Majed ( @majeeeeeeddddd / @majedelsleybe ) asked me to create a fundraising campaign for him after @buildabear had to close their gfm because of bank issues. I made it on chuffed and you can find it here:
Majed has previously been vetted by association through his friend @ahmadresh2 , see #3 here
Anything helps so please if you can! Donate and be so so so cool
" Please donate and share to help treat Abdulrahman 🙏🏼❤️ "
Mothers day is just a week away, please support and help evacuate disabled mom Nara and her family!
Send support to givebutter.com/NaraMedicalAid
They need $17,500 to evacuate their family and the rest will go towards medical treatments for her Pancreatic cancer and MS which were both brought on by a white phosphorus exposure in 2008.
Please support this verified give butter that I verified myself and please share with your networks! Sending direct messages to people, texting and calling with specific asks for support work the best, so please take a little time out of your day to share mindfully!
Nara cannot share her own campaign because only her immediate family knows of her disabilities and cancer, so it is our responsibility to get her funded!
[Image Description: a digital illustration by @k8deciccio of Nara, a Pal-eh-stienian woman wearing a black hijab/outfit with purple highlights. She has a breathing apparatus that is bulbous that goes in her nose. Text Reads: Help Narawith Cancer and MS Treatment, She Must Evacuate with her family of 4. $30k goal givebutter.com/NaraMedicalAid . There is a QR code in the bottom right corner that goes to her support link.]
I’m Farah, a young woman from Gaza living through unimaginable suffering. The war has brought famine, disease, soaring prices, and constant danger. We’ve been displaced multiple times, our home is damaged, and basic needs like clean water, electricity, and medical care are nearly impossible to find.
I was a medical student, but the war stole my education and dreams. I come from a family of seven, and while two of my brothers study abroad, I remain here, struggling to survive.
To my kind friends around the world — your support, even the smallest amount, can help me endure this tragedy. Thank you for standing with us.
#Free gaza
✅️Vetted by @gazavetters, my number verified on the list is ( #549 )✅️
My daughter could not sleep because of the severity of hunger. What is the fault of the children who are dying of hunger in Gaza and the world cannot do anything?
@dirhwangdaseul @b0nkcreat @tamamita @chokulit @3000s @apas-95 @pitbolshevik @ot3 @punkitt-is-here @vampiricvenus @turtletoria @paper-mario-wiki @valtsv @omegaversereloaded @i-am-a-fish-stinks @catsgifsarefun @spongebobssquarepants @postanagramgenerator @feluka @nyancrimew @90-ghost @beserkerjewel @neechees @memingursa @certifiedsexed @afro-elf @11thsense @sawasawako @spacebeyonce @skipppppy @beetledrink @fools-and-perverts @dailyquests @evillesbianvillain @wolfertinger666 @taffybuns @ankle-beez @sabertoothwalrus @meshugenist @isuggestforcefem @hotvampireadjacent @marxism-transgenderism
I am Hanaa, a resident of Gaza City, specifically in the northern Gaza Strip. I am 38 years old. I live with my eight children and my husband in the Gaza Strip. Before the war on Gaza began, I was living a happy life with my children and my husband. We had a monthly income that was sufficient to meet our needs and fulfill our requests. When the war on Gaza began on 10/7/2023, we lived as homeless people after our entire house was bombed at the beginning of the war. We were displaced to countless areas since the first day of the war. After more than 200 days of the war, one of my sons was martyred and two others were injured while trying to find us food to satisfy our hunger. I became fully responsible for him after my eldest son was martyred and the other two were seriously injured. My children, my husband and I live in displacement camps. We have no other shelter. For the sake of God, help me feed my children and build a home for us. Donate to me, even if it is a little, because I need your help.
https://www.gofundme.com/f/hanaa-family
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
The last loaf of bread for five people. A kilo of flour costs $10, and a whole bag costs $300. Please don't leave my children hungry. Donate via the link in our bio. Please, please 🥺🙏
pakehas when i tell them being maori is about recognising your maori ancestors, back to the first arrival and percentages didnt matter
Idk, I feel like reverse racism is a thing but its nowhere near to the scale of real racism. In my country people are offered scholarships if they are 'Maori'. And by that the government means if your great great great gran was maori then you're maori too. Idk its something thats always irked me, I feel like you shouldnt be handed money for something you had no control over ya know?
Reverse racism isn’t real
always searching, for serenity, now im on the; edge of reality.
193 posts