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Battle Of Wills

She had done it a thousand times before.

When Emma was younger, she would carefully and slowly roll her body down the two steps of our sunken living room, from the foyer of our apartment. But as she got older, she evolved into scooting down on her bottom, with some semblance of graded control. It was a sight to see. Her four foot, seventy-five pound, lanky frame, propelled itself by pushing off the floor with the back of her hands while simultaneously pumping her legs, in what appeared to me as a painfully uncomfortable movement, much like a caterpillar.

She never did take to the hand splints that were custom-made for her when she was a little girl, to keep her wrists straight, and to prevent the contractures, that partly defined her life. Even as a small child, she was not going to be restrained and somehow always managed to remove the limiting splints–using her teeth to pull apart the velcro. A veritable Houdini.

I marveled at her determination to get to where she wanted to go, with all of her physical limitations, as she would lower her diapered tush, first one step and then the other, bouncing and closing her eyes in anticipation of the not so soft landing.

I would spot her from the corner of my eye, as she would rhythmically make her way to the couch where I would be sitting, attempting to go unnoticed as I would to try to sneak in yet another episode of the Housewives of NY, or Orange County, or Beverly Hills or Atlanta—my one guilty pleasure. Caught in the act, Emma would determinedly pause at my feet, reach for the remote control sitting next to me on the couch, place it, matter of factly, into my hand, and, without skipping a beat, turn her head to look at the television. And even though I always knew how this story ended, I would make an unenthusiastic effort at redirecting her from her goal, by placing the remote control behind my back.

There was no dissuading this persistent, then teenager. Survival was the name of the game for Emma—from the day she was born. With every obstacle that presented itself to her, she would somehow, with ingenuity, find a way of overcoming it, by resorting to the limited skills she had learned over the years.

Precisely the reason she learned to pull herself up on the couch by planting her forearms and elbows into the cushion of the couch and with nothing less than sheer superhuman strength, throw her body up, while pivoting it 180 degrees, so that she could land with aplomb, on her padded behind next to me. The next movement involved her reaching for the remote control behind my back, retrieving it, and triumphantly, and with a deliberate gesture, placing it in my hand once again, so that I could comply with her wordless command, to change the channel to Sesame Street.

It was an impressive battle of wills, and one that I invariably lost—secretly happy that I did.

I Lost Her, But I Feel Her

Hi everyone.

I feel strange saying what I’m about to be saying. I feel my late girlfriend’s body on top of me.

Yes, you read that right. I literally physically feel my girlfriend, even though she is no more.

Doctors haven’t been able to help me with this.

It started about six months ago. She was taken away from me in a car accident. Three days later, I was in no shape to do anything or move anywhere, and I suddenly felt her. I felt her head on my chest, her arms hugging me really tight, her feet on top of my feet.

She loved doing this. If there ever was such a thing, this was our thing. I know this was the same sensation because I could feel her hair poking my chin, like it always did. She didn’t like long hair, so she would cut it really short, and it would poke me irritatingly in my chin when she hugged me like this.

The funny thing is, I sometimes did not hug her back. Just. Just because I was irritated about something or the other. I know she didn’t like it when I didn’t, but she put up with me.

And now, I feel her arms, her feet, her prickly hair, just like before. But she’s not there.

I know she’s not there but I feel it so strongly! It comes and goes, but when it’s there, it’s like she’s back. I can see there is nothing but air in front of me, but she is the air around me. I hug the air back, and it all feels real.

I am left with so much conflict about this. On the one hand, I am glad to have her back in whatever way. But in another way, I am just grieving all the time. Because of this, I just break down and talk to her. I tell her I love her and how much I miss her. But I feel like her soul is attached to me, and I’d like to free her soul.

I miss Ragini. I just wish I knew what to do with her ghost.

My Son Has Autism, Now WTF Do I Do?

I work in therapy and I can’t even spell Asperger’s. I had to google that in fact because I spell it so poorly spell check can’t even help it. Jenny McCarthy would be so pissed. But now that we are on just the “spectrum” crap, Blair is just flat out considered mildly autistic. I personally think they dumped Asperger’s because it’s so hard to spell.  But enough about that.

I have a beautiful, loving, I can’t say enough great things about him 4 year old named Blair.

Truth is, I’ve always thought Blair was different. Well, not always. I guess around 18 months is when I started my “something is different” speech. Truth is, my speech was sometimes a rage because I couldn’t believe no one saw what I was seeing. There were meltdowns. Oh the Blair melt downs. And then the Blair moods, as I called them. You could tell what kind of day it was going to be within 5 minutes of him waking up. Of course now I go back and look at videos of him as a like 8 month old and can see differences between him and Jules, for example. Not just simple differences because they are different kids. But different because Blair is…different. Blair didn’t engage with you. Blair looked at you. He looked content, but wasn’t happy all the time. He didn’t copy you. He was quiet, he was…there.

Blair’s moods and outburst over the most asinine things have caused conflict between everyone involved in his care. My dad has become so frustrated he started blaming us having dogs for Blair’s stress. My mom flat out once said she was scared that we were “losing him mentally.”

I, of course, have cried more than anyone thought possible. I’ve yelled at Adam countless times for his “oh, he’s just shy” bullshit when Blair would walk away from kids trying to play at the park or when he’d blow me off about how awful taking him to preschool was because he’d scream and growl and hold onto things to avoid other kids or leaving his regular schedule.

I thought once there was a diagnosis I’d feel relief, but that’s not true.

I answer shopped; at least that’s what it felt like.  I’ve found the good news locally is that no one wants to label a child autistic.  The bad news is that no one wants to label a child autistic.

Discovery – I am an ACON

Discovered, after 40+ years that I am an ACON (Adult Child of Narcissistic Parent)I guess I knew along that something was wrong with our family growing up, at least, with my relationship with my father, I just never knew what it was. I guess I just never knew that my “normal” was not normal.

Happily married for 12 years with 2 wonderful children, there were so many episodes with father in my adult life. Episodes between him and my wife, episodes between him and me and then the deal breaker, the last and final episode when he started on my 10 year old son. It was like something inside of me let go, something changed. I was furious at him, I was enraged like I had never been before. I thrust myself into a quest for answers, to answer the ultimate question as to why, why is my relationship with my father a complete disaster, why can’t I have a normal relationship with him?

In my search I stumbled, by accident, across narcissism. As I read the definition and characteristics of a narcissist it was like I was reading about my father. The more I read, the more I was blown away about what I had discovered. It was all there, every bit of it, all the criticisms, the one-upping, the belittling, the obsession with money, the gambling, the down-talking, the tone of his voice, the disregard for boundaries, the fits of rage, the inability to take criticism, the ego-driven decisions, the lack of common sense, the lack of empathy, the threats, triangulation, the control of information, all of it was there…. and so, my journey to recovery began. I have much more to say, much, much, more….

Still Alive and Thriving

After going through what was quite possibly the most difficult year I’ve had so far, Things are finally settling down.

I’ve lost a child, was denied access to a child and have fought all year through to get it back.

I faced some of the most horrific gas lighting abuse imaginable,  I work in a position of trust and have done so for many years and my former abuser decided that they would try and get me fired with some of the worst false accusations you could imagine.

I’m now at a point where child protection services no longer believe my former abuser and have some solid boundaries in place to protect myself.

They tried so hard to pretend they were the victim whilst I watched them send constant mixed messages, cheat on me, control every aspect of my hard earned wages, my professional life and personal life alike, and I watched my friends disappear everyday, then when enough of my support had gone they turned on my family.  They were constantly redirecting the blame for everything onto me and making me feel responsible for every bad situation they created by abusing others as well.

The final straw was when I recognized that they were trying to set me up to make the biggest move of gas lighting abuse imaginable, I’ll be the first to admit that it didn’t go as far as accusing me of Satan worship or cults where children were sacrificed, but it got pretty close and was all to try and control and limit my access to my child.

I then identified defining factors of Munchhausen by proxy in their behavior and had no choice but to try and protect my child as best as I could whilst fighting off these organizations that she used to further victimize me.

My child was ill, in accident and emergency or was at emergency appointments almost every week.  I noticed that the universal factor was that my former abuser would always press for me to have contact with HER, not my child.  When I tried to be there for my child without seeing them even under the supervision of medical professionals, I was told that it’s unacceptable and I have to see my former abuser.

I am still clearing up the shrapnel in my life but it’s back.

MY LIFE.

I’ve been studying the past year to help real victims of domestic violence as a McKensies friend, as well as help both mothers and fathers hold onto their children when courts become involved, offer practical and emotional support for the men women and children whilst maintaining my own contact with my child and jumping through those hoops.

I’m in a fairly successful band and still retain my job in a position of trust, I’ve trained as a volunteer children’s speech therapist and rebuilt all of those broken bridges from my friends and family and I’ve brushed up on my cooking skills a great deal, and I still donate blood as often as possible.

If I had tried any of this over the past years during my victimization I would of crumbled and broke under the pressure.  But now,  now I can do all of this with an ease that belies my former victimization.  Now it’s all as natural as breathing to me.

I received a shock on valentines day, It was an act that helped me realize how far I’ve come and how much stronger I am.

My former abuser sent me a valentines card…….

Are they sure about that?

I suspect that they have either the final screw has come loose, lost the ability to exert their manipulation of others and want to try again with me, or want to try and set me up again.

Well, Not Gonna Happen.

I did not build all of this to watch them break it again.

Not this time.

Find someone else to fall victim to you’re disillusion, faux perception and toxic miasma of a personality because I am free.

Thank you to The Band and Aunt Becky

I’m sorry for my silence since my last post I’ve just been so busy.

Until next time,

Stay strong all of you