What I Want You To Know About Postpartum Psychosis

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

yyellowbird via Compfight cc

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.

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.

On Hiring A New Therapist

ΞSSΞ®®Ξ via Compfight cc

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.

Five Minute Friday {14}: Lonely

I was lonely back then, back seven and a half years ago when I had just been told I was facing mental illness. Two stints in a psych ward and it was apparent to the doctors but I was still in denial. I was so lonely.

I longed for someone to talk to who knew what I was feeling. Someone other than a psychiatrist or a therapist or a group leader in an outpatient program. They only studied these symptoms in a textbook. How could they really know what I was going through? They didn't, in my mind.

Writing would become my call for help. My attempt to erase the loneliness by telling my story to see if there were others out there feeling my same feelings.

There were. There are. And it's a relief to no longer feel lonely in this life with mental illness.

Today, nearly two years to the day from when I started this blog, I feel so far from lonely. Instead, I feel the compassionate hugs this community of readers, fellow bloggers, friends and family have wrapped around me.

#OK2Talk: Join the Mental Health Movement

Experiencing a psychotic break can be an isolating and debilitating event. If I talk about it, will everyone think I’m “crazy”? Will I lose my friends? Will I lose my job? Will I ever get better?

When mania grabbed a hold of my brain at the age of twenty-six, I thought my life was over. I had been hospitalized for three days and had to be tranquilized in order to force sleep, my mind brought back to reality only through the use of antipsychotics. The details were not pretty. I practically suffocated from the weight of keeping my pain bottled up inside. It seemed like no one in my immediate circle of family and friends understood what I had just gone through. My close friends tried, but the truth was everyone was so scared to talk about it.

I wanted desperately to find someone, anyone other than my psychiatrist and therapist, who knew what I was feeling. Wasn’t there anyone out there, a peer, who was like me?

My emotions pummeled my personality to the ground with their negativity. Thoughts raced through my head and nothing I did could make them stop.

Fear of the future. Guilt over what I had put my husband and family through. Sadness for the career that I had to leave behind. Disbelief in the words the doctors kept repeating. Anger that this was happening to me. Why me? Why?

I remember visiting bookstores with my parents where we’d search the Psychology section for titles that might help us understand what was happening to me. On one trip, my dad bought three thick paperbacks with promises on the cover which gave us hope. We went home and flipped through the pages, eager to find the answers to our questions.

We did find some, but they were clinical in nature. I was searching for different answers. I wanted to read personal stories of recovery and inspiration. I wanted to know that others had walked in my same shoes, had lost touch with reality, came crashing down to the darkest place they’ve ever felt, and made it out okay.

I wanted to know I’d be okay too.

Back then, in 2007, there weren’t many people blogging openly about bipolar disorder. There were women bloggers who were starting to open up about their experiences with postpartum depression, but blogging wasn’t nearly as prevalent as it is today. Social media was in its infancy, at least for regular Internet users like myself, so the ease in sharing information wasn’t quite there yet. You had to do the digging yourself, and my efforts at finding stories of hope and inspiration from other mental health consumers weren’t successful.

Back then.

The times, how they’re changing.

Today there are more and more people opening up each day about their journey to recovery from mental illnesses. There are blogs and vlogs, online support groups, Tedx talks, Facebook groups, and community performances which are educating the public on what it’s like to live with a mental illness. I’m proud to have opened up on my blog, sharing my true identity because I can now celebrate being a part of this change.

I can feel the change as its happening. I feel it in every email I get from a friend thanking me for writing about my story because they’ve been through something similar. I feel it in every message I receive on Facebook or Twitter from someone I’ve never met who has read my words and felt inspired to share their own.

This is how a movement starts.

It starts with one person who is brave enough to share,

who inspires others to share,

which in turn inspires the world to change.

On Tuesday I attended the launch event on Capitol Hill of #OK2TALK, a national media campaign produced by the National Association of Broadcasters in an effort to spread mental health awareness and teach young adults that sharing our stories of hope and healing can help others who are struggling. The campaign includes PSAs in both English and Spanish featuring teens and young adults talking openly about their experiences with mental illness. At the end of the ads, there is a call to action directing you to create the conversation about mental health online via social media.

NAB President and former Senator Gordon H. Smith described the campaign as “bringing the issue of mental health into the sunshine,” and I couldn’t agree more. I applaud the NAB for its commitment to increasing the awareness and understanding of mental health and I encourage you to contribute to the conversation via the blog, www.ok2talk.org.

Help is available and treatment is effective, and by encouraging society to be supportive of those struggling we will save lives.

 

The Truth About Living Openly with Bipolar Disorder

Me & my little firecracker on July 4th

I will never regret my decision to write openly about living with bipolar disorder. Never. There is something to be said for reaching a point in your life when you take an important leap. One you can tell your kids about someday. When I realized it hurt too much to keep it bottled up inside was the point when I realized that I wanted people to know I’m not perfect but I still love my life just the way it is, mental illness and all.

I love the moments right before I fall asleep. My mind replays my day’s highlights, as if to ingrain the smile or giggle or kiss in a corner of my brain, so that I won’t ever forget it. Tucked away safe so that I can unwrap it again when I need that memory.

Lying still, listening to the steady rhythm of the one I love beside me, I think about the day that awaits me when the sun rises.  I soak up all the sleep I can because chances are, I was up too late writing the night before. I no longer set an alarm; the sweet voices of my kids will wake me when the sunlight pours into their rooms.

The truth is, even though I will never regret my decision to tell the world about the chemical imbalance in my brain, I still wonder if I chose the right time in my life to open my heart.

Living openly with a mental illness means you’ll always wonder if the world is judging you. You’ll wonder if you will ever be looked over for a job you applied to or a promotion you earned because of the fact the employer knows you have bipolar disorder. You might wonder if you will ever work a regular job again now that you’ve written about the darkest and also the most manic times of your life.

These are the things I’ve been worrying about lately.

The truth about living openly with bipolar disorder is that even though I know my husband loves me with his entire heart, someday he might not because my illness might get in the way one time too many. My entire world would come crumbling down around me.

And if my world did come crashing down, if I was left to manage on my own, how would I do that? Again, the future employment picture bubbles to the surface. How would I support myself financially when my loving husband has been the main provider for the last six years? And would my symptoms suddenly break through the surface again, like a volcano that has been dormant but now is ready to explode?

These are the big, scary thoughts that sometimes make me wonder if I did the right thing.

Because the truth about living openly with bipolar disorder is that once you’re diagnosed, it’s yours to live with for the rest of your life. It’s yours to manage, to curse, to medicate, to appreciate. There is no erasing a mental health condition. Therein lies both the beauty and the beast.

The truth about living openly with bipolar disorder is that it’s shown me how far I’ve come as a person. How I’m no longer afraid of showing my true colors. I love my brain and all the creativity it has allowed me to express. Even though it may break down from time to time, I love this piece of me which has shown me what I’m capable of. And that is overcoming my fears and insecurities.

For this I say, I’m glad I’ve decided to be open about the fact that I have bipolar disorder.

No looking back. There’s only the beautiful mystery of what lies ahead.

An Open Letter to My Former Psychiatrist: On Being Right

Mukumbura via Compfight cc

Dear Dr. H***,

You were right. Seven years ago this August, I left your office with my husband, round belly bulging with my nearly full-term first child, cursing your name. It was our first appointment together and you basically told me I was going to fail. When I explained to you that I had been off meds and symptom-free from my bipolar disorder for almost a year and that I wanted to stay off medication to breastfeed, you nodded with a sympathetic smile on your face, scribbled in your notebook and simply said we needed to have a plan.

A plan for which hospital I’d go to when I became manic to the point of needing that level of care. That level of care that you were so sure I’d need.

You were right.

At that stage of my fight, Dr. H***, I was still in denial about the fact that I had been diagnosed with a mental illness. I thought maybe, just maybe, since I had nearly a full year of stability without meds, the past had been a misdiagnosis. Perhaps those eight psychiatrists I had seen over the years since my two hospitalizations for mania were all wrong. I mean, I hadn’t experienced any significant episodes of depression or mania since 2006 and most importantly, I felt solid and stable. Didn’t that count for anything?

Didn’t that make me normal again?

I was so excited to be a mom and every spare moment I had was spent preparing for this new little life who would soon enter the world. His crib was set up, clothes had been washed and lovingly put away, and diapers and wipes sat waiting on the changing table in his nursery. One of the last things on my list was meeting with you, a psychiatrist who agreed to treat me without medication for the remainder of my pregnancy and beyond, according to my wishes.

Man, am I glad we met when we did. Because you were so right. And when the time came, four weeks after his birth, when the compounded lack of sleep and absence of meds in my bloodstream caught up to me in the form of full-blown postpartum psychosis, my husband had someone to call for help.

He called you.

How terrifying it must have been for him to see me unravel the way I did. How helpless he must have felt watching me slowly lose touch with reality, my eyes glazing over, unable to focus on the simplest task of taking a shower or eating a bowl of cereal. And when the psychosis reached its peak, he saw me scrambling to pull together every journal I had ever written in, piling them up before the blazing gas fireplace in our family room like an offering before I died. My legacy, scrawled in ink for my son to read someday since in my mind, I wasn’t going to make it back to the surface. I was hurling to the depths of hell which to me felt like being dragged to the floor of the ocean, my ankles cuffed with a ball and chain pulling me to the bottom. I was sinking faster than I could breathe. And I was so scared it was my day to die and I’d never see my baby again.

Mania to the point of psychosis can do this to a person.

I was taken under a Temporary Detention Order to the Emergency Room where I was held handcuffed to the bed. The doctors and nurses eventually determined I was a threat to myself or others and the green light was given to find me a bed. I was lucky, beds aren’t always available, as the Deeds’ family tragedy recently and unfortunately proved. I only had to wait overnight and the next morning I was transferred to our local hospital’s geriatric psych ward, the only open bed in the surrounding area.

I made it through. It wasn’t easy, in fact, it was pretty awful being in a psych ward for a week of my new baby’s life. My mental illness had landed a forceful blow to the gut, showing me it was in control of my body. Still, wandering the halls at night I’d stumble, groggy from the antipsychotics, to the nurses station to ask for another dose of whatever sleeping pill they could give me. I knew sleep was my friend in there. After a week, I got well with your help, and with support from my husband and family.

I focused on getting stable. I followed my treatment plan and took my meds religiously. Then it happened again. I thought I knew what was best for my next baby. I didn’t. Acute mania reared its ugly head to the point of psychosis, repeating the nightmare a year and a half later when I found out I was pregnant with my daughter because I had stopped my medication.

You were right again. At five weeks pregnant I landed in the psych ward again.

Those days are tough for me to look back on, the times I was in the hospital and the weeks and months of recovery afterwards. But I wouldn’t trade them for anything because they are a part of who I am now and they tell the story of how I’ve evolved. Those slices of my life do not define me, but when added into everything else that makes me the person I am today, I am grateful for those agonizing, terrifying, heart-wrenching experiences.

You are the expert when it comes to psychiatry, Dr. H***. Me, I’m just the patient. But when it comes to making life decisions, I asked for your opinion but of course only I could make that call. You expressed the same sadness that so many in this world share over the injustice mentally ill people experience when they expose their conditions. I was looking for justification that it would be okay if I wrote openly about what I had been through, but I didn’t get that from you. In fact, you recommended that I keep my illness hidden, lest I be discriminated upon because of it. Once more, it was as if I were hearing “destined to fail” all over again.

Good thing I didn’t listen that time.

I’m writing now, Dr. H***. Remember when I told you I wanted to write a book? Well, I still do, but first I’ve started self-publishing online, to gain experience. I have a blog, and over the past two years my readership has grown tremendously, all organically, due to my dedication to sharing my story in order to help others.

I’ve met so many incredible people through blogging and social media. It blows my mind how I can write about the struggles I’ve gone through and in return, I get emails from people saying, “Me too!” and “Thank you so much for being so brave.” My heart is blissfully content because I know I’ve uncovered my purpose in life and my words are having an impact on people, a positive impact. I can feel it. And every time I put my thoughts out there for the world to read, my voice grows a little stronger.

I’ve created a show and non-profit organization called This Is My Brave where others like me who live with mental illness can stand up on stage and share our personal stories, our suffering and our breakthroughs, the hope we’ve found in long-term recovery. This is our chance to show the world our vulnerability in an effort to raise awareness and acceptance.

For years after I was handed my diagnosis I feared the backlash of people who knew me finding out about my mental illness. Conversations were uncomfortable, I cared too much about what other people thought of me. It didn’t take me very long to realize that living in fear is not really living. Taking off my armor and choosing to expose myself and my story was one of the best decisions I ever made about my mental health and my life in general.

Revealing my vulnerability freed me to follow my dreams.

And I have you to thank. Thank you for being right. Thank you for letting me fall. Thank you for being there when I needed you. Finally, thank you for doubting me and advising me to stay silent. Because I needed my chance to prove someone wrong and you were that person for me.

Respectfully yours,

Jennifer Marshall (your patient from 2008-2011)

 

A guest post from Mary: Almost Together

I connected with Mary through the power of blogging and social media, and am so excited to share her story with you today. She’s talking about her truth, and my hope is that you’ll listen.

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Hi all! My name is Mary Leaphart and Jennifer has been incredibly kind to let me share a bit of my story with you. I am 37 and a single mother to a 7-year-old rescue dog named KC. She is my baby as I do not have any non-furry kids! I taught high school math for about 11 years and now write curriculum, working mostly from home in order to maintain a lifestyle that helps keep my mental health in check.

See, when I was in college, my bipolar disorder showed up. It would be twenty years before I knew what to call it. But trust me; this disease did not need a name to wreak total havoc in my life. And even though I didn’t have a name for it yet I had a lot of labels I used to describe it – despair, self-loathing, euphoria, deceit, laziness, hopelessness, ecstasy, crazy…you get the picture. I could remember the strength, joy and fearlessness I had know as a child, but now all of a sudden I could not conjure it again, no matter how hard I tried. I thought I had lost myself forever.

I know I don’t have to tell you, but bipolar is brutal – it will rip your guts out, tear you to shreds, bring you to your knees and somehow convince you that you were the one to blame for it all. But of course, by the very nature of the disease it will also take me to some of the highest heights I could ever imagine. The blessing and the curse of my bipolar is that it is type 2 – meaning that my highs have never gotten high enough for me to do something to get hospitalized. Oh, but I fantasize about it – driving my car into a guardrail. Not enough to kill me, but just enough to give me a reason to lie in a hospital bed for months. A reason to not have to work so hard to live the life that everyone around me seems to manage so easily. A reason to get put in a hospital where someone might finally be able to “fix” me.

Of course, there is no fixing bipolar but there is a happy “ending” to this story. It started when a very wise, very dear friend of mine finally had the courage to look me in the eye and tell me that I needed real help. She brought me to her house for dinner and literally held my hand while I called my first therapist. I was terrified.

Finally, in 2007, I found the right doctor for me and got my diagnosis and began the long and painful journey to find the right medication for me. I spent the next two years swimming through a sea of medications trying to find just the right cocktail. It took time, and a great deal of hard work, but I did eventually find the right combination and most importantly, found an amazing therapist who I visit religiously every two weeks.

Throughout my journey with bipolar, I have always gone back to my music, my singing, as a way to help me cope. I connect with the music in a very deep way and am able to express feelings that I am not normally able to talk about in day to day conversations. Once I realized that, I discovered that I might have a very unique way to share my story.

And hence, Almost Together, was born. For the last year I have been putting together a cabaret show about my life with bipolar disorder. I use songs from all different eras and genres that have touched my soul and short monologues between to weave the story of my journey. This July, I am honored to be able to perform my show in the Capital Fringe Festival in Washington, DC.

As I look back through history and see how change has happened, how stigmas have been removed, how stereotypes have been lifted – I see that most change came through simply talking. Talking about what matters most. And what matters most to me is survival – my ability to live a full and abundant life with bipolar disorder. And I want to share that story with everyone who needs to hear it.

If you are local to the area, I hope that you will be able to come to the show. I believe that it will be a show that resonates in some way with everyone and I also believe that it will be a true celebration of what life can be for each of us. You can find all the information you need about dates, locations and tickets at:

https://www.capitalfringe.org/festival-2013/shows/139-almost-together

I hope to meet many of you there and please feel free to connect with me before then – www.facebook.com/maryleaphart

Blessings and strength to each of you along your journey!

Mary

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Mary knows she still is, and always will be, on the road to recovery, but feels that she’s come so far in the last several years to realize that now is finally time to share her story in big way. She’s opening up about the truth - not the misconception, not the stigma, not the stereotype - but the raw truth of life with a mental illness.

I’m so thankful to have met Mary online and look forward to giving her a hug after one of her shows next month.  If you’re near DC, or are in the area in mid-July, I hope you will consider supporting Mary and the movement to end the stigma surrounding mental illness by attending her show.

 

Our lives begin to end the day we become silent about things that matter.

- Martin Luther King, Jr.

 

 

Five Minute Friday {12}: Rhythm

kokoperry via Compfight cc

Right now, in this moment, I'm ready to make the climb.

I am ready to rise up at the end of the longest day of the year to make a statement.

With my family by my side, the steady rhythm of our hiking feet choosing measured steps along the trail, we will make the trek to honor the path I've walked in the past and the recovery journey I am still taking and will continue to fight for as long as I live.

I am a warrior mom. I climb to show that I am brave, that no one should be afraid to talk about mental illness, and because I passionately believe in the mission of Postpartum Progress, the non-profit sponsoring this event and the world’s most widely-read blog on postpartum depression and all other mental illnesses related to pregnancy and childbirth: to focus on positive messages of empowerment and recovery.

Today I am reminded that every day is a climb. Every day brings new challenges to face and overcome. Every day is a gift which I am honored to receive. Every day I will answer the call to climb because making the trek to the top, however impossible the obstacles to the summit may be, will be well worth it in the end. I know now from experience that what lies ahead holds more potential than I could have ever imagined.

See you at the top.

#ClimbOut

Linking up with Lisa-Jo Baker's

Let's Talk

[youtube http://www.youtube.com/watch?v=EH9meoWmAOM?rel=0]

 

Are you lost or incomplete?

Do you feel like a puzzle, you can’t find your missing piece?

Tell me, how do you feel?

Well I feel like they’re talking in a language I don’t speak

And they’re talking it to me

…

You’ll tell anyone who’ll listen, but you feel ignored

Nothing’s really making any sense at all

Let’s talk, let’s ta-a-alk

Let’s talk, let’s ta-a-alk

~ Lyrics from “Talk” by Coldplay

Lately I’ve been hearing from people who’ve been reading my blog. I’m so honored to learn their stories. I read each of these emails, comments, and texts with a deep respect for the story they’re sharing with me. They’re trusting me with their pain, their struggles, their fears.

And I can totally relate because I’ve walked in their shoes.

It’s a scary thing to have to deal with mental illness. It can rock you to the core. Make you question your future. Turn your world upside down. Turn your family upside down. Your friends may even shy away from trying to help. Not because they don’t care about your well-being, but because they don’t know how to help. They are clueless as to where to start, even though they want desperately to have their old friend back. They feel helpless.

The same emotion the person who was handed the mental illness card feels: helplessness.

When a chemical imbalance occurs in someone’s brain, of course the first thing a person feels is helpless. A band-aid won't fix this. It’s not something visible from the outside that a regular doctor can address. The brain is mis-firing. Something is deficient within the cells and synapses and it will likely take some time, effort, therapy, and a good doctor to figure out how to get things back to the baseline.

WHY ME???

Is inevitably the question that screams out from within. This isn’t fair. What did I do to deserve this plight? It’s not fair.

Friend, I’ve been there. I’ve been through the pain and fear that comes along with hearing you’ve been diagnosed with a mental illness. I’ve trudged through the thick, seemingly never ending mud pit of despair that is clinical depression. And I’ve felt the prickly, rushing waves of anxiety roll over me countless times, rendering me into an immobile heap, unable to decide what to do next to squash the distress. My mind has lost touch with reality when mania caught hold of my brain with her fiery grip, only to be brought back down through injections of antipsychotics in a psych ward. I even wrestled with several bouts of suicidal thoughts, when I hit rock bottom.

That, my friend, is what it took. The lowest low you could ever imagine. Weeks of wanting to just curl up and sleep forever. I’d pray that I wouldn’t wake up. But each morning, the world kept turning and the cycle would start again. I’d loathe the chore of taking a shower and picking out clothes for the day ahead of me. I’d put myself on autopilot in order to get through my morning routine. If I thought too much about it, I’d crawl back into bed, my safe cocoon. Episodes of anxiety at work would cause me such stress I could barely eat. I internalized so much, keeping my hurt bottled up inside because I was afraid of what people would think if I told the truth. Countless nights of red eyes from tears that had flowed so hard, there was nothing left. My body ached with the weight of it all. It had become too much to bear.

That’s when I realized: I can’t do this anymore.

I was sick of feeling the way I was feeling. I made a conscious decision to listen to what my doctors had been telling me. I chose to try a new medication and I committed to a treatment plan. And do you know what?

It worked for me.

It took several months of seeing my doctor consistently, taking my meds religiously, and following up with feedback for my doctor so that we could tweak the dosages. Sure, there were plenty of unpleasant side effects. I’ll spare you the details. The important thing is that I got back to well. I got my life back. Definitely not the same one; my life is completely different now than when I was first diagnosed. But in my opinion, this life I’m living now is ten million times better.

Because of what I’ve experienced, I now get to help people realize that they can get well too.

I realize it’s not always that easy. Sometimes there are so many other factors involved. It’s not my place to give out medical advice to my readers. Ethically, I don’t think it’s right. But there is something I will always share with anyone who reaches out to me: hope. I believe everyone is capable of overcoming a mental illness. We can do this by learning to live with it, accepting it for what it is instead of letting it beat us down. And we can help each other by talking about it.

We can do this. We’re much stronger together than we are solo, wouldn’t you agree?

If you or someone you love is struggling with mental health issues, please don’t hesitate to reach out to someone you trust. Whether that person is a blogger you only know from reading online, or someone much closer to you. Just talk. It’s the first step to getting back to well.

Let's talk.

There is Hope

If someone had asked me back in the summer of 2006 whether I ever thought I’d become a mental health advocate, I probably would have responded with tears instead of words. Because crying is what I did the most of that year. It was as if I were trying to cry out my severe depression. Cry all the tears until there were no more left to cry. Smiles, laughter, and happiness hid deep inside of me, dying to emerge, but too suppressed by the pain.

Back then, I couldn’t see hope. I couldn’t see my future because I was blinded by the tears of my sadness over losing my old self to my mental illness. I had a very difficult time accepting the fact that I was sick and needed help and medicine to get me back to well again. Each and every day of that year felt like a lifetime. I flew back to my parent’s house in Florida and spent several weeks with them while they helped me get treatment. The constant anxiety over my future, feeling like things would never get better, the intense darkness inside my heart made 2006 the longest and most challenging year of my life thus far.

The Overnight walk this past weekend was a night I will remember forever. I was honored to be among such an incredible group of nearly 2,000 walkers who each had been impacted by the loss of someone they loved to suicide and/or their own personal struggles with mental illness. The mood was solemn yet so full of inspiration. I met new friends and learned their stories of loss but also heard their dedication to spreading the message of hope and encouragement to those struggling. Hugs flowed freely everywhere you looked.

We talked as we walked, about the friends we had lost, about our own struggles, and about our hopes for the future: that we can help to break down the stigma that surrounds mental illness so that people won’t be afraid of reaching out for help when they need it most. Tons of photos we took during the night, posted to social media for the world to see, tell the story of our journey. I will treasure these images because they remind me how important it is that I’m sharing my story.

I walked with my friends Cristi @MotherUnadorned, Kiran @kferrandino, Jenni @zrecsmom, and Angel @mediamatson from dusk to dawn. We passed many of the gorgeous monuments and they lit the way for us as we made our way through our nation’s capital, passing the White House before making it to the dinner stop at 1:20am. At Farragut Square, we sat and ate for twenty minutes before heading out to finish the trek. We crossed the finish line at 4:15am and entered the finishing area where over 2,000 luminaries lined the walkway, each glowing with a loved one’s image and words of love and hope. It brought us back to the reason we were all there. To pay tribute to those we had lost and to strengthen our commitment to the cause of preventing suicide.

Without the help and support of my husband, my parents, my in-laws, my brother and sisters-in-law, and countless other family members and friends, I may not be where I am today. Because when things became so hopeless for me, when I wanted to give up my fight to get well, they kept fighting for me. They stood by me, and fought hard. I’m so grateful that they did.

They gave me hope to keep going. To keep fighting. To keep trying to fly again.

I’m proud to say that today I am flying. And the only reason I’m looking back is to help others. To show them there is hope. That they can get well with help and hard work.

This luminary caught my eye on the steps of the stage waiting for the closing ceremony. It sums up perfectly what the Overnight is all about:

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

PS. Thank you to all those who supported me on this walk. Collectively, the walk raised $2.6 million dollars - which is SO AWESOME! Donations are still being accepted though, for all the important work they do at the American Foundation for Suicide Prevention. If you'd like to donate, my walker page is available here.

On Staying Up All Night

Over the course of the past three months, I’ve made the transformation from Mental Health Consumer to Mental Health Consumer/Advocate, and from anonymous blogger to someone who finally realized she was entitled to call herself a writer. A writer who was no longer afraid to write her truth.

And I’m only just getting started.

Here’s a quick re-cap of the intertwining events of the past few months which led up to what is taking place this weekend.

Back in March, I attended the Wild Mountain Memoir Retreat as a newly self-proclaimed writer. It was on the Friday the retreat began when I read the email that I had received my first offer to join a major parenting website as a contributing blogger. A paid contributing blogger. They were going to pay me to write for them.

I was at the top of the highest high possible without actually being manic. It was blissfully refreshing.

This was my first post: My Love/Hate Relationship with Sleep. It was featured on the AOL Homepage on April 11th, and although it wasn't the post I had hoped would be my "coming out" piece to the world, I was still very appreciative for the exposure and was in complete awe of the avalanche of love and support that followed from my family, friends, and readers I had never met before.

The following day I posted what I would have chosen as my reveal post, had I been given the choice. My Time to Stand Up to Stigma was my big announcement to whoever was willing to listen. I stood at the top of the platform that is my blog and said {well, wrote, actually}: "I have bipolar disorder, and I'm no longer ashamed about it. I'm ready to finally show my true colors and talk about that piece of my life because I believe it's important for me to do so."

After having met an incredible person and fellow writer, Natalie, who happened to be my roommate at Wild Mountain, I had purpose to make my next leap. Natalie had overcome a suicide attempt last year, and her story inspired me to sign up to walk the American Foundation for Suicide Prevention's Overnight Walk {this weekend!} in Washington, DC. I had heard the commercials on the radio prior to meeting Nat, but it was only after listening to her tell me the harrowing narrative of what she went through that I actually logged onto AFSP's site to register to walk.

I've raised $2,025 for the walk thus far, and will be meeting up with several blogging friends (and meeting new ones!) over the weekend who have also made the same commitment to the cause. We believe in the importance of speaking out, of telling our stories, of starting the conversations about mental illness so that we can help others. I am so proud to be a part of this amazing event. {Follow me on Twitter (@BipolarMomLife) as I live-Tweet during the event.}

I'm a part of a movement that is changing the world. One word at a time. One day (& night) at a time. One reader at a time. If I were never diagnosed with bipolar disorder, I might not be writing right now. I consider my mental illness a blessing in disguise because at first diagnosis I became a prisoner of my condition. But over the years I've learned that condition doesn't have to take over my life. In fact, it enriches my life.

Over the past few months, I've chosen to stop wasting time being scared of being vulnerable because life is too damn short. I've realized that it’s my life to live and I control the end of my story. Staying up all night - for ONE night* - this Saturday into Sunday is only the beginning.

*I have put several precautions in place for this weekend, including asking my parents to be here so that the kids will be taken care of while I nap before and catch up on sleep after the walk. Staying healthy for myself and my family is my number one priority. 

My latest post for WhatToExpect.com's Word of Mom blog is live! Please stop by & check it out if you have a few minutes. It's got an important message. 10 Reasons I'm Thankful I'm a Mom Fighting a Mental Illness Thanks so much!