The Stomp
June 2009

Welcome to The STOMP!, the newsletter dedicated to stomping out stigma by providing education and raising awareness about mental health issues.

Crisis Planning: Safety is the Name of the Game!
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Stomp OutIdentifying and responding to symptoms early reduces the chances that you will find yourself in crisis. It is important to confront the possibility of crisis, because in spite of your best planning and assertive action in your own behalf, you could find yourself in a situation where others will need to take over responsibility for your care. Writing a clear crisis plan when you are well, to instruct others about how to care for you when you are not well, helps you maintain responsibility for your own care. It insures that your needs will be met and that you will get better as quickly as possible.

Elements of a Crisis Plan:

Part 1 Feeling well—Write what you are like when you are feeling well. This can help educate people who might be trying to help you. For someone who doesn’t know you well—or at all—it is very important.

Part 2 Symptoms—Describe symptoms that would indicate to others that they need to take over responsibility for your care and make decisions on your behalf. This is hard for everyone. No one likes to think that someone else will have to take over responsibility for his or her care. Yet, through a careful, well-developed description of symptoms that you know would indicate to you that you can’t make smart decisions anymore, you can stay in control even when things seem to be out of control.

Part 3 Supporters—In this next section of the crisis plan, list these people who you want to take over for you when the symptoms you listed in the previous section arise. Before listing people in this part of your plan though, talk with them about what you’d like from them and make sure they understand and agree to be in the plan. They can be family members, friends, or health care providers. They should be committed to following the plans you have written.

Part 4 Health care providers and medications—Name your physician, pharmacist, and other health care providers, along with their phone numbers. Then list the following—the medications you are currently using, the dosage, and why you are using them; the medications you would prefer to take if medications or additional medications became necessary—like those that have worked well for you in the past—and why you would choose those; the medications that would be acceptable to you if medications became necessary and why you would choose those; the medications that must be avoided—like those you are allergic to, that conflict with another medication, or cause undesirable side effects—and give the reasons they should be avoided. Also list any vitamins, herbs, alternative medications (such as homeopathic remedies), and supplements you are taking. Note which should be increased or decreased if you are in crisis, and which you have discovered are not good for you.


Part 5 Treatments—There may be particular treatments that you like in a crisis situation and others that you would want to avoid. The reason may be as simple as “this treatment has or has not worked in the past,” or you may have some concerns about the safety of this treatment. Maybe you just don’t like the way a particular treatment makes you feel. Treatments here can mean medical procedures or the many possibilities of alternative therapy.

Part 6 Planning for your care—Describe a plan for your care in a crisis that would allow you to stay where you like. Think about your family and friends. Would they be able to take turns providing you with care? Could transportation be arranged to health care appointments? Is there a program in your community that could provide you with care part of the time, with family members and friends taking care of you the rest of the time?

Part 7 Treatment facilities—Describe the treatment facilities you would like to use if family members and friends cannot provide you with care, or if your condition requires hospital care. Also include a list of treatment facilities you would like to avoid—such as places where you received poor care in the past.

Part 8 What you need from others—Describe what your supporters can do for you that will help you feel better. This part of the plan is very important and deserves careful attention. Describe everything you can think of that you want your supporters to do (or not do) for you. You may want to get more ideas from your supporters and health care professionals.

Part 9 Recognizing recovery—In the last part of this plan, give your supporters information on how to recognize when you have recovered enough to take care of yourself and they no longer need to use this plan.
You can help ensure that your crisis plan will be followed by signing it in the presence of two witnesses. It will further increase potential for use if you appoint and name a durable power of attorney–a person who could legally make decisions for you if you were not able to make them for yourself.


Source: www.samhsa.gov

Stories of Success: Debra Demeyere
By Margaret Thele

Stomp OutBefore 1995, Debra Demeyere knew she was having trouble with her mental health. She was having mood swings, making poor choices, and having trouble dealing with her family. She went to a private psychiatrist and was prescribed medications.

Unfortunately, the combination of meds she was put on was not helping her. Debra gained over 100 lbs., had debilitating physical side effects, and as she puts it, “I was a mess.” She decided to go off the medications and became enmeshed in a negative spiral of insomnia, moods, and the effects of bi-polar disorder. In 2003, her relationship with her husband came apart and she was divorced.

Debra moved in with her mom. “She didn’t know how to help”, Debra says. Debra was hospitalized and felt, “The longer I stayed in, the more paranoid I became.” Unfortunately her insurance ran out before she became stable. So her mother, not knowing what to do, took Debra to a homeless shelter in Pontiac, thinking she would get help. Luckily, the intake worker recognized that Debra didn’t belong there and steered her to the crisis center at Common Ground. She was again admitted to the hospital.

“I’ve been through hell—but it has made me stronger.” After seven hospitalizations, living in two group homes, and an attempt of suicide, Debra was finally referred to Community Network Services (CNS) and credits the agency with her recovery. “CNS turned my life around, within a year I was a normal person.”
Debra says she “had an awesome case manager”, who helped her reach her goals one step at a time with the help of her person-centered plan (PCP). “It was baby steps”, Debra says, “until little by little I achieved my goals.” One of her first goals was to get out and get better connected with people. Debra joined the CNS Art Group and says of the experience, “it let me know that I’m not the only one, it made me feel less isolated.”

As Debra became stable her goal was to get a job. She hadn’t worked in 10 years and was anxious about a new venture. Her case manager encouraged her to just go out and do it. Debra went to an Arby’s restaurant for an interview and was hired on the spot. She continued to work there for 2 years. Her next goal was to get a job that was less physically stressful and Debra is now employed with the CNS Empowerment Zone as a facilitator and coordinator of group activities.

“My last goal on my PCP was to get a place of my own.” In October of 2008, Debra moved into her own apartment. “Now I have a room with a view”, she says. Debra has also developed a great relationship with her family, her ex-husband, her kids and grandchildren. “Now I am back with my family, my kids are in my life.”
Goal oriented, and determined to reach them, even with baby steps, Debra Demeyere has advice for others on their recovery journey. “Never give up hope, there’s always a reason to live. Trust your heart and go with your feelings. There’s always a light at the end of the tunnel.”

CMH Corner: Taking the Twist out of Twisted Thinking
By Jackie Castine

stomp!At what point in your life did you figure out that you have very little control over other people? You can’t control what they think; you can’t control what they feel; you can’t control what they choose to do. And the more you try to control others, the more inadequate, angry, frustrated and depressed you will become.

If this is headline breaking news to you today, don’t despair! All is not lost. The good news is that you do have control over YOU! You can control what you think, what you feel, what you do AND how you choose to respond to what others directly say and do. The magic formula is CBT!

Today that principle is the foundation of a therapeutic model called Cognitive Behavioral Therapy. Ted Faris, a practicing psychotherapist, uses this treatment model successfully with his clients, many of whom suffer from mood disorders and addictions. He says it works because “our thoughts cause our feelings and behaviors, not external things, like people, situations and events. The benefit of this fact is that we can change the way we think to feel/act better even if the situation does not change.”

I asked Faris what motivates a person to make the leap from blaming other people for their problems to take on the responsibility (and the cost) of changing themselves. Faris replied, “Most folks don’t get into therapy until all the different ways they have tried to cope no longer work for them. They get sick and tired of trying to manipulate all the people, places, things, and situations on the outside and come to realize that they will never have any peace of mind until they make changes from the inside out.”

Faris describes CBT as “mastering the art of mindfulness.” CBT trains people to analyze the thoughts that run through their head. “It’s like becoming your own self-appointed lawyer, whose job it is to challenge your internal thought process and cross examine your beliefs. The question is ‘what real evidence supports your conclusions?’” Faris reports. Further, the therapist says that, “without this ability we remain like emotionally immature children. We react mindlessly to whatever comes into our head. We respond without thinking. All of life becomes a knee jerk reaction to outside stimuli.

CBT is designed to help clients recognize some of the self-defeating thought patterns and emotional triggers that have kept them caged in behaviors they want to change by being conscious in the present moment and become more flexible in their thinking.

Cognitive behavioral therapy educates clients about habitual patterns of “twisted thinking” that create conflict in their interpersonal relationships. Faris's list includes: 1) Black or White Thinking, i.e. “all or nothing” when shades of interpretation are more likely to give variety and flexibility to the way we interpret situations. 2)Over Generalizing—it is a “you always” or “you never” dialogue instead of the more user friendly “sometimes” or “perhaps.” 3) Mental Filtering occurs when one significant emotional experience blocks our ability to take in new information. The result is obsessive thinking. 4) Jumping to Conclusions sets you up as mind reader or a fortune teller. Not a welcome communication skill. 5) Magnification is a thought habit that makes “mountains out of mole hills.”

Faris says “sloppy thinking allows negative emotions to create a false reality.” For example, if you feel afraid of flying you are likely to conclude, erroneously, that flying is dangerous. Likewise, if you feel angry you may conclude that you have been treated unfairly.
Many people in therapy have learned to recognize how much psychic damage is done by their common mental habit of “shoulding” on themselves and others. Albert Ellis, Ph.D., calls this “musterbation.” We’ve internalized the do’s and don't’s we heard growing up. Now we believe that without the negative self-talk, we wouldn’t get anything done. Faris says, “could’a, should’a, ought’a thinking” is self-defeating. It escalates feelings of guilt and frustration. And when our critical mindset inevitably spills over onto other people, it produces resentment and anger in them.

Cognitive Behavioral Therapy trains us to pay attention to what we are thinking and feeling. “mindfulness” gives us a much greater range of “response-ability.” CBT won’t take always all of life’s problems but gives us many more options to interact with people and be comfortable in situations which used to frighten us.”
Jacqueline Castine, B.A., is a Community Education Specialist at the Oakland County Community Mental Health Authority. She is the author of I Wish I Could Fix It, But … (Phoenix Publishers, 2005).

She can be reached at castinej@occmha.org


Monthly Footprints: June 2009
By Malkia Maisha Newman & Emily Smith

Stomp outThe month of May was filled with plenty of activity for the Community Network Services’ Anti-Stigma Program. It was a great way for us to celebrate National Mental Health Month.

The team participated in two special advocacy events. The first was an advocacy training workshop that was sponsored by NAMI Michigan and AstraZeneca. The workshop was held at the historical Central United Methodist Church located right across the street from the Capitol Building in Lansing. The sessions were taught by Gabrielle King, Vice President and CEO of GDK Associates LLC located in Ellenwood, GA. We were excited and ready to engage our legislators with the tough issues that are facing us all.
After the workshop the team was able to join hundreds of consumers for the Walk a Mile in My Shoes Rally on the Capitol Building’s front lawn! This advocacy event was very powerful. It was inspiring to hear stories from several people across Michigan and see each county’s flag displayed.

Some other highlights from the month include:

An information table at the Oakland County Council for Children and Adults with Psychiatric Disabilities (OCAP) meeting

An information table at WHRC Elementary School in Pontiac

Our presentation, “The Power of Recovery”, at the CNS Consumer Celebration of Excellence breakfast

We wrapped up the month by being present at two faith-based events. First, NAMI Downtown Detroit had their faith-based conference. Malkia represented the team at our information table there. The team also spoke at the 2nd Annual Collaborative Mental Health Education Suicide Prevention Conference designed to foster partnerships between the mental health system and the faith-based and educational communities. Margaret and Malkia presented about mental health stigma and how the faith-based community can help those diagnosed with a mental illness.

Our desire is to continue our message of hope, education, and recovery to those throughout Michigan and beyond. If you are aware of any agency, organization, school, or community group you feel would benefit from the workshops that the CNS Anti-Stigma Program shares, feel free to contact us either by phone, 248-409-4227 or email mmaisha@cnsmi.org .

Stigma In Action: You Can’t Make This Stuff Up!
By Amy Yashinsky

Stomp outSocial Networking websites are all the rage these days. They are a great way to find old friends, stay in touch with people, and generally be connected. Aside from the networking aspect of these sites, some of them offer games to play, bands and TV shows to follow, and quizzes to take. These quizzes range from “which actress would play you in a movie about your life” to “which state should you be living in?” They are harmless and fun, and an easy way to pass some time. Not too long ago, I received a message on one of these sites from my boss. She was forwarding me something she had seen, but could not believe. One of her friends on this site had taken a quiz, and it wasn’t about what profession they were meant to pursue. The name of this quiz was “What Psychological Disorder Are You?” Hold on a second!!

First of all, nobody IS a mental illness! By naming the quiz “What Disorder ARE you?” it implies that a person is their illness. In this world of person-first language and erasing mental health stigma, we need to stop referring to people as BEING their illness. People have an illness, deal with an illness, live with an illness, SURVIVE an illness...they are not now, nor will they ever BE an illness.

When I first saw this quiz I thought to myself “Seriously?! This isn't real!” Who thought this up? Who was sitting around thinking of fun things a person could do online and came up with this? It is not from a medical website, it does not offer reputable information or sources about mental illness. It is not meant to be a place people go to get information about mental illness. It takes normal, every day issues people have, puts them in a list, and labels them (and the person) as an illness. In the example I saw, the person had taken the quiz and the result was “Schizophrenia.” I would like to know what this person answered to generate this response. Assuming this person does not really have a diagnosis of Schizophrenia, this quiz took her average behavior and experiences and turned them into a clinical diagnosis.

Mental health is a spectrum, and we all fall somewhere on it. Very few people are completely at one end or the other. Whether we have a mental health diagnosis or not, we all have days of feeling very down or extremely happy, we all have days where we feel like people are talking about us everywhere we go, or could swear we keep hearing someone calling our names, but nobody is there. If these days outnumber the days when we don't feel or experience these things and start to impair our daily lives, we need to seek help for them. If not, however, we understand that life is full of good, bad, and confusing things, and we go about our business. In the world today, many people are not informed about the real facts of mental illness. This “fun” quiz created to pass the time takes very real, very serious, very treatable experiences and turns them into a joke. It denormalizes normal behavior. It devalues the experiences of those who truly deal with these illnesses. Maybe these websites should stick to the social networking thing, and leave the mental health education to those who are trained. As advocates, it is our job to call these things out when we see them, bring them to people’s attention, and continue to educate and inform others on the power contained within our words and actions.

The Power of Your Story
By: Jenifer Strauss

Stomp outWhen you tell a story that touches me, you give me the gift of human attention—the kind that connects me to you, that touches my heart and makes me feel more alive.” (From The Story Factor by Annette Simmons).
Human beings have one very important and powerful thing in common. From the time we begin to communicate or express ourselves, we share our lives in story. In fact, current brain research indicates that human beings think, learn, and remember in narrative or story. We share stories informally each day, about the people who are important to us, the places that hold memories, and the events or turning points in our lives that have had impact or meaning in our lives.

I make my living telling stories to help people learn, heal, and connect. Lately, I have been paying attention to the stories that people tell about themselves. When I ask them about their life, how do they answer? What part of their life story do they choose to share? What part of their story are they leaving out? Are their stories about limitations or are they about possibilities? Are they telling their whole story?

Our stories are a vast accumulation of experiences that we have had along the continuum of our life’s journey so far. Our lives are one long, changing story. We can stop at many points along that continuum and find a story about an experience that impacted our lives. Each stop is like a portal, or a “door” that can be opened to a story that will give us new insights about ourselves. Think of three things that happened to you in your life so far, from the time you began remembering, to this very day. What are three important or impacting events you have experienced so far? Could you tell a story about each of these events? How did these particular events cause you to grow, learn or change?

Choosing Stories along a Personal Life Continuum


Your earliest memories Today!
Some of the stories we tell about ourselves are joyful. Some are sad. Some are painful, and some are full of hope and inspiration.

Some of our “story doors” take courage to open. Some we may not be ready to open until later. Each of us has a whole story, and telling our personal stories, can help us see our lives as whole. Listening to the stories that others tell, can do the same.
For those of us dealing with the challenges of mental illness, our story can start to feel heavy and lopsided. And so, the recovery stories that we tell should include all the facets of who we are. Not just our challenges, but our joys and successes too. Recovering from mental illness is not our whole story but it is an important part of our story.

To understand how all parts of our lives create our Personal Story Continuum, try this. Create “Your Own Personal Top Twelve”. Take a piece of paper and number it 1-12. Everything you write on your list is a potential story. Write down three things that you love to do. Now write down three people who are important to you, who have impacted your life. Next, write down three places that hold memories for you. Finally, write down three ways to describe who you are by completing the prompt, I am a___________.
When you finish generating the list, look at each item and ask yourself, “is there a story about that?” I think you will start to see that our lives are made up of a series of experiences that are connected and can be shared in story.
So for those of us in recovery, why is it important to share our stories? I believe that when we know and tell our own story, we understand ourselves better. When we listen to and witness the stories that others tell, we understand others and ourselves better. Our life experience is mirrored “in the stories that others tell, for the truth, clothed in a story, is always easier to tell and to hear.

So for those of us in recovery, why is it important to share our stories? I believe that when we know and tell our own story, we understand ourselves better. When we listen to and witness the stories that others tell, we understand others and ourselves better. Our life experience is mirrored “in the stories that others tell, for the truth, clothed in a story, is always easier to tell and to hear.”

Why Tell Our Story?
The stories that we share from our life experience speaks to the truth about living with, and recovering from mental illness.

Our stories can help break through the stigma about the causes of mental illnesses by breaking down barriers of ignorance, prejudice and unfair discrimination, and promoting education, awareness and action.
Our stories can be the advocacy tool that protects against the abuse of rights and mistreatment of consumers.
Telling our story, and listening to the stories of others in recovery, can promote our healing and the healing of our peers.

Suggestions for Consumers:
Use storytelling and story writing activities with peer groups, or in your Club House settings to support and empower each other. Make it a weekly or monthly event.
Speak to groups of adolescents who are dealing with mental health issues to mentor them in recovery.
Write your story and post it on a blog, or place your story on other mental health related posts.
Send your story to magazines, newsletters, or publications that print recovery stories that others can read and benefit from.

Create an inspiring story piece for You Tube!
Suggestions for Mental Health Providers and Recipient Rights Advocates
Use narrative writing and telling as a healing tool for those you provide mental health care for.
Provide a listening space for your clients in group therapy so individual’s stories can be heard in a safe, supportive environment.

Involve family members of consumers in story telling and story listening sessions to help create awareness and understanding.

Ask consumers to share stories, or use stories, with permission, to help dissolve stigma, create policy, and advocate for the protection of rights for mental health care recipients.
In his book, “Listening for True Treasures in the Wind”, author Ron Collins says, “When we take our time and focus on our fellow human beings and give of ourselves, we can truly connect our inner core with another inner core. It is empowering…True listening connects living souls, enhances healing, reduces loneliness, empowers, and impacts all of our lives in the most positive ways…The person you come across can be impacted by the true listening you give to them. Both of our lives can be impacted in ways you can only imagine due to the gift of true listening”.

When we know where we have come from and understand our past “story”, we can understand our present story with greater clarity. Our present story can be one of possibilities, not limitations, for the most powerful way to connect with other human beings, at the core, is to tell and listen to each other’s stories.

Jenifer Strauss is a keynote speaker, storyteller, and workshop facilitator from Hastings. A mental health care consumer, she is currently pursuing a masters degree in Counseling Psychology and serves on the MIAPSRS Board. Jenifer can be reached at jenifer@storybetold.com.


Thank you for your support of the Stomp Out Stigma program. We hope that you have gained valuable information that can help in erasing stigma and look forward to seeing you at one of our upcoming events. If you have any comments or questions about The STOMP!, please contact us at lfarwell@cnsmi.org

In This Issue

Mental Wellness

Success Story

Stigma In Action

CMH Corner

Team Update

Guest Columnist


Stomp out stigma

NEED Help in a CRISIS?

In Oakland County, MI:icon
Common Ground
Sanctuary
24 hr. Crisis Line
800-231-1127

National Hopeline Network
24 hour Crisis Center
800-784-2433

Save The Date

2nd Annual
Stomp Out Stigma
Fundraiser
Run/Walk

Saturday
September 12th, 2009

walk

Mark your 2009
calendars!

 

run

www.
Getme
registered.com

Anti-Stigma Team
Upcoming
Events

 

6/10 - CMH New Hires

6/17 - MORC

6/17 - African American Men’s Health Event

6/18 - Green Path Credit Counseling

6/23– 6/24 - Michigan Peer Support Specialist Conference

7/6 – 7/10 - NAMI Conference

7/8 - CMH New Hires

7/23 - Consumer Conference

 

“Unlocking the Mind”
on CMN TV

This month we will be showing
The Award-winning video Did You Know
Comcast Ch.52
WOW! Ch. 18

Tuesdays 2:30 pm


Get a copy of our VIDEO!!
“Did You Know?”

movieThe video is filled with stories from people who have had a first hand knowledge of what it like to live with a mental illness and how stigma personally affects them. Designed to help promote awareness of
mental health issues, the film could be used at trainings, group meetings or in the classroom.


**$10.00 suggested donation


Contact: mmaisha@cnsmi.org

Do you have a story or article
You would like to see in
The Stomp?
Contact Laura Farwell at:
lfarwell@cnsmi.org
Or call 248-745-4900 x1035

Myth or Fact?

There is no connection between our mood and the weather.

Myth!

Sunshine provides us with Vitamin D, which has a proven effect on our mood. So go outside, take a walk, and soak up the Vitamin D!

Source: www.mayoclinic.com

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

CMH
cns
CNS Waterford:
279 Summit Drive
Waterford, MI 48328
248-745-4900 x 1058
CNS Farmington Hills:
38855 Hills Tech Drive
Farmington Hills, MI 48331
248-994-8001

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