When You’re More Nervous Than Your Child On The 1st Day Of School

Crowds of kids gathered with their parents at the bus stop snapping photos of their elated children.  Some even took video.  I stood with my daughter giving a hug and kiss on her cheek.  I did this as support, support she didn’t ask for. Why? Because today was the 1st Day of School, the first day in a new school district for her and I was worried.

I was very nervous, bordering on anxious… wondering if she had everything.  I think I was more nervous this year than she was because I can actually remember Junior High (New York’s version of Middle School) and I remember starting Junior High not knowing anyone.  I remembered the fear, the anxiety, the pure terror.  You see, I didn’t go to my zoned Junior High where I would have had friends from my elementary school, I went to a ‘Gifted & Talented’ Junior High for my creative writing abilities.  And although my daughter was starting a new school system as we moved in late spring to give her a better education, unlike myself, she already knew a few people.

I worried about my daughter.  With every new thing she would panic over… What if I can’t open my locker? What if the kids make fun of me? What if I am late to class?… my worry grew.  I only want her to be happy and to succeed.

As the days passed and the 1st Day approached, I repeatedly asked her questions:

“Do you remember how to open your locker?  Tell me.”

“What bus do you take from school to the YMCA in the afternoon?”

And then I started to make blatant statements:

“Don’t forget you will need lunch.”

“You only need a pen or pencil the first day. Why are you bringing so much other stuff?!”

I think I was beginning to drive my daughter batty as she began to roll her eyes at me and sigh.

I just wanted her to be prepared.  Middle School is not Elementary School.  You are given more responsibilities in Middle School.  You have to go to more than one classroom.  You have a set time to get to each class.  You have reports and projects.

And most important… you must figure out who you are sitting with at lunch!

This last item was what was making my daughter more anxious the last few days.  She doesn’t want to hurt anyone.  She was debating between her oldest and dearest friend (they have been friends since they were babies), our neighbor across the way and a friend from her former camp in the city we used to live in that relocated too.  She questioned me repeatedly about this.  I suggested her old camp friend as she would see her bestie on the bus and well, our neighbor lives right across the way from us.

A mass chaos of questions, things to purchase, items on a To-Do list and my brain was foggy (it has been for the last couple of months already).  I couldn’t concentrate to get everything organized, I just couldn’t think.  With that I became irritable.  With the irritability, I grew more anxious and had several anxiety attacks.  It felt like my brain was playing a hyper speed game of Atari’s Pong in my head. But I tried to keep my anxieties from my daughter. We didn’t need her GAD to start.

It was official. I was more nervous than my daughter.

As I stood at the bus stop this morning with her and the gaggle of other kids and parents, I internally told myself this is it.  She is ready and if she forgot something, there is always tomorrow.  Tell your Anxiety that she is fine.  She will make friends. She will open her locker.  She will find her classes. You know she is ready for this and so are you.

Then the bus showed up. I waved to my friend, the bus driver.  I watched her get on and smiled. I walked away feeling calm and content and whispered, “Good luck my love.”

What Happens When A Dream Turns Into A Triggering Nightmare


Suddenly, I was back there.  That place, both a saving grace and a hell.  I was walking down the hall.  Bare concrete block walls.  Gray, solemn, just like the people that dwelled inside.  Doorways on both sides leading to rooms with aging office waiting room furniture that was once comfortable but now forlorn like their occupants.  I was one of them again.  An empty void, emaciated, internally crying for help.  Tempered glass and a counter to my left held those that treated us.  Their faces ranged from a gentle smile to a stare as if asking, “What is this person doing?  Am I safe?”  Slowly, I walked toward the end of the hallway where a window was.  Large, a glimpse to the outside world.  If only it was not right across the street from a cemetery.  

My eyes were welling up with tears.

Why was I back here?  There was no reason to be.  I have been doing well mentally and emotionally.  If this was the case, why was I, without warning, plunged into the short term psychiatric ward once again?  I was dreaming and being triggered.  Being both on the outside looking in and on the inside dying to get out.  

I have a love-hate relationship with the hospital’s psych ward.  When I was first there over ten years ago, I wondered why I was there.  I never thought I was experiencing the same problems as the other residents at the time.  I thought I was normal.  Ha, ha, good one Steph!  When I went back over two years ago, I begged for it.  I know being there would help me.


There are things I would rather forget about the hospital aside from the bare walls and gloomy atmosphere:  


The bed checks every 15 minutes… even if I was deep asleep, like clockwork I was awakened to a flashlight shining into the small glass panel in the door.  


The psychiatrists… although there to help, none of them appeared like they cared to help you. I spent all of five minutes a week day (they did not work on weekends or holidays) talking with them while their eyes looked elsewhere as if saying “You’re wasting my time.”


The wake-up time and routine… it was a bit rough waking up at 7am with all the medications I was given and then to go through the process of waiting in line to get weighed and our blood pressure taken.  


Lack of outdoor time… depending on your mental and physical state that day, you may be allowed to go for a short walk circumnavigating the hospital building viewing the nearby cemetery and emergency room.


But, where there is bad, there is also good.  As I mentioned, I knew I needed to be hospitalized again.  For some reason, I felt safe there.  I was only responsible for myself.  I could focus on my much-needed self-care and work on getting better even if it took a psychotic break to get me there.  I knew I would get the medications necessary to sedate me, stop my brain from its incessant thinking… you’re worthless, helpless, not worthy of love.  These medications would also stop my hysterical, borderline delusional, thoughts… take that screw, just jam it in your head, who cares if it kills you?!


Although the psychiatrists were lacking in care, there were some nurses that were a pleasant gift.  They would talk with you about your life focusing in on your face, treating you like a human being.  They remembered things you told them and asked you about it days later.  They were concerned about your care.  Sometimes they even sat and watched TV with us.


Aside from two very special nurses (1 each hospitalization), I made connections with fellow residents.  We talked about our experiences, gave each other advice, was there as a person who knew what it felt like.  I still, from time to time, communicate with my last roommate.


And yet, this dream triggered me.  I awoke with rapid breaths, scared, worried, panicked.  What did it all mean and why was it affecting me so badly?  I was somber the whole day.  Was this a prelude of another hospitalization to come?  Because of my Anxiety diagnosis, of course, here I am jumping to the worst conclusion instead of calmly thinking this through.  And if it is a premonition, why am I so fearful?  The hospital helped me.  Ultimately, I think I will have to consult my therapist on this.

When False Information On A Meme Makes You Angry…

Originally posted on Stigmama on Tuesday, June 20th:

The other day on Facebook I came across a meme… actually calling it a meme is too nice. I came across a shitty ad that basically told me and others that are Mentally Ill and medicated that we are now drug addicts. While addiction is a Mental Illness, I have not been diagnosed with it. I am a long time Depressive and Anxiety-ridden Mom that will fully disclose any part of my history because people need to know what it is really like to be Mentally Ill.

When I saw this, I was outraged, furious, and this was at 10am on a weekday morning in my cubicle at work:

What made this worse, was this was the pinned post in this group ‘The Free Thought Project’. My blood was boiling. I wanted to break something. Instead I decided to use this as an oppurtunity to educate.

I have seen many versions of this ad before (see below) consciously telling people that medication is evil and while I find them offensive, it didn’t hit me as hard as saying I now have a “lifelong addiction”:

                                        

Is medication shit… well I will flat out admit I wish I didn’t have to take it but comparing it to the stuff that would be on my daughter’s diaper years and years ago is a bit much.

Nature as an antidepressant… I agree wholeheartedly that nature is very rewarding.  I am an avid walker and hiker (and snowshoe-er in the cold winter months).  I love being outside.  After a hike, I usually find myself rejuvenated, feeling alive and most importantly happy.  A hike or a walk outside at lunch can ‘turn my frown upside down’.  There are just a couple of things wrong with this statement:  Nature does not have the same effect on everyone and when you are severely Depressed, it ain’t going to work, trust me, I’ve been there.

Being an Alpha personality, a control freak, a perfectionist, I will fully admit that I hated being on meds.  I couldn’t fathom the idea that a little pill (or four) controlled me.  I was only ‘normal’ because of them.  I thought I could get better without them.  I was wrong… very very wrong.

The first time I was prescribed medication was shortly after my 18th birthday.  It came in the form of a half white and half aqua capsule known as Prozac.  I was quickly told not to tell anyone I was taking it.  This was after I held a case cutter I stole from work to my wrist debating whether I should live or die.  This event, I was also told, to not speak of.  Ah, you got to love the stigma associated with being Mentally Ill.  Because of this, I thought medication was wrong, bad, sinful.  How stupid of me.

It wasn’t until my recent episode of Major Depressive Disorder and Severe Anxiety almost three years ago, that while getting better I finally said “Screw it!”  I didn’t care who knew.  If I had a megaphone, I would probably be screaming it.  There is nothing wrong with being medicated.  I really should create (or order if it exists) a shirt that reads: “Medicated & Proud Of It”.

These people that create these offensive and naïve memes have no idea what it is really like to live with these conditions.  Because it is invisible it doesn’t actually exist.  Because there is no official blood test or genetic test, we all must be making it up.  It is all in our heads… why yes, it is.  Because of a lack of Serotonin, something produced in my brain (i.e. my head) I live daily with two severe illnesses.  I am not making it up.  Who would make up paying monthly for medications, weekly psychiatrist & therapy appointments, being hospitalized, becoming severely delusional, considering hurting or killing yourself?!  Yes, I totally want all of this!

But we live in a society that believes Mental Illness is not on the same level as a Physical Illness.  It is okay if you take lifelong medications for illnesses such as Diabetes, Multiple Sclerosis, Lupus, and Cancer and that is not seen as an addiction.  Why is it okay for them but not for people like me?  Why am I considered ‘an addict’?  Why am I ‘faking it’?  I wonder if there was a real test that proved a Mental Illness diagnosis if these views would change.

I have weaned off medications a handful of times.  It can happen.  I lived 4 years med free before I entered into my 6th Major Depressive Episode.  Once on medication again, I took a hard look at my husband, my daughter, and my parents and told myself I didn’t want to see them suffer anymore.  I didn’t want to suffer anymore.  I decided then and there to never ever go off my antidepressant.  Lexapro and I will remain the best of friends.  I am not ashamed of my med.  Without it, I would be in a very dark place or not here at all.

To ‘The Free Thought Project’, research more on what is truth and what is fiction.  I don’t care if you lean liberal or conservative.  The Mentally Ill are a large population and by posting this, you are making us want to hide more.  Because of this, many people will stay silent.  Because of this, many people will not get the help they need.  Because of this thinking, more deaths by suicide will occur.  Remember that old adage “Stop and think before you speak”?  It would have come in handy here.

To all my fellow people with Mental Illness, please do not hide.  Do not believe a word of this absurdity.  There is help.  A walk in the woods can help, but it is not a cure.  It will not help as much as therapy and medication.  Remember:

 

Struggling To Help My Daughter…


My daughter is a bright, caring, empathetic, preteen girl.  Most days she has a smile on her face that melts her mom’s heart.  She is typical preteen, mostly caring about binge-watching shows on Netflix or catching up on her friend’s latest YouTube videos featuring her fave, Beanie Boos.  She does well in school, is friendly to everyone, and is respectful of others.
She also has Generalized Anxiety Disorder (GAD).
When she was diagnosed at age 6, I did everything I could to help her.  I got her into a special group at her school, inquired information from her doctor and read up on anything I could get my hands on.  I have plenty of experience with adult GAD, but I haven’t a clue on what to do for childhood Anxiety.  The school group helped immensely and then she aged out of the program.  She was doing well until a major life event occurred in our household.  We were fostering-to-adopt but had to give this child back to DCF because of my declining mental health.  Her GAD came back full force.  This time we sought out therapy.  While she got help, so did I for my Depression and Anxiety.
In the last 2 ½ years, my daughter has been doing great with only minor hiccups.
Then we decided to move to give her a better education as she starts Middle School, another major life change.
My husband and I do not hide things from her and she knew from the beginning about the move.  She helped us in choosing where we would live (ultimately her input was minor).  We wanted her to embrace this change.  She was excited as she will be in school with her best friend now.  We thought she was handling this well.
And then sleep disturbances set in.  
My daughter has always been a good sleeper; I have never experience this before even with her past episodes of GAD.  As the moving date approaches, her sleep disturbances have become full fledge episodes of Insomnia and I, as her mother, feel completely helpless.  Here I am, a woman who has struggled with Depression and Anxiety for most of my life and I can’t help her.  For me, the solution comes in the form of medication that I take nightly.  For her, at age 10, there is no medicinal help.  At first we tried simple solutions by telling her to read, it will tire her eyes.  That didn’t work.  
As night 3 was approaching, I became extremely concerned.  I could vividly remember what I felt like and how I reacted to night 4 of Insomnia for me.  I remember the tears and the strong desire to sleep.  I remember the immense amount of thoughts that bounced in and out of my mind.  I remember the extreme irritation and delusional thinking I had during the day.  I was desperate to give my child relief.  
I suggested she use my weighted blanket.  She refused.
I suggested mindfulness meditation.  She refused. 
I suggested my Therapist’s 4-square breathing technique (breathe in for 4 seconds, hold for 4 seconds, breathe out for 4 seconds, repeat 4 times) which has worked for me a few times.  She was hesitant but decided to give it a shot.  It didn’t work.
Night 4 brought on the only pseudo-medicinal thing I could try with her… Melatonin.  I cut my 3mg pill in half.  Nope, still didn’t work.  She was in tears.  She just wanted to sleep and I completely understood this all too well.  I explained that she needed to distract herself, try not to just lay in bed.  I suggested reading, writing, journaling, drawing, coloring and lastly, watching stuff on her Kindle (which I set to the night mode that turns off the harming blue light).  She slept only 7 hours that night, barely enough for an adult.
Last night, night 5, I finally convinced her to use my weighted blanket.  I thought we may have found the solution as all was quiet.  Then I heard her come downstairs at 11pm.  After about 15 minutes, she returned to her room.  This morning she said that she sat crying in her room and eventually fell asleep around midnight.  She woke up at 6:10am.  6 hours of sleep.
I don’t know what to do.  She is declining rapidly.  The recommended amount of sleep for a child her age is 9-12 hours.  She has not had anywhere close to this in five days.  My sleep is becoming disturbed worrying about her.  I do not know how to help her anymore.  I am struggling as I feel the sense of blame coming back… she is like this because of me.  My GAD worries that she will never sleep again, always jumping to the worst conclusion.  I cry for her.  I blame myself for her struggles with this illness.  I am pondering therapy again, but that isn’t going to fix her problem quickly.  How can I help my daughter?  

A Letter To My Former Foster Son As You Turn 5

 

My Sweet Little Boy,

I can hardly believe it has been a little over two years since you left our home. I can still remember your toddler-self walking in circles around the house. I can still hear your voice so vividly as I would come down the stairs in the morning, you pointing at me, saying, “Look, it’s a Mommy!”. I can still feel the soft skin of your cheeks as I would hold your face in my hands right by your dimples and then place my lips on them.

And then I remember what happened next. I never wanted you to be a trigger for me. Countless hours as I would hear you talk yourself to sleep or cough made daggers pierce my heart. It was as if I was falling down, out of an airplane with no parachute, into another episode of Postpartum Depression. First, the severe anxiety that left me emaciated and riddled with shaking and hyperventilating. Many days towards the end, as you sat in the living room watching TV with Sophia, you remained oblivious of the delusions my mind and body played on me. Once you left, Depression set in… Badly.

Oh, my sweet boy, it was never you. You were never the problem. I was. Every day since you left, I wake up with you on my mind. You are also one of my last visions when I go to bed at night. Please know, I never stopped loving you since the moment I met you in August of 2014. I still love you that much now.

And now you are turning 5. I am completely in awe of this. In my eyes you are still this toddler discovering the world. I remember seeing you learn how to eat real food, how to interact with children your age, learning the true meaning of love. You made friends, you experienced holidays, you finally had a family who truly loved you and in return, you learned how to love back. I can only imagine the little boy you’ve turned into, with your tousled dark brown hair and deep sienna eyes.  This big boy who will be starting Kindergarten in the fall.  I wonder how much taller you’ve grown, if your reading, what you are into.

Everyday my heart yearns to see you, to know you are okay, cared for, loved for certain.  And other moments, just when I think I would be okay seeing your face, my heart reminds me of my longing for you, the pain, the ache, the realization that you will never come back to me.

My Tyler, on your 5th birthday, I want you to know how loved you are. I don’t want you to ever feel abandoned. You are still adored by us. You are cherished by your forever family. You are cared for and loved deeply.  You will always be special, especially to me.  I did not birth you, but in those few months I had the pleasure of interacting with you, you gave me a new view on life and compassion.

Today, we will light 6 candles on a cake for you… five for your age and one more for good luck because Tyler, you deserve all the luck in the world and so much more.

Happy 5th Birthday my boy!

Love eternally,

Your Former Foster Mommy

What My Daughter Knows

My daughter knows I hated her just two weeks after she was born. Pure hatred, where using the actual word ‘hate’ is valid and not taboo. She knows I wanted to leave her and never ever see her again. She knows I wanted to turn back time and never have her, completely obliterate her existence.

My daughter knows what suicide is. She learned this at age 8 because she overheard something on the radio. She knows that I have thought about committing suicide a handful of times and that one of those times I came very close to slitting my wrist with a case cutter I stole from work (and still have). She knows I was a teenager then, almost 18, a legal adult, only 8 years older than she is now. She knows that these ideations have blown into my mind like a breeze and have quickly left several times in the last twenty years.

My daughter knows I am sick. She has seen me at my worst, a vision I never wanted her to lay eyes on. She has seen me shaking, rocking back and forth, nails digging into my head spewing delusions out of my mouth left and right. She has seen the tears, witnessed the dry-heaving runs to the toilet, heard my self-loathing.

My daughter knows I have been hospitalized, twice. She accompanied my parents this latest time when they visited me, being forced to stay in the cafeteria with my father because she was deemed ‘too young’ for the short term psychiatric ward. The hospital feared the patients there would hurt or scare her by saying or doing something. This means they feared I would hurt or scare her too. She knows the emotional pain one feels when the only communication we had was through a phone… a phone that would cut you off if you moved wrong, a phone so desperate in need of replacement. She understands that the hospital is my safe place, when our home is unable to be just that.

My daughter knows she is an Only child because of me. She knows I was barely able to raise her in the beginning due to Severe Postpartum Depression and Anxiety. She knows at times I have been unable to care for her in the episodes of Major Depressive Disorder since. She knows that she lost her little brother, my beloved former foster son, because my illnesses prevented me from being able to function, let alone parent. I became a third child for my husband then, a childlike creature in an adult body that my daughter started to take care of, becoming a Mommy to her own mother.

What I didn’t expect for  this wonderful, kind, and loving child to learn was acceptance. Every time I had to explain these things, every time I hurt her, I expected anger and rage in return. I expected her to ignore me, shout “I hate you Mommy”, rotating the knife deeper into my back.  I expected extreme tears over losing her brother, many more than she shed (and she cried quite a bit).

Instead, she shocked me by becoming my protector of sorts, a role I never asked her to take and tell her now she can relinquish.  She truly cares if something will affect me, triggering me back to those dark dismal days.  She has true compassion and empathy, two traits I am happy she learned, although I wish she learned them with something other than me as the subject.  She is the Wise Fairy that her name, Sophia Faye, connotes.

There are so many things she has had to learn at the tender age of 8, 9 and now 10.  These things I would have liked to have postponed.  I have been called out by a select few saying she was too young for these strong topics.  Yes, I know.  But, I have to say, if by telling her about being mentally ill, suicidal & hospitalized has made her into the awesome kid that she is today, I am happy she knows.  I am happy she knows, because she won’t have to live in the shame and stigma of it if it happens to her.  She knows she has a loving mother who has been through hell and back that can help her.  And she knows that although at one point I hated her, wanting to leave, I couldn’t bare to live without her now.  She is my heart, my strength, my love, my Sophia Faye.

Mommy’s Sick… Does Anyone Care?!

A few days ago I stayed home sick.  No, I didn’t actually have a fever, but my nose was constantly draining as if someone forgot to turn the shower off and my body was achy everywhere.  I was involuntarily stretching because of these aches and knew that I would accomplish nothing, zero, zilch, nada at work.  I was lightheaded and nauseas.  From the moment I woke up, I knew I was doomed.  I texted my boss and informed him I would be out apologizing because I have a project deadline approaching.  I then crawled up the stairs and informed my husband that he would have to drive our daughter to school.

“I’m sick.  Can you please drive Sophia to school?” I voiced weakly, “I’m dizzy, achy, and my nose needs to be permanently attached to tissues.”

I should’ve known what his response would be, after all I have been married to the man for over 12 years and with him for over 20, but I was still a bit awe stricken…

“Ugh, do I have to?!” he whined.

Really?!

I love my husband, really I do.  He really is my rock.  So many times my Depression and Anxiety have told him to leave, that he would be better off without me.  But he never did.  He stepped in as primary parent and let me get the help I needed whether in the form of visits to my therapist or psychiatrist, a phone call to my parents or even a couple of hospitalizations.  He truly is my best friend and an awesome man with exception to this one thing.

During my hospitalization for Severe Postpartum Depression and Anxiety 10 years ago, I finally learned I am not Wonder Woman, I cannot do it all.  I mean ALL is a considerable amount.  The media will have you believe that mothers can do everything.  I haven’t met a mother yet that does everything and those that come close usually have large quantities of coffee or wine in hand.  Once I arrived home from this hospitalization, I put the phrase, “I need help” to use.  I mean, I honestly needed help.

“Jimmy, can you help me with this?” I asked my husband.  For awhile, he did (remember, this was a decade ago).  Then he would get whiny.  Once he started to get whiny, I stopped asking for help.  Without asking for help, my Mental Illnesses got worse, but I kept them relatively under control.  After all, I was forever in debt to him for being hospitalized and leaving him with a newborn to take care of for 12 days… at least I thought I was.  Then, I was hospitalized again and once released, he and my daughter questioned me how they could help me.

Ah, finally, they were asking how they could help, not waiting for me to beg them.  This, unfortunately, didn’t last.  I was once again asking them for help, not a lot, and I was using “please” and “thank you”.  They are the magic words you know.  My daughter usually obeyed, but lately, with prepubescence, it is becoming more difficult.  My husband…

And we’re back to… “Ugh, do I have to?!”

I tried not to get angry by this response.  I was completely drained anyway, but inside I was beginning to boil.

“Yes.  Thank you.”

He proceeded to do as asked.  I then called him at work around noon, after a nap and forcing some food into me, to make sure he was going to pick her up from school.

“You’re picking Sophia up from school, right?” I inquired.

“What? Me? Why me?  You’re home.  You pick her up.”

“I’m sick.  I’m not leaving the house.”

And once again… “Ugh, do I have to?!”

When this is a response you constantly receive, it makes it hard to ever ask for help.

Then, he added, “What are you making for dinner?”

What?!  Yes, I know I am home, but really, I don’t even have a desire to eat.  After explaining if he would like his food with snot on it (because, hello, drippy nose), I hoped he would understand that dinner making was not happening from me.  That wasn’t the end of it though… somehow he did guilt me into marinating the steaks I wasn’t going to eat.  With tissues stuck in both nostrils and my hands lathered in antibacterial gel, I got the steaks marinating.

It didn’t end there.  When these two people I love to infinity and beyond arrived home, their understanding of Mommy being unwell left the house.  I was constantly needed for something.  I don’t understand… the two of them functioned fine when I was away on business a couple of weeks ago.  But somehow they can’t understand the idea of me becoming sick.  To them, if I am present in the house, I should be able to function at 100%.  This, too, was the case 3 years ago when I had the flu.  They both couldn’t fathom why I wasn’t cooking and cleaning the whole house since I was home.  At that time, I put myself in quarantine… for 3 days all I did was sleep, go to the bathroom, and munch on toast.

And now, the tables are turned.

Hubby left work early 2 days ago feeling icky, deep into a case of the ‘Man Cold’ with the symptoms I had.  For those who are questioning what the heck ‘Man Cold’ is, I am pleased to tell you.  ‘Man Cold’ is the common cold when it presents itself in male humans.  Instead of acknowledging that they have a cold, they think they are dying.  They believe their sneezes and coughs are much more than a common everyday germ.  They somehow get the idea that this germ, the germ us females have just had, has mutated into a superbug.  They will continuously whine about how awful they feel and try to make you believe that they deserve to sit on the sofa and binge watch Star Trek and Mythbusters.

He stayed home yesterday to nurse said ‘Man Cold’ and mainly because school was canceled due to a couple of inches of slushy snow and ice.  He questioned why I wasn’t staying home too so I could take care of him and our daughter. I just looked at him oddly.  Home all day and he didn’t even salt the walkway, driveway and sidewalk.  Made for quite a theatrical performance for me getting to my front door last night after work.

This is the same person that only a few days ago was having me drive my child to school, make dinner, clean, pick up the child from school and wanted to know why I couldn’t go to work.  But I don’t whine when he asks for help.  Why?  Because I am Mommy.  I am the caretaker and my heart aches when those that I love are ill.  I just want to help them feel better.

I am sure there are men out there that do not act like they are on their death bed, that do not suffer from the dreaded ‘Man Cold’.  But, I haven’t met one yet.  Anyone who is married or with one of this special men, hold onto them tightly.  They are a rare species.

I’ve Always Wanted To Be An Architect… And Other Shit 

I remember my first Lego set.  I was six and my family had just gotten back to my Aunt & Uncle’s house from the mall.  I am not sure why I wanted this set so badly, but I begged, I pleaded, and now it was lying on the floor of the bedroom I was sitting in.  It was a medieval boat that came with two men in helmets.  I stared at it in awe.  Could I build this?  At six?

I worked hard on it but sure enough, I completed it.  I stared at it in amazement thinking, Wow, I built this!

This teeny-tiny itty-bitty Lego set started it all.  I wanted to become an Architect.  I made a major life decision at the respectable age of 6.

Through the years, I challenged myself.  The sets got bigger and my time to build them got shorter.  I would follow the directions, quickly erect the Lego building, look at it with pure elation and then take it apart.  At this point, I would be my own creations.  I was, after all, a budding Architect!

As I became a teen, I shifted from Legos to hand drawings.  I would draw floor plans just for fun.  Soon, I developed into drawing the front elevations of houses.  I received several home plan books and computer programs for my birthday and holidays.  I even received a drafting table.  Yes, this is definitely what I wanted to do.

In the fall of 1998, I started the 4 year Bachelor of Science in Architecture degree at the University of Maryland.  I was on my way.  For the next few years, I lived in the Architecture building, taking a particular interest in my Architectural History courses.  I became fascinated with buildings, mainly homes, from the Colonial and Federal time periods.  I graduated in May of 2002 and after a month started my career in Architecture.

But, I was far from my desire to be a licensed Architect.  I kept my work records and when the time came, I began to study for the exams.  7 exams at over $200 each.  I took my first exam when my daughter was 2.  I anxiously waited for my results.  The day finally came…

…FAIL.

I was heartbroken.  I was also in the midst of my 5th episode with Major Depressive Disorder.  I decided to take a break and wait for my daughter to get a bit older.  After all, the 5 year rolling clock didn’t start until you passed one of the exams.

1 year after I failed the first exam, I took a different one.  I felt confident going in.  I felt happy when I left.  I felt defeated when the results came…

…FAIL.

The word ‘fail’ and the fact that I am an Alpha with perfectionist tendencies, didn’t ease this situation.  I decided then and there, I was done taking exams until I had the money to pay for the review courses and the exams.

Years went by.  My job growth continued, although minimally.  I began to really think about my career.  Would being licensed make a difference?  At that point, no.  My pay would not increase.  My responsibilities would not increase.  Why spend the money?  Just so I could put ‘Architect’ after my name?

A few years ago, I was struggling with my career.  Where I was working was affecting my Mental Health greatly.  It was not a healthy place for me anymore.  So I once again thought about the question:

What do you want to be when you grow up?

Suddenly, the answer was no longer Architect.  I had become increasingly interested in hiking and nature.  Being outside rejuvenates my soul.  Researching, I realized that maybe a career in Forestry, like becoming a Park Ranger would be for me.  Lacking funds to go get a degree in it, I decided to start small and take a Certificate Course in Forest & Wildlife Conservation.  Most of the material intrigued me.  And then reality set in… there were very little, if any, paying positions in the Northeast, and we were not moving.

Next up in line, a Groupon became available to become a Certified Personal Trainer.  I studied and miraculously passed the exam (an exam that most of its material was not covered in the books the course came with).  To this day, I am still certified.  To this day, I have not used it.

Why?  I changed jobs.  I found a job that still uses my knowledge in Architecture that I enjoy.  Is it my passion?…

…No.

I feel like we stress deciding a career so early in life.  Of course, I made the decision even earlier than necessary.  I graduated college when I was 22, but one had to declare a major by the end of sophomore year.  I look at my daughter now, and can’t even believe that in less than 10 years, she will have to decide what she wants to do with the rest of her life.  How can we decide so young with so little knowledge and experience on what life really is?  She is already starting to decide.  So far she has narrowed it down to Fashion Designer, Illustrator, and Teacher  (Fashionista dropped off the list a couple of years ago).  These are her current passions, but when she is my age (a few years shy of the big 4-0) will she still feel that way?  I don’t.

If I could turn back time (someone send me a Time Turner from the Harry Potter world), I would change my major, knowing what I would endure in the years to come.  Becoming an Architect would fade away.  After suffering severely with Postpartum Depression and Anxiety and with Major Depressive Disorder and Generalized Anxiety Disorder, advocacy is my new passion.  I only want to help others to not suffer the way I have and to get better.  I want others to know they are not alone.  I want to be one of the many people to break down the stigma wall, block by block.  If money were not an issue, I would go back to school now.  I would get a degree in Mental Health Counseling.  I would become a Mental Health Counselor.  Since money does not grow on trees, I will do what I can, maybe one day going back to school.

For now, I am an Architectural Project Manager who advocates for Mental Health and Maternal Mental Health through my writing. And, I am content this way.

November 16th… How Far I’ve Come

It’s been a decade, 10 years, and still on this date every year I think about it, the day I admitted myself into the hospital for severe Postpartum Depression and Anxiety.  Every year I would cry.  The last few years, I got angry.  None of the years did I listen to my therapists (last and current) and actually focus on how far I’ve come instead of how forgone I was.  I focused too much on “Why me?” or “It isn’t fair” all the while knowing life isn’t fair.  I didn’t grow up in some naive protective bubble.  

Many tears have dripped down my cheeks.  I stir up memories of having a panic attack in the ER.  I visualize the days, even weeks, leading up to this moment.  I never wanted to experience this.  I never wanted to hate my daughter.  I never wanted to contemplate running away.  I never wanted to think of myself as unworthy, a disgrace.  I never wanted to cause pain to my husband and parents.  I did though and I carried all that guilt, that blame, that shame, with me on this day for the last 10 years.
The anger I had toward myself would revisit me on this date every year.  The anger I had because I was given this experience set in only the last year.  The anger that because of the Postpartum Depression and Anxiety, the dream of a larger family ceased to exist.  I would no longer have my two, three, four kids I planned I would since childhood.  The anger that because I suffered this, I missed a typical postpartum experience… being that doting mother who adored being around her baby, rocking her, singing to her.  The anger that I missed almost 2 weeks of her life because I was in the hospital.
 
This year, though, I think it is finally time for a change.  Time to not dwell so much back to that moment in time.  Time to sit with the thoughts and feelings for only 10 minutes max and move on.  Time to focus on the good that came from my experience:
 
1)  I got the help I so desperately needed… even if I couldn’t see it at the time.  I’ve dwelled on the lost time, the hate I had for myself and this little baby that took away my life.  But, where would I be if I never went into the hospital?  Would I have run away, contemplated suicide, or worse, took my life like so many other women?  With the hospital stay, I got to focus on getting myself better and I did.
 
2)  My daughter and I have a great relationship.  Years I agonized the fact that because I missed two weeks of her life we would never have a tight bond  or she would use that time lost against me.  I also worried that she would despise me for once hating her.  None of the above happened.  In fact, she appreciates my honesty and knows how much I love her now (to infinity and beyond, forever & always).
 
3)  I am not alone as I thought.  Ten years ago resources in this area were limited.  The hospital, my psychiatrist and therapist were not trained to deal with a focus on postpartum.  The internet was not what it is now with social media and information.  I thought I was alone.  Feeling alone is the worst thing to ever feel.  The isolation, the lack of hope.  Turns out, there is a whole community of us who have experienced Postpartum Illnesses.
 
4)  I get to help and advocate for others.  Once I discovered this community, I wanted to give back.  I wanted to let others know they were not alone and they should never feel like they were.  I wanted to be a friendly ear, a warm hug, a trustworthy soul.  I became a voice for thousands of others who fear(ed) speaking up.
 
After 10 years, I am finally focusing on how far I have come!

When Specific Dates Are Excessively Triggering

I’ve been a Depression sufferer for most of my life. Because of this, I tend to live in the past.  At the moment I am coming up on certain months in my life that cause me guilt, anxiety, regret, and deep sadness… 

October 26th (2014): The day Tyler moved into our house

October 31st (2015): The day I left my new job early to rush my little boy to the Pediatrician because he wouldn’t eat or drink.

November 12th (2014): The day Tyler got kicked out of the first daycare because he wouldn’t follow their schedule. 
November 16th (2006): The day I admitted myself into the hospital for Severe Postpartum Depression and Anxiety 
December 5th (2014): The day at work where I had my cell in one hand talking to Birth to 3 about Tyler and my work phone in the other talking to the nurse at Sophia’s school about an anxiety outburst. 
December 30th (2014): The day I went to the ER for a severe panic attack. 
December 31st  (2014): The day I moved out of my house to my parents waiting on Tyler to be removed from our house.  The day my psychotic break started.  The day I didn’t want to leave work early to go home.  The day the delusions took over. 
January 2nd (2015): The day Tyler left us. 
January 3rd (2015): The first day I started to die inside. 
January 14th (2015): The day I went to the Behavioral Crisis Center at the hospital and spent the night there. 
January 15th (2015): The day I knew I could not be left alone by myself.  The day I went back to the Behavioral Crisis Center.  The day I laid on the bed there and tried really hard to come up with a way to removed a screw from a table and jam it in my head.  The day I admitted myself again to short term psych. 
I try hard every year to look at how far I’ve come, but these dates and the images associated with them instantly pop into my head if I don’t keep my brain busy.  It’s amazing how quickly I can forget the good.  How images of my daughter’s euphoric birth are pushed aside with memories of the postpartum months that followed.  I sit with them, the hurt, the pain, the shear agony, ignoring the good.  Each year it does get slightly better.  EMDR therapy has made a world of difference in how I process these memories.  
Then the dates quickly approach.
Somehow, even with all my effort to push away these negative moments, there is always a moment where I find myself sitting with the anger and the frustration, and of course the guilt, and it seems nearly impossible to focus on the good.  So many happy memories.  
… An intensely cute little cherub of a boy, a dimple in one cheek… instead my focus goes directly to how in the end he was a huge trigger for my Anxiety and Depression. 
… Hearing him speak, seeing him learn how to eat solid food, seeing him discover how to love and loving him back…  to the point it hurt so much to let him go.  To the point I put my Mental Health aside again to try to save my family of four.  To the point I almost sacrificed my life as I admitted defeat, as I raised my white flag and surrendered to my Anxiety and Depression… 
The struggle is in how long I let the negative memories sit with me.  How long to let them dwell in my house, eat my food, drink some tea.  The longer they sit with me, the more deeply rooted they become, and the harder the struggle to pull myself out of them.  I am still working on this step.  Still having issues letting the guilt I have for myself over these events go completely.  After decades of dealing with Depression, I am learning how to live with it, instead of fighting to remove it from my body, mind and soul.  That latter battle is pointless.  It will never fully leave.  I am learning to control it, instead of it controlling me.  
As each of these dates approach, I will let in all the emotions and memories and will work my hardest at not letting the negative ones become permanent house guests.