Hello my friend, my name is Jaafar from North Gaza, I am 24 years old, and finally after waiting for a whole year of killing, displacement, hunger, massacres and genocide against us, the time for a ceasefire has come, thank God we are still alive after all the exhaustion, and during the next week we will return to our homes in North Gaza, which was completely destroyed, unfortunately our area was completely and brutally destroyed and we have nothing left, neither a home, nor property, nor furniture, nor clothes, nor any other clothes, I know that returning to the north will be very painful and difficult due to the lack of the necessities of life, and we will start building our lives from scratch, but we are happy for the war to end.
Please 🙏, donate to my campaign to save my family, even a small amount will help us stabilize ourselves a little, and buy some supplies 🥹, I hope that God will protect your family and friends, thank you 🥰🩵
✅️Vetted by @gazavetters, my number verified on the list is ( #299 )✅️
Hello lm hamdi ,I humbly ask for your support by reblogging this post on your account to help me and my family. As newcomers to Tumblr and GoFundMe, we are in desperate need of your kindness and support. 🙏🇵🇸🍉😔Please donate 🙏🏼Let's reach the goal as soon as possible .
I am sorry but i have no banj account so i cannot donate but i will reblog your posts
After visiting the hospital and seeing the doctor, it became clear that Ahmed needed urgent surgery, but the cost was expensive and we didn't have enough money. I don't know how long Ahmed will be able to endure the pain. Please help me get the surgery. Ahmed was born through IVF and was admitted to the incubator due to holes in his heart. He was exposed to artificial oxygen, which affected his eyesight and caused vision problems. You are my only hope with your donation and sharing this post.
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We need your help. The situation is very difficult. You are our last hope. Food, clothes, milk, rent, everything has become very expensive. My son Ahmed needs heart surgery and eye surgery. Save my son so he can complete his treatment and undergo the operation. In addition to my family in Gaza, my father, mother, brothers and sisters are living in very difficult conditions as a result of the war and continuous bombing. We hope you will help by donating and sharing the post 🙏🙏
we're all aware of hypermobility right?
well let's raise awareness for hypomobility.
as a person born with cerebral palsy that left me hypomobile in different areas of my body, it can be debilitating. I can't do certain things without feeling my muscles stretch and being in severe pain. sometimes, different joints lock up in place and won't move. it's scary, there's been times where I thought it would stay stuck forever. I have less range of motion than an average person.
but nobody ever talks about hypomobility. all the attention goes to hypermobility. which has made me feel left out and less valid in the disability community.
lets raise awareness for hypomobility. we need all the same support and recognition hypermobility has
feel free to reblog <3
i think terfs should go eat glass
Transphobia almost always has collateral damage towards cis women.
This person claims she cares about "women's rights."
But her little jokey post basically threw every tall and broad-shouldered cis woman under the bus.
This took 10 seconds of googling.
These posts represent thousands of women struggling with the exact same issue. The US has nearly 2 million women over 6 feet. And this "women's rights" advocate is telling them they don't have a woman's body.
*Just not tall women or muscular women or wide shouldered women.
Bathroom bans are creating the same problems. I keep hearing about cis women who are being harassed because they have features deemed too masculine.
Sports bans have led to invasive medical testing of cis women. They need to get testosterone checked. Schools ask about menstrual cycles. And now with more bans going in place, they are requesting private medical records to prove the sex of young children.
And don't get me started on self-appointed trans police.
Imane Khelif is still getting harassed even though the entire controversy was proven to be Russian disinformation. She's "dangerous" even though that style of boxing is point based and much safer than punch-until-they-go-to-sleep boxing. Quick punches are preferred over powerful ones. It's literally designed that way so people get bloody noses instead of chronic brain injuries. JK didn't know that and didn't care because she had to make an example of someone.
These people will hurt and harass and lie about *anyone* if it furthers their agenda.
If cis women or girls get harmed in the process, they do not give a shit.
That is bigot behavior.
So, yes… BIGOT!
basically, not all of us people with eds are hypermobile, and we shouldnt reduce ehlers danlos to just being hypermobile with stretchy skin.
I have hEDS, the most common type of EDS, where you do get hypermobility, but even hEDS is more than that.
i really wish that ehlers-danlos syndrome wasn't basically just thought of as the "bendy" disorder. firstly, there are more than 13 types of eds, and they all have varying relations to and degrees of hypermobility. secondly, eds are a collection of congenital connective tissue disorders - connective tissue makes up a vast majority of your body and, because of this, eds, hsd, and other congenital connective tissue disorders like loey-dietz, marfans, stickler syndrome, and osteogenesis imperfecta are multi systemic.
having eds or another connective tissue disorder is SO much more than just some flexibility and it's especially frustrated that they're often thought of solely in relation to that one aspect of them because it leads a lot of people down the path of misdiagnosis.
as an advocate and educator regarding ctds and especially eds, i have spoken to SO many people who simply wrote the possibility of them having a ctd like ehlers-danlos off simply because they aren't flexible. it's such a dangerous misconception and really frustrating to see especially given the fact that the muscles of hypermobile people often overcompensate to make up for joint laxity, which can actually lead to a lack of flexibility/high tone/spasticity
so yeah, tl;dr: if you have a bunch of multisystemic symptoms that seem largely unconnected, look into connective tissue disorders. they're much more common than people think, frequently go under the radar, and can really wreck havoc on your body - ESPECIALLY when you aren't aware that you have one
Please, please, look at my donation campaign and help me. I have newborn children and my son Ahmed needs treatment. He is a heart patient and suffers from two holes in the heart. He needs help and treatment. We do not have money and we are stuck in Egypt because of the Gaza war. My wife and I lost my jobs and there is no source of income. I would like you to help. To care for my children and provide the necessary treatment for my child Ahmed, please donate even a little thing to save my child’s life
I cant donate, i have nonbank account. i hope somebody can though
Hello, I am Hani from Gaza, Palestine, I speak to you with a sad and heavy 🥺 heart about what happened to me and my family. I was seriously injured in the war on Gaza and did not receive treatment from the moment, I am married and have three children, Abdullah, Salma and Saleh, and my wife gave birth to a baby girl named Tulip, but unfortunately she died at birth from the effects of war and famine, more than a year and seven months ago I was unable to buy my children's needs of milk and life necessities. We live in a torn tent and winter has come💔😭 and the bitter cold hits my children very cold, because we don't have winter coats and winter clothes, we lost everything we had in our house destroyed in the war, please my friend don't ignore my story Donate and share my campaign I will be grateful to you 🫶🇵🇸🍉
Read more about us in the following link, please donate to us on it and share it 👇
Please help us get out of life's crises and the woes of war
✅ Vetted by @gazavetters, my number verified on the list is ( #99 ) ✅
https://www.instagram.com/hane1986_10_26?igsh=MWs4Zzd1d3UyM3V3ag==
vote for the armadillo fir minecraft live. why? Cute new savannah animal, we have barely any savannah critters in minecraft, Plus, Armour for your pet wolves, it keeps them safe!!!!
No safety. No food. No aid. No water. No healthcare. No education. Is this what it means to live? Is this what world accept as life?
If a group of animals were trapped, starved, and cut off from the world like this, people would be outraged. But because it's us—human beings—somehow, the world looks away.
These are unbearable days. Everything feels heavy. Each hour presses on my chest like I’m being suffocated.
My family needs urgent help.
Basic survival has become nearly impossible. Bread—just bread—now costs over $25 a day to make.
We are not asking for luxury. We are begging for life.
#crisis #humanrights #emergency #donate #pleasehelp #tumblrcommunity #survivestories #reblogtohelp #signalboost
just wanted to share the National Down Syndrome Society’s message for this year’s World Down Syndrome Day (21st March) 💛💙
always searching, for serenity, now im on the; edge of reality.
193 posts