Thank You!

Call it part of a Depressive’s “12-Step” Program, but I feel the need to say thank you to the people in my life that have contributed to my better health and wellness.  Considering the decades that I’ve struggled, this list can become rather lengthy but I will narrow it down to my latest and greatest (note sarcasm) episode of Major Depressive Disorder.  Some people listed may shock you, but all have helped in bringing the strength trifecta back to me.  I now feel strong.

Thank You To:

My Parents:  You have never given up on me.  Although we all struggled to understand exactly what was going on with me in my teenage years, you never pushed my thoughts and feelings aside.  You never told me to “suck it up”.  You never told me to “just get over it”.  From the beginning you both have sought out ways to get me help starting with group therapy, to Cognitive Behavior Therapy and even medication.  You helped when I was a few states away in college.  You both have cried with me, constantly worried about me but never ever left my side.  I am extremely thankful to have you two as parents as many others do not have such caring and understanding parents in their lives.

My Husband: Oh, what we have been through… first and foremost, thank you for never taking me up on my offer to leave me.  I must of told you dozens of times to go, take Sophia and run.  But you didn’t.  You stayed and took our wedding vows seriously.  You loved me when I was “crazy”.  You sacrificed so much when I was hospitalized.  You never gave up on me.  Although now you are unsure of what to say or do when my illnesses make themselves present, I know you care.  As Bon Jovi said, “Thank you for loving me”.

My Sophia, my baby girl:  How did I get so lucky?!  You are the light in my darkness.  So compassionate, kind and empathetic.  You have never made me feel guilty or unloved by you.  You worry about me to extents you shouldn’t but I appreciate it.  You are always there for a big hug.  Thank you for being  you.

My Therapist:  Hmm… I don’t think I would be here without you.  I came to you in the darkest moments of my life.  Lost and completely hopeless that I would ever recover this time.  CBT therapy wasn’t working this time.  I needed something more.  It was fate that all I did was Google EMDR Therapists and narrow it down to who was more convenient in location.  It just so happens that the most convenient turned out to be my saving grace.  I had huge doubts that EMDR would work.  Highly emotionally draining in the beginning, you helped me to reprocess the loss of Tyler and in turn, the loss of Sophia’s infancy, my Postpartum, loss of more children and even the loss of my former self.  Thank you!

My Friends: From visiting me in the hospital to checking in on my through social media and texts, I am grateful for each and every one of you.

My Gym:  Again, another choice of convenience to work and home, the gym has been a wonderful addition to helping me get strength in all areas of life.  Aside from building up my physical strength (I can barbell squat 135lbs currently!), all the trainers, instructors and the owner have made me feel welcome, like I belong.  I am not just a number lost among many.  It is a close knit family that I am thankful to be a part of.  Thank you!

My Medications:  Although the stubborn weight gain and selective side effects are an annoying pain in my ass, I am completely grateful that they exist.  I used to hate taking these tiny pills to feel ‘normal’ but now I am thankful they help me to feel like myself.  We have a strong bond that will never be broken.

And lastly…

Myself:  I think this was the hardest person to thank.  I spent years hating myself, years internally abusing myself.  I didn’t matter.  I didn’t deserve love.  At points in my life, I thought I didn’t deserve to live.  I have come a long way.  Battling Depression and Anxiety both physically and mentally, sometimes draining myself into complete despair…  I’ve finally learned acceptance and because of this have become kinder to all aspects of myself.  I am now happier and understand I cannot change the past.  I am starting to live in the present, enjoying the little things in life… my daughter’s smile, a chirping bird, pretty flowers.  I want to live.  I want to see what the future brings.  Thank you Stephanie, for learning to live.  You are truly an amazing strong being!

 

When All You Can Do Is Blame Yourself For Your Daughter’s Diagnosis

I tried to hold my tears back as I stared into my daughter’s oceanic blue eyes.  I could feel them welling up, feel the moisture increasing.

Not here, not now, not in public, Stephanie.

But, to be cliché, the dam was about to break.  A tear or two escaped.  My daughter was concerned and relayed this to her father on the phone.  She handed my cellphone back to me and my husband proceeded to ask, “Are you okay?”  No, no I wasn’t okay, but do I tell him that?  The silence was broken as he asked again.  I told him the truth because even if I lied and told him I was okay, he knew I wasn’t.

I am about to cry,” I uttered quietly so the other patrons could not hear me.  My daughter and I were waiting for our dinner order to be ready at our favorite sandwich shop in town.  It was last Friday evening, the start of the weekend, and my husband’s Friday to geek out and play Magic.  He wanted to stay home with me.  I told him no, I didn’t want him to blame me for not being able to play (even though he wouldn’t, it was all in my head).  I told him this knowing full well that I wanted his support but feeling I didn’t deserve it.

Our food order was ready and we went home passing my husband’s car on the way.  When we pulled into the garage, my tears flowed like a high pressure hose.  My daughter wanted to know what was wrong although she could somewhat guess as she has been a witness to me, her mother, for the last eleven years.

“It’s my fault, it’s all my fault.”  My lamentation increasing as these words escaped my mouth.

“What is your fault, Mommy?”

“That you are the way you are.  It is my fault.”

My daughter has been diagnosed with Generalized Anxiety Disorder since she was 6 and has struggled off and on with it over the last 5 years.  This year has been extremely hard on her and because of it, hard on me.  She has been in therapy since the fall and because of some reactions she has had during her anxiety attacks the past month, it has recently been suggested that she get evaluated by a psychiatrist.

When the recommendation was first made to me by her therapist, I have to say I was a bit shocked.  I guess I never thought that her Anxiety warranted a psychiatric evaluation.  After a few hours, I have to admit the stigma against Mental Illness set in; her seeing a psychiatrist would really mark her as someone who is mentally ill.  I hurt for her.  My husband and I discussed the evaluation with her.  She has learned about the stigma, has learned to stand up to it (from her Mom of course).  But even this, having the word “psychiatrist” associated with her name, caused her to want to hide.  She instantly thought she would be medicated.  Eventually, she became okay with the evaluation that is set to be done in another week and a half.

All this got to me.  It pulled at my heart, tore holes, ate away at it.  The biggest fear I had when becoming a parent is that I would pass on my Depression and Anxiety to her and I have.  Her being in therapy never bothered me.  I am a firm believer that most people would benefit from therapy regardless of a Mental Illness diagnosis.  It was the mention of “psychiatrist”.  To me, like my daughter, I associate “psychiatrist” with “medication”.  Throw in the word “evaluation” and I was losing it.  I held back my emotions for the sake of my daughter, but I knew eventually they would become very visible.

I spoke with my therapist about it.  He told me it wasn’t my fault.  I said, “How?  How is it not my fault?!  She suffers the way I do.  I never wanted her to and now she is.  It’s only going to get worse.”  He logically said that this is something I did not give her on purpose.  There was no way of knowing whether she would be Mentally Ill or not.

“But I gave it to her.  It is my genetics that did this.  She is becoming me.”

No matter how many people tell me it is not my fault (heck, even my intelligent daughter tells me), I still cannot stop blaming myself.  I can’t kick this feeling.  She is already experiencing more than I ever did at her age.  I mean, I wasn’t even diagnosed until 14 and here she is at 11 with 5 years of Anxiety under belt.  Maybe I am transferring myself onto her to an extent, already predicting more suffering in her future getting worse and worse as she ages like it has for me.  No parent wants to see their child endure pain and illness.  In this case, I didn’t want her to endure the thoughts that I have felt, the fear I have felt, the hopelessness that I have felt.  I didn’t want her holding a case cutter to her wrist.  I didn’t want her desiring to stick something in her brain to end the constant negative thinking.

And yet it is beginning.  The fear is already inside of her.  And it was all my fault.  How could I, someone who has battled Depression and Anxiety for over 24 years, not feel blame?  More importantly, how can I stop feeling blame?

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?  

Awaiting My Emotional Aftermath…

I am sitting here nauseated.  Stomach churning.  Gurgling.  Body repulsed and mimicking regurgitating motions when thinking of eating my breakfast.  It is almost 11am and I have not eaten anything yet.  I have been up since 6:40.  I am anxious.  Anxiety has been building in me since this past weekend started.  There is so much to do and, frankly, not enough time.
On Thursday, I leave for Atlanta.  I am going for pleasure, not business this time.  I will be spending three days there interacting with a wonderful group of Warrior Moms at the 2nd Annual Warrior Mom Conference.  This is indeed a no judgment zone, more so than Planet Fitness.  All of us have empathy.  All of us can relate to each other in some way because all of us have suffered and survived a Postpartum Mental Illness.  I have enthusiastic anxiety.  I am elated to see all of these mothers I met last year and to meet so many more this year.  I can’t wait to learn more about what I can bring to my community.  And, of course, see a little bit of Atlanta while enjoying some Southern fare.
One minor problem that weighs heavily and what is causing my anxiety to grow… I decided to have my daughter’s birthday party the day after I get back, this Sunday.  I did this for numerous reasons.  Sunday is her actual birthday.  I also wanted to get this party stuff over and done with.  By doing this, I left the last minute party details in the hands of my husband, a guy who is wonderful, but has never helped me with planning any of our daughter’s parties.  Now in addition to my packing list, I have to create the “You Need To Do This On Saturday For The Party” list.
And, I am at work… getting overwhelmed with what I need to do here and the above mentioned.
I’m worried.  No, scratch that, I am fearful that I stretched myself too thin.  I am very worried that I’ll snap and like a stone released from a slingshot, be propelled backwards even deeper into that sinking hold of my Anxiety Disorder.  That quicksand, suffocating.  Drowning in the depths of my Frenimies… Anxiety and Depression.
And I did it anyway.  I created this.  I could have easily made my daughter’s party another weekend.  What the heck was I thinking?!  My flight home won’t arrive back at the airport until 11pm on Saturday.  I won’t get back to my  house until 12am, 1am on Sunday the 16th, my daughter’s 10th birthday.
And then there is that… the fact that my baby, my Only, is turning 10.  Double-digits.  I am extremely excited to celebrate this with her, but devastated that this is the beginning of the end of her young childhood.  From this point on she will get moodier, meaner, more secluded.  First with prepubescence and then with becoming a full-fledged teenager.  My sweet little girl will start to not want to be seen with me.  She’ll start to pull away from hugs and avoid kisses.  Yes, 10 starts my grieving process.  Grieving for the baby, toddler, and young child she isn’t anymore.
So many emotions going through me in this short period of time.  I will be fine, yes extremely anxious, but fine until I come back from the conference and get through her birthday.  Then all hell will break loose.  This has happened to me numerous times before.  I did take measures to try to relieve the affects of all these emotions, feelings and side effects from this Anxiety.  I decided to take Monday off of work too.  Crazy, I wasn’t going to do that originally.  I scheduled a massage and have therapy that day.  I am hoping to hike, weather permitting.  All things that help me cope, that relax me, rejuvenate me.
Now I wait… wait to see how bad my emotional aftermath will be.  Wait to see how dead tired and irritable I will be on Sunday as I entertain about 10 girls age 8-10 of course putting on a happy face and pleasant demeanor.  Wait to see when it all will hit me.
Going to try to force myself to eat breakfast now (at 11:30am)…