My Only Sister Alice Died When I Was 14. Nineteen Years Later As A Reporter, I Went Looking For Answers.

My sister and me riding a pony as children. (Photo courtesy of Pete Earley.)

(2-13-23) My only sister, Alice, died on this date  fifty-seven years ago after being struck by an automobile. I was 14 years-old at the time and it was my first experience with death. Nineteen years after her death, I awoke one night calling out her name. I realized that I had repressed most of my memories about Alice because her death was so painful. My good friend, Walt Harrington, who was an editor at the Washington Post, suggested I return to Colorado and investigate my own sister’s death as a reporter. The Post published my account in 1986. I am posting it today in her memory. With the passage of time, the hurt and memories fade, but in your heart, you still feel the loss.)

Missing Alice: The Story of My Sister

By Pete Earley for The Washington Post

Midway across Ohio, the man beside me on the DC-10 asked where I was going.

“Fowler, Colorado. A little town of about a thousand people near Pueblo.”

“Why would anyone go to Foouuller?” he asked, grinning as he exaggerated the name.

“A death. My sister.”

“Sorry,” he mumbled and turned away.

I was relieved. I didn’t have to explain that my sister had been dead 19 years. Alice was killed when I was 14. She was two years older and we had been inseparable as children.

I couldn’t talk about her death at first. My voice would deepen, my eyes would fill with tears. My parents would cry at the mention of her name, and we rarely spoke of her. Then it seemed too late.

After I left home, my mother would phone me each February 13 and remind me that it was my sister’s birthday. Year after year, I would forget — and find myself angry with my mother’s insistent reminders. It was just before last Christmas, as I shuffled boxes in the basement, that I ran across Alice’s picture and clipping describing her death.

“A tragic accident Tuesday, June 14, about 7:05 p.m., took the life of Alice Lee Earley…” I sat down on the concrete floor, closed my eyes and tried to picture her. I couldn’t. I tried to focus more sharply. Alice eating Sugar Pops beside me at the breakfast table. Alice washing the green Ford Falcon. Alice stepping on my toes while singing in Church.

The events I recalled vividly. Alice’s face I recalled not at all.

I could only see the girl in the photograph — an image I had never liked, the face being without joy or expression. But in my mind I found no other. For the next week, I seemed to think of Alice constantly.

One night I awoke in bed, turned to my wife, and said, “Alice, are you there?” It took me an instant to realize what I had done.

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Inspired by “No One Cares About Crazy People,” upcoming documentary exposes faults in system & heroes demanding change

2021 Promo Reel – No One Cares About Crazy People from Gail Freedman on Vimeo.

(2-06-23) Please watch the powerful and moving clip from the documentary No One Cares About Crazy People by Gail Freedman, a talented director, producer, and acclaimed documentary maker who hopes to finish the film by year end.

Freedman’s documentary was inspired by Ron Powers’ 2017 nonfiction book by the same name, but the film quickly expanded into a story about multiple families struggling with serious mental illnesses and their tireless efforts to get help for their loved ones.

If you have a family member with a serious mental illness, love someone who does, or have a diagnosis, you can’t help but be moved by the familiar plight of the families and inspired by their gritty determination to improve our mental health care system.

Freedman told me she wants to harness “the power of documentary storytelling as a tool for change – to help galvanize public discussion, awareness and action around our profoundly broken systems of care for those with serious mental illness.” Thankfully, she accomplishes her goal.

Freedman began by interviewing best-selling author Ron Powers, the father of two sons with schizophrenia. Kevin, his youngest son, ended his own life at home just before his 21st birthday. That tragedy thrust Powers and his wife, Honoree Fleming, along with their surviving son Dean, who continues to struggle with the illness, into what Powers described as the “sub-nation” of those with serious mental illnesses.

“The madman is a man, in effect, without a country,” Powers said. “Certainly without a country that gives a damn whether he lives or dies, as long as he just stays the hell out of sight.”

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A Rational Approach To Fixing The IMD Exclusion That Limits Beds For The Seriously Mentally Ill

Image by Ben Kerckx from Pixabay

(1-25-23) A critical shortage of hospital beds for individuals with serious mental illnesses has prompted repeated calls for the elimination of the Institutions of Mental Disease or “IMD Rule.”

The National Alliance on Mental Illness supports getting rid of it, while consumer groups and disability advocates oppose changing the law. The last serious attempt in Congress to end the IMD exclusion happened when former Rep. Tim Murphy (R-Pa.) introduced the Helping Families in Mental Health Crisis Act, back in 2015, but Murphy’s efforts were blocked by Democrats and civil rights groups.

Now newly elected Rep. Dan Goldman (NY), is considering reintroducing legislation to repeal the IMD rule,  and the hope is that he will instead introduce a bill to limit its reach, rather than attempting to eliminate the rule.

 The fact that Goldman is a Democrat and the bill is named in honor of a woman who was pushed in front of a New York subway by a man with untreated mental illness may help it get some traction.

But while the debate about the IMD exclusion always focuses on fears that our nation will return to mass re-institutionalization, another stumbling block will be the expense to Medicaid if the IMD is dropped. Supporters of the IMD Rule claim it will cost the federal government billions of dollars if Medicaid starts paying for mental health hospital beds.

Cheryl Roberts recently wrote about Goldman’s efforts in a New York Daily News editorial. Judge Roberts runs the Greenburger Center for Social and Criminal Justice, which I’ve written about on this blog.

Congress must stop blocking mental health clinics from needed money 
An Editorial by Cheryl Roberts. First published in the New York Daily News

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“I pulled the needle out of my arm for the last time and embarked on an arduous journey of recovery.”

(1-5-23) A skilled author can use fiction to tell powerful truths about the reality of serious mental illnesses and those whose lives are touched by it in ways that nonfiction often can’t convey. So I was delighted when I learned that Jordan P. Barnes, already an accomplished author, had written Late Blight in the Koʻolaus: A Novel. 

Because of his own experiences with addiction, he is especially well-suited to pen a novel about the challenges that individuals face after leaving a hospital and returning to a community. I asked him to tell me about his novel since I’ve not had a chance to read it yet.

Dear Pete,

A little over eleven years ago, I pulled the needle out of my arm for the last time and embarked on an arduous journey of recovery that would change and challenge me in ways I could never foresee. Now, with over a decade of clean time behind me, I am fortunate in many ways and owe much of my success in overcoming heroin addiction and homelessness to the endless support of my parents.

My parents never gave up hope on me, despite the fact I’d long given up hope on myself. I was also facing multiple felonies at the time, but with my parent’s support, I entered a two-year inpatient treatment program in 2011 and have been working on bettering myself ever since.

Today I am a husband, homeowner, father of two, and an independent author.

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Losing My Son Broke Me. Telling Our Story Opened The Door To Healing

(1-3-22) I’ve always enjoy promoting books about mental health, including those that I’ve not yet read but pique my interest. This week, I’m posting guest blogs by two authors telling their personal stories.  I’ve asked them to describe why they wrote their books and provide a short excerpt. 

For the Love of Jeremy — A Memoir of a Family Affliction: Mental Illness and Addiction

By Renate LeDuc

Losing my son broke me at the deepest level and something just emanates from your heart and soul when that happens. I was driven to write this book for several reasons.

First and foremost, of course, was my own healing. It is a mother’s instinct to protect her child. If that child dies, it is a mother’s instinct to protect that child’s memory. This book is a part of that process.

For the Love of Jeremy: A Memoir of a Family Affliction: Mental Illness and Addiction is about unspoken truths. It has opened the door to healing my family’s somewhat secretive past of suicide and mental illness. Opening the lines of communication will promote knowledge, awareness, compassion, and progress.

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Lessons About Serious Mental Illnesses That I’ve Learned As A Parent

(1-1-23) I continually get emails from parents who are desperate for help. I am not a psychiatrist, therapist, or a neuroscientist. I am a father. I listen and try to comfort those who I can. Most often, I feel frustrated because helping others successfully navigate our mental health care system is extremely difficult. 

More than a decade ago, I posted a blog about the lessons that I had learned helping my son. I reprint it each year with the hope that it will help others who have discovered that they are on the same rocky road that I have and am traveling.

Happy New Year fellow travelers!

Helping Someone Who Has A Mental Illness: Lessons I’ve Learned

It’s difficult helping someone with a mental illness.

My relationship with my son,  Kevin, has not always been easy. Those of you who have read my book know that I was forced to lie about him threatening me in order to get him taken into a hospital rather than put in jail. During a later break, I called the police and my son was shot twice with a Taser. These events hurt parent-son relationships.

So what have I learned?

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