adoption

Bio Dad Visit Success!

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We finally did it! We pulled off a bio-dad visit for Carl. It started with a closed Facebook group where I posted pictures and report cards for Carl and Mary. I invited bio family into the group, when I could find them.  Bio mom joined, but only looked at a few pictures. She hasn’t watched the video I posted of Marcus graduating high school. It breaks my heart.

“Hate me,” I want to say to her. “Go ahead. It’s OK. Just please, please watch him walk. It’s one of the few things he really wanted. For his family to see him graduate.”

But I say nothing. It’s not my place. Bio Dad, however, has been as involved as he can. He has looked at everything I posted. He’s made comments and asked questions. He isn’t Marcus’ biological father, but he watched the video and congratulated him. Bio Dad sends cards if I remind him about a birthday or holiday. He was very open in asking me to tell him when their birthdays were. That’s OK. He’s trying.

I’ve asked the kids if they would like to write a letter or make a phone call. The response is usually “no.” But I float it out there, just in case. Luke and I often say however the kids feel is fine. We support them. This is their biological family. It’s their choice. It’s fine to have more than one set of parents. It’s good to have many people who love you. The door is open.

Finding Bio Dad was tricky. The address he gave to DCF for the open adoption agreement isn’t valid anymore. Nothing we sent to the department got picked up. He had himself listed under an animal on Facebook. Let’s face it, I was looking under his name, not searching for something like “The Stallion.” Eventually I skipped through the “Friend” lists of enough relatives to find him. Waiting for him to respond was the most nerve-wracking thing I’ve ever done.

Bio Dad’s response was amazing. I couldn’t have even hoped for this. He wanted to do whatever he could to contact the kids. He thanked us for taking care of them, which he didn’t need to do. He opened up about the bad place he was in when DCF was involved. He told me about his own family history, and why he didn’t have any support when he lost his case. He never mentioned why he stopped coming to the visits at DCF. I never asked. It’s not important.

The only important thing is what kind of relationship, if any, the kids want to have with him.

Bio Dad was very nervous about the visit. He kept texting me about how nervous he was. How emotional he was. After all, its been 3 years since he saw Carl. He was so open and emotional, I started to feel like I maybe accidentally adopted a 40-something-year-old man.

“He’s going to hug you, you know,” I say to Luke, “just you wait!”

The visit, itself, was amazing. We all sat together at a McDonald’s in the mid-point of our 2 addresses. When Bio Dad saw Carl, he practically ran to him. Carl got swooped up into a big hug and Bio Dad shook with tears.  He silently cried behind his sunglasses many times. We stayed right there through the visit in case Carl needed us.  I’m happy to say that he didn’t. We got to meet Bio Dad’s new wife of a month. She was lovely. He says that meeting her and becoming religious are the things that made a difference in his life. I’m glad.

He also brought Carl’s little brother from another previous relationship. The little guy is 5 and was terrified of the whole situation. He burrowed into his stepmom’s side. He was meeting Carl for the first time he could remember. He had a little yellow cast on is left arm. Stepmom and Bio Dad both rushed to tell us it had been an accident from riding a bike. We told them we know all about little boys playing rough. Carl broke his leg playing soccer 2 years ago. They looked relieved.

After eating lunch and talking, we encouraged Bio Dad to take his boys out to the playscape. He almost hesitated to take them on his own.

“It’s fine,” I told him, “We will stay right here.”

That’s all he needed to take the two kids out and play a rousing game of tag. This was a much better visit than sitting in a DCF visit with a social worker watching. Stepmom chose to sit inside and chat with us. It was pleasant and eye-opening. She had been in foster care as a child. She was happy that Mary was getting treatment. She told me about how they always prayed for the children. She told me they prayed Bio Dad would see them again someday.

“I have a question to ask you,” Bio Dad said over ice cream. They boys came in sweating and happy for some ice cream before we left. Bio Dad looked nervous as he asked me, “Would it be alright if I posted some of the pictures we took? Can I share them with anyone?” I was dumbfounded. Luke and I looked at each other.

“Your camera, your pictures, your kids. Yes, Of course! Do whatever you’d like!”

It wasn’t all puppies and roses, though. To be honest, the kids have a history of being hurt by this father. And they never forget. He has since apologized, but some things can’t be wiped away. Yes, Carl had a good time at the visit, but he was relieved to go home. Although we were open about the visit with Mary, she adamantly did not want her own visit, and did not want to see pictures from this one.

Mary says that she is afraid of Bio Dad, but that she likes him “as a person.” For now she only wants to get letters and cards. She does not want to write back. We never lie to our children about their Bios. Everything is an open book, including the reasons they came into care, which oddly enough, social workers never told them. No matter how uncomfortable to us, we share whatever information we have. We offered Mary a visit when she gets to the weekend pass stage of her program at the therapeutic treatment facility. She declined. She isn’t ready, she tells us. That’s fine.

This visit went better than I could have hoped. Even if it didn’t, we’d still offer another to the kids. Carl had fun. We were all safe and I think our families built some mutual trust.

And of course, before walking off, Bio Dad clasps Luke’s hand and pulls him in for a hug. As they walk away I arch an eyebrow at Luke. “Told you so!”

FTTWR                                                         Vote For Me @ The Top Mommy Blogs Directory

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

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adoption, family

Cocaine Donut Mom

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I wanted to be the homemade chocolate chip cookie mom. Before the children were placed with us I practiced. I tried all different recipes. I used different ingredients. Organic flour, cake flour, semi-sweet chocolate chips and dark chocolate chips.

I practiced making cookies from scratch like it was my job. Then I brought batches of cookies to my actual job. I let everyone weigh in on the best kind. You see, I believed that having perfect homemade cookie skills was essential to being a good mom.

I wanted to be a cookie-ninja mom. I wanted to welcome my kids home with the smell of fresh cookies baking in the oven. I wanted to mix dough with my children and teach them to measure ingredients. We would wile away the long New England winters in our cozy kitchen, just baking away. Chocolate chip cookies. The ultimate comfort food. I wanted to be THAT mom.

How naive was that? I held on to that cookie dream until the kids came home. Acquiring three/sometimes four children at once is a bit like getting hit by a truck. Mary only slept for 45 minutes at a time. She and Sean both woke up screaming from nightmares all night long. Carl raged whenever I was out of his sight. He would scream and throw his food at me during every single dinner. The dinnertime meltdowns cost me many-a-meal. I lost close to 20 pounds in those first months! Carl would hoard croutons in his room to eat later. “I want my REAL mom to make me food,” he’d say.

I never slept. On the off night the house was quiet I would jolt awake terrified something had happened to the kids. I was so used to their nightmares I didn’t know how to sleep without them. Going to the bathroom started meltdowns galore. I couldn’t even pee, let alone utilize my cookie ninja skills.

At some point I gave up. It was a Saturday morning and I was dragging my weary carcass around on autopilot. We must have been out of coffee. With dark circles under my eyes, I shuffled the children into the nearest Dunkin Donuts. I figured everyone could have a donut. It wasn’t homemade comfort food, but it was something.

And then I did the bad thing. I ordered a powdered jelly donut. Gasp. Somewhere a trauma-trigger alarm sounded, unbeknownst to me. Carl looked askance at me and bellowed, “Don’t do it, mom! Don’t eat the cocaine donut! Cocaine makes you crazy!!!”

Record. Scratch. I blinked a few times. Then I glanced around at the shocked patrons all staring at me. I looked down at my disheveled clothes hanging loosely from my skeletal frame. I did indeed look the part. Cocaine Donut Mom. So I ordered a different donut.

And right then and there I gave up the dream. I gave up the fantasy. No, I wasn’t the cookie ninja mom. This definitely was not the parenting journey I expected. It didn’t matter what the white-haired ladies at the corner table thought about me. It mattered to me that Carl felt safe. Thus began my foray into chocolate glazed donuts. Which, by the way, I got to actually eat without anything being thrown at me.

Sitting in the coffee shop, eating my donut in uninterrupted bliss, I found my comfort food. Maybe we didn’t spend hours happily baking together as a family. But we did get eat our donuts (in their entirety!) without a single meltdown. It was something. It was a start. Being the Cocaine Donut Mom wasn’t the worst thing, after all.

Over the years we finally joined together on several family baking endeavors. Some were great, like our Christmas cookies. Some were a blackened mess of would-be snickerdoodles that stuck to the cookie sheet. I never again made the perfect chocolate chip cookie. But we made memories.

Yes, this is a different kind of parenting. It’s different from the path I thought adoption would lead us down. Accepting an alternative parenting journey has made all the difference. Plus, I have great stories to tell, like the time I was a cocaine donut mom!


**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

Parenting With Puke: and Other Food Issues

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Our children have some pretty significant food issues. It’s fairly common for children who come from an environment where they often went unfed. To this day we have to explain to doctors why Mary doesn’t know how to drink a beverage. She will hold a bottle or cup to her lips and chug until the entire thing is gone. Then she gasps for air and clutches her stomach, feeling sick. We have to portion out water or give her straws to encourage sipping. Because of the way she attacks drinking, Mary hates liquid and assumes it will make her sick. It’s like pulling teeth to keep her hydrated on a hot day.

When Marcus and Sean lived here they each had to know they had their own food available. For Marcus, we bought him a huge package of Clif bars at Costco. He kept it under his bed and never touched it. It was helpful just to know it was there. Sean, on the other hand, had a mountain of perishable food items under his bed. He had half eaten tubs of frosting, boxes of crackers, uncooked pasta that he ate raw. We found a molding tub of cream cheese with a spoon cemented to the middle. Sean could, and did, throw up at will. He was always eating or holding food in his hand. We never knew how severe the problem was until we cleaned out his room and found the food. Having a box of non-perishables did not make him feel safe.

For Carl, the issue is a bit different. He scarfs food down like a baby velociraptor. He shoves bite after bite into his mouth without stopping to chew or even swallow. His cheeks are puffed out to the max and he eats everything within a few minutes. If you aren’t careful he will try to move on to your plate next! When he is upset it’s impossible to slow him down or stop him. Carl will eat 5 helpings if we let him, and then promptly get sick. And then eat some more.

This is how Carl ended up with a tear in the lining of his stomach. It caused him to vomit everything, even ice chips. We took him to the pediatrician, and later the hospital for tests. I won’t lie, it was really scary. At first we just thought it was his trauma-eating. As it turns out, over time, this kind of eating can do some serious stomach damage. We try to give him small portions a little at a time. We space out snacks, meal courses, etc so he has time to digest. We make a big deal to count his “chews” and encourage him to chew really well. It’s very difficult to re-teach the eating habits a child learns in the first 5 years of life.

So I was home with the little guy all of last week. He’s 11 now, but when he’s sick his emotional age is somewhere around toddler. Because of this he was extra sweet and snuggly. He could only eat soup, jello, tea and other clear fluids. I made him tiny meals and gave him medication throughout the day. The poor guy missed field day, but no way could he go.

Call me a terrible mom, but I loved it. I got the opportunity to take care of my little guy. I wasn’t just providing care, I was providing care that was working! I can’t tell you how good that made me feel, especially with what’s going on with Mary right now. I felt like I was being a good mom. I could see my efforts pay off. And best of all? Carl and I got to hang out stress-free, and without physical danger. I’m not happy Mary is at RTC but I am happy that Carl seems so much more at ease. That’s right. Vomit is not as scary as murder.

Even with all of the vomit, Carl and I had super fun! We played CLUE, and Beat the Parents and Monopoly Deal. Papa came for a playdate and taught Carl to play Yahtzee! We read books and watched the Harry Potter movies. I rubbed his back and kept him hydrated. He is such a neat kid to spend time with. Although I love and miss our daughter, I am truly grateful for this one-on-one time with Carl. I hate the fact that it took puke to get me some individual parenting time with him.

As he grows up he will want to spend more and more time with his friends. But while we are on the cusp of adolescence? I’ll take all the parent-time I can get.

Not even puke could keep me away!!

 

**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

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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.

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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, and we snuggle, and I giver 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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