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Why Kate Spade’s Suicide Doesn’t Matter
Kate Spade had it all.
Met a cool guy named Andy. Started a business with him (and they later married). Business skyrocketed and became a household name (at least, in any household including teens or young women).
A New York Times headline describes her as the woman “Whose Handbags Carried Women Into Adulthood,” passionate and approachable.
She and Andy seemed to be unbelievably well-matched partners. He came up with the rough draft. She ran with his ideas and crafted the finished product.
Friends said the couple were “perfect” partners in business and life.
She sold her stake in the business shortly after the birth of their daughter. Even in her absence, the website still seems to draw from her unassuming, quirky, vibrant personality.
The designer told Moneyish last year she wouldn’t trade the time with her only child in exchange for her self-titled brand “in a million years.”
In almost every article, Kate is described as the driving force of a fashion empire, impacting young ladies across the globe and in every layer of socioeconomics. “Attainable” fashion, with something for everyone from British Royalty and Chelsea Clinton to high school students. Fans like Jonquilyn Hill, now a producer, are reminiscing about buying their first Kate Spade bags.
Kate Spade was famous. Kate Spade worked hard and attained success. Kate Spade was a fashion phenom.
These are the reasons news of her apparent suicide is splashed across every web page around the world.
But Kate Spade’s suicide doesn’t matter.
At least, not for the reasons listed in many of the articles.
Kate was a mother, wife, sister, daughter, friend. Kate Spade’s suicide matters because she was a PERSON.
According to a CBS story, she may have been a person battling mental illness.
Most of us did not know Kate personally. 99% of The Web Collective freaking out right now did not know Kate.
Kate’s suicide doesn’t matter because people everywhere are mourning memories of their first handbag or wallet. Kate’s suicide doesn’t matter because she was a success. Kate’s suicide doesn’t matter because she is proof the American Dream comes true.
Kate’s suicide matters because people cared about her. Really cared. Not because famous people bought her products.
EVERY suicide should receive the same coverage. We should all mourn EVERY life lost to depression, to mental illness, to bad choices made in a moment of hopelessness.
Kate Spade’s suicide doesn’t matter any more than the suicide of my friend or of your parent or of that guy’s brother or of the kid from the neighborhood.
Her suicide also doesn’t matter any less.
The loss of a bright female leader (who chose to take time away from her fashion empire to focus on her daughter) is heartbreaking.
The fact that she is one of 45,000 individuals in one year to commit suicide is devastating.
According to the National Institute of Mental Health,
- Suicide was the tenth leading cause of death overall in the United States, claiming the lives of nearly 45,000 people.
- Suicide was the second leading cause of death among individuals between the ages of 10 and 34, and the fourth leading cause of death among individuals between the ages of 35 and 54.
- There were more than twice as many suicides (44,965) in the United States as there were homicides (19,362).
At-risk children, including those in the foster system, are even more likely to commit suicide.
In one study, children in foster care were almost three times more likely to have considered suicide and almost four times more likely to have attempted suicide than those who had never been in foster care.
Perhaps “Kate Spade’s suicide doesn’t matter” isn’t really what I want to say. I think, “my friend’s suicide should matter just as much as Kate Spade’s” is closer to my true intent.
My adopted son’s declaration last September that he’d rather not be alive opened my eyes to the need. IN MY OWN HOME. Maybe in your home, also.
Hopelessness is rampant.
Be Hypervigilant.
Pay attention to the people around you—especially if they belong to an at-risk population like kids who’ve been in foster care.
If family members seem a little “off,” don’t wait to ask if they’re okay.
If friends admit to feeling depressed, encourage them to seek help—and don’t walk away.
You might be the light that draws them back to life.
Here are a few resources for help:
If you are in crisis, call the toll-free National Suicide Prevention Lifeline at 1-800-273-TALK (8255), available 24 hours a day, 7 days a week. The service is available to anyone. All calls are confidential. http://www.suicidepreventionlifeline.org
https://www.christianitytoday.com/ct/2013/april-web-only/when-suicide-strikes-in-body-of-christ.html
https://answersingenesis.org/sanctity-of-life/christians-and-suicide-prevention/
Sending hugs your way.
Success…for now
THANK YOU for your prayers and encouraging words.
In case you’re just joining us, I presented this week to a group of eleven professionals appointed by the government to ensure children receive appropriate services. They hold the power to choose the best route of treatment for our son.
My meeting went well, although the current residential facility representative maintained the opinion the best option for our boy is a step-down to a group home. After hearing about his current outbursts, the team agreed a step-over to a different facility is warranted. This was our desired outcome. As one of the members noted, he is still not in control of his anger.
The current facility’s mindset is that he’s made great progress since January. However, they’re ignoring the huge swing he’s experienced since admission. In some ways, his behavior is now worse.
We admitted him because he expressed suicidal thoughts, and his actions were harmful to himself and others. When he became angry, he usually expressed it verbally (or in writing, as I often sent him to his room to write in his journal).
From November through January, his expression escalated to physical. He began provoking and fighting with the other children—specifically those he saw as weaker than himself. We worked with the therapist to create a reward/consequence system to eliminate the physical aggression (“TV time” is his most effective motivating factor; an altercation = no TV).
Although the therapist agreed with and supported the plan, getting the general staff on board proved difficult. Part of the issue stemmed from attempting to communicate the plan with the large number of individuals involved. In addition, not everyone agreed with our tactics. They felt barring him from TV made him feel as though he were not “part of the group” and minimized his “socializing” opportunities.
I argued that punching another kid in the face might also limit his social acceptance.
We had very little success. Enforcing rules from a distance is difficult, especially without buy-in from staff.
He figured out that his physical aggression was keeping him in the center longer and occasionally affected his TV access, so he stopped punching kids and started punching and kicking the walls when angry. He hasn’t yet cracked the sheet rock, partly because some walls are cinder block. This week, he bruised his hand badly.
To the center, this is progress. To Hubby and me, not so much. He’s still expressing his anger in inappropriate ways, with the threat of property damage looming just one kick away.
This week, he sat down at a table in the classroom and refused to get in his seat because he wanted to color. When the teacher explained this wasn’t an option, he walked out of the class. Staff informed him he may not refuse school (the center allows them to refuse certain activities) and he flipped out, punching and kicking windows and walls. Call me crazy, but this does not feel like progress.
Thankfully, the team agreed with our concerns; we can move forward.
Next steps involve obtaining admission from the desired facility and sending a description of why this is our best option to yet another government employee for final approval. She knows our story, so I have hope for limited delays. Having the team’s backing also gives credibility to the request.
The road to healing is long and it hasn’t been easy, but I have hope.
I write our story to be a support and to help other families in similar situations feel less isolated. YOU ARE NOT ALONE.
I write our story to show the individuals who support these families: YOU ARE NEEDED.
Adoptive parents AND adopted children—we learn from those who’ve gone before. Please feel free to give your opinions and guidance.
We need each other.
You have a story. Chime in.
- Change ChangHe’sfThe c
Monopoly on Happy
The problem is that you are putting in all the effort to see me and I’m not doing any effort to show you that I want you to visit.
This was my son’s explanation of the main problem in our family relationship during a phone call.
He continued, “when I don’t do what I’m supposed to do, I’m sending the message that I don’t care if you come to see me.”
The kid is smart. He knows what he’s doing.
In the beginning of his residential treatment stay, we visited our son every weekend. However, his behavior escalated and his actions became increasingly violent. We reduced the frequency of visits based on his behavior.
His therapist agreed he needed to have some responsibility in our family connection, unrelated to other behaviors. As part of his therapy, we created a behavior plan which required our son to do a chore and a lesson in a Bible devotional each day in order to earn a visit.
Because our main objective during that time was also to ensure his sister’s safety, deleting the visit was a negative consequence if he had a violent outburst during the week. Assuming he did not assault anyone, we would show up.
Our son agreed to the plan.
The therapist ensured the chore would take fewer than 5 minutes. The devotional page also required about 5 minutes. In order to fulfill his behavior plan, our son needed to put in only 10 minutes of effort each day.
We purposely kept his responsibility simple, to ensure that he would easily be able to attain success. We wanted to show him that when he did what he needed to do, he would get what he wanted.
As the therapist worked with him to prevent thoughts from becoming behaviors, he stopped assaulting other humans. Instead, he began beating on the walls, doors or windows when frustrated. Sometimes he threw or flipped chairs.
He made the mental connection that we were not visiting during times when he had been violent with another person and assumed that we would visit if he didn’t hit someone else.
By this time, though, the behavior plan was in place and he needed to complete those two simple actions in order to have a visit. Instead of complying with the plan, he became angry that we were not visiting even though he had not hit anyone. He refused to complete chores or the devotional.
For weeks, we encouraged him during nightly family calls—as well as during family sessions with the counselor—to complete his plan.
Eventually, he began doing the chores but still refused to do the devotional work. He said he didn’t see a point because he already knows who God is. No amount of reasoning worked.
It became a power struggle and I asked the counselor if we should simply give up, but he agreed that if we did so, our son would simply see us as liars, even though we would be breaking our word in a positive way.
The counselor and I began to wonder if he was simply convinced we wouldn’t visit and was making sure that he was in control of the situation.
I wanted to make sure that he knew we would visit, so the counselor and I came up with a compromise. If our son did not finish seven lessons by Thursday, I would do the rest of them on the phone with him so they would technically be completed.
We were able to get him to do three of the lessons on his own by Thursday. On our evening call, I told him to get the book and completed the last four lessons with him on the phone so that we could make a plan to visit him on Friday.
Last night, I saw my son for the first time in over a month. Waiting until he completed his behavioral plan may seem extreme, but we wanted him to grasp the necessity of putting effort into the relationship. We also wanted him to see that we would immediately reward that effort.
We want him to know that he can trust us to show up. We also need him to grasp that relationships take work.
Last night, we had the best visit we’ve had since his treatment began. He was thrilled to see us and knew that he had completed what was required of him in order to make it happen. He had done his part and we had done ours.
Interactions weren’t perfect, and he was still less than truthful when it came to owning up to behaviors during the week. However, I have never seen him so happy.
I believe he experienced the kind of joy you feel when you know you’ve been responsible and done your part.
We played a couple of card games and spent the rest of the time playing Monopoly. It was the first time we’d ever played the game as a family, mostly because I wasn’t sure he would react well to some aspects of the game.
He amazed me, interacting and trading and paying rent and going to jail without flipping out.
I had a foot-in-mouth moment the third time his sister went “straight to jail without collecting $200.”
“I never expected you to end up in jail a bunch of times; I always thought it would be your brother,” I grinned at her.
Then, horrified, I realized what I’d said and slapped a hand over my mouth.
He cut his eyes at me, then cracked up with a true belly laugh.
He patted my arm. “It’s ok, Mom. Don’t feel bad. That was pretty funny.”
For the first time since October, I think perhaps we are making headway.
I know it’s a long road ahead. Expecting things to be perfect (or even to consistently go well) would be ridiculous.
But for the first time in months, I believe we will be able to have game night in our own living room, together. Not tomorrow, but someday.
I have hope, because last night, for a few hours, we had a Monopoly on Happy.
Guilty
Continued from Desolate
When the kids first came to live with us, I clocked three to four hours of sleep a night. The girl wailed until after midnight; the boy woke screaming around in the wee hours.
Every. Single. Day.
The initial sleep deprivation lasted about six months; four months for social services (still the legal guardian) to approve meds and two more months for the doctor to find the correct dose.
I still remember the relief I felt the first morning after we found the right combination, waking around 6 instead of 4 am.
I’d forgotten how it felt. September brought it all rushing back.
This time, I think, was worse.
Digressing a bit: I’ve had a recent epiphany that I experienced almost no change in stamina from the time I was seventeen. Until now.
Sometime this year, I looked in the mirror and realized I am no longer twenty-seven. Or thirty-seven, for that matter. Am I too old for a ponytail?
Apparently, up to this point my brain has been convinced I’m a decade younger, and the shock of realizing I am OH NO middle-aged was a bit too much.
This time, sleep deprivation almost killed me.
Ok, that’s hyperbole.
But I was beyond exhausted. By the end of September, I started telling Hubby I might like a weekend in the acute center, if they actually had white padded rooms available. 48 hours sleeping in a soundproof room…sounds like heaven.
Unfortunately, checking myself in at one of those places wasn’t an actual option. Hubby took over on weekends and let me nap as much as possible while he was home.
Finally, after weeks of phone calls and meetings and waiting, we got the approval call from the treatment center.
Because we were concerned about what our son might do if we informed him ahead of time, I packed him a suitcase during the night. I crept into his room and slipped his stuffed dog from under his arm. The next day, as we drove to the treatment facility, we explained.
-
We are not counselors or psychiatrists; we have researched and prepared as much as possible, but we are not trained to provide the care you need.
-
We care very much about you and want to give you the best chance to succeed in life. The people at this facility have the qualifications to help you.
-
We are NOT giving you up, letting you go, abandoning you or sending you away.
Our son responded with little emotion.
Like I said before, you’ve tried everything. We might as well try this.
His absolute lack of reaction still stymies me.
The experience at this treatment center was a complete change from the acute center. We met the director, head nurse and several staff. While the nurse completed the intake with our son, we toured the facility.
The staff explained to our son that the initial stay would be thirty days; he perked up and I watched determination firm his jaw.
At the time, we didn’t realize this would become a problem.
He thought if he could “act good” for thirty days, they’d release him. And he decided to make it happen.
He hugged us goodbye without a tear, then walked through the metal door with a staff member. It closed behind him with a heavy thud.
We walked to the car.
I expected to feel guilt at leaving him with strangers.
I expected to feel great sadness at leaving him behind. For almost seven years, we’d been four. Now, at least temporarily, we were three.
I expected to feel lonely, to feel his absence, to experience a boy-shaped hole in my existence.
I expected to feel that I was a failure as a mother, having not been enough to help him.
But here I must admit: I felt nothing but relief.
I truly believed the people in that building would be able to help him in a way Hubby and I could not. I knew we weren’t leaving him permanently; we would, soon enough, once again be four. I understood that I’d exhausted every possibility available, turned over every proverbial stone.
As for missing him—maybe this sounds awful, but…I didn’t.
My only source of guilt: the relief at being able to relax.
No checking every thirty seconds. No worrying whether he’d wake before I did. No concern about destruction or harm to property or living creature (including his sister) if my visit to the loo lasted an extra minute.
The first three days after drop off, I slept like the dead.
A week later, Hubby looked ten years younger.
And the nurse called to tell me our son was the best behaved child in the center.
He is so polite. He is kind to everyone. I wish they were all just like your son.
I was gobsmacked. Flabbergasted. Shocked.
How could this be the same child?
Until now, I’d never realized how determined he could be.
Guess how long that dogged kid kept it up.
Excruciating Ride, Part 2
Continued from Excruciating Ride
I often search Flickr for just the right photo, but I don’t always find what I want. In this case, the picture is worth about a million words.
The roller coaster we’re riding with our son right now isn’t any fun.
As I walked into the hall, my son whipped the pencil away from his chest.
“What are you doing?” Reaching for the pencil, I leaned over to see whether he’d progressed through his school work. I used the pencil to point, summoning as much nonchalance as I could.
“You need to fill in these blanks in pencil, please.” I handed the pencil back, adding, “Pencils are for paper; pencils are not for poking people.”
He nodded and took it.
After he finished his school work, I gave him a journal assignment. He wrote about suicide by a pencil stab.
An hour later, he growled in frustration when I wouldn’t believe an obvious lie. He left the house and headed down the driveway. The timing worked well, because we needed to head to an appointment, so I pretended to think he was going to get in the car.
Unlocking the vehicle, I called, “Hey, thanks for getting out of the house so quickly so we can be on time! Do you want me to meet you at the end of the driveway?”
He froze, then turned slowly and shuffled back to the car, muttering, “wearing the wrong shoes, anyway.”
His sister gave him a sharp look. “Were you trying to run away?”
“Yeah, but I need my other shoes.”
She shook her head. “Running away is stupid. What are you going to eat?”
In a cool, flat tone that gave me chills, he said, “Dead squirrels, probably.”
…
By late August, I was spending an average of seven hours per day closely monitoring our son. Completing tasks became almost impossible; he didn’t want to move, so he began a sabotage campaign. When we put the house on the market, we asked the kids to try to keep things neat for the showings. He thought buyers would refuse to purchase the house if he worked against us. He trashed his room, wrote on the walls in permanent marker, decimated a large planter…every time he wasn’t by my side, I looked for the next bit of destruction.
He did the opposite of whatever we asked and began doing things he’d never done in the past, like climbing out of his window to leave the house. Hubby and I did our best, but…have you ever tried to keep an 11 year-old in sight at all times? It’s even harder than it sounds.
Cameras and a newly-installed alarm system helped, but we still couldn’t supervise 100% of his day. Showers became especially problematic, because he’s really too old for one of us to stand there. He plugged the drain with toys and toilet paper, defecated in the tub and filled the curtain with water, letting it go when it became too heavy (all over the bathroom floor).
Because he is diagnosed as “on the edge” of the Autism spectrum, the in-home counselor suggested we apply for ABA therapy for help with behavior modification. Good ABA therapists have successfully helped non-verbal, low-functioning children learn to communicate and to perform self-care tasks. If his apparent inability to follow directions stemmed from the autism, the therapists would be able to help. And maybe, once he had a habit of doing the right things, he would feel better about himself.
While I sat outside with the supervisor, outlining the challenges of the last several months, another staff member sat with our son to evaluate him. I explained to the supervisor that he’s great one-on-one with an adult, so I expected the other therapist to find nothing. Sure enough, when she joined us, I saw The Look.
The Look, n., facial expression indicating the parent must be out of her mind, as this child is brimming with intelligence and compliance.
Thankful for backup from the in-home counselor, the supervisor and I explained there is more to this kid than becomes obvious in one meeting. We were approved for services, but staffing shortages meant ABA wouldn’t start for several weeks.
…
A week later, the threats of suicide came almost daily, sometimes several times a day. His moods swung between anger and depression. I couldn’t leave him alone with his sister for even a minute because he started lashing out at her.
ABA wasn’t going to be enough.
We began looking for residential treatment, this time for a program that lasted more than a few days.
Continued
Excruciating Ride
Continued from Roller Coaster, Part 2
Angela Duckworth, author of Grit, believes we reach “expert” level by practicing our craft for at least 10,000 hours; K. Anders Ericksson specifies those hours are spent in “deliberate practice.”
Therefore, I would like to announce that
I am an expert.
For at least thirty years, I have deliberately practiced…procrastination.
Don’t even have to try anymore; Hubby agrees my practical level of procrastination is unbelievable—even mind blowing.
Blog procrastination happens when I know it’s time to write but I’d rather pretend nothing is happening.
Writing about the last six months is painful, terrifying, discouraging.
I’ve been procrastinating.
As I mentioned earlier, the roller coaster with our girl has morphed into a super-fun ride most days. (And yes, I know that super-fun is technically not a word.)
The roller coaster ride with our boy…not so much.
Right now, his roller coaster is excruciating.
When we began our journey, people supported us in the best ways they knew. However, few had the experience to understand, so we stopped trying to share our angst, because conversations went something like this:
Me: “Our foster son won’t stop screaming. Anything sets him off. He won’t let me touch him until he’s out of his mind—then, still screaming, he clings to me like the earth is falling away and I’m the last thing standing. Sometimes it lasts for hours; I don’t know what to do.”
Friends my age: “Yeah, my kid does that, too. I just turn on the TV and he settles down,” or “Put him in his room, tell him he can come out when he’s done, and shut the door.”
Friend my mom’s age: “Tell him if he doesn’t stop crying, you’ll GIVE him something to cry about.”
Friend my grandmother’s age: “He probably has gas. Have you taken him to the doctor?”
Social worker: “If he’s too much for you, we’ll find another placement.”
The above suggestions didn’t help.
But those kinds of conversations prompted me to start this blog, because Hubby and I agreed no one should feel as alone as we did.
Have a troubled kid? You are not alone.
Terrified of the future? Wondering whether your child will have the ability to function in society? “Cautious optimism” is your motto?
You’ve come to the right place.
Everyone’s story line is a little different, but the internal conflict connects across all boundaries: parents want beautiful life to happen for their kids, but we don’t always know how to best assist.
We want them to thrive, be mentally healthy and happy, be successful, have a great future.
Three months ago, the main life plan for our eleven year-old son was
stay alive.
His roller coaster almost went off the tracks in August. The happy boy who lived with us during the summer of 2016 was long gone. He used his intelligence to charm and manipulate adults but could not stand his peers. Aggressive behavior caused his expulsion from two summer camps.
Several life alterations (loss of Hubby’s dad, job changes, selling our home, moving) or hormones may have something to do with the downward spiral that held a tenacious grip on his personality; we don’t really know the cause. Hindsight sometimes holds clues and answers, but in this case, we can’t find any triggers.
I once read that talking about suicide is “just” a cry for attention unless the person has a plan. (We can discuss “just” another time…if a person is reaching out, there’s a reason.)
Our son had a plan.
Several plans, actually.
When he was upset, I often sent him to write in his journal; after he finished, he allowed me to read it and we took time to discuss his thought processes. As he found that I would not give him a consequence for anything he wrote (he tested this with a list of swear words), his writing became darker and included plans to run away or harm himself.
His list of ways to die included throwing himself in front of a vehicle, drowning himself in the pond or stabbing himself in the heart with a pencil.
Because of his extreme behaviors and inability to function appropriately in most settings, he had an in-home counselor ten hours a week. She became an invaluable presence in our family, mostly for me. (I no longer had to wonder whether I might be overreacting.)
We monitored him closely, working with the in-home counselor with the goal of keeping him with us.
We were, in a word, Hypervigilant.
We installed an alarm on the house to alert us if he tried to leave in the middle of the night, and cameras so I could keep an eye on him when I had to be in another room. Most of the time, I slept only when he slept, woke before he did and kept him in my physical sight almost all day. If I needed to use the restroom, I took the monitor, and only took showers when another adult was in the house. Hubby took over when he got home from work so I could get a little rest.
We were exhausted but determined to do everything we could to prevent residential care.
We believed our love could be enough.
Our in-home counselor agreed he needed immediate and urgent help after he acted out a detailed suicide scene in front of a camera in our home. We aren’t sure whether he chose the setting intending a manipulation, since he knew the camera was there. Regardless, the underlying issue remains the same: his thoughts were focused on ending his life.
As I explained that we might need to seek help from a facility outside our home, he shrugged.
“You’ve done all you can. You’ve tried everything else. We might as well try this.”
We checked him into an acute care psychiatric facility that afternoon. We visited every chance possible and each time he fed us lies (people hurting him, taking his shoes, trying to fight him). After a visit on day 5, Hubby and I resigned ourselves to the knowledge he’d be there a while as his mindset was obviously not changing.
Less than 24 hours later, a nurse called and told me they planned discharge that day. I was shocked.
“He told the doctor he’s not thinking about suicide anymore, so he can come home now,” she chirped.
I asked to speak to the managing director, who told me they could only keep the child if the child continued to want to hurt himself or someone else. Since our boy knew the right words, he had to come home.
The next day, as I painted a closet, I glanced at the monitor to see him trying to shove a pencil through his ribs.
Continued
Meet & Greet…Hypervigilant Style
Photo by Peter Nijenhuis
**We’re up to $35; see below!
We’ve all seen (and occasionally participated in) a Meet & Greet post. You know, “drop your link in the comments and maybe someone will click.”
Instead of posting a hit-or-miss link, let’s change it up. Your mission, should you choose to accept it:
1. Describe your blog in nine words or less.
2. Paste a link to a post you’re proud of writing. Bonus points for adoption, mental health or parenting themes*, but it can be anything.
*With your link, please note the post theme, e.g., “Adoption,” “Mental Health,” “Parenting,” “My Happy Place,” “Honey Badgers are Misunderstood,” etc.
3. Reblog this to increase the number of participants. For every comment below, I’ll donate a dollar* to Compassion International, a fabulous organization committed to child development and rescuing kids from poverty.
*If the comment number rises beyond my ability to personally donate, I commit to raising the money.