the strongest bond is probably pad wings to themselves. the weakest is probably pad wings to your underwear
Not today Justin
Cosmic Funnies

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One Nice Bug Per Day
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hello vonnie
PUT YOUR BEARD IN MY MOUTH

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Love Begins
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we're not kids anymore.
styofa doing anything
AnasAbdin
he wasn't even looking at me and he found me
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@extravagantexx
the strongest bond is probably pad wings to themselves. the weakest is probably pad wings to your underwear

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i honestly dont get why people stopped reblogging things they like on here bc like what are you afraid of??? people thinking youre cringey?? guess what bitch! youre on tumblr! it's all cringey! reblog everything you like and do it shamelessly no one fuckin cares
Bc I know some of y'all are about to have a fit in the notes
Little does he realize that I have on my discourse-proof vest.
Puthykraken got dithintegrated by the dithcourthe
shoutout to the person in my building that left their halloween skeleton on their balcony and proceeded to dress it up for other holidays
thanksgiving
christmas
not pictured: when I came back from the holidays and thereād been a huge storm while I was gone, so all that was left was a pelvis
but we persist. valentines
st patricks day
and the latest, easter
when thinking about how oppression works, on a structural level, my guiding principle is that I must spend at least as much time looking down as I do looking up.
what do I mean by this? here's an example. when my surgery is delayed multiple times, I spend a little time looking up (there is only one surgeon in the entire area who will perform this surgery on trans people, so every trans person's surgical timeline is bottle-necked and delayed by months every time he goes to a conference or takes a vacation or experiences an injury. in other words, if I was cis, I would not encounter this difficulty in accessing surgery). and then I spend time looking down (due to nonstop harassment and legal threats, this practice now only treats adults and will no longer perform surgeries on minors. in other words, my access to surgery is predicated on adult privilege I have at the direct expense of trans youth's lack of access).
if you do not build a habit around thinking in this way, you will become the person Audre Lorde describes as "so enamored of her own oppression that she cannot see her heelprint upon another woman's face." If we are seeking to dismantle structures of oppression, rather than to simply use and climb them, then we absolutely must make a practice of looking in both directions, especially when we feel like we're on the bottom.

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Sees your 3racha question and then notices your Mr Muffins pfp. Keep on being rad af!
omg thank you!!! I love finding my people!
stay rad y'all š¤
"we live in an uncaring universe." sorry the special planet full of beauty and animals and food literally growing out of the ground isnt good enough for you. i guess
No, but seriously. If whenever you get up from wherever you start to feel faint, get palpitations, get numb, get nauseous, get light-headed and/or literally feel your blood drop to your feet, check the symptoms of Postural Orthostatic Tachycardia Syndrome.
Also add more salt to your diet lol. With or without the POTS unless you have hypertension in which case Iād be more cautious.
Actually, itās not just that you can reblog this. I want people to reblog this.
My poor mom went by years without knowing why the fuck she was having all these debilitating symptoms.
All it took was me making her add some more salt to her diet and have an isotonic drink daily and she IMMEDIATELY (as in, less than an hour) stopped feeling faint whenever she got up from kneeling down and her hair is slowly falling off less and less.
She used to need at least 5 minutes to recover from kneeling down and now she kneels down and stands up like itās nothing. Even her joint pain from EDS and brain fog have improved tremendously and she has much more energy.
Itās not normal to always get dizzy when you kneel down and then get up, or when you get up from bed or a chair.
Itās not normal for any of that to make you light-headed or nauseous, or get blurry vision, headaches or palpitations.
Itās not normal for your body to suck at regulating its temperature and for your heart rate to go insane if youāre just mildly stressed.
Itās not normal to want to be active and āproductiveā but be unable to get your body to do anything so you just lay there, or if you manage to get anything done, youāll need a whole week to recover.
Itās not normal to be tremendously tired all the time no matter how much you rest and sleep, even if people think youāre just ālazyā.
Iām pointing all these things out as abnormal because chronically ill people tend to not realize that our symptoms are symptoms.
Our individual bodies are the only bodies weāve experienced and since most of us donāt look any different from others and arenāt taken seriously when we complain of any ailment, we assume our symptoms happen to everyone. They do not.
People with no physical conditions (at least not impairing ones such as being a bit short-sighted) do not have their bodies make life difficult for them, unless theyāre temporarily ill. But we are ill ALL the time.
Take yourself seriously. Doctors and healthy people already donāt, so if you donāt take yourself seriously, who will?
If your body is making life difficult for you, thereās probably something going on with it, and if it persists and nothing makes it go away, it may be a chronic illness.
POTS can develop in previous healthy people after a Covid infection. If you have had Covid recently or know someone who has, please keep this in mind.
ya boy had Covid and my Doctor thinks I may have POTS as part of my Post-Covid Syndrome. He has me drinking pedialyte to help with it because of the sodium content and I gotta say, itās expensive but at least it fucking works.
No wait, itās really not normal to feel lightheaded and see everything in a blur for a minute when you stand from being laid down ????
Nope, itās very much NOT supposed to happen.
The whole āsalt is badā stigma is from the campaign during the boomer generation when there was too much salt in peopleās diets and caused blood pressure issues etc. So now the entire population has gone to the other extreme with ālow sodiumā and āno added salt!!ā as if its a health benefit and THATS JUST SIMPLY NOT TRUE.
With this fear of salt, people all over are developing POTS- salt deficiency disorder for the laymen. Some other symptoms include partial or total blackouts and what i refer to as heat sickness. Salt regulates your hydration and body temperature. If you DONāT SWEAT you have POTS. If summer months are almost impossible for you to enjoy because of the heat and sun, you probably have POTS and need more salt. If salty foods like puckles, fries, and chips taste absurdly good and/or addictive and/or SALTLESS, YOU NEED MORE SALT. Your tastebuds are literally telling you that you arent getting enough salt for your body. How do you know enough is enough? When your tastebuds go āew thats TOO much saltā. Thats your sign you finally have enough in you for now. Yes, you can literally eat a teaspoon of salt and it STILL NOT BE TOO SALTY if you are very salt deficient.
Stop being afraid of salt, its a VITAL MINERAL TO OUR BODIES, WD NEED IT TO FUNCTION AND REGULATE OURSELVES.
*flapping hard* Iiiii gotta talk to my doctors again. I keep forgetting how many adults in my Cerebral Palsy support group have these issues.
Reblogging SO FAST. I wish I had seen this years ago. To my past self and current you (if you need to hear this): you do not need to faint to have POTS. POTS UKās website has lots of helpful info. Hereās their page on diagnosis. You can literally do anĀ āactive stand testā on yourself at home + that should give you a good indication of whatās going on with your heart rate. Pulse oximeters are relatively cheap (I got mine for under Ā£20 from Argos).
and itās more important to self-diagnose now in the UK because thereās an active move in the NHS not to diagnose POTS, specifically because so many more people have it now thanks to covid - so your GP often canāt refer you for an assessment because most regions simply arenāt Doing That any more
I love how it doesn't matter what expedition it is.
They all turn into excited kids when they meet penguins.
The Penguin: GIANTS! no way! Iām gonna wave at them THEY WAVED BACK! Holy Shit theyāre dancing with me! My Wife is never gonna believe this OMG I got to dance with a Giant today so cool.
The Humans: Penguin! No way! Iām gonna wave at it IT WAVED BACK! Holy Shit itās flapping with me! I got to play with a Penguin today; so cool.
where's the joy and whimsy guy? Have they found this one yet?
@joy-and-whimsy-official
Joy and whimsy detected! This post is joyful and whimsical!
Who am I to deny a penguin some joy and whimsy š§
ill show you my tits if you stop asking ai to do things

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"Because I said so" straight up isn't as good an answer as you think it is.
school uniform codes extending to what colours youāre allowed to dye your hair, and what piercings you can have and stuff is so crazy. you HAVE to go to school and youāre not even allowed to have pink hair or pierce your nose about it????
āoh itās to prepare you for the workplaceā okay. i donāt think any workplace should be dictating what you can and canāt do with your body either and i think itās strange to decide to teach children that their body is not their own
this pissed me off like nothing else. one's sense of self is so crucially important in figuring out who they are as individual people. the younger you are, when being able to learn about yourself and express yourself, the better it will be for you as an adult. not to mention that if there's a specific career you want, you most likely know if they would or would not hire you with gauges in your ear. you don't need a school regulating that which they don't even know. I have multiple facial piercings (starting in my sophomore year of high school) and have been dying my hair very unnatural colors since 8th grade. it has not once hindered my ability to do anything! I've gotten multiple jobs, graduated with straight A's, and got a full ride to college. I want to be a teacher or an editor. How I express myself, I've seen, has only encouraged others to do it as well.
I'm just pulling your chain. I mean yanking your leash. I mean jerking you off. uh I mean I'm just messing around with you,
Iām doing all of the above if you ask me nicely
the only one i trust i knew sheād never let me down
Hudson Williams is really out there redefining "to be known is to be loved" and it might just have been the thing that undid me in the most beautiful way in the past weeks.
I know it's been said before (and I've said it before, even), but I cannot stress enough what an absolute gift it is that he is portraying Shane the way he does - unapologetically, lovingly, unflinchingly and with so much utter reverence. And how he doesn't back down. Not once. How he keeps defending Shane in interviews, like no, this is important, he needs people to know Shane is autistic and that this is not a character flaw. Because this is personal to him. Because his dad is autistic and he loves his dad, and he understands autism and it's important to him that people can see it through his eyes, that people show up with the same kindness and love and respect he has for both his dad and Shane as a character and he will to great lengths to ensure that.
And what I'm saying: you deserve people like that in your life, you really do. You deserve someone who sees you, all of you, and loves you as you are, not in spite of it, even on the harder days, and I'm eternally thankful for people like Hudson who carry so much love and empathy and compassion within them and are willing to unapologetically share that part of themselves with others

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fuckfuckfuck can we talk about how shane could barely make eye contact at all while he was talking with his mom ??? because hudson williams im going to kiss you on the fucking mouth thatās EXACTLY HOW IT GOES FOR US. i have adhd not autism but jesus they really nailed it. the way yuna begged him to look at her. the way he was trying so damn hard to do it but could only slide his eyes across her face for a few seconds before giving up and looking at the sky or down at her shirt⦠iāve done that so many times. hudson williamsās portrayal of shane as an autistic person this whole season has been incredible and if connor storrie got his flowers for episode five by GOD hudson williams better get his. him and jacob tierney are my heroes i really hope they know how much this shane means to so many people
yk ive been seeing a lot of people on tiktok and twitter talk about how "bad" hudson williams acting is in heated rivalry and then when they elaborate on what they thought was "bad" it ends up being the deliberate autism traits hudson is acting out
no a character having a flat affect and being less expressive does not automatically mean the actor is doing a bad job especially when both the creator of the character and the actor have publically stated this character is autistic and he is acting with that knowledge
and btw hudson williams does a fucking FANTASTIC job representing autism in this, i have never related to a character's mannerisms and shit more, like he absolutely nailed that shit and im getting kinda sick of non-autistic people ignoring this about his character