Winter sunset...
Hope you have a good weekend everybody!
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Photo credit: Marisa Farnsworth
Winter sunset...
Hope you have a good weekend everybody!
Ty
Michigan has passed Kevin's Law. The first time it passed was in 2004. Then it was updated, by lowering requirements, in 2017. Kevin's Law, basically, allows the court to order outpatient treatment. Court orders can include a mandatory long acting antipsychotic shot, usually once a month, for a seriously mentally ill person — especially for those who lack insight into their own illnesses (anosognosia).
Unfortunately if you walk into most county probate court offices, the staff won’t know about Kevin’s Law. They’ll tell you to call county mental health, hire a lawyer or just kick you out. This was my experience today at Muskegon County Probate Court. I asked “May I please have the forms to fill out for Kevin's Law.”
The clerks and a judge began to communicate lots of incorrect information. The judge was intimidating. His sheriff’s deputy, was standing next to him as he yelled, “Get an attorney.”
I said, “I don't need an attorney.”
He said, “You have to go to Healthwest, County Mental Health.”
I said, “Sorry, the law doesn’t say that. A parent, neighbor, friend, teacher, doctor, social worker, sister, brother, uncle, or anyone, can file Kevin's Law. My husband and I have guardianship and the record of an independent forensic psychiatric exam.”
The reality is, it’s the responsible thing for a parent and guardian to do. Apparently, they didn’t understand that. They shooed me away. The experience shook me up. Blame lack of education and training and Michigan's policy of underfunding important initiatives. What’s the point of passing a law that is improperly funded?
Our sweet 19-year-old bi-racial son, Tyler, is a graphic artist and a musical genius. He was born drug addicted and adopted through the state of Michigan as a medically fragile baby. He has autism, bipolar disorder with psychosis, ADHD, and has suffered six traumatic brain injuries.
The state knows Ty well. We were promised a medical subsidy whereby the state would help us with his medical and psychiatric care if it was an expense that our insurance or Medicaid didn’t cover. When he needed extra treatment, we were denied. When the time came that he needed a supervised group home, the state refused. Michigan Adoption Subsidy denied us all help. County Mental Health (CMH) failed to recognize our guardianship and failed to file for group home placement and residential treatment.
We found out mental illness with autism is considered a co-morbid disease. The state is required, by law, to help. We also found out all denials were required to be done in writing not orally. CMH did not comply with this requirement.
We requested CMH to file Kevin's Law, through the Muskegon County probate court on Feb. 17th, 2017. CMH said, “We don’t know how to file Kevin's Law. We don’t know what it is.”
Our son was arrested and incarcerated while in psychosis, Feb. 18th, 2017. He was arrested for a home invasion as he was sleeping on our neighbor’s sofa. Our neighbor almost shot him but, in a split second, recognized him as the kid next door. This is the second time our son was almost shot.
Tyler had an ER doctor diagnose him with acute psychosis. He’d tried to hang himself. He had intrusive thoughts. He was delusional. We were in the ER, doctors’ offices and psychiatrists’ offices, 15 times for emergencies. CMH canceled three psychiatric appointments. CMH workers tried to access crisis care with a doctor but the psychiatrist had quit or taken a leave of absence. CMH prescribing psychiatrists were not accessible by phone when medications interacted dangerously. Ty was hospitalized only twice, for short term treatment.
The first time he was admitted, Ty was catatonic. He hadn’t eaten in almost two weeks. He was admitted to Pine Rest for a week. The second time he was admitted to Saginaw White Pines for a week. No one called us from Saginaw White Pines to say he’d be released even though HIPPA releases were signed. Our son was still in psychosis, still delusional. He was almost 4 hours from home and released without a phone call.
Our son has been found NGRI (not guilty by reason of insanity) by a forensic psychiatrist. He’s still awaiting trial. His trial's been postponed for almost a year. Speedy trials are not a reality for the mentally ill. Michigan has a rule that, after 15 months of incarceration, they can release NGRI inmates without ever providing treatment at the forensic center.
Our 17-year-old son, Ty, was in psychosis and incarcerated in February 2017 with adult inmates and assaulted. Today, I went to probate court, again, to request assisted outpatient services. Please, state of Michigan Governor Snyder, and Lt. Calley, train your judges, mental health workers, lawyers, clerks, politicians, and doctors about Kevin’s Law.
We dream of the day our home is filled with Ty’s piano music again.
Note: Kimberlee West and her family have been informed that Ty has to undergo a second forensic psychiatric exam by the state — the first exam was "incomplete." It could take another 60 days for Ty to be examined. Ty's trial date had been set for January 23, 24, and 25, 2018. It's been postponed. Again.
Read more of Ty's story in the archives in the right hand column.
November 15, 2017: Hope One Day We'll Have Real Choices by Kimberlee West
August 22, 2017: Walk a Mile in Our Shoes by Kimberlee West
Ty and his friends
This is rough...but it's my heart…
I got angry at a woman, today. I don't know her, and she doesn’t even know I'm alive. And yet, her very existence, well, more to the point, the existence of the bumpersticker on her car, filled me with a stupid, unreasonable rage.
That f@cking bumpersticker.
You know the one. It’s festooned with the same innocuous slogan that is plastered on every minivan in America. “My kid is an honor roll student at YourTownHere Middle School.” Really? Who cares? Who really f@cking cares?
My daughter is an inmate at Clifton T. Perkins psychiatric hospital in Jessup, Maryland. There’s no bumpersticker for that.
So, good luck to you, lady, and your honor roll student. Believe me, that sh@t changes without warning. My daughter was an honor roll student, a world-class musician, an actress, a funny, well-loved kid with a beautiful smile and laughing eyes. Now she has schizophrenia.
Or is it bipolar? Or borderline? Or schizo-effective disorder? Or none of the above? The fact that she was diagnosed — or misdiagnosed — under virtually every category in the DSM-V (or is it IV?) is part of the tragedy that has tormented my daughter and my family since she was a child. Because after a being let down and abandoned by medical systems on both sides of the Atlantic, my beautiful daughter could fight no longer and succumbed to the demons that have haunted her for nearly all of her short life.
They raged through her body and soul, writhing like snakes beneath her skin, robbing her of the ability to think, go to school, work or even show the most basic of human compassion and emotion. Her life became a wasteland of days spent searching for and then wallowing in whatever she could find to self-medicate her pain and fear away. The demons had won, it seemed.
Despite our best and constant efforts, my good wife and myself, weary from the fear-filled days and sleepless nights felt like all was lost. At least, we would often console ourselves, things couldn't get any worse.
Until they did.
Ray
Photo credit: Jim Moon
Well, hello. Somebody said it's a new year.
Hope you have a good weekend everybody!
My son, James, is 34. I'm so proud of the man he's become, and grateful to everyone who's helped him get where he is today. Mostly though, I'm grateful for him.
You see, although I'd take away his illness if I could, his journey's made me a better person. Although I'd eliminate all the pain he's walked through, his pain's enabled me to be more compassionate. Although I'd give him back the life he knew before his symptoms took it all away, I'm grateful each day that he is alive and able to give and receive love.
This picture was taken in January 2017. James looks the same except that he's thinner now. There were so many times along the way that I never, in my wildest dreams, thought he could enjoy such a wonderful quality of life. Don't get me wrong, he can't hold a full time job and will never be totally independent, but he's accomplished so much more than we dared to hope for.
James
A wise man once told me that what I needed to do was give my son something he didn't want to loose. This was what I built everything on. It's a solid foundation. Of course, as you well know, doing it takes a village!
Just a little back story because I understand how hopeless and overwhelming caregiving for our loved ones can be — the pain, the endless stress, the blocked paths to treatment, the grief, and the feeling of isolation. For my son, his journey started before his birth, really. I was high risk due to having placenta previa and he was in fetal distress during labor. They couldn't find a vein for an IV so I could have a C-section so other methods had to be used. James was blue from a knot in the umbilical cord that was wrapped around his neck.
When James was in second grade, he was diagnosed with ADHD and we started behavior modifications along with medication. He continued with behavior modifications until he became so ill that they didn't work well.
James was always a gifted athlete. In his freshman year of high school, his coaches told him to look for college scholarships in basketball, baseball, and football. But, by age 15, his symptoms were severe and he was put in a locked down facility out of state because he was still a minor. I appealed to the court to release him into my care so I could get him treatment. He needed treatment, not punishment, and it's in the right treatment that we found our hope. That's why I do what I'm able to help more find their treatment in time.
My son's been and continues to be one of my greatest blessings and the best teacher I've ever had. I'm honored to know him and to have the privilege of being his mom. At long last, he's at peace with his life. He's on the other side of his horrific journey. His kindness, gentleness, and his never giving up have lead him here. He's able to enjoy the present and let go of what once was.
Photo credit: Marisa Farnsworth
One last 2017 moon.
Hope you have a good holiday weekend everybody! Happy New Year!
At year's end, I'm so proud of this blog and the storytellers who've made it happen: Marie Abbott, Margie Altman, Gilbert Anderson, Jr., Janet Wood Asbridge, David Bain, Mary Barksdale, Tama IsesaJah Bell, Joyce Berryman, Ronni Blumenthal, Judy Waldo Bracken, Kendra Burgos, Crystal Burks, GG Burns, Robin Burton, James Callner, Sylvia Charters, Laurie Lethbridge Christmas, Elizabeth Courtois, Deborah DeLash, Sonia Fletcher Dinger, May Enos, Deborah Fabos, Laural Fawcett, Anne Schmidt Francisco, Heidi Franke, Mike Gaeta, Patricia Gager, Sheila Ganz, Deborah Geesling, Val Greenoak, Jeanne Gore, Donna Hairston, Janet Hayes, Gloria Hill, Sherry Hunter, Dj Jaffe, Joe IV, Amy Kerr, Kevin, Nikki Landis, Ray Maternick, Maggie McGurk, Lynn Nanos LICSW, Linda Olivia, Teresa Pasquini, Laura Pogliano, Donia Que, Diane Rainbowitz, Patrick Ranahan, Ryan Reyes, Karen Riches, Frank Robbins, Kate Schultz, Joann Strunk, Andrea Turner, Sandy Turner, Cheri VanSant, Laurie Lamsus Vogel, William Vogel, Lynne Warberg, Christi Weeks, Kim West, Craig Willers, Mindy Willers, and Maggie Willis.
Storytelling is ancient. Over time, storytellers, who are good at chronicling the important events of their tribes, come to reach positions of respect and power within their communities. Storytelling is one of our most important traditions because stories instruct and inspire. Stories help us feel what others feel when we haven't experienced what they've experienced. Stories help others feel what we feel when they haven't experienced what we've experienced. Stories help all of us feel not so alone.
Sometimes it's not easy being storytellers. We don't know if anyone is reading our stories. It can seem like we're writing our stories in sand. But look at the photo below. The "story in sand" represents someone's anonymous time and effort. At water's edge, this undertaking will be washed away. Before it vanishes, however, it's been captured by at least one photographer and I'm posting the image here and passing it on. The artist has no idea of the reach and impact of his/her/their soulful expression. Likewise, our stories can resonate in ways beyond our comprehension.
I hope, in 2018, you'll continue to tell your stories. I hope, in 2018, your stories will include accounts of improvement in the lives of your loved ones and in mental illness care. Thank you so much for writing for and reading this blog. And, if you're inclined, please share Sooner Than Tomorrow with your families and friends.
Photo credit: Marisa Farnsworth
Marisa is my daughter. She's taken most of the photographs I've used for HAPPY PICS.
Thank you, Marisa.
#ShatteringSilence4SMI- Sharing a final reflection of our family’s 2017 Christmas Miracle. I think it is clear that Danny enjoyed being home with family and friends and we enjoyed having him home.
I was able to sit alone with him on Christmas morning and show him his Facebook fan club. He had never seen a Facebook page. He loved the picture of me holding the “My Danny Matters” sign. He loved reading the comments from old friends and new friends. He loves knowing that people care.
He was sad to pack up and go back to California Psychiatric Transitions (CPT)* but he knows that he has to complete the program before he can step down to community placement. We made the two-hour drive back feeling love and gratitude for the time we had together while holding onto big hopes and dreams for 2018.
We arrived back at CPT to see families like ours visiting their loved ones onsite. We were welcomed back with such kindness by staff and observed how they helped Danny transition back behind the locked doors. A final big hug for mom and dad and he was gone from sight.
I drove home while my exhausted husband slept feeling at peace but knowing that the road ahead for our Danny will be bumpy. I will be working on smoothing out Danny’s future journey and hopefully, we will find the right path for him and all families like ours. I will also never forget those who have no family to pick them up and bring them home to sleep in their own bed.
I will never give up the fight for #OneCare #Everywhere because I love someone with a serious mental illness.
Thank you all so much for the #DannyLove ❤️
*CPT is a mental health rehabilitation center in Delhi, California, Merced County (cptmhrc.com). Teresa says, "We need a CPT in every county in the state and yet our Governor and legislature cut the budget for these facilities in the 2017 budget. These are also the facilities that the Feds refuse to fund because of the Medicaid Institutions for Mental Disease (IMD) Exclusion.** Discrimination!"
**The Medicaid Institutions for Mental Diseases (IMD) exclusion prohibits the use of federal Medicaid financing for care provided to most patients in mental health and substance use disorder residential treatment facilities larger than 16 beds. This limits the number of beds available for the those with serious mental illness. For an overview go to lac.org
Danny with his Mom & Dad Christmas 2017
Photo credit: Dede Ranahan
Mormon Tabernacle Choir on PBS.
Hope you have a happy holiday weekend everybody!