Confession: My greatest fear is that I will lose my life to suicide. I don’t say that to be melodramatic, I simply state it as a fact. As a person living with bipolar disorder, it is a fear that silently … Continue reading
I’ve been in a depressive episode for nearly 8 weeks. The decline has been gradual. There have been good days scattered throughout, but I’ve been edgy, tense, fatigued….my mind has been too loud some days, eerily silent during others. I’ve been crying off and on in my bathroom to hide my breaking from my kids…in my car as I drive from one errand to the next. I’ve had to shift to auto-pilot to just get through hard moments, root myself in detachment to keep from getting swallowed up by the stress. I’ve spent the last two weeks cycling rapidly between hypomania (marked mostly by agitation and a mind packed with too many thoughts), and a dragging depression that swallows me up and sends me into its belly for a few moments then spits me back out into the sun and air where I can breathe again. And then everything’s still and quiet…I feel “normal” and then the cycle repeats itself hourly, daily, weekly….and so it’s been for nearly 2 months now. Rinse. Settle. Repeat.
I’m still in that critical postpartum window. I just weaned nearly a month ago. My body and hormones are in flux and adjusting as a result. I hate it.
Stress is both motivating and crippling for me. I can handle 10 things going on all at once with ease. It’s once the 11th shows up demanding my attention that my mind starts to split and scatter off into darker corners. I think about my life these days and chide myself with all kinds of “should” statements for feeling and being overwhelmed by all I manage on a day-to-day basis: baby is teething & raging, middle child with special needs, oldest was just diagnosed with ADHD and his enthusiasm for school has waned significantly, trying to overhaul our home and parenting lifestyles to accommodate and support their needs (like increasing structure and making our home more sensory friendly), supporting my husband while he deals with stress at work. New therapy schedules, trips to the pediatrician, and comprehensive psychometric testing have dominated our lives over the past month. Up ahead there is more testing to be done, and meetings with the school district to discuss accommodations for Brennan and evaluations and placement for Alex who is gearing up for preK this fall…
It’s not all stressful. I’m involved in birthing great projects. I’m taking my mom’s advice on avoiding burnout by feeding my spirit so I don’t fall prey to losing myself, you know? I’ve joined writing & art communities online, I’m painting at 11pm, I’ve signed up for retreats and writing eCourses, done a couple of write-ins with groups, and I’ve done a juice cleanse to try to reset my body and mind. I’m re-reading Daring Greatly by Brene Brown as well as books on painting, sensory processing disorder, creativity, and feminism. I’m trying to find my way here still, in this space as far as my writing is concerned. I’m trying to learn how to embody all the parts of myself that have come alive over the past few years-artist, writer, advocate-in the midst of the daily demands on my person and time as a mother and wife. I’m trying to bloom where I’m planted. At 31, it’s still a stumbling process though.
I’m searching for my flow amidst the rhythms, rocking and swaying as the ebb and flow of my life’s current carries me throughout my days. But the stress of everything gets triggering and I find myself cycling with the ebb and flow as a result sometimes. That’s when my knees buckle and my head spins. My chest constricts and my brain starts to feel like it’s suffocating. My grip gets weak. Fatigue sets in and my steps forward get heavy. Taking care of myself gets harder, and usually becomes the last checked off item on my must do list-if it’s checked off at all. I end each day feeling as though I have no safe place to come up for air and just process my thoughts, fears, and anxiety…I end most days feeling unsettled and bottled up, stuffed to capacity and as I close my eyes to sleep I’ve found myself starting to pray like Jabez, asking God or whoever is listening for an increase in capacity…in ability…in might…
My hair is pink again with some blue added for extra fun. My hair and color are always my first lines of defense against the disorder of my brain chemistry and mood.
I visited my psychiatrist last week at the VA. This is another area that I can’t seem to find solid footing. We’ve lived here for nearly two years and I’m on my 3rd psychiatrist. Obtaining talk therapy has been a fail. The appointment scheduling system here is confusing and useless to me because I have very little say in what days and times fit into my schedule that’s already inundated with the kid’s school and therapies. I’ve had to fight to get treated, and I’m constantly having to say “but if you read this and go here, research and experts agree that….”. I feel lost in a system that I’m constantly told is for me to use and that I should trust. But the bureaucracy I face with nearly every interaction chips away at that trust. I have no confidence in my mental health care these days, in the professionals assigned to my care. And yet, at my appointment last week, I sat in front of her desk and allowed myself to become undone. Completely and unapologetically. I unloaded nearly 24 months of thoughts and stress right there in her office in 20 minutes while my smiling baby squirmed and cooed in my arms. She listened to every word. Asked some questions that dug a little deeper. Apologized for all the trouble with the system I’ve had and for not really hearing me 6 weeks ago when I told her my anxiety was becoming a problem. She admitted that lack of knowledge about medications while breastfeeding restricted her ability to really give me what I was needing. We decided now that I’m no longer pregnant and breastfeeding we could get more aggressive with my meds again-go back to finding a more therapeutic dose. So over the next two months I’ll be doing that-going up on lamictal and prozac and trying out an additional med for anxiety. I started the increase yesterday. I’m hoping by the end of the week my brain and mood will start to grab ahold and adjust accordingly.
I’ve struggled today to pick everything back up and keep walking. To push past and through. To square my shoulders and lift my chin. To turn a deaf ear to the tape playing in my head that has all kinds of lies and frenzied talk on a loop.
But I’m doing it-picking up and pushing. I’m moving forward. Slowly. The sun is shining outside despite the cold front that’s moved through. I’m working my way out into the sun, breathing in deep as I go.
Dear Miriam, My head and heart have been reeling since your death. Upon seeing your picture and hearing details emerge about your struggles mentally and hospitalization, I sat crumpled in my bathroom, sobbing for you, your daughter, and for myself.
You see, I saw your face, your brown skin, and I saw a reflection of myself-a mother battling a mental illness. Having lived in the darkness of postpartum depression I know the hopelessness, fear, confusion, and pain that consumes you from the inside out. Although I’ve never experienced psychosis, I have and do experience the chaos, scattered and fragmented thoughts, paranoia, and such that comes at times with having bipolar disorder. I know that my having such a mood disorder puts me at a much more significant risk of psychosis postpartum, and that terrifies me. Like you, I’ve been hospitalized, trapped in my own mind, wandering the halls and monotony of the psych ward, getting help, but also wanting OUT and have some sense of normalcy back…whatever’s left of it in your life at least.
I know how triggering and taxing an unplanned pregnancy can be on your psyche, even when you’ve accepted and embraced the new life growing within you. I know the disconnect you can feel once you’re holding that new life in your arms minutes after delivery and long after you’ve been sent home. I know how difficult those first few months can be, and even that first year. And I know what it’s like to need help, be in treatment, but not have anyone you can really talk to about it, no one who “gets” the upheaval your mind and well-being is in. I know what it’s like to have to live with mental illness for the rest of your life. I know what it’s like to have to make a conscious choice to fight for your life daily, and being too tired to make that choice most days. I know the stigma that comes with being sick, and taking medications. I know side effects and having to rely on meds is exhausting and at times can chip away at your feelings of self-worth, and leave you doubting your capabilities to mother, to accomplish goals and dreams…to LIVE.
I know all of these things and that is why I sat in my bathroom crying for you…for me…for your daughter, and for my unborn son squirming in my belly.
After my tears came questions: were you getting help after your hospitalization? Were your boyfriend, mother, and sisters supportive? Did they encourage you to stick with treatment-were they themselves educated on your meds and illnesses? Did you have a therapist and adequate access to other mental health resources? Did you have anyone, ANYONE to talk to? Were you afraid to talk to anyone? Were you compliant in your treatment? Did you decide to stop treatment because you figured you could do it on your own, or were you pressured to by those around you? Did anyone tell you the dangers of quitting meds cold turkey or talk to you about weaning? Were you given speeches about bootstraps and soldiering on? Did your doctor think you were getting better and miss something? Were you even properly diagnosed and given the right kind of treatment? What led you to DC that day? WHAT HAPPENED?
I know that because you are no longer with us to tell your story, we won’t ever really have the answers to these questions-we won’t ever know the full truth. My heart aches with this knowledge. My heart breaks that the events that took place unfolded the way that they did and that your life was taken.
Since your death I’ve seen lots of discussion in the media about the state of your mental health, and lots of misinformation and a lack of distinction between postpartum depression and postpartum psychosis, which is what it appears to be that you might have suffered from, or possibly some other form of mental illness. I’ve seen anger and outrage over how the police responded to your actions, and calls for an investigation on their use of force policy. I’ve seen what happened to you become politicized and I’ve seen people make ugly, disgusting comments about you, a woman they’ve never met.
I’ve seen all of this and all I can think about is your precious daughter. When I do anger wells up in me and boils, but not for any of the reasons I see it embodying others. My anger is with our community, with our people. I’m angry that within the black community there is no focus placed on our mental well-being and on mental illness. We fight to quell violence and hardship in our communities but do little to nothing to fight for resources that can help us deal with the mental impact violence, abuse, and hardship has on us. We don’t talk to our children about mental illness, other than to point to “Crazy Ray” who lives down the street and further cement stigma about mental illness in their minds. We are misinformed and uneducated. We are ignorant. We think therapy and medications are for whites only. We are held hostage by a code of silence that throughout our history has kept us safe and helped us survived but is now killing us. Our churches tell us to pray more, have more faith, live right, strive for prosperity…but say nothing about the mental illness that is often quietly sitting amongst us in our congregations.
We will fight for Trayvon and for our black boys. We will march against those who believe it’s better to close our schools and build more prisons. We will rage at police brutality and systemic racism across the board. But when it comes to our mental health and the facts on mental illness, particularly for the WOMEN’S mental health, we are cold…silent…apathetic…hushed…disbelieving and ignorant of the science and biological roots of mental illness and how vital a role environmental factors play in the manifestation of illnesses like depression, anxiety, bipolar disorder, and schizophrenia.
Our national black leaders and organizations speak little on this issue and make no demands for change. I would go as far as to say it’s not even on their radar or list of priorities. Narratives and dialogue on mental health in our communities is driven and dominated mostly by white advocates. Those of us who live with mental illness and choose to face the stigma within our community and society at large often aren’t given the same platforms and amplification as white advocates. Our outrage and concern for other issues drown out suicide prevention and mental health awareness. Campaigns and efforts are not targeted at us, in OB offices we don’t see our faces on pamphlets on PPD or other perinatal mood disorders, and our doctors rarely screen us effectively for it. Medicaid provisions often keep our single mothers from being able to get adequate treatment and access to resources on the mental health front. (I speak from experience)
All of this…has me angry. Has me raging on the inside, and pushes me to do more with the space I have here. As a woman and mother of color with bipolar disorder who has survived PPD, I look at you, your daughter, and what happened, and the role mental illness might or might not have played in this, and I rage and I feel a responsibility. To your memory and most importantly to your daughter who witnessed such horrific violence that day, I feel an obligation to do more, say more, fight for better within our community. Others can rage and decry the actions of the police if that’s what they feel is most important. Speaking from experience I can say that law enforcement officials are not adequately trained on how to respond to situations when a possibly mentally ill person is involved. But I will rage and decry the lack of education and honest dialogue about mental illness on a national level and within our own community. I will rage and push for you so that your daughter and other women of color get educated and aren’t ashamed to get help. I will rage against the “strong black woman” archetype that keeps so many of us from acknowledging we need help and treatment on this front. I will speak up, I will fight, I will advocate for you so that your death will not have been in vain.
I will do this because I know, Miriam, what it’s like to be touched by madness and struggle to survive in its death grip. I will do this because your story and your death have shown me that its past time we rise up, get real, and take responsibility for our mental health….and take action. I will step up Miriam. I will continue to speak in the vacuum until our stories and experiences with mental illness are heard and taken seriously instead of dismissed or trivialized.
I’m so sorry we lost you. I’m so sorry you lost yourself. I’m so sorry your daughter will no longer have you. I’m sorry we couldn’t do better by you both. But know that now? We will.
I am a Warrior Mom.
I have sat in the darkness of postpartum depression and anxiety feeling hopeless and lost. I have felt them rip my identity as a mother and a woman apart, leaving me feeling like a shell of a person, empty.
I’ve hid in closets, and cried on my bathroom floor because being near my children felt impossible to handle.
I’ve endured thoughts so intrusive I still can’t speak of them to anyone, let alone myself.
I lived with guilt over my inabilities to play, laugh, and hold my children-it feasted on my insides for months….and still comes back for more when I find myself on the low end of the bipolar mood spectrum.
I still live with shame over the rage that engulfed me for over a year, often over the trivialest things, in the most unexpected of moments. The screaming, the yelling…If there’s one part of my experience I wish I could erase it would be that.
And yet, in spite of the darkness I lived in after Alex’s birth, despite how sick I was, I survived. With support and treatment I overcame. I climbed out of that darkness. I became a Warrior Mom.
Tomorrow, I’m celebrating that accomplishment with over 100 other women across the United States and in 6 other countries.
My family and I will be heading to Wild Basin Wilderness Preserve here in Austin for a 2 mile trail hike. With each step I’m sure I’ll be emotional as I look at my boys and my husband around me and reflect on my experience with PPD…and I’ll again be overwhelmed with gratitude for Postpartum Progress and Katherine Stone.
If you’ve been a reader for any amount of time here, you know how much I credit Postpartum Progress and Katherine Stone with essentially saving my life and helping me come into my own as a mother. In January 2011, it was THE lifeline I needed that started to pull me out of the darkness of PPD & anxiety and eventually led to my diagnosis of bipolar disorder. You can read more about how Postpartum Progress helped me here and at the end of this post if you haven’t already.
3 weeks ago I joined fellow survivors and even those still fighting PPD in a campaign to raise funds for two very specific projects Postpartum Progress is working on. In those 3 weeks, we’ve managed to raise over 36K, and basically create a movement to honor our experience and give hope to others still finding their way out of the darkness Postpartum Progress helped us come out of.
We are Warrior Moms. We are climbing out and pulling others up with us today, the longest day of the year, to stand tall in the light of hope. I’m honored and humbled to be a part of something so significant with the most amazing women I’ve met in my life.
Let’s do this.
To learn more about Climb Out of the Darkness, what the donations are funding, and to donate to our hike on Saturday click here
Sorry I haven’t stopped by here since May 20th. Life’s been pretty consuming as of late, and I’m not as good about writing my way through periods like this as I was a year ago. Things are busy busy busy and I’ll be honest-sitting down to write has proved to be more difficult than I would like it to be. The words are there, waiting to be given life, the stories are stacked up on shelves in my brain, the desire is there, but it all just becomes a jumbled mess when I sit down to type or even write in my journal.
Part of it is because my brain is so scattered, thanks to my disorder and my recent hypomanic episodes and cycling. Part of it is because I become to preoccupied by my compulsions to clean, organize, and rearrange everything in our apartment. Part of it is because I’m fatigued and the energy I do have is poured into being pregnant, mama, wife, housekeeper, cook, errand runner…the desire to create or give anything back to myself lingers quietly in folds of my heart, but never finds its way to execution. My mind is scattered and my hands feel inadequate, empty, unable to form the words or images that are mixed in the chaos.
Part of it is because I’ve become completely immersed in a new parenting approach with Alex and in implementing new routines and techniques I hope make like easier for him…and for all of us, really. I’m seeing how different and significant some of his needs are and in a lot of ways re-learning this whole parenting thing. From how I discipline, to the words and tone I use when speaking to him, to even how much pressure I apply when I touch or hug him, my whole posture towards parenting and mothering him has changed. Most of my days are consumed with being engaged with him in ways I wasn’t before. Learning about sensory processing disorder, autism, and what we’re learning from his therapists since April has given me new ways to engage and interact with him that are different from how I did before. It’s been quite the learning curve-there’s so much more to be aware of these days! I’m more watchful, taking note of the slightest change in attitude or behavior (positive or negative), more apprehensive and mindful about how changes in routine, however slight, will impact him from moment to moment. In some ways I feel like I’m on high alert from the time he wakes up until he finally falls asleep after I’ve put him back in his bed and given him a deep pressure squeeze for the fifth or sixth time. I’ve had to become much more patient, learning to move at his pace, and how to move him along faster in a way that he can understand when we’re short on time. I’ve found that all of this has taken an energy that I, especially being pregnant, barely have the reserves for. The simplest things from washing his hands to getting dressed to helping desensitize his facial muscles before his speech therapy sessions is all a process; exhausting and consuming, but one I’m committed to helping all of us navigate and learn as best we can.
Part of it is because I’m committed to being well during this pregnancy and am forcing myself to focus on self-care. This becomes increasingly difficult when pregnancy is kicking my ass, particularly when migraines attack, and my blood pressure is low. The migraines have been pretty frequent this pregnancy; during a good week I only get one, during my worst I’ve had them for 4 days straight. Functioning when I’m a wreck physically feels impossible, but I somehow get through making sure the kids have what they need for the day and that’s about it. Aside from eating and taking my medications, taking care of myself takes a backseat and I have to fight to make things like taking a shower, combing my hair, getting in any kind of exercise or leisure activity a priority. Overall I’m doing better on the self-care front than I have in the past, especially during my last pregnancy.
All of this focus on concentration on these other areas of my life leave little for my writing here and painting….advocating even. I had all of these plans for my creative pursuits this year but the mental and creative bandwidth I need to execute them isn’t what I’d like it to be. For some reason I can’t seem to find space for those two to fit in my life as of late and this does sadden me. Frustrates me. Leaves me to wonder how I’ll fit them in when there are THREE children to give my time and attention to. I’m hoping I can find a way….I’m in awe of those who’ve found a way to balance and navigate it all.
At any rate, while I find it hard to write and paint these days, I have found it easy to keep up with vlogging-probably because I can just do it on my phone while I’m on the go and have a few minutes alone. So I think that’s just what I’m going to have to do for now because it’s the one thing that I can keep up with that fits in best with everything else. It’s the one thing I feel I can keep up with right now on this front. I’m hoping to write here during the summer, but know that if you don’t see me here, you’ll be able to find me on my YouTube channel, addyeBeesWorld, where I’ll mostly be sharing the nitty-gritty of navigating bipolar disorder while being a pregnant mama. Feel free to watch and subscribe-I’ve done videos for weeks 15, 16, and 17 so far (I tell you what we’re having in my second video for week 16!) And of course, I’ll always be on Twitter :) (@addyeB)
So that’s where I’ve been, what I’ve been up to, what’s going on. I’m still here…I’m just consumed is all.
Maybe I just need to Lean In…anyone have Sheryl Sandberg’s number?
I decided to take “My Bipolar Life” in a new direction and turn it into a video diary of sorts for this pregnancy.
As with my other videos, this one goes against all vlogging rules-it’s just me, talking, unscripted. I hope you don’t mind the lack of editing, the “ums” and my losing my train of thought at times :)
My goal is to do at least one of these a week. There might be more-just depends on what’s going on, if I have some thoughts I want to share, where I’m at mentally, etc. Hold me accountable? Oh and subscribe? Thanks.
Fear has become my constant companion these past months, sowing seeds of doubt, confusion, and discouragement that have taken root deep down inside of me where my essence and passions are conceived. It has choked my creativity, inhibiting my freedom … Continue reading
Before I spill my guts here today I want to make sure you understand something from the very beginning: What I’m going to talk about speaks solely to MY experience as a mother who’s lived with antenatal depression and PPD and who has a child with developmental delays and is on the autism spectrum. I can’t speak for other women and their experience or how their illness-treated or untreated-may or may not have had an impact on their child’s development. I’m choosing to share this because honestly? I’m having a hard time processing it on my own. I don’t have a therapist to talk with about it right now, and keeping it all to myself is only allowing shame to breed ugly thoughts and emotions; thoughts and emotions I definitely don’t need right now considering I have a family to take care of, am currently off of 2 of my meds until my 2nd trimester, and I have a new baby growing within me. This is how things have played out for us-I’m in no way claiming this is how it will play out for others.
11 months ago, I wrote a post about Alex’s 2yr well visit and how his pediatrician at the time had expressed his opinion that the developmental delays we were concerned about were linked (at least in part) to my untreated antenatal depression, PPD & anxiety. You can read it here; doing so will give you more context.
When I wrote that post I was hurt, wracked with guilt and defensive. I was confused-I didn’t know what to make of what he had said and I honestly didn’t want to believe it. I didn’t want to believe it because I was afraid to. Allowing myself to acknowledge he may have been right would’ve just ripped the band aid off of the wound I had worked like hell in therapy to stop bleeding.
But like I mentioned in my post last year, I had read the studies, the articles, what the experts had to say about untreated depression in mothers and it’s effects on their children. I had read the stats about low birth weight and premature labor and caught my breath every time, knowing how small he was, how I’d gone into labor 3 weeks early-but I secretly hoped he wouldn’t “fit” the others about developmental struggles. (Again, links to some of those studies and articles are in the post linked above.) The knowledge pulled and gnawed at me every time I struggled to engage with Alex. The shifts in mood, the struggles to get him to do simple things like eat, wash his hands, or even just accept hugs and kisses from Bertski and I without withdrawing first. Every time I watched him shut down around people, or scream in terror when approached by children on the playground, my insides, my heart twisted. When he stopped eating nearly everything and would only touch hard, rough textured food….when we were told by early intervention he was delayed at least 25% in speech and possibly more in other developmental areas….as I watched his symptoms become more pronounced over the course of the past 11 months, my mama gut begged me to turn a deaf ear to fear and just face reality, listen to what it was trying to tell me. I wasn’t going to be able to help Alex if I didn’t. I wasn’t going to be able to be the mother he needed me to be if I didn’t.
So I did, and I started talking to Bertski about it a few months ago. He expressed that he had been watching Alex and having the same thoughts about his behavior and development and what had possibly caused him to develop the way he had. We agreed that in addition to my illness being untreated for so long possibly being a factor, the instability of our relationship during Alex’s first two years was likely a factor as well. It was a tough set of conversations…thinking about them still makes me cringe. But I’m glad we had them because it enabled us to move forward in seeking help. We knew Alex needed more help than we could give him and WE as his parents needed help parenting him. His issues had started to become beyond us and the daily struggle of trying to navigate them was overwhelmingly frustrating and discouraging.
His 3 year visit was two weeks ago, with a new pediatrician here in Austin. We told her everything, with her interjecting a question or two every now and then. She listened attentively until we finished spilling our parental guts out to her. She was quiet for a few minutes and then started to give her thoughts: “It’s obvious he’s very smart-I can see that for myself in just the short time he’s been in here. But from my brief observation and what you’ve told me I would go ahead and say he’s definitely on the autism spectrum. My initial guess would be high functioning but he does have significant speech and socialization deficiencies. Further evaluations will give us more information. The good news is we’re catching it now-early intervention is crucial. We’ll get him into various therapies and by kindergarten I’m confident he’ll fit in just fine with other kids in a regular classroom environment. He’ll catch up, he’ll excel. I’m sure even within just 6 months we’ll see significant improvement.”
We walked out of that appointment with an answer, with hope even, but also with some sadness. A heaviness rested on us for the remainder of the day. Even though we had been preparing ourselves to potentially hear such a diagnosis for Alex, the reality of it still hit us pretty hard. I can’t speak for Bertski, but I know for me, the guilt was excruciating that day. I called and talked with the pediatrician about it some more, explaining my illness and how it impacted my ability to bond and interact with him during my pregnancy and his first year and a half. I expressed to her what my difficulties had been and she didn’t shame me for them:
“Based off of the research, your history, and where he is developmentally, I’d say it is highly likely that there’s an association. Being depressed and not having effective treatment can definitely have the kind of impact on a child’s development and behavior like we’re seeing in Alex. But you don’t have to blame yourself for it. You’re helping him now-he’s older and you’re recovered and managing your Bipolar as best you can-that’s what’s important. Yes, this happened, but it’s ok, you’re getting him help just like you sought help. It’s not your fault, Mrs. Nieves.”
No, being depressed during my pregnancy and struggling with PPD and anxiety the first 2 years of Alex’s life wasn’t my fault.
I would even go as far as to say that not being treated for so long wasn’t my fault either-there was so much I just didn’t know, and when I did express what I was enduring to those around me and my OB, I was told it was all “normal,”…given time, I’d be “fine.”
You know, they say we can only do better when we know better. Given my circumstances, I know I did my best and when I couldn’t, I fought to.
I don’t think I failed Alex. I do think my illness failed both of us-it robbed us of having a strong start and that’s what hurts me the most when I think about how it’s impacted him.
But I’m learning now how to use the hurt to lay a new foundation for us to build upon. I’m learning how to advocate for him and learn all I can to help him like I’ve done with myself and my illness. Alex has started ABA therapy and is already showing progress. He has upcoming evaluations with speech therapist to work on improving his language and an occupational therapist to help with his autistic and sensory related struggles.
Accepting that there’s possibly an association between my illness during pregnancy and Alex’s development struggles is a hard truth to stare in the face y’all. I know it’s not everyone’s truth, but it’s MY truth and I’m working hard once again to process it, heal from it, ditch the guilt over it, and move on now that I know where he’s at. I’m not sharing this to say that what’s true for me and Alex is true for all moms with untreated antenatal depression & PPD. It’s not at all. But I am sharing it to say that you know those effects they talk about in those studies? I’m watching my son live with them. It DOES happen. It’s in the minority, but it does happen-I wish it was talked about more-not to shame anyone, but to help women understand that they don’t have to BE ashamed that this happens. Does that make sense? I hope it does.
I’m not here to scare anyone or have you think that you and your child are in the same boat as we are. Definitely not. But I am here to say that if you ARE in the same boat we are-It’s ok. It’s not your fault. Illness may have robbed you and your child of a strong start, but don’t let guilt rob you of anything else. I know it hurts like hell, and you feel like you could’ve done more, but you did your best with what you had and don’t let shame deceive you into thinking otherwise. You’re still an amazing mama to your child. You’re not a bad mother. Our children will be okay because they have us and they have others to help them get to where they need to be.
If your child is showing signs of delays-don’t let shame keep you from getting help. Ask for evaluations and resources. Talk to their doctor and ask about Early Intervention. Be open. Be honest. Be their advocate just as you’ve been for yourself.
I hope this made sense. It’s late and I’ve had a rather emotional day. Also? I could REALLY use a friend in this particular boat.
I gots some thangs to say…..forgive me if this just kinda tumbles out, I’m not in the mood to filter much today. Here we go:
Yesterday I listened to a heart whisper and submitted two pieces for BlogHer’s 2013 Voices of the Year, one visual, one written.
I submitted them because one of my words for this year is “pursue,” and when it comes to my writing and art, my intention this year is to pursue opportunities for them to be showcased. Why? Why the hell not? I write and paint for myself first and foremost and will always do so even if I have zero readers and the world thinks my art is a travesty, BUT I’m also a storyteller who believes in the power of sharing your experiences with others. Writing and painting save me from the parts of myself that thanks to illness are hell-bent on destroying me-and so does sharing about my life through the written word and visual art. Sharing my stories here and through paint are my way of giving back-I hope that at some point, what I share and convey in what I create helps someone on some level, in some area of life be it motherhood, mental illness, abuse, or just life in general.
I also submitted because hey, who doesn’t like to connect with others and be heard? And who says it’s wrong to be proud of what you’ve created? What’s wrong with just going for it, JUST BECAUSE you never know what will become of it? YOLO! Am I right?
I said all of that to say that I didn’t submit my pieces because I think other people will find them moving and valuable, worthy of attention. I shared them because I FIND THEM VALUABLE, MOVING, AND WORTHY. Maybe if my piece on being bipolar and a mother is selected, maybe another mom who was just diagnosed will find it and find some comfort-or find a way to contact me so she can find someone to talk to or ask questions. Maybe if my piece is selected people will stop believing people with an illness like bipolar disorder are incapable of being quality parents and raising healthy kids. But if I had decided to NOT submit that piece, then the chances of that happening are significantly reduced considering how “small” I am in the blogosphere. So I saw an opportunity to be an advocate, be a storyteller, honor MYSELF for owning my story, and took advantage of it-Like Nike, I just did it. Insecure, vulnerable, and all, dammit I sat my ass down, read through my stuff and submitted.
Maybe for you, it’s not about any of this. Maybe you just want your work to be heard, be seen, be validated, be recognized. Maybe you wrote some funny shit and you want others to recognize you’re the next Richard Pryor or Sarah Silverman. That’s OK. It really is. Go ahead-submit! Honor your work. Pat yourself on the back, man. Be proud.
For those of you who are discouraged by this whole VOTY thing, hear me: STOP WAITING FOR OTHERS TO VALIDATE YOU AND YOUR WORK AND VALIDATE YOURSELF. STOP DRINKING THE DAMN VOTY KOOL-AID. I’m watching so many of you flog yourselves and doubt your self-worth and value as a blogger, writer, and fucking human being because no one is nominating your work. I get why it’s a downer, and trust me, I think the voting aspect of the process is asinine and I know that’s what’s discouraging so many of you from submitting. But I learned a couple of years ago that sometimes you can’t wait for others to celebrate and honor you, you’ve got to do it yourself, fuck everyone else. THROW YOUR OWN DAMN PARTY. Stop waiting for an invite. NO ONE will take pride in you or what you’re putting out there if you don’t.
96 of the pieces that will be selected as VOTY will be selected by the committee-guess what? They are reading each and every piece submitted whether it has 500 votes or 0. So even if you’re small potatoes like myself, your work will still be seen. Shouldn’t that matter more than some damn votes? Even if your piece isn’t selected, you never know who will become a fan of your work just because they were on the committee and read your piece. You don’t know what kind of opportunities could come out of this. And even if nothing comes out of it, shit, pour a drink and cheer yourself for having the balls to do something so many people wouldn’t.
I know when you’re a small fry in the blog/writing arena it’s easy to get intimidated and feel left out because those with bigger platforms are being nominated, called out, read, and recognized-and recognizing their own peers. But hear me: SMALL DOES NOT EQUAL INSIGNIFICANT and is in no way an indication of the value and worth of your work and your story.
So STOP DRINKING THE VOTY KOOL-AID. Submit something if it’s on your heart to do so. (Heart whispers are meant to be listened to-unless it’s telling you to go kill someone. If that’s the case, get a new fucking heart ASAP.) Go find a favorite piece from someone you read and submit it to honor them-if they’re a fellow small fry, I can guarantee you it will make their day and probably encourage them to keep writing, sharing, owning their story.
So. What are you still doing here reading this? GO. Bye!
“How many more copycats are waiting in the wings for their moment of fame from a national media machine that rewards them with wall-to-wall attention and a sense of identity that they crave, while provoking others to try to make their mark,” LaPierre said. “A dozen more killers, a hundred more? How can we possibly even guess how many, given our nation’s refusal to create an active national database of the mentally ill?”-Wayne LaPierre, NRA lobbyist
The NRA sickens me. Truly. They just gave a completely tone-deaf and disrespectful response to what occurred a week ago today. They believe arming school officials and having armed guards at school will prevent such tragedies. I don’t agree with this perspective at all for varying reasons, but I know there are those of you who do. I don’t want to debate that with you today. I simply want to address the question asked at the end of the above statement.
I’m a mother of two boys.
I’m a USAF disabled veteran and former police officer.
I’ve survived Postpartum Depression and Anxiety.
I currently live with mental illnesses called rapid cycling Bipolar Disorder type II and OCD.
I take medication for these illness. 4 of them. Every day. Every.Single.Day.
I go to therapy. I see a psychiatrist.
There are days I struggle to keep it all together and not let the fact that I have some chemical imbalances stop me from living life.
There are days when I want to give up.
I have been hospitalized-not because I was a threat to those around me but because I was a threat to myself.
I am not a violent person, although I have been traumatized by and have experienced violence first hand.
I am not a threat to society.
I have no desire to own a weapon, and never have despite my knowledge of how to use, clean, and take them apart, and being properly trained and qualified on several of them-ranging from the M9 pistol I carried on my hip every shift to the M203 grenade launchers, M249′s, and M4′s I was trained to use in combat during deployments.
I do not belong in a database because I have a mental illness.
My mental illness does not mean I am a violent person.
I am a compliant, law-abiding citizen who still manages to function just like everyone else despite the effects my illness has on me.
My friends who also have mental illnesses? They don’t belong in a database either.
They are just like me: men and women, mothers and fathers living with a painful “invisible” illness but still living their lives, working, raising their children, loving, helping others, and being productive members of society.
If our mental health records should be put into a database, then every person who applies for a weapons permit or who purchases a weapon, should submit to a comprehensive mental health evaluation, comprehensive background check similar to what’s required to obtain a security clearance, and a weapons safety course. You can’t say I should be registered in a mental illness database but not even mention that a more rigorous and comprehensive screening of those applying for weapons permits and buying guns is needs to be monitored as well.
It shouldn’t take less than 20 minutes to walk in to WalMart and walk out with a gun, I don’t care what you’re using it for.
Also? No one should be allowed to own or put together an assault rifle or semiautomatic weapon. I don’t understand why such a deadly weapon should be in the hands of the man who lives next door to me.
Yes, you have the right to bear arms, but maybe the kind of arms you’re entitled to bear should be re-evaluated. Yes, you have the right to protect yourself in case of a threat or danger…but we all saw how that played out with the Trayvon Martin incident, didn’t we? Maybe we start redefining what a threat is and what self-defense actually looks like. Maybe we start asking ourselves some hard questions and making some compromises. Not saying I’m right. Not saying the solutions or answers to this are simple. Just thinking out loud here.
You have the right to bear arms, but guess what? I have rights too. I have the right to have access to mental health services and resources that aren’t underfunded and understaffed; services and resources that have qualified professionals working for them who treat us with the respect and dignity we deserve just as much as “normal” people.
You have your rights. What about mine? And the other 1 in 5 people who live with some form of mental illness in this country? You have a right to arm yourself…we have our rights to privacy…and to the same life you do.
Those who live with mental illness are not all dangerous. We don’t all need to be tagged and stored in some database. If you REALLY think we do, then I say you should be too. Because while you may not have a mental illness you could be just as capable of violence. ANYONE with access to a gun can quickly and easily become a criminal-yes, even “responsible good guy gun owners.”
I am mentally ill. I am not violent. I don’t belong in your database. Stop stigmatizing me and those just like me. Stop using us to redirect criticism and calls to action by saying we are the problem. We are not your scapegoat.
I guess the old cliché is true: “you can’t teach an old dog new tricks.” No you can’t. Not when their greed disguised as advocating for”rights” is stronger than their desire to admit they could stand to learn a few things.
Go fuck yourself, NRA and hold another press conference when you have something more substantial to say.