adoption, family

Imperfect Family

When my daughter came home I found myself well out of my depth parenting the girliest of girly-girls. She loved pink and Disney princesses. She owned a pair of sparkly high-heels and wore them despite being unable to walk very far. She was seven. I hated those heels with a fiery feminist passion. They wreck a woman’s spine. They represent a misogynistic ideal and so on. However, she brought them with her from foster care. She loved them. They were hers and therefore taking them away would be a violation of her possessions and her past. I was trapped.

As a brand-new mom to a child already seven-years-old I struggled to bridge a divide. She’d already had seven years without me and now I needed to find a way to connect. I favored bare feet and Bob Marley over nail polish and tea sets. Light mascara and a bit of translucent face powder was the sum total of my makeup repertoire. Mary came to me asking about perfume, blush and something called “contouring.”

The boys were always easier in this way. They wanted to be outdoors exploring or working on projects. We’d all put on comfy sneakers and take off for the day to explore a museum exhibit, petting zoo, or aquarium. Inevitably someone would end up carrying Mary because her shoes were uncomfortable.

She’d wonder aloud why I didn’t have more “boyfriends” while her new feminist mom fretted about teaching her the truth behind a woman’s worth. (As an aside Luke was constantly baffled at her lack of understanding around the “marriage” concept. Poor guy!)

People would say to me, “All those boys! At least you’ve got your girl.”

I would think to myself, “Yes, but what do I do with her?? I hope I’m doing this right!”

Mary loved to wear matching clothes. She was delighted at thinking we looked the same. She said it marked us as family. We bought all manner of matching outfits in pastel colors. I happen to love long flowing skirts or dresses with flip-flops. Luckily for me, Mary picked up my penchant for hippie-clothes and Bob Marley music. It seemed like we met somewhere in the middle. Although I still gritted my teeth through “Barbie: Life in the Dream House” on TV, I found I could play actual barbies with finesse.

One of the cardinal sins in adoption is trying to order up your perfect child. Sometimes parents envision a certain kind of future with their child only to face reality  involving an imperfect child. I’m sure we all do this to an extent. We’d like for our children to take after us. Then we find we have a unique individual with their own ideas. Letting go of my peace, love and political-activism ideal wasn’t exactly easy.

One day it all came to a violent end with those god-awful high heels. You see, from the time Mary came home she would experience intense, violent rages. Mary, and the other children, were always on high alert for danger. The slightest thing could trigger a volcanic eruption from her that resulted in blood, bruising, and property damage all around. If she felt my attention was elsewhere, intense fear of abandonment would start a chain of destructive behavior.

It was startling and baffling to the rest of us. She’d begin to laugh in a loud and strange way. The laughing would reach an uncontrollable frequency and an ear-piercing decibel. Then the rage would start as the laughing turned to screaming, hitting, biting and head-banging. This could go on for hours.

The demise of the high heels came on a day like many others. It was a weekend, which was usually the time Mary found unbearable. Lot’s of close family time was difficult for her. Having a really fun time turned to intense fear and anger quickly. On this day, Luke was at work all day so I took the kids out by myself. We’d all done something fun like a trip to the park before coming home for lunch.

Spirits were high and everyone was laughing. I should have noticed then that Mary had begun the laughing sequence that never ended well. I was a new-mom though, and I didn’t. When I started preparing lunch, she couldn’t handle it anymore. She attacked me with full force hitting, kicking, and biting. She chomped into my exposed leg with the strength of a rabid racoon. Thanks a lot, flowing skirts!

Around this time I had been reading a book by Heather T Forbes that explained regulation and explosive behavior in traumatized kids. She had this suggestion that you contain the child in a room and get below eye level so they didn’t feel threatened. I took/dragged Mary into the safety of her room, speaking in a soft voice. I closed the door for the safety of the other kids. Kneeling down below eye level, I softly repeated, “you’re safe, I’m here,” while she raged.

And rage she did, in spectacular fashion. Before the adoptions were finalized we were unable to place her in a protective hold. The best we could do was mitigate the damage and wait for the on-call crisis worker to come.

After knocking over her book shelf she sort of flew at me and then BAM! something hit my head. It all happened so fast I couldn’t understand why red blood was clouding my vision. I (smartly) stood up and felt around at the wet patch on my throbbing, burning, skull. Mary stood screaming and thrashing with one bloody high-heel in her hand. She’d landed a blow with the heel of the shoe right on top of my head. I stood up and grabbed the heel while clutching my sweater onto the blood. Her rage went on for another hour and I fended her off as best I could.

By the time I was able to disengage, the storm had passed. Mary lay in a tiny 44 pound heap under her blankies. I cleaned up my head and applied ice. The emergency crisis clinician arrived to find a straitened room and a shaken mom with wet hair. Mary had gone mute and wouldn’t talk at all to the responding clinician.

This was maybe the fourth time they’d responded to a sad, quiet child and a shaking, nervous mom. I didn’t realize it at the time but so far as they could tell, nothing was wrong at all. When they asked Mary if anything had happened she would shake her head “no.”

“Was it just that she didn’t want to eat lunch?” the clinician asked, looking skeptical. I shrugged. I had no idea.

When Mary was finally hospitalized in the psychiatric ward, the therapists didn’t understand. I overheard one say to another, “Well, the mom didn’t get exactly what she wanted. She wanted a little doll to dress up and look like her. When these kids aren’t perfect playthings, the parents give them back.”

Four years ago I was stunned to realize that people didn’t believe our tiny daughter was violent and dangerous when dysregulated. At home she felt safe to let her feelings out. In public she was selectively mute, small and unassuming. People in public thought she was the sweetest thing and we just didn’t like her. It was quite the opposite. We loved her and she was beginning to love us. She was terrified.

Four years later and those high heels are GONE. Mary is still here. So is the tiny round scar on my scalp from the heel of her shoe. She may be in a residential therapeutic school, but she is in this family. Therapeutic school is what she needs for treatment. If she needed a kidney, I’d give her that. Instead, she needs intense treatment in a place she can be safe. She is still our beloved daughter. She is always a part of this crazy, imperfect family.

Luke and I did listen to Heather Forbes. We listened to Karyn Purvis and Deborah D. Gray. We learned about trauma and we continue to connect with our daughter the best we can. Mary has a psychiatric condition, though. Her trauma, like my scar, will always be there.

I don’t know what this means for our family long-term. We have a moratorium on heels now. We have the best relationship with Mary that she will allow. Maybe she thought she’d get a perfect mom. Maybe I did think we’d all have that perfect happy ending. I don’t know.

What I know is this: We have a perfectly imperfect family. For now, that’s enough.

**Names have been changed to protect the privacy of those involved

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adoption, family

The Prodigal Son is Homeless

He’s been sleeping in his car, apparently in a cemetery. Marcus is in another state, in a slum, sleeping on the street in his car. I cannot understand this choice for the life of me. Why does Marcus prefer living in his car to learning or skill to help him get gainful employment? He honestly can’t visualize his future at all.

He’ll say/shout, “I told you what I want for my future. I want MY CAR! I need to work on MY CAR! That’s what I need for my ‘future.’ I don’t have a future if I don’t have MY CAR!!!”

It baffles me and I feel as if we are always speaking a different language. Either way, we aren’t supporting him financially so that he can buy more pot and “soup up” the rusting Honda Civic from the 90s that has become his whole life.

I made a throwaway comment the day that he left. I sent him a text message (because he refused to talk to me) trying to convince him to go to his interview with Job Corps. I was so mad that he blew it off to work on his car. I said, “Unless you want to LIVE in your car…blah blah blah.” I didn’t mean that Marcus should literally live in his car. He did it anyway.

Marcus took off. I only saw him once since then. One Friday morning I found him asleep with some guy, in his car. He’d spent the night in his car, in our driveway. His bed was right there and he chose to sleep in the car. Marcus was wrapped up like a burrito in the fuzzy purple blanket I bought for him when he was a teenager. He didn’t really pack anything from his room but he took that blanket with him when he left.

Now, he calls because his car has been towed in the city where he’s been staying. He didn’t switch his license plates over from his first junker to his second. This means he was (recklessly) driving  an unregistered car when he got pulled over.

So, now he is sleeping…?

Marcus called begging for us to pay for the car to be towed to his biological dad’s house. His BD is a mechanic and tries to help Marcus on occasion. Marcus had no plan to go to his court date for this infraction, or register his car, or deal with his overdue emissions. As usual he had no plan for the future, no matter how immediate. It wouldn’t be so bad if he’d let us help him plan these things but he refuses to plan. Instead he calls and yells awful things at us.

Despite the fact that he called swearing and cursing me out, we knew he needed help. Unfortunately we couldn’t quite understand what he needed through all of the yelling and the obscenities. He is, of course, still refusing to come home. Marcus is clinging to the  phrase, “I was kicked out!”

He still won’t agree to any certificate program or apprenticeship. He is determined to…? His only plan is about his car. He says he needs to, “Get MY CAR back!”

Luke says that Marcus is like the fox. He heard a quote by Voltaire (and I am heavily paraphrasing here) that fits our son perfectly.  Marcus is like a fox you’re trying to free from a trap that bites you:

“It’s difficult to free fools from the chains they revere.”

**Names have been changed to protect the privacy of those involved.

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adoption, family

While She is Gone

So many things happen while she is gone. There are birthdays, holidays, and family outings. There is so much lost time. And yet, I ask myself: what really happens while she is gone?

Mary has been at a psychiatric residential treatment facility (PRTF) for 5 months. People will ask me, “Do you get to see her?” Yes, of course we get to see her. She isn’t in jail. We have visits and day trips and we’ve even made it up to almost 8 hours at home on a handful of occasions. Ok, maybe just 2 occasions, but we are working on it. It’s just not enough.

Luke and I travel the hour drive one-way to see her about 3 times a week. Once is for a day-trip visit. once is for a family therapy session at the PRTF. The third is for an attachment-focused therapy session “off-grounds” with a psychologist. This last one is the ONLY therapy session in which she will participate. I’m almost certain the psychologist is part wizard.

In the PRTF session she mostly screams at the clinician, Mrs. T. Mary runs away, laughs uncontrollably and then smashes things during Mrs. T’s sessions. Afterwards she asks me to take her to lunch as if nothing has happened. Instead, I’ve begun to call in for the PRTF sessions because nothing beneficial is happening during that time.

Mrs. T has decided that whatever happens in therapy will be Mary’s choice but if she won’t go to session her “level” will drop. So Mary goes and sits in the room. She screams and slams things. Mrs. T assures her they will only talk about what Mary wants to talk about. They will only do what Mary wants to do. Not being a therapist herself, Mary makes some interesting choices. She chooses a lot of yelling and foul language at said clinician. Eventually she colors some pictures about why she hates therapy. Mrs. T praises Mary and sends her on her way.

I know they care about Mary at the PRTF. Mrs. T wants her to do well. Everyone wants Mary to improve. Everyone except Mary. Maybe she is too scared to try. So all of us keep trying while she is away. Mrs. T acquiesces and cajoles to no effect.

Not so with Dr. P, the off-grounds psychologist. He calls Mary out for her avoidance tactics. He lets her know that mom and dad will go to lunch and she will stay behind if she won’t participate. After all, it’s her session. She has to finish it but we do not. Oddly, she isn’t upset by this. Instead, she responds fully. He somehow magically draws her out of her shell. She would never scream at him. So Luke and I attend this weekly session together, every week. Dr. P has Mary sit in between us to “feel the love all around her.”

Dr. P has many insights into why it’s so hard for Mary to share Mom. He is very, very good. I still spend so much time wondering: what is really happening with her? How much progress is really taking place while she is there? While she is gone, we are all safe. Are we really accomplishing anything else?

Because life is happening while she is gone. Our family is healing while she is gone. The world continues while she is gone.

https://fulltimetired.com/roundup/?vote

**Names have been changed to protect the privacy of those involved.

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adoption, Attachment Disorders

Too Young to Die


“I don’t want to die yet. I mean, I’m too young to be dead. There is still a lot of stuff I want to do.”

This is Carl’s pragmatic view on why he doesn’t want Mary coming home for visits. Why he doesn’t want to see her. He is “not ready to be dead yet.” Currently Mary is at a therapeutic program for a few months. It’s a short term program and we are working towards home visits. The longer she stays away from home, they say, the harder it will be for her to transition back.  There is a danger she will become “institutionalized.”

So here we sit, at dinner to celebrate our adoption anniversary. I’m sipping a glass of sparkling moscato. Luke is holding my hand discretely under the table. If the kids see they will surely tell us to “keep it PG!” Catlyn and Seth are tucking into their creamy alfredo pastas. We are all in a happy bubble of contentment. Except…except….Mary isn’t here. I can’t decide how I feel about it.

We visited Mary earlier in the day. She was wearing her adoption T-shirt, but hadn’t realized it was Adoption Anniversary day. She was in a good mood, hugging us and snuggling into my hair. Mary had just gotten glasses. She picked the brown ones so they would look like mine. A part of me is melting over this. 

 In all the years we had her, she never would complete a vision test. Doctor’s appointments tend to leave Mary shut-down, mute and staring at the floor. By the time the vision test came she would be entirely unresponsive, not even attempting to stand on the marked line. Don’t even get me started on the scoliosis test.

But when the nurse from the institution took her? She was fine. Mary said she “felt safe,” and that she “had been telling us” she needed glasses all along. Color me confused. It seems that her trauma is always triggered by, well, us. Being in a family, with a mom is hard. Being in an institution with strangers? That’s easy.

Her clinician says they have seen a lot of the drastic mood swings. They notice when Mary’s speech is so pressured that her words blend together and they don’t know what she is saying. She’s had to be restrained once so far, for attacking staff members who tried to break up a fight she was having with another girl. There is no way I could restrain her like that at home. I have a (possibly permanent) spinal injury, and my husband is going back to work full time. We can’t afford for him to just work the odd shift now and again. He can’t stay home all the time anymore in order to protect us from Mary’s violent rages.

What on earth will we do? After the murder planning, Carl is traumatized. So am I. Things are just starting to settle nicely. We are sleeping without the deadbolts locked on the doors. We haven’t had to secure the locks on the kitchen cabinet where the cutlery and glassware is. Things are quiet. Things are safe. I can allow myself to exhale.

But there is another side to this. The side where I see one of Mary’s little stuffed owls lying on the floor. I am gut-wrenchingly sick with missing her and simultaneously glad she isn’t here. I, like Carl, feel that I am too young to die. There is so much left to do.

 

**Names have been changed to protect the privacy of those involved.

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adoption, Attachment

What Are We Fighting For?

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You can’t fight a war on all fronts. Or so I’m told. Lately we’ve been fighting that way, though. Everywhere I turn there is something else to confront, another battle to win.

On the one hand, I don’t want to die. I don’t want Carl to die. And I most certainly don’t want to see that haunted look on his face ever again, where he says, “She sounds just like Mom G. (Bio-mom)” Carl is referring to Mary. After her 8th acute psychiatric hospital stay since 2017 began, we installed cameras all over our house. With motion sensors and night vision. We find a dog to be trained as a PTSD service dog. We find a trainor. We spend thousands, thinking “this has to work!”

After the 8th hospitalization, Mary came home with a murder plan. She’d written it down with pictures and words while inpatient. Despite our best efforts to monitor and keep our cupboards locked, she found a weapon. And she planned to find it, planned to use it, all around her father’s work schedule. When Luke wouldn’t be here to protect us. She wasn’t out-of-control. She was casually discussing getting rid of the people who cause her the most emotions. Because love hurts Mary. She fears it. She hates it.

We need more help, we tell providers. We need more help we tell her insurance company. We need more help we tell the Department of Children and Families Voluntary Services program. We need more help we tell the state Office of the Child Advocate. (That last one actually worked.)

We can’t take her home yet, we say to the Emergency Department. She’s too dangerous. We have another child in the home.  Luke cannot work because he stays home to protect the family when she is there. Carl doesn’t sleep. We’ve been putting the service dog in with him at night. “Her violent rages are increasing,” we say. That isn’t the scariest part. The part that terrifies us is when she is smiling and happy, but you find her with a knife.

We fight to get her services. She will be going to a short-term residential treatment facility. (Thank you, child advocate!) The director tells us that they are trauma-informed. They’ve worked on cases of RAD before. I’ve heard that before from providers with little to no experience. “But,”he says, “we can’t cure your daughter. Once we’ve exhausted all of our treatment options, you have to agree to take her home.” Huh?

“She’s not a renovation project,” I find myself defending her, “She’s a traumatized little girl. And, no, you can’t keep her.” But it’s said over and over again. “In cases like this we have to insist that the family agree to take the child home. If not, you may be charged with child abandonment.” What?!

“Do you know how hard we fought to adopt her in the first place? Why is this even a conversation?” So I’m battling again. To show others the good inside of her. To show them that we love her. She’s not a “bad kid.” She’s not a mistake. She’s just very, very dangerous right now. But she’s our daughter, so hands-off!

We fight to show the intensity of our struggle at the same time we fight to show the validity of our family. We fight for services. We’ve had trauma focused, in-home, and partial hospitalization programs galore. She isn’t getting any better. She’s having more intense periods of mania. No more SSRIs. We are fighting about med changes.

In the end we are fighting for her not to return/but then to return home. “What outcome would you like?” says the Residential Center director.

“Less homicidal,” we say, “less dangerous.”

If we can be safe we can handle the rest. I think. At least, we’ve managed so far. It’s probably too much to hope the girl I knew will be coming back anytime soon.

And I’m fighting with Luke. We hardly ever argue. Sure, we get upset sometimes but after a decade together, we work it out. Luke has always been my safe place. It’s just that I can’t seem to conceptualize “safe” anymore. Instead , I’m irrationally fearful. I still want to sleep with the deadbolt on, even while Mary is away. I walk Carl across the road in an empty parking lot. I’m irritable. I don’t like it when she calls Luke from the hospital to calmly argue her points on all of the reasons I should die and that “It was only a little knife.” Why even take the phone calls? So Luke stops taking calls until we can meet with a clinician. They are just too disturbing. And he is too much of a good man to listen if it hurts me.

I feel as though I’m fighting for my life. All the time. I’m fighting for Carl’s life. The hospital thinks we should live apart. Carl and I should take up a separate residence. Luke should stay with Mary and keep her safe. “You’ll have to agree to take her home” they repeat. Why do they keep saying that? Now Luke is fighting.

“I live with my wife! I live with my family!” He is fighting for me. He is fighting for Carl. He loves us. He will not have us separated.

I am fighting to muddle my way through EMDR therapy. It’s supposed to help my stress levels. Help me to cope. “But if I’m still in the same stressful situation, can it really be helped?” I ask the therapist. She has no answer.

Instead she asks, “what would you like the outcome to be? How would you like to respond to these incidents?”

“How would you respond?” I ask, “If someone was planning your death?” The therapist just shakes her head. She doesn’t know. Nobody knows how to do this.

And I’m still fighting back pain. My injury has nothing to do with Mary. It happened at work. And yet, it has everything to do with Mary. She cannot be near me so Luke always has to be home when she is. For safety. The neurosurgeon tells me that I will “probably never be asymptomatic” because my “reaction is very rare.” We won’t know for months. Mary worries that I will die. It’s better if she can control when that happens. That way her grief can’t surprise her like it did with Mom G. So Luke has to fight to keep Mary away from me. We literally can never be alone together. So even if I’m not dying, I’m slipping away from her. This only feeds her fear.

At the same time I fight to help Mary, I’m fighting to regain my own balance. I’m fighting to remember that I’m a good mom, a good wife. Mary is still mad at that other mom. The first one. Her biological mother who hurt her so much. It’s just that, well, why do I always have to pay the price? Why does Carl? Because she assumes I love him more. Because I talk to him and this makes her panic. Therefore I should watch him get hurt. To pay for all the hurts Mom G doled out to Mary.

So I’m fighting. We are all fighting a war. But the question is, what are we really fighting for?

**Names have been changed to protect the privacy of those involved. 

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adoption, mental illness

Mania and Matricide: It’s Not OK

cdadlock

Installing deadbolts

It’s not OK to hit me. It’s not OK to bite me. It’s not OK that I have a scar on my head from where you split it open with a high heeled shoe three years ago. It’s not OK that our son has to live at my parents house because he isn’t safe here. It’s not OK for you to plan on stabbing me and stabbing your brother. Not with a kitchen knife OR with a bottle opener.

It’s not OK that we’ve installed cameras with motion sensors and night vision in all the public areas of our house. It’s not OK that we have combination locks on the cabinets where we keep all the “sharps.” It’s not OK that we had to install deadbolts on the doors to our bedrooms. It’s not OK that the motion sensor alarm goes off to wake me up at 12:30 AM when you are wandering the house in search of a “stabbing weapon.”

It’s not OK that you told your therapist today that “Mom has to die!” and then threatened to kill yourself and your brother. You’ve been planning this ever since your last few hospitalizations. Last time they called you “depressed” and started a course of SSRI medications. Not OK!

When you came home your depression became a manic state. You became a child with pressured speech so fast that you stopped using consonants. You started your “hyper phase,” which means you never sleep. You laugh harder and harder until you are screaming and then breaking things. It is not OK that we had to “toss” your room and remove all of the hard furniture and sharp objects. It is not Ok that your service dog found a jack-o-lantern carving knife and gave it to us (well, actually it’s very OK with me that the service dog probably saved our lives.) Did you find it during a night of wandering around the house? Your hand was always holding things under your blankie, ever aware of the cameras. This is not OK.

dakota1

Dakota Blue, the service dog

You want to know what else is not OK? It’s not OK that the inpatient doctors refused to call your PHP, your psychiatrist, your trauma therapist, or your in-home service team. It’s not OK that they sent you home with an active murder plan and a spiraling state of mania that escalates into more grandiose and diabolical schemes. It is not OK that the state’s voluntary services program we applied for does not consider planning murder to be “clinically acute” enough for a short-term residential placement.

There are some other things that are not OK. It was NEVER ok for you to be neglected as a baby. It wasn’t OK that your pediatrician never reported to anyone that you were in the 12th percentile for weight and selectively mute. It is NOT ok that DCF had been involved with your bio family for 10 years before removing all of you. They were getting hotline calls before you were ever born! It is not OK that any attention you got from your bio mom often became abusive. It is not OK that you lived in terror and learned how to survive the ever-rotating bevy of strange men in your home.

It is NOT OK that I wasn’t able to be your mom in the beginning, when the bad things were happening. It’s not OK and it is not your fault.

Here is what is OK. It is OK that we knew about your mental health concerns when we adopted you. We chose you because you are more than a diagnostic label. You are an amazing girl. You are OUR girl. It is OK that you need to be somewhere safe right now until you stabilize. It is OK to need medication to help you do that. It is OK to grieve the first mother you ever had. God, I wish I could give some of that back to you. The good parts at least.

Our family is going to be OK. It isn’t easy getting there. Yes, we “chose” this life. But I still say we chose the best children. Nothing in life is easy. The best things are hard. I’ve seen parents with profoundly disabled children flourish. I’ve seen severely autistic children learn to read. So yes, we will be OK. It is OK to decide we are not going to try for a biological child. It is OK to stick with the family we have.

it’s OK that it takes an attachment-disordered child a long time to overcome the fear of love. It’s Ok that you inherited some of your bio mom’s mental health concerns. It’s OK because you will never struggle on your own the way she had to. It’s OK as long as we can all stay safe. And I pray that we can. We have done everything in our power. The rest is up to you, sweet girl. Don’t doubt yourself. Mental health can be a manageable illness. Love will always be there for you. No matter what.

ycameran

night vision camera

 

**Names have been changed to protect the privacy of those involved.

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adoption, Attachment Disorders

If I Die Before I Wake

I pray the lord my soul to take. I wish these were just the words of a bedtime prayer. In my case, these words are real. If you’ve been following my blog, you know that our children have experienced an intense level of unspeakable trauma. Luke and I know this. We know how to parent therapeutically. We know how to get as many services as possible for our daughter. It doesn’t matter. She is a real danger to me and to her brother right now.

Our daughter has learned to survive. Her current diagnosis are PTSD-dissociative subtype and Reactive Attachment Disorder, with periods of psychosis. There is a lot of chatter about the RAD diagnosis, which I won’t get into here. Because I don’t care. Whether it be Developmental Trauma Disorder  (DTD, which never made it into the DSM-V) or RAD or PTSD or DMDD or any other diagnosis she’s had, it doesn’t matter. She still wants to kill me. A mother’s love is something she craves so badly that it hurts her. It twists her happy feelings into anger and possessiveness.

It all started the month we needed to buy her bras. She’s only 10 but here comes puberty. And so it began. In with the bras. Out with the effectiveness of her medication. She began hearing voices. She started to journal about my death. She began to tantrum and scream and fight invisible foes that only she could see. Oh, my dear little Mary, how I wish I could fight them for you.

Her love for me is desperate and all consuming. She needs me every second of every day. If I take a shower, she tantrums, if I leave the room, she explodes in a fit of rage. If I ask an innocuous question such as, “Do you like your new shorts?” She hears, “I hate you. I no longer love you. I am abandoning you.” When I turn to her brother for a momentary comment, she attacks. She will circle me and chase me with her little fists flying. She is trying to hit me in the spine. She will cripple me before allowing me to speak to Carl. So far, it hasn’t worked.

“If I can’t have you, ” she tells me, “no one can. I will stab us both.” In the night or early morning, she will loom over the bed, watching me sleep. “Mama?” she whispers, “Do you love me?” Of course I do. But I can never show her enough to quell her fear of losing me. She will make comments on my facial expressions. Why did my eyebrow twitch? Why did I move my top lip? Am I trying to get away? Have I stopped loving her?!The last 3 years of Trust Based Relational Intervention made all the difference, until now. TF-CBT made all the difference. Until now. Her anti-psychotic medication made all the difference. Until now.

The worst part is that it becomes unpredictable. We play mirroring games,we snuggle, and I give her all of my attention. Our time is spent connecting. As close as I stay to her, and as much love as I provide? I can never guess when a momentary glance at another person or thing will invoke her uncontrollable rage. We keep our knives and “sharps” locked up. You need the combination for a screwdriver in this house. Only, she finds other things. She shows me a bottle opener I’ve overlooked.

“You know this is sharp enough?” she casually quips, “I could stab you with this.”

The part that gets to me is how she discusses my murder without any observable emotion at all. Her brother tells me that earlier that she’s tried to figure out the combination for the lock on the knife cupboard. We only use plastic silverware in our house now.

As far as I can tell, nothing has changed. Nothing except the onset of puberty. Her intense violent rages happen every day. She injures herself most frequently.  She rips out her hair or punches herself in the face. She screams about murder. And blood. And the death of everyone on this planet who has ever hurt her. The bio-mother who abandoned her and hurt her. The mother she has now who sometimes needs to shower.

She is being released from the inpatient psychiatric hospital for the 5th or 6th time tomorrow. I’ve lost track. We have in-home services. We have an amazing trauma therapist who has worked with her for 3 years. We have a parent therapist for Luke and I. We have a partial hospitalization program set up that she has used more than I could even count over the last 3 years. There aren’t anymore services, unless the state agrees to help. Her medication no longer works. Today the inpatient hospital program told us they are releasing her tomorrow because there isn’t anything more they can do for her on the unit. Ever.

We’ve called a meeting with all of her providers for safety planning. We have PHP, Trauma team, And IICAPS (Intensive In-home Adolescent and Psychiatric Services) all concerned for safety is she is home. I miss my girl. I want her home. I’d just like to remain alive for her childhood. She hasn’t managed to truly hurt me yet, beyond a few arm and leg bruises. She hasn’t hurt Carl yet. It isn’t for lack of trying. It’s because Carl and I are too quick. We lock ourselves away and call for help.

Luke and I are doing the only things we can do. We are installing security cameras in all of the common areas of the house. Everywhere except for bedrooms and bathrooms. We need to objectively see what is happening. It’s entirely possible that we are unwittingly triggering her in some way. It is entirely true she doesn’t want anyone to see the things she does in the privacy of our home.

It is also highly probable that she’s spent a lot of time talking to “Josie” the “ghost” who orders my death (and possibly that of her brother.) The therapists in our home see her mood fluctuation and dangerous actions. So does her long term trauma therapist. But to most other clinicians? She is the sweetest most charming girl of all. She has always had to be this way, in order to survive her biological home. My Mary is a fighter. A survivor. For this, I am proud. I only wish she didn’t feel the driving need to survive being loved. 

Mary flipped out and began to yell at us and her inpatient therapist in the hospital today. She doesn’t like the cameras. She doesn’t want others to see her violence and destruction. She doesn’t want anyone to see her try to hurt Carl or try to attack me. When we don’t make progress with her on-call crisis team, we call 9-1-1. She will scream at the police and yell at the EMTs, but they never hear her plan my murder. Once we get to the psychiatric ward she is completely calm. Perhaps the video will help us to show what happens. After all, she only threatens or attacks those she loves the most. This kind of deep attachment-related trauma won’t be seen on a psychiatric ward. She simply does not require or crave deep relationships with revolving staff.

What she really needs from me is proof of my unconditional love. I try to give this as much as I can. Is it enough? It never is. What she is getting is 24/7 surveillance. Just in case. Because our daughter is trying to literally love me to death.

So if I never blog another post? Well then, I guess you’ll know why. 

yletter3

**Names have been changed to protect the privacy of those involved

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