I actually chose the image, as the editor that published the story. The feeling it captured for me was the disorientation and overwhelm of a sensitive person besieged by strange forces and judging eyes all around them, so it felt like a fit with the themes in Odette’s story.
We have options for publishing anonymously (usually with an abbreviated version of the name, and an obscured or otherwise non-identifying photo). If you follow the links to submit a story there’s a checkbox to let us know you need to publish anonymously: https://www.madinamerica.com/submitting-personal-stories/
As the person who edits the personal stories section I thought I should respond here and clarify a few things.
We do offer the option to publish somewhat anonymously, usually under an abbreviated version of the author’s name (such as their initials, or first name and last initial, etc). Although we try to avoid outright pseudonyms, in some cases we have allowed them, as well as pen names and artist names. On our personal stories submission form, one of the main questions a potential author is asked is whether they need anonymity.
We do ask for an actual photo, but it does not need to be a head shot that shows their face if an author isn’t comfortable with that. It might be a photo taken from a distance, from behind or with their face averted, for example. Or it might be run through artistic filters until it’s no longer recognizable as them (at times I have done this myself, if the author isn’t able to).
Sometimes an author is comfortable publishing with their real name and photo but later on their life situation changes and they need more anonymity. So I will work with them to change the name and photo on their account and scrub identifying details from their story, their bio, and even the comment section if needed. We try to avoid taking down a post altogether, but in a few cases we’ve even done that when an author felt that their safety was endangered by it remaining online.
Maybe these options don’t go far enough – I’m certainly open to ideas about how we might protect people better. But to suggest that we don’t offer any sort of protection is simply incorrect.
Regarding the rest of your criticism, I honestly don’t know what you’re talking about when you say things like “if one truly overcomes the experience, this type of diversity is not allowed.” A great many of the personal stories we’ve published – maybe even the majority – are by people who have come out the other side of their negative experiences and consider themselves recovered.
The members of our science news team can all be seen on our staff page. Their job is to report on new studies and other developments in psychiatric research each week, which is a valuable service since the public would generally never even hear about such research otherwise. They do a great job and we couldn’t be more proud of them here at MIA.
Hi Surviving and Thriving. We’re definitely open to publishing blogs by people with lived experience of chronic pain. If you’d like to write one, or know someone that might, feel free to get in touch via our contact page.
fred77, it’s simply not true that survivors don’t get a chance to post or contribute here. Almost all of the personal stories on this site are written by survivors, and many of our regular bloggers (and some of our staff) are survivors as well.
Hi everyone. We heard from Matt’s sister that it meant a lot to their family to read about people’s interactions with him. She also shared his obit which I will paste here:
It is with great sadness that the family of Matt Stevenson announces his passing on Thursday, September 21st at 32 years of age.
Matt graduated from Marymount University with a degree in English. He then turned his lifelong passion for tennis into a career as a tennis coach. Matt loved coaching and was very popular with his students, especially the children. He was an inventive teacher and created many games to teach his young students new tennis skills through fun activities. Matt also volunteered teaching English to new Americans , and he organized many socials for young people in his community .
Through his struggles with mental health, Matt became passionate about helping others in crisis and working towards a new paradigm for mental health treatment . He pursued this passion through his involvement with several organi z ations , including Mad in America, The International Society for Psychological and Social Approaches to Psychosis (ISPS), and the International Society for Ethical Psychology and Psychiatry (ISEPP).
Matt was an intelligent, thoughtful, and caring young man with a quirky sense of humor. He is mourned and will be greatly missed by his mother Judith, his father Hugh, his sister Catherine, and his many friends.
A service to celebrate Matt’s life will be held on Thursday October 5th, at 7 pm, at the Celebration Center, 2840 Graham Road, Falls Church, VA 22042. All are welcome to the service and reception to follow. As this is a celebration of his life, please do not feel the need to wear black.
For those who wish to contribute, we will collect donations to support the International Society for Psychological and Social Approaches to Psychosis (ISPS), an organization that was dear to Matt’s heart.
Just to clarify, this change was not implemented due to James and Brett’s feedback — it had already been decided at a staff meeting several days prior. The discussion here about writers leaving due to the comment section just seemed like a good place to mention it.
We can and do moderate comments that cross a line, but that doesn’t undo their damage when authors have already seen them. The only real solution for that would be to make all comments go into the moderation queue to be approved before they appear, which would result in considerable delays in communication.
No one’s arguing that it’s “the job of readers to provide ‘safe space'” (whatever that means). It’s the responsibility of this organization to manage our website in the way we think is best. And that’s what we’re doing.
This just goes back to the “thick skin as a requirement to write here” thing. Maybe you can ignore people who are trying to tear you down, but not everyone can or should.
That would be ideal, yeah. But as you might imagine it can be pretty challenging, and moderating is already very difficult work. We’ve burned through a string of moderators at this point — it requires an even thicker skin than being a blogger, and a pretty specific skill set. It also takes up a lot of organizational resources, which are not infinite.
As for your other question: we do see value in bloggers participating in discussions, and we could make that more clear in our invitations. But we’re not going to make responding to comments a requirement or attempt to persuade writers to do anything they don’t have time to do or don’t feel comfortable doing. They are already participating in the ‘give and take’ by sharing their work here.
Richard, I’ll reply to your last question as it pertains to me. The role of MIA moderators is ultimately just to remove comments that aren’t in line with our posting guidelines. When I was the moderator I did attempt to mediate between authors and commenters at times, and generally tried to help people understand where others were coming from. So maybe that’s where you got that impression.
As for allowing writers to close the comments, we’ve actually been doing that for some time now, when it was requested, and a few blogs have been published that way. The main difference with the recent decision is that we’ll be offering this as an option rather than waiting for writers to get so fed up with the comments that they request it. This way comments will effectively be “opt-in.” So far, everyone offered the option has opted in, and that will likely remain the case for the most part.
Many online publications have actually closed their comment sections altogether these days. I think the solution we’ve come up with is preferable and takes the needs of all sides into account.
Hi Stephen. We won’t be stopping comments altogether, it will be per post and up to the author. I expect that most authors will prefer to keep comments open, but this way they’ll at least have a choice.
By the way, it isn’t just mental health professionals who have issues with the comment section. Writers with lived experience sometimes do too, and it becomes a barrier to participation here.
I hear you on professionals not always being willing to make the effort to see things from the perspective of people with lived experience. But the reverse is also true — people making no attempt to see the good in what a professional is doing, instead bending over backwards to find fault and assume the worst, sometimes missing the point of a blog entirely or reacting to things the writer didn’t even say. Certain topics become a flashpoint for rage, which is certainly understandable, but not always constructive.
Jim, I just wanted to say that MIA staff share the concerns you and Brett have expressed here. We strive to maintain a space where people can “speak truth to power,” but when such speaking drives people who have power to change the system away from participating in the conversation at all, that goal is undermined, as is our mission to rethink and remake the mental health system. We recognize the difficult position that many ‘dissident’ professionals are in, often risking their careers and facing condemnation from their peers when they break away from the pack, only to be met with a barrage of criticism from the other side for not being radical enough. It’s understandable that some are unwilling to put themselves through that.
There is no easy solution for this problem, really. But we will now be offering writers the option to turn off comments for their posts if they want to share their work and their experiences without facing the firing squad, so to speak. This way, “unusually thick skin” will no longer be a requirement for writing here. We hope that this will broaden the range of writers we can bring in, and also help raise the caliber of comments as people learn that keeping things constructive is the way to keep the conversation open.
Matt, I’m not sure what you mean by ‘original version’ — this article has not been modified at all since it was published, and it never took the extreme position that some seem to be reading into it.
Hi LavenderSage. Feedback about the site can be directed to our operations manager Chris Page. You can get in touch with him via our contact page: https://www.madinamerica.com/contact-us/
As for the tagline, we’ve received a lot of feedback about this and will be changing it within the next few days. We’re open to community input if anyone has suggestions about what might be more fitting.
Hi everyone, I’m stepping in as moderator to say that I won’t be allowing further comments alleging that the authors are promoting any products or companies. Since that allegation has been addressed and rebutted, I consider the matter settled — to continue pursuing it would be to engage in misrepresentation, which is against our posting guidelines: http://www.madinamerica.com/posting-guidelines
I’ll give Bob a heads up that you’re looking for a reply. You can also contact him or other staff via the contact page: http://www.madinamerica.com/contact.
Thanks for your work in helping get these ideas out there! The Holistic Mental Health Network you mentioned sounds very promising.
Joel might be disappointed to learn that the delay had nothing to do with a conspiracy to suppress dissenting viewpoints, but was simply a matter of the “editorial woman” (as he put it) being busy that day.
“Hardly ever”? Are you not aware that the comment section you wrote this in is a space created for precisely that purpose — for people with experience of the labels and the drugs to say what they think about it? And that our forums also serve that purpose? And our entire Personal Stories section, and a number of our blogs? Inclusion and amplification of the survivor voice is a key part of the mission of this organization that Robert Whitaker started, so your criticism seems pretty misplaced.
Folks, the comment section is for discussing the issues raised in the blog posts, not for ad hominem arguments (no matter how true they might be) and slinging insults at other commenters. I realize the discussion started out with something of a provocation, but we need to keep it clean and stick to the issues. It’s unfortunate that some comments making valid and important points also contained personal attacks and had to be removed.
Would something like “chance” be preferable to “risk”? If you have more suggestions about less-problematic wording, I’m sure that Justin would welcome you getting in touch with him via the contact page. We’ve discussed some of the responses to this news item and what efforts we could make to address the concerns. It’s challenging to make everyone happy with word choices, especially when reporting on studies that use diagnostic terminology (as many of them do). And we do need to report on studies like these, because people have a right to know how the drugs they take may affect the fetus they’re carrying.
The article is about an app, and this discussion about the author’s stance on ECT is basically off-topic and ad hominem. I don’t want to suppress legitimate criticism, and criticism of ECT is certainly legit, but the comment section is not an open forum for the character of authors to be put on public trial every time they write a post.
As for authors responding to comments, it’s true that many do and this is definitely appreciated. But they’re under no obligation to do so. Like it says in our posting guidelines, “A person’s choice not to acknowledge or respond to specific arguments will not be assumed to be malicious, or a sign of a character flaw, or otherwise held against them.”
Some of these comments are getting pretty personal — which is not to say they’re not making valid points, but with so much to discuss regarding the Murphy bills and the systems of power behind them, I hope the conversation can focus on that rather than on individuals in the comment section.
Snowyowl and Oldhead, please feel free to get in touch with more details about your ideas. I’m not sure what you’re envisioning — something like a temporary content block on the front page where content related to the Murphy bill would be gathered?
I need to clarify that MIA as an organization can’t create such content ourselves or advocate for or against specific legislation. It’s just not our role — but as Leah pointed out, it is the role of other groups, and they’re doing a good job taking the lead on that.
So my suggestion for you would be to come up with a plan for where the content would come from, and then we can talk about where it would fit on the site. We’ve already published a number of pieces related to the Murphy bill and more are certainly welcome.
While I’m not interested in silencing anyone, as the moderator of this website I need to be clear that this is a trans-inclusive space. Everyone’s unique perspective is welcome, but we can’t allow comments that are oppressive to marginalized groups — which includes cisgender women, transgender women and all trans people. So this is not the place for the ‘who qualifies as a woman’ debate, and I ask for everyone’s cooperation in keeping this space as oppression-free as it can be.
Oldhead: yes, of course. “Rethinking” is pretty broad and can encompass calls for abolition as well as reform. I’m sure you’re aware that the people who blog on MIA come from a variety of perspectives on that.
Jonathan: I don’t want to derail the conversation from Sera’s post too much, but as a member of the MIA staff I’d like to address the concerns you brought up here. We are very much interested in bringing more diversity to the group of writers on the site. While most of our writers have come to us, we’re putting a plan in place to do more active outreach to potential writers in underrepresented groups. There’s a lot of energy around this right now, so hopefully you’ll be seeing some changes soon.
Of course, the challenge for any organization or project that wants to become more diverse is to reach out in ways that are respectful and non-tokenizing. And the challenge for us at MIA is to find people who are specifically focused on “rethinking” psychiatry. If you have any suggestions for people we could be reaching out to, please feel free to get in touch with me via the contact page.
I’ve removed a number of comments that I felt were needling, baiting, personally attacking etc. I realize there’s a fine line sometimes between legitimate criticism and sniping, but I hope people can try to keep the critique civil, constructive and non-personal.
Bernadette, as the moderator of this site I’m not sure what you’re talking about when you say “trying to silence varying points of view.” If you’re referring to editorial policy regarding what stories are published, obviously there’s a focus on “rethinking” or taking a critical view toward psychiatry since that is this organization’s mission. There’s no shortage of pro-psychiatry views elsewhere (in fact, they heavily predominate) so it would not make a lot of sense for this site to merely echo what can be found pretty much anymore else.
If you were referring to the comment section, I’d like to clarify that we do not moderate comments based on a person’s position on psychiatry — there is no “censorship” of pro-psychiatry views.
We do, however, moderate comments according to our posting guidelines, which are mainly concerned with civility and being on topic: http://www.madinamerica.com/posting-guidelines/. Please note that discussion of moderation in comment threads is generally considered off-topic, however, if you have concerns about site moderation you can contact me or any staff member directly via the contact form, or leave feedback in our feedback forum: http://www.madinamerica.com/forums/forum/feedback/
I don’t think it’s accurate, or appropriate, to call it “race baiting” when people talk about racism and violence against people of color. Used in that way, the term is an attempt to deny the reality of racism and shut down conversations about it.
These are all expressions of racism, conscious or otherwise. I want to be clear that racist views are not welcome on this site — they contribute to the harm and oppression of people, and that’s the opposite of what we’re about.
My request for everyone taking part in these difficult but important conversations: if the issues of racism or racist police violence don’t impact you personally, if they’re invisible to you (much as psychiatric violence is often invisible to people who haven’t experienced it), I ask that you make an effort not to disrespect or minimize the struggle of people whose lives are impacted, every day, sometimes in deadly ways.
What’s the difference between power and authority? The workers who perform the labor have power; the bosses who tell them what to do have authority. The tenants who maintain the building have power; the landlord whose name is on the deed has authority. A river has power; a permit to build a dam grants authority.
There’s nothing oppressive about power per se. Many kinds of power can be liberating: the power to care for those you love, to defend yourself and resolve disputes, to perform acupuncture and steer a sailboat and swing on a trapeze. There are ways to develop your capabilities that increase others’ freedom as well. Every person who acts to achieve her full potential offers a gift to all.
Authority over others, on the other hand, usurps their power. And what you take from them, others will take from you. Authority is always derived from above.
In this society, power and authority are so interlinked that we can barely distinguish them: we can only obtain power in return for obedience. And yet without freedom, power is worthless.
I also really like the idea of presenting material from fact-heavy, academic books in more condensed and maybe unconventional forms, like in the blog Jessica linked above, or like this Rat Park comic: http://www.stuartmcmillen.com/comics_en/rat-park. Sometimes you just have to meet people where they’re at, and those pop culture forms can be more accessible to a broader range of people. But once you pique someone’s interest with some kind of “teaser” they might be more inclined to read the book. Ever since I read Anatomy I’ve been wishing there was some kind of Cliff’s Notes version of that book that I could hand out to everyone I know. Of course, authors should be fairly compensated for their hard work and it could be problematic to undercut that, but ultimately I think that getting the info out there is the most important thing.
This comment thread has gotten pretty sidetracked — I’m hoping we can bring it back to the topic of book activism. In her concluding remarks Bonnie asked readers to share suggestions about how best to do book activism, and one thing I thought of is audio books. A lot of people lack the time or attention span to sit down and read a book, or the money to spend on books about topics they’re unfamiliar with or skeptical of, but might download a free audio book and listen to it while driving or doing things around the house etc.
Looks like they’re pretty easy to make: http://www.makeuseof.com/tag/how-to-record-your-own-audiobook. In fact, I’ll volunteer to try it out and make one, if any authors want to send me a book? I actually used to record audio books for kids when I was little, at the request of my school library (I guess because I was such a good reader) — it might be fun to do that again.
I’m stepping in as moderator to point out that this comment thread is on a blog post about book activism. These side conversations may be interesting but they’re also off-topic — if anyone would like to continue them, please take the discussion to our forums so this comment thread can get back to the topic of book activism.
Jeffrey, yes, I am asking you to add a valid email address to your account, because that is a requirement for posting comments here. I am not going to continue to discuss moderation issues in the comment section — that’s not what the comment section is for.
Jessica, I love the idea of presenting the information from Anatomy of an Epidemic in a pop culture context with humor and pictures like you’re doing. It could help make that information more accessible to people who haven’t read the book and might not understand why it’s important. Very cool!
He’s on facebook, and it looks like his page is set up to allow people to post to it (posts appear in the “POSTS TO PAGE” section on the sidebar, under Photos).
Where the line is drawn at MIA is described in our posting guidelines: http://www.madinamerica.com/posting-guidelines. Please note that registering with a valid email address is a requirement, and that discussion of moderation in comment threads is considered off-topic and may be removed.
I’m not going to go into what the problem was with the removed comment, but discussion of issues of justice was not it.
Hi everyone. Due to an increasing number of comments that attacked persons rather than practices, comments for this post are now closed. There can be a fine line sometimes between discussing practices and discussing their practitioners or proponents, but that’s the line we’re trying to maintain here (perhaps a bit clumsily in this instance, and I apologize for that). We’re interested in providing a platform for the hazards of all psychiatric practices to be thoroughly discussed, not for people in the movement to be raked over the coals, because in the end, despite our differences on certain issues, we’re all part of the same fight. And so, with respect for the passion, insight and devotion to the cause that everyone brings, we ask for your understanding as we close this comment thread.
Kermit, thank you for this. I recognize that for many this site is a kind of sanctuary from the status quo, so it’s understandable that people might resent the status quo showing up on our doorstep. But I believe as you do that this can and should be embraced as an opportunity — after all, shifting the dialogue to bring about change is essentially the whole point of what we’re doing here.
I’d like to ask that people please refrain from labeling pro-psychiatry newcomers as “trolls.” If someone is in fact here to troll rather than dialogue, they will eventually make that clear through their pattern of behavior and it will be dealt with by the moderator (me). In the meantime, let’s try to give people the benefit of the doubt.
Hi there, I’m sorry you felt ignored! I just saw your question in the forums and replied to it there. Not sure what happened with your attempts to contact folks, but I know we all get a lot of email and occasionally something might slip through the cracks.
It’s still there at http://www.madinamerica.com/contact/ — under “Select message recipient” there’s a drop-down box, click the arrow and a list of names should appear.
I’d say it’s to a person’s credit if they rethink an initial off-the-cuff response and come back with a more measured and thoughtful reply that offers someone the benefit of the doubt, as AA did. It’s a shame you couldn’t respond in kind.
Link fixed! Thanks for the heads up Madmom. Carina, your webpage is beautiful and it’s so exciting that you’re doing this festival! I wish I could go there, but I’ll hold out hope for Eugene.
LoveLife that’s so great that your husband is supporting you in your decision! One resource I would recommend is this guidebook you can download, it’s helped many people get started in their journey to come off psychiatry drugs: http://willhall.net/comingoffmeds/
You’re so not the only one! The trajectory of your story is unfortunately very common, with negative reactions to SSRIs being labeled as “bipolar,” resulting in more drugs and worse reactions until everything spirals out of control. But many of us were able to stop that cycle and find our way out — I hope that you can too.
B: There hasn’t been a rule prohibiting it. Looks like we’ll have to add one, since it’s been used as a way to get out of moderation on a moderated site. I like to give everyone the benefit of the doubt, and many chances to understand what the boundaries are and try again, but after a certain point if a person is just not willing (or maybe able?) to respect the boundaries of a space, they can’t be in it anymore.
If anyone has more questions or feedback about what is or is not allowed on the site, please feel free to get in touch with me via email or using our contact form.
Alex, what I’m hearing is that certain needs might not be met by this discussion platform. I want to acknowledge that those needs are real and valid, while also acknowledging that this platform has been created for a specific purpose, and people are free to choose for themselves whether it meets their needs or not.
My feeling is that if healing or emotional safety are what a person seeks, the comment section of a blog site might not be the most likely place to find them. There are inherent limits to text-based internet communication. There are inherent hazards in debate, and (especially) in interacting with people who represent a role that you’ve been harmed by (such as psychiatric survivors interacting with psychiatrists). It can all feel very draining or even triggering. Ultimately a person needs to weigh those risks for themselves and make their own decision about whether it feels worthwhile, constructive or healthy to participate in such conversations. That is the responsibility of the individual.
Of course, the creators of a space also have responsibilities. While I personally believe that emotional safety and the internet are mutually exclusive to some degree, I also believe it’s important to be thoughtful and aware of the risks and make a good faith effort to mitigate harms. I think we do make that effort.
What I’m hearing is that for you, and maybe others, it’s not enough, or there’s a need for a space that’s very different than this one. I hope you can find that space, or create it if it doesn’t exist. Recently I’ve been hearing talk among survivors about creating a survivor-led (and maybe survivor-exclusive) space for discussion, support and information sharing. I think that would go a long way toward meeting some of the needs you identify, and would be a good complement to what we’re doing here. But in terms of empathy, I believe that face-to-face connection is more likely to facilitate that than anything that could ever happen on the internet.
If you would like to draw attention to published research, please do so in a comment that is free from personal attacks and within our posting guidelines for the site: http://www.madinamerica.com/posting-guidelines/
Moderator chiming in, but first I would like to point out that discussion of moderation in comment threads is in most cases considered off-topic to the blog posts. Readers are encouraged to use the report button for problematic comments, or contact us directly for feedback on moderation or editorial decisions: http://www.madinamerica.com/posting-guidelines/. I’m pointing this out because by sharing my perspective there’s a risk of sparking a debate about whether a moderation issue exists here or not, and I don’t want the conversations about the issues discussed in Richard’s or Timothy’s posts to be derailed.
That said, my perspective is that I don’t see persons being attacked here. I see ideas being criticized. I think it’s okay for Richard to write about how he thinks Timothy missed the mark, just as it was okay for Timothy to write about how he thinks Robert Whitaker missed the mark. I’m quite certain that both authors understood that their viewpoints would stir the pot and generate controversy, but I feel that they’re attempting to engage in respectful debate (and for the most part succeeding, although both occasionally used terms such as “dogmatic” or “absurd” to describe positions they disagree with).
I view the resulting discussions in the comments similarly — while there are very strong feelings around these topics, and some pointed critiques, I see an effort to keep it civil and largely non-personal.
I do think it’s important for people working as clinicians or counselors etc to be mindful about how they address people with lived experience, though. While there’s no power differential among authors on this website, there can be one in the roles people represent.
Excederin, please take a moment to review our posting guidelines for the site: http://www.madinamerica.com/posting-guidelines/. Personal attacks are not allowed, and “armchair diagnosing” is a personal attack, regardless of how enamored with diagnostic labels one might be. Since Steve’s replies have been instructive, I will allow your comment to remain for context, but any further attacks or baiting will be removed. If you are unable to keep your comments within our guidelines, this may not be the right conversation environment for you.
ps: blakeacake, please get in touch with me via our contact form. I have attempted multiple times to contact you regarding moderation issues and the emails have bounced, as I’ve mentioned before.
Edited to address your questions: yes, your contact info will be kept private and confidential, and no, nobody needs to “divulge personal, protected medical information to MIA” in order to post here. You do need to have a valid email address that you can be contacted at. Comments that are not within our posting guidelines will be removed, and anyone posting a high volume of such comments will be placed on moderation. More information about our policy can be found here: http://www.madinamerica.com/posting-guidelines/
As someone who once was given a diagnosis of adult ADD (no h, and I am not endorsing the diagnosis by mentioning it), I can say that diet changes made all the difference for me, particularly eliminating gluten and dairy. It was something I figured out on my own in college — I’d be working on a paper and take a break to eat pizza or pasta or something, and come back to find that I could barely even follow what I’d written. I also avoid artificial colors and sweeteners, MSG, soy and various other things. It helps.
I should note that I never had any attention or concentration issues as a child though. It wasn’t until I’d been on psych drugs (“antidepressants”) throughout my teen years that the issues developed, so they might be iatrogenic in origin. But having this basis of comparison, I do know that there’s a difference between being bored with a topic, and finding that your brain simply. will. not. work. when you try to focus on something. It’s incredibly frustrating. Occasionally I still experience this when stressed or overwhelmed, but I’ve learned various techniques for getting things back on track. Sometimes it’s as simple as taking a break to play a computer game or watch a relaxation video. Therapy and journaling can help too, because it’s certainly more difficult to attend if you’re struggling with some kind of chronic internal war like Dr. Berezin talks about in his post.
No worries! I do look pretty different without the glasses.
My title is community manager, which basically means moderator for the website. That’s why I tend to weigh in on issues like this, but for the most part stay on the sidelines of the discussions.
My feeling is that if someone is truly here to disrupt, not to dialogue, they will eventually make that abundantly clear through the pattern of their behavior, and when they do it will be dealt with. But I would like to set a high bar for designating people as “trolls” in this space, and ask that we try to give the benefit of the doubt. Not just because this is the respectful thing to do, but because one of our goals here is to contest and counter mainstream thought about psychiatry, and as such we should expect opposition from those adhering to the status quo. Ideally, we would be prepared to address or rebut their arguments.
Of course, no one (including site authors) is obligated to respond to anything they aren’t interested in, don’t have the patience for or find pointless or baiting. I’m just saying that, generally speaking, when someone challenges our views they offer an opportunity — the opportunity to strengthen our case. Such a person can serve as a useful “foil” in a way. Maybe not useful for ourselves so much as for the thousands of unique visitors who read this site every day and may be encountering these challenges to the status quo for the first time.
Just something to think about. I realize that it’s generally more enjoyable and interesting to have conversations with like-minded people who’ve put a lot of thought and study into these topics, but there’s a bigger picture to keep in mind too.
“First they ignore you. Then they laugh at you. Then they fight you. Then you win.”
Thank you for sparking such an important conversation. Maybe you could explore the topic of loosening polarizations in a future post? I’d be curious to hear your ideas about that. My feeling is that building coalition around points of unity, while respecting differences on certain issues, will make our movement(s) stronger and more effective without compromising any principles.
I’m not sure what you’re getting at, and am not interested in getting embroiled in a debate with you, but to answer your question I don’t really watch television. I do read articles from a wide variety of sources, but am more likely to read those that take a more critical perspective than the “featuring the wonders of a drug” point of view you describe.
Very good point about the use of diagnosis and “treatment” as a means of blaming the victims of oppression, not to mention effectively compounding it by decreasing likelihood of recovery — which as B pointed out, can make it more difficult for people to fight against the oppression they face. This is a key intersection that people committed to anti-oppression work should be grappling with, not deflecting.
I see it as one of the keys to rethinking psychiatry too. We need to focus on the harms and the alternatives but also the root causes of the experiences that get labeled and drugged. So in that sense I very much agree with the author’s call for a focus on structural violence, which obviously is a huge source of trauma, but disagree that the issue of psych drugs can or should be detached from this. Similarly, I agree with “loosening up polarizations” but disagree that “shifting attention from debates about [psych drugs]” is the way to go about it.
Blakeacake, you’re certainly free to share your opinions (as long as they’re within our posting guidelines for the site). I was pointing you toward resources where you might find the proof you say you’re looking for, and suggesting that that might be a more productive use of your time than trying to demand proof from people who may not be interested in (or have the patience for) engaging with you.
Robert, I’m sorry, I should have put the name of who I was addressing my comment to — I was referring to the commenter Blakeacake singing their praises, not you! Much appreciation for your approach toward psychiatry. I’ll edit my comment so it’s more clear.
Ted, I’m not sure what you mean by “no encouragement” from MIA for the involvement of psychiatric survivors in our own liberation. We recently added an Organizing for Social Change forum at the request of psychiatric survivors: http://www.madinamerica.com/forums/forum/organizing-social-change/. This comment section itself is also a form of involvement, which psychiatric survivors regularly avail themselves of, as you know. Since resources are devoted to the very thing you say we aren’t encouraging, I don’t really understand your assessment (maybe you’re just talking about the number of survivors among the mix of bloggers?). At any rate, if you have ideas for more ways that involvement of survivors could be encouraged, please feel free to share them with us. I think we’re all open to hearing them — I know I am.
Blakeacake, I can understand how disorienting and off-putting these conversations might feel for you. After all, you’re encountering a new and unfamiliar perspective that calls into question everything you know. Meanwhile you’re trying to share your own perspective, but it isn’t a new one for the people you’re conversing with — they’re already familiar with it, and have strenuously rejected it.
If you’re interested in learning more about this new perspective, my advice would be to seek sources of information that state the case in a calm and objective manner, rather than attempting to sing the praises of psych diagnosis and drugging to people who have been harmed by diagnosis and drugging. One place to start would be right here on this site, in our archives: http://www.madinamerica.com/news-archives/all/adhd/
Best of luck to you. And ps: please make sure that the email address you’ve signed up to the site with is a valid one (I attempted to contact you about a moderation issue and the email bounced).
I’m not entirely certain what you mean by users (readers? commenters?) but it almost sounds as though you’re suggesting that their agreement is a requirement for blogging here… that’s definitely not the case. I think I can speak for everyone on the staff of MIA when I say that we value Sandra’s perspective — a perspective that is much more thoughtful and nuanced, in my opinion, than “always in favor of enforced psychiatry” — and are grateful that she chooses to share it here. To really change things, we need to be aware of the dilemmas and unintended consequences that may result when people attempt to put principles into practice on the ground, in complex and less than ideal circumstances. And we need to understand how a person’s thinking can evolve over time as they grapple with these issues. I’m glad that Sandra is willing to be so open about her process here, because I think it can serve as a model to others in the field who will hopefully come to change how they practice psychiatry too.
Understood. The arguments here are somewhat one-sided in the sense that what we’re trying to offer on this site is a counterbalance to the monolith of mainstream perspectives on psychiatry. That ground is more than sufficiently covered elsewhere — in fact it’s pretty much all you can find elsewhere — what we’re presenting is an alternate, more critical view. (Or in the case of the comment section, an oppositional view, but the comments do not necessarily represent the site itself.)
I can see how it might come across as something of an echo chamber. Respectfully, I would suggest that the same is likely true of the professional circles you travel in, and that there might be some confirmation bias involved. As one person pointed out in response to your claim that you’d never seen a return to premorbid states — if the prescribed treatments are in fact causing chronicity and iatrogenic illness, as Robert Whitaker argues in his book Anatomy of an Epidemic, and if you only interact with people who prescribe or are prescribed such treatments, might that not be a possible explanation for why you’ve never seen a return to premorbid states? Aren’t you at least curious about how other treatment approaches such as Open Dialogue are able to produce such drastically different results? I would think that the prospect of full recovery would be intriguing to someone who’s devoted their life to helping others, even if it shakes up everything you thought you knew about what was possible.
Although you seem pretty attached to your position and I can understand why others are finding that frustrating, I think that to come here and engage in dialogue with people whose views are so different from your own takes guts, and it suggests to me that your mind is not entirely closed. I’d be curious to see what you might make of books such as Anatomy if you read them.
Sleves, I’m curious — if one of the authors were to donate a book to you, would you be willing to write something about how it influences your perspective, and have that published here on MIA?
We invite anyone who would like to share their reflections on Leonard’s life and work to post them on the special memorial page that was created for him, so that all the remembrances can be together in one online tribute to this man who will be so missed: http://www.madinamerica.com/2015/01/memoriam-leonard-roy-frank/. Some comments that were posted here have been moved to the memorial page. May all find comfort in the wake of this loss, and may his spirit live on in our work.
These are all great ideas! Here’s a link to our submission form if you’d like to suggest any of these songs for Song of the Week: https://www.madinamerica.com/song-week-community-submissions/
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The image was actually created by AI. The prompt I used was something like “oceans of consciousness” if I recall correctly.
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I actually chose the image, as the editor that published the story. The feeling it captured for me was the disorientation and overwhelm of a sensitive person besieged by strange forces and judging eyes all around them, so it felt like a fit with the themes in Odette’s story.
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Your research would make an excellent article as well!
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One resource you could look into is our Provider Directory here on MIA: https://www.madinamerica.com/provider-directory/
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We have options for publishing anonymously (usually with an abbreviated version of the name, and an obscured or otherwise non-identifying photo). If you follow the links to submit a story there’s a checkbox to let us know you need to publish anonymously: https://www.madinamerica.com/submitting-personal-stories/
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As the person who edits the personal stories section I thought I should respond here and clarify a few things.
We do offer the option to publish somewhat anonymously, usually under an abbreviated version of the author’s name (such as their initials, or first name and last initial, etc). Although we try to avoid outright pseudonyms, in some cases we have allowed them, as well as pen names and artist names. On our personal stories submission form, one of the main questions a potential author is asked is whether they need anonymity.
We do ask for an actual photo, but it does not need to be a head shot that shows their face if an author isn’t comfortable with that. It might be a photo taken from a distance, from behind or with their face averted, for example. Or it might be run through artistic filters until it’s no longer recognizable as them (at times I have done this myself, if the author isn’t able to).
Sometimes an author is comfortable publishing with their real name and photo but later on their life situation changes and they need more anonymity. So I will work with them to change the name and photo on their account and scrub identifying details from their story, their bio, and even the comment section if needed. We try to avoid taking down a post altogether, but in a few cases we’ve even done that when an author felt that their safety was endangered by it remaining online.
Maybe these options don’t go far enough – I’m certainly open to ideas about how we might protect people better. But to suggest that we don’t offer any sort of protection is simply incorrect.
Regarding the rest of your criticism, I honestly don’t know what you’re talking about when you say things like “if one truly overcomes the experience, this type of diversity is not allowed.” A great many of the personal stories we’ve published – maybe even the majority – are by people who have come out the other side of their negative experiences and consider themselves recovered.
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The members of our science news team can all be seen on our staff page. Their job is to report on new studies and other developments in psychiatric research each week, which is a valuable service since the public would generally never even hear about such research otherwise. They do a great job and we couldn’t be more proud of them here at MIA.
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This is actually in our “Around the Web” section, which is where we repost articles from other sites.
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Looks like there was an unclosed html tag in Chaya’s bio. I fixed it.
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Hi Surviving and Thriving. We’re definitely open to publishing blogs by people with lived experience of chronic pain. If you’d like to write one, or know someone that might, feel free to get in touch via our contact page.
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fred77, it’s simply not true that survivors don’t get a chance to post or contribute here. Almost all of the personal stories on this site are written by survivors, and many of our regular bloggers (and some of our staff) are survivors as well.
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Hi everyone. We heard from Matt’s sister that it meant a lot to their family to read about people’s interactions with him. She also shared his obit which I will paste here:
It is with great sadness that the family of Matt Stevenson announces his passing on Thursday, September 21st at 32 years of age.
Matt graduated from Marymount University with a degree in English. He then turned his lifelong passion for tennis into a career as a tennis coach. Matt loved coaching and was very popular with his students, especially the children. He was an inventive teacher and created many games to teach his young students new tennis skills through fun activities. Matt also volunteered teaching English to new Americans , and he organized many socials for young people in his community .
Through his struggles with mental health, Matt became passionate about helping others in crisis and working towards a new paradigm for mental health treatment . He pursued this passion through his involvement with several organi z ations , including Mad in America, The International Society for Psychological and Social Approaches to Psychosis (ISPS), and the International Society for Ethical Psychology and Psychiatry (ISEPP).
Matt was an intelligent, thoughtful, and caring young man with a quirky sense of humor. He is mourned and will be greatly missed by his mother Judith, his father Hugh, his sister Catherine, and his many friends.
A service to celebrate Matt’s life will be held on Thursday October 5th, at 7 pm, at the Celebration Center, 2840 Graham Road, Falls Church, VA 22042. All are welcome to the service and reception to follow. As this is a celebration of his life, please do not feel the need to wear black.
For those who wish to contribute, we will collect donations to support the International Society for Psychological and Social Approaches to Psychosis (ISPS), an organization that was dear to Matt’s heart.
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Yes, we will be posting a tribute to Matt tomorrow, now that we have the okay from his family.
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Just to clarify, this change was not implemented due to James and Brett’s feedback — it had already been decided at a staff meeting several days prior. The discussion here about writers leaving due to the comment section just seemed like a good place to mention it.
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Not sure how that would work exactly, with a volunteer doing the same work as paid employees, but we can look into it — I’ll email you.
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We can and do moderate comments that cross a line, but that doesn’t undo their damage when authors have already seen them. The only real solution for that would be to make all comments go into the moderation queue to be approved before they appear, which would result in considerable delays in communication.
No one’s arguing that it’s “the job of readers to provide ‘safe space'” (whatever that means). It’s the responsibility of this organization to manage our website in the way we think is best. And that’s what we’re doing.
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This just goes back to the “thick skin as a requirement to write here” thing. Maybe you can ignore people who are trying to tear you down, but not everyone can or should.
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That would be ideal, yeah. But as you might imagine it can be pretty challenging, and moderating is already very difficult work. We’ve burned through a string of moderators at this point — it requires an even thicker skin than being a blogger, and a pretty specific skill set. It also takes up a lot of organizational resources, which are not infinite.
As for your other question: we do see value in bloggers participating in discussions, and we could make that more clear in our invitations. But we’re not going to make responding to comments a requirement or attempt to persuade writers to do anything they don’t have time to do or don’t feel comfortable doing. They are already participating in the ‘give and take’ by sharing their work here.
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Richard, I’ll reply to your last question as it pertains to me. The role of MIA moderators is ultimately just to remove comments that aren’t in line with our posting guidelines. When I was the moderator I did attempt to mediate between authors and commenters at times, and generally tried to help people understand where others were coming from. So maybe that’s where you got that impression.
As for allowing writers to close the comments, we’ve actually been doing that for some time now, when it was requested, and a few blogs have been published that way. The main difference with the recent decision is that we’ll be offering this as an option rather than waiting for writers to get so fed up with the comments that they request it. This way comments will effectively be “opt-in.” So far, everyone offered the option has opted in, and that will likely remain the case for the most part.
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Many online publications have actually closed their comment sections altogether these days. I think the solution we’ve come up with is preferable and takes the needs of all sides into account.
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Hi Stephen. We won’t be stopping comments altogether, it will be per post and up to the author. I expect that most authors will prefer to keep comments open, but this way they’ll at least have a choice.
By the way, it isn’t just mental health professionals who have issues with the comment section. Writers with lived experience sometimes do too, and it becomes a barrier to participation here.
I hear you on professionals not always being willing to make the effort to see things from the perspective of people with lived experience. But the reverse is also true — people making no attempt to see the good in what a professional is doing, instead bending over backwards to find fault and assume the worst, sometimes missing the point of a blog entirely or reacting to things the writer didn’t even say. Certain topics become a flashpoint for rage, which is certainly understandable, but not always constructive.
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Jim, I just wanted to say that MIA staff share the concerns you and Brett have expressed here. We strive to maintain a space where people can “speak truth to power,” but when such speaking drives people who have power to change the system away from participating in the conversation at all, that goal is undermined, as is our mission to rethink and remake the mental health system. We recognize the difficult position that many ‘dissident’ professionals are in, often risking their careers and facing condemnation from their peers when they break away from the pack, only to be met with a barrage of criticism from the other side for not being radical enough. It’s understandable that some are unwilling to put themselves through that.
There is no easy solution for this problem, really. But we will now be offering writers the option to turn off comments for their posts if they want to share their work and their experiences without facing the firing squad, so to speak. This way, “unusually thick skin” will no longer be a requirement for writing here. We hope that this will broaden the range of writers we can bring in, and also help raise the caliber of comments as people learn that keeping things constructive is the way to keep the conversation open.
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Matt, I’m not sure what you mean by ‘original version’ — this article has not been modified at all since it was published, and it never took the extreme position that some seem to be reading into it.
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If you’re trying to insinuate that this blog was deliberately bumped off the front page to give it less exposure, you could not be more wrong.
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They disappeared somehow when the post was updated and then had to be republished… hopefully our tech guy can retrieve them. 🙁
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Hi LavenderSage. Feedback about the site can be directed to our operations manager Chris Page. You can get in touch with him via our contact page: https://www.madinamerica.com/contact-us/
As for the tagline, we’ve received a lot of feedback about this and will be changing it within the next few days. We’re open to community input if anyone has suggestions about what might be more fitting.
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Hi everyone, I’m stepping in as moderator to say that I won’t be allowing further comments alleging that the authors are promoting any products or companies. Since that allegation has been addressed and rebutted, I consider the matter settled — to continue pursuing it would be to engage in misrepresentation, which is against our posting guidelines: http://www.madinamerica.com/posting-guidelines
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Hi Bill. I’m the comment moderator on MIA. It looks like you may have posted your comment on a different page — is this the one you mean? http://www.madinamerica.com/2013/11/about-mad-in-america/#comment-85267
I’ll give Bob a heads up that you’re looking for a reply. You can also contact him or other staff via the contact page: http://www.madinamerica.com/contact.
Thanks for your work in helping get these ideas out there! The Holistic Mental Health Network you mentioned sounds very promising.
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I fixed the ProPublica link, thanks for the heads up. Not sure about the other one so it’s removed for now.
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Fixed — thanks Donna.
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Joel might be disappointed to learn that the delay had nothing to do with a conspiracy to suppress dissenting viewpoints, but was simply a matter of the “editorial woman” (as he put it) being busy that day.
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Fixed the link, thanks for the heads up.
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Hi Oldhead, here’s the address for our office (you can also find it on our contact page):
Robert Whitaker, President
Mad In America Foundation
763 Massachusetts Avenue,
Cambridge, MA 02139
Checks can be made out to Mad in America Foundation Inc. Much appreciation for your support!
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“Hardly ever”? Are you not aware that the comment section you wrote this in is a space created for precisely that purpose — for people with experience of the labels and the drugs to say what they think about it? And that our forums also serve that purpose? And our entire Personal Stories section, and a number of our blogs? Inclusion and amplification of the survivor voice is a key part of the mission of this organization that Robert Whitaker started, so your criticism seems pretty misplaced.
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Folks, the comment section is for discussing the issues raised in the blog posts, not for ad hominem arguments (no matter how true they might be) and slinging insults at other commenters. I realize the discussion started out with something of a provocation, but we need to keep it clean and stick to the issues. It’s unfortunate that some comments making valid and important points also contained personal attacks and had to be removed.
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Would something like “chance” be preferable to “risk”? If you have more suggestions about less-problematic wording, I’m sure that Justin would welcome you getting in touch with him via the contact page. We’ve discussed some of the responses to this news item and what efforts we could make to address the concerns. It’s challenging to make everyone happy with word choices, especially when reporting on studies that use diagnostic terminology (as many of them do). And we do need to report on studies like these, because people have a right to know how the drugs they take may affect the fetus they’re carrying.
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People do not actually have to support any particular cause to post comments here. Critical voices are welcome too.
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The article is about an app, and this discussion about the author’s stance on ECT is basically off-topic and ad hominem. I don’t want to suppress legitimate criticism, and criticism of ECT is certainly legit, but the comment section is not an open forum for the character of authors to be put on public trial every time they write a post.
As for authors responding to comments, it’s true that many do and this is definitely appreciated. But they’re under no obligation to do so. Like it says in our posting guidelines, “A person’s choice not to acknowledge or respond to specific arguments will not be assumed to be malicious, or a sign of a character flaw, or otherwise held against them.”
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Fixed — thanks Chuck, good catch.
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Hi folks, a friendly reminder: http://www.madinamerica.com/posting-guidelines/
Some of these comments are getting pretty personal — which is not to say they’re not making valid points, but with so much to discuss regarding the Murphy bills and the systems of power behind them, I hope the conversation can focus on that rather than on individuals in the comment section.
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Snowyowl and Oldhead, please feel free to get in touch with more details about your ideas. I’m not sure what you’re envisioning — something like a temporary content block on the front page where content related to the Murphy bill would be gathered?
I need to clarify that MIA as an organization can’t create such content ourselves or advocate for or against specific legislation. It’s just not our role — but as Leah pointed out, it is the role of other groups, and they’re doing a good job taking the lead on that.
So my suggestion for you would be to come up with a plan for where the content would come from, and then we can talk about where it would fit on the site. We’ve already published a number of pieces related to the Murphy bill and more are certainly welcome.
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While I’m not interested in silencing anyone, as the moderator of this website I need to be clear that this is a trans-inclusive space. Everyone’s unique perspective is welcome, but we can’t allow comments that are oppressive to marginalized groups — which includes cisgender women, transgender women and all trans people. So this is not the place for the ‘who qualifies as a woman’ debate, and I ask for everyone’s cooperation in keeping this space as oppression-free as it can be.
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Oldhead: yes, of course. “Rethinking” is pretty broad and can encompass calls for abolition as well as reform. I’m sure you’re aware that the people who blog on MIA come from a variety of perspectives on that.
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Jonathan: I don’t want to derail the conversation from Sera’s post too much, but as a member of the MIA staff I’d like to address the concerns you brought up here. We are very much interested in bringing more diversity to the group of writers on the site. While most of our writers have come to us, we’re putting a plan in place to do more active outreach to potential writers in underrepresented groups. There’s a lot of energy around this right now, so hopefully you’ll be seeing some changes soon.
Of course, the challenge for any organization or project that wants to become more diverse is to reach out in ways that are respectful and non-tokenizing. And the challenge for us at MIA is to find people who are specifically focused on “rethinking” psychiatry. If you have any suggestions for people we could be reaching out to, please feel free to get in touch with me via the contact page.
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Fixed: the end tag just needed a / to turn the italics off.
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Fixed the links, thanks for the heads up.
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Adventures in editing! I kind of want to change it to CZ now just for fun…
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That was my fault — sorry for the confusion. It’s fixed now. 🙂
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Added.
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Hi folks. A friendly reminder: http://www.madinamerica.com/posting-guidelines/
I’ve removed a number of comments that I felt were needling, baiting, personally attacking etc. I realize there’s a fine line sometimes between legitimate criticism and sniping, but I hope people can try to keep the critique civil, constructive and non-personal.
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They’re linked to text in the post, for example, “very lively demo” links to Chile’s video. Feel free to email me if you’re still not seeing them.
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Update: I added a bunch of links to the post, if folks want to check out more photos, video, interviews and reports about the protests.
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For me it was computer games! A few years back there was some research suggesting that focusing on highly engaging visual-spatial tasks can prevent the symptoms of PTSD, makes sense that it would help with anxiety too: https://www.scientificamerican.com/article/tetris-shown-to-lessen-ptsd-and-flashbacks/
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Bernadette, as the moderator of this site I’m not sure what you’re talking about when you say “trying to silence varying points of view.” If you’re referring to editorial policy regarding what stories are published, obviously there’s a focus on “rethinking” or taking a critical view toward psychiatry since that is this organization’s mission. There’s no shortage of pro-psychiatry views elsewhere (in fact, they heavily predominate) so it would not make a lot of sense for this site to merely echo what can be found pretty much anymore else.
If you were referring to the comment section, I’d like to clarify that we do not moderate comments based on a person’s position on psychiatry — there is no “censorship” of pro-psychiatry views.
We do, however, moderate comments according to our posting guidelines, which are mainly concerned with civility and being on topic: http://www.madinamerica.com/posting-guidelines/. Please note that discussion of moderation in comment threads is generally considered off-topic, however, if you have concerns about site moderation you can contact me or any staff member directly via the contact form, or leave feedback in our feedback forum: http://www.madinamerica.com/forums/forum/feedback/
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Fixed, thanks for the heads up!
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I don’t think it’s accurate, or appropriate, to call it “race baiting” when people talk about racism and violence against people of color. Used in that way, the term is an attempt to deny the reality of racism and shut down conversations about it.
Similarly, expressions of outrage about property destruction/riots often amount to denials of the legitimate reasons the unrest is occurring, or they mask the sentiment that inanimate objects somehow matter more than the lives of black people. http://phillynow.com/2015/04/28/why-your-friends-criticizing-the-baltimore-riots-are-either-ignorant-or-racist/
These are all expressions of racism, conscious or otherwise. I want to be clear that racist views are not welcome on this site — they contribute to the harm and oppression of people, and that’s the opposite of what we’re about.
My request for everyone taking part in these difficult but important conversations: if the issues of racism or racist police violence don’t impact you personally, if they’re invisible to you (much as psychiatric violence is often invisible to people who haven’t experienced it), I ask that you make an effort not to disrespect or minimize the struggle of people whose lives are impacted, every day, sometimes in deadly ways.
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Another way to frame the difference is power vs authority: https://www.youtube.com/watch?v=S0Rj4mMMSYI
What’s the difference between power and authority? The workers who perform the labor have power; the bosses who tell them what to do have authority. The tenants who maintain the building have power; the landlord whose name is on the deed has authority. A river has power; a permit to build a dam grants authority.
There’s nothing oppressive about power per se. Many kinds of power can be liberating: the power to care for those you love, to defend yourself and resolve disputes, to perform acupuncture and steer a sailboat and swing on a trapeze. There are ways to develop your capabilities that increase others’ freedom as well. Every person who acts to achieve her full potential offers a gift to all.
Authority over others, on the other hand, usurps their power. And what you take from them, others will take from you. Authority is always derived from above.
In this society, power and authority are so interlinked that we can barely distinguish them: we can only obtain power in return for obedience. And yet without freedom, power is worthless.
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Just wanted to link Bob’s reply here: http://1boringoldman.com/index.php/2015/04/28/just-stop/#comment-261509
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I also really like the idea of presenting material from fact-heavy, academic books in more condensed and maybe unconventional forms, like in the blog Jessica linked above, or like this Rat Park comic: http://www.stuartmcmillen.com/comics_en/rat-park. Sometimes you just have to meet people where they’re at, and those pop culture forms can be more accessible to a broader range of people. But once you pique someone’s interest with some kind of “teaser” they might be more inclined to read the book. Ever since I read Anatomy I’ve been wishing there was some kind of Cliff’s Notes version of that book that I could hand out to everyone I know. Of course, authors should be fairly compensated for their hard work and it could be problematic to undercut that, but ultimately I think that getting the info out there is the most important thing.
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This comment thread has gotten pretty sidetracked — I’m hoping we can bring it back to the topic of book activism. In her concluding remarks Bonnie asked readers to share suggestions about how best to do book activism, and one thing I thought of is audio books. A lot of people lack the time or attention span to sit down and read a book, or the money to spend on books about topics they’re unfamiliar with or skeptical of, but might download a free audio book and listen to it while driving or doing things around the house etc.
Looks like they’re pretty easy to make: http://www.makeuseof.com/tag/how-to-record-your-own-audiobook. In fact, I’ll volunteer to try it out and make one, if any authors want to send me a book? I actually used to record audio books for kids when I was little, at the request of my school library (I guess because I was such a good reader) — it might be fun to do that again.
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I’m stepping in as moderator to point out that this comment thread is on a blog post about book activism. These side conversations may be interesting but they’re also off-topic — if anyone would like to continue them, please take the discussion to our forums so this comment thread can get back to the topic of book activism.
http://www.madinamerica.com/forums/
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Jeffrey, yes, I am asking you to add a valid email address to your account, because that is a requirement for posting comments here. I am not going to continue to discuss moderation issues in the comment section — that’s not what the comment section is for.
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Jessica, I love the idea of presenting the information from Anatomy of an Epidemic in a pop culture context with humor and pictures like you’re doing. It could help make that information more accessible to people who haven’t read the book and might not understand why it’s important. Very cool!
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He’s on facebook, and it looks like his page is set up to allow people to post to it (posts appear in the “POSTS TO PAGE” section on the sidebar, under Photos).
Just saying. 🙂
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Where the line is drawn at MIA is described in our posting guidelines: http://www.madinamerica.com/posting-guidelines. Please note that registering with a valid email address is a requirement, and that discussion of moderation in comment threads is considered off-topic and may be removed.
I’m not going to go into what the problem was with the removed comment, but discussion of issues of justice was not it.
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Hi Jeffrey — please get in touch with me via the contact form, I’m unable to reach you at the email address you signed up with.
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Hi everyone. Due to an increasing number of comments that attacked persons rather than practices, comments for this post are now closed. There can be a fine line sometimes between discussing practices and discussing their practitioners or proponents, but that’s the line we’re trying to maintain here (perhaps a bit clumsily in this instance, and I apologize for that). We’re interested in providing a platform for the hazards of all psychiatric practices to be thoroughly discussed, not for people in the movement to be raked over the coals, because in the end, despite our differences on certain issues, we’re all part of the same fight. And so, with respect for the passion, insight and devotion to the cause that everyone brings, we ask for your understanding as we close this comment thread.
In solidarity,
Emmeline
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Kermit, thank you for this. I recognize that for many this site is a kind of sanctuary from the status quo, so it’s understandable that people might resent the status quo showing up on our doorstep. But I believe as you do that this can and should be embraced as an opportunity — after all, shifting the dialogue to bring about change is essentially the whole point of what we’re doing here.
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Friendly reminder: http://www.madinamerica.com/posting-guidelines/
I’d like to ask that people please refrain from labeling pro-psychiatry newcomers as “trolls.” If someone is in fact here to troll rather than dialogue, they will eventually make that clear through their pattern of behavior and it will be dealt with by the moderator (me). In the meantime, let’s try to give people the benefit of the doubt.
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Hi there, I’m sorry you felt ignored! I just saw your question in the forums and replied to it there. Not sure what happened with your attempts to contact folks, but I know we all get a lot of email and occasionally something might slip through the cracks.
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It’s still there at http://www.madinamerica.com/contact/ — under “Select message recipient” there’s a drop-down box, click the arrow and a list of names should appear.
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I’d say it’s to a person’s credit if they rethink an initial off-the-cuff response and come back with a more measured and thoughtful reply that offers someone the benefit of the doubt, as AA did. It’s a shame you couldn’t respond in kind.
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It’s a link to a change.org petition to the UN Committee on Human Rights. Here’s the full link: https://www.change.org/p/the-un-committee-on-human-rights-we-demand-to-recognize-psychiatric-coercion-as-the-crime-against-humanity-and-on-this-basis-to-exclude-it-from-acceptable-in-the-human-community-measures?just_created=true
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Link fixed! Thanks for the heads up Madmom. Carina, your webpage is beautiful and it’s so exciting that you’re doing this festival! I wish I could go there, but I’ll hold out hope for Eugene.
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LoveLife that’s so great that your husband is supporting you in your decision! One resource I would recommend is this guidebook you can download, it’s helped many people get started in their journey to come off psychiatry drugs: http://willhall.net/comingoffmeds/
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You’re so not the only one! The trajectory of your story is unfortunately very common, with negative reactions to SSRIs being labeled as “bipolar,” resulting in more drugs and worse reactions until everything spirals out of control. But many of us were able to stop that cycle and find our way out — I hope that you can too.
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B: There hasn’t been a rule prohibiting it. Looks like we’ll have to add one, since it’s been used as a way to get out of moderation on a moderated site. I like to give everyone the benefit of the doubt, and many chances to understand what the boundaries are and try again, but after a certain point if a person is just not willing (or maybe able?) to respect the boundaries of a space, they can’t be in it anymore.
If anyone has more questions or feedback about what is or is not allowed on the site, please feel free to get in touch with me via email or using our contact form.
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Alex, what I’m hearing is that certain needs might not be met by this discussion platform. I want to acknowledge that those needs are real and valid, while also acknowledging that this platform has been created for a specific purpose, and people are free to choose for themselves whether it meets their needs or not.
My feeling is that if healing or emotional safety are what a person seeks, the comment section of a blog site might not be the most likely place to find them. There are inherent limits to text-based internet communication. There are inherent hazards in debate, and (especially) in interacting with people who represent a role that you’ve been harmed by (such as psychiatric survivors interacting with psychiatrists). It can all feel very draining or even triggering. Ultimately a person needs to weigh those risks for themselves and make their own decision about whether it feels worthwhile, constructive or healthy to participate in such conversations. That is the responsibility of the individual.
Of course, the creators of a space also have responsibilities. While I personally believe that emotional safety and the internet are mutually exclusive to some degree, I also believe it’s important to be thoughtful and aware of the risks and make a good faith effort to mitigate harms. I think we do make that effort.
What I’m hearing is that for you, and maybe others, it’s not enough, or there’s a need for a space that’s very different than this one. I hope you can find that space, or create it if it doesn’t exist. Recently I’ve been hearing talk among survivors about creating a survivor-led (and maybe survivor-exclusive) space for discussion, support and information sharing. I think that would go a long way toward meeting some of the needs you identify, and would be a good complement to what we’re doing here. But in terms of empathy, I believe that face-to-face connection is more likely to facilitate that than anything that could ever happen on the internet.
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I think a list like that would make a great blog post, if you’re ever interested in putting one together…
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If you would like to draw attention to published research, please do so in a comment that is free from personal attacks and within our posting guidelines for the site: http://www.madinamerica.com/posting-guidelines/
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Moderator chiming in, but first I would like to point out that discussion of moderation in comment threads is in most cases considered off-topic to the blog posts. Readers are encouraged to use the report button for problematic comments, or contact us directly for feedback on moderation or editorial decisions: http://www.madinamerica.com/posting-guidelines/. I’m pointing this out because by sharing my perspective there’s a risk of sparking a debate about whether a moderation issue exists here or not, and I don’t want the conversations about the issues discussed in Richard’s or Timothy’s posts to be derailed.
That said, my perspective is that I don’t see persons being attacked here. I see ideas being criticized. I think it’s okay for Richard to write about how he thinks Timothy missed the mark, just as it was okay for Timothy to write about how he thinks Robert Whitaker missed the mark. I’m quite certain that both authors understood that their viewpoints would stir the pot and generate controversy, but I feel that they’re attempting to engage in respectful debate (and for the most part succeeding, although both occasionally used terms such as “dogmatic” or “absurd” to describe positions they disagree with).
I view the resulting discussions in the comments similarly — while there are very strong feelings around these topics, and some pointed critiques, I see an effort to keep it civil and largely non-personal.
I do think it’s important for people working as clinicians or counselors etc to be mindful about how they address people with lived experience, though. While there’s no power differential among authors on this website, there can be one in the roles people represent.
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Excederin, please take a moment to review our posting guidelines for the site: http://www.madinamerica.com/posting-guidelines/. Personal attacks are not allowed, and “armchair diagnosing” is a personal attack, regardless of how enamored with diagnostic labels one might be. Since Steve’s replies have been instructive, I will allow your comment to remain for context, but any further attacks or baiting will be removed. If you are unable to keep your comments within our guidelines, this may not be the right conversation environment for you.
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ps: blakeacake, please get in touch with me via our contact form. I have attempted multiple times to contact you regarding moderation issues and the emails have bounced, as I’ve mentioned before.
Edited to address your questions: yes, your contact info will be kept private and confidential, and no, nobody needs to “divulge personal, protected medical information to MIA” in order to post here. You do need to have a valid email address that you can be contacted at. Comments that are not within our posting guidelines will be removed, and anyone posting a high volume of such comments will be placed on moderation. More information about our policy can be found here: http://www.madinamerica.com/posting-guidelines/
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As someone who once was given a diagnosis of adult ADD (no h, and I am not endorsing the diagnosis by mentioning it), I can say that diet changes made all the difference for me, particularly eliminating gluten and dairy. It was something I figured out on my own in college — I’d be working on a paper and take a break to eat pizza or pasta or something, and come back to find that I could barely even follow what I’d written. I also avoid artificial colors and sweeteners, MSG, soy and various other things. It helps.
I should note that I never had any attention or concentration issues as a child though. It wasn’t until I’d been on psych drugs (“antidepressants”) throughout my teen years that the issues developed, so they might be iatrogenic in origin. But having this basis of comparison, I do know that there’s a difference between being bored with a topic, and finding that your brain simply. will. not. work. when you try to focus on something. It’s incredibly frustrating. Occasionally I still experience this when stressed or overwhelmed, but I’ve learned various techniques for getting things back on track. Sometimes it’s as simple as taking a break to play a computer game or watch a relaxation video. Therapy and journaling can help too, because it’s certainly more difficult to attend if you’re struggling with some kind of chronic internal war like Dr. Berezin talks about in his post.
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No worries! I do look pretty different without the glasses.
My title is community manager, which basically means moderator for the website. That’s why I tend to weigh in on issues like this, but for the most part stay on the sidelines of the discussions.
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My feeling is that if someone is truly here to disrupt, not to dialogue, they will eventually make that abundantly clear through the pattern of their behavior, and when they do it will be dealt with. But I would like to set a high bar for designating people as “trolls” in this space, and ask that we try to give the benefit of the doubt. Not just because this is the respectful thing to do, but because one of our goals here is to contest and counter mainstream thought about psychiatry, and as such we should expect opposition from those adhering to the status quo. Ideally, we would be prepared to address or rebut their arguments.
Of course, no one (including site authors) is obligated to respond to anything they aren’t interested in, don’t have the patience for or find pointless or baiting. I’m just saying that, generally speaking, when someone challenges our views they offer an opportunity — the opportunity to strengthen our case. Such a person can serve as a useful “foil” in a way. Maybe not useful for ourselves so much as for the thousands of unique visitors who read this site every day and may be encountering these challenges to the status quo for the first time.
Just something to think about. I realize that it’s generally more enjoyable and interesting to have conversations with like-minded people who’ve put a lot of thought and study into these topics, but there’s a bigger picture to keep in mind too.
“First they ignore you. Then they laugh at you. Then they fight you. Then you win.”
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Thank you for sparking such an important conversation. Maybe you could explore the topic of loosening polarizations in a future post? I’d be curious to hear your ideas about that. My feeling is that building coalition around points of unity, while respecting differences on certain issues, will make our movement(s) stronger and more effective without compromising any principles.
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I’m not sure what you’re getting at, and am not interested in getting embroiled in a debate with you, but to answer your question I don’t really watch television. I do read articles from a wide variety of sources, but am more likely to read those that take a more critical perspective than the “featuring the wonders of a drug” point of view you describe.
I read this today and found it quite interesting: http://www.theblaze.com/contributions/adhd-definitely-doesnt-exist-but-if-it-did-i-would-have-it/
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Very good point about the use of diagnosis and “treatment” as a means of blaming the victims of oppression, not to mention effectively compounding it by decreasing likelihood of recovery — which as B pointed out, can make it more difficult for people to fight against the oppression they face. This is a key intersection that people committed to anti-oppression work should be grappling with, not deflecting.
I see it as one of the keys to rethinking psychiatry too. We need to focus on the harms and the alternatives but also the root causes of the experiences that get labeled and drugged. So in that sense I very much agree with the author’s call for a focus on structural violence, which obviously is a huge source of trauma, but disagree that the issue of psych drugs can or should be detached from this. Similarly, I agree with “loosening up polarizations” but disagree that “shifting attention from debates about [psych drugs]” is the way to go about it.
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Blakeacake, you’re certainly free to share your opinions (as long as they’re within our posting guidelines for the site). I was pointing you toward resources where you might find the proof you say you’re looking for, and suggesting that that might be a more productive use of your time than trying to demand proof from people who may not be interested in (or have the patience for) engaging with you.
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Robert, I’m sorry, I should have put the name of who I was addressing my comment to — I was referring to the commenter Blakeacake singing their praises, not you! Much appreciation for your approach toward psychiatry. I’ll edit my comment so it’s more clear.
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Ted, I’m not sure what you mean by “no encouragement” from MIA for the involvement of psychiatric survivors in our own liberation. We recently added an Organizing for Social Change forum at the request of psychiatric survivors: http://www.madinamerica.com/forums/forum/organizing-social-change/. This comment section itself is also a form of involvement, which psychiatric survivors regularly avail themselves of, as you know. Since resources are devoted to the very thing you say we aren’t encouraging, I don’t really understand your assessment (maybe you’re just talking about the number of survivors among the mix of bloggers?). At any rate, if you have ideas for more ways that involvement of survivors could be encouraged, please feel free to share them with us. I think we’re all open to hearing them — I know I am.
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Blakeacake, I can understand how disorienting and off-putting these conversations might feel for you. After all, you’re encountering a new and unfamiliar perspective that calls into question everything you know. Meanwhile you’re trying to share your own perspective, but it isn’t a new one for the people you’re conversing with — they’re already familiar with it, and have strenuously rejected it.
If you’re interested in learning more about this new perspective, my advice would be to seek sources of information that state the case in a calm and objective manner, rather than attempting to sing the praises of psych diagnosis and drugging to people who have been harmed by diagnosis and drugging. One place to start would be right here on this site, in our archives: http://www.madinamerica.com/news-archives/all/adhd/
We also have a new search function: http://www.madinamerica.com/?s=adhd
Best of luck to you. And ps: please make sure that the email address you’ve signed up to the site with is a valid one (I attempted to contact you about a moderation issue and the email bounced).
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I’m not entirely certain what you mean by users (readers? commenters?) but it almost sounds as though you’re suggesting that their agreement is a requirement for blogging here… that’s definitely not the case. I think I can speak for everyone on the staff of MIA when I say that we value Sandra’s perspective — a perspective that is much more thoughtful and nuanced, in my opinion, than “always in favor of enforced psychiatry” — and are grateful that she chooses to share it here. To really change things, we need to be aware of the dilemmas and unintended consequences that may result when people attempt to put principles into practice on the ground, in complex and less than ideal circumstances. And we need to understand how a person’s thinking can evolve over time as they grapple with these issues. I’m glad that Sandra is willing to be so open about her process here, because I think it can serve as a model to others in the field who will hopefully come to change how they practice psychiatry too.
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Understood. The arguments here are somewhat one-sided in the sense that what we’re trying to offer on this site is a counterbalance to the monolith of mainstream perspectives on psychiatry. That ground is more than sufficiently covered elsewhere — in fact it’s pretty much all you can find elsewhere — what we’re presenting is an alternate, more critical view. (Or in the case of the comment section, an oppositional view, but the comments do not necessarily represent the site itself.)
I can see how it might come across as something of an echo chamber. Respectfully, I would suggest that the same is likely true of the professional circles you travel in, and that there might be some confirmation bias involved. As one person pointed out in response to your claim that you’d never seen a return to premorbid states — if the prescribed treatments are in fact causing chronicity and iatrogenic illness, as Robert Whitaker argues in his book Anatomy of an Epidemic, and if you only interact with people who prescribe or are prescribed such treatments, might that not be a possible explanation for why you’ve never seen a return to premorbid states? Aren’t you at least curious about how other treatment approaches such as Open Dialogue are able to produce such drastically different results? I would think that the prospect of full recovery would be intriguing to someone who’s devoted their life to helping others, even if it shakes up everything you thought you knew about what was possible.
Although you seem pretty attached to your position and I can understand why others are finding that frustrating, I think that to come here and engage in dialogue with people whose views are so different from your own takes guts, and it suggests to me that your mind is not entirely closed. I’d be curious to see what you might make of books such as Anatomy if you read them.
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Sleves, I’m curious — if one of the authors were to donate a book to you, would you be willing to write something about how it influences your perspective, and have that published here on MIA?
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So whoever disagrees with you is cognitively incapacitated? Interesting theory. 🙂
This would probably be a good time to offer a friendly reminder about our posting guidelines:
http://www.madinamerica.com/posting-guidelines/
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We invite anyone who would like to share their reflections on Leonard’s life and work to post them on the special memorial page that was created for him, so that all the remembrances can be together in one online tribute to this man who will be so missed: http://www.madinamerica.com/2015/01/memoriam-leonard-roy-frank/. Some comments that were posted here have been moved to the memorial page. May all find comfort in the wake of this loss, and may his spirit live on in our work.
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Rest in peace, courageous fighter.
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