LETTER CAME IN FROM THE COURTS TODAY!! I AM NOW LEGALLY MALE!! WE FINALLY DID IT, FELLAS
we’re celebrating now
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LETTER CAME IN FROM THE COURTS TODAY!! I AM NOW LEGALLY MALE!! WE FINALLY DID IT, FELLAS
we’re celebrating now
reblog if ur bi, ur not biphobic, or ur best friend is a beautiful valid bisexual
please may i have some coochie
NEW PAYPAL LINK
Proof + Extra Information
Please Reblog this new version my post and discontinue reblogging the old version
From the bottom of my heart ty for reading. Thanks to you all I’ve ordered a cane. Let’s keep the goodness coming.
two new things!
1. my birthday is May 8th. I have a gift wishlist. (however some of the money will be be put to the bank+recovery funding)
2. i am now selling items on depop
thanks again! love you all!
it’s ldov! please help a funky lil lesbian out!
$262.84/$600 (4/26/19) thank you all ily!!!
Please help raise awareness about a serious illness that hides in plain sight
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:
https://m.youtube.com/watch?v=JvK5s9BNLzA
You can also see her speaking here on TEDtalk.
https://m.youtube.com/watch?v=Fb3yp4uJhq0
Here are organizations you can donate to:
https://solvecfs.org/donate/
https://www.meaction.net/donate/
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.
Hi, guys. I don’t usually reblog stuff like this, but this is really important. Someone I really care about, Ang Vondra, has been dealing with an absolutely horrific illness for the past several months. Ang is an incredibly kind, sweet, and all-around awesome person; you may remember this sweet drawing that they did for my birthday earlier this year:
Please spread this post around to share awareness about this illness.
This boy got ZAPPED!!! ⚡
I know this isn’t the type of content I post normally but I really love how these guys turned out and thought I’d share them with y'all.
This is my Ghost Sal design! I wanted to toy with the idea of his mask expressing emotion and shit.
you’re my home now
4 Lunar New Year mobile headers.
Likes and reblogs are appreciated but not needed.
RB IF YOU SUPPORT HER
☆reblog for luck during your next gacha☆
Prom Night! 🎉
I’m really upset this arc was skipped so I made it myself.
They’re going to try and kill him.
He’s probably already dead
BOOOOOST THIS
YOOOOO
seriously guys boost this
I don’t care if it looks ugly on your blogs THIS COULD POSSIBLY SAVE LIVES
Nigerians are about to save the world
Governments are gonna kill this guy.
his name is Maduike Ezeibe, a professor at the Michael Okpara University of Agriculture Umudike, Abia State. this is huge
The world won’t get serious about this unless a post goes viral and that’s sad af You rather talk about a vine video or popular culture ok that’s fine and all but there’s a cure for HIV/Aids and america is lying There is a cure for HIV/Aids and no one will spread the news for those who are diagnosed with it, so that THE WORLD COULD WAKE TF UP There is hope for those who have been diagnosed with a disease that may have given them 20 or so years to live For the first time in the history of the world there’s is a possible preventative cure for one of the most deadliest viral diseases
Most def had to reblog this. I’m supporting him 1000%
https://www.naij.com/455113-nigeria-professor-claims-to-have-cure-for-hivaids.html
Repost & Save a Life!!!!!! Repost
There is hope .Amen Repost this would help a lot of people…
God bless this man. I hope this saves lives.
Reblog it saves lives
The tumblr app closed on me TWICE when I tried to reblog this
coincidence?
(THREE TIMES)
!!!!!!!!!!!!!!!!!!!! cool shit !!!!!!!!!!!!!!!!!!!
REBLOG THIS SHIT OR BLOCK ME
Reblog please
@madhattey @princeofmints @androgynousblackbox @ryuronny @mrgoldsdearie @blogthegreatrouge @ship-is-love @askoswaldandedward
WHAT I S THIS
REBLOG REBLOG REBLOG
WHATSHDJD–
Is this real? Because god damn!
I don’t think a lot of people understand how frustrating memory and concentration problems are. It’s not cute or “ditzy” or whatever to forget what you were doing or thinking about moment after you were doing it. Being able to complete a task or thought because you can’t remember or focus long enough to finish it is a terrible feeling.
blingee rainbow hatsune miku aesthetic board !
Please reblog, this is so important.
I needed this
Is this foreal?
Yes it’s a real service. I do volunteer work for a rape crisis support service in my city and texting is one of the features we provide as well. But just to boost its credibility, I tried it myself:
reblog to save lives!
You can also text “Steve” to 741741 if you’re a young person of color. The website for more info is stevefund.org
My understanding is that it’s more multicultural and some folks feel more comfy with that in mind!
^^^^^THIS
get help guys, please. if you’re hurting, don’t let that hurt consume you. seek help.
I never knew this. It’s spectacular.
THIS is what I was looking for a few weeks ago when I was in crisis; reblog to save a life!