I Landed in the ER after watching '13 Reasons Why'

Four days ago I finished watching the Netflix series ‘13 Reasons Why’ and drafted an opinion piece which I published Monday morning. The show rocked me to my core. So much so, that I landed in the Emergency Room of my local hospital. This is the story of how and why that happened. I live with type 1 bipolar disorder. For those who aren’t aware of the various types of bipolar disorder, Bipolar Hope Magazine is an amazing resource and they have an informative section on their website which describes the types of bipolar and different symptoms. In a nutshell, my type of bipolar disorder means that I lean towards the manic side of the condition. If I’m not careful to protect my sleep, I could find myself launching into a manic episode. It doesn’t happen overnight, rather, over the course of several nights of getting little to no sleep.

As I mentioned in my opinion piece, I put my mental health at risk by choosing to watch the show. I didn’t know how risky it was to begin watching the show because I’ve been mentally healthy for the past 7 years. The last time I was hospitalized for a manic episode was, ironically, exactly seven years ago this month, when I was 5 weeks pregnant with my second child. I thought since I had been so stable for so long, it couldn’t possibly be that risky to watch a few episodes.

I was wrong.

I started watching the show Friday evening, and got through four episodes (binging) before forcing myself to shut it off so that I could get some sleep before flying to Cedar Rapids, Iowa for my nonprofit’s show the following night. Our Iowa Corridor This Is My Brave show was incredibly moving and inspiring, as all of our shows are, and I was so excited to get to spend time with the show’s producers and cast members afterwards. We went out to a local bar and played Cards Against Humanity while eating and hanging out. I had a blast. But unfortunately didn’t get to sleep until 2am EST, and awoke at 6am Sunday morning. I usually sleep well when I’m on the road, but I had so much on my mind having started watching the show the night before and wanting to continue watching.

I pushed play on episode 5 shortly after waking up, and was able to finish the series in the airport on my way home on Sunday. I was furious by the time I finished, and reached out to several of my friends via text to see if they had watched and to get their thoughts. Everyone seemed to have similar feelings, but slightly different reactions. Overall, the few people I was able to connect with directly were shook up by the show, but were glad it was out and was opening the eyes of the public.

At that point I began thinking about those in my circles who were already vulnerable, sensitive. How would they take it if they had watched? How would teenagers react to the show? Especially if they didn’t have solid support systems in place, if they were already in a tough place, if they didn’t have the energy or resources to access proper mental healthcare.  

I landed around 8:30pm and grabbed an Uber home. I normally enjoy chatting with the driver, but on this particular ride I needed to connect with one of my close friends. I called my This Is My Brave Co-Founder Anne Marie Ames. She and I have been friends for four years, and I needed to tell her how the show affected me. We talked the entire ride home, and agreed to catch up again during the week.

My husband had let our kids stay up late so they could see me, so I hugged and kissed my little people and got them tucked in by 9pm. My husband knew how I was feeling because I had called him from the airport, and he knew that I wasn’t sleeping well. The plan at that point was to focus on sleep all week, make it a priority again. On the flight home from Chicago I had jotted down my feelings and initial reaction to '13 Reasons Why', and I told him I felt that if I was able to get them organized into a piece that made sense, I’d likely sleep better. I started pulling my thoughts together, tapping away at my laptop, and he went up to bed.

I crawled into bed around midnight, as it had taken me longer than I had hoped to draft my reaction. But I did feel better once I got it out, so I was hopeful I’d be able to get some quality sleep.

Only, instead of crashing and sleeping hard, my sleep was broken and riddled with nightmares. I woke at 5:30am, and since my husband was already downstairs doing his normal early morning workout in the basement, I grabbed and pen and paper and let my feelings flow again. I shot off a draft of my revised piece to two friends and by then it was time to wake the kids and get them off to school.

I recognized my symptoms of hypomania and immediately told my husband that I was going to call my psychiatrist at 8:30am when they opened to get an appointment. He said that he thought that was a good idea and off my family went to work and school. I normally find relief in the calm of the morning once the house is quiet and I’m on my own. But instead I found myself feeling that familiar current of mania beginning to rush through my blood and anxiety creeping in.

I still hoped I could relieve some of these symptoms by publishing my reaction to the show. I felt a little better after hitting Publish on Medium, but things escalated quickly from there.

I picked up my kids from school and took them out for frozen yogurt, one of our favorite treats. I hadn’t seen them all weekend, so it was fun to catch up. As we were sitting there, Kelly, my best friend from college called to see how our Cedar Rapids event had gone. I told her it was amazing, as all our events are, but that I had a lot on my mind. She caught on immediately that I wasn’t in a good place, probably based on the tone of my voice, but I told her I couldn’t talk because of where we were and the kids were with me. She offered to pick up the groceries I said I’d be running out for later that evening, so that I could head to bed early instead. She agreed to meet me back at my place in ½ hour.

{One of the things Kelly asked was critical for her to know how I was doing mentally, and she knows this from being there when my very first manic episode came on back in December of 2005. She asked me where I was on a 10-point scale. I was at a 6-7.}

When a person with type 1 bipolar is at a 6-7, it means that they’re in a hypo-manic state. A person can very quickly go from a 6-7 to a 9-10, meaning they need to be admitted to a psychiatric hospital, if things aren’t addressed in an urgent manner.

Once we were home, I did my best to summarize for Kel why the show '13 Reasons Why' affected me so deeply. She’s a teacher, and hadn’t heard of the show, but when I told her how I had met a friend of mine for coffee that afternoon, she had a better understanding. The friend I met up with had been directly impacted by suicide, as her son Jay took his life last year, and now the family is pursuing a lawsuit because Jay’s guidance counselor had been alerted by a friend three weeks before he took his own life. The counselor had neglected to contact Jay’s parents. You can read about it in the Washington Post.

Little did I know, Kelly had already set an emergency intervention plan into place, even though she may not have noticed it at the time. While she was picking up the groceries for me, she called my husband and let him know that she was concerned about me. She also texted another one of our close friends from college who had a friend who was a pharmacist. (What can I say? It takes a village.)

When Ben got home, he found the kids happily playing video games, while Kelly and I were sitting in the dining room trying to figure out a plan. I needed Ambien to ensure that I got a solid night’s sleep. The only problem was that I hadn’t used a sleep medication in seven years, so we didn’t have anything (expired or otherwise) in the house. We called my psychiatrist’s office to see if we could get through to an after-hours line. We left a message for my doctor’s medical assistant, but by then it was already 6pm and we were running out of time. We called my regular pharmacy, but my psychiatric medication info was out of date. (Side note: I use a mail-order pharmacy to fulfill my regular mood stabilizer prescription which I’ve been on for the past 7 years at the same dose.) The pharmacist at my regular pharmacy recommended an over-the-counter sleep aid, but we weren’t convinced that would work for me given my level of hypomania.

Our friend who is the pharmacist (in California) communicated by text that if I didn’t have Ambien on hand at home, I would need to go to the Emergency Room to get a prescription for it, and that was what she recommended given my symptoms. I argued it was overreacting, but based on my experience living with this condition for eleven years now, and my past 4 psychiatric hospitalizations for mania, I also knew she was right.

Kelly offered to drive me to the hospital while Ben held down the fort at home. I resisted at first, as it seemed dramatic and unnecessary. I wanted to just get an OTC sleep med, and said we could get Ambien the next day from my psychiatrist. But looking back now, it's a good thing I didn't resist as I could have ended up in handcuffs again, being carted off to the Emergency Room and then the psychiatric hospital. I didn't want my kids to have to see that happen, so I happily went along with the intervention plan. 

We joked on the drive over about how efficient my intervention team was and how I was voting her President of the team based on her stellar performance. (In college, Kelly was President of the water polo team and I was Vice President, so it seemed fitting.) We were immediately admitted to the ER, the intake nurse took my vitals, and I was sent back to a triage room with a bed. By that point I had called my parents to let them know what was going on, letting them know the plan and that we had everything under control. They were worried but relieved, and asked that I keep them posted.

The ER doc was really great, and got us in and out quickly with a script for the Ambien that hopefully would do the trick and get me through until I saw my psychiatrist on Wednesday. Ben had called his mom and she was already at our house by the time I was getting my discharge papers, and he met us at the hospital right as I was released so that he could drive me to get my script and Kelly could head home to her family.

Ben’s mom got the kids in bed as I called my parents to update them once we got home around 8:30pm. I ate a little something for dinner, and was crawling into bed by 9:30, ready to let the meds do their trick and lull me into a deep sleep.

Only it didn’t exactly work as planned.

I slept from 10pm until I woke at 1:30am, unable to get back to sleep. Hypomania/mania has a way of doing that to a person. I woke my husband and told him I couldn’t sleep, so I took another dose of the sleep med. I woke groggy at 6am Tuesday morning. Concerned that I had to take two doses, when in the past one dose had worked for me, we called to bump up my psychiatrist appointment, and luckily she had a slot in her schedule for Tuesday afternoon.

My husband was able to take time off from work to drive me to my psychiatrist appointment. We filled her in on everything that had happened, and made a new plan including medication changes. She provided us with her emergency contact info in case we needed it, and answered all our questions. We were in and out in an hour total. My mother-in-law was able to help us with our kids while my husband went back to work for the afternoon and I went to run a few necessary errands, including picking up my new prescription. My therapist (who I haven’t seen since December, because I’ve been “busy”), has an awesome online scheduling tool for current clients. I grabbed one of her only two open appointment slots for Thursday.

Tuesday night we followed the plan. It was extremely difficult to get out of bed Wednesday morning due to the side effects of the medication changes. I haven’t had trouble getting out of bed because of my mental illness for so many years that I forgot what it felt like. It’s hell.

My anxiety has returned due to this “almost-episode,” which is totally normal. It’s just been so long since I’ve felt it that it’s been a little overwhelming. Uncomfortable, yes. Manageable, yes. Especially when I have such an incredible support system and so many resources at my fingertips.

I may have been able to stay mentally healthy for seven years, and yes, that's a long streak. But if this week has taught me anything it's that I'm not immune to relapses. I live with type 1 bipolar disorder and I'll always have it. Like any other chronic condition, it's lifelong. I'll continue to kick bipolar's ass, I know I will. I'm even a little grateful for this week's experience because I had been feeling like a bit of an imposter lately, having not felt symptoms for so long and getting to do this nonprofit work where I hear stories of individuals overcoming mental illness every week. I'll forever be a member of the club, my tribe, as I call it. And together we're ending the stigma surrounding mental health disorders. One true story at a time.

*****

About a year ago, I wrote a guest post for a website called OC87Recovery Diaries, and in it, I stated that we didn’t have a plan. The reason I’m publishing this post is not to highlight how fortunate I am, but to point out how I almost landed in a psychiatric hospital this week, but didn’t, because we had a plan. It may not have been a formal, executed WRAP (Wellness Recovery Action Plan), but it was darn near close, and it worked.

If you or someone you love lives with a mental illness, it's important to have a plan. And if you're in a tough place right now - here are some things I find helpful:

• Know your local and national mental health resources, including the crisis hotlines. This Is My Brave's Resources page is a great place to look, or even just Google it and keep that info handy.
• Make sure you know how to contact your psychiatrist after-hours in case of emergency.
• Keep a journal that lists the meds you're currently taking and what's working for you. Allow those closest to you to have access to this in case of emergency.
• Don't be afraid to be completely honest about how you're feeling. Feeling overwhelmed, triggered, fragile, etc., and sharing your feelings with those you trust is NOT weakness. In fact, it's the complete opposite. It's brave to allow yourself to be that vulnerable and it leads to deeper, more close-knit relationships with the people you love.
• Don't lose sight of self-care. We often get so wrapped up in our day-to-day lives that we forget to take time out for ourselves, and being too "busy" can lead to burn-out and mental health issues.

Letting Go of the Secret

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Living a life with an ever-present fear of revealing a certain secret part of yourself isn’t truly living. I know, because I’ve been there. Being caught up in an inauthentic version of myself wasn’t the way I wanted to live my life. And so I made some changes. The results were incredible.

At twenty-six years old, newly married and at the peak of my career as an agency recruiter, I was hit with mania. It came without warning, and felt exactly the same as slipping on black ice and landing flat on my back, the wind sucked out of my lungs and a searing pain pulsing through my bones. I was terrified of what was happening in my brain. I had lost control of everything and my career and reputation were on the line, not to mention my relationship with my husband who didn’t see this coming.

How would I ever recover from this mess?

I would, although recovery eluded me several times. Following my diagnosis, I spent a full year in what felt like an extended visit to a deserted island: the isle of depression. It seemed like no one could possibly understand what I was feeling. I fought waves of anxiety each morning, and would calm myself down from my afternoon anxiety by collapsing on the couch in front of the television, tears soaking the oversized pillow which my head rested on.

I saw many doctors, so many that I can’t remember most of their names. My parents pushed for second, third, fourth opinions. Not because they didn’t trust the doctor’s opinions, but because we hadn’t figured out what would bring me back to my baseline. My normal. Finally, after seeing one of the top doctors in our area, a national specialist in the study of bipolar disorder, I was ready to follow his advice, the same medication recommendation that the previous few psychiatrists had been urging me to try.

Within two months I felt better than I had felt in an entire year. Slivers of my old personality were coming back. When I laughed, it felt genuine and amazing, better than it had felt even before I became sick. When several weeks had passed and I realized I hadn’t cried, I was shocked. The drug was actually working for me.

There would be two more hospitalizations in the years that followed, only because I had taken myself off my medication during pregnancy to protect my kids. When my daughter was only 8 months old, I decided I was ready to tell my story in order to help other women who might think they couldn’t have a family because of their mental illness. I launched my blog and began writing, but kept my identity a secret because I feared the repercussions of the stigma associated with mental illness.

I kept writing and sharing my experience as a mom raising two small kids while at the same time managing my bipolar disorder and over the next year and a half, I realized that keeping my identity a secret was only adding to the stigma surrounding mental illness. It was a part of my life and I wanted to show society that I’m a real person with real emotions and I believe that people who live with mental illness should be treated like any other person living with any other life-long disease. We didn’t ask for these conditions we were dealt, and the last thing we need is for society to look the other way when we’re suffering and need support to find recovery.

I was no longer ashamed.

And so in April of 2013, I announced on my blog that I was “ready to not be anonymous anymore,” and I took a brave stand against stigma. The support that poured in from my family and friends, and people I didn’t even know but who had read my post, was overwhelming. The words of gratitude for sharing my story so courageously were like fuel to me, as I kept writing about my experiences and connecting with people who appreciated my transparency.

Six months ago I launched a project and couldn’t have imagined the response it has generated. This Is My Brave is a live theater production where people from the community will take turns at the microphone to share their story on stage via personal essays, original music and slam poetry. This Is My Brave is more than just a one-time performance. We have become a platform and a community for people living with mental illness to speak out in an effort to end the stigma associated with brain illnesses.

Our mission is to ignite and actively promote―through actions and social media― a positive, supportive national conversation about mental illness for those who live with, or love someone who lives with, a brain illness. Through the sharing of stories and experiences of those in recovery, we expect to provide a sense of community and hope; encouraging others to share their stories. We believe that each time one of us talks openly about living with mental illness, we create another crack which helps to break down the stigma. We’re currently in the process of converting to a 501(c)3 non-profit organization and have been actively planning the pursuit of our mission beyond the debut of This Is My Brave in Arlington on May 18th.

It’s time we bring mental health issues into the spotlight because they’ve been in the dark too long. Please visit www.thisismybrave.com to learn more about the show. Auditions are currently being scheduled (www.thisismybrave.com/auditions) and tickets to attend the show are on sale now at EventBrite.com.

Follow the show on Facebook, Twitter and Instagram for all the latest news!

My {In}voluntary Commitment and Why You Should Care

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Our bedroom door creaked slowly open at 6:35am this morning and my little man crawled under the covers next to me while my husband finished getting dressed for work. As I felt the chill of little toes brush my warm legs, I thought back to this same day, five years ago, when my mania had reached the breaking point.

I had begun to cross the threshold, going from highly manic to the inevitable psychosis, when my husband took matters into his own hands and called 911 for help.

What a stark comparison to today, I thought, as I reached into my sock drawer to fish out my psych ward socks. I pulled them on this morning as a way of honoring my past, while at the same time recognizing how far I’ve come and how I don’t ever want to go back.

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If your father were having a heart attack, or symptoms consistent with those of a heart attack, you would rush him to the hospital where he would receive treatment. If your child had a 104 fever and was gravely ill but refused to take any medicine, you would call your pediatrician who would tell you to rush the child to the Emergency Room where he would receive medical assistance.

But if someone you loved were experiencing a mental health crisis and needed to see a psychiatrist or be involuntarily committed to a psychiatric facility to receive treatment, you wouldn’t believe the obstacles you have to surpass in order to get them the care they need to get well.

I know, because my family and I plunged head first into these roadblocks in the U.S. mental healthcare system five years ago when I was hospitalized for postpartum psychosis after the birth of my first child in 2008. Writing about this experience was something I wanted to do in order to educate people about the policies surrounding access to mental health care in the state of Virginia. {The laws vary by state. A good resource with links to studies and comprehensive information is MentalIllnessPolicy.org.}

In researching my mental illness and the treatment I received during my hospitalization, I requested copies my medical records from the hospital. I’d like to take you back to the week of October 22nd, 2008, approximately four weeks after I had given birth to my son. Belly still swollen, breasts leaking milk, I lost touch with reality during the early hours of that cool fall morning, but remained silent about my growing sense that this would be my last day on earth.

I was terrified of being taken away from my baby even though there was a little voice in the far corner of my mind urging me to go. I just didn’t want to listen.

That morning my husband knew from my past two manic episodes that I needed to be taken to the hospital. He called his mom and sister to come over and help, as we had been through this before and he knew my erratic manic behavior would require more than one person assisting in the effort to get me ready to be transferred. His next call was to dial 911, where he explained to the dispatcher that I had a bipolar diagnosis, was off my meds because of having just had a baby, and was now rapidly deteriorating and we were in need of help to get me to the hospital. He then called my psychiatrist, leaving her a message to tell her what was going on. And lastly he called my parents in Florida to alert them as well.

I remember being on the phone with my Dad while sitting on a chair in the kitchen, talking to him on speaker phone while the two female police officers who had been dispatched to our house were standing right before me. He was pleading with me to go with them. I don’t recall much, other than being afraid. I don’t know exactly how much time passed, but eventually they were able to take me, in handcuffs, under a Temporary Detention Order (TDO), to our local hospital for an evaluation.

I was clearly manic to the point of psychotic. It was well documented in the detention order paperwork that I had reported hearing voices and seeing ghosts in the baby’s room. My husband had told the officers that I had only slept 3-4 hours a night for the four nights leading up to his call for help. His sleep estimates were correct - it had been the weekend of our son’s baptism and I was trying to prepare for out-of-town guests along with getting everything ready for the party we were hosting. On top of learning to care for our new baby and suppressing the mania that I had felt since the night he had been born, it all caught up to me.

The Temporary Detention Order allowed my husband to have me sent to the hospital for an assessment. My husband was my Petitioner - the person asking that I be involuntarily committed. We were led to an empty hospital room where I was handcuffed to the metal bars of the hospital bed. My husband stayed by my side the entire time. The nurses assessed me and it was determined that there was substantial likelihood that, as a result of my mental illness, in the near future I would suffer serious harm due to a lack of capacity to protect myself from harm. I refused all meds in the Emergency room and I met the criteria for involuntary admission to a psychiatric ward of the hospital, not to exceed a 30-day stay.

I was taken by police car, still handcuffed, to our local hospital’s geriatric psychiatric ward, the nearest facility with a bed available. By the time the bed had become available, it was late at night and I remember being terrified upon entering the facility because of the Halloween decorations festively decorating the glass doors which were pulled open for me. My throat closed and I struggled to breathe, leaning all my weight back, attempting to keep them from guiding me in. They eventually coaxed me in and a young attendant began working with me to get me through the intake process. I remember her arms, covered with tattoos. Her name was Jenny.

They tried to give me drugs to force me to sleep, but my mania was so rampant and I continued to refuse oral medication, so I was given an injection to tranquilize me and my body succumbed to the rest it so desperately needed. I woke groggy, and still very ill.

The Temporary Detention Order meant I could be held involuntarily for one to five days, until a commitment hearing could be held. I was admitted the night of October 22nd, and my commitment hearing was scheduled for 9am on the 24th.

After only thirty-six hours of psychiatric care, I was still extremely sick and my mania was apparent to everyone close to me. But the chemical imbalance that was still working itself back to balanced with the help of the meds and forced rest, wasn’t severe enough to present me as a threat to myself or others during the trial, and despite my family’s strong arguments that I was not well enough to go home and care for myself, let alone a newborn, the judge still deemed me well enough to not be held against my will.

I was free to go home. Case dismissed.

My father spoke with the judge immediately following the trial’s conclusion. He was shocked and couldn’t believe the judge was going to send me home in the condition I was in. My father then asked if they (my family) were able to convince me to stay in the hospital, voluntarily, would I be able to stay?

The judge informed him that yes, I would of course be able to stay on a voluntary basis, but on the same token, I’d be able to sign myself out at any time.

This news was plenty good enough for my family and they immediately began encouraging me to stay and rest, so that I’d be able to return to my newborn baby in a much clearer state of mind. They knew that with just a few more days of treatment and solid sleep, I’d be in a significantly better place to where I could continue to see my outside psychiatrist and work on making a full recovery.

Fortunately, I was well enough to rationalize their concern for me and that was all it took to convince me to sign myself in. I stayed for three more days. My husband and dad came to visit me every day to check on my progress. They used my somewhat still disoriented state to their advantage as they were able to remind me each day that “we all needed to be in agreement that it was the right time for me to go home,” and I was too fragile mentally to process what had happened in the hearing so I followed their lead. I had signed myself in to stay and could leave when I was ready, but I didn’t really comprehend it all at the time.

I called home daily to check on my baby and asked them to bring pictures to the hospital. He changed so much in that week that I missed. His wispy brown hair on top fell out, so he had a bald head with only hair on the sides and around to the back. I cried at a picture they brought me of him smiling on his back laying on a blue and green striped baby blanket. Desperate to get back to my son, I eagerly took my meds each day and night, and did my best to be a model patient.

I signed myself out of the hospital on the 27th, after a 5-day stay, and walked into the kitchen of my house where my mom was stirring a pot of homemade chicken noodle soup cooking on the stove. I made my son a bottle of formula and sat on the couch to learn the art of bottle feeding him after having spent a month perfecting breastfeeding. I will never forget that moment. While feeding him and gazing into his eyes I silently vowed that I would do everything in my power to stay healthy for him. I never wanted to be taken away from him again.

Some people might say that involuntary commitment laws take away a person’s constitutional right to freedom. I completely disagree.

My family sought help for me because they knew I was so severely ill. The system initially determined I was a threat to myself, but the judge at the commitment hearing determined that was no longer the case. Situations like this happen all the time due to the current state of our mental health system and unfortunately, these holes in the system are what contribute to tragedies like Virginia Tech, Sandy Hook or the Navy Yard shootings. It’s the subjective “threat to themselves or others” which is determined by someone who has never met the mentally ill person, which is what needs to change.

People who are aware of family or friends who have mental health issues (and we all know someone given the statistic of 1 in 4 Americans living with a mental illness) need to be more proactive when they sense a change in someone’s behavior. By paying attention to the fragile mental states of people within our own environments, we will be able to push for help before it’s too late. The mental health laws need to be reviewed and modified to permit family and friends to have the ability to have people in trouble involuntarily committed for longer periods of time, so they are better able to make bigger strides towards recovery during the time in which they are under the hospital's psychiatric care. Until this done, we will continue to see more tragedies.

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On this fifth anniversary of my TDO and subsequent voluntary psychiatric commitment, I’m able to smile at my son’s insistence on dressing up as a ghost for Halloween. Five years ago I was not taking my medication and therefore went through hell, reportedly saw ghosts, and thought the world was coming to an end. But today I’m cutting eye holes out of a white sheet to dress my little man up on the last day of this month. A costume which serves as a gentle reminder of my past, while allowing me to appreciate the invisible challenges which inevitably lie ahead.

What I need: meds and sleep

My poor husband. Being married to someone who has Bipolar Disorder has got to be a teeny bit nerve-wracking at times. Take last week for instance. I contracted Baby Girl's lovely stomach bug and on Wednesday night (really, the wee hours of Thursday morning) was up puking my guts out from 1am until 4am. It was horrendous. I swore up and down that I don't think I want to have another baby because throwing up is the most awful thing in the world and I know I'd have morning sickness if we decided to go for #3.

The next morning I tried my hardest to get the kids up for Mom's Morning Out but I could barely walk ten feet without my head spinning. My husband had a 9am meeting that he HAD to be at, so I decided that I'd just keep the kids home and would let them watch TV all day until he could come home early in the afternoon.

And then I remembered my wonderful Mother-in-law. She's retired and she loves the kids and they adore her. I called and she said she would of course come over to watch them so that I could catch up on my sleep.

I couldn't even make the kids breakfast. My husband gave Mister Man a bowl of cereal and Baby Girl a sippy cup of milk and he was out the door. They were distracted with the TV until my Mother-in-law arrived and I crawled back in to bed. I didn't even come out until almost 2pm.

By then I only had a few hours until my husband would get home. I hadn't been able to eat anything, but was able to drink apple juice on ice. It tasted like pure heaven but it was bad news for my blood sugar. My husband got home around 4:30pm and I went straight back to bed. He made me a piece of toast and I was able to keep it down, but my body still ached from the heaving the night before and then there were the chills. I couldn't get warm despite two layers of clothes, socks, and a fuzzy bathrobe. Under covers. Eventually I fell asleep again.

I woke up at 9:30pm and picked up my phone next to me in bed to text my husband so he would check on me. He came up and when I was so delirious in the way I was asking him to get my phone charger, he started to get concerned.

Not about the stomach bug I had. He was concerned that I may be manic. I could hear it in his voice.

He tried to force me to take my Lithium, but I refused. I got angry. I called him names for trying to force me.

I realized I had forgotten to call his mom back about the next day and whether she should come help me again, so he offered to call her. He'd stay home with me and the kids.

When he came back up with another piece of toast for me, I took a bite and apologized for my rant. I was just so afraid of the medication making me throw up again like I had the night before. I promised to take it the following night. I know how much I need it.

Just not when my stomach is rejecting anything that goes into it.

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Sleep is my #1 trigger. I know this after years of managing my illness. As much of a night owl that I am, I cannot pull all-nighters like I did in college anymore. I can't even take care of multiple newborn feeding shifts (lucky for me). Because of this, I do everything I can to protect my sleep. If I don't, my health is at risk. Same thing with taking my medication. I may just need a small amount of Lithium every night, but if I go a week without it, I am most-likely going to become manic.

I don't blame my husband for trying to get me to take my medication and for worrying that I could have been becoming manic. He is just doing his job of looking out for my well-being and our family's well-being. I am very thankful that he realized that my irrational behavior was due to my frustration in him not being able to find my cell phone charger and also my haywire blood sugar levels from surviving on nothing but apple juice and a piece of toast all day. He is a wonderful, loving partner and father to our kids who has done a tremendous job of helping me to manage my illness.

Within a few days my sleep was back to normal and my stomach is almost back to normal. I was only off my medication for one night do to this nasty stomach bug (which I wouldn't wish on my worst enemy, btw). This week I am preparing for Daylight savings by going to bed a little earlier each night starting tomorrow. The following weekend (St. Patty's weekend!) I am heading to a memoir writer's retreat in Seattle and this will be a bit of a challenge for me, sleep-wise. But I am well-prepared and I have my trusty sleep-aid to use since the time change will definitely disrupt my sleep. When I get home on the 18th I'll have a good week of work to do on my sleep to get back on schedule, but I know I will be okay.

I am a fighter. I monitor my sleep and take my medication because it is my responsibility to my self, my spouse and my family.

And it's getting to be past my bedtime, so I need to wrap this post up so that I can log some quality ZZZZ's.

Living with bipolar disorder

I don't think a day goes by that I don't think about the fact that I am living with a mental illness. Not because I worry about what other people think of me, it's not that at all. It's because I have to constantly be taking the pulse of my mood so that I can manage my illness to the best of my ability. Over the last seven years I've gotten pretty good at it. I like to describe my experience living with bipolar disorder as a scale of one to ten. A simple ten point scale tells so much for someone like me. Think of it this way: 1 = completely depressed, can't get out of bed; 5 = in the middle, balanced (this is what I strive for every day); and 10 = completely manic, need hospital. I won't lie, I like being in the 6-7 range, but when I do have those times when I creep up to the 8's, I start to crumble. I know that when I get to 8, I need to make time for sleep or else I could tip over to 9 or 10 and that would be incredibly awful. Just because I've been there before. And now we have two kids and I would hate for them to see me in a manic state. Just as I would hate for them to see me depressed. But with my version of bipolar disorder, Bipolar I, my moods swing on the higher side of the scale versus the low side.

Nighttime is the hardest. The kids have been asleep for an hour and within that time I've cleaned up the kitchen and (of late) collapsed on the couch in front of my favorite show right now: XFactor. Some nights I am motivated enough to do a workout and then am filled with so much serotonin that it's almost impossible to turn off the endorphins enough to sleep right afterwards.

I'm trying to curb my evening leftover work/facebook surfing/twitter gazing/blog stalking to a minimum so that I can hopefully join the 10pm bedtime club.

When I do climb into bed, I get super jealous of my husband who, within exactly two minutes of us shutting off the lights, is snoring away happily. I'm a different story. My eyes close, my breathing slows down, and I shift around until I get into a comfortable position to try to nod off. Thoughts pop up and a running to-do list keeps flashing before me. I've learned coping mechanisms over the years so now I am able to turn down those things and find sweet sleep. If ever an hour goes by and I am still not asleep, I know that I must pop a sleeping pill to help me get the zzz's that I need.

I've just been thinking lately about how I live with this each and every day, and will for the rest of my life. Nothing I can't handle, just thought my readers might be interested in knowing a little bit about what it feels like.