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.

Why I Declare My Goals

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Back in June, my husband and I went on vacation with our friends to celebrate our 10-year wedding anniversaries. One night at dinner, Tim asked us go around the table and share our goals out loud. Studies have proven that when you declare your goals, the act of simply vocalizing them to people, you have a much higher probability of actually reaching them.

I used to love goal-setting, but had fallen out of the habit since leaving the corporate world to become a stay-at-home-work-from-home-mom.

Ten years ago, in my career as an agency recruiter, I witnessed the power of setting goals. I’d talk about them to my boss and colleagues, and would work my tail off to attain them, seeing the direct results of my tireless dedication displayed on reports each week, month, and year of sales numbers.

These days, I am my own boss. There is no promise of a paycheck for the advocacy work I’m doing. Only the pure sense of accomplishing something that will hopefully help other people on their journey to recovery.

“Act as if what you do makes a difference. It does.” - William James

Which is why I am so thankful to Tim for putting us up to the challenge of declaring our goals. I had said I wanted to write an e-book before the end of the year and self-publish it to be able to offer it for free on my website, but also to sell it on Amazon to reach people who might not have heard of my blog yet but found me via searching for books on mental health.

I’ve accomplished two of the three parts of that complex goal. The book is written and is available by signing up for my blog newsletter (which I haven’t yet officially launched - another goal in the works!), and it’s also available via the This Is My Brave website by signing up for the newsletter which will keep people informed of the progress of the show.

I hope to finish the process of self-publishing it to an online distribution channel (most likely Amazon, but I’m researching other avenues as well) by the end of November.

Right now I’m focusing on another recent goal that came to life: creating a Kickstarter campaign to fund our show, This Is My Brave. We have until November 15th to raise $6,500 which will be used to create the most inspiring, thought-provoking, entertaining show about mental illness the public has ever been invited to. If the show gets funded, we’ll have the capability of not only putting it on live in the Washington, DC area, but also reaching countless others by sharing the video of the performances after the initial debut.

Because of goals my life has meaning. No goal is too big. Take small steps and you’ll reach your dreams.

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What goals are you working on? Shout them out in the comments and create some accountability. I'll support you and cheer you on!

#ForMiriam I Advocate: World Mental Health Day

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When I think of what happened in DC last week, I keep coming back to the same feelings of anger, frustration and sadness.

Her life shouldn’t have ended that way.

There is something called Crisis Intervention Team (CIT) Training, which is a training program developed in a number of U.S. states to help police officers react appropriately to situations involving mental illness or developmental delay. The Washington, DC chapter of the National Alliance for Mental Illness has a page on their website describing the District’s Crisis Intervention Officer Program, as having "had 5 graduated classes of officers so far, as well as new recruit trainings."

I can’t help but wonder if the officer {or officers} who pulled the trigger had gone through CIT training.

If they had, or maybe had remembered the training during the incident, maybe the outcome would have been different.

Maybe not.

The only good thing that can happen as a result of this tragedy is advocacy in Miriam’s memory.

Advocacy to prevent something like this from happening again.

We can speak out. People like myself, who have experienced the hell of an inexplicable train of discombobulated and paranoid thoughts running through our heads. The hallucinations that come and go as fast as the minutes flying by on the clock next to the bed. The feeling that we’re invincible and don’t need sleep.

I've been there and I will continue to speak out about my experience in an effort to raise awareness for the signs and symptoms of postpartum psychosis. Because if even one person is helped through my writing, than it is worth all the effort.

Just because I experienced postpartum psychosis doesn’t make me a bad mother. It doesn’t make me a monster. It is an illness and my brain was sick. The important thing is that I got well and I made it through with treatment and support. I'm now able to help others by my work as an advocate.

And Miriam should have had that same chance.

But instead her friends and family are left to mourn this beautiful person who touched their lives and left behind is a constant reminder of her legacy, her baby girl.

It is my hope that once the darkness of their grief begins to dissipate, however far in the future that may be, the family will assume the role of advocate in their dear Miriam’s honor.

History, despite its wrenching pain, cannot be unlived,but if faced with courage, need not be lived again. - Maya Angelou

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Brave Because I Want To See Society Change

I learned of yesterday’s shooting here in Washington, DC, via the news pouring into my Twitter feed about the woman who had crashed her car into the gate surrounding the White House. There was speculation that a child was in the car with her at the time. There was also speculation that she suffered from mental illness.

Then she was shot by police and died soon after. The baby, thankfully, was unharmed in the ordeal and is now in the custody of child protective services.

I am so utterly heartbroken for this woman, her child, her family and friends and our society.

This needs to stop.

But unfortunately, until our country stops blaming people with mental illness for their conditions and starts providing the mental health services they need to get well, incidents like what happened yesterday will continue to occur.

We need to come together as a society to talk openly about mental health issues. If you notice someone exhibiting the signs and symptoms of a mental illness, do what you can to help them get the treatment they need. I guarantee you they are too sick to realize they need help.

We need to stop hiding our mental illnesses, because by hiding we are adding to the stigma.

Earlier this year I made the choice to go public with the fact that I live with Type 1 Bipolar Disorder. That I’ve been hospitalized a total of four times for mania, once was postpartum psychosis after the birth of my first child in 2008. That I once was afraid and ashamed to speak openly about my illness.

Today, I am neither afraid nor ashamed of my illness. I am proud to talk openly about my experiences because my openness helps others. They've told me so.

When we come together to share our stories, we propel a movement forward. A movement to shift the way people view the mentally ill. A movement to bring desperately needed changes to the state of mental health services in our country. A movement to stop the loss of innocent lives - both the mentally ill themselves and the people they harm when they are sick.

You see, yesterday’s news could have been me. I suffer from mental illness. But unlike Miriam Carey, I received proper treatment.

And with proper diagnosis and continuous treatment, people with mental illness can lead perfectly productive lives. They can be {and ARE} valuable members of society when they have the support and services they need to get well and stay well.

I don’t like to think about what could have happened if my husband hadn’t reached out for help. But the reality is that whenever a story like this hits the news and the person involved is thought to have “a history of mental illness,” I am brought right back to the torment and the excruciating emotional pain of what we went through as a family the times I was sick.

We need to change the public's misconceptions about mental illness because when people get treatment, lives can be saved.

I recently wrote a manifesto on my experience living with bipolar disorder. It's called Find Your Brave and I hope you'll take a moment to download it here and share. It's part of my effort to encourage people to stop hiding and seek support because we're so much stronger when we come together.

Let’s come together and show the world This Is My Brave.

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What I Want You To Know About Postpartum Psychosis

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Five years ago today my little man was born.

As for any first-time mom, the excitement and energy of the rush to the hospital to meet him is a bit of a blur, especially given the five years that have flooded my memory since then. Sure, we had the same fears and concerns as any new parents: is he sleeping and eating enough? Are we using the right baby products? When will his umbilical cord heal? Are we doing enough tummy time? But for us, the beginning of our story is quite different than that of most new families starting out.

Because right after he turned four weeks old, I had to be hospitalized for postpartum psychosis.

I knew I was experiencing hypomania from the time that he was placed in my arms around four a.m. the morning after he was born. He tried nursing for the first time and the physical exhaustion and emotional release of having just given birth started to set in. We sent him to the nursery so that I could try to catch up on sleep, but with the nurses checking my vitals every hour due to the C-section, sleep was nearly impossible.

Some people may wonder why I hid my symptoms from the people who could help me. The doctors and nurses who saw me when they came to check on the baby while we were still in the hospital never noticed that I was struggling. My therapist, who saw me when I was three weeks post-partum didn’t detect anything unusual. My husband and my parents could sense something was different about me, but we were all so caught up in the new baby that we pushed my mental health issues to the side and put the needs of the baby first.

I love my son with everything in me, but I know from all that I’ve been through over the past eight years living with bipolar disorder that I need to put my mental health first in order to be the best mother I can for him and his sister.

But in the first few weeks of his life, I didn’t know this. I was just a new mom. Trying my hardest to not screw up. And at the time I thought that meant staying off medication to protect my baby.

I was absolutely determined to breastfeed him. I put so much pressure on myself to make it work that the first week I was barely producing any milk because I was so stressed out and the internal fear that my body wasn’t going to be able to actually make food for my baby was doing just that: stunting my ability to lactate.

We did finally figure the whole breastfeeding thing out, me and Owen. And I nursed him for the first four weeks until I was no longer able to hide the fact that I was losing touch with reality.

I felt as though I was invincible and hardly needed to eat or sleep. The less I slept, the more energy I seemed to have. I never napped when the baby napped because I’d always find something to do around the house that was of course more important than catching up on sleep.

Everything around me had a certain sparkle to it. It was as if I were living in a dream world where everything was amplified and so vivid that I had to stay awake to soak it all in. There was no pain, only the soothing sounds of my baby cooing or crying softly before I picked him up.

It was all very surreal. But when hypomania turns into mania, and mania escalates to psychosis, things can go very wrong.

I am so thankful that my husband realized what was happening and knew exactly what to do in order to fix me.

As hard as it was for him to call 911 and have the police and EMT’s take me to the hospital, he knew that I needed to be separated from my baby for a week in order to get well.

And as much as I mourn the week that I lost with my son, I’m grateful for what I learned and how sharing my story has the potential to help other moms and families out there.

Not enough is shared about postpartum psychosis. Even though it is not nearly as common as postpartum depression, doctors still should discuss the potential chances of the occurrence, specifically in patients like me who had a previous bipolar disorder diagnosis.  Society doesn’t understand it and therefore, families aren’t on the lookout for symptoms in new moms. And I’d like to change that.

Women who experience postpartum psychosis are just normal moms who unfortunately have a chemical imbalance in their brains. Some of these women have thoughts of harming their children, and some of them act on those violent thoughts. I was one of the lucky ones who didn't have those intrusive thoughts, but even if I did - that doesn't make me a monster, as my friend Robin wrote on her blog recently.

I’m just a mom, with a 5-year old little man, who wants to prove to the world that our struggles don’t define us. They only provide us with opportunities to make a difference in the world. I’m beginning to work on explaining this to him every chance I get.

I’m loving watching my son grow into a smart, funny, caring, determined and stubborn little guy who has stolen my heart with his hugs and his smile. I’m still in complete awe of the fact that he grew inside of my belly, remembering the pressure of his little feet apparent from the outside. Bringing him into our lives was a miracle and we couldn’t imagine life any other way.

The other day I asked him what he thought it would feel like to turn five. “I’ll be all grown up! A big kid!” was his response. So much like me, he’s eager to make his way in the world, try new things and move mountains. I’m trying my best to just let him be little, to enjoy the carefree afternoons at the playground or the library. To linger over snacktime at home with him while his sister is still napping. And to savor every small moment we have together like our morning hugs and bedtime stories.

Five years have gone by so quickly but I’m not sad about them passing. The collection of countless precious memories which I’ve tattooed onto the inside of my mind are what I carry with me in my heart from the past.

I’m eager to see what the years ahead hold. Both for him, and for his mom who will always be looking on with pride.

 

The Hospital Badge

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When I meet other people who live with mental illness, it’s inevitable that at some point the topic of hospitalizations comes up. It’s as if the number of times you’ve been committed is like a badge of honor.

It’s not, but it is at the same time.

When you’ve been in the hospital, you learn how to fight to get well. You learn to have compassion for other people’s struggles. You learn to realize that your brain just doesn’t work like a plain old regular person’s brain works.

And so you learn coping mechanisms for how to manage your illness.

In group sessions you’re taught how to listen and be present in the moment. You're shown how to use art to express your feelings and work through your emotions in art therapy. During the exercise class you might appreciate the calmness that comes from the breathing exercises and stretching of yoga.

But it doesn’t mean that you’ll be fine when you’re released. For me, having been hospitalized for mental illness was... a very traumatic event, each of the four times it happened.

When I came home from the hospital each time, I’d hide my feelings of guilt and shame, not really opening up about what I had been through to anyone but my therapist. It would take weeks to return to stable, and I was constantly desperate to talk with someone else who understood what I had gone through.

Luckily, I have met some friends through support groups and other avenues, who have also been through hospitalizations for mental illnesses, and it’s always interesting to compare notes. But when it comes down to it, those types of stays are all the same. Meds, therapy, paperwork, release. Then you’re on your own.

Through blogging I’ve had the privilege of hearing from some of my readers who've reached out to me via email saying they’re so glad I’m writing because stories like mine are important to share. They’ll sometimes tell me how hard of a time they’re having, and how they wish they could just go to the hospital for a week or two, maybe it would help.

What I want those readers to know is that going to the hospital may help take the edge off momentarily. But when you get out, and you’re back at home, it’s sometimes easy to fall right back to where you were before you were admitted.

Life goes on. The world keeps turning. And we have to keep on learning to lead the dance with our conditions, lest they turn us in the wrong direction.

For me, this means protecting my sleep. Last night my allergies were in an uproar, given the change in the weather this past weekend. My fitbit displayed a horrendous sleep pattern. I went to bed at 9:15pm (the earliest I’ve been in bed for the past three weeks by an hour) but yet it was quite possibly the worst night of sleep I’ve had in that many weeks.

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But I won’t give up. I'm working on staying on top of my triggers to ensure I stay mentally healthy. For myself, for my family, and for my community.

And on that note, it’s time for me to hit the sack.

I Advocate for a World Without Suicide

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Photo from the Fairfax AFSP National Capital Area Chapter's Community Walk this past Sunday, September 8th.
 
 

I never believed suicidal thoughts were truly a real thing until I experienced them myself. To me, it was unbelievable for someone to want to take their own life. It seemed so horrid, so severe, so final.

What gives a person the right to take their life in their own hands, anyway? God says how much time we get, not us.

Plus, how could a life feel so worthless that someone would think dying was the solution? I just couldn’t comprehend it.

Until it happened to me.

Being diagnosed with bipolar disorder at the age of twenty-seven changed my perspective...on the topic of suicide. I slipped into a deep depression and would spend my nights curled up on the couch, tears streaming down my face until I was so exhausted from the hurt that I’d fall asleep. I had lost my will to keep going because I didn't think there was hope. I was so scared to reach out for help that I hid my painful feelings from everyone.

Everyone except my husband and my parents, thankfully.

They kept fighting for me to get the treatment I needed in order to get well, even when I could no longer fight for myself. I don’t know if I’d be here today without their incredible love and unwavering support back then.

Looking back on that time in my life, it’s apparent that I feared the stigma surrounding mental illness and because of it, I hid my depression and suicidal thoughts from my friends.

I was terrified of what they would say if they knew the thoughts running through my head. I was convinced they’d turn away from me, too afraid of my mental illness to help me out of my darkness. It was stigma that kept me from opening up to my friends about my depression.

I am one of the lucky ones that made it out of the darkness. I survived depression and made the decision to become an advocate for those who are still suffering. Because in my heart I believe everyone is capable of overcoming mental illness and that no one should feel ashamed about living with mental illness.

By educating the medical community and society in general to better recognize the signs and symptoms of depression and other mental illnesses, we can and will save lives.

If a friend seems to be struggling, ask them if they’re okay. Take time to really listen and offer support. Don't accept "I'm fine." for an answer if you know they aren't. Share the National Suicide Prevention Website and Hotline with them: 1-800-273-TALK (8255). It’s staffed 24/7 with trained professionals who offer free and confidential emotional support to those in crisis.

Social media can be another avenue for support if someone is in crisis. There are groups and organizations that lead chats on Twitter to help people who are struggling with suicidal thoughts. By searching the hashtags #suicideprevention, #suicidechat and #AFSP, streams of conversations  on how to get help become available and you’re able to join right in the conversation. In 2011, Facebook unveiled a tool for friends and loved ones to be able to report a suicide threat posted online which has been credited for saving lives.

Please don't be afraid to speak up. Start the conversation. Join the conversation. Keep the conversations flowing.

The only way we’re going to end the stigma that surrounds mental illness is by promoting open dialogue so that people are not afraid to open up and ask for help.

Suicide is preventable. Let’s pull together and join the movement to bring suicide prevention into the light.

Because every life matters. Don’t ever give up hope.

Help is available if you need it. If you are in crisis, call 1-800-273-TALK (8255) National Suicide Prevention Lifeline.

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I was invited by the University of Southern California's School of Social Work to join in their Suicide Awareness Blog Campaign. Please visit their website for information on how you can also participate.
 

Playground confessions

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I don't know what it is about me that makes me want to tell people my life story when I first meet them. Sometimes I wonder why I'm so open, why I wear my emotions on my sleeve, why I have such a strong sense of trust in people I may have just met.

Why do I think my life is so important that everyone I meet needs to know about it?

Take yesterday afternoon for example. Vivian woke up from her nap a complete disaster, so upset that I dared come in her room to get her before she had fully woken up. After fifteen minutes of a terrible-two's-almost-three tantrum, I was finally able to calm her down and convince both kids to let me push them in the double stroller to the playground.

Let's talk about who got the better deal here for a moment. They got to enjoy a tasty snack of a cherry-vanilla cereal bar and a generous handful of sweet red grapes, along with a beverage of chilled water fresh from the fridge in their water bottles filled to the brim by yours truly, while I had the luxury of pushing them for thirty minutes in 85-degree, muggy heat to the playground.

I was happy to do it though. I've made a commitment to myself to be more active in September (and beyond, but I'm taking it one month at a time). My new therapist says I need to schedule self-care into my day or else I will end up neglecting myself and I know this is true. I've felt it lately. I can definitely tell a difference in my mood, my parenting, and my overall enjoyment in life when I take time to do things for myself each day.

So pushing the kids to the playground and back home is my way of having some time for myself (great exercise and fresh air) while also allowing them to burn off some energy.

The bonus was meeting a really cool mom and her two kids who were the only other people there when we arrived.

I didn't expect to strike up a conversation with her. When we got there... she was talking on her phone. But as our kids began to interact she wrapped up her call and a few minutes later I found myself asking her the customary playground ice-breaker among moms:

"How old are your kids?"

Her son, a year older than mine, jumped right into my son's imaginary fire-fighter rescue scene, while we pushed our daughters (also close in age) on the baby swings as we chatted. I asked her if her son had started Kindergarten this week and she admitted he was actually repeating it since he had some issues focusing last year. I told her how my husband and I had decided to hold Owen back a year since he was so close to the cut-off for enrollment. "He just needs another year to mature a little bit more," I said and she nodded sympathetically.

Then she revealed that she and her husband suspect that their son may have ADHD and they had consulted a child psychiatrist this summer and he had recommended trying meds, but she wants to see how he does this year. Maybe it's a maturity thing. But she also mentioned his lack of awareness of personal space which he demonstrated a few minutes earlier when he playfully tugged at Owen's arm to get him to follow him over to the slides.

Owen didn't seem bothered by it, although the mom said sometimes her son can be aggressive with other kids. It was at that moment I had to bite my tongue.

Just listen, I told myself. And so I did. And I'm glad I made that choice.

But at the same time I felt a connection to this wonderful stranger I had just met and I wanted to tell her that there is nothing wrong with mental illness, and if he does have ADHD it does not define him and there are treatments that can and will help. I wanted to tell her that it's going to be okay and that she will get through this.

I can't help it. The advocate in me always wants to speak up.

But I didn't this time because I sensed from the way she was telling me all this about her son that she got it. She's on my side. And in that moment it was such a joy to simply watch our kids play pretend together on the playground.

Her husband called and I noticed it was already five-thirty and I still had a half-hour walk home. We had been talking for forty-five minutes like good friends and I hated to have to say goodbye.

My kids reluctantly made their way down the slides one last time before walking over to hop into the stroller. As I walked over to buckle Vivi, my new friend's son ran up beside me and took my hand. Looking up at me he asked in the sweetest voice, "But why does he have to go?"

It melted my heart.

His mom and I looked at each other and smiled. We both said how it was getting close to dinner time but maybe they'd see each other at the playground again sometime.

A part of me wishes I would have asked for her email address and maybe we could have set up another playdate. But for some reason I didn't and now I'll just hope we'll run into that lovely family again in the future at one of our local playgrounds.

Because I'd love the chance to tell her my story. I'd love the chance to tell her why I'm passionate about mental health advocacy and most of all because I'd love to just watch our kids have fun pretending to be fire-fighters again.

On Hiring A New Therapist

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Change has always been a hard thing for me. When one season comes to an end, and another sweeps in to take its place, I usually need a good few weeks to adjust and settle in. Take this weekend, for example. I loved celebrating the end of August with our anniversary date night and the two days spent soaking up the end of summer at the pool with friends. But until we ease into our new school routine I’ll be fidgety and uncomfortable with the newness of it all.

Speaking of change, I had to break up with my therapist of five years because she stopped accepting my insurance and there was no way I’d be able to pay the regular office visit amount out of pocket. I’m sad about not seeing her again, and feel terrible about not having the chance to say goodbye at our last visit. But I guess that’s just the way life goes sometimes.

Tomorrow I’ll meet a new therapist who I’ll share details of my life with. It feels like the first day of school when everything is new and I’m excited and nervous at the same time for all the learning I know I’ll do while I’m there. I’m sure I won’t be able to cover my entire mental health history in our first visit. But in the event we do continue on after tomorrow, I have a few expectations for our sessions.

I hope she helps me figure my complicated self out.

I hope she challenges me to see things from a different perspective.

I hope she teaches me how to be more forgiving of myself.

I hope she realizes that just because for the past three years I’ve been a “high-functioning” bipolar 1 patient, doesn't mean I don't struggle with my symptoms on a regular basis.

I hope that we’ll hit it off and have a long-lasting patient-therapist relationship.

I know this is a tall order and I have high expectations... for how this will work out. The truth is, we may not have chemistry and I may have to try several therapists before I find one who meets my needs. I’m prepared to do that if I need to. I'm prepared to work through change.

I believe I didn’t invest enough effort with my last therapist. I didn’t go to the appointments with something in mind to work on. It was more like going to monthly appointments where I sat and blabbed about myself and what I had been doing since I had last seen her. It didn’t do me much good. I didn’t grow the way I believe therapy should help a person grow.

This time I want things to be different. I’m ready to work this time.

The sun is setting on one season and will rise with the next. Bring it on. I'm ready.

My love anchor

10thAnniversary

I woke up before anyone else in the house did on my wedding day. It was six o’clock and my nerves had driven me to the bathroom. Back in bed, I pretended to go back to sleep, but my mind kept running through the events of the day ahead of me. I wanted our kiss to be perfect.

We got married at twenty-four. Some may say that’s young, but I knew I wanted to be with him forever after we had only been dating for three months. I’ve always said I’d be ready to take the next step, build my life, when I knew we were right for each other. My anchor. He’s always been my anchor. This is what I’ve learned after fifteen years together, ten of those as husband and wife.

I didn’t know back then how many obstacles we’d be faced with in the years ahead. Neither of us saw mental illness in my future. How could anyone predict that? And even if we could, it’s not like it would have changed our minds about wanting to be together.

It's not easy being married to me. I have tumultuous moods, get frustrated easily, am the most stubborn person I know, and I'm sure sometimes... he just wants to shush me because I'm exhausting. But he doesn't. Because he knows that's just who I am. And he loves me for me. I like to think I'm all the excitement he'll ever need.

He is my support, encouraging me with his love. He is my balance, guiding me back to the middle when I sway off course. He is my steady, gently pulling me up when I fall back. I am more in love with him today than I was the day I married him.

Happy Anniversary, Honey. You’re my anchor through life’s storms. And I love being tied to you.

xoxoxoxoxo

 

Starting Over

Starting-OverThe show will go on in DC this coming May, 2014. I'm simply taking some time to figure out where to go from here, as my partnership unfortunately did not work out due to our vastly different work styles. I have an incredible team surrounding me here in Virginia and I know that with all the hard work and passion that is going into this project, it most certainly will be a success. I may have failed at a partnership, but I will not fail at executing my vision for this show.

I envision this show to become a community of people coming together to embrace mental illness so as not to let it define them, but to propel a movement forward. A movement built on the belief that those of us living with mental illnesses are real people who simply need help. By coming together as a supportive society which fights for mental health services and programs, we will

change and save lives.

Please follow along here, and/or via Instagram and Twitter for updates as they become available. For now, if you're local to the DC metro area, or you're interested in coming in from out of town to see the show, mark your calendar for the weekend of May 17 & 18, 2014.

Thank you for all your support and I hope to see you at the show!

Five Minute Friday {15}: Small

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I can’t help but think about how one decision always leads to the next. Some things, which may seem small and insignificant at the time, have the ability to change the trajectory of our entire lives. Choosing a major at the age of 18, going on that blind date that your friends set you up on, deciding there will never be a perfect time to have another baby and so you just go for it even though the house and cars are too small and you don’t know how you’ll ever afford college for them all.

Sometimes you have to stop over-analyzing and just pick a direction, hoping for the best.

I’m glad that I’m able to uncover and pay attention to that soft whisper of my conscious in the back of my mind. A tiny part of me believes it’s Him helping to guide me make the right choices. Yet, I’m constantly doubting myself. I’m constantly doubting my faith.

But He hasn’t let me down.

I’m still trying to comprehend my reason for being here, but I believe the decisions in my life that have made me who I am. All the left turns when they should have been right, and the right turns when I could have gone straight, the year and a half when I would take two steps forward only to fall back and not be able to get up for weeks. These small moments of my life have brought me here.

And I’m loving this place. Five Minute Friday