Mental Illness

darnold1975

Silencing The Lambs

The Silencing of the Lambs

3.16.15

“What makes psychopathy so different, so surreal…that it knocks her head off?  The inability to wrap her head around the emotional-physical-spiritual-sexual gang bang that just happened when she thought she was the most wonderful person.”

—Sandra Brown, Women Who Love Psychopaths

I was trying to decide on a quote this morning for this particular blog post about trauma that would cover the spectrum of how trauma effects different developmental stages from a personal perspective.  While quite blunt, this quote pretty much describes the ‘rape’ on so many levels of each of my personal traumas.  When people ask, “If things were so bad, why didn’t you leave? Or, why didn’t you just tell someone what was happening?”  Honestly, I just have to see and understand that I’m talking to someone at that moment who doesn’t and might not ever understand unless in that position themselves.  Individuals who have never been abused or been so scared that the last thing they would or could ever do is tell the ‘little secret’ to expose their perpetrators, can’t comprehend that level of fear.

Keep in mind that the ‘little secret’ about my molestation by our preacher’s sons was mentioned in passing only a couple times until I told what happened, not even in detail, less than 10 years ago.  That secret I had been holding since I was a 5.5 year old child.  Why do kids do that if they know and are confident that their parents can help?  The problem is not with the child or the parents.  The problem lies with the perpetrators.  If the perpetrators are the parents, then that’s a separate topic.  Even when I got older and new no physical harm could come to me, the seed of fear was planted many years ago.  All I knew was that the topic scared me.  I knew what had happened through broken memories.  But, I was completely detached emotionally except for the emotion of fear.  My parents being the very loving and understanding couple that they are were revealed additional pieces of that time in my life last summer for the first time.  Can you imagine how they felt knowing some additional information about things that transpired?  Then how do you think, as a child, I felt with it being done to me?  The fact that they were connected to religion has always had an influence on my view of religion and religious figures.

In my abusive previous relationship and consequently a marriage, I kept holding on to the false hope that one day I would again be in the relationship with the person that charmed me.  I was so young and naive that I couldn’t see what was happening to me every single day.  His grip just became more and more tighter emotionally until I had been convinced that I was too stupid, dumb, uneducated, ugly, retarded, unwanted by anyone else and whatever else he could come up with in the moment to call me that I felt too weak to be able to stand on my own two feet.  My view of survival was…..well….him.  I was also extremely scared, at that time, of the repercussions of his or his family’s anger.  But, he had his own techniques about how he would ‘raise’ me as his wife.  He just didn’t know that there was a term called gas lighting that would describe parts of his abuse.

A very common form of brainwashing in which an abuser tries to falsely convince the victim that the victim is defective, for any purpose, such as making the victim more pliable and easily controlled, or making the victim more emotional and therefore more needy and dependent. {You’re reading “Definition of Gas lighting” by J. E. Brown.}

Often done by friends and family members, who claim (and may even believe) that they are trying to be helpful. The gas lighting abuser sees himself or herself as a nurturing parental figure in relation to the victim, and uses gas lighting as a means for keeping the victim in that relationship, perhaps as punishment for the victim’s attempt to break out of the dependent role.

Here’s an example…If an abusive person says hurtful things and makes you cry, and instead of apologizing and taking responsibility, starts recommending treatments for what he or she calls “your depression” or “your mood swings,” you are in the presence of a gas lighter.

So, next time, when someone says, “If it’s true, why didn’t they tell?” or “Don’t feel sorry for someone who just stays in a situation like that!”  Understand, that there is so much more going on psychologically that you nor anyone else who’s never experienced brainwashing can comprehend.  True the victim does protect the abuser most of the time.  Trust me…..”IT’S OUT OF FEAR.”  This is how perpetrators ‘silence the lambs.”

Mentally and physically, the effects of 14 years of ‘gas lighting’ took a big toll on me.  My ‘alters’ protected me from feeling much more of the abuse than was felt.  Did I develop maladaptive coping skills from a very young age?  Yes, of course.  They worked well at the time to help me survive some of the horrific traumas of my life.  Now, they just interfere with daily life.  PTSD, social phobias, OCD, rages, flashbacks, body memories, etc. are what my days and nights consist of these days.  Life is better on some days rather than on others.  This, however, are the effects of a lifetime of abuse perpetrated on who ‘had it all’ and became a ‘head case’ over time.  Look at the events of many forms of abuse in my life and tell me who were and still are the ‘head cases?’

Dissociative Identity Disorder is in no shape, form or fashion an easy thing to deal with on a daily basis.  It’s scary as hell for me most of the time.  I won’t nor can I even begin to imagine what it’s like for my wife.  Our son, he’s learning on a different level all of Momma D’s parts.  Every single day our family is in a battle with this disorder.  On an individual level, we’re in a war to put the pieces of the memories back together and deal with them as they should’ve been dealt with many years ago.

Every morning, as long as I choose to put one foot in front of the other, they don’t win.  The day I lay down directly or indirectly in a permanent manner is the day they win.  I think you know enough about me to know that I come from a long line of coaches that demanded and would accept nothing less than winners.  ‘Winners’ in their eyes were more than just numbers on a scoreboard.  There’s only one way I know how to operate….”Get knocked down 1000 times.  Get back up 1001 times.”  This too is a gift.

This lamb is no longer going to be silent.  Abuse is real.

#Thispuzzledlife

darnold1975

Happy “Legal” Anniversary

Happy “Legal” Anniversary

2.25.15

 “If someone could reach into my chest and tear out my heart and turn it into a living, breathing person, “Melody” would be it..”

– Airicka Pheonix

February is a month on my calendar that will always be remembered specifically because of Sarah’s passing.  There are very few dates that I remember that hold so very close to my heart.  Mel and I have been “legally” married for 4 years now.  I really don’t know what the exact date is not because marrying her wasn’t important but rather that was the day that the government said we were married.  The horrible date of May 17, 1997 when I legally signed my own “abuse warrant” by marrying my “EX” husband, was replaced by a beautiful date of May 28, 2007.  This was the date that Mel and I married each other in our hearts.  There are soul mates as friends and family.  Nothing can compare to soul mates with the right spouse.

We were instantly friends and devoted to each other.  I have always been one where the term “friendship” isn’t just thrown around like a household word.  There was something different about her and I knew it but was afraid to admit that I loved her.  Firstly, I hadn’t stepped out of the elusive closet as being gay.  All I knew was that there was this person who I was finally “safe” with both emotionally and physically.

I told her at the beginning of our relationship that I had a lot of emotional baggage from a very long and very abusive relationship.  She didn’t care.  She loved me for me and everything that would come with it.  I’ve tried pushing her away in every way possible to prove to her that I’m not worth loving.  I was someone’s “sloppy seconds” after a 14 year stretch.  I felt as though there was nothing good left of me.  I knew that I could be her friend, but “marriage” scared the absolute hell out of me.

I had a hardness about myself that was meant to keep people away.  For some reason, she had me melting like butter on the inside.  I knew how the rumors, comments and bibles would be thrown at us as a couple.  I had dealt with that for many years and really just didn’t care.  This was a whole new experience for someone that I loved dearly.  I told her I could handle it again and I tried to help paint a picture of what this would look like as word got around.  She didn’t care about that either.  She just wanted to be with me.  Needless to say, I just couldn’t understand that.  What I had just experienced for many years was totally the opposite.  My idea of a “marriage” was one that had nothing but fear attached to it.  My thought was that no one is accepted for who they are without strings attached.  And once you’re legally married, that means you’re property.

Things have been difficult to say the least about us being a gay couple.  People were not going to be happy for us because we each had found someone who loved and respected us.  To put it quite bluntly, our genitals were put on display instead.  As you can imagine, our families were not thrilled.  I actually think my mom went and put her head in the oven and turned it on.  Not really, but pretty close.  Even at the thought of being rejected by family members couldn’t deter us from wanting to be together.  Have she and I both lost “friends” and “family” because of our relationship?  Yes, of course.  However, neither one of us are responsible for their feelings nor how they choose to act.  We CAN determine whether or not we will be an audience to their ignorance and hatred.

Six months later, in the privacy of our house where we living together, on Christmas Eve, I proposed and she said YES!  We wanted to get “legally” married and have children.  We had no idea what all was involved both financially and legally to make this all happen.  She very eagerly said that she had always wanted to carry a child.  I very eagerly said, “Good because I didn’t.”  I wanted to be a mom, but I had no desire to be pregnant.  My ex-husband took the joy out of wanting to start a family which turned out to be a blessing in disguise.  We didn’t have to really tell anyone because you could just see the happiness that we both shared.  We also didn’t have the luxury of proclaiming our engagement because of such conservative views in that area of the country.  And so the journey of being each other’s only support when it came to our relationship began.

My mental health issues seemed to get somewhat better from just being in a supportive environment with someone that genuinely loved me.  We were both in graduate school and that was our first priority to finish.  What was becoming increasingly evident was the PTSD that had developed from a lifetime of abuse.  The safeness that I felt with her slowly started to reveal just what kind of damage had been done.  All I wanted to do was finish school, get as far away from that area of the country and start a family.  So, in June of 2009, Melody and I headed out to Albuquerque, NM to begin a new life.  We didn’t know how anything was going to turn out.  We just wanted to live life as a couple without all the stares and harassment.  That, I can say, has happened since we moved west.  Do we both miss friends and family? Yes more than anyone will ever know.  Moving back there would come at a cost that we’re just not ready for as a family yet.

We would soon realize firsthand what the long term effects of abuse would manifest.  She was fortunate to get a job with a company that provides fertility insurance.  This was how we would make our dreams of having children a reality.  On December 3, 2011, our little 5 lb preemie baby boy was born.  Here we were as brand new parents to a preemie that we knew nothing about.  We were out here by ourselves and had just entered the world of parenting.  No one could’ve ever prepared either one of us for the feeling of having to leave the hospital without our baby boy.  Every day I would drop Mel off at the hospital to spend the day at “Camp Marshall” while I went to work and then pick her up on the way home from work.  Mentally, I couldn’t handle the thought of losing our newly born son so I just avoided seeing him at all costs.  I was terrified of our son dying and tried to distance myself. This I now regret.  We were both on auto pilot in different ways.

She continues to be the same very sweet and kind hearted woman that I initially met.  She has a beauty within her that is hard to find in most people.  She loves me despite my mental disorder and continues to want nothing but the best for me.  What she and I have been through as a couple and now as a family is more than a lot of couples go by themselves in a lifetime.  We can read each other like we’ve been together for 30 years or more.

People often wonder how we have made it as a couple.  The truth is, since the very beginning of our relationship, we have always had to depend on each other for support.  When you’re 18 hours from where you were raised and have no desire to go back to small town living, you’re forced to sink or swim.  We have struggled both emotionally, physically and financially just like “straight” couples.  We are in the process of raising a very energetic, superhero of a kid that only knows one thing….he is loved by his mommies and that he’s not going to have a baby “sisser” much to his displeasure.  Mel melted my heart when I met her.  Now 8 years later both she and our son continue to melt my heart.  The way I try to make sense of a deep traumatic past regarding a marriage is that there will always be challenges in any relationship.  Had I not had a horrible and abusive marriage, I wouldn’t be able to fully understand how my mom and dad have their own loving connection.

Thank you, Melody Landrum-Arnold for just being you!  Thank you for continuing to love me despite the hatred for myself.  Thank you for helping to make our dreams of becoming mothers a reality.  Thank you for always having my best interest in mind while we walk this treacherous road of trauma recovery side by side.

My mom always told me growing up, “If you find a man a tenth of what your daddy is, you’ll have a good man.”  My answer is, “I did find HER.”

#Thispuzzledlife

darnold1975

Mel’s Corner: The Diagnosis

Mel’s Corner: The Diagnosis….

Often times I can be asked questions about how it is living with a spouse with dissociative identity disorder, well let me assure you it’s never a dull moment.  When I met Dana over 8 years ago and we started our relationship just a few months after that, neither one of us knew she had DID.  She had been given many different diagnosis at that time and even had someone give her a rule out of DID, which we quickly dismissed, she just didn’t seem like a “Sybil”.  The first time I met an alter, I had no idea.  I thought it was just a PTSD flashback.  There would be 6 years pass before the official diagnosis.  The latter of those years proved to be very challenging.

   I’ve learned to appreciate each alter and the specific needs and talents they bring.  For instance, there is only one alter who likes ketchup, everyone else hates it and often blocks the alter who likes it from getting ketchup.  I learn likes and dislikes when it comes to food, and there have been times that one requests a certain meal only to have another come out while I’m cooking or we are eating and decide they want something else.  I’ve learned to cook what Marshall and I want and that usually works out.

   In the early days of diagnosis, there was one alter who had no idea who I was, but that has been the only one who had no idea  of me.  Now that’s not to say that I’m the “spouse” to everyone.  To the littles, I’m “Momma Mel”, to others “I’m a friend”, and even others see me as ‘the one who takes care of Dana.”

   Around the start of 2012, Dana started having large gaps of time missing and often times during this time there was a lot of aggressive/ angry behavior.  At one point it was thought she might have a seizure disorder.  We had started psych medications to stabilize her mood starting in 2010, however if a medication worked, it only worked for just a short time.  We even tried lithium and ended up in the hospital one month prior to our son being born for lithium toxicity.  That was one scary time.  Even the mental health system was no help.  We were on our own trying to figure this out and get help that was desperately needed.

  In September 2013, when dissociative identity disorder was first given as a diagnosis, I was a bit in denial.  I had to take everything in and then decide for myself based on the research and facts, did this diagnosis fit?  Having a masters in counseling my first go to was to see if Dana met criteria as listed in the Diagnostic and Statistical Manual.  I kept an open mind and I started to consider that this might be correct.  The more I met alters and got to know them, the more this diagnosis made sense.

   Most people would have no idea that Dana is a multiple.  In fact I would say unless we came out and said it, most people wouldn’t have a clue that she is a multiple.  The switching is very subtle and sometimes it’s not until later that I put it together that I’ve been talking to someone other than who I thought.  They like to try to trick me into thinking they are someone else in the system at times.  I’ve learned to adapt but even now I have moments of difficulty.  I’ve been told that the roughest time is in the beginning and the system will settle down and things will get much more manageable.  I’m starting to see that take place, I think in time we will learn more about how to deal with this disorder.

#Thispuzzledlife

darnold1975

Out Of The Darkness, Into The Light Part2

Out of the Darkness, Into the Light Part 2

1.29.15

“I want everyone that has been abused by someone in their childhood to know that you can get past it. Having DID is not the end of the world; it’s the beginning of your new life. DID allows the victim of exceptional abuse the ability to “forget” the abuse and continue living. Without it, I may have gone crazy as a teen and spent my life in  a psychiatric hospital.” 
― Dauna Cole, A Shattered Mind: One Woman’s Story of Survival and Healing

One of the major issues with this disorder are what most people refer to as ‘alters’ or other personalities.  What I’m going to try to do is to paint the picture for you in a way that I’ve been learning how to understand this.  So, imagine you have an apartment complex and each person has their own room.  Except in these rooms, there are horrible memories that are behind doors and no one can get in without a key.  The only people that have these keys are my therapists and my alters which help keep anything else from hurting me.  This is what has protected me throughout the years.  However, some of the coping strategies that worked then DO NOT work now.

Alters can also range in age depending on at what age the abuse occurred.  As dysfunctional as things can get at times the alters as a whole are referred to as a ‘system.’  Until consciousness together can be shared, there might always be memory loss.  The amnesic episodes are, at the very least, scary as hell.  The memories that I often have include only flashes of pictures of the day or days. The information date, time and situation is usually not available.

Alters and systems are as individual as a finger print.  There is no ‘cookie cutter’ way of treating DID.  The most important thing to me hands down is the relationship with my therapists.  Without that relationship, recovery is futile for any issue or disorder.  I trust my therapists enough to take me into the depths of the most terrifying events that have ever happened to me.  This relationship that has been  allowed to happen, as close to trusting, as possible has taken 2 years now with one therapist.  However, both the ups and downs of these relationships has lead to the progress now being made by leaps and bounds.  Painful as this process is, I can only hope that things actually get better.

The tenets in these rooms represent parts of the person you know as Dana.  I will not get into discussing how many or their names.  I can tell you that while growing up with some of those reading this blog alters were already formed or forming.  Not only do these alters hold memories, but they also function in different ways.  However, sometimes the problem with the alters is that they function completely independent from the individual known as the ‘host.’  This is usually the mood swings that you might see. Alters develop out of traumatic events and sometimes more than one during a single traumatic event.   Just to put to rest for those that don’t know my parents, no they were not any part of the abuse.

Alters actually develop when the brain compartmentalizes the traumatic event, memories, etc.  The trauma is so overwhelming and the mind and body both have to survive, that the only way the individual knows instinctively to survive is by developing a new alter even though they may be unaware at the time.  Often times, it is many years down the road that survivors even realize that they have alters.  Therefore, many survivors are trapped in the cycle of the mental health system being misdiagnosed for years and much money spent on treatment for the wrong diagnoses.

Often times, many people say, “I’ve been through worse things and I don’t have alters.”  The only answer I have found is that what’s traumatic for one person may not necessarily be traumatic for another person.  There is also a genetic predisposition to being able to dissociate.  And dissociation is key to the formation of alters.  What is known is that trauma of any kind effects the brain permanently.  Severity depends on how long and what type of trauma was occurred.

You can most definitely have PTSD without meeting criteria for DID.  DID cannot exist without a diagnosis of PTSD since that is a large part of how the disorder forms.  DID also usually always entails some form of early childhood sexual abuse although ‘splitting’ in adulthood is uncommon.

“Another of the difficulties of having DID is the denial. DID is a disorder of denial. It has to be because if the original person knew about the alters and felt their pain, they would either go crazy and be hospitalized permanently, or would die.” 
― Eve N. Adams, A Shattered Soul

#Thispuzzledlife

darnold1975

Out Of The Darkness, Into The Light

Out of the Darkness, Into the Light Part 1

1.1.2015

 “Dissociative parts of the personality are not actually separate identities or 
personalities in one body, but rather parts of a single individual that are not yet 
functioning together in a smooth, coordinated, flexible way. P14” 
― Suzette Boon

Since this begins a new year, I thought I would start it off with a ‘boom’ of reality from our world.  The topic that I will discuss is one that has such stigma attached to it that it’s has taken me months to muster the guts to discuss it.  This is a topic that hits home in the best/worst kind of way.  I’ve written for months now explaining some of the many symptoms that I experience mostly on a daily basis.  2014 was no doubt one of the most difficult for me, Mel and Marshall.  However, we as a family including my brother have shed tears together, as well as, have a lot of laughter. I have also smoked a ton of medical marijuana just to be able to live day to day.

I figured that a few months ago when I ‘came out’ out as a medical marijuana consumer, the thought crossed my mind that even though people can be cruel when it comes to mental illness, that since this blog is about MY healing I would ‘come out’ about my particular illness.  Many have read my blog since day one and for that I thank you.  I would also like to say that while reading this particular post that you just keep an open mind.  I’m not going to try to change your opinions or perceptions of mental illness.  I’m simply going to try and paint you a picture of mine to the best of my ability.

I have Dissociative Identity Disorder (DID).  Now for those with no therapy background, I can tell you that this is the same thing as Multiple Personality Disorder.  And now your opinions and thoughts begin to race. The only references that most of you have are those of the books/movies The Three Faces of Eve and Sybil.  Hollywood did a horrible job painting a picture of what those of us with this disorder look like and how we function on a daily basis.  Guess what?  I’m still the same Dana that you grew up with and loved.  I just have a world that has formed inside my brain that I didn’t realize everyone didn’t have.  I didn’t question it because to me that has been my normal.  Does this diagnosis make me ‘crazy?’ Should it make you fear for your family’s life if I happen to be around? Does this make you want to run as fast as you can in the opposite direction?  I can promise you that all of that energy would be wasted.

The symptoms that I have mentioned in other posts are all true and are a part of daily life for me.  I can’t tell you what it’s like living with a spouse with this particular disorder because only my wife can answer that.   I can tell you that it’s the most intricate puzzle I’ve ever had to try and figure out.  Having only had this correct diagnosis for almost 1.5 years we, as a family, have had to adjust.  We were already adjusting prior to Marshall being born.  His birth somehow set off a bomb inside my brain that retriggered everything that has happened to me.  Not his fault or mine, just our reality.

With both my wife and I having Master’s Degrees in Counseling, we were baffled when we never even considered this diagnosis as one that would fit.  Even in graduate school, because of limited time to study the Diagnostic and Statistical Manual of Mental Disorders we didn’t see the signs.  If you want to know why we had limited time to study on this manual, just take a look at it one time and you’ll see that it could take years to be taught thoroughly and it’s like computers changing all the time.  This diagnosis is still part of a great debate about whether or not it’s an actual diagnosis. I can’t answer for other families but for our family it’s very much a REAL diagnosis.

Some people have, in fact, asked Mel if she felt safe around me with Marshall.  The answer is always the same….yes.  There’s a lot of self education we’ve had to do because of the stigma within the mental health communities, as well as, those outside that community.  We don’t have all the answers yet to how and why and neither does science. I can tell you that the very slow journey of recovery from a lifetime of trauma actually began when the correct diagnosis was given.  Now I finally had answers to why sometimes I would answer myself and had what I thought were ‘loud’ thoughts.

To see me today, I’m the same goofy ass, class clown that was and still is friends with Levi Pierce.  I have scars on my arms.  It’s nothing to be afraid of, it’s how I survived.  You don’t have to be afraid to have your kids around me. I’m not going to cook them and eat them.

DID, as I’ll refer to the diagnosis from now on, is not near as scary as the picture that has been painted.  Does it have scary moments? Of course.  So does Bipolar, Major Depression, Schizophrenia and any other disorder.  This disorder requires a very patient and understanding spouse, as well as, professionals to be able to deal with some unpleasant moments.

The title of my blog “This Puzzled Life” is all about putting these scary pieces back together enough for me to be able to enjoy doing what I love…..helping people.  Once piece at a time is how I’ll learn to live with this disorder.  Trial and error is how it’s been for almost 1.5 years now with the correct diagnosis.  Prior to the correct diagnosis it was and still is at times a total nightmare.  Also, life continues regardless if I have a disorder or not.  Friends and family still pass away which can complicate things.  But, this too, is just the way life operates.

 With very patient but firm therapists, I’m finally being able to look very closely at some of the horrors.  The ‘alters’ or other personalities, if you so wish to call them, have their own story because they were created by the mind at very key times in the abusive history.  Alters together are called a ‘system.’  Each ‘alter’ has his/her own function within the system.   Each person with DID has a system much like that of a finger print.  Not every therapy works the same like a cookie cutter.  Do not be afraid to ask what you don’t understand.  Your fears come from what you don’t understand.

“DID is about SURVIVAL.  As more people begin to appreciate this concept, individuals with DID will start to feel less as though they have to hide the shame.”

–Anonymous

There are also no psychotropic meds that are specifically designed for this disorder.  This also explains why for the first 3 years of seeing a psychiatrist none of the meds worked for an extended period of time.  Some antidepressants, anti-psychotics, axiolitics work well for some alters and not for other alters.  I was taking Parkinson’s medications for the side effects of other medications while feeling horrible from the side effects.  So, that represents toxicity to me.  My psychiatrist offered as a last resort the state’s Medical Marijuana Program because of all the mood swings, PTSD, hallucinations and every other symptom I would have at that time.  Now believe what you want about medical marijuana, but I can personally tell you that that medication as it is so treated, is one of the reasons my wife, son, friends and family still have someone they love living.  The memories of the trauma alone are more than I can handle.  The effects of PTSD steal your sanity one image, smell, thought or sound at a time. The body memories while very painful become a little more tolerable with the marijuana and acupuncture.

This is why I’m also so big on people recognizing and working on their own trauma.  That way people like me who set out to enjoy life don’t have to wait 40+ years to understand what that means.  I’m representative of people who were too proud or stubborn to face their own demons.  This too was not a “choice.”  I understand the concept of ‘free will.’ Where was my free will?  That’s right, there was none.

People from all walks of life have this diagnosis but go on for years with the wrong diagnosis because so much can mimic other diagnoses.  There are also those still that live with this diagnosis and are very successful members of society.  The trauma didn’t just occur overnight.  It’s has happened my whole life so, the process won’t resolve itself overnight.  There is a lot of painful elbow grease that has to be put into this recovery.  The point is to keep putting one foot in front the other.  I’ve never backed down from a fight and won’t start now.  You just can’t take the athlete out of me.

I will take you through the victories and the setbacks of this journey.  Hopefully, I’ll help educate you while also healing me.  The only thing I ask is keep an open mind.

#Thispuzzled

darnold1975

The Birthday That Will Never Be Forgotten

The Birthday That Will Never Be Forgotten

12.4.2014

 “How much tragedy has to happen before I slip wide open?” 
― Alisa Mullen, Unrequited

As much as I want to celebrate another year of survival from both physical and mental issues, sadly it has been overshadowed by the loss of one of our twin children.  My wife, Melody and I weren’t really concerned about the doctor’s visit because there was never a problem with any of the previous visits.  She is considered high risk every time because of us doing invitro fertilization.  We see the perinatologists which basically knows every time the babies hiccup.  We are also at about the 12.5 week stage so, chance of miscarriage was much lower.

My brother Levi Pierce and wife are in the exam room while I’m frantically trying to get there in time for the measurements and everything that entails.  We had been preparing Marshall for two babies while he was trying to reassure us that there were four. Toddlers are just funny.  I get there in time for the technician to tell me that she was waiting to take all the measurements until I got there anyway.

After having my regrets about not really knowing how to bond as a first time parent with Marshall, this pregnancy was just different.  I could feel it so strongly on an emotional level that I had never experienced.  It was so beautiful.  It wasn’t something that I ever discussed with Mel or anyone else.  For some reason because that level of emotion and bonding with such little creatures I wanted to enjoy all by myself.  I had already completely embraced the reality of us having twins and the ways that we would have to work even more as a team.  We hadn’t told anyone yet for some realities just don’t match our realities.  Nevertheless, these babies already had our hearts.

With all three of us eagerly waiting for all of the measurements, I was so excited to get to have my only somewhat physical contact with our children.  She goes through each thing she measures, stomach, legs, head circumference, etc.  “Baby B” as it was named by the doctors for twin pregnancy,  was measuring a little smaller but not a big deal because this is a twin pregnancy.  And then even though she passed the words off as really no big deal that the doctor could probably detect it, the words “I can’t find a heartbeat came out of her mouth.”  My heart hit the exam room floor.  I could only think, “Did she just say that one of our babies is dead?”  In my heart, though, I knew.  Neither I nor my brother could hold the tears back as my extremely emotionally strong wife did. Hopes were there but the doctor also confirmed that there was no heartbeat.

I will forever remember December 4th not only as my birthday but also the day one of our children was born in Heaven.  2014 had been an extremely emotional year but this, I must say, has knocked the wind out of me.  This venture was new and I didn’t know how to comfort me or my wife.  All I could think about was, “Our baby will never get to meet any of the amazing people in our lives.” I was a snot crying mess to say the least.  I had never allowed myself to be this vulnerable in public.  It felt as though, I had just been shot in the chest.  My brother just simply got up and left the room.  Mel was able to hold it together until we left the doctor’s office.  And then it was my turn to try and comfort my grieving wife.  Any additional information they might’ve given us, I never heard. I could do nothing but feel my own soul crying out for our baby.

From that day, the term “miscarriage” will never been the same as it did before it happened to us.  The few that knew were trying to be encouraging by telling us that we had another baby still left to take care of.  The anger that flew all over me was the thought that the statement meant, “You can just go get another one at the store. No big deal.”  My initial thoughts were, “That was our child, not a broken toy.”  That instant reaction was valid but completely due to grief.  I don’t remember the rest of the day.  And really, it’s ok with me.  In the following days, I laid my head on her stomach and sobbed.  I realize that “this is just part of life” and “lots of people have miscarriages.”  But, we still just lost OUR  child.

We will no doubt love this other little baby and welcome him into the world with open arms just like we did Marshall.  Our hearts will never forget the day we lost our precious little 12 week baby. Happy Birthday to me.

#Thispuzzledlife

darnold1975

Illusions of Halloween

Illusions of Halloween

10.21.14

“The moment of betrayal is the worst, the moment that you know beyond any doubt that you’ve been betrayed:  that some other human being has wished you that much evil.”

—-Margaret Atwood,  The Empathy Trap book page

These last several months has left me both mentally and physically drained to a low that I have never experienced.  Sometimes I have wondered if the universe is trying to point out something that I just can’t seem to see or understand.  The stress alone has left me 40 lbs lighter.  No complaints from me about that.  I think both me and my wife have felt every emotion possible at its highest intensity.  Have I allowed myself to do too much at times? Undeniably, yes.  Have I neglected my own needs psychologically, physically, mentally and emotionally?  Indeed I have.  Do I regret it? Not one minute of it.  I don’t feel compelled or obligated.  I am who I am. And I do what I do out of love for other people.

I’ve been told over the last few months, “No one ever said you had to do it or you weren’t asked to do it.”  My response has always been, “Why should I have to be asked to do something for someone that’s just the right thing to do?”  I don’t feel that I deserve any pats-on-the-back or high fives for simply taking some time to comfort someone in need.  Should I do this more in moderation?  Yes of course.  But, I know only one way to be a friend…..110% at all times when possible.

I’ve tried to figure this entire struggle lately with very few satisfying answers.  The only things I have become “one” with are my own tears.  I think that whatever emotional block that I had been struggling with prior to going back south for a visit has certainly been remedied.  I have emerged someone different and even more confused.  How do I deal with my own trauma like I need to while continuing to be supportive to those in need?  Well, right now, I don’t have those answers.  I just know that promises were made to both friends and family that I would stand by and support them in any way possible.  And since I don’t know how to turn my back on people, I’ll continue to be there for them while also trying to find my balance.

This time of year has many unpleasant anniversaries and memories associated with it.  I have always loved the fall and Halloween.  This year the familiar smells in the air are enough to turn my stomach.  I normally would be hunting for the best haunted house, haunted barn, haunted corn maze or anything that I was hopefully to get a good scare from in the region.  However, at this point in my life, there are very few days that are fun and enjoyable.  All I can seem to attribute this lack of contentment to is just where I am on my path of healing.  The word “trust” is one that has become again a word that is attached to the word “fear.”

Just this past weekend, our family went to McCall’s Pumpkin Patch in Moriarty, NM that we have been going to since before Marshall was born.  It has always been a place where my “inner child” comes alive and enjoys having fun.  Since Marshall was born, we always take this time to have fun taking fall pictures of him.  This year was different.  I was very apprehensive about all the people that would be there and just the thought of going scared the absolute shit out of me.  I didn’t totally understand but I think back to the sacrifices that my parents always made to attend all of my many softball/basketball games.  Instantly, I put on a smile and thought, “I, too, must do this for our son.”

Mel had all medications ready just in case.  And I will also add that I was medicated before we even left the house.  Secretly, my goal was to get through this as quickly as possible and get back home to my place of “safety.”  I must admit that seeing our son having such a good time brought joy to my heart.  The fear that I had from just being there was beginning to make me nauseous.  I sipped on my medical marijuana shooter to try and help combat all of the anxiety and nausea that was beginning from somewhere deep in my soul.  Something was beginning but what and why?  I knew that part of it had to do with being around so many people that was for sure.  I knew, though, that there was something more painful attached to this reaction, but what?  Halloween had always been something fun for me or had it?  I tried to ignore everything as best I could for the sake of Marshall and Mel to have an enjoyable day.

The last thing we always do before leaving is the hay ride.  However, after being around what seemed like ½ of the total population of New Mexico, I was done.  I told them to go ahead  and I would just wait under a covered area where a lot of families were eating and taking a break from the activities.  Never going anywhere in public without my IPod, I sit at a table and try to do some deep breathing and try and enjoy some music until they got finished.  Apparently, I was seen as an easy target to squeeze out because a rather large family decided that they would occupy the rest of the space at the table.  So, I politely got my shit and left them with the damn table.  I would like to interject that there is not a whole lot that I miss about where I was raised.  The common courtesy of simply asking if it was ok to sit there was something that I truly missed at that exact moment.  I would’ve gotten up anyway but, you know, the whole “principle” of the matter thing.  Anyway, I find a place on a hay bale and sit there in eager anticipation for the return of the pumpkin hunters.   I soon realize that I’m not able to keep an eye on everything but this time I’m alone.  My mind begins to panic and all I can think is, “Get me out of here NOW!”  Then the flashes of images that I can’t seem to connect with begin.  Really?  All I knew was that I was terrified.  The nausea sets in and I keep swallowing to prevent the ultimate embarrassment of vomiting in public.  I was scared and alone and that was all I could comprehend.  I felt like at any moment someone was going to do something horrible to me.  I just didn’t feel protected.  My deep breathing quickly became like a dog panting.  My eyes searched the area like a tiger looking for a meal.  And then…….I’m in the truck almost back in ABQ not remembering if something had happened.  I had a really bad headache and tried to put the pieces together and couldn’t.  Yea…..Happy Halloween.

#Thispuzzledlife

darnold1975

Winners

Winners

8.14.14

“It isn’t the mountains ahead to climb that wear you out; it’s the pebble in your shoe.”
-Muhammad Ali

Today is one of those days where I regret being able to open my eyes.  I rolled out of bed this morning and felt like I had been at war all night.  My body feels like I’m detoxing from a chemical that I haven’t taken.  And it’s already begun happening at 6:00am.  I feel the overwhelming sense of sadness mixed with anxiety.  The nausea is hitting like a gulf coast wave from Hurricane Katrina.  I feel that overwhelming sense of needing to vomit.  Halleluer! I must not have eaten before I went to bed last night! I didn’t see any remnants of anything.  So, I grab my cannabis wax pen and take a couple of hits off it to settle my entire system down.  This has also helped to combat a horrible headache that was beginning to hit like a thousand hammers.  Then the diarrhea hits like some kind of ‘shock and awe’ attack on Iraq.  How soon until I have another acupuncture session?

I’m actually catching a break from these symptoms right now.  The medical marijuana is just like any other medication, it too has its limits.  However, the combination between both mmj and acupuncture and a drastic slow down in therapy seems to be slowing everything but my mind.  What was started about a month ago and was exacerbated when we traveled home has continued to plague every inch of my mind.  This blog, no doubt, is an exit for both frustration and education on certain topics.  But, for now, certain things must be kept hidden to ensure safety on several different levels.

Am I just trying to have a “poor, pitful me” moment today? Hell no! You’re just getting a ‘firsthand’ look at what some people’s days are like.   Like I’ve said before, “writing about these topics on my own abuse has had numerous effects on me both mentally and physically.”  Yes, I realize that I had an awesome life up next to others who have had some horrific things happen in their own lives.  I’m not going to compare stories because this blog is not about minimizing anyone’s personal traumas.  Have I cried about feeling so guilty about being upset over seemingly insignificant things? Absolutely!  But, the fact is that things did happen.  I’ve held that shame and guilt so long that my mind and body feels like I’m melting.  And I’ve stuffed and stuffed feelings for so long that I’m not only nervous….I’m terrified to work with them.

The “special” people helping to guide me through this process must either be angels from God or “gluttons for punishment.”  LMAO!!!  I feel like I’m really just beginning this treatment even though, I’ve been in therapy for a few years now.  I just don’t have the ability to keep my defenses up like I use to.

As an athlete, “YOU NEVER GIVE UP!” You play until you hear the whistle blow.  This drive is not one that can be taught. You must be born with a love for the game and the athletic ability to become the best ballplayer you can become.  I got my softball playing nickname ‘Charlie Hustle’ from one of my earliest and dearest coaches assigned to me by Nick Kolinksy.  He always told me that I played a lot like Pete Rose and never gave up.  I smile every time I remember as a kid playing ball for him and always feeling a sense of ‘safety’ around him.  He would tell me sometimes, “Dana, that was a $100 catch and a .10 throw.”  He made his point very clear but didn’t crush my self esteem as a ballplayer or as a person in the process. He and other coaches are on my list of ‘special’ people that had a dramatic and positive impact on my life from a very early age.  I never complained about going to practice or games.  That was a way out for me.  Playing ball was my life.  Pete Rose said it the best way that I know how to describe the love that I had for the game.  

“I’d walk through hell in a gasoline suit to play baseball.”

—Pete Rose

Occasionally, that old, washed up athlete comes alive in me again with reminders about how “putting one foot in front of the other is still considered progress.” I get caught up a lot on what the definition of ‘progress’ or ‘winning’ is about in regards to therapy.  Sometimes, the best I can do for that day is just get out of the bed.  Even doing that means that I made progress because one foot had to be put in front of another foot for that to be accomplished.

Sometimes people ask me what it’s like to process trauma.  To me it’s all about going to war, except this time, I know what I’ll be faced with.  I have survived it once so, it can be done. Do I have the strength? That remains to be seen.  I relive everything all day everyday anyway. What makes this situation different?  I have actively made a choice to volunteer to go through it again.  The fear can make me angry, frustrated and paralyze me at times.  I must admit that it’s very unfair to be almost 40 years old and still paralyzed in many ways by what others have done.  I can hear some of the old, southern biddies saying, “She made her bed, now, she can lie in it.” And that’s fine, if that’s your reality.  My reality is this….”I don’t care what the circumstances were…No one deserves to be abused in any way….EVER!  My ex-husband, teacher, baby sitters and birth mom didn’t deserve the abuse that they suffered at the hands of their family and people they trusted.  When the effects of the abuse begin affecting them then, the new generation of abuse is born and is taken out on other people who become their victims just like I did.”

This time….”I WILL NOT ONLY SURVIVE, I WILL WIN!”

#thispuzzledlife

 

#Thispuzzledlife

darnold1975

Family Day

Family Day

9.8.14

“Some people’s lives seem to flow in a narrative; mine had many stops and starts. That’s what trauma does. It interrupts the plot. You can’t process it because it doesn’t fit with what came before or what comes afterwards.” 
― Jessica Stern 

And then you have a random day where everything seems wonderful.  I’ve been in public without getting sick.  I’ve stopped and talked to a friend and laughed.  I’m only dealing with minimal physical ailments this morning.  Maybe the weed, klonopin, Valium and ativan are working.  I’m not asking questions. I’m just going to enjoy the ride.  Reality will be back soon enough.  At least I’m not sick despite all of the medication.

I wish I had had the break from some of the side effects from when we went and took pictures on Sunday.  I was all dosed up and ready to face the people and overstimulation of my brain.  The plan was to take Marshall to the botanical gardens and let him ride the choo-choo.  Off our little family goes to find the choo-choo.  Did I mention that I had been dosed with a good bit of meds before I left the house?  I vaped on my wax pen all the way to our destination at the Botanical Gardens.

Everything was going fine. Marshall was enjoying running around being a kid.  Mel was…well….being a mixture of a professional photographer and a mommy.   Today was going to be the day that Marshall and I had “mommy/son pictures.”   Other families were there having picnics and just enjoying a nice, cool Sunday late morning and taking in the scenery.  The people were spread out so, at least, I wouldn’t have to worry about them touching me.  I had my wax pen ready, my sunshades to hide my life full of shame and my IPod ready to face any type of external or internal stimulation.

Marshall was showing me things and asking, “Bite you?” So, our conversation was typically, “No, baby, flowers don’t bite.”  Then he sees the koi pond. The koi have instantly become sharks.  He starts shouting to get our attention, “Sharks, Sharks!” Yep, this momma was proud that our son knows the difference between a fish and a shark.  I look behind me thinking because I thought I heard someone call my name.  It was a seemingly peaceful pathway filled with small trees, bushes and ground covering.   “Here we go,” I thought but not knowing why.  I notice my stomach getting a little nauseated but took a couple of vapes off my pen and hoped that the feeling would go away.  I soon noticed that my jaw began hurting. The muscles in my body began cramping. The nausea became stronger.  I told Mel that I was going to sit down a few minutes to rest, but really hoping that I just didn’t throw up.

 The longer I sat there, the worse I felt.  As a tear, dropped from my eye underneath the sunshades and shaky voice, I told Mel we needed to go home.  An unimaginable fear I must’ve been ‘triggered’ but I hadn’t realized it. Then, the headache hit.  Not as bad as the one last week, when I had acupuncture where I never remembered the visit, but plenty bad enough to feel miserable.

Once again, my physical symptoms have messed up another family outing. And soon the shame and guilt hit me like a “tornado propelled bumble bee.”  I had no warning but thought it was probably in the lineup somewhere.  I felt like collapsing from just sheer embarrassment, even though, people around me didn’t seem to notice. I just sat down again and tried to wait for the feeling to pass. After several minutes, I decided no more waiting and listening to music. I suddenly had to GET THE HELL AWAY FROM WHERE I CURRENTLY WAS!  Something still seemed to scare me, but I didn’t know what.

I tried to remember what we were doing, and what had just happened to cause such a scare.  I couldn’t remember what I had said, done or thought. All I could do was hope that ‘it’ was over soon.

MY wife, being the very understanding person she is, told me everything was ok and we could come back another day.  The disappointment laid somewhere deep within me, not her.  She had no idea the level of disappointment I was experiencing.  Everything was fine and now it wasn’t.  Marshall didn’t seem to notice and neither did the people passing by. So, now I act like everything is fine, right?  I stood up and the familiar feeling hit me but this time it scared me. My body didn’t feel like I could control itself but I was moving.  It was as if I was watching this awkwardly walking human being that I didn’t recognize. ‘Things’ just weren’t ok for some reason.

We were still able to get some good pictures of me and Marshall.  But, the disgrace of the signs and symptoms of disorders can be embarrassing even if other people don’t seem to see them.  Some things can’t be hidden.  Some things have been hidden for years and are now noticeable.  I just wanted to get back to my ‘familiar’ surroundings….HOME!

#Thispuzzledlife

darnold1975

I’m Not Alone

I’m Not Alone

8.23.14

“A bird doesn’t sing because it has the answers, it sings because it has a song.”

—Maya Angelou

I don’t normally blog on Saturday mornings at 5:30am.  This morning I was awaken to what felt like my insides twisting.  I felt nauseous but lay still to make sure it was real and not a dream.  I decided very quickly, “Nope, that wasn’t a dream.”  I also noticed that my whole body was hurting with what seemed like “growing pains” as my pediatrician use to call it.

I go through my morning routine of turning on my vaporizer and the coffee pot.  But, this morning, I decided against coffee and would have a diet coke.  Since, everyone else was asleep, now was the perfect time to read some of my library books.  I started vaping but at a higher rate because the pain in my body was becoming ever more painful by the second.  I once again felt like I was in full detox from some chemical.  I also have these symptoms randomly attack me at different times of the day.  I’m starting to get a headache but get busy trying to keep it at bay.

I think I finally begin to feel my medication beginning to work after a few minutes.  My nausea begins to subside somewhat, my headache is doing ok for the moment but my muscles and tissues of the rest of my body seem very angry at me.  I pick up my book and begin reading.  Due to the types of abuse, I endured both as a child and adult, I’m constantly looking for answers for why things happened the way they did.  The book I’m currently reading is Wife Rape. It’s an older book but I need answers.  This was the same book that had me reliving a scene from my former marriage the other night. So, I kept that in mind and agreed with myself that I started feeling anything familiar in my mind or body; I would put the book down. Deal!

I’m instantly sucked into that book again. These women had stories like mine.  Some were much different, but the “acts” were about control.  This I already knew. But, seeing things in black and white can sometimes be the one thing that makes things “click.” I kept reading some of the sentences and paragraphs over and over.  I thought, “How do they know how I felt in that moments or those surround those types of events?” I just had to read more. The book not only describes the actual accounts of abuse from the survivors. But attempts to explain why this “secretive, abuse happens and how the abuser also views this as both their “biblical and societal RIGHT as a man.”

I want to make perfectly clear that I am sensitive and also understand that this can and do happen in ALL kinds of relationships.  Since this book is older, I’m not distracted by the fact that they use information from heterosexual relationships.  But, since I’m discussing my previous heterosexual relationship, I won’t make a big deal about what types of samples they used regarding gender.

These women describe, in detail, how they felt, hurt and emotionally survived their abuse.  It was like looking in the mirror again.  My instant thought was, “How do they know this much? I’ve told only a couple of people some of what happened?  Who betrayed my confidence?”  I very quickly realized was how much I identified with all of these survivors.  Not only what they did but what they thought.  They also seemed to “lose time” with some of the attacks on their body. Their worth as a human being has been severely damaged.  They also spoke about how much easier it was to just “go along” instead of fight.  That fighting back always seemed to make everything worse in every way.  I knew and felt that too.

I had ignored my body but soon realized that I now feel like someone is trying to tie my body in a knot.  EVERYWHERE was and is still hurting like I’m being hit with a bat.  The nausea is back. My stomach is cussing me repeatedly and my head is pounding.  My upper back feels like I was just shot and just breathing almost brings me to tears because of the anxiety.  I prefer to think that my body is ‘bleeding’ many years of emotions that I never felt ‘safe’ enough to release.  I feel like every day I don’t write, that my body is filling up with toxins.  But, I’m physically miserable too.  My body feels very conflicted.  Do I have that much “stuff” to process that I haven’t started getting better physically yet?  From somewhere deep inside me, I hear…”Someone please stop this NIGHTMARE! I can’t handle reliving it again!

Most people would say, “Just put the book down and it will get better.” I really wish it was that easy. My body and mind are remembering every single vivid detail of everything that has happened.  It’s not just the book.  But, the book is really helping me understand what exactly happened to me the 14 years I was in a relationship with my ex-husband.  I relate to so many of those women though which makes me feel like I’m in a group therapy session in my own little way.  Sometimes you do stuff knowing that it’s going to hurt because you seem to understand and long for more understanding.  Do the benefits outweigh the risk?   I don’t know what the right answer is right now.  Maybe I’ll take what I have read and read it more at a later date.

#Thispuzzledlife