend told me, definitively, before switching to the far more compelling topic: medication. “So are you going to take Adderall and become super skinny?” “Are you going to sell it?” “Are you going to snort it?”
The answer to all of those questions was no. I would be taking Concerta, a relative of Ritalin. Dr. Ellen Littman, author of Understanding Girls with ADHD, has studied high IQ adults and adolescents with the disorder for more than 25 years. She attributes the under-diagnosis of girls and women—estimated to be around 4 million who are not diagnosed, or half to three-quarters of all women with ADHD—and the misunderstandings that have ensued about the disorder as it manifests in females, to the early clinical studies of ADHD in the 1970s. “These studies were based on really hyperactive young white boys who were taken to clinics,” Littman says. “The diagnostic criteria were developed based on those studies. As a result, those criteria over-represent the symptoms you see in young boys, making it difficult for girls to be diagnosed unless they behave like hyperactive boys.”
ADHD does not look the same in boys and girls. Women with the disorder tend to be less hyperactive and impulsive, more disorganized, scattered, forgetful, and introverted. “They’ve alternately been anxious or depressed for years,” Littman says. “It’s this sense of not being able to hold everything together.”
Further, while a decrease in symptoms at puberty is common for boys, the opposite is true for girls, whose symptoms intensify as estrogen increases in their system, thus complicating the general perception that ADHD is resolved by puberty. One of the criteria for ADHD long held by the Diagnostic and Statistical Manual, published by the American Psychiatric Association, is that symptoms appear by age 7. While this age is expected to change to 12 in the new DSM-V, symptoms may not emerge until college for many girls, when the organizing structure of home life—parents, rules, chores, and daily, mandatory school—is eliminated, and as estrogen levels increase. “Symptoms may still be present in these girls early on,” says Dr. Pat Quinn, cofounder of The National Center for Girls and Women with ADHD. “They just might not affect functioning until a girl is older.” Even if girls do outwardly express symptoms, they are less likely to receive diagnoses. A 2009 study conducted by atThe University of Queenland found that girls displaying ADHD symptoms are less likely to be referred for mental health services.
In “The Secret Lives of Girls with ADHD,” published in the December 2012 issue ofAttention, Dr. Littman investigates the emotional cost of high IQ girls with ADHD, particularly for those undiagnosed. Confused and ashamed by their struggles, girls will internalize their inability to meet social expectations. Sari Solden, a therapist and author of Women and Attention Deficit Disorder, says, “For a long time, these girls see their trouble prioritizing, organizing, coordinating, and paying attention as character flaws. No one told them it’s neurobiological.”
Often, women who are finally diagnosed with ADHD in their twenties or beyond have been anxious or depressed for years. A recent study published in the Journal of Consulting and Clinical Psychology found that girls with ADHD have high rates of self-injury and suicide during their teenage years, at last bringing attention to the distinct severity of ADHD in females. In Pediatrics, a large population study found that the majority of adults with ADHD had at least one other psychiatric disorder, from alcohol abuse to hypomanic episodes to major depression. This poses a particular threat to females, for whom ADHD diagnoses tend to come later in life.
For the two decades prior to my diagnosis, I never would have suspected my symptoms were symptoms; rather, I considered these traits—my messiness, forgetfulness, trouble concentrating, important-document-losing—to be embarrassing personal failings. Matters really deteriorated in college, when I was wrongfully allowed a room of my own, leaving me with no mother to check up on “that space between your bed and the wall,” where moldy teacups, money, and important documents would lie dormant. I maintained a room so cluttered that fire inspectors not only threatened to fine me 200 dollars if I didn’t clean, they insisted it was the messiest room they had ever seen (boys’ included!) in their twenty years of service. Throughout college, I would lose my ID and keys about five times a semester. I’d consistently show up for work three hours early or three hours late. I once misplaced my cellphone only to find it, weeks later, in a shoe.
“Often, if girls are smart or in supportive homes, symptoms are masked,” Solden says. “Because they’re not hyperactive or causing trouble for other people, they’re usually not diagnosed until they hit a wall, often at college, marriage, or pregnancy. A lot of things that are simple and routine to other people—like buying groceries, making dinner, keeping track of possessions, and responding to emails—do not become automatic to these women, which can be embarrassing and exhausting.”
As a recent college graduate cautiously negotiating adulthood in New York City, I am both embarrassed and exhausted by my struggles to keep track of objects and time. While the stakes have become significantly higher—credit cards, passports, and cameras have slipped through my fingers—medication has minimized the frequency of these incidents.
I can’t say that I know what part is ADHD, what part is me, or whether there’s a difference. I can say that ADHD medication (in conjunction with SSRIs) has granted me a base level of functionality; it has granted me the cognitive energy to sit at my jobs, to keep track of my schedule and most possessions, and to maintain a semblance of control over the quotidian, fairly standard tasks that had overwhelmed me—like doing laundry, or finding a sensible place to put my passport.
Medication is certainly not a cure-all, but when paired with the awareness granted by a diagnosis, it has rendered my symptoms more bearable—less unknown, less shameful. And while I’m certain I’ll continue to misplace and forget objects, I have discovered the virtues of a little self-love, a lot of self-forgiveness, and even using different drawers to store different things.
The drawer thing, though, is a work in progress. The next time I misplace my keys, the fridge will be the first place I look.
—Maria Yagoda
Month: July 2014
“One of the best examples,” Jackson said, “ is that at the end of WWII some librarians decided that they wanted to put books on tape for people who lost their vision. Those were the first audiobooks. And today, there’s Audible.com, there’s Amazon, there are so many uses for audiobooks outside of those who are visually impaired.”
There are dozens more examples. Under Armor recently acquired the patent for a one-handed zipper. NPR added transcripts to their site for the hearing-impaired, and their traffic increased 7%. Inclusivity is a good business move.
I survived because the fire inside me burned brighter than the fire around me.
Narvi and Vali
Today has seemed like a very important day for me to honor Narvi and Vali, so I decided to write about it and share with you all. UPG ahead.
———
This morning, I woke up groggy and dragged myself off the couch and upstairs to grab clothes for the day, and upon arriving in my room, I was almost immediately pulled towards my altar. Something was compelling me to go over to it. So I shuffled over, still half-asleep, and asked why I’d been called over. Because I was still so asleep, all I could make out were lots of jumbled voices, not making any sense. But I felt like Loki’s whole family, as they were represented on my altar, was all there, asking me for the same thing. I went over each part of my altar, first Hela’s portion, then Sigyn’s, Angrboda’s, and Loki’s, all getting no specific calls until I realize that something’s missing.
Narvi and Vali. Their portion of the altar felt empty. It was then that I realized at least part of why I’d been called over.
In the past, there have been certain aspects of the topic of Narvi and Vali that Loki has specifically not wanted me to think or know about, but today, I got the feeling like I was very much supposed to do something for Them.
The song “Always Gold” by Radical Face has been in my Loki playlist for a long time. But the first time I tried to listen to it, I got the distinct feeling that Loki didn’t want me to. Since then, I hadn’t touched it, but on my morning commute to school, I played it. This time it felt like I was very much supposed to, and it broke my heart.
“We were tight knit boys
Brothers in more then name
You would kill for me
And knew that I’d do the same
And it cut me sharp
Hearing you’d gone awayBut everything goes away
Yeah everything goes away…”The next thing that I heard from Loki was a request. He wanted me to paint Them. He wanted something done to honor Them and make sure They were not forgotten. Since then, I’ve been planning two pieces for Them. One of Narvi on a sailboat, ready for adventure, and one of Vali in the forest, surrounded by small animals.
I felt Loki around most of the day. To say that He felt full of grief wouldn’t quite explain it. It was the sort of grief that comes with the anniversary of a death that may have happened long ago, but…the pain is still there. Still an ache in the soul where something was crudely torn from you…
And I realized the way to help that feeling was to do what was requested. To paint the boys and make sure They weren’t forgotten.
And that’s why I’m sharing this. I want to make sure that Narvi and Vali are remembered and honored. I want others to carry Them in their hearts. Sing for Them. Make art for Them. Give some time out of your day to do something for the boys that didn’t deserve Their fate.
And don’t forget our own children here. If you have your own children, hug them. Remind them they are loved. Do the same for your young siblings, if you have them. If you can, donate your time, talent, and money to charities for children who are sick and poor. Especially this holiday season. Remember Them.
Because in remembering Them, we do Them honor and make sure Their tragedy was not for nothing.
——
Below are some charities to which you might donate your time, talent, and money if you are able to. I’ve especially tried to include charities that don’t require a donation of money, so that those who might not have it to give can still find ways to help.
http://freerice.com/content-group/lovers-loki
A FreeRice group set up for Lokeans. FreeRice is an educational website that donates 10 grains of rice for every quiz question answered correctly.
The Courage Lion Project donates a stuffed lion named Duffy and a storybook about him to children who are critically ill, traumatized, abused, grieving or in crisis. The stories help the children to identify, validate, and communicate their feelings.
http://www.afghansforafghans.org/
From the website:
afghans for Afghans is a humanitarian and educational people-to-people project that sends hand-knit and crocheted blankets and sweaters, vests, hats, mittens, and socks to the beleaguered people of Afghanistan.
This is unexpectedly not about make-up haha
reblogged before it was even finished.
SUPREME
If someone doesn’t “seem” disabled to you, maybe it’s because they’ve been forced to develop a huge and complex system of coping mechanisms in order to try and survive in an ableist world. It’s probably that.
Stressed Out: Americans Tell Us About Stress In Their Lives
NPR, the Robert Wood Johnson Foundation and the Harvard School of Public Health conducted a poll in March and early April to find out how stress is affecting people in the U.S. Here’s what we found.
Not surprisingly, people with poor health, chronic illnesses or who are disabled have the most stress.
Seriously though, it’s interesting to look at the various breakdowns of things, and how having any sort of illness or condition affects one’s stress levels exponentially.
الدموع
Do not tell me
that crying is a
sign of weakness.If I can use water
to keep my body
free from dirt,then I can also
shed tears to
remove the burden
from my soul.
“Well I know what you were thinking
You thought you’d watch me fade away, away
When you broke me into pieces
But I gave each piece a name, a nameOne of me is wiser
One of me is stronger
One of me’s a fighter
And there’s a thousand faces of me
And we’re gonna rise up
Yeah we’re gonna rise up
For every time you wronged me
Well you’re gonna face an army, army of me”
Stop Hurting Kids
End Restraint and Seclusionthis is very important.
*
Students deserve to be treated with respect and dignity, and those with challenging behavior, which can include children with disabilities, should be treated with the same respect and dignity that everyone is entitled to. Yet students across the U.S. remain at risk of being subjected to traumatic, dangerous and dehumanizing procedures, referred collectively as restraint and seclusion, as a means of managing challenging behavior in school.
We encourage you to visit the resources section of this website for a deeper understanding of restraint and seclusion, and the wealth of information available on this subject. On this page we’ll provide an overview of restraint and seclusion, and why these practices should be eliminated from use in our schools…
