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In addition to 15-year-old Nour’s ongoing health issues, Nour’s sister Noha recently developed a severe stomach ulcer due to an infection induced by drinking unsanitary water. This ulcer is causing Noha extreme pain and digestive issues, and if it is not treated very soon, will lead to internal bleeding. This ulcer has gone untreated in order to allot more funds for Nour’s ongoing nebulizer treatments, but it has progressed to the point of literally debilitating pain and serious complications. Let’s raise the cost of treatment ASAP so Nour can continue nebulizer treatments and Noha can live her life again!!
Current: $4,927 out of $5,290 usd (28 June)
Need: $363 usd
Nour is a 15-year-old girl living in a fragile tent in Gaza.
… Zachary Morgan needs your support for Help Nour: A 15-Year-Old Girl with Hea
Maha and her family previously had a verified GFM to pay for basic necessities like food, medical care, and some form of shelter. Horrifically, the person running their former GFM has stolen from them and hijacked their campaign.
Below is Maha’s new GFM. Her previous GFM was vetted by el-shab-hussein and nabulsi on their vetted campaign master list, on line 163.
I am physiotherapist Ahmed Khalil Al-Habil
from palestine _Gaza
I have been dis… Ahmed Alhabil needs your support for Support My Family To
Maha has been hospitalized due to serious complications from an infected tooth. She is particularly vulnerable to this type of infection, which almost killed her last year. Thankfully her husband has returned from Egypt, but both he and Maha are unable to work and thus cannot pay for her hospital bills. They are over $700 usd in debt for her treatment and Maha is about to be kicked out of the hospital.
As I said, last year a very similar infection almost took Maha’s life. If she is expelled from the hospital, a worsened infection is an inevitability. She still has a high fever and needs to remain hospitalized. PLEASE help her continue life-saving treatment!!
the default way for things to taste is good. we know this because "tasty" means something tastes good. conversely, from the words "smelly" and "noisy" we can conclude that the default way for things to smell and sound is bad. interestingly there are no corresponding adjectives for the senses of sight and touch. the inescapable conclusion is that the most ordinary object possible is invisible and intangible, produces a hideous cacophony, smells terrible, but tastes delicious. and yet this description matches no object or phenomenon known to science or human experience. so what the fuck
"touchy" is also a word! however it's mostly used for things that aren't objects, like subjects of conversation. it either means "oversensitive and irritable" or "requires careful handling/wording, delicate"
i think the second one works well for our hypothetical object. so we can use that.
therefore, the Default Object is:
beautiful
makes a horrendous sound
smells absolutely awful
is very fragile
tastes delicious
and i still cannot think of anything that matches this
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When I was diagnosed at age sixteen, after having one period in the eighth grade and then never again till a medically induced one my junior year of high school - my uterine lining measured in centimeters because it was so thick, my mother turned to me in the car. She was upset. Literal tears in her eyes. And she told me her friend had PCOS, but was still able to have kids. That this was still a possibility for me if I did injections and fertility treatments, etc. My mom had never asked me if I wanted kids, she just assumed.
My first conversation about PCOS with my new endocrine/OBGYN was about weight management and how that could improve my fertility when I eventually wanted kids. It wasn't asked what my goals were for my health or if I wanted kids, just assumed.
I was a hormonal, depressed mess. I hated my body. My body dysmorphia was so bad that I cloistered myself away from so much. I wore hoodies and jeans in the 90°F, 80% humidity summers. This was considered fine. I was given metformin and birth control pills and told this was all that could be done. That PCOS wouldn't affect my life until I wanted to be pregnant. I wasn't asked if I wanted to be pregnant, just assumed.
I don't know how many PCOS groups I joined on my early 20s hoping to find community and commonality for body dysmorphia and symptom management, only to be bombarded with fertility treatments and tips and 'inspirational conception' anecdotes. They never asked if I was attempting to conceive, just assumed.
It's a problem. It's been a problem. And thank god I learned to speak up and find medical professionals that would help me with *MY* goals. I shouldn't have had to, someone should have recognized the needs of that sixteen y.o. and protected her, but I can only hope the conversation changes as awareness increases.
19-year-old Khalil Al Habil's liver and kidneys are failing. Shrapnel damage from the bombardment that killed his baby brother Omar has gone mostly untreated due to a lack of funds and resources. The ill effects of this damage have progressed to the point that the organs are losing their ability to function. Khalil urgently needs 3 rounds of treatment to combat the effects of his deteriorating liver and kidneys.
We've paid off the first round of treatments but Khalil has two treatments that he still needs. The second costs about $1,250 usd, but we haven’t made much progress in more than a month and his condition is getting progressively worse. We need to meet this second goal ASAP!!!
Current: $10,052 out of $10,407 usd (12 May)
Need to raise: $355 usd
Hello, my name is Khalil, I'm 19 years old, from Gaza.
Vetting information linked in the last reblog of this post, courtesy of murderbot
Khalil is in so much pain that he can barely access the internet to contact me.
The lethargy and fatigue caused by his deteriorating organ function only make reaching out more difficult. He is in very, very bad shape, and I’m extremely worried about him.
He has gone so long between sessions that he requires additional medications to sustain him between treatments. With a price of $1500 for the treatment for his failing organs, and $500 for supplementary medications, this is where we are for round 3:
Please, before you keep scrolling, give me just one minute of your time.
My name is Enas Hajjo. I am 30 years old, from Gaza. I am a wife, and the mother of a little girl.
Our beautiful home،،the place where we dreamed, laughed, and built our lives،،was destroyed during the war. Nothing is left. Every memory we had was buried beneath the rubble.
Since then, we have been trying to survive in circumstances no family should ever have to face.
Then another nightmare began.
In the middle of the war, my husband, Ahmed, became seriously ill. After many tests, the doctors told us the heartbreaking truth, he has lung cancer.
Today, Ahmed is lying in a hospital bed, fighting for his life. The doctors say he must travel outside Gaza as soon as possible to receive treatment. Without it, we could lose him at any moment.
The cost of his treatment is far beyond anything we could ever afford.
At the same time, I am suffering from severe malnutrition because of the famine. Our bodies are growing weaker every day.
Now we live inside a small tent beneath the burning sun.
Every night, I watch my little daughter fall asleep, and my heart breaks. Rats and insects crawl over her tiny body while she sleeps. I try to protect her, but I cannot protect her from everything.
Can you imagine watching your child live like this?
Can you imagine not knowing whether your husband will still be alive tomorrow?
My daughter is too young to understand cancer.
She only knows that she doesn't want to lose her daddy.
And I don't want to lose my husband.
Please... pause your day for just one minute and look at us with compassion.
If you cannot donate, please don't underestimate the power of a reblog. Sharing our story may help it reach someone who can save my husband's life.
Please reblog our post.
Every reblog gives us another chance to be seen.
Every share brings hope.
Every kind heart brings us one step closer to saving Ahmed.
From the bottom of my heart, thank you for reading, for caring, and for standing with my family.
With love and hope,
Enas Hajjo from Gaza ❤️
✅Vetted by @gazavetters, my number verified on the list is (#425)✅
My name is Ahmed Al-Nabeeh. I am 33 years old, a husband and a father t… Amanda Marsh needs your support for Help Ahmad, Enas, and Their Bab
Until this moment, I have not received a single donation in more than a month.
Please, don't leave us alone. You are our only hope. Please don't scroll past our story.
My husband is battling cancer, and his condition is getting worse every day. Our little daughter cries constantly because she is terrified of losing her father. As a mother and a wife, watching them suffer is breaking my heart.
We are desperately asking for a chance to save his life. If you are unable to donate, please share our story. A single share could help us reach someone who can.
Please don't ignore our plea. Every share, every kind word, and every act of support gives us hope.
From the bottom of my heart, thank you to everyone who stands with us during this incredibly difficult time.🥹🙏
We no longer have the strength to endure what is happening to us.
This is one of the worst tragedies in history.
Please speak up for us. Share, comment, and let the world know that two million people are suffering every day.
I’m not only trying to survive…
My father is sick, and I can’t afford his treatment. Watching him get worse while I can do nothing is breaking me.
I just need to buy medicine and food for my family.
📌📌📌Fundraiser vetted (#167 by el-shab-hussein & nabulsi), But we created a new GoFundMe page because GoFundMe suspended the beneficiary’s account on the platform, which put us in a very difficult situation.
Ahmad, a SIXTEEN years old boy had been fundraising on this site for such a long time, and still he wasn't able to reach the goal required for him and his family! Please, do whatever you can to support!!!
In addition to 15-year-old Nour’s ongoing health issues, Nour’s sister Noha recently developed a severe stomach ulcer due to an infection induced by drinking unsanitary water. This ulcer is causing Noha extreme pain and digestive issues, and if it is not treated very soon, will lead to internal bleeding. This ulcer has gone untreated in order to allot more funds for Nour’s ongoing nebulizer treatments, but it has progressed to the point of literally debilitating pain and serious complications. Let’s raise the cost of treatment ASAP so Nour can continue nebulizer treatments and Noha can live her life again!!
Current: $4,927 out of $5,290 usd (28 June)
Need: $363 usd
Nour is a 15-year-old girl living in a fragile tent in Gaza.
… Zachary Morgan needs your support for Help Nour: A 15-Year-Old Girl with Hea
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
✓ Live Streaming✓ Interactive Chat✓ Private Shows✓ HD Quality✓ Free Actions
Free to watch • No registration required • HD streaming
genuinely so frustrating when youtubers swear or say something like "kill" or "suicide" out loud uncensored, but the subtitles censor it. like why the fuck, if YouTube is gonna get your ass for writing "kill myself", literally who wouldn't it get you for Saying It??? all it does is make me feel babied as someone who has sensory processing issues, and I can't imagine how much worse I would feel if I was completely deaf. why do hearing people get the uncensored version but we get the toddlerified end??? how is that fair?
I keep fucking thinking about this. people with hearing loss are treated as children who would fucking ignite if they saw the words Fuck, Suicide, or Kill. if the original material uses it uncensored, and the subtitles censor it, that's about as fucking blatant as it can be
not even getting into the subject of fucking "unalive"... if you don't want to say "murdered" or "suicide", English has many euphemisms for either??? unalive sounds like a word a kindergarten teacher came up with and the fact that so many people use it unironically is beyond confusing.
As a reminder, July is disability pride month! This pride month, I want us to especially think of:
Those with long-term/worsened disabilities because of their parents telling them to just work through it/get over it/"it's not that bad"
Those with disabilities stemming from childhood abuse
Those who know that they're disabled or suspect such, but can't get it diagnosed or checked out because of their parents/guardians disapproving
Those who know/suspect that they're disabled, but won't be diagnosed or checked out because they're "too young"
Those who struggle in or had to drop out of the harsh and mostly unaccommodating school system because of their disability or disabilities
Those who were lied to or not told they were disabled growing up so they could be raised "normal"
Those who have their privacy and autonomy violated as a combination of being disabled and being a child, as both of those groups are seen as not deserving their autonomy
Those who are disabled or had their disability (or disabilities) worsened because of the school system pushing them too far
Those who feel that they can never be one of the "normal" kids and that they'll always be isolated because of their disability or disabilities
Disabled folks who don't know or didn't know much about their disability as a kid because doctors would only explain to the parents/caretakers and no one bothered to talk to you
All disabled children having to deal with the intersectuality of being oppressed by both ableism and adultism.
Happy disability pride month and please start treating children and disabled people with basic respect and dignity!! They are autonomous beings! Act like it!
By the way it's like. Really fucked how society's thoughts on epilepsy is just "get over it." Seizures can cause permanent brain damage. Seizures can kill people. Seizures hurt like hell. Allow me to reiterate that seizures can kill people. And you're just gonna casually put flashing lights, a common trigger for seizures in your advertisement, in your animation meme, in your edit, on your billboards, without even thinking about putting a simple disclaimer? That's unbelievable. Your little anime edit could deadass cost a life and you're not gonna put a warning because it's "inconvenient" or "people like that shouldn't be on the internet" (ableist) (the problem exists outside the internet also). Or you'll give insufficient ones like putting it in the captions or only giving like one second before the flashing lights appear, meaning that the trigger's already in motion before anyone who needs the warning can read it and save themselves from literal physical danger.
We need to start commenting under other people's posts about how to properly warn for flashing lights and eyestrain. We need to be emailing and calling companies about their possibly triggering advertisements that could induce seizures. We need to stop tolerating ableism and start speaking up for the more vulnerable.
Also, stop putting epilepsy warnings. That's like saying "warning: schizophrenia" on a post including unreality or "warning: dyslexia" on a post with a typing quirk. First off, the disability mentioned isn't the only group of people that this could trigger. Second, it doesn't truly get the message across and instead makes it worse for those with the disability-- scrolling through the epilepsy tag on Tumblr should get you to view the content of other epileptic people, but no, you just get a bunch of flashing lights and eyestrain, even though you could instead tag for, oh I dunno, flashing lights and eyestrain.
Anyways this Disability Pride, and for every month that comes after, think about epileptic people and others who are triggered by flashing lights/eyestrain. Happy pride to those who experience seizures too frequently due to the unaccommodating and ableist societies we live in!
WHEN THE MODERN FRAMEWORK OF GENDER, SEX, AND SEXUALITY WAS LITERALLY BORN OUT OF 19TH CENTURY RACE SCIENCE YOU CANNOT DISCUSS FEMINISM OF ANY KIND WITHOUT HAVING TO FIRST DISCUSS THE RACIALIZATION OF GENDER ASSIGNMENT/PERCEPTION
like i cannot stress enough that when "man" and "woman" got codified "scientifically" in the 1800s as intrinsically seperate categories within western society THEY EXPLICITLY STATED BLACK AND BROWN PEOPLE WERE TOO PRIMITIVE TO DEVELOP THIS DISTINCTION. WE WERE QUITE LITERALLY SEEN AS A THIRD UNDIFFERENTIATED CATEGORY BELOW (WHITE) MEN AND WOMEN.
Like you CANNOT divorce gender as a construct from race as it was literally born out of the social construct of race. Black/Brown Trans Woman and White Trans Woman are, for all intents and purposes, discrete gender identities historically speaking. And the worst part is that this way that both Black/Brown women of ANY gender have had to fight to be recognized as people - much less women - should be a point of solidarity between white trans women and black/brown women. but every time we try to have this discussion it turns into a fucking flamewar bc of white fragility
okay but we can't know for sure that the loud noise and bright flash offstage—which occurred after the character who was holding the gun exited the stage with it—was a gunshot, because we didn't get to directly see it
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Everyone talks about how queers have got to get meaner but as soon as someone says “hey that sounds polyphobic” or “hey that sounds aphobic” it’s all “oh it’s not that deep this is the internet grow up and stop being such a child”.
ppl say "the queers have got to get meaner" and mean "i should be allowed to be an asshole to everyone, including other queers, just because i am queer", when it's supposed to mean "we should stand up to bigotry instead of politely letting it slide"
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