It’s time to activate it…
Bites The Dust! now this entire post will be reversed!
holy fucking shit
I hate all of you.
What in the fuck

It’s time to activate it…
Bites The Dust! now this entire post will be reversed!
holy fucking shit
I hate all of you.
What in the fuck
I hope Forretress gets a mega form because then we’ll all be forced to use
I’ve made the Autumn cookies before, so now it’s time to tackle the Winter cookies! I know it’s after the holidays, but these cookies could technically be eaten any time of the year. Difficulty: Easy, 4 hours (mostly fridge time). Makes about 2 dozen, depending on size.
-1 cup white sugar -½ cup cocoa powder -¼ cup (60mL) vegetable oil -2 eggs -A few drops of peppermint flavouring or 1 tablespoon brandy (I did brandy and added a teaspoon of vanilla for extra flavouring). Optional. -1 cup flour -1 teaspoon baking powder -¼ teaspoon salt -¼ cup icing sugar
In a medium bowl, combine the white sugar, cocoa powder, and vegetable oil. Mix until fully combined. It’ll look gritty, don’t worry about it.
Add the eggs and flavouring (if you’re adding any). Mix well, then add the flour, baking powder, and salt. It will be kinda runny. Again, don’t worry.
Cover the bowl with a teatowel or plastic wrap and stick it in the fridge for at least 3 hours. This might seem a bit excessive, but the dough is very sticky, so working with it right away would create a mess.
After the 3 hours or so, preheat the oven to 350°F and grease a couple cookie sheets. The icing sugar will stick to the pans, so it’s important to grease them well. Put the icing sugar in a small bowl. Do this all before removing the cookie dough from the fridge, so it doesn’t have much time to warm up (and thus get really sticky) while you’re working with it.
With a spoon and your hands, roll the dough into balls and then roll them in the icing sugar until fully coated. Shake off the excess sugar before placing on the cookie sheet. Just keep in mind if you make them really small or really big you’ll have to estimate a change for cooking time.
Bake the cookies for about 10-12 minutes. When you remove them they’ll look very soft and fudgy. Let them sit on the pan for 10 minutes, and then refrigerate them for 20 minutes. This will allow them to harden a bit but still remain soft and fudgy in the centre.
These cookies are really, really good. They’re soft and rich with a neat look to them. I don’t think holly grows up here, so I grabbed some Oregon Grape leaves from my backyard instead. Close enough.
-SVR
My name is Ang. If you’ve been following my story then I’m sure you’ve heard about this, but I’ve come down with a chronic illness. I have severe-spectrum MECFS. Myalgic Encephalomyelitis, or cruelly called Chronic Fatigue Syndrome, which downplays how much of a devastating, horribly disabling and terrifying disease this is.
It is an illness that affects millions, leaving a good portion of us housebound or bedbound, some so sick they are paralyzed and need to be tubefed and others die from the illness or complications.
I’ve been bedbound almost 3 months now since my illness has been progressing (which is nothing compared to how quickly it can become years), so sick some days I cant lift a spoon to feed myself, talk, or tolerate light and sound. I can’t draw anymore which was my passion in life as an artist, let alone take care of myself. I can’t even tolerate watching TV or play games most days to distract myself from the trauma caused by being confined to a bed in this sort of agony.
I got ill like this after getting the flu in January, and it’s been downhill from there as I started having bizarre neurological symptoms and collapsing episodes where I was unable to move, the energy draining from my body as the days went on until I needed a cane to walk, then a walker, then I was housebound with a wheelchair, and now I am bedbound and the severity steadily worsens with no let up so far despite doing everything I can to stop or slow the progression.
It is a level of sickness that is overwhelming me and my life is uncertain, but it’s looking grim from this point. I’m in severe pain constantly, on top of having horrible dysfunction in every other part of my body. I’ve only been steadily declining.
I lost my entire life right as it felt like it was starting. I was an artist working my dream job at Cartoon Network, and now I may never be able to return to the animation industry or live out my dreams of telling the stories I wanted.
The worst part is this illness could have been treatable by now! But it’s not, due to a deliberate choice of abuse and neglect by medical institutions. Most doctors aren’t trained to treat or diagnose M.E. and it gets practically no funding. Most sufferers are told it’s all in our heads (wrongfully diagnosed with conversion disorder or functional neurological disorder) even with evidence coming out that it’s a physical neurological disease and the only treatment we are given is get told to take anti-depressants, see a therapist, and exercise (despite exertion intolerance being the hallmark symptom and dangerous).
So the only way people like me have any hope of getting better is if we get a surge in awareness and understanding, and hope it leads to more funding and research. With decades of neglect and lives lost, this can’t go on.
At first I asked for donations when I was trying to figure out what was happening to my body as I threw money at doctors appointments begging for help only to get turned away and given no help, dwindling away my savings from when I used to work. And while donations were loved and helped significantly in my financial situation, it will not give me access to effective treatments if they don’t exist.
That is why I am asking you to help spread awareness. Please educate yourselves and donate if you can to organizations that research M.E.
People like me are suffering with a monster illness as debilitating as late-stage AIDS or cancer, hopelessly sick and dying with little help and living in severe medical neglect. I can’t even get a caregiver which I need now because my family can’t care for me longterm, all because my illness isn’t taken seriously by health insurance companies!
We need help. People with M.E. need help so bad because a lot of us are even too sick to advocate for ourselves.
If you want to know more there’s a wonderful documentary on Netflix made by M.E. sufferer, Jennifer Brea called Unrest (2017). Please give it a watch.
Here’s the trailer:
You can also see her speaking here on TEDtalk.
Here are organizations you can donate to:
Please share this. I am one of the #millionsmissing and while I have not been suffering with M.E. for very long compared to others, the trauma and destruction this illness brings is great and no one should have to go through this. I would not wish this suffering upon even my enemies.
We need awareness. We need advocacy. We need understanding. We need funding. We need diagnostic markers. We need research. We need effective treatments and hopefully one day a cure.
I may never have my old life back, and I don’t want anyone else to keep suffering the way I have since I’ve gotten sick. The pain is indescribable. I want one day for someone to get sick like I and others have, only to learn they can be diagnosed and effectively treated or cured.
Please help bring our stories to light. Please help save our lives.
Thank you.
mario collects his last star
i need both of these now
the reason these exist (iirc) is because peppa pig is banned in china for “promoting gangster attitudes”: peppa was popular (for whatever reason) with “shehuiren” (anti-establishment internet users), who made a lot of memes involving peppa and even got tattoos of her because it’s funny. the result of banning peppa is that shehuiren-types liked peppa even more afterwards, and now she’s a bit of a counterculture symbol in china. hence these shirts.
this is the EXACT kind of knowledge i absolutely had no idea i so badly needed
Just a quick reminder that the 10 minute power hour is a national treasure
A lot of games suffer from this,
HOWEVER
recently I’ve noticed that many games have a little secret inside the box…
You see, on the inside, when you open the case, some of these titles will have an alternate box art!
Simply open the case, *carefully* pull out the paper…
And on the other side…
:O
Now doesn’t that look like a much better representation of what playing DOOM is like!?!? The best part is theres no mountain of text on the back, the art just keeps going!
Best DOOM cover ever.
Other examples include Final Fantasy XV, The Last of Us, The Evil Within, Fallout 4, etc.
Not all of my games had this, but the ones that did had such cool art. I love the lack of “advertising text” on the back. Some of the alternate box art just paints a scene from the game so well you dont even need the title to know what it is.
Reblog to save a life! You might have some badass alternate box art in your games and you just never knew it :D
Let trans men be as feminine or as masculine as they want
also let trans women be as masculine or feminine as they want
bi/lesbian solidarity
inspired by this
lesbians love and support our trans sisters 💖💖
PLEASE tell me someone got pics of brendon wearing like 26 pride flags in portland tonight djdjdjjdjddjs
When your best friend tells you all she had for breakfast Was a packet of Splenda and a Diet Coke, And she tells you that she’ll stop after she loses five more pounds, Do not believe her. Tell her mother. It does not matter how angry your friend gets. The pain of that will always be preferable to the pain Of seeing your best friend in four years Weighing as much as she does now Half-dead in the hospital.
When your father sneaks into your bed in the dead of the night, And he tells you that this is how fathers love their daughters, Do not believe him. Tell your English teacher. She will have read millions of stories of girls like you. There is a one in six chance that she will be a girl like you. There is a five in six chance that she will know what to say to you. There is a six in six chance that she will help you.
When your veins whisper to you in the moonlight And say that there are so many nightmares inside you That could be free If you would just open your arms, Do not believe them. Tell your school’s guidance counselor, No matter how scared you are Because whispers are liars, And opening your arms will only open the passage For more nightmares to climb in.
And when the therapists say that you are better, Totally better, And you don’t need to worry about the sadness again, Do not believe them. Always be cautious, because sadness has a way Of sneaking up on you When you’re not looking. Be careful. Be careful.
Woah
this fucking made me cry fuck
Note to everyone. Not just 13 year olds.
!!!
OBGYN: Yeah, you are exhibiting all the signs of Polycystic Ovarian Syndrome. I’m so sorry.
Me: Huh? Oh, yeah. Insulin resistance, impossible weight loss, pre-disposition to type II diabetes, painful AF periods. Likelihood of bleed outs. Crap. That blows.
OBGYN: Yeah, well that too.
Me: *blinks* What?
OBGYN: Well, PCOS makes it very difficult for a woman to conceive and carry.
Me: BWHAHAHAHA. Yeah. No. No babies. Ever. Never wanted them. At all. Maternal instinct is not strong with this one. Only upside today.
OBGYN: Well then. Not exactly problem solved, but we’ll run with it.
Me: So about the MIND-SEARING PAIN and occasional HEAVY AF BLEEDING. When can we deal with that.
OBGYN: Not until you are 35.
Me: Dah fuq?
OBGYN: Not my rules. Hospitalization won’t even consider any treatment unless it’s life or death until you’re 35.
Me: Why?
OBGYN: Because you might want to have a baby.
Me: I’m 31. I didn’t want kids when I was 11, I didn’t want them at 21, and I sure as shit don’t want them now. Can’t I just sign a form that says “I don’t ever want a baby take it out, take it out now”?
OBGYN: Nope.
Me: Why?
OBGYN: Government rules. No removal of baby making parts before 35 unless your life is in immediate jeopardy.
TL;DR: The government knows better about your baby making parts than you do.
This is just evil. They are literally refusing to treat a potentially life-threatening condition, not just without the patient’s consent but despite the patient’s protest. Evil.
According to the National Women’s Health Network, there’s no legal age restriction- “Technically, any woman of legal age can consent to the procedure, but it should be medically justified. It’s incredibly unlikely that a doctor will perform a hysterectomy on women ages 18-35 unless it is absolutely necessary for their well-being and no other options will suffice.” Of course, this is in the US. Other countries may have different rules.
If you’re in the US and your OBGYN says “government says no,” look for a new one because they lied to you. If your OBGYN says that “hospital says no,” look for a new one because this one doesn’t respect your bodily autonomy. It is true that most surgeons don’t like to perform hysterectomies until you’re in your late 30s at the earliest, but a respectful surgeon will listen to their patient and not just write them off. Sexism in hospitals is alive and well- and it’s not just anecdotal evidence. There’s been a history of looking at it academically/professionally since the 70s (look into Mary Halas as a good place to start if you’re curious), and it crops up all the time in articles in the Journal of Women’s Health and Women’s Health Issues, and the International Journal of Women’s Health all of which are peer-reviewed, well-respected medical journals. It’s absolutely a real thing.
Anyways, I guess what I’m getting at is this: here’s a list of doctors (mostly US-centric) who perform different sterilization surgeries without giving their patients trouble. While even a surgeon on this list might caution anyone under 35 away from a hysterectomy, at the end of the day it’s your body and your pain. (And some of the docs here have been known to perform hysterectomies on people in their 20s with no fuss.) While this list won’t be practical for everyone- after all, medical treatment is ridiculously expensive in this country, it might help someone.
Holy shit fam Holy S H I T
SIGN ME THE FUCK UP I’VE BEEN TOLD THIS IS NOT ALLOWED FOR YEARS
Oh god
QUICK REMINDER THAT I HAD A HYSTERECTOMY A FEW DAYS AFTER MY 26TH BIRTHDAY B/C I HAD CANCER AND I DID EXACTLY THIS. I HAD A DOCTOR WHO DIDN’T WANT TO DO IT AND THEN I WENT TO A NEW DOCTOR AND AFTERWARDS SHE MORE OR LESS SAID MY LIFE WOULD HAVE BEEN IN DANGER HAD I NOT DONE IT.
Sometimes it’s not the doctor, it’s the hospital. For example, my OBGYN worked at a Catholic hospital, so they couldn’t perform any type of sterilization onsite unless it was an emergency situation.
So if your doc feeds you this BS line about not being allowed to, ASK IF IT’S THE HOSPITAL POLICY. If it is, ask if they are able to perform the procedure elsewhere. If they are not, ASK FOR A REFERRAL.
I was 28 years old when my OBGYN explained that he wasn’t allowed to perform a sterilization procedure onsite, and then he proceeded to tell me what a crock of shit it was and referred me to someone else who was able to. And even though I was under 30, his referral listed me as “an ideal candidate” for the procedure.
If they pass off this line and insist when you know otherwise, FIND A NEW DOCTOR.
Frequently I encounter non Native folks who tell me they think reservations are some form of reparatoins to Natives from the US government. I even had someone close to me tell me they thought reservations were places to “reserve” our cultures.
Where I’m from (South Dakota) reservations were concentration camps where they sent us to die after they stole and colonized all of the land every US citizen occupies. In the early SD Rez days our ppl had to get permission from district agents (white settler men) to get food, fix our homes, or even leave our community to travel to another community on our Rez to visit relatives. We couldn’t hunt cuz they killed millions of our buffalo. If we didn’t get permission from the white settler agent we couldn’t eat, fix our homes or visit relatives because we would be violating US law & could be arrested. Also our cultures & ceremonies were illegal under US law until the Indian Religious Freedom Act in 1978.
So plz educate the ppl you love and care abt because everyone in the USA is living in an illegal settler colony, Indigenous ppl survived their genocide & we’re her to say these settlers never gave af abt us & never will.
~ @FrankWaln
Point made
a masterpost
as someone who experiences the passage of time i really relate to this
You don’t fuck with the tray master
HOLY SHIT
This is what the Exotic Weapon Proficiency feat looks like in real life.

