Bipolar disorder

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AfterShocks (…Smile) From our ECT Series

Reference cat

I am hoping to get a running stream of references for those interested in finding out more about ECT.  To start, some are:

  1. As relayed in our last blog post, check out Mayo Clinic
  2. Kitty Dukakis: Shock Therapy Saved My Life – ABC News on abcnews.go.com
  3. Kitty Dukakis And ECT – CBS News Video
  4. Kitty Dukakis And ECT video – CNET TV
  5. Katherine Kitty Dukakis on ECT | Psych Central
  6. Kitty Dukakis & Shock Therapy | World of Psychology
  7. Shock: The Healing Power of Electroconvulsive Therapy – Amazon …
  8. Kitty Dukakis Backs ECT for Depression : NPR
  9. Scientific Articles on Neurogenisis From ECT as described on PubMed
  10. Mortality Rate From ECT
  11. University of Maryland describes their understanding of ECT as a treatment option for Bipolar Mood Disorder and Depression
  12. Currently under research at Duke University, “Not-So-Deep Brain Stimulation:  Transcranial Magnetic Stimulation (TMS)
  13. I also really love the 1st hand words from    Here is one of her excellent statements – “No one really knows how ECT works. For the longest time everyone just said it “rebooted” the brain. Hardly scientific. What we now know is that ECT creates neurogenesis, in other words, neuron growth. And this is needed because long term depression kills brain cells and shrinks the brain. (Antidepressants also induce neurogenesis, FYI.) So ECT is able to make connections in the brain that weren’t previously there, and it makes them very, very quickly compared to any other method.”  She has done her research.
  14. Also, enjoy reading The Bipolar Badger who is going to be writing more on his experience with ECT this week (he’s promised).  The Badger says, “there is very little positive or objective is more like it out there on the interwebs. While I do not expect every post out there to be positive as not everyone has a great experience with ECT. It as important to mention positive outcomes as well.”
If you know of more, please tell us!
Be a friend to yourself.  🙂

 

 

 

 

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The Gift of Desperation

Life (23/365)

LIFE

Misty sounded relieved,

Yes.  That’s it.

She had just realized that life isn’t fair.  Sure.  She knew that before, but she just realized what she knew.  Don’t we all love that moment when our senses join up – sight, hearing, taste, touch, smell, emotion, intellect, spiritual and the rest.  That is a lot to coördinate after all and sometimes some of them don’t make the train.

Misty was a single mom of three.  Her ex-husband was what she called, “Disney-Dad,” and her kids relished their time with him.  Misty complained that she didn’t get to spend the special times with her kids.  She mainly took care of them, but missed out on irresponsible fun.  She was sure her kids wouldn’t look back and think of her like they would their father.  She was getting angrier about it all the time, ruminating about it and it was getting in the way of her ability to connect with others and feel pleasure.  There it was in front of her blocking her from seeing her kids even, let alone herself.

Then after weeks of this along with medication and talk therapy, she told me,

Yes.  That’s it.  Life is not fair.  There are many other things in my life that aren’t fair either and if I look for them, I could spend my whole day every day counting them off.  

It broke my heart a bit to hear her and see her there.  Humble like that; she would I think affect you the same way.  So real.

Yesterday, Carl D’Agostino replied to our post about growing our understanding of our choices beautifully.

…we wait until we are at our wit’s end before we seek assistance…. considering reaching out as personal failure or inadequacy re: our own self-esteem…. Foolishly we wait until our way just is not working anymore. That is why AA calls this a gift: the gift of desperation. …For many, the depths into which we have succumbed are now found not to be so deep at all and in fact, ladders are readily available if we use them in recovery. 

Ah Carl.  Say it again.

The gift of desperation.

Too good.  Don’t you think?

Questions:  Have you ever received the gift of desperation?  What did it bring you?  Where did it take you?  What did it do to you?  Do you still have it?  Please tell me your story.

Self-Care Tip – Celebrate your gift of desperation.

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A Testimony of “Being A Friend To Yourself,” From Bipo Blogger

You might recognize these five questions from yesterday’s blog-post.  Thank you for your testimonies.  Is there anything more powerful than hearing someone’s personal story?  I think not!  Here is what Bipoblogger has to say.

Q1:  What does being a friend to yourself mean to you in real-time life practice?

A1:  That’s easy, but not so easy, LOL!  Being “a friend to yourself” means that I acknowledge I need to respect myself, just like I do other people.  It means not sabotaging my self, plans, job, relationships, etc.  I love myself enough to not kick myself when I am down. 

Being bipolar can be so detrimental to my being, but just like normal people, I still have the need to …allow for room and time to grieve about whatever horrible circumstances (were) caused (by) the bipolar disorder.  

…Stop every once in a while to acknowledge my accomplishments and own that.

Q2:  What helps you do this one time vs. another?

A2:  Yes, I have found that BPD is in part an anger disorder and knowing the true source of the anger can help me go forward.

I have chosen to no longer hurt myself cause when I do, and anyone else, I build up layers of hurt and it hurts to start to take the layers off when I’m ready, so why even do it? …

Also it helped me so much to learn that God doesn’t deal with me the way I deal with myself or another.  I’m not a fanatic, but I just believe in what makes sense.

Q3:  What still hinders your efforts?

A3:  Wanting to be better than I already am.  Not accepting that the balance I have is better than having less or no balance at all, …(which means various kinds of) risky behavior.

Q4:  What has pushed you past those barriers?

A4:  Really just forgiving myself for how I was affected by BPD and remembering that I am breakable and valid as a human, just like all of us.  If I keep practicing a constructive way of life, I will be okay, and that has been true for the last 3 years.

Last push.

Q5:  How do you understand the interplay between biology and choice in being “a friend to yourself?”

A5:  I was created with the choice to choose how I live my life and I do, BPD or none.  Natural inclination is to do the wrong thing because I am imperfect.  I seek power, fame, notoriety and in someway someone, including myself is gonna get hurt in the process.  …People without mental deficiencies don’t experience or don’t carry out to this degree.  So in short, biologically the deficient brain makes more extreme choices, overly withdrawn or overly outward and destructive.

Whoa, I smell smoke.  I never think that hard.  LOL.

Questions for you:  

  1. Anything you’d like to share with Bipo Blogger? 
  2. If you had a blank page for this, what would your own questions be?  What would you answer?  
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Me! Where Emotions and Behaviors Come From

steps 15

Image by Erik - parked in Cairo these days via Flickr

We are doing a narrative series on understanding where emotions and behaviors come from:

  1. Emotions Are Contagious – Emotions shared
  2. Our own Emotional Junk – Emotions hidden
  3. Positive Emotions and Behaviors are Contagious Too 
  4. Our Conscious Self is Our Board and Paddle at Sea – Small conscious self and BIG unconscious self
  5. Biopsychosocial Model – Biological, Psychological, Social selves
  6. Me!  (Today’s Post)

What we have covered so far in our series is that we know emotions are contagious.  We know that if we take care of our own first, we might not be as “susceptible” to negative “contagion” in turn and perhaps, be more available to giving and receiving positive “emotion-contagion.”  Further, we hope that if we do this, we might be able to choose to be with people we love even if they don’t do their own self-care.  We can have that connection without personalizing what isn’t about us.  Sigh.  That is nice, isn’t it?  Then …out at sea (away from our narrative for a day,) we talked about the pleasure in engaging with what bits of biology are directly available to us and the relationship we maintain with the big expanse of our unconscious biology.  Yesterday we reviewed our biopsychosocial model as a tool for further understanding where our emotions and behaviors come from.

Self-Care Tip #272 – If you are ever unsure about where your emotions and behaviors are coming from, it is always safe and true enough to say, “Me.”

Where do emotions and behaviors come from?

Me.

For example:  Me <–> Emotions Shared <–> Me <–> Emotions Hidden <–> Me <–> small conscious self and BIG unconscious self <–> Me <–> Biological, Psychological, Social selves <–> Me… round and round, starting and ending and starting with Me.

Rob and Yesenia were both breathing hard.  Rob was pale and Yesenia flushed.  Where to start?  With Me.  This is what I shared with them both.

Put your spouse down and take three steps back!  Own your own self.  Take care of your own self.  In the process, you will be able to pick each other up again and share love.

Questions:  What are you holding, carrying, using to explain where your emotions and behaviors come from?  How have you been able to put those down and hold yourself?  Please tell me your story.

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Be Aware of Your Feelings and Your Body Function When Getting Friendly With Yourself

Self-Care Tip #202 – Be aware of your feelings and your body.

symptoms and signs

Image by madamepsychosis via Flickr

Wordsmith SuziCate commented to our post three days ago on finding depression in those of us who appear “fine.”

It can be more apparent in what is not said…. When I was depressed it was the absolute last thing I wanted to talk about. I evaded the subject, and if forced to talk it was about anything but what “I” was feeling.

Yet again, the comment completing the post.  It was on my mind and in my face somehow over these sum of days.  When I would start thinking about something else, a patient would nearly quote SuziCate and I wondered if you all have met behind my back on some other blog site with intent to trip me out.  (Grandiose delusions….)

Margo said yesterday in clinic, with hands moving, eyes wide and leaning in,

When I was really down, I just quieted down, stayed low, did my thing.  The last thing I wanted to talk about were my feelings.  I felt afraid of the Nothing that waited there.

She was talking more quietly now and her whole body receded a little.

You aren’t interested or interesting to anyone.  You don’t have anything to say.

We were both quiet for a bit.

These flattening-of-the-spirit symptoms used to be called “Pseudodementia” because they resembled dementia so much.  A muting of the mental and physical function.  A disease progression slowing the nerves and body.  We now refer to them as “Neurovegetative Symptoms.” **

When thinking about getting friendly with ourselves, we can’t forget about what we don’t say or feel emotionally.  We remember also, that the brain is connected to the rest of our body.  Brain is sick, the rest of us is sick too.  This can be a good check point once we start realizing that something is wrong either by insight or by comments from others.

It can be more apparent in what is not said….

Hear more than words.

Not all depressions are these muting processes.  Some of them are activating and agitating types leading to anger and irritability.  Those are hurtful too.

All types of depression are dangerous when left untreated.  The reason isn’t only the risk of suicide or the distance it creates from others.  The reason also includes the less familiar brain changes that it causes on the brain function.  The sooner we are able to pull out of a depression, heal and return to ourselves, the better health our brains will have the long term.  The longer a depression is left untreated, the more damage is caused to the brain’s health.

Questions:  How did you figure out you were depressed now or then? Or that someone else was depressed?  Please tell me your story.

**Neurovegetative Symptoms are the things about affective disorders that most of us don’t know about.  We think about emotions – depressed, sad, happy, angry and calm when we think about mood or anxiety.  We don’t think about the body.  We don’t think about cognition, concentration, memory and what SuziCate or Margo described so well.

It can be more apparent in what is not said….

Neurovegetative symptoms are called “neurovegetative” because they are caused by the changes in the nervous system and they limit our ability to function.

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Go Toward Mental Illness and Take It To The Floor

Sean and Cheryl: Drama on the dance floor

Image by gwilmore via Flickr

Self-Care Tip #155 – Go toward the real issue.  Be a friend to yourself.

Little woman, she had pinched toes in her four-inch heals and wonder what her size has done for her.  Mindy was anxious.  Even though I wonder about her stressors, like possibly her height and the history she is telling me, I know something else.  Even though I wonder about her parenting and marital stressors, and about growing up in a small town but now living with giants, I don’t wonder what she thinks.  Mindy describes these giants as people with large accomplishments, things she would not try herself and that means something to her, but not what she thinks it does.  Mindy wanted to see how things went.  Apparently six months of this wasn’t long enough.

We could spend the next five years breaking all this up and apart and tossing it like a cranberry salad.  But Mindy’s anxiety is mostly not about the salad of life.  Mindy’s feelings are a bit about the stressors and a lot about her brain.

Mental illness is not a small thing.  We trim it down when we say otherwise.  The unfavored sister, Mental Illness isn’t spoken to much at the table.  Her more popular sisters, Stress and Life-Triggers, get a lot of the attention.

With some effort, people who once worked around Mental Illness like it was barely there take a chance and go straight at it, full charge, and swing that woman onto the ballroom floor.

I went for that dance with Mindy.  And she wasn’t talking about waiting and seeing how things went for long.  I told her, like I’ve told you, that how we feel and interpret our stressors comes from our brain.  I told her that mental illness gets worse if it isn’t treated and treated to as full a response as possible.

We weren’t talking about life stressors at that point.  We were talking about her medical condition.  Once treated, Mindy will continue to have life stressors.  We will hopefully also see however, that she responds to life stressors differently.

Question:  How do you make sense of the seemingly meaningfulness of how stress affects us with the seemingly less meaningful concept that we feel that way because of our brain and not because of the stress?  Please tell me your story.

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Pebbles to Diamonds

 

yourloosediamonds.com

Self-Care Tip #117 – Notice, you got diamonds out of stones!  Be a friend to yourself.

Cindy replied to yesterday’s post (that had some discussion on functional mental illness,) “I understand Miranda’s feelings completely.  Some days it’s all I can do not to down tools and scream ‘What about ME?’”

That is one of the lovelies that these illnesses bring to us.  In our honest moments, we can, like Cindy did, perceive our own traits that resemble them.  Perhaps, if we are lucky, that will lead to empathy, one of the great human experiences.  To be able to put yourself in the hypothetical place of someone else.  To imagine what they think and feel.  “If I were in your shoes…” and so forth.  If you’d like, read more on this at this post.

Illness is often considered a step in the dyeing process.  Others see it as part of the living process.  Of course, it is both.  We are all on level ground when it comes to having been born, coming into life, and knowing we will equally die.  Illness reminds us of our like-natured frailty and of course the opposite – resilience.  Whether seeing our own illness or someone else’s, we have this privilege of being blessed this way.

My Dad used to tell me a story (author unknown) when I was little.  It’s been a long time but I remember it this way.

Three travelers were walking when they heard a voice telling them to bend down, pick up pebbles and put them in their pockets.  The voice told them further that in the morning they would be both happy and sad.  The travelers did but not equally.  Some pockets were more full than others.  In the morning when they awoke, their stones had turned to diamonds.  Whoever gathered many stones were happy even though all of them wished they picked up more stones.  But whoever gathered few, well, they were not happy.  They still had diamonds but the comparison soured them and they finished their journey full of “what if” thoughts and not thoughts about the obvious.  They got diamonds out of stones!

We are all similar, with the opportunity to say thanks in seemingly off times, such as mental illness.

Question:  What have your “stones” turned into?  Please tell me your story.

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When Suicide Almost Made Sense

Hello world. Please comment.

nancy says:
November 17, 2010 at 8:01 am (Edit)
I could write a book….but suffice it to say, to the day she died, my mother never even told her best friend that I had had a breakdown and was on medication, my sister said I couldn’t possibly be a Christian and be mentally ill, people at church have told me that they actually walked across pews to avoid talking with me when I was sick, and, even though I’m off all medications but Klonopin and seeing a therapist only every three or four months “just to keep in touch”, I can’t go anywhere or meet anyone new without feeling as if I’m wearing a sign saying “Mentally Ill” around my neck. My attitude about people with emotional problems? God bless them…and I pray that they have a really good connection with HIm. It (and the love of my family) is the only thing that kept me alive.

Question: aside from the obvious nausea and anger that stigma and prejudice bring on, what do you have to say? Please tell me your story.

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When It Is Time To Take Medication

"Yard with Lunatics"

Image via Wikipedia

When is it time to use medications for mental illness?

It is time to consider a medical cause for your behavior and mood when:

1.  you can no longer control them

2.  they affect the various areas of your life

3.  you start having other physical symptoms not accounted for through medical exam and studies, such as:

  • sleep changes (Pearl:  Sleep is known as the vital sign in psychiatry.)
  • change in energy
  • gastrointestinal – stomach upset, nausea/vomiting/diarrhea, change in appetite
  • neurological – headache, numbness, tingling, shaking, change in response time physically or verbally

I’m sure I missed a few things, but roughly, these are guidelines that can apply to most mental illnesses on multiple spectrums, such as anxiety, mood, psychosis, addictions, and even character pathology.

According the numbers count done by NIMH:

…about one in four adults — suffer from a diagnosable mental disorder in a given year. When applied to the 2004 U.S. Census residential population estimate for ages 18 and older, this figure translates to 57.7 million people.  …mental disorders are the leading cause of disability in the U.S. and Canada.

When you next go outside and walk in a crowd, count them.  One, two, three, mental illness.  One, two, three, mental illness.  And so on….  If you suffer from mental illness, you are not alone.

If you buy any of this, if you see these things in yourself, consider seeing a physician for further evaluation and possible medical care.

Self-Care Tip #108 – Take medication if it’s medical.  Be a friend to yourself.

Question:  How has your definition of mental illness affected your ability to get treatment?  Or how has it affected your interaction with those who are in treatment?  Please tell me your story.

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Related Articles from FriendtoYourself.com
  • Mental Illness Relapses When Medications Are Stopped http://bit.ly/pA4kxo
  • Number One Reason For Relapse In Mental Illness  http://bit.ly/rt1qJf
  • Are Your Meds Safe?  http://bit.ly/lh1cBh
  • Say Yes to Medication And No To Drugs  http://bit.ly/oX12i0
  • Fears of Addiction To Medications for Brain Illness http://bit.ly/oWY8i4
  • Other Fears of Medication For Brain Illness  http://bit.ly/qdHksR
  • Afraid of Meds  http://bit.ly/rjt7wY
  • Full Treatment Response Means a Better Future  http://bit.ly/ph84ZU