self-compassion: an antidote to shame mb

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@iamkindtomyself
self-compassion: an antidote to shame mb
other people’s inability to love you does not reflect how lovable you are. it says something about their emotional availability, not your value.
Ellen Bass and Laura Davis, The Courage To Heal
["GETTING IN TOUCH WITH YOUR ANGER
If you're willing to get angry and the anger just doesn't seem to come, there are many ways to get in touch with it. A little like priming the pump, you can do things that will get your anger started. Then, once you get the hang of it, it'll begin to flow on its own.
It's often easier to get angry for someone else's pain than for your own. That's fine for a beginning. Imagine a child you love being treated the way you were treated. Read the writings of other survivors in anthologies and feminist journals. You can listen to their stories at conferences, workshops, and in small support groups. You can look at the expressions of grief on their faces and be touched. You can hear their fury and be incited. Know that any time you cry or get angry for someone else, it taps your own grief and anger as well.
Getting into an angry posture also helps. Physically taking an angry stance, making menacing gestures and facial expressions, invites genuine anger to arise. One woman, who described herself as much more prone to feeling hurt than angry, was quietly weeping during a therapy session. As she relates:
My therapist scooted her chair toward me so that her knees almost touched mine. Then she put out her hands, palms facing me, and instructed me to put her palms against hers. "Push," she said. "Push against me." I pushed against her palms and she pushed back. As I pushed harder, she met me with equal pressure. It took all of my strength to maintain. Within seconds, I was angry. The tears were long gone. I was mad! And it felt powerful.
Therapy and support groups can be ideal places for stirring up anger:
I felt incredible anger, but I never allowed anger my whole life. It was really a difficult thing to let out. One day my therapist got up out of her chair, and she said, "Your father's in that chair." And she handed me a rolled-up towel and she said, "I want you to hit your father."
It took me a long time to psych myself into doing that, but once I started, I couldn't stop. I pounded and screamed until I couldn't move anymore. It was such a relief.
(...)
FEAR OF ANGER
Many survivors are afraid of getting angry because their past experiences with anger were negative. As one survivor put it, "I don't get the difference between anger and violence yet. When I hear loud noises, I think they're coming after me." In your family, you may have witnessed anger that was destructive and out of control. But your own anger need not be either. You can channel your anger in ways that you feel good about and respect.
Even women with no history of violence are often afraid that if they allow themselves to feel anger, they're liable to hurt or kill someone.
I know the anger is there. I'm too scared to let myself experience it. I'm scared that I won't be gentle with myself. That I'll turn the anger on myself. And I'm so used to watching other people hurt people. I don't want to be a perpetrator. I don't know how to discharge my anger in a way that's safe.
It is extremely rare for women to violently act out their anger toward the people who abused them as children. And for women with no history of violence, the fear that you might hurt someone with your anger is usually unrealistic.
Anger is a feeling, and feelings themselves do not violate anyone. It's important to make the distinction between the experience of feeling angry and the expression of that anger. When you acknowledge your anger, then you have the freedom to choose if and how you want to express it. Anger does not have to be an uncontrolled, uncontrollable phenomenon. As you welcome your anger and become familiar with it, you can direct it to meet your needs— like an experienced rider controlling a powerful horse."]
no disabled person should have their parents be their only choice for support/caregivers. it’s not a privilege to be stuck with them and you don’t have to be grateful.
guy who has chronic pain and fatigue: man why can't i do more stuff
guy who has chronic pain and fatigue: man i'm so tired today for some reason
thinking about how when you experience a lot of shame in your formative years (indirectly, directly, as abuse or just as an extant part of your environment) it becomes really difficult to be perceived by other people in general. the mere concept of someone watching me do anything, whether it's a totally normal activity or something unfamiliar of embarrassing, whether I'm working in an excel spreadsheet or being horny on main, it just makes my skin crawl and my brain turn to static because I cannot convince myself that it's okay to be seen and experienced. because to exist is to be ashamed and embarrassed of myself, whether I'm failing at something or not, because my instinctive reaction to anyone commenting on ANYTHING I'm doing is to crawl into a hole and die. it's such a bizarre and dehumanizing feeling to just not be able to exist without constantly thinking about how you are being Perceived. ceaseless watcher give me a god damn break.
sorry to put your tags on blast on this insane breach containment post I have since muted, but you're right and you should say it.
It is defeatable. Go for the throat.
Crips for eSims for Gaza is a collaboration between Jane Shi, Leah Lakshmi Piepzna-Samarasinha, and Alice Wong.
Please boost. This is urgent. There is a need for esims more now, than ever.
if you ever find yourself thinking “wow I scraped the bottom of the barrel with my energy with that and came out okay!” that’s the devil talking. you did not come out okay. you borrowed energy from the future. you will repay it if you don’t rest and replenish the borrowed energy first.
this one took off quickly - are you guys ok
WIZARD PSA: Chronomancy might be weird and confusing, but one of the few solid rules of the discipline is keep your promises. Time is a library, and you don't want to meet the librarian.
Reblog if you have met the librarian
astonishing how good it can feel to get some chores done sometimes. you’ll be sitting there like damn i am some type of horrid little smeagol like creature who should be crushed to death. but then you do some laundry and you’re like wrow. im actually gods most fuckable soldier.
when the fatigue-out-of-nowhere-disorder causes you to get fatigued out of nowhere
Unusual but sympathetic paper:
Language Matters: What Not to Say to Patients with Long COVID, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, and Other Complex Chronic Disorders
https://www.mdpi.com/1660-4601/22/2/275
"Please don't fucking say fhat."
Love this.
Long COVID and ME/CFS folks, and disability allies:
I have something you can do in 15 minutes that will be very helpful to those of us with these disabilities!
The Canadian working group putting together recommendations for Post-COVID Condition (PCC) have released some bad recommendations regarding exercise as a treatment for Long COVID and cognitive behavioural therapy (CBT) to treat Post-Exertional Malaise (PEM).
The UK just recently managed to get these recommendations out of the NICE guidelines for ME/CFS, and we should try to prevent them from getting embedded in the Canadian ones for Long COVID.
They have a survey out until Nov. 27 at 11:45pm EST asking for public input. If you can manage it, please fill out the survey explaining why these are both bad recommendations. The survey is open to people internationally, and anyone interested in the topic. Please mark #2 and #8 as "Major Concerns" and provide a sentence or two explaining why (in your own words).
Draft Recommendation #2 - recommends exercise as a treatment for Long COVID, and only briefly mentions the existance of post-exertional malaise (PEM). Given how many people with long COVID meet the diagnostic criteria for ME/CFS, this is entirely backwards. PEM should be evaluated first and regularly thereafter and exercise should only be suggested once everyone is confident that PEM isn't present.
Draft Recommendation #8 - Recommends CBT as a treatment for PEM. This is recommending a psychological treatment for a physical issue, which is inappropriate. It also contributes to the long history of treating the fatigue in ME/CFS as self-inflicted. And is an activity that can also worsen or cause PEM.
The recommendations and links to their evidence charts are inside the survey itself, or you can open the PDF link on the first page and write your answers before copying them into the survey.
Survey:
https://www.research.net/r/CAN-PCCRecommendationCommentPublic
Here's a blog post explaining one person's responses to the survey:
https://thesciencebit.net/2024/11/21/my-submission-on-the-new-canadian-draft-recommendations-for-long-covid/
And here's one on the history of these "treatments" for ME/CFS and why they're based on bad science.
https://mecfsresearchreview.me/2021/01/12/the-expert-testimony-to-nice-that-took-apart-the-case-for-cbt-and-graded-exercise-for-me-cfs/
If you see this before the November 27 end date, I'd really appreciate some help getting the word out.
@thebibliosphere @covidsafecosplay @myalgicencephalomyelitiscfstom @snorlax-and-co @covid-safer-hotties @spoonfulofhannah @theoverstimulated
i simply need everyone to understand that i am tired all of the time. literally at all moments. if i ever go somewhere and do something, it is not because i am somehow full of energy, but instead that i have carefully stored up all of my little bits of energy like a dragon collecting jewels, and am now vaporizing them all at once
autistic folks when their routine gets disrupted, and they don't get alone time when they're supposed to get alone time
job search is bad for your health. get high and jack off instead
I swear to god I am going to (remembers nothing) (stares directly at the fucking
heartbreaking: local thing has to leave the house even though it is so tired and sleepy and full of joint pain