Re-establishing My Credentials: Psychiatric Survivor Activists are Needed by the 100%, Now!

The popular blog site Mad In America just published my post about my psychiatric survivor #MadPride #Disability journey since I broke my neck in 2012: (If you would like to hear this as a voice synthesized podcast, click play below.) 

By David W. Oaks

David W. Oaks, Revolutionary, Aciu!

For more than four decades, I have worked as a psychiatric-survivor human rights activist. Then, at the end of 2012, I broke my neck. As readers of my blog posts, such as those on Mad in America, know, I have devoted the past few years to rehab and activism. But it has been a while since my last personal blog. Let me sum up my Mad Pride journey today, because a lot is changing.

As a quick background, all of my grandparents were immigrants from Lithuania. Both of my grandfathers were coal miners for a combined 31 years. I was raised in a very working-class neighborhood on the south side of Chicago, and got a scholarship to Harvard. During my sophomore, junior, and senior years, I experienced the psychiatric system. This included involuntary psychiatric drugs, such as on the sharp end of a needle while being held down on a bare mattress on the floor in solitary confinement.

During my junior year, Harvard’s volunteer social change agency, Phillips Brooks House, referred me as an intern at Mental Patients Liberation Front in nearby Central Square. MPLF is one of the very early psychiatric survivor activist groups from the 1970’s. After a total of five psychiatric lockups I graduated with honors in 1977, and studied community organizing with the infamous group ACORN, based on the methods of Saul Alinsky. Community organizing with psychiatric survivors became my career.

MindFreedom International: Winning Human Rights in Mental Health!

Fast forward: I co-founded and was Executive Director for 25 years of the independent nonprofit coalition, MindFreedom International (MFI) which fights for human rights in mental health. MFI has always been wide open to everyone who supports human rights, including attorneys, mental health workers, family members, and the general public. But surveys show that a majority of MFI members identify as having personally experienced human rights violations in the mental health system, that is, psychiatric survivors.

Because MFI’s constituency tends to be low-income, most groups in this field need to rely on government support to exist. That is understandable. But an amazing thing about MFI is that it has always mainly been supported by donations from individuals, poor and rich, and some private grants.

Because of this independence, MFI has always had a different center of gravity than most similar groups: Revolution! We at MFI always attempted to connect with other movements for social justice, such as prisoner’s rights, LGBT+, anti-racism, anti-poverty, and environmentalism. For the last few decades, one of our closest connections has been with people with disabilities.

A Tale of Two Movements: Psychiatric Survivors and People With Disabilities

Frankly, the connection between psychiatric survivor Mad Pride and the physical disability movement has been a bit complex, and sometimes even challenging. For example, there appears to be a difference about the issue of diagnoses. Don’t we radical psychiatric survivors reject all labels? Don’t people with physical disabilities often rely on their labels? Yes, “disabilities” are socially constructed; it is our society that is disabled. But I am aware that some leaders do not always understand our unity.

Unfortunately, I have even seen a leader of a disability Independent Living Center falsely say, repeatedly, that MindFreedom pushes people to quit psychiatric drugs. Wrong. In fact, there are many MFI members who willingly choose to take prescribed psychiatric drugs, and they have told me they feel totally comfortable and accepted.

Both the psychiatric survivor movement and the movement for people with disabilities are united in their goals. Both support the empowerment and choice of the Marginalized And Disempowered (MAD). I’ve written about this before, and I will again, but this is not my point now.

For now, I will point out that calling someone a name they do not want is labeling. Asking for a diagnosis from a pro you trust, willingly, ain’t labeling. More later, but for now, understand that the unity between psychiatric survivors and people with disabilities is more than theory for me. It is my life.

Our Cat, Bongo, Plays a Key Role in My Life

Bongo & Debra (David’s wife)

At the end of 2012, in an attempt to retrieve our cat, Bongo, I fell and broke my neck, becoming a very disabled quadriplegic in a power chair with impaired voice and hands. I do not recommend this drastic approach, but one silver lining is that now I have absolutely no problem at all bridging both the psychiatric survivor movement and the entire disability movement!

As some of us activists have joked about ourselves when we encounter challenges again: I have “re-established my credentials.”

Because of my profound disability challenges, I needed to retire from MFI in 2013. During the past seven-and-a-half years, I have been working on rehab.

I have improved my breathing by twice-daily exercises with heavy weights and an incentive spirometer, bringing my capacity from one-fourth to one-third typical breathing. A great improvement, but I am of course, at the age of 64, one of the most vulnerable folks during the COVID-19 crisis.

I have sought to improve my impaired speech. This has involved years of speech therapy and a surgery on my vocal folds.

Before my fall I could type 120 words per minute, now I cannot type at all. So I have worked to improve my memory because projects and writing need to stick up there, in the mind. Now, in one sitting, I can pretty easily and reliably memorize two shuffled decks of cards (a total of 112 cards, counting jokers and promo cards). I can repeat the memorized order of cards, blindfolded, in about five minutes. I have recited shuffled double decks perfectly 37 times.

There are many other ways I have applied the lessons I learned in our psychiatric survivor movement to my own rehab. For example, back in 1989, I started a men’s support group called the BUBS. During this COVID crisis we have been meeting weekly via Zoom. This sort of small group, mutual peer support, as we know from our movement, is invaluable to rehab and surviving a crisis.

Before my fall, as a fiercely independent Pagan, I relied on my occasional trips to the Oregon wilderness for three days of fasting and reflection. In fact, after one of these trips, I recorded a brief statement, which can be found on YouTube by searching for: david w oaks neptune beach.

Since my fall, to make things easier, I have joined the nearby Unitarian Universalist Church. Yes, a church. I am glad I did, because the UU philosophy works for me, and they are very supportive of people with disabilities. For example, I helped re-start an Access Committee at our church with support from the reverend.

But What Would Judi Chamberlin Say?

Judi Chamberlin

As I have expressed, and many other psychiatric survivor activists know, I have always fought against involuntary and unscientific diagnoses. “Label jars, not people!” as my friend in MPLF, the late Judi Chamberlin, liked to say.

After my accident, I clearly had thoughts and feelings consistent with classic Post-Traumatic Stress Disorder, such as recurring vivid nightmares of falling off my bed that would continue after I woke up. Folks, I cannot even budge once I am lying in my bed!

I have found my psychotherapist, Dr. John Bundy, to be very helpful in addressing these problems. Finding a psychologist that works for me took a bunch of my skills and networking from our movement. Dr. Bundy is superb, and because of a childhood accident, is 100% blind. Perhaps we connect more as peers because of our disabilities.

Yes, many friends and family have encouraged me to write a book, because there are many other tools from our movement I have used in my rehab journey, that may help the general public now.

Silver Linings of Planetary Crises: No New Normality!

Looking for silver linings is one of the lessons I gained as a psychiatric survivor with major physical disabilities. Today, as the whole world struggles with COVID-19, there are quite a few silver linings. One of these is that undeniably we are all connected in one planetary community, obviously and deeply.

To the right are images of my home care team wearing masks. This montage is a tribute to these truly essential workers, crucial for my independent living and our household. One of my home care workers pointed out that essential workers have always been essential, even before this pandemic. Good point. Mainly, I need help thanking and giving credit to my home care team.

Ačiū! Ačiū! Ačiū! This is an ancient Lithuanian word that means “thanks.” This gratitude is why I named my consulting business Aciu! Institute. Thank you, everybody, for your support!

During this rehab, I have attempted to blog now and again. But I will now try to do this more frequently. I believe there are real life lessons from the psychiatric survivor and disability movements which can assist the general public right now, in this era of viruses and climate crisis. I have often heard media outlets say people with disabilities or mental problems make up ‘x’ percent of the public, such as 18% or 15%. But, for example, everyone on Earth addresses the severe trauma of how we treat nature. Scientists suggest that none of us have, or even can, get a grip on reality.

We are now all the 100%. In today’s world, if you are not crazy you may be nuts!

Today we often hear about how “normality” is gone. But normality never really ever existed. Kind of like a unicorn. Many are now talking about a future “new normality.” But this is a lie! Normal is dead forever. One way or another, for better or worse, we won!

This year, my consulting business, Aciu! Institute, LLC, has its second major client, MindFreedom International! I report to their superb director who has taken my place very well, psychiatric survivor Ron Bassman of Colorado. I am helping build their network of Affiliates and Sponsors, updating the list of past groups and finding new ones. One of the uniting tasks that Ron is encouraging for these groups is to support a retooled MindFreedom Shield. Shield is a campaign to support individuals who are expressing concerns about their involuntary psychiatric procedures, issuing human rights alerts that encourage action, similar to pressure campaigns by Amnesty International.

Here in Eugene, Oregon, USA, we continue to build our own MFI local affiliate, MindFreedom Oregon and MindFreedom Lane County. We meet every month by Zoom now. Contact me if you are interested: revolution@aciu.info.

MindFreedom has always called for a global revolution. Wouldn’t a planetary revolution be a nice thing to try? Is there any other way? We can discuss what kind of revolution, but at least talking openly about this would be a start.

As well as MindFreedom, my Aciu! Institute consulting business is assisting a variety of disability and mental health groups. I will blog about this in future posts. Even though I only work a few shifts a week from home, working remotely with my superb administrative assistant Fian Peng, launching Aciu! helps my purpose and meaning. I last ran a for-profit back when I was a little kid, selling seeds and lemonade. I then worked for decades for wonderful nonprofits. It is a blast returning to a for-profit dedicated to social and environmental change!

Building Support for the Next Phase: Revolution!

After I broke my neck, the values and wisdom from our movement helped me each day in my real-life endeavors. Many call this inspiring. I call our social change Mad Pride movement inspiring. Once in a while, someone will question the whole idea of “Mad Pride.” (I sometimes wonder if they like “Normal Shame.”) But for the last few years, our Mad Pride crazy wisdom has helped support and sustain our home, my independence and my life.

One skill I learned in our movement was grassroots fundraising, from many people, poor and rich. While I was in Craig Hospital rehab, we held a number of support drives to raise funds. For instance, quick support from people like you is how I bought my wheelchair van.

Since then, I have not done much fundraising. For one reason, my wonderful wife, Debra, and I live a comfortable life on our quarter-acre homestead we call Mad Swan. One of the absolutely best things in my early adulthood was falling in love with the amazing and always-fascinating Debra.

But while we are not struggling for food, I do want to use my background and experience to help justice and transformation today.

My family created a “David W Oaks Irrevocable Medical Trust” that supports my independent living. Support from this trust is helping me launch my Aciu! Institute consulting.

I pledge to post more often to my own personal blog (www.davidwoaks.com), my consulting business blog (www.aciu.info), and of course Mad in America, which has helped amplify my concerns over the years, so that I know my leadership is still here and helpful.

More than ever, I especially value your feedback. The Mad in America community is vibrant, and I look forward to your comments here. I will try to reply to as many as possible. You will now also find me frequently on Facebook, including our group UU Mental Health Justice. On Reddit we have created subreddit r/MadPride. On Twitter and LinkedIn, let us explore what challenges and opportunities can be found in the intersection of #MadPride and #Disability. (You may comment here, and/or join the lively debates in the comment area at the end of my post on Mad In America.)

Ačiū!

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Editor’s Note: If you wish, you can make a one-time or monthly donation to David W. Oaks Irrevocable Medical Trust. Your gift is not tax-deductible, but is very important to his independent living. He is launching his consulting business, Aciu! Institute.

For more information about donating to David W. Oaks Irrevocable Medical Trust, go here: http://davidwoaks.com/welcome/support

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Ruby Rogers Center in Danger of Being Defunded by Massachusetts

Ruby Rogers Center in Danger of Being Defunded by Massachusetts

One of the very first community centers run by and for psychiatric survivors is at risk of losing its funding from the Commonwealth of Massachusetts. I know about the roots of this user-run space, because as a senior at Harvard College back in the 1970’s, I was placed at Mental Patients Liberation Front as an intern by Phillips Brooks House, Harvard’s social service group.
MPLF, with the leadership of the late Judi Chamberlin, author of a book on empowered mental health centers, created the community gathering locations that eventually became the Ruby Rogers Center in Somerville, Massachusetts. Here are some of the highlights as we created the center:

  • In the mid-1970’s a handful of us in MPLF came together for weekly mutual support. We were gratified to see that Judi’s book, On Our Own, was published. We often met at the storefront of an early activist space, Vocations for Social Change, near Central Square, Cambridge.
  • For a while we created a center at Stone Soup Art and Poetry storefront in Boston, thanks to the generosity of Jack Powers, proprietor. I recall briefly meeting poet Allen Ginsberg when he visited Jack. Activist Ted Chabasinski, survivor of forced electroshock, also visited.
  • Thanks to a grant from Haymarket Fund, we established an office and community center across the street from Boston Common.
  • As a group we met with state-employees at Department of Mental Health headquarters to explain our deep concerns about human rights violations and the need for humane alternatives.
  • About at that time, 1981, I left Boston, but the MPLF members won an agreement from Massachusetts to create a community center that was eventually named after Ruby Rogers, one of the early psychiatric survivor plaintiffs in a key lawsuit against forced psychiatric drugging. I saw Ruby, a charismatic African American psychiatric survivor, who I heard spoke up while locked up in a psychiatric ward, supported by MPLF organizing and a petition by other folks who were locked up.
  • During the three decades since then I have been very delighted to hear that the Ruby Rogers Center, keeping alive the name of MPLF, has continued to do great work. You can read about the details here.

Now the center is in danger of being eliminated by DMH, even though there is a need more than ever for independent living centers run by and for people diagnosed with mental health issues. Not only are such alternatives cost effective for taxpayers, anyone may someday need to have such a welcoming place for their own well being. If not you, then perhaps a loved one may benefit.

I remember a few years ago when I was chatting with a employee of the small, activist-friendly foundation, Resist. They were unfamiliar with our movement, but I knew they were located in Somerville. I asked them if they were familiar with the Ruby Rogers Center, and it turns out that was right across the street. Perfect to illustrate how our movement was widespread but little known! We got the small grant for MindFreedom International, and I recommend other grassroots groups in our movement apply for a Resist grant.

You can read about the Ruby Rogers Center on Facebook here: https://www.facebook.com/rubyrogercenter/

Thanks to a Facebook post from Harry Agritha, shared by Karen Langley, that alerted me about this. Charlie Carr commented and this brought my attention to the danger, here.

I encourage all those who support the disability and prison justice movements to speak up about the importance of the Ruby Rogers Center, now! I especially call out for support from disability activists in the hundreds of independent living centers, which form the backbone of the funded disability movement in the USA today.

You are invited to join me in emailing a civil but strong message to DMH of Massachusetts via this address: dmhinfo@massmail.state.ma.us

 

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Mental Health Revolution, or Why Humor is Necessary if You Are Really Serious About Overthrowing the Corrupt System: My Stand-up Comedy, Ghostbusters Satire, and Dead Family & Friends Such As Leonard Roy Frank

David W. Oaks portrait by Isaac Paris c 2016

David W. Oaks portrait by Isaac Paris c 2016

More than 42 Months After I Broke My Neck, I Do a Stand-Up Comedy Act this Saturday, 30 July 2016

Or perhaps I should say “sit-down comedy”? My intro for my act by the MC will be this:

“From right here in Eugene, our next sit-down comic is David Oaks, also known as PsychoQuad. That means he can slay any audience and then plead insanity!”

If you live in the Eugene-area, or know someone here, get there early to save your seat at Sam Bond’s Garbage, the bar Blair! I will bring my own seat. The monthly show, Bleepin’ Funny, is hosted by an indisputably leading comedic talent in our area, Leigh Anne Jasheway-Bryant. And it is a free event.

I have been going with my loving wife, Debra, for most months to Bleepin’ Funny, for years. I have been in the audience, in fact Sam Bond’s saves a table or two for my friends and me. But this Saturday, 30 July 2016, when the show starts at 5 pm, I am slated to take the stage about the fourth slot.

I have been practicing my stand-up. Before my fall I had the disadvantage of speaking “seriously” in about a dozen countries, for a fee. But humor is better and more fulfilling than boring non-stop seriousness. Or not?

Today, 27 July 2016, above we scoped out the stage at Sam Bond's, where I am to perform this Saturday. I have two plans for getting on the stage. They involve four strong, sober volunteers with strong backs. I will bring a hold harmless clause printout so they will not worry about lawyers. But should I wear a bike helmet?

Today, 27 July 2016, above we scoped out the stage at Sam Bond’s, where I am to perform this Saturday. I have two plans for getting on the stage. They involve four strong, sober volunteers with strong backs. I will bring a hold harmless clause printout so they will not worry about lawyers. But should I wear a bike helmet?

Bleepin’ Funny always features some stand-up, plus Leigh Anne takes the stage with a crew and does some lively, fresh improv. The show ends about 7 pm. It is all-ages, so bring the kids and do not worry about blue material. Call me crazy, but, I say get there early. Heck, even if it is nearly empty you might volunteer for my chair-hoisting crew! See Ian if you want to help out.

The comic Isaac Paris drew me to this amazing possible career, if these weird people known as stand ups can tolerate a professional weirdo. Move over Josh Blue, you no longer are the king of cripple comedy.

Isaac helped arrange for me to do comedy and be on this show. He is up in his native Alaska this week, so he will miss this Bleepin’ Funny. My documentarian and good friend David Zupan plans to video my act, with permissions of course!

Last week, I rehearsed at the Lane Independent Living Alliance (LILA) Peer Support Club, and Zupan was out of town so I did not pursue the documentary. But a relative shot me with their laptop for my own edification. You would think we had somehow violated the law, because an unsmiling employee had her boss e-mail me a verbal unfriendly terse note, I guess government-funded places like that can never have documentaries? My friend Mark Roberts is the brother of the famous Ed Roberts! I guess if Ed were still alive, and tried to speak at a Center for Independent Living, he would not be able to be taped for broader distribution. Hey, protect those privacy rights, cash our taxpayer-money checks, and let us celebrate there are now several-hundred Center for Independent Living (CIL’s) in the nation today, the backbone of the USA disability movement. I love CIL’s, but it is time to start an ADAPT local chapter; I hear you ADAPT headquarters in Austin, Texas.

Humor is Necessary: Please Laugh Once Per Minute (Just Joking!)

Anyway, the good humor, at least we hope it is good humor, will be at Sam Bond’s Garage, a down-home community center with good beer, great little menu, and even great outdoor seating in the back during warm months when it is appropriate. See you there, I will get there very early to save a place or get drunk.

Some Actual Real Humorous News! Well, True Anyway, and I Think it is News-Worthy Mental Health Revolution News

During my rehab, over these more than 42 months, I have had one (1) paid gig doing my work. Incredibly, probably because of a recommendation by my good friend, psychiatric survivor New Yorker Celia Brown, of MindFreedom, my solitary paid gig during my rehab has been to be one of the many independent contractors in the mental health reform field to review and comment on drafts of several manuals, mainly about mental health peer support, by the World Health Organization (WHO), based in Geneva, Switzerland.

The WHO, yes, the same global health agency that tackled some nasty viruses in recent years, has a small but active division working for global mental health. Five years ago, I had the good fortune to visit WHO headquarters in Switzerland, because a number of us psychiatric survivor activists met with and consulted for the head of WHO mental health at that time, the passionate and brilliant Italian psychiatrist, Dr. Bendetto Saraceno. The doctor now directs a psychiatric non-governmental organization in Europe, and has retired from WHO.

This year, the WHO mental health manuals have not yet been released to the public, and so the content is private. However, for my generous independent contractor fee, I tried to provide online input for all the draft manuals. I tried to provide written comments that were both practical and revolutionary.

Some of the non-normal written comments that I made about these drafts, as an actual official paid WHO consultant, were:

  • The world very much needs a revolution, especially because the climate crisis has been so ignored for too many years. Yes, as the Pope recommends, I also suggested revolution for our planet in my official written comments to WHO, as a contracted consultant. In fact, since another round of input is to be requested, I currently still am an WHO independent contractor. Of course, I am speaking for myself and my opinion alone here, not in any way for WHO.
  • Repeatedly, I made sure that my position was crystal clear, that one hundred percent of all people, all the time, every moment, from womb to tomb, are in a state of mind that is in extreme, life-threatening crisis. That is right, my 42 years of activism in psychiatric survivor revolution provided me with four words as my lesson: “We are all nuts!” Nothing wrong with being nuts, if that word has any meaning at all. We may always all of us be nuts, but we can choose what kind of nuts we will be. Will we be creative positive nuts? Or destructive divisive nuts? We must choose.
  • Everyone alive, everyone, has a crisis. Maybe your’s will be very short, but we all have at least one crisis. We are moral. We love. So, prepare for your crisis! Hey, all you need to do is get ready for the unexpected. May I humbly suggest building your community of friends and family?
  • We must act now! We cannot wait for perfect information, in fact science has a theme: Mystery! Whether it is quantum physics, black holes, fractals, chaos theory, string theory, dark matter, dark energy, etc.: As Socrates noted over and over, we do not know much, to this day. But we still need to act, we still need to ask questions. Just as the wing of a butterfly can later influence the course of a hurricane, we must flap our wings! Note we have enormous influence, but not control.
  • The other side of the Butterfly Effect is that as the climate crisis triggers dozens of positive feedback effects, we are entering unpredictable chaos. No way I am giving up hope! Hey, that was me lying on the floor with a broken neck 42 months ago! But my paralysis is mild next to our society’s paralysis. Everyone, all of us, get off the floor!
  • A first step is to realize that internal revolution in our hearts and minds, is not stoppable. Let us make this shared goal more visible now, to help our global morale. I am not saying we will win a quality revolution, but I am sure we can try right now! I believe in you, you all are Supreme Commanders this time! OK, not all of that went into my comments to WHO.
  • But, I made it very clear in my written comments to WHO as an official consultant, that the thing we the public have been calling “normal” does not actual exist. Yes, like some horrible nightmarish virus, “normality” has been eliminated, it does not exist. Since I know that several WHO people have a great sense of humor, it turns out they are human, then I hope they take some credit for finding their funny bone and realizing the seriousness of saying, “There is no normal!”
  • Yes, normal is not in fact, well, normal. Eliminating all traces of “normal” is not the same thing as going after a virus. Yes, some people choose to take drugs to address mental and emotional issues. That is their choice. But “normality” and mental wellness in general, is about something far deeper and more profound than any “normal” medication.
  • I encourage folks to use the easy online interface with WHO to provide resources, suggestions, feedback, important points about the mental health industry, and more important the revolution in mental well being, which uses choice/freedom as a kind of umbrella for recovery, and once shielded there are thousands and thousands of approaches! Just use your search engine to search for the following phrase and then type in your comments: World Health Organization Contact Form. Dr. Saraceno told me, that every comment made to WHO must be treated with respect, and logged. Yes, even so-called irrational comments. Please send your favorite empowering alternative, ask WHO to send this to their mental health division! At the bottom of this is a three-minute video to promote reaching out to WHO. The revolution does not apply only to us consultants, but to everyone, even non-human animals, plants and maybe every particle.
  • Hey wouldn’t it be cool if the whole universe, you included, are equals all working as one? Now that is a Revolution!

On the Birthday of My Friend Leonard Roy Frank (LRF) 15 July 2016

David W. Oaks and his wife Debra react to publicity about the debut of Ghostbusters 3 on July 15, 2016, which is also the birthday for the late and amazing Leonard Roy Frank, psychiatric survivor, editor, friend, revolutionary.

David W. Oaks and his wife Debra react to publicity about the debut of Ghostbusters 3 on July 15, 2016, which is also the birthday for the late and amazing Leonard Roy Frank, psychiatric survivor, editor, friend, revolutionary.

I first wrote this on the 8th day of Creative Maladjustment (CM) Week, which was 7 to 15 July 2016. Yes, Creative Maladjustment Week is now eight days long to end on the 7/15 birthday of this psychiatry-surviving, electroshock defying, mystic-being, beatnik-pioneering, quote-editing San Franciscan Leonard Roy Frank (who would have turned 84 this year of he were still alive).

During these three and a half years of my deep recovery I estimate that I have listened to more than 4,000 hours of National Public Radio news, tuning in every morning via our local KLCC-FM. For example, I feel as if I am personal friends with John Hockenberry, host of Takeaway, because he first got his start here in Eugene KLCC-FM, he is in a wheelchair, but he only exchanged one message before he moved to the East Coast and became a national radio star. He still seems to support revolution, and you do not have to use your imagination much to hear that.

So, for better or worse, I have had more time to think, with my brains, heart, great support folks. Leonard, you showed us that after incredible torture the human spirit can still come back and help humanity. Every time I spoke privately with Leonard, we laughed and laughed. What a keen and at times wicked sense of humor, informed of course that near-biblical personal moral code.

A bunch of my friends in our movement are now dead, or as some of us joked very, very disabled: Rae, Judi, Howie, so many more, and now Pat Risser. If we remember to reform the corrupt mental health group, NAMI, even half as much as Pat wanted, always keeping our sense of humor and outrage, think of all the loving parents who we can support, now being tricked by this drug company front group!

More info about Leonard can be found all over the web, or go to any major bookstore and ask for their huge book Quotationary. Leonard lovingly edited this book of thousands of quotes, and subversively inserted dozens of great quotes very critical of the mental health industry, psychology, psychiatry, electroshock, etc. While he did not hide his identity as a psychiatric survivor during his work as one of the world’s experts on quotes, the fact is that he ended up gathering quotes as part of his strategy to re-create his incredible mind after psychiatry tried to destroy his loving spirit, unsuccessfully.

Sounds like LRF got the last laugh on the mental health industry torture machine. Since this apparatus apparently lacks a spirit of humor, getting the last laugh may be very winnable! I know that so many people have been cheering me on and sending support in so many ways, thanks! My Mom used to send out personal thanks with hand-written cards. As Mom got into her late 90’s she stopped sending cards. Her death last year really put a crimp in her card writing!

But do MindFreedom members really know that this shy Mom of mine worked for years as a volunteer in the main office, sometimes three days a week! Truly, Violet Oaks, my Mom, was MindFreedom’s top volunteer. So far.

For those of you who have read this long post, despite my many severe disabilities, or perhaps because of my creative maladjustment to these extreme challenges, I am talking with board members about coming back in some way, perhaps as a consultant. If I can crawl back to the work place, with extreme accommodations, so can anyone!

So a MindFreedom folks, do you want me back helping on our ship after these 42 months? If you can work together with other members, and ask me to come back, maybe I will, in some way. Before I fell, during my 25 years at MindFreedom’s helm, I raised about one million dollars for this grassroots human rights coalition.

We always prided ourselves about being independent of government money, and working for donations, often from very poor folks. Now, your feedback is appreciate, here, or via Facebook, or with your hearts. And the Oddsquad Advisory Team, and others, I need your advice right now. I must find the tight rope between recovery and revolution.

You may also refer to MindFreedom’s portal about Leonard.

Breaking your neck is never a good idea but if you must break your neck, I would recommend Eugene, Oregon, USA. I have so very many of you to thank! Surprisingly, the absolute winners in the “Support David W. Oaks During His Recovery,” is the Fair Family connected to Oregon Country Fair.

This message is to you all: The rest of my life could be weeping tears of joy thanking you all, every moment! How do I know? I can’t wait, I must act now and thank you! Thanks, thanks, thanks. The word for thanks in Lithuanian, origin for all my grandparents, sounds like a sneeze:

Ah-h-h-h-h Ch-o-o-o-o-o! That word is spelled “aciu,” with some pronunciation marks. Sorry, no time for that, just thanks thanks thanks!

DISCLAIMER: Thanks to homecare worker Sara and my admin for taking my raw notes and fashioning that into the blog, though I take full responsibility and finished my final edit today 27 July 2016. Because of the coincidence of Ghostbusters 3 debuting on 15 July 2016, I was eager to get something out that day. Thanks everyone, especially my darling wife Debra, when I fell, I know that we fell. I hope people give you, Debra, support that is even better than the amazing support so many have given me this past 42 plus months!

 

OK, Here is a Three-Minute Free Video Encouraging You to Contact the World Health Organization, Now!

It is easy, you can suggest your favorite humane alternative to the inherently flawed, corrupted-beyond-comment mental health industry to our World Health Organization, just direct your search engine to their Contact Form:  http://www.who.int/about/contact_form/en/

 

Above entry was a originally posted on my personal blog, which can be found here: 

www.davidwoaks.com

Protected by Creative Commons, only for non-commercial use with attribution. 

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My Friends Hold A Fun Benefit For Me, Here In Eugene!

This fundraising event for me went very well and we want to thank everybody who helped: The bands, poster-makers, donors, participants, and too many to mention here. Friendship gave me such a vision of joy that clearly this gift of community won that day!

Here is my original message:

Below, my friends have sent out this announcement about a benefit with two great bands, on Thursday, June 26, 2014. Please spread the word and if possible join me for the festivities! You may want to arrive early because the event is only two hours long.

By the way, there are musicians in both bands who have had decades at the Oregon Country Fair. Hopefully, both will play songs they have written with an OCF theme!

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Please HELP us promote this event by spreading the word, and by printing and posting the attached 8×11 flyer: oaks-201406-poster-8×11

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The Friends of David Oaks Fundraising Committee invite you to enjoy a very special evening of entertainment at Cozmic featuring STEEL WOOL and THE REFRESHMENTS on June 26, 2014 from 6 to 8 pm.

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My Event on February 21, 22, 23 in Eugene Oregon

If you have a contact who is within driving distance of Eugene Oregon…or if you are local…please support donate to and attend the below fundraising sale to help me.

Here is the announcement from Friends of David Oaks (FODO):

Her is a PDF color poster you may download or view of the event:

OAKS sale214 fnl1

If you are on Facebook, get out this Facebook event to your contacts and say you will attend: https://www.facebook.com/events/188931397984319/

The Friends of David Oaks fundraising committee invite you to a Living Estate Sale in North Eugene, starting Friday, Feb. 21 through Sunday, Feb. 23rd.

WHAT: Living Estate Sale to raise money for David Oaks’ medical/rehabilitative care needs

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