Month: May 2019

My New Family… The Barnes & Noble Book Event

On By spaige08In Advocacy, anxiety, depression, funny, hospitalization, humor, maternal mental health, medication, mental health, mental health awareness, mental illness, postpartum, postpartum anxiety, postpartum depression, PTSD, relatives, silly, stigma, suicide, Uncategorized, writing2 Comments

I can’t lie, I have fantastic parents. They have grown so much in their views on mental illness. From telling me to keep my mouth shut to being proud about how open and honest I am with my suffering. I have a great husband, whom I chose. He is truly my best friend. He has seen the worst in me and the best and has always stood by me. My daughter is amazing, an old compassionate soul. A kind loving artistic creature and a huge support for me, her mom.

With their support, there has also been some great disappointment with other family members. Since I do not want to upset anyone, I am going to leave them alone and respect them for who they are even if they aren’t very supportive.

They say blood is thicker than water, but I do not believe that. There are plenty of people I know who are adopted or have been adopted and have terrific relationships with their adoptive families. There are many I know that chose friendships over their blood because their blood is just toxic.

I am lucky because I get to have a mix of both. Something a lot of people do not have.

I first ‘adopted’ my oldest and dearest friend ‘J’ as my younger sister. We met when she was 4 and I was 6. For the next few years we had many playdates that included dolls, dollhouses and Lego. Even though there were some years where we were apart, we rekindled our strong friendship and have since been in each other’s weddings and have supported each other with our children. I consider her 3 kids like my own, even though I haven’t met her youngest yet. We try to see each other every year although sometimes it goes longer. And you know what, we pick up conversation as if time hasn’t passed.

Recently, I am choosing to ‘adopt’ more siblings into my tight-knit family.

We all first met online. I know, creepy, right?! You never know who is really behind the online person. We were joined together by who we call our Supreme Leader… CEO and founder of both Stigma Fighters and our publishing company, Eliezer Tristan Publishing. I first met the Supreme Leader through Stigma Fighters as I am a frequent contributor… usually at least twice a year. We met in person at a reading in NYC at the NYU bookstore (wow, that is a lot of letters!) a few years back. What an amazing woman!. I totally love and admire her.

Well, she created this publishing company and was seeking authors who wanted to publish their books. Um, hi, hello, me! I jumped at the opportunity. And hence Rising From the Ashes, the book, was born on October 23, 2018. It is a collection of many of my blog posts here from its birth over 4 years ago until the summer of 2018.

Because of this book, I have met some great people. These people are my family now, including our Supreme Leader.

It all started one day a few months back with a text from the Supreme Leader, “Can you do a book signing in CT on May 17th?” Well, hell yeah I can! She proceeded to tell me that a few other local ETP (Eliezer Tristan Publishing) authors would be there as well. Awesome! I’ve read quite a few of their books and was ecstatic to meet them in person. Well, it got closer to the event, like May 13th closer, when the Supreme Leader didn’t know if she could make it. Usually flying standby, there were no available standby seats.

Panic commenced between the rest of us. We can’t do this without her! It was as if the sky was falling and we were Henny Penny. A group chat was started between us authors to try to raise money for our Supreme Leader and her 2 children, the Little Supremes, to get her here in CT for this event. This chat started out as the “I’m confused” chat because, frankly, we were all very very confused with the situation.

With some begging, a decent donation from myself, and pure luck, we were able to fly the Supreme Leader here. Sadly, one of our fellow authors remained back in Oregon to watch the Little Supremes. This author was my cover designer as well.

Well, in the mass confusion of whether or not our Supreme Leader would make it, Sarcastic Asshole (author of 100) was in a bit of a panic on where he was going to stay the evening of the 16th. Him and the Leader were supposed to be sharing an Airbnb. He was going to back out of coming. Well, I couldn’t have that… no Supreme Leader and no Sarcastic Asshole! No way. I invited Sarcastic Asshole to stay with me.

We had never physically met before. (Insert my mother panicking right now)

So after some mass confusion of which Union Station in CT he was coming into (Yes, we have more than one) and an Uber ride, Sarcastic Asshole landed on my doorstep. Honestly, it was like we were old friends. Conversation was easy with him. We were both very sarcastic people, and some of the oldies of the group of authors. He did think I was going to kill him though as he found my list of what not to do when committing a crime (expect that follow up blog post soon, see the first one here) and quickly took a swig from his bottle of Fireball. But all was well the next morning as we continued our sarcastic banter.

It was time to pick up Young Possum at the train station. After confirming which Union Station we were going to, Sarcastic Asshole and I popped in my car for what would be a fast trip up to Hartford… hahaha. Fast trip on a Friday?! No, CT believes that rush hour starts at 3pm on that day. It took some time but we made it there just in time as Young Possum exited the train station. Now Sarcastic Asshole, of course, started to be a sarcastic asshole with Young Possum but it was all in good fun.

We arrived in West Hartford and was quickly met by Lucky Rabbit’s Foot, her husband, best friend and the cutest toddler you have ever seen. Rabbit was the editor on my book. I admire her so much. What she has gone through and she always seems to have such a cheery positive disposition. Honestly, everyone from this event has gone through so much… so much that some of them shouldn’t physically be here. But that is their stories to tell.

Soon after, Corpse Bride and her mother arrived. I could tell she would fit in perfectly on the sarcasm meter.

But where was our Supreme Leader?!

As the event commencement time was approaching, again, all of us began to panic. What the heck were we going to do without her?! Our anxieties were quelled when she literally popped up in the room.

It’s funny though. If you had attended the event, you would never know that we all had met in person that night. Conversation flowed between us. We read from our books, clapped for each other and had a great panel discussion with the representative from NAMI (National Alliance on Mental Illness).

I was saddened to see the night end. The drive back from West Hartford to my home was a depressed one for this depressive. I missed my new family greatly. None of us knew when another ETP event might happen. The thought of meeting these great people, brought together by mental illness, and not seeing or hearing from them for who knows how long overwhelmed me with sadness.

This sadness quickly dissipated as our private messaging has continued. I have totally ‘adopted’ all of them. They are not only friends. Each one of them… Supreme Leader, Sarcastic Asshole, Young Possum, Corpse Bride & Lucky Rabbit’s Foot, are now close family.

Totally looking forward to our next family event!

I believe it involves breaking things…

Note: I have used nicknames that we have given each other through our messaging and time together. If you would like to know, my given nickname is How To Get Away With Murder because of the above mentioned list and my true crime obsession. They can call themselves out, but I would like to keep their privacy if they do not want to.

And because I love them, I would like to promote their books (which kind of gives away their names):

100

In The Gray Area of Being Suicidal

Nobody

Stigma Fighters Anthology IV 

Untranslatable

Redeeming The Anti-Fairytale

And although my cover designer couldn’t be there, his book:

Cultural Savage: The Intersection of Christianity and Mental Illness

You will not be disappointed!

The Reality of Being a Shorty

On By spaige08In funny, genetics, humor, short, silly, Uncategorized, writingLeave a comment

I’m not going to lie, I’m short. I was never the tallest in class growing up and through the years, I slowly moved towards the front of the line (the short side) in height. Genetics were not in my favor. My mother is a shorty too. My father is not tall. I guess I should have known what to expect.

When I was school-aged, I watched my older sister grow up and admired her final height of 5′-7″ (although I am not sure where she got it from?!). Those recessive genes became my biggest desire. I would compare my stature to all of my friends and get disappointed as each one surpassed me in height. In 7th grade when my ‘special friend’ came to visit, I thought “This is it! Now is my time!” Every morning I would wake up and look in the mirror. I looked taller. I felt taller. I mean my body was maturing in many other ways so why not height, right?!

And then I went for my yearly physical to only be disappointed. “You grew 1 inch.”

What?! Wait a minute?! I got my period so shouldn’t I be going through some sort of growth spurt?!

Height was never meant to be part of me.

After many years of complaining to my parents about my height, how it was their fault I was such a shorty, I finally gave up. What was the point? Complaining wasn’t going to make me taller. I arrived at my final height of 5′-1 1/2″ at 16 and remained there until I hit 30. It has only been downhill since then. At my latest physical (age 39) I only measured 5′-0 1/4″. Don’t ask me how I shrunk 1 1/4″ already. I am a bit shocked myself.

Being a shorty has its pros and cons. Not going to lie, it does suck most of the time.

The Cons

  • I am constantly getting neck aches from looking up at tall people. At home, I am currently the shortest. My husband is over a foot taller than me and my pre-teen (almost teen – EEK!) daughter surpassed me about a year ago.  At work it seems as if every person there is ten times my height. Not only do I look up all the time, I take 4-5 steps back. At my in-laws I am the shortest as well. For once it would be nice to be taller than someone.
  • Clothes… not sure who created Petite sizes but it wasn’t a short person. According to most fashion lines, Petites is for those 5′-4″ or under. Basically, no matter if I buy Petites or Misses, I am hemming my pants. It is a good thing I come from a long line of women who sew. I have gotten really good with a needle and a sewing machine.
  • But pants are not the only item that there are issues. Tops are usually too long and well, you can’t hem a top that has writing on it. You might hem part of the inspirational quote off and be left with “Strong As A…” (wait a minute, I am sure the word ‘Mother’ was there before…).
  • Then there is the kitchen. I have gotten very used to climbing on top of the counters and praying there is no food on them when I do. It just seems that everything I need is on the top shelf of the upper cabinets. Why do you ask? Because my husband is selfish when it comes to the kitchen. He puts what he needs on the other two shelves of the upper cabinets because that is his eye level and my stuff winds up in the heavens of the top shelf. He does this with the fridge too. For now I am mobile and in shape enough to climb the counters but what happens when I am 80?!
  • Cars. We are a 2 car household and we never share because of our height differences. We would constantly bitch when we would need to share our cars. My husband’s car is set for a tall person: seat all the way back and low. My car is set for a short person: seat all the way up front and high that you wonder how a person can fit in the car to drive. Driving to Florida in one car this past October was a nightmare.
  • The aisles of the grocery store are fun as well. The product I need is always, ALWAYS, on the top shelf. And half the time, in the back on the top shelf because supply has run out. If you see a woman scaling the racks in  your store, it is most likely me, Spider Woman. I climb the metal racks, the freezer racks, any and all of the ones I need to reach. I don’t care if I get yelled at by employees. Hey, if the shelf isn’t full and the item is on top, that isn’t my fault. And yes, I know of liability. Just make sure the shelves are built correctly. I am sure they can hold my petite shortiness.
  • I look young. I look so young and being short just aides in how young I look. I have never looked as old as I am. Some see this as a good thing, but honestly, it hasn’t been. When I had my daughter at 26 I was often mistaken for a teen mom. I saw the dirty looks I got from people in the mall as I walked around with my daughter in a stroller. Even now, many think I am 29 instead of 39. I remind people I have a 12 year old child but it doesn’t help. Embarrassingly, I can fit into kid clothing. Couldn’t you just picture me wearing clothes from Justice?! The worst part of being short and being mistaken for someone younger is I have never ever felt like a real adult. Sure, I am a loving wife and mother and am an adult in that sense but when I dress or wear makeup, I feel like a little girl playing house. In prior employments I was never taken seriously because I was the short little girl. I’ve been viewed this way so often that I see myself as that.
  • You become someone’s arm rest. Everyone thinks that since the top of your head is available that it is an invite for their elbow or arm. Let me just say this… no, my head is not your armrest. Do not stick it there or I will smack you.
  • And… I am always the last one to know when it is raining…

The Pros… Yes, There Really Are Some

There aren’t many. But when looking at the reality of something, even though I am a hardcore pessimist (hello depression!), I should look at the positives. At least that is what my therapist tells me…

  • I can fit in kids clothes.  Yes, this is both a con and a pro. Although it is embarrassing, it can also be helpful financially since children’s clothing runs cheaper than adults. My womanly hips are not fitting into any pair of jeans in that section but I have bought several plain tanks and tees. It helped as well in Disney World when I wanted a sweatshirt with Donald Duck (my fave!) on it. The kid size was $5 cheaper. Score!
  • I can fit in small spaces. Hide and seek proved well with me. If I need to be alone, I can just squeeze myself into the bottom of the coat closet. And, being serious now, God forbid, if an active shooter came through at work, I could easily fit in the corner underneath my desk. Maybe not so positive is that I am the only one who can fit in our crawl space. Not exactly a grand beautiful place to be but it does house the wine we are aging. So if I wanted to, I could sit down there, hide and get drunk.
  • My tall child can’t complain to me that’s she’s tall. She has done this and I just stared at her perplexed. I actually asked her why she was complaining about this to me, the short one. Then I sent her whiny butt over to complain to her father for passing on his genetics.

My list of pros are short (ha ha, see, I used a pun there!) as am I, but I don’t let it bother me as much anymore. I will never be able to change it and at this point, I am not sure I would want to.

They Should’ve Warned Me… The PMAD Addition

On By spaige08In anxiety, depression, hospitalization, maternal mental health, medication, mental health, mental health awareness, mental illness, Mother, parenting, PMAD, postpartum, postpartum anxiety, postpartum depression, stigma, suicide, Uncategorized, writingLeave a comment

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I recently read a blog post (written in 2015/revised in 2017) by Jenny Studenroth Gerson on the Huffpost which left me slightly angry and annoyed. Actually, ‘slightly’ is an understatement. I was pissed. In the post, They Should’ve Warned Me, Jenny explains that throughout her pregnancy, she was told to “sleep while you can”, “enjoy your husband now”, and “You’ll never have time to shower.”

Then she proceeds to explain how ‘they should’ve warned her’ about the immense love she would have the second her child was born. About how crying is happy thing. About how you would love your husband so much more. About how eating healthy would create enough milk to nourish your child. About how even being extremely exhausted, waking up in the middle of the night to take care of your child is so rewarding. About how the little cries and screams wouldn’t piss you off but make you feel like a rock star… and so on and so on.

As someone who suffered from two PMADs (Perinatal Mood & Anxiety Disorder), I was angry after reading this. First off, you do not need a ‘warning’ about loving your child. Everything she lists in this post are happy things (and frankly I can’t buy that all of them are true). Who needs a warning that you are going to cry at your child’s birth because you are happy?! Really?! With all this anger, I decided I needed to counteract this post with one of my own that deserves the word ‘warned’ in the title:

They Should’ve Warned Me: The PMAD Addition

12 years ago, I suffered. I suffered first from severe postpartum anxiety that slowly morphed into severe postpartum depression. This is what ‘they’, whoever ‘they’ are, should’ve warned me and, in turn, you about:

  • They should’ve warned me that my anxiety would start right after birth. That I would constantly worry if my daughter was getting enough colostrum. That I would have anxiety attacks in those first few hours in the hospital about why after 2-3 hours she wasn’t brought to me for a feeding.
  • They should’ve warned me that the anxiety would only grow as I had to identify the color of her poop. Is it green? Is it mustard in color? Is it brown?
  • They should’ve warned me that breastfeeding is hard work and sometimes it is not the right answer to feeding your child and that that is okay. Why is she falling asleep on my boob after 5 minutes? Is she eating enough? Oh God, what’s wrong with her?!
  • They should’ve warned me that although crying is normal, keep an eye on it, it could develop into something more than Baby Blues. I cried from day one. Sure it started out being 3-4 times a day but it slowly grew in excess of six times a day.
  • They should’ve warned me that sleep is important and to push for it. Yeah, I get it, you’re not going to sleep much when you have a newborn, but if you have a prior mental health condition (such as myself with depression) then those around you should know the importance sleep plays in your life and allow you to rest for a few hours.
  • They should’ve warned me that my anxiety would worsen that no matter what I tried to eat, it wouldn’t stay down. That vomiting would become my new way of life. That Ensure won’t cure it all and that the smell of chicken cooking would have me running to the bathroom.
  • They should’ve warned me about how my love for my infant would grow into hatred. That with each shriek, I would want to pull out my hair or bang my head against the wall.
  • They should’ve warned me that I would become hysterical enough to make plans to run away, that my husband and daughter would be better off without me. That the whole world would be better off without me.
  • They should’ve warned me that I would scare my family and friends with my hysterics.
  • They should’ve warned me that I would see myself as useless, unworthy and undeserving of love.
  • They should’ve warned me that all this would occur in the first month postpartum and would culminate into admitting myself into short-term psych.
  • They should’ve warned me I would have to be inpatient for 12 days.
  • They should’ve warned me that I would go through many therapy & psychiatry appointments after my stay.
  • They should’ve warned me that I would go through multiple medication changes that first year to find just the right combination.
  • They should’ve warned me that it would be a few months before I loved my child again.

And…

  • They should’ve warned me that it would be a year before I would smile for real.

PMADs deserve warnings. The things Jenny Studenroth Gerson mentions in her article do not. It took me to one year postpartum to feel like myself again. To fully embrace my daughter with infinite love. To know my life is the way it was meant to be. For some women it is longer. Although most women will not be affected by a PMAD, there is a high percentage that are. About 1 in 5 women will experience postpartum depression. That’s just one PMAD. Let’s not forget about postpartum anxiety, postpartum OCD, postpartum PTSD, and postpartum psychosis. These are things to be warned about.

If I could tell Jenny Studenroth Gerson one thing it would be:

Research your definition of ‘warn’. Most women understand and have the immense love for their partner and child at birth. Most women will successfully breastfeed. Most women will cry tears of joy when their baby coos or cries. But you need to realize that over 20% of the postpartum population will not feel that. They will not see these items as warnings (and they didn’t, I took to my Warrior Mom community with this one). Some will find your article cruel, like if they didn’t feel what you did, they weren’t as loving as a mother as you are. And, if they read this while going through a PMAD, it would just make them feel worse. I understand you enjoyed your postpartum stage (and around 80% of mothers will) but please show compassion for the rest of us.

If you are someone you know is suffering from a PMAD (Perinatal Mood and Anxiety Disorder) resources can be found at the sites below:
The Bloom Foundation for Maternal Wellness
Postpartum Support International
2020 Mom
If you know a mother or are a mother considering suicide, please call the National Suicide Prevention Hotline at
1-800-273-8255
or text 741741

This Time is Different

On By spaige08In depression, medication, mental health, mental illness, stigma, Uncategorized, writingLeave a comment

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“I feel different.”

I wake up most days and this is the first thought that pops in my head. Since my depression has returned like a cyclone attacking a house this January, I have not felt like me. Most people with depression will understand this. I mean, I’ve been through this countless times before. Why is this time different? Why am I struggling so much? Why isn’t it over yet?

The last diagnosis I was given by my therapist happened about a year ago before depression became a guest in my head once again. He had told me when I asked that he considered me as having, “Persistent depressive disorder (PDD) with episodic major depressive disorder (MDD).” At the time I agreed. Even though I was content with life, I wasn’t ever fully happy. I had immense amounts of love for my husband, daughter, family & friends, but there was always something missing… small, tiny, minuscule as it was, it was a constant reminder that depression was still lurking in the back of my mind awaiting its next visit.

This was PDD. The constant low-level depression that I have lived with over the last few years once my MDD episode #6 was over.

And then January occurred. My husband broke down, broke a few cups by slamming the top rack of the dishwasher and cried. He expressed his anger toward me about everything that happened with my former foster son 4 years ago. The event that sent me into MDD episode #6. I listened. I felt compassion for him, empathy. And while he was shedding tears (which he had every right to) it suddenly hit me that I wasn’t.

Damn Lexapro! A drug I have been on since January 2014. A drug that has stabilized me. A drug that kept me sane. It stole something from me that did not bug me until then. It stole my expression of emotions. I honestly have not cried in 2 years and it has slowly gotten worse to where I can’t even express my compassion and empathy. I just look cold.

While my husband felt better by the next day, I did not. I felt worse. So much worse that I took up the art of cutting. Ashamed the first few times I did it after the act, it was a way for me to feel, for me to know I wasn’t an empty void, that I was human. If I cut and bled, that meant I was human.

Each month, the cutting has been less often. I thought I was done with it. Only 4 times in April, but May has proved me wrong. Because this time is different.

This depressive episode has not been classified by my therapist as “Major”. My psychiatrist is not sure she agrees or not with my therapist’s diagnosis. I would call it moderate to major, only throwing in the word “major” because of the cutting. But it is different. Very, very different.

It has become cyclical.

One week I will be so happy, almost euphoric, and the next I am down in a shit hole. It will be days of not wanting to get out of bed, not wanting to eat, and not caring about anything. Then there will be days when I can function but that emptiness and funk is still there. Until one day, I wake up happy and elated. And the cycle repeats.

I had started to Google cyclical depression which led me to cyclothymia. I read the description and thought, “Hmm, this could be me, but maybe not.” My therapist did not agree with my self-given diagnosis because I did not show anything that was related to hypomania and I hadn’t had this cycling for over 2 years.

Yet, still, I complained about the cycling. I have no hope whatsoever that I will get better because every time I have a good week and get slightly hopeful, it is ruined by the bad week.

Through all this, I have consulted my psychiatrist. She put me on Wellbutrin along with my Lexapro to see if that would help with my emotions returning and wake me out of my intense brain fog and lack of concentration and motivation. I took it for 2 months and recently stopped with her blessing. It was not working. In fact the brain fog and concentration has gotten worse. I can’t think of the right words for objects. I switch words around when I speak sometimes. I’ve stood in front of cabinets wondering why I went over to them when I knew 2 seconds prior.

This Wednesday, I asked her, “What now?”

I had 2 options… go back on a anti-psychotic or try a mood stabilizer. After living with almost 2 years of constipation because of the anti-psychotic (Seroquel) I was on, I had no desire to relive that again. I opted for the mood stabilizer. Commonly used for those with biopolar disorder, I wondered why she suggested it. Then I asked her, “Do I have bipolar disorder?”

“No,” she said, “You have never exhibited anything related to mania or hypomania, but what you are explaining to me is cyclical, like bipolar disorder, so I think this will help to stabilize your moods.”

Last night, I took my first dosage of Lamictal (or the generic version). As with all the SSRIs I have been on (every one of them through the years) I will have to wait 4 – 8 weeks for it to fully kick in. This will be months 3 and 4 of my trial-and-error phase with medications. An issue I never had before.

All because I feel different. All because this time is different.