DAY 24 - You're Alive For a Reason

Place your hand over your heart. Can you feel it? 

That's called purpose. You're alive for a reason, so don't ever give up.

- Joyce Meyer 

Here is a partial list of resources for suicide attempt survivors. You are important. You are important. You are needed in this world.

And you are not Alone.

AFSP (American Foundation for Suicide Prevention) provides many suggestions for attempt survivors. You can find that information by clicking here.

The Suicide Prevention Crisis Line offers many resources for suicide attempt survivors. You can find that information by clicking here.

The American Association of Suicidology offers a list of resources for attempt survivors. Click here to learn more.

Live Through This is an excellent source for finding the stories of suicide attempt survivors.

SAVE (Suicide Awareness Voices of Education) provides resources for suicide attempt survivors. You can learn more by clicking here.

The organization PH&S (psych help and safety) offers a downloadable document that provides support and suggestions to those who are dealing with thoughts of suicide and/or are a suicide attempt survivor. Click here for that document.

If you would like to find more information and posts on the Lighting Up the Sky blog related to suicide attempt survivors, click here.

DAY 15 - I am a suicide attempt survivor.

 

Our deepest wounds surround our greatest gifts.
― Ken Page

When I first published What I Want To Offer in 2018, I was nervous about its response and uncomfortable with the vulnerability of the writing.

Since then, it has become the most popular post on this blog. This personal essay about my own suicide attempts has been particularly helpful to those who have lost someone to suicide and are struggling with questions like 'How could they do this to me?' and 'Why wasn't my love for them enough?'

Because of this, I have gone from feeling uncomfortable with the essay to being honored that I can help loss survivors in this way. So, I am sharing it with you again, today. Click here or on the image above to see the essay.

DAY 27 - Changing the World

We are rewarded for hiding ourselves. 
 The fact that we can function, at great cost to ourselves, is used to beat up the people who cannot function.

S.E. Smith

 

Not quite six months after John died, I reached a turning point in my anger. Up until then, most of my anger was focused on the mental health care systems that had failed him. I was enraged at the lack of information, lack of adequate treatment, and the industries that prioritized cost effective measures over making mental health resources available to those who need them.

I was also angry at the lack of resources and support available to those who love someone with a mental illness. I hated that much of the messaging for partners and loved ones is that they either leave, love perfectly, or assert boundaries that are nearly impossible to manage. All of these messages fell terribly short of respecting the imperfection of being human.

I have come to believe that the suggestions that are made to the loved ones are born of the fact that we don't have adequate treatment for mental illness itself, and we don't have adequate resources to foster universal suicide awareness.

These illnesses inflict pain and suffering on not just the person with the illness, but also on their loved ones. Trying to mitigate this suffering, loved ones often treat the person with the illness as if they are the enemy. Sadly, this dynamic exacerbates the shame and fear that mental illness already imposes.

And if we lose someone to suicide? We disect in excruciating detail the ways in which we'd been in conflict with the person we'd lost. We continue to confuse the illness with the person we loved. How could they have done this to me? But we must begin to replace the words 'him/her/they' with 'the illness,' in order to have an accurate reflection of what was going on.

Similarly, we ask ourselves: how could I have said this to him? How could I have done this to her?  The answer is that we weren't fighting with the person we lost, we'd been engaged in an argument with an illness.

Still, whether we are loss survivors or we are attempt survivors - we agonize over what we could not do, what we did do, and what we believe we should have done. We blame ourselves for not having tools and resources, despite the fact that they do not yet exist. We blame ourselves for not knowing many things that are still unknown. We blame ourselves for not being the cure for mental illness - as if that were even possible.

So yes, in the months following John's death I was angry. And I was also ashamed. I survived only because the people who loved me held me up. I know too though, it was often a struggle for them. 

My guilt was so incredibly heavy, it dragged me down again and again. I'd lost my mother to suicide. I'd nearly lost my own life. And now I'd lost John. I didn't understand why life was so unfair. Not in a self piteous way, but in all earnestness. How could this be happening? How would I ever be able to incorporate the reality of these losses into a life that might include hope and joy as well?

It was exhausting. The grief was exhausting. My self flagellation was exhausting. I was tired of the confusion. And then one day I realized that I would never overcome the worst of my pain, if I didn't better understand what had happened to John, and myself, and my mother.

It is important for me to point out that amidst all of this emotional exhaustion, I remained motivated by wanting to defend John. Because he died by suicide, there was this constant inference that he was selfish. But I knew him well. He was human with many flaws, but selfishness was the least among them.

If nothing else, I understood that John had lost his life to a mental illness that was beyond his control, and yet he was being blamed for it. I knew that he'd fought extremely hard to rebound from the ways his illness impacted him. I knew this because he told me, I knew this because I saw it.

When John died, I knew he deserved far better than the fallacy that he'd been weak or selfish.

I thought about when my mother had died by suicide 15 years earlier. When she died, I was beside myself with grief and guilt. My lack of understanding set me up for years of feeling responsible and years of feeling as if the similarities between her illness and my own meant that I would lose my life to suicide too.

And then I thought about my own suicide attempt, which had happened less than five years prior to John's death. In the weeks following my attempt, family members stopped speaking to me. People unfriended me on Facebook. I received one anonymous text: "Don't do this to your son." To this day, I don't know if that was supposed to be instructive or accusatory.

I changed my phone number and stopped replying to messages.

The truth is, I hadn't known the answers to the questions people were asking. I agreed with the premises though. There was something terribly selfish/bad/wrong with me. I was not worthy of friendships or forgiving. I couldn't understand how I had 'let' this happen either. I, like John, had tried desperately to stay alive, for years. What went wrong and how could I have failed so terribly? The accusations from others and the self blame on my end was agonizing.

I had bursts of blaming others for my despair, and bursts of feeling defensive of myself. Mostly though, I agreed with what the world at large says about those who are suicidal: I was selfish. All I cared about were my feelings and I was incapable of thinking about the feelings of others. I was rash and weak and not to be trusted. I was not worthy.

When my mother died, initially I was convinced that I should have 'done something different' to save her. Fifteen years later when John died, I believed that I should have 'loved him better' in order to save him. With my own attempts, I just knew I'd failed everyone who loved me. In all three, I still struggle with guilt some days. This is common for people whose lives have been touched by suicide. Guilt offers very few people mercy.

Our culture tells us that death by suicide is driven by choice. This belief creates an agonizing contemplation on the part of the loss survivor. 'Why didn't the person I lost choose me over death?' And for the attempt survivor, the stigma driven suggestion that they made a selfish choice only serves to add a layer of shame on top of what is likely already profound self hatred.

How do we challange stigma and change the unhelpful premises that exacerbate it? We speak up. 

After John died, I realized that my voice was important. I am the voice of someone who has experienced all these facets of suicide and stigma. I am a multiple loss survivor. I am a suicide attempt survivor. And I am a person who, at times, still struggles with suicidality.

I have experienced first hand the misunderstanding, the accusations, and the insensitivity. But I have also experienced the support, the understanding, and the love that carries people like me from one day to the next.

This is why I use my voice. Because it is those who speak up who are making a difference. If those who read learn something, that can potentially lead to life saving advocacy and action. And for others, knowing that they not alone and that they are understood can save a life too.

There is an African Proverb: Not to know is bad; not to wish to know is worse. If suicide has touched your life, I encourage you to reach out, ask questions, and learn more. Educating yourself is the first step toward compassion.  

And I believe that knowledge and compassion have the capacity to change the world.

[The essay above was first written in June of 2018.]

If you are looking for resources and organizations that promote suicide awareness or prevention - click on the image below to reach our Links/Resources/Learn More page.

Many Busy Days

Hold me closer, tiny dancer
Count the headlights on the highway
Lay me down in sheets of linen
You had a busy day today

There is a story here. It is the story of a journey. A seven year journey. And a six year journey. And a one year journey. And a seven month journey. This is the story of one journey and many journeys. 

I'll start at the beginning, seven years ago.

In 2013, inspired by the counselors who (I believe) helped to save my son's life, I registered with CCAPP (California Consortium of Addiction Programs and Professionals) to become a drug and alcohol counselor. As with many social service vocations, certification (credentialing) was going to be necessary to work in the field. At the time, this required taking 12 academic classes and working just over 1,800 practicum (internship) hours. And all of this needed to be completed within five years. These requirements were non-negotiable. As soon as I registered, the clock started ticking.

But I didn't take any classes in 2013 or in 2014 either. You see, in late 2013, I'd had a relapse and overdose. So the year of 2014 was dedicated to creating a foundation for not just my son's recovery, but my own recovery, as well.

After my overdose, I moved into a sober living house (SLE) and I lived there for close to two years. In 2015 I spent many late nights sitting at the kitchen table of that house, studying for classes and exams. My roommates (also in new recovery) were very patient with me when, night after night, half that table was taken up by textbooks and note paper.

In May of 2016, I was taking one of my last classes at Cal State University, East Bay. At that class, (the amazing) Jimmy Isch was invited to speak. He was recruiting interns for the agency he worked for - Second Chance Recovery Center in Hayward, California. When he talked about Second Chance, he explained that they worked with underserved communities, including the homeless. Many clients were dual diagnosis, as well (dealing with illnesses such as PTSD in addition to their addictions). And there was one other thing he emphasized when he was recruiting interns. "You need to be able to write," he said. I knew then, this was the internship I wanted.

I started right away, but only worked a few hours each week. My plan was to complete the bulk of the hours I needed by working full time, starting in April of the following year (2017). Everything went as scheduled and I was set to begin my full time hours on April 3rd. But then something happened.

On April 2, 2017, John died.

Everything in my life came to a halt as I tried to recover from his loss. My practicum hours had to wait. Second Chance was incredibly supportive. Everyone was very patient, taking my shifts when needed, and helping me with my work on the days that I did make it to the office. So I continued as I had before, a part time intern. It was all I could manage. Suicide loss stays with you always, but for me, the first year was particularly hard. By the time 2018 rolled around, I was in trouble. I simply wasn't going to complete the hours I needed in order to apply to take the statewide chemical dependency counselor exam (the IC&RC). My five years were up.

So, I filed an application for a one year hardship extension. Armed with medical records from my 2013 overdose and a copy of John's 2017 obituary - my one year extension was approved. I made plans to work more hours. I believed that I could do it. That I could finally complete the bulk of my hours.

But 2019 was another brutal year. Loss after loss, yet again. Family members, dear friends, clients, and many other people I knew. Midway through the year, I was on the verge of a breakdown. Still, in August of 2019, I was finally ready to apply to take the official IC&RC exam. I filled out my application papers, and added documentation. The documentation included my transcripts from Cal State, and signed proof of those 1,800 internship hours. As I was filling out the application, I re-read the requirements in order to ensure that I had everything needed. As I read, I noticed there was a discrepancy between what I was submitting and what was required. I was confused. I still remember that moment. I was at work sitting in the room where staff completed their notes after a counseling shift. No one else was in the room, and I was glad. Because suddenly, I couldn't breathe. I fought off tears.

You see, in the six years that had passed since I first registered to become a counselor - the requirements had changed. For the first time, I realized that I was missing multiple required classes, and I was over 300 hours short of those that were now required in a practicum. I was already deeply overwhelmed by the grief of loss, and desperately fighting to control the beginnings of an eating disorder relapse. I was too ashamed to talk to anyone about the fact that I was likely to lose the six year long goal of becoming a fully credentialed counselor, too.

I was angry and overwhelmed and extra sensitive to absolutely everything. I lashed out at people I loved. One particularly hard night, my son asked me if I would go into the hospital. So, I did. The truth is, I didn't want to live anymore. I just wanted to be done.

I did live through the next several months though, but only because of the unwavering love of my son and my closest friends. More than once, the people who cared about me sat me down and said, 'Please make it through this.' In fact, on Christmas night, my son told me this same thing. "Mom, I need you to live." It was the greatest gift he could give me, I suppose, telling me that he needed me in his life. So I kept trying, even when I didn't want to. I complained to one friend that it was too much to ask of me. She told me something that we often hear in our circles of recovery. "Well, act as if," she said. "Act as if you want to live. That's enough for now."

I have two close friends whom I met in eating disorder treatment many years ago. Each one reached out to me. They buoyed my hopes when it came to the eating disorder part of my treatment this time around. "You can do it" really means something when the words are coming from people who've done it before, themselves.

Another friend came to my house one night with two matching pairs of pink onesie pajamas. She told me that we were going to put them on and sit on the couch and watch a stupid movie together. You don't have a choice, she said. It is amazing to me that there are times when I have no idea how to help myself, but sometimes there are others who know exactly what I need.

Equally important, John Macaluso's mother (and we'd lost John only two and a half years earlier) called me every single day for months. She wanted to make sure I knew that when a person deals with mental illness - even if, while suffering, they lash out at people they care about - it doesn't mean that they themselves are less lovable, less forgivable, or less of a valued person. My own mother is not living, but there were many nights that I spent at Jo Macaluso's house, just so I could be near a mother who loved me.

Always, all of these people reminded me that even if did cruel things while sick - those actions did not determine who I was as a whole. One friend reminded me that what you do while having a nervous breakdown does not take away the value you have as a friend.

I was in day treatment when my counselors encouraged me to apply for a second hardship extension. They believed in me, they said. They believed I would be able to complete the additional classes and the additional hours I needed in order to take the IC&RC exam. I was desperately trying to find a will to live and they were telling me I should be applying for something that would happen in the future. I knew enough about suicide prevention to know what they were doing. Any step I took that spoke to the promise of a future, was a good step. And so that is what I did. I applied for a second extension. It can be hard to get the second extension. If you are approved, it's your last chance. You will get no more extensions beyond the two years. That's it. Period. Once again I gathered transcripts and medical records, and once again I submitted a copy of John's obituary. I included a letter from my supervisor at Second Chance that verified that I was a good intern with lots of promise and who was well liked by staff and clients alike. I submitted the application. Two weeks later, I received a letter telling me that the second extension was approved.

October 5th of 2019 marked six years since the day in 2013 that I'd overdosed. And the next day, October 6th, 2019, marked six years from the day that I began my journey of recovery. Meanwhile I was bouncing between inpatient and outpatient day treatment. Just like they had done six years earlier, my treatment team and the people who loved me made sure I lived through the last months of 2019 and the first months of 2020. I sure didn't know how to do it on my own, I leaned into all these people and learned to pick up the pieces of me that shatter when grief is too heavy for me to bear. And I leaned into this too - the one thing that has remained constant from October 6th, 2013, until today:

I stayed sober.

Staying clean and sober when you are in eating disorder treatment can feel so very unfair. My primary addiction had been to anxiety medications, and for the past six years I have had to manage learning to eat again and all the accompanying anxiety inherent in that, without medication.

This time around, it felt too hard. Just getting to day treatment felt impossible on most days. Seven years ago when I went through this process, even my doctors and my treatment team were at a loss as to how to help me. How to keep me in treatment at a time when my PTSD was so activated that I could barely breathe, much less eat. At that time, they suggested a service dog. So, from 2013 - 2015, I'd had a wonderful service dog - Butter - who came with me everywhere. He came with me to the hospital when I was in treatment. He came with me to the meetings that supported my sobriety. He came with me to work and he came with me to school. Butter ushered me into the life that I have today. But Butter was an older dog. In 2015 he passed away. Although I was heartbroken, I knew I was ready to move on without a dog at my side.

She needs a service dog again, is what my doctor said this time around. And so, that is what we did. We trained my tiny dog Peanut to be of service. Most often, the service she provides is to sit quietly for hours at a time. Peanut is a spitfire ball of energy, but she learned her service skill right away. That dog can sit beside my chair or in my lap for up to six hours, without complaint. So again, a dog accompanied me to treatment. Slowly, we noticed that I could eat again. Soon after, I could sit through a day of treatment without crying the entire time. One week though, people were particularly scared for my life. Once again, the people who loved me pleaded with me to go into the hospital. So in I went, yet again. My doctor knew that my efforts at eating would be lost if I was hospitalized without help for my anxiety. So my sweet little service dog came with me. She slept beside me in my hospital bed. Sometimes in the middle of the night she would bark at the nurses as they passed by my bedroom door. One of the nurses put a sign on my door, so that others wouldn't be startled.

"Beware of Service Dog," it said. "She may bark if you enter the room."

Beware of service dog. I thought that was the funniest thing. I just laughed and laughed.

I left the hospital two days before Thanksgiving, but I was in day treatment for a total of seven months. I've never been in treatment for so long. I just couldn't find purchase for a way to forgive myself for struggling so much.

Perhaps the beginning of my true journey toward healing began one February day, while I was at day treatment. I was sitting on the floor, leaning against the wall, with my face in my hands. I didn't know what to do with the self hatred that had been so unrelenting. Sarah, a fellow patient, sat down beside me. She knew that I couldn't forgive myself when my mental illness has impacted the people I love. "Maybe you can't do anything to change the way you behaved when your struggles were at their worst - but today you can do the thing that you wish your boyfriend who died could have done for you, and the thing that the people who are in your life are asking of you, now." She looked at me, and then she finished. "Find a way to stay alive."

During those seven months that I was in treatment, I continued to work towards my counseling credential. I had to complete multiple classes. My friends and family cheered me on as I completed one class, and then another, and then another too. I was still in treatment, but I had to work as many hours as I could. Second Chance accommodated me every step of the way. At one point I apologized to one of my supervisors. I couldn't return to taking day shifts, because my treatment was going to last for yet another month. And his response was to tell me that he didn't care how long it took, Second Chance just wanted me back healthy and ok. So I worked as many part time hours as I could. My little Peanut came with me to work, and soon she became more popular than I was. More clients at Second Chance know Peanut's name, than they do mine. By March, I'd completed the last of the hours I needed in order to apply for the IC&RC exam,.

Staff at Second Chance Hayward Recovery Center.

Left to Right, Andrea Caracol, Wendy Love, Chelise Stroud, Jimmy Isch

Dan Castro in the right forefront.

With all of this love and support surrounding me, and because of the extraordinary team at Alta Bates Herrick Hospital, in April of 2020 I was ready to leave day treatment. My feet were shaky but they were there, underneath me, once again. That same month, I submitted my shiny new application to take the statewide IC&RC exam, so that I could finally be fully certified as a drug and alcohol counselor. I held my breath and waited. Within a week, I received notification that all of my requirements had been met, and I received my hard-fought Candidate Admission Letter. Now I could schedule my exam. Except for one thing. There was a worldwide pandemic and all exams had been suspended. So I waited. I worked at Second Chance. I played with my dog. I mended some relationships, and I surrounded myself with lots of love. Maybe not physically, but through the phone, and zoom, and even through the mail. Week after week passed, I waited, still. With the expiration of my second hardship year looming, I began to get worried. I called the credentialing agency. What if I can't take the exam in time? Will I be allowed another extension, even just for a few months, because the exams had been suspended? The answer was no. The state had not, as of yet, made any allowances for that. So, I kept waiting. Finally, in mid May, they opened up exam registration. The first appointment I could get was two months away, on July 10th, 2020.

The next two months were a flurry of studying. I'd taken so many of my academic classes five years earlier. I was worried that I wouldn't remember what I needed to know in order to pass the exam. Did I remember anything about pharmacology? The difference between agonists and antagonists and the partials of both? What about the differences between statewide and federal regulations and assembly bills? 42 CFR Part 2? AB109? It was disconcerting when I realized how little I'd retained of these types of details. I read and I researched and I pre-tested, nonstop for eight weeks in a row. People worked with me as I memorized hundreds of flashcards. My job gave me time off so I could study. On the week before the exam, one person stayed up, twice, until the wee hours of the night, so that he could quiz me on 450 potential exam questions. Likely, he could pass the exam himself, now. Finally, the exam day came. I prepared the people close to me for the inevitability that I was going to fail. I just could not remember enough. Too many flashcards and too many practice exam questions. My brain couldn't take it all in.

The exam was three hours long, and it was harder than I expected. It did cover a great deal that I hadn't studied. There were many questions where I wasn't sure about the answer - I just had to pick the best one I could. When I finished the last question, I still had time left. But I used every minute of the three hours in order to check and re-check my answers. I was still checking answers when 'Time is Up' flashed on the screen and locked me out of the test. I blinked, and then the exam result appeared.

Congratulations! Your scores indicate you have passed the IC&RC exam.

I realized I was holding my breath. I don't know. Maybe it was the only real breath I'd taken in over a year. If you had sat down with me one year ago, I was so enmeshed in all the loss in my life, in many ways I myself had become the walking dead. But that is not who I am today. How beautiful it is, what can happen if you just don't give up.

So yeah. I did a thing. A great big little 'ol thing that was seven years in the making. That same night, one of the women in my online suicide loss survivors group posted a request. In that group, we do whatever we can to share hope. This was her request:

Share something positive that happened today.

So I wrote it down there, first.

I passed my IC&RC exam to become a fully credentialed drug and alcohol counselor here in the state of California. ❤

That was where I wanted to write it. On that thread, in that group. I know there are a lot of people who are proud of me. That amazing man who is in my life, and John's mom, and the people I work with, and even more friends. And I know that wherever John is, he is proud of me, too.

I also know this: Whether you are a suicide attempt survivor, a suicide loss survivor, or someone who is dealing with thoughts of suicide right now - I have been where you are. Please hold on. You may have a lot of heartbreak ahead of you. But, you will also have many busy days ahead, and there will even be moments of joy, and miracles too. I promise.

Look What Happens With a Love Like This

Even after all this time the sun never says to the earth, 'You owe me.' 

Look what happens with a love like that. It lights the whole sky.”
- Hāfiz

This morning, the Lighting Up the Sky blog crossed a threshold. The number of times the blog has been viewed surpassed 100,000.

It's an amazing thing, that what is written here has touched so many people. Not quite three years ago, I started this blog. I wasn't sure where it was going. At first I thought I'd share parts of the journal I'd kept in the months after John died. I did that because of the number of people who were telling me that my writing about suicide was helpful to them. The most powerful feedback then remains the same today. When I hear someone say 'I learned something important about suicide by reading your blog,' it motivates me. But when I hear someone say 'when I read your blog, I felt less alone,' I am humbled by those words. I am humbled by the fact that this blog has impacted people in this important way.

So I stepped back and paid attention to what was being said. People told me they appreciated that someone was talking about suicide. They told me they didn't feel they had a voice. Many survivors of suicide loss felt they didn't have a right to mourn. Nearly every person I spoke to said they were hurt by the ways that people didn't understand suicide. Whether they were a survivor of attempts or a survivor of loss, they reached out to me to talk about the agony that this lack of understanding can cause.

Quickly I realized I could do more with this blog than I originally intended. I recognized that there were an immeasurable amount of people whose lives had been touched by suicide, not just me. Asking those people to share their own experiences with suicide was important. The more lives and voices that this blog could share, the more of a reminder that none of us are alone.

"People don't understand!" is what I was hearing.
"So, tell them," has always been my response. 

I understood too, the importance of being allowed to grieve a suicide loss. To be sad, angry, hurt and sometimes relieved. I knew firsthand that the stigma around suicide complicates grief. Often, we are told we shouldn't be talking about the loss. We are told that we should be mad at the person we lost, that we should forget about them.  Or sometimes the opposite - we are told we can't be mad at those who die by suicide, at all. We can't rage against a person's mental illness and we are not allowed to celebrate the beauty of who the person was, either. It is an excruciating paradox. So, I wanted this blog to give people permission to react to their grief in any way they needed. And I especially wanted to celebrate and encourage the beautiful side of grieving and the beautiful side of healing too.

I am both honored and humbled that so many people have been interested in what we, those whose lives have been touched by suicide, have to say. Our voices matter. As Robin Williams once said, "No matter what people tell you, words and ideas can change the world."

Speaking of quotes, many people have asked me why I named this blog Lighting Up the Sky. The name is derived from a quote by the Persian poet, Hāfiz. 'Even after all this time the sun never says to the earth, you owe me. Look what happens with a love like that. It lights the whole sky.'

When I started the journey of writing this blog, I was struck and saddened by the often held notion that those who die by suicide are selfish. As a survivor of a suicide attempt myself, I knew that many of us truly believe that by leaving, we are doing something good for those we love. I struggle with this to this day. If I hurt someone, I wrestle with wondering if my loss would be an adequate reparation. The pain of this deliberation cannot be put into words. We think we are relieving our loved ones of a burden. We believe that we don't deserve love or to be cared about. In this sense, though misguided, our actions are the opposite of selfish.

I considered the lack of understanding about suicidal ideation, the lack of resources available to those who need them, and the lack of effective treatment. Given all of the prior, I believe that we often look at suicide from a faulty and painful perspective.

But what will happen if we flip that perspective? How much more will be accomplished if we stop blaming the ones we've lost? I believe that often it is not those who are losing their lives to suicide who are failing us. Instead our culture, the stigma, and the silence around suicide, failed them.

What if instead of focusing on their owing us forever unfulfilled promises, we focus instead on the beauty their presence in our lives had once offered? I would think if we did this, while their loss would be no less heartbreaking, it would be a measure less dark.

That's how I want to think about the people I've lost to suicide. Not that they have darkened my life, but instead, I want their memory to light up my sky.

I can't let this milestone of 100,000 go, without saying this:

I started this blog for John Macaluso. I loved him. I love him still. He was needed in this world when he lost his life to suicide. And I know he'd be proud that this blog has had an impact on so many people.

I continued this blog for my mother. She was a writer herself. She was smart and funny. She was needed in this world when she lost her life to suicide. She would be proud of my writing too, I know.

And I write for this blog still, for me. It has been much easier for me to write about being a survivor of suicide loss than it has been for me to write about my own attempts and my own thoughts of suicide. It is important to be able to talk about these things without feeling ashamed. Speaking up is one of the most important ways to fight stigma. My words, like those of all others who've been touched by suicide, are needed in this world. 

I know.

To all of you who have cheered me on, or supported me when I've been hurting, and to those of you who have told me that this site means something to you, thank you.

And thank you especially to all of my fellow suicide attempt survivors and suicide loss survivors. You are the bravest people I know.

And finally, to all those who have lost their life to suicide - know that we are fighting for you. You are not forgotten. The sky lights up for you, today and every day.

Owning My Story - DAY 14

If we can share our story with someone who responds 

with empathy and understanding, shame can't survive.

- Brené Brown

I am a survivor of suicide loss. I have written about that. I am addict and alcoholic in recovery. I have written about that. I have an eating disorder. I have written about that, too.

But, until last year, I didn't write much about my own suicide attempts. Actually, I did do some writing in 2013, following my second and last attempt. I made some of that writing public, but within a month or two I removed the writing from public view.

I removed the writing for the same reason that I rarely write about my attempts now. I was ashamed. At that time, people contacted me and told me that they disagreed with my point of view, others contacted me and told me that I was being disrespectful toward my son by violating his privacy. Not that I was writing about him (I wasn't) but because he would undoubtedly be ashamed that his mother had attempted suicide. Out of respect for him (he was 16 at the time) I needed to hide the fact that I'd had an attempt. That is what I was told.

Every reluctance to write about my suicide attempts had been grounded in shame. The stigma in our culture is so strong. We are routinely told that those who attempt suicide are selfish, attention seeking, weak, sinners, inconsiderate, cruel, etc.. Those who die by suicide are taking their pain and without giving it a second thought, they are handing all that pain to someone else. That's what our society tells us.

Those who attempt suicide are everything that I don't want to be.

I can write about a lot of stigmatized issues that are close to home, but writing about my suicide attempts is one of the most difficult things I have ever done. I am not alone in this. In Jamie Brickhouse's article Overcoming The Shame of a Suicide Attempt (New York Times, May 2016), he says:

"As a recovering alcoholic I know that admitting to my behavior and owning my story is the only way it can no longer own me. I’m not ashamed of being an alcoholic, but I’m still ashamed of trying to kill myself."

For me, despite having feelings that were similar to Jamie Brickhouse's, there was a point about a year and a half ago, when I knew it was time to share my personal story. I was knee deep in suicide prevention advocacy, and I regularly bemoaned the stigma that deterred people from reaching out for help. But that wasn't my primary reason for talking about my own attempts. I was frequently exposed to people who were angry at those who'd taken their life. But, that wasn't my reason for talking about my own attempts, either.

I decided to write about my experiences with being suicidal, because in my suicide loss survivors groups, I kept hearing people say: "How could they leave me like this? Why wasn't I enough? Why weren't our children enough? How could they not have told me what they were planning to do?" These questions were agonizing for the people who were posing them.

I wrote about my attempts because people who didn't understand the complexity of  suicidality were in excruciating pain. And by and large, this pain reflected a general misunderstanding of what it is like to be suicidal. I wrote about my attempts because my fellow survivors of suicide loss, who were already in so much pain, exacerbated their grief by tormenting themselves over the possible answers to their questions. And I knew, most of the questions didn't actually apply to the circumstances under which a person loses their life to suicide. I knew I wasn't going to speak for all who have attempted suicide, but I also knew I was speaking for an awful lot of us.

I wrote about my attempts with the great hope that my story might help someone else who was suffering.

So today I will share my story again. It's long. (I'm 'wordy' as someone once told me.) But, it is thorough. Others have told me that my story was very helpful as they processed their loss. I am so glad. If you would like to read what I wrote, simply click on the picture below:

One Less Day

I'm not afraid of getting older  I'm one less day from dying young  I see the light go past my shoulder  I'm one less day from dying young  I'm one less day from dying young
 - Rob Thomas One Less Day
My mother died seventeen years ago, today. It was a cold Wednesday afternoon. Cold at least for the month of April, in Oakland, California. That day, the temperature outside never rose above 56 °F. My mother took her life sometime during those cold daytime hours, while she was home alone. My step father would find her when he came home from work, later that evening. I, however, did not find out that she'd died, until early the next morning.

I remember bits and pieces of that morning. It was just after 7 a.m. when my phone rang. My brother was on the other end of the line, and he said that he had bad news. Then he told me that my mother had taken her life. Needless to say, 'bad news' was far from an accurate description.

Over the next several days, I would vacillate between disbelief, anger, and grief of course. It was the grief that seeped in between every other feeling. It would rise until it took over where my other emotions couldn't manage to hold on. The disbelief eventually settled into acceptance. The anger eventually turned towards forgiving. Forgiving my mother, and forgiving myself as well. But the grief, it never went away. Not completely. Seventeen years later, and I still grieve, today.

Still, as time went on, it was not the grief that wrecked the most havoc in my life. It was something different. It was fear.

For years after she'd died, there were times when fear dictated every aspect of my life. And the fear was very specific. I was afraid of all the ways that I was like her. And I am like her, after all. We share some physical attributes. Many would say that you can tell by looking that I am my mother's daughter. And we both had a sharp sense of humor, though hers was more dark than my own. And this too. She was a writer. She wrote sophisticated fiction and less complex but equally powerful poetry. We were similar there too, of course. My writing style is different, but we always shared a love for pen and paper - or, later, for a keyboard and the accompanying screen that would fill so quickly with our words. This adoration of the possibility inherent in the written word - we shared that, my mother and I.

Me, with my mother, El Collie Kress. 

Saint Clair Shores, Michigan, 1978.

It was my mother's disease that scared me the most, though. Her mental illness that had steadfastly stolen her from me and from so many other people who'd loved her. I agonized over the deterioration of our relationship during the years before she died. And I agonized, even before she died, over the thought that we shared the illness that was taking her from me. The illness that would eventually take her life.

I once confided to a counselor my fear that because my mother had taken her life - it was inevitable that I would also take mine. Perhaps not right away, but one day, I said. I was truly afraid that I would leave my own son with the same loss that my mother had left with me.

"Your fear is not an omen," my counselor had tried to explain. "It is not a predictor of the future. It's normal, it's common, when a parent takes their life. Their children then must contend with the fear that they might lose their life to suicide as well."

Predictor or not, the truth is, I did eventually attempt to take my life. Afterward, I was absolutely wracked with guilt over the attempt. "I've done to my son what my mother did to me!" I'd often weep when talking to counselors, and doctors, and anyone else who would listen.

No, no, no, they'd correct me.

"How am I any different than her? How is what I've done not the same as what she did?" I'd ask.

"Chelise, it is very different." people would tell me.

"But how?" I'd cry. 

"It is different, because you are alive," they would explain, pointing out the obvious.

Of course. There it is.

I am alive.

There is evidence that my mother planned her death over a period of time. She'd acquired the means weeks earlier. She wrote a lengthy note. She'd likely been composing her last words, for days ahead of time. And she was fastidious in the execution of her plans. A fastidiousness that suggested pre-planning. 

I don't know why she chose this particular day in April. Likely, I never will understand. But I do suspect she'd chosen the date well in advance.

I would imagine that once she decided upon the day, then her measurement of time stopped flowing smoothly and became instead a chipping away of sorts. Suddenly, every day that passed represented one less day until the date she had chosen to die. 

So there are times now when I look at life through that same lens - counting time backward instead of forward. It is just that our start and end points are different - as different as the very natures of life and death.

It would be easy to sit back and blame my mother for my mental and emotional woes. It seems likely that I have a genetic predisposition toward both mental illness and addiction, and those genes both appear to originate on the maternal side of my family. And I could blame much of the childhood trauma I experienced on her as well. Living with a parent who was so severely mentally ill meant that I lived in a constant state of chaos with little structure or support. My mother's untreated illness tore my childhood away from me. This is true.

But my anger at my mother has softened. By and large, I am much more forgiving now. My mother lived with an illness that was (and still is) misunderstood and stigmatized. She was provided with very few resources and no hope for a cure. The universal lack of understanding when it came to mental illness meant that she was blamed for her symptoms. Blamed by society, blamed by myself, and blamed by other loved ones as well. Looking backward is where I find my compassion for her. As my mother got older, her symptoms increased. Her anxiety and pain were joined by delusional thoughts that often bordered on psychosis. Her despair was relentless. In fact, without any hope for relief, in many ways it is amazing that she lived as long as she did.

So it is guided by this compassion that I allow my own countdown to begin. Unlike my mother though, I am not counting down to a final day. Instead, each day that I wake anew, I recognize that it is one less day until I live past the day that she died. And tomorrow will once again afford me the opportunity to say that I haven't just survived so far, but that I will continue to survive. I am my mother's daughter, I am a part of her legacy. So, despite her death, I will do everything in my power to carry her legacy forward as one that speaks of survival instead of one that speaks only of loss.

My mother died seventeen years ago, today. It's a sad day for me. This is true. But if someone asks me how I did today, a day when the absence of my mother is so prevalent - I am glad that it is one less day until I can say that I made it through.