greyshadowquestionsbeing:

thebibliosphere:

sophies-sideshow:

thebibliosphere:

thebibliosphere:

Also, to any men reading my posts who are horrified and want to know how they can help—offer to go with your female friends and relatives to appointments. Explain to them you’ve been reading about medical neglect towards women and let them know that if they ever want emotional support, you are there for them.

No, really, you have no idea how differently doctors react when there is a man in the room. Some female doctors will give ETD the side-eye and try to find ways to ask if I am okay (which, bless them) but once they are made aware that he is there at my request for emotional support, they are perfectly happy to have him there, and don’t talk to him unless I need them to. 

Male doctors? Whole other ball game. They spot him sitting there and their whole demeanor shifts, and if they do talk over me to him, he quickly sets them right and doesn’t engage in their misogynistic comments, he just stares them down and steps in if he thinks I am being gaslighted, words and phrases like “is this the usual treatment for symptoms like this?” forces the doctor to explain usually what they’d do for him, at which point I am able to ask “so why am I not being sent for XYZ testing/why am I not being prescribed pain treatment?”

But also remember, you are there to be my ally, not to tell the doctor what you think is wrong with me, but to make them pay attention to me. Direct the conversation back to me, and if it’s not working, repeat exactly what I am saying and make them listen.

It’s entirely fucked up, but your mere presence could mean the difference between misdiagnosis and proper medical treatment.

And just because I am seeing it in the tags “#this shit doesn’t happen with female doctors” oh it absolutely fucking does.

Misogyny in the medical world is fucking ingrained. It’s in the very teachings of modern medicine.

Some of my worst gynecological experiences were at the hands of other women who thought I was bullshitting my pain levels when it comes to certain procedures and illnesses. 

I’ve been told to “stop making a fuss” while I have screamed on the table from a speculum insertion (by the way, HUGE warning sign there is something majorly wrong with your muscle walls, pain upon insertion is not “normal” do not accept it if they tell you agony is normal upon insertion of anything) for a “routine” exam. And to give you some idea of my pain tolerance levels, I’ve had two root canals without anesthesia (cause 

anesthesia doesn’t work for me) and I breathed deeply through them. I left nail marks in the chair and had to tap out a few times for a rest, but I’ve never screamed and shot out the chair like I was being murdered.

I’ve had female doctors tisk at my medical file and tell me I want to “get myself together”, like I’m having an autoimmune collapse for funsies. I’ve had female doctors tell me I “just need to have a baby” because that will “calm me down” and also “what does your husband thing of all this?”

Which speaking of, I’ve also had female doctors turn to my husband and say “wow you sure are good to be coping well with this” like eXCUSE YOU, HE’S NOT THE ONE WHOSE BODY IS EATING ITSELF ALIVE???!! BUT OKAY, SURE, I’M THE ONE WHO NEEDS TO “BE MORE POSITIVE AND TAKE A TYLENOL”. OKAY THEN. 
(also as an aside: if they do ask your male friend/loved one to leave the room to ensure your safety and you aren’t being controlled, remember to ask for him to be brought back in. Sometimes they “forget” and you’re left on your own again)

And all of this? All those things I posted up there? Those apply to white women as well. 

Women of color and women with disabilities, are more likely to be neglected and gaslighted than cis white able bodied women are—and we (I use the term losely when it comes to able bodied re: myself, heh) already get the short end of the stick when it comes to appropriate medical care. Be aware of your fellow women (all your sisters, not just your cisters) and if you are in a position to offer help and go to appointments and sit in on exams, know that it would be greatly appreciated. 

And again, remember, it is not your place to talk over your friend, this is not about you or what you think is wrong.

This is about you using your privilege by your mere presence alone, to make sure your friend is going to get adequate medical care, whether it’s pain management or diagnosis. 

Be a witness and hold those in the medical industry accountable for their neglect and actions against the vulnerable. Because by gods no one else will.

@thebibliosphere, are you aware most doctors won’t allow someone else in the exam room?  Sometimes even spouses?  Even if the patient specifically and verbally allows it?  At least, that’s how it works where I live, in the south-east USA.

Besides that, though, good advice.

Oh they can tell you they’re not Allowed but they’ve no legal leg to stand on. If you want someone in there with you, you are absolutely legally allowed to do so. If you explain why you want your spouse in the room with you (you don’t need to say “I don’t trust you” just “I want someone else here to remember things/I get nervous”) and they downright refuse to let your partner in with you? That’s a huge red flag to me.

The only doctors who downright refused to let ETD in the room with me were the ones who ended up being dangerous and abusive in their behavior and I stopped the exams to demand someone else be allowed in the room with me as is my legal right. They might not be behind the curtain with me but they are absolutely allowed to be in the room by US law, regardless of state.

If a medical professional pushes for someone to leave, that is a massive red flag and I will walk out. Any professional worth it wants their patient comfortable – and the only professionals who ever asked someone to leave with me have ended up being assholes.

The last time I agreed to send someone out of the room and be alone, I was then held down and sexually assaulted not a minute after they closed the door behind him. And all involved were women. I still remember in full them talking and laughing about having taught me a lesson and the shocked look on J’s face at the amount of blood on bed. Every case of medical abuse and neglect I’ve dealt with involved women professionals. At minimum for check-ups/tests with nurses/lower risk situations, I let them know I have someone in the waiting room that I may bring in if I feel I need help.

thebibliosphere:

sophies-sideshow:

thebibliosphere:

thebibliosphere:

Also, to any men reading my posts who are horrified and want to know how they can help—offer to go with your female friends and relatives to appointments. Explain to them you’ve been reading about medical neglect towards women and let them know that if they ever want emotional support, you are there for them.

No, really, you have no idea how differently doctors react when there is a man in the room. Some female doctors will give ETD the side-eye and try to find ways to ask if I am okay (which, bless them) but once they are made aware that he is there at my request for emotional support, they are perfectly happy to have him there, and don’t talk to him unless I need them to. 

Male doctors? Whole other ball game. They spot him sitting there and their whole demeanor shifts, and if they do talk over me to him, he quickly sets them right and doesn’t engage in their misogynistic comments, he just stares them down and steps in if he thinks I am being gaslighted, words and phrases like “is this the usual treatment for symptoms like this?” forces the doctor to explain usually what they’d do for him, at which point I am able to ask “so why am I not being sent for XYZ testing/why am I not being prescribed pain treatment?”

But also remember, you are there to be my ally, not to tell the doctor what you think is wrong with me, but to make them pay attention to me. Direct the conversation back to me, and if it’s not working, repeat exactly what I am saying and make them listen.

It’s entirely fucked up, but your mere presence could mean the difference between misdiagnosis and proper medical treatment.

And just because I am seeing it in the tags “#this shit doesn’t happen with female doctors” oh it absolutely fucking does.

Misogyny in the medical world is fucking ingrained. It’s in the very teachings of modern medicine.

Some of my worst gynecological experiences were at the hands of other women who thought I was bullshitting my pain levels when it comes to certain procedures and illnesses. 

I’ve been told to “stop making a fuss” while I have screamed on the table from a speculum insertion (by the way, HUGE warning sign there is something majorly wrong with your muscle walls, pain upon insertion is not “normal” do not accept it if they tell you agony is normal upon insertion of anything) for a “routine” exam. And to give you some idea of my pain tolerance levels, I’ve had two root canals without anesthesia (cause 

anesthesia doesn’t work for me) and I breathed deeply through them. I left nail marks in the chair and had to tap out a few times for a rest, but I’ve never screamed and shot out the chair like I was being murdered.

I’ve had female doctors tisk at my medical file and tell me I want to “get myself together”, like I’m having an autoimmune collapse for funsies. I’ve had female doctors tell me I “just need to have a baby” because that will “calm me down” and also “what does your husband thing of all this?”

Which speaking of, I’ve also had female doctors turn to my husband and say “wow you sure are good to be coping well with this” like eXCUSE YOU, HE’S NOT THE ONE WHOSE BODY IS EATING ITSELF ALIVE???!! BUT OKAY, SURE, I’M THE ONE WHO NEEDS TO “BE MORE POSITIVE AND TAKE A TYLENOL”. OKAY THEN. 
(also as an aside: if they do ask your male friend/loved one to leave the room to ensure your safety and you aren’t being controlled, remember to ask for him to be brought back in. Sometimes they “forget” and you’re left on your own again)

And all of this? All those things I posted up there? Those apply to white women as well. 

Women of color and women with disabilities, are more likely to be neglected and gaslighted than cis white able bodied women are—and we (I use the term losely when it comes to able bodied re: myself, heh) already get the short end of the stick when it comes to appropriate medical care. Be aware of your fellow women (all your sisters, not just your cisters) and if you are in a position to offer help and go to appointments and sit in on exams, know that it would be greatly appreciated. 

And again, remember, it is not your place to talk over your friend, this is not about you or what you think is wrong.

This is about you using your privilege by your mere presence alone, to make sure your friend is going to get adequate medical care, whether it’s pain management or diagnosis. 

Be a witness and hold those in the medical industry accountable for their neglect and actions against the vulnerable. Because by gods no one else will.

@thebibliosphere, are you aware most doctors won’t allow someone else in the exam room?  Sometimes even spouses?  Even if the patient specifically and verbally allows it?  At least, that’s how it works where I live, in the south-east USA.

Besides that, though, good advice.

Oh they can tell you they’re not Allowed but they’ve no legal leg to stand on. If you want someone in there with you, you are absolutely legally allowed to do so. If you explain why you want your spouse in the room with you (you don’t need to say “I don’t trust you” just “I want someone else here to remember things/I get nervous”) and they downright refuse to let your partner in with you? That’s a huge red flag to me.

The only doctors who downright refused to let ETD in the room with me were the ones who ended up being dangerous and abusive in their behavior and I stopped the exams to demand someone else be allowed in the room with me as is my legal right. They might not be behind the curtain with me but they are absolutely allowed to be in the room by US law, regardless of state.

naamahdarling:

real-live-dragon:

timepunkspg:

the chemical mentioned in the article… like only if you ate 100kg of mac and cheese in one sitting… that’s how much it’d take to be toxic.

well i know what the fuck and how the fuck much im doing for dinner today

Shit, man, we have formaldehyde in our bloodstream at all times. Our own blood is full of dangerous chemicals.

I fucking hate these fearmongering food purists who want us to subsist on air and organic kale. Especially when these same dipshits are the ones on the health food bandwagons that promote eating large amounts of real weird superfoods. Like apricot kernels. Which contain a shitton of a substance that is converted in the body into CYANIDE. But hey, amygdalin/laetrile is supposedly a cancer-fighter, so we should take it so we don’t get cancer. Right?

At this point I don’t have a problem just coming out and saying I HATE health culture. No really. I hate it. I want people to just not be so fucking invested in the health of strangers.

Like, I’m old and dying. Let me be old and die and eat my mac and cheese in fucking peace please.

I truly, truly don’t give a shit if my food is killing me. Not eating would kill me sooner, and easy-fix stuff is pretty much the only way to keep myself fed. Come to my house and fix me healthy food I don’t have to pay for or shut the FUCK up.

I actually got triggered worse by one reblog, partly talking about how much less than seriously gyno problems get taken pretty much across the board.

Yeah, I’ve strongly suspected for yesrs that I might have endo, with increasingly worse symptoms over time. Which have never gotten taken remotely seriously.

(Surprise, it may be even more common in people with EDS, and/or the worst of the symptoms may actually be coming straight from that with endo possibly overdiagnosed! “Menorrhagia reported by 77.6% of the patients” 😱)

Seeing another version of that post again now was not the best timing, a couple of days after getting another routine pap smear “invitation” letter. When not only do I not have any confidence that they would actually listen to what I am saying about those problems, I do not trust them at all and have not felt safe going back since what happened the last time. In 2005. (No really. It was that traumatizing. Pretty much all the content warnings you might imagine, for both those links.)

So yeah, literally anything could be causing this, and I cannot trust them far enough to even go for a routine exam. Much less try to look into the symptoms again, with the invasive stuff required if they do take it seriously. Even with backup along, and you can bet I really wouldn’t go into that room without someone I trust along now.

Getting brushed off and treated like a particularly stupid naughty child some more is not even the worst case scenario there. And it makes me very angry.

Do you know what pisses me off the most about the dreaded “Autism Moms”?

c-squared2911:

Let me tell you, as an autistic adult who also was a main caregiver for an autistic boy (my brother). 

For the record:  I swear that if you use this post to say autism makes people violent and abusive, I will send 12,000 angry geese to flock in your bedroom and destroy every item that you treasure the most. AND I will eat the leftovers you had planned on eating for lunch tomorrow. Don’t you fuckin dare miss the point of this post. 

Listen up. I got a story for you.

Bit of background first.

My boy, my little hobbit, was born when I was ten years old. My mother left him alone with my grandparents and me. She legit abandoned him. 

My grandparents weren’t sure they could take him in. 
I begged. I pleaded. I asked as hard as I could to let us keep him and not give him back to my mother. 

Of course, they said yes. 

I dutifully became the protective older sister.

I would bathe him up until the week I left for college. I measured his medications and crushed them into his favorite yogurt. Blue, if you were curious.I made sure his food was perfect – french fries made just like he wanted, a chicken fry sandwich complete with his favorite McDonald’s sauce we bought in bulk.  
I went to his speech and occupational therapies several times a week, and practiced the things he learned. I went with him to his first day of school.

I even did a middle school project all about autism (which I am slightly embarrassed about, as I mentioned A$ in it ugh). I read all the autism books a 12 year old could find, and immersed myself in the Vanderbilt paperwork. I delved into the world of IEPs, visual schedules, and basic sign language.

And now, I’m still sending them resources and information on medications, papers for teachers, and going over doctor notes for him – despite being six hours away. 

(Of course, I was an undiagnosed autistic girl who also needed quiet. When I wasn’t needed to do these things, I was often in my room away from the loud television and people. I wasn’t a perfect caregiver, but I did do a lot.)

All of that to say: yeah, it wasn’t easy. But since when is raising a kid ever easy? I started looking after this boy when I was ten years old.

But here’s what infuriates me.

I read all the time about these autism moms who complain about how terrible their lives are. They say they’re afraid of being hurt and their lives are destroyed. Some even talk about killing their kids.

You know what?

Yeah, I got hurt by him or when helping him. I got bit, scratched, hit, and everything else. Usually it was just him being frustrated over lack of communicating his needs, so I was rarely angry. 
I ran after him when he went out the door straight for a lawnmower and I fell to the concrete. I grabbed him right before he ran into a street and ended up with my arm covered in blood.

I was kicked in the head and given a traumatic brain injury that requires me to now use a cane, and has caused a ton of nervous system issues. I even use a wheelchair part-time due to another condition that occurred afterwards. I’m only 20, and my health is pretty comparable to someone with congestive heart failure.

And you know what? 

I never in a million years thought about hurting my little brother.

I still don’t blame him. He was often overwhelmed, and had meltdowns. As an autistic person myself, I understood it – even if I didn’t know I was autistic at the time. (I suspected, but was too focused on other things.) 
I don’t know if I’ll ever get better health-wise, and that’s okay. I don’t know if I’ll get to run and dance again, or if there’s worse effects to come. It’s just what it is, and I’ve accepted that. 

He’s a child. It’s not his fault. He once asked me if it was, and I hugged him tight and said absolutely not. 

I say all this not to demonstrate how violent autistic people can be, but to demonstrate that I get where these autism moms are coming from.

  Again, for the record, autistic people are far more likely to be abused and assaulted. 

Remember how I said  I get where they’re coming from?

Yeah, that’s still not an excuse to be harmful toward your child. Ever.

You don’t give your babies bleach, shock them, or starve them. You don’t talk about them as if they’re literally a death sentence for you. And you sure as hell don’t want to murder your little ones. 

And if you literally want to kill your kid, if you would rather have a dead child than an autistic one, I have news for you.

You don’t deserve that child, and you better back up and understand this.


You autism moms need to stop. You need to listen. 

Your kids are going through a world that wants to “cure” them, force them into suffering so they can look “normal.” Your kids are going to spend their entire lives dealing with a world that is hostile to them. People try to assimilate us to save their own pride, at the expense of our own comfort and stability. 
Your kid is going to go through life being told that they should be literally “treated” with electroshock therapy because of their neurology. They’re going to be told that they shouldn’t reproduce. They’re going to be told that they’re not worth having space in this world. Your kid is going to grow up one day, and they’re going to hear this and internalize it. 

I know that, because that’s what I hear every day. 

You say it’s so hard to have an autistic kid?

Well, of course it is. But you know what?

Kids are hard.
They’re going to kick, hit, pinch, and everything else. Even neurotypical kids do that. I don’t know a single kid who hasn’t bit their caregiver or thrown something when grumpy. 
(I’ll say it again for those in the back: autistic kids are way way way more likely to be abused and hurt.)

When you have a kid, you sign up for this. You love that little one unconditionally, you protect them with all your heart. You give them support. You love that child even if they have a disability, especially when they have a disability.

You teach them that they are allowed to exist, that they are just as valuable and needed in this world like anyone else. We need all the neurodiversity in this world we can get. 

You teach your child that they’re not a burden. You teach them how to say no and that autonomy is often more important than compliance. You teach them that you love them, and that they will always have someone in their corner to back them up when times are tough.

I don’t care how hard you think it is raise an autistic child.

Trust me, I know full well it’s hard. Parenting is hard. It’s not easy, and it’s not always roses and fluffy kittens. That has nothing to do with having an autistic kid; that’s just a fact of life. 

The fear of getting hurt is valid. I can attest to that, and I don’t think I can downplay that. But that behavior is communication, and you have to learn how to read it. I did. You have to fight for better supports, for ways to make it easier on your kid – and by doing this, easier for you too. 

Sure, it’s hard.

But you know what? Your kid’s going to have it much harder. 

ASAN’S Anti-Filicide Toolkit

neurowonderful:

What is filicide?

In the past five years, over fifty [70+ as of 01/03/16] people with disabilities have been murdered by
their parents, relatives or caregivers in the United States alone.

These acts are horrific enough on their own. But they exist in the context of a larger pattern:

  1. A parent kills their disabled child.
  2. The media portrays these murders as justifiable and inevitable due to the “burden” of having a
    disabled person in the family.

  3. If the parent stands trial, they are given sympathy and comparatively lighter sentences, if they
    are sentenced at all.

  4. The victim is disregarded, blamed for their own murder at the hands of the person they should
    have been able to trust the most, and ultimately forgotten.

  5. The media sends a message that if you kill your disabled child, you will receive attention
    and sympathy. The justice system sends a message that if you kill your disabled child, your
    punishment will likely be minimal.

  6. Parents of kids with disabilities see these messages.
  7. A parent kills their disabled child.

What does the term “filicide” mean?

“Filicide” is the legal term for a parent murdering their child. In the disability community, “filicide” is
used when talking about a parent or other relative murdering a child or adult relative with a disability.
This toolkit is specifically about filicide in the disability community. When we say “filicide,” we are
talking about a pattern of violence that starts when a parent or caregiver murders their child or adult relative with a disability and continues in how these murders are reported, discussed, justified,
excused, and replicated.

How common is it?

We don’t know. Filicide in general is very difficult to track, and filicide in the disability community is
notoriously underreported. We are aware of over 50 filicides in the United States from the last 5 years
where the victim was disabled. We know that the numbers we know of are much smaller than the
reality.

Why are we only talking about filicide against people with disabilities?

Typically, when a child without a disability is murdered by their parents, everyone stands united in
condemnation. No one attempts to understand, justify, or explain the murder. No one expresses
sympathy for the murderer. No one argues that every parent has had moments or thoughts like that.
No one understands. No one suggests that if the child had been easier or the family had had more
support, this could have been avoided. The crime is punished harshly, and the victim is remembered
and mourned.

When someone with a disability is murdered by their parents, the opposite happens.

Why does it happen?

Because we live in a world where disabled lives are valued less than the lives of people without
disabilities.

Because we live in a world where people think it is better to be dead than to be disabled.

Because we live in a world where killing your disabled child is excused, minimized, and normalized.

Because we live in a world where this is okay.

Frequently Asked Questions About Filicide

  • Isn’t this caused by lack of services?

It’s absolutely true that people with disabilities and our families don’t get enough services. But that’s
not what causes these murders.

There are thousands of families across the country with insufficient or nonexistent services who
refrain from murdering their disabled family members. In addition, most high-profile cases have
occurred in upper-middle-class communities and have been committed by parents who either refused
services, or had more family services than is typical. This is not about services. Suggesting that
murders could be prevented with more funding holds people with disabilities hostage: give us what we
want, or the kid gets it!

When disgruntled employees take guns into their workplaces and murder their colleagues, we don’t
use that as a launching point for a conversation about how Americans need better employee benefits
or more paid leave. When students shoot people in their schools, we don’t use this as a launching
point for a conversation about anti-bullying policies. This doesn’t mean that we don’t care about
worker’s rights or student safety; it means that these are separate conversations, and combining
them makes excuses for murderers. We feel that drawing a line between filicide and lack of services is
equally inappropriate.

  • Is it a hate crime?

Yes and no. A hate crime is a crime that is motivated by bias; disability hate crimes are defined as
crimes that are committed because of a bias or prejudice against disability. Filicide in the disability
community is almost always about the person’s disability, so in that sense, yes, this is a hate crime.

Legally, disability-related hate crime can only be persecuted on the federal level if it is inter-state, and
individual states vary in their state-based hate crimes laws. Check your state to see if filicide related
to disability can be considered a hate crime under state law; if not, consider lobbying your state
legislature to include disability in your state’s hate crimes statute, or to adopt one if your state does
not have one.

  • Why is it bad to try to understand why someone might do this?

Filicide is a horrifying act, and wondering how someone could do this is a natural response. But when
we progress to saying “I understand why someone would do this,” or “but you have to understand,”
we are not just saying that we have thought about what motivated the killer – we are saying that the
killer’s actions make sense to us.

Our society’s reactions to filicide reflect our beliefs about disability. When parents of kids without dis-
abilities murder their children, we are universally united in condemnation. It is only when the victim
is disabled that we pause. It is only when the victim is disabled that we are encouraged to understand.

This is a double standard, and it reveals dangerous things about our beliefs.

When we say every parent of a disabled child has had moments like this or walk a mile in our shoes or the
system failed everyone
or but you have to understand how hard it is, we are excusing a parent murdering
their child. It does not matter how many times we say not that I would ever condone this: if we attempt
to make a parent murdering their child understandable, if we ever attempt to position it as a
comprehensible or inevitable or normal thing, if we take and normalize the perspective and the side of
abusers and murderers, we are minimizing and excusing this act. Doing so puts the lives of disabled
people everywhere in danger.

There are absolutely things we should understand about filicide. There are absolutely people with
whom we should empathize. We should understand that filicide is not committed by loving parents.
We should empathize with the victims. But to say, “I don’t condone the murder but I understand it,” is
to say, “This is bad, but it isn’t so bad if we put it in context.”

We do not believe that this is a good way to talk about murder.

  • But anyone who would kill their child, or try to kill their child, must have
    a mental illness. Doesn’t that change how we should think about this?

Filicide is not a symptom of mental illness. Filicide indicates a decision to murder. These decisions are
deliberate and often premeditated for days or weeks. The perpetrators of filicides are often evaluated
and found competent to stand trial.

Saying that only mentally ill people would commit a murder can make some people feel better, but it’s
not true. People with mental illness are no more violent that the general population – but, like people
with developmental disabilities, they are often the targets of violent crimes. When we’re talking about
cases where people with disabilities are murdered by parents, invoking mental illness is just a way of
blaming one group of people with disabilities for the murders of other people with disabilities, and
shifting the blame away from the person who is actually responsible – the murderer.

How do we talk about this?

Names: to discourage copycats, don’t use the full name of the murderer. Do use the name of the
victim.

Sympathy: as with any other murder, do humanize the victim. Do unequivocally condemn the
murder. Do mourn the victim. Don’t sympathize with the murderer.

Be mindful of anti-disability bias: don’t imply that it is better to be dead than disabled, that
disabled people experience a lower quality of life, or that we cause other people to suffer. Do use
respectful language, and do consult with people with disabilities.

Focus: don’t give the murderer a platform. Do center the victim.
Don’t refer to filicide as mercy-killing.

Don’t talk about services in the context of filicide.


Do
be mindful of the potential for copycat murders:

  • avoid using the killer’s name or giving them a platform
  • focus on the victim, and
  • avoid grisly sensationalism.

Do write about filicide against a disabled victim the same way you write about any other filicide.

How Can We Prevent This?

1. Change the conversation

Center the victim. Condemn the murderer. Refuse to “understand,” excuse, justify, minimize, or
normalize a parent killing their child. Refuse to accept this. Refuse to allow this to become our new
normal.

2. Prosecute

Call for these crimes to be prosecuted to the fullest extend of the law, similarly to other filicides.
Demand that people with disabilities have equal protection under the law. Consider lobbying your
state legislature to include disability in your state’s hate crimes statute, or to adopt one if your state
does not have one.

3. End ableism

Challenge ableism (anti-disability bias and prejudice) everywhere you see it. Challenge the idea that
it is better to be dead than disabled, that disabled people are a drain on society, that disability means
suffering, and that disabled lives are not worth living. Promote inclusion, community integration,
and acceptance.

4. Self-report

If you think you are going to harm your child or adult relative, turn yourself in. Call 911 or child
protective services and say “I am thinking about killing my child.”

5. Community reporting

If someone you know is talking about killing their child, turn them in. Often in the wake of a filicide
people come forward to say that days or months before the murder, the perpetrator made a comment
to them suggesting that they were contemplating homicide: “I’m despairing about my child’s
condition – I think this is the end for him,” or “kids like mine should be put down,” or even “I am
thinking about killing my child.” In addition, report any indications you might see of child abuse or
child neglect. Abuse and neglect of children and adults with disabilities is very common and extremely
under-reported, and many filicides are preventable escalations.

What do I do if this happens in my community?

1. Get the language right

Change the conversation: challenge poisonous ideas and help prevent copycat crimes. Read “How do
we talk about this?” for more.

2. Hold a vigil

Mourn the victim and call for justice. See our vigil guidebook at the end of this toolkit for more.

3. Watch the media

Encourage journalists to speak to disabled people, follow best practices for preventing copycat crimes,
center the victim, and treat this filicide like all other filicides. Refer them to this toolkit. Push back
when they make mistakes.

4. Push back

If someone attempts to justify, minimize, or normalize the murder, challenge them. Don’t let them
interpret your silence as agreement.

5. Sentencing

Call for the harshest possible sentence under the law. Emphasize that people with disabilities have a
right to expect full and equal protection under the law.

6. Call for hate crimes legislation

As appropriate, advocate for expanding state and federal hate crimes legislation to include disability
and filicide against disabled victims.

7. Hold the justice system accountable

Contact your local protection and advocacy agency, your local FBI field office, and your district
attorney. Let them know that the disability community is watching. Let them know that we are
outraged. Tell them to do their jobs.

 – ASAN’s Anti-Filicide Toolkit

fierceawakening:

argumate:

birdblogwhichisforbirds:

birdblogwhichisforbirds:

birdblogwhichisforbirds:

on the one hand free speech in academia is very, very important.

on the other hand, if i ever once swore in front of a customer at any job i’d ever had, or called a coworker a d*ke, or loudly speculated about a customer’s sex life apropos of nothing, i would have been fired on the spot and nobody would have questioned it.

the lady in this article is a goddamn snowflake. she is being held to a far, far lower standard of politeness than any cashier, office worker, nurse, cleaner or person in any other kind of job would be held to. 

imagine you phone up a your bank’s customer services and the person on the phone starts dropping f bombs. imagine the cashier in waterstones told a pregnant customer one of their books isn’t for “mommies and wives.” imagine the receptionist at your local dental surgery said it was “bullshit” to ask for accomodations from your dentist. 

none of those people would have jobs the next day. not one.

this woman thinks she should get special treatment for some unexplained reason.

she wasn’t fired for academic opinions. making fun of a student for being pregnant is not a political or philosophical stance. neither is making fun of someone’s trousers.

if she’d said, as an academic opinion, “mothers shouldn’t study or do paid work outside the home” i’d think that was a shitty opinion but i’d defend her right to say it. but sh didn’t she just made fun of someone for being pregnant. if she’d said “same gender relationships are wrong because something something thomas aquinas something something bodily union” that would be a shitty philosophical stance but i’d defend her right to express it, but “lol your trousers make you look gay” is just being rude for no reason.

also if multiple people are leaving meetings with you in tears, and they don’t complain about any of your specific opinions but just the general way you talk to them, then you’re not being fired for unpopular opinions.

Ginn was describing her service project—a coat drive that had brought in 300 coats for needy kids—and mentioned that her fiancé had helped her out with it. “Well,” Buchanan told her, according to LSU documents, “he might support you now when the sex is good, but trust me, he won’t support you in five years when it’s not as good.” Ginn was “mortified” that a professor would make assumptions about her sex life—and she was too afraid of Buchanan, she said, to confront her about the matter.

But other allegations fell into different bins—mostly professionalism and abuse of power. In Ginn’s meeting with the associate dean, which was recounted during the hearing, she mentioned that another young woman in her class, Kaitlyn B., also felt traumatized. And soon, Kaitlyn reported to the university that during her own assessment team meeting, Buchanan upbraided her until she burst into tears and then began filming her with her cellphone, saying, “You need to see how unprofessional you look.” Another young woman, referred to in LSU documents as Student C, reported that in a 2012 class, Buchanan declared that only a “dyke” would wear brown pants, and that the female students shouldn’t expect to pass if they got pregnant, even offering to purchase them condoms to prevent it. The student, who was expecting her third child, met with Buchanan to discuss whether she should quit the program; the professor told her that it wasn’t really designed for “mommies and wives” and further discussed her learning disability in class, calling the special accommodations granted her because of it “bullshit.”

Students complained that Buchanan canceled classes and one day brought in her yoga teacher as a guest speaker. “I learned nothing, besides I should not wear brown pants, her kid smokes weed, and she is getting a divorce,” one student wrote. Other evaluations mentioned that Buchanan announced that she didn’t care if people completed their assignments because she probably wouldn’t have time to look at them.

yikes

Yeah. When I read the “when the sex isn’t good” bit I thought that was icky, but not worth firing someone over. But if someone pulls shit that makes people consistently uncomfortable and isn’t presenting it as something to debate or discuss in the class… yeah, after a certain point, the problem is you.

andreashettle:

outsider-my-ass:

via [x]

[The Women’s March on Washington Disability Caucus tweeted:

“A few points around why removing people from their wheelchairs is [police brutality]:

Wheelchairs are sometimes the only form of movement disabled people have.

Removing them from it can mean they have no way to move. No way to use restrooms or get out of the way in emergency.

Wheelchairs can be the only way a disabled person can sit correctly. Reduces stress on body.

Many have cushions 2 reduce pressure/hot spots. Pressure sores can lead 2 severe illness and even death.

It shouldn’t be our fault they don’t have accessible vans/don’t know how to use our chairs.

Recently, a person was charged with resisting arrest because police didn’t know how to use wheelchair. Even after she explained how to drive it.

Stuff like this is ridiculous. If u talk abt [police brutality], make sure you talk abt how disabled community is affected.

Especially disabled people of color #blacklivesmatter #policebrutality #disabilityrights”]

@accessibledeedadee  @captioning-action