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- Penny Positive #79
- The Springtime Crazies
- It’s My Life…And I’d Like To Make A Return
- Stranded By Dollar Signs
- Workshop 2
Daily Archives: April 9, 2017
At first you don’t even realise what is wrong with you. Overcome with a cold shudder, accompanied by fluttering palpitations, palms sweaty and confusion. Utter confusion. You can’t move. But hold on, 5 minutes ago you were fine? But now,…
Daily Prompt – Heal The word “heal” can take on a whole different meaning when you have a chronic illness. I remember the first thing they told us at my pain management program was “We are not here to take … Continue reading
Daily Prompt – Heal The word “heal” can take on a whole different meaning when you have a chronic illness. I remember the first thing they told us at my pain management program was “We are not here to take … Continue reading
When you’re facing bipolar disorder – which is, when you have it, nearly every day – there are some things you can do to lessen its hold on you. But in order to do so, you’ve got to have the right tools. Try to collect as many as possible for best effect.
The Usual Suspects
- medication – to tame your symptoms, level your moods, get your brain back in gear, and/or regulate your energy
- psychiatrist – to prescribe your medications (a primary care physician may also do this)
- psychotherapist – to discuss with you the issues you haven’t resolved, the problems you still have, and the things the medication can’t do
The two most important tools you need for self-care are sleep and food. Without either, the body can’t function properly, and if the body doesn’t function, the brain is less likely to function properly either.
Ideally, the food should be nutritious and eaten regularly, but let’s face it, that doesn’t always happen. But you’ve got to give your body something to run on. If there are carrot sticks there, eat them; if there is mac-n-cheese, eat that. If there’s Raisin Bran, well, it’s easy to eat and requires no preparation. Try for at least one substantial meal per day – two is better, if you can manage it.
(Of course, this advice doesn’t count if you have an eating disorder. In that case, see your doctor or psychotherapist or support group.)
Find support where you can – a friend who’s willing to listen, a support group online or in real life. Try for a combination of these and don’t rely on any one of them for too much. Maybe you have a friend you can phone once a week; a support group that meets every two weeks; and an online group or two of people who really understand, with links to helpful articles and blogs. Before you know it, you’ve got a support system, especially if you count your therapist (which I do) or have a supportive family (which I don’t).
If you don’t know what this is, see https://butyoudontlooksick.com/articles/written-by-christine/the-spoon-theory/. Basically, Spoon Theory is a way to measure how much energy you have on any given day – and an understandable metaphor for explaining your symptoms to others, and a shorthand for other people who are also up on the theory. It can also help alleviate the guilt of not being able to do all the things you are “supposed” to do in a day. It’s not an excuse, but an explanation.
Let’s face it, it’s all too easy to dwell on your symptoms and how miserable you are. And if you’re at the bottom of the depressive well and your meds haven’t kicked in yet, there may be nothing you can do about it.
But maybe there is. Do you know a person who tells good jokes – or really bad ones? Do you have music you used to play but have forgotten about? Do you know of a TV show that features people whose lives are an even worse train wreck than yours? Do you have a go-to movie that never gets old no matter how many times you see it? (Mine is The Mikado. )
If that distraction involves creativity, so much the better. Coloring books and pages for adults have been the trend for a while now. (Some of them are really for adults.) Jenny Lawson draws and also puts together tiny little Ferris wheels. I know someone who can make little sculptures out of drink stirrers or paper clips. The point is, you don’t have to paint masterpieces. Just keeping your brain and your hands occupied is a good idea.
Soft warm, fluffy things and smooth, silky things are soothing. They just are. Cats and dogs come instantly to mind (they also provide distraction). But I also have a collection of teddy bears and other plushies that I sometimes cuddle with. These are “comfort objects,” which is an actual psychological Thing. (I wrote about them once: http://wp.me/p4e9wS-k9.) I even took a plush bunny with me when I went to have a sleep study.
This may be the most important tool of all. Be stubborn. Take those meds, even if you hate them. Eat that egg, even if you don’t feel like it. Go to that appointment, even if will take all your spoons for the day. Call that friend, even if you don’t think a joke will help. Post on your support group, even if you feel you are alone.
We can’t let bipolar disorder beat us. Not when we’ve got so much to beat it back with.
Filed under: Mental Health Tagged: being overwhelmed, bipolar disorder, coping mechanisms, creativity, depression, friends, mental illness, mutual support, my experiences, Spoon Theory, support systems
“The Holmes side is … crawling with spies. The Mycroftian branch … spends so much time undercover, they never travel anywhere without a duvet.” – Dr Margeurite “Daisy” LeStrade, from “Sherlock Jones & the Hound of the Basingstokes”.
Today’s tune is “A Cup of Brown Joy,” by Professor Elemental. Because you can’t get much more Steampunk, and jolly, than this. Plus, I love tea:
Dressing up at a Steampunk, Doctor Who, Cosplay, etc, convention, can be a way of letting our child-self out to play, in a safe environment. Safe, because we’re surrounded by other people who are also playing in the same colourful sand pit. Plus, our play time is limited: just for that day, that weekend, that week.
Alternatively, are adults who dress up seeking ways of covering up the grief of living? Of gift wrapping our fear of mortality, and loss?
If you’re wondering where the bit about grief came from, in a blog about creating a Steampunk character, and her costume, well, join the club. I was planning to chat about my initial steps to put together a costume for myself to use at several Steampunk festivals this year. Here’s what I’ve got for Doctor Daisy LeStrade so far:
I also have a handkerchief I carried at our wedding, and which no lady would be without (because, otherwise, she cannot properly deal with a touch of catarh):
Someone who knows me well, or just follows this blog, will know I’ve had a long(ish) running interest in Steampunk. I love colour, creativity, and people having a good time in ways that doesn’t harm anyone, including themselves. And Steampunk has this in teacups, with an added emphasis on manners. I’ve attended at least two, more likely three, of the Doncaster Steampunk conventions. Cross fingers, Dr Daisy and her costume will be making their debut at this year’s, which is on 8 July.
My amateur photographer side – very amateur – is thrilled at the thought of taking photos of people in full Steampunk attire in such a lovely old Georgian building. Sadly, it looks like my hopes of having a stall with other writers is unlikely, as the trade off for such a historic location is fewer stalls than usual. So it looks like myself, my writer friends, & Dr Daisy are going to have to find another convention(s), if we want to sell books.
Those books include my upcoming collection, “A Yorkshireman in Ohio”, as well as “Koi Carpe Diem”. Both include stories about Sherlock Jones, and his cousin Daisy, as well as artwork by the magnificent Tom Brown.
For the time being, though, all that’s going to have to wait, as I sort out my US taxes. It’s not something I like doing: indeed, it’s a major trigger for my mental health, which is a bit wonky just now. Has to be done, though. Still, it’s a beautiful day here in Donny, so at least I can escape to the garden, if and when things get a bit difficult.
Whatever you decide to do with your sunny Sunday, I wish you joy, and peace.
Tagged: A Yorkshireman in Ohio, Boswell Badger, conventions, cosplay, Daisy LeStrade, Doctor Who, Doncaster, fiction, grief, Koi Carpe Diem, loss, mental health, Professor Elemental, Rewind, Sherlock Holmes, short stories, short story collection, Steampunk, taxes, tea, Tom Brown, triggers, writing
(GUEST POST) This piece is brought to you by the lovely guest author and writing/publishing/feminist extraordinaire, Alaina Leary, who interviewed me for this piece. If you’ve ever wondered who the heck I am or where I came from, these (super thoughtful!) questions are a great introduction. I cried a lot while answering. Which will surprise absolutely no one.
As a disabled and transgender writer, Sam Dylan Finch is passionate about amplifying the voices of marginalized people, as well as drawing from his lived experience to educate and empower.
Currently, Sam is an editor at RESIST and Social Justice U, and the founder of Let’s Queer Things Up!, a blog exploring the intersections of queerness, feminism, and mental illness. His work has appeared in the New York Times, Huffington Post, Everyday Feminism, The Establishment, Rewire, and many more.
I’ve been following Sam’s work since around 2015, and have watched him talk about mental illness, trauma, recovery, transitioning, gender identity, and feminism on multiple public platforms. I’ve been fortunate to work with Sam in a few professional capacities and have had the pleasure of getting to him know on a personal level, which is an absolute joy, because he radiates the same love and light in his everyday life that he does in his work.
I had a chance to ask Sam some questions about writing, activism, and being radically vulnerable in his work.
AL: How did you get your start in writing and activist work?
SDF: I’ve always been writing, but I actually have been blogging since I was 13 years old! Back in the day, we had Freewebs and shitty graphics and used the font “terminal” a little too much. (laughs)
I’ve loved blogging for all these years. As a mentally ill and queer youth, being “seen” was extremely powerful, and was critical in my survival. It was the ultimate way to take up space in a society that didn’t otherwise offer me that visibility or validation.
As for my activism, it really began when I was participating in a walk to raise awareness about mental health with NAMI (National Alliance on Mental Illness). I think I was 18 years old at that point?
I was so excited to be visible as a mentally ill person for the first time. But I quickly noticed that the stigma persisted, even there. People signed into the walk with fake names. When cameras flashed, they ducked out of the way or hid behind posters. When the news crews came, many people scattered or ran away.
It was my first real political action of any kind. These were my people, my community. And even in that space, people were afraid. Terrified. Afraid of losing their jobs, afraid of being recognized by family and friends and colleagues, afraid of being seen. And I thought, “This isn’t right. This isn’t the kind of world that I want for mentally ill people.”
Not everyone can be visible. But whatever the personal cost, I promised myself that day that I would be. I haven’t looked back.
AL: A lot of your work has followed your journey—transitioning, being diagnosed with mental illnesses, dealing with your recovery. What has it been like to share yourself so vulnerably and honestly in your writing?
SDF: Recently someone messaged me and told me that, because I’d written so openly about my psychiatric hospitalizations, they had found the courage to admit themselves and get help.
So whenever the trolls try to tell me that no one cares about what I have to say, I remember how it felt to get that message – to know that this person was safe that night and that I played a part in that. Even if this one person was the only one that cared about my words, their survival is worth it to me. (pauses) Their life is worth that much.
Being so honest in your writing can be scary. It opens you up to criticism and hostility that can wound the most tender parts of you. But it’s also an incredible process, because I get to remind folks that they aren’t alone in their struggles, and in return they remind me that I’m not alone, either. We build community. We build connection. We build strength. We build safety.
Society wants marginalized people to believe that sharing their stories is playing a card, playing the victim, or telling lies. But I believe that being visible as mentally ill and transgender has helped illuminate some important truths. And I hope that it’s made folks in my community feel held and affirmed along the way. I honestly can’t think of anything I’d rather be doing.
AL: What has your journey with intersectional feminism been like? Tell me a little about how you came to find feminism and embrace it.
SDF: I found feminism in college. (laughs) Cue all the groaning about those damn “liberal arts” schools. I double-majored in Anthropology and Women’s & Gender Studies, and that radicalized me. When I realized that my personal struggles were deeply political ones, I started to connect the dots. A lot of folks resent “identity politics” (boohoo for them), but understanding that our lived experiences are shaped by a larger system was mind-blowing and important to me.
My studies taught me the ways in which identity, power, and privilege affect us personally, systematically, culturally. I never looked at anything the same way after that – I never looked at myself the same way again.
In particular – and it’s really important for me to mention her – I wouldn’t be the writer or activist that I am today without Dr. Suzanne Bergeron, who taught my first gender studies course in undergrad and was there every step of the way as I navigated university. As mentally ill and queer, academia was not always a safe place for me, and having a fierce mentor like her is why I was able to succeed despite so many obstacles.
Institutions like universities are not always built with marginalized folks in mind. In fact, when I was a student, we didn’t even have an LGBTQIA+ center on our campus. That’s why mentors are so critically important for the survival of marginalized folks in spaces like universities. I can’t tell you how many times I wanted to drop out, or how many times I showed up for Dr. B’s office hours and had to be talked down. (laughs) She was so patient.
And that’s what feminism has come to mean for me. It’s not just a philosophical worldview that remains abstract, but a daily practice and a commitment we make to one another. (pauses) It’s a commitment that we make so that we can resist these systems together and allow marginalized folks to come into their own and truly thrive, especially when these systems aren’t by and for us.
I learned that from her. And I’ve tried to be that person now, like, showing up for folks in my life but also through the public work that I do. I’m trying to carve out space where people like me can show up as themselves, like my mentors did for me.
AL: Has anyone ever reached out to you to tell you how your work has impacted them? What does that feel like?
SDF: Every day. I cry about it. It’s especially intense when it comes from a queer and/or mentally ill youth, because that’s such a difficult and powerless place to be. You know, I was there.
And back in my day… (laughs) I know, I sound old when I say that, but the world has changed a lot in the last decade. I was never able to find people like me with stories like mine. I genuinely believed that I would never see 18, because I’d never seen an adult like me surviving.
When I started writing publicly in these spaces, the most important thing to me was making sure that young folks who weren’t sure if they could make it would see what might be possible for them. That they could reclaim their power. That they could get older. That there was a future with them in it, maybe even a bright future at that. That you could grow up – like me, severely mentally ill and transgender and traumatized – but still be soft, be brilliant, be alive.
I want that for everyone. That when you reach the end of your rope, you can see other possibilities. You can see them, because you’ve seen someone living them. Someone like you, someone who knows how you feel. (pauses) I didn’t see those possibilities once upon a time, because I couldn’t find them, and I almost ended my life because of that. So I’m trying to create a world where those possibilities are known, never out of reach, never hard to find.
So when someone tells me that I’ve done that, there’s no way to describe how it feels. There just aren’t words… (long pause) I’ll never have words to explain what that means to me.
AL: How do you come up with topics for your blog posts and writing you pitch? Where do you draw that inspiration, especially for deeply personal writing?
SDF: My writing just comes from my very messy life! (laughs) When I started my blog, I wasn’t sure if I’d have a lot to say or how long I could keep it up. But that was a few years ago now, and I haven’t run out of ideas yet.
Being mentally ill, gay, non-binary, and transgender – considering where we are situated historically and culturally, you know, the “transgender tipping point” and the new administration and all that – means that there’s an important place for marginalized communities in the narrative we’re writing about this moment.
And with online media at the center of it all, marginalized folks like me have more power than ever to write that story instead of allowing others to write it for them. That’s the inspiration: making history through our words, to ensure that our lives and our struggles aren’t erased.
AL: What’s the hardest piece you’ve ever written?
SDF: Anything that I’ve written about suicide, to be honest, is the most difficult for me. It’s the most difficult because I know suicidal folks are going to find it, read it, and weigh their options. That feels like an enormous and important responsibility, and I take it very seriously.
Suicide as a topic makes me deeply emotional. I mean, I look at everything I’ve been able to do – and I imagine the other scenario where I never lived to see 18, and everything that might be different otherwise. “Sam Dylan Finch” as a person would’ve never existed. That’s not even a name I had claimed until, I don’t know, four years ago.
My whole body of work, and all the good that it did… (pauses) There’s an alternative timeline where none of that happened. I can’t even wrap my mind around what that timeline looks like, how many people are affected.
Honestly, I didn’t know I had any potential. Most of my life, I haven’t even had very great self-esteem, because depression can rob you of that. And how many people out there are like me, not even aware of what they’re capable of? So I imagine the collective potential of ALL survivors – everything we could do together, the ways we could shape the world – and the weight of that feels so heavy.
I’ll be honest: I don’t want to lose anyone else to suicide. I understand better than anyone why people end their own lives, but that doesn’t make it any easier to let folks go. Because that’s not just an individual loss, but a collective loss for us all. We’ll never know what you had to offer. We’ll never know what you could’ve done, the life you could’ve led. And whether it was just for you or for all of us, you deserve to know what you were capable of in this life. That matters to me. Survivors matter to me.
When I write about suicide, it’s the hardest thing of all, because I just want to reach through the screen and say, “We need you. You need you.” It’s gut-wrenching. It’s life and death, for real. It will never get easier to write those words, but I also know they’re the most important words that I write.
AL: What do you like about being on the editorial side of the writer/editor relationship, in your past work at Everyday Feminism and your current role at Resist? Is it more satisfying to you to be an editor or a writer?
SDF: I’m always asking myself, “What needs to be said?” And of course, “Do I need to be the one to say it?” If not (as is often the case, because I have my own privileges), I’m doing everything I can to support the folks who are saying it.
That’s why I pursued editing in addition to being a writer – my voice isn’t the only voice that matters, and I want to do everything I can to get diverse voices out into the world. I learn so much through the process. I don’t think I could ever just write or just edit. I see both as critically important work to be doing.
AL: What are some of the things you’d like to accomplish in the next ten years? How do you want to make your mark?
SDF: This interview is making me cry a lot. (sighs) So many feelings.
Because I’m imagining that like, I’ll be 35 in ten years. That sounds young to a lot of people, but when you aren’t used to imagining yourself getting older, it feels immense. I never thought about getting there. (pauses) And more queer, trans, and mentally ill kiddos are coming up in the world, and they’re going to need folks to show them that they can make it, too. Now more than ever.
In those moments when I can’t live for myself, I live for them. Every time my heart beats, it’s like a signal – it’s like morse code or something – just making sure they know they aren’t the only ones out there. That’s how I want to make my mark. I want to survive, for all of us. In ten years, twenty years, fifty years. With every beat, telling them: “I’m here, I’m here, I’m here.”
If you want to let Sam know how his work has made a positive impact on you, he’s just relaunched his Patreon campaign, which allows readers to personally connect with him while supporting the very important work that he does!
We need you. You need you. If you ever need support, please consider the following crisis resources:
The National Suicide Prevention Helpline: 1-800-273-8255
The Trevor Lifeline for LGBTQIA+ youth: 1-866-488-7386
Trans Lifeline: 1-877-565-8860
Or check out Sam’s favorite mental health apps at this resource list.
Alaina Leary is an intersectional feminist activist, editor, and publishing professional based in Boston, MA. She is currently a social media assistant for We Need Diverse Books, and is completing her MA in Publishing at Emerson College. Her career focus is on how to increase inclusive, authentic, intersectional representation in the publishing industry. She also edits for several online magazines, including Her Campus, Luna Luna Magazine, Germ Magazine, and Doll Hospital Journal. When she isn’t busy reading, you can find her at the beach or curled up with her girlfriend and their two adopted literary cats. Read her articles here.