Fuck Indiana. Me and my homies despise Indiana
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Fuck Indiana. Me and my homies despise Indiana
WATCH INFINITY TRAIN ON HBO MAX
We have a week to get enough views to continue this show. If you have an at&t subscription you can get hbo max. If you have hbo max I’m begging you to stream it because this is one of the few GENUINLEY good kids shows and if you haven’t watched it I suggest you do. It focuses on so many real life problems on a kids show and talks about so many important topics that should be talked about nowadays. If you can’t watch it on hbo max I suggest spreading awareness about infinity train since it’s pretty underrated
OUR LIVES MATTER
BLACK LIVES MATTER
Let's say it's been one hell of a week.
***** ***
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Abortions in Poland are now illegal in cases of severe damage to the fetus. It means that women and other pregnant people will be forced to give birth to deformed fetuses, even if they die in suffering.
They changed the law in the middle of pandemic and instead of taking the legislative route they used the Constitutional Court.
The abortion law in Poland was already one of the strictest in Europe and now it's one if the strictest in the world.
The ruling party and pro-life organizations might want to ban abortion completely, even when the pregnancy is a result of rape, incest or when the mother’s health and life is at risk.
There are protests all across Poland. There are many cases of police brutality used against the protesters.
It’s inhumane.
(source ig: @stonewall_poland )
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My friend and I were talking about how messed up America is right now. They kept saying that we can't do anything about it, but that isn't true. Don't tell me that you can't do anything about our messed up world right now. If we want to change something, we can change it. If we want to change something, we need to do it ourselves. Letting it just go by and thinking that it's going to fix its self is wrong. I want to be the change in America. I want to fight for what is right. Martin Luther King has been dead for over 52 years, and his dream of everyone being treated equally is still not complete. I know that he is looking down at us and thinking, 'How has the world come to this?' The answer, is that people are not using their voice. Everyone has a voice. For some people, they haven't found it yet, for others, it's being silenced. For those who already have found their voice, use it. Stand up for those who need it. We are the future of America, and we need to fight for what is right. I am not going to involve myself in protests because I am scared. Instead, I am going to hold up a black lives matter sign on the side walk of a busy road. I dont like talking, but writing is just as powerful. Using your voice, whether it's talking or writing or drawing, your standing up for those who need it most. I hope that you start to use yours.
Spread the word. If we want a change, we need to be the change. We were given a voice for a reaso, and that reason is for helping others. I will not just stand by and watch the world aroubd us crumble.
You can repost this if you want to, just spread the word. Black lives matter✊🏿 ✊🏾✊🏽✊🏽✊🏾✊🏿
My non Australian follower, please know what’s happening right now. It’s the worst we have seen & it’s only expected to get much worse!
October is dysautonomia awareness month! I created this especially for those SW fangirls, like myself, that suffer from POTS (postural orthostatic tachycardia syndrome). In order to be diagnosed a tilt table test is administered, in which you are strapped to a table and inclined to 70 degrees while hooked up to a bunch of machines that measure your blood pressure, heart rate, breathing, oxygen, and sweat response. When I saw this scene in TFA I had recently been diagnosed, and my first thought was “that literally looks like torture!”, because I quite literally started having full body convulsions after being lifted for only like 5 seconds!
To learn what POTS is please take a few minutes out of your day to watch the short vid in the link below. If you don’t want to watch the vid, I will give my best attempt to explain it in layman’s terms.
https://youtu.be/ch6ipV3M4yo
Dysautonomia is a group of medical conditions that are characterized by a loss of proper function of the autonomic nervous system, which is in charge of everything that should happen automatically in the body without you consciously thinking about it, such as heart rate, blood pressure, blood vessel contraction and expansion, core body temperature, digestion, pupil dilation, organ functions, pain response, sleep (my circadian rhythm is all out of whack!) etc. etc. This is not a rare disorder, which primarily effects young women, usually starting in mid teens-early 20’s, but there is so little research no one knows how many people have it. In fact it is so misunderstood that most doctors don’t even know what it is! (I cannot tell you how many doctors I’ve had to explain it too 🤦♀️). POTS specifically is characterized by the body’s inability to maintain blood pressure when you stand up. You know that feeling when you stand up too quickly and you get really dizzy and have to sit down? That happens because in order to keep enough blood going to your brain, a complex series of things needs to happen when you change to a vertical position. When you stand up your brain tells your blood vessels in your legs that they need to constrict to prevent blood from pooling in the feet and keep the blood up in the head, then the heart needs to beat strong and fast to push the blood back into the brain within 2-3 beats. When the body fails to do this properly, if even a small percentage of blood falls from the brain, you are in danger of passing out, or at the very least feeling extremely dizzy, lightheaded, confused, nauseous, or a headache. People with POTS experience this every time they stand up! Many faint multiple times a day, and suffer from injuries such as bruises, sprains, whiplash, even broken bones and concussions from falling when passing out. When a person with POTS stands up, the blood vessels in the legs either expand instead of constricting, or simply fail to constrict, making the blood fall down to the feet (ppl with pots often have purple or red flushed feet). The heart starts doing its thing to pump the blood up to the brain, unawares that the blood vessels did not hold up their part of the bargain! Then the heart realizes the blood is gone, there’s not enough to pump up to the brain! So it freaks out and starts beating like a jackhammer (this is called tachycardia) desperately trying to pump enough blood up to the brain so you don’t lose consciousness. This releases a ton of adrenaline, and you then often start breathing heavily as if you’ve just run a marathon, only you can’t keep a rhythm, so you’ll be hyperventilating one second, and the next just fast deep breathes, the next slow breathing, then hyperventilating again, then holding your breath, then breathing slowly, and back to hyperventilating etc. If the heart still fails to pump enough blood to the brain, to prevent permanent brain damage or death, the brain presses the off button, and you pass out..
But people with POTS also suffer from other symptoms related to dysautonomia, such as digestive issues like IBS and gastroparesis (paralyzed gut), inability to sleep or keep a sleep schedule (body does not understand that sun means awake, dark means sleep!), chronic fatigue, brain fog, chronic pain, over active adrenal glands, and so so much more (a lot also have Ehlers-Danlos Syndrome, a connective tissue disorder characterized by a genetic fault in collagen production, creating weak and loose tendons, ligaments, skin, and in severe and deadly cases, organ structure. This makes exercising difficult...)
So in order to treat POTS there has to be a very holistic approach, which modern medicine tends to not do very well, everything is very compartmentalized. Doctors specialize in one thing, and won’t treat anything else or communicate closely with doctors in other fields.
Treatment right now is not very effective. Most people take a medicine to retain water volume, drink 2 liters water/day, and eat lots of salt, potassium, and magnesium so that with increased blood volume less blood will fall from the head, in theory anyway. Intense specialized physical therapy is needed, which includes intense cardio (that makes you pass out sometimes... super fun), moving the digestive tract (it doesn’t know wtf it’s doing), strengthening muscles that start to weaken and atrophy from prolonged bed rest (it’s hard to do anything when you pass out every time you stand up, but the longer you spend on bed rest the worse pots gets), strengthen leg and core muscles to pump the blood which the blood vessels suck at doing, breathing practices to prevent hyperventilation or breath holding, and meditation to calm the parasympathetic nervous system (which is in charge of fight or flight). All very Jedi like actually. So to motivate myself to do up to 2 hrs of pt throughout the day, I tell myself I’m training to be a POTSie Jedi. Lol
Please help spread awareness and educate yourself! We need more research to find better medications and hopefully one day a cure! Feel free to dm me with any questions, especially if you’ve ever experienced any of the symptoms described in the video!