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@evenonthedarkestdays

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“Take a shower, wash off the day. Drink a glass of water. Make the room dark. Lie down and close your eyes. Notice the silence. Notice your heart. Still beating. Still fighting. You made it, after all. You made it, another day. And you can make it one more. You’re doing just fine.”
— Charlotte Eriksson
reblog if you support feminine trans men and masculine trans women!

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Dependency does not equal addiction.
My mom has to take thyroid medication and will have to take it for the rest of her life. Because her body will not function without it.
That is not addiction, that is dependency.
I am on Lyrica for my Fibro. If I stop taking it for even 24 hours, I will experience massive withdrawals that could cause seizures and even death. (And I’ve had to go off it suddenly 3 different times. Thanks USA HEALTHCARE!)
That is not addiction, that is dependency.
If you take your pills as prescribed, you are not an addict. Most medications cause withdrawals when you stop taking them because your body has become dependent on them to function normally. That also doesn’t make you an addict.
If you can’t understand the distinction, refrain from speaking about it until you do. Or at least don’t do it around me.
What have I been up to since I last answered messages? Dealing with POTS of course, my hr increase is more mild for POTS but you can see here that my lying hr is 81 and it goes up to 116 when standing.
I just wanted to share it and if anyone sees themselves in it please contact a doctor and ask to be tested for POTS.
Those with POTS also experience symptoms like:
High/low blood pressure
High/low heart rate; racing heart rate
Chest pain
Dizziness/lightheadedness especially in standing up, prolonged standing in one position, or long walks
Fainting or near-fainting
Exhaustion/fatigue
Abdominal pain and bloating, nausea
Temperature deregulation (hot or cold)
Nervous, jittery feeling
Forgetfulness and trouble focusing (brain fog)
Blurred vision
Headaches and body pain/aches (may feel flu-like); neck pain
Insomnia and frequent awakenings from sleep, chest pain and racing heart rate during sleep, excessive sweating
Shakiness/tremors especially with adrenaline surges
Discoloration of feet and hands
Exercise intolerance
Excessive or lack of sweating
Diarrhea and/or constipation
It can be very debilitating. If you have any questions feel free to ask. I also have an Instagram where I share my chronic illness journey: @chronically_ash. Not trying to self promote just trying to share more about POTS and what I have been doing since I last answered. I also have been doing an internship and just started school.
I hope you all are doing well,
Ash
Repeat after me:
I have enough,
I am doing enough,
I am enough
https://blue—rain.tumblr.com/
via weheartit

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Sometimes the problem isn’t so much finding the time for yourself, but allowing for there to be time for yourself. It’s in believing that you deserve the time. Acknowledging that you, too, deserve to be happy.
Nicole Addison @thepowerwithin
Me @ my body: I don’t take 21 pills a day for you to behave this way.
I Stood Up and Immediately Regretted It: a Memoir
“Arent you too young to be sick?”
Hi yes my illness doesnt discriminate based on age and neither should you.
You know what? I wish I didnt have a chronic illness. I wish that I was completely healthy, and able to keep up with all of my abled peers that are passing me by. But I’m not. I am not completely healthy. I am not able to keep up with abled people. I’m just now, after all these years and setbacks, beginning to accept it.
Its okay to wish that you didnt have this chronic thing.
Its okay to not be okay with the circumstances surrounding you.
But I’ve gotten myself through the last week by reminding myself that:
I will go at my own pace.
I will persist.
I will keep trying to keep myself at baseline.
I will accept my flares, and I will get through them.
Ive got nothing left in me but pain and spite, and goddamn it, I’m gonna make it carry me through as long as I need it to.

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I wish healthy people understood that getting a diagnosis ≠ getting an effective treatment.
There are so many chronic illnesses for which there aren’t very effective medications or therapies. Even if your chronic illness has a few good treatments available, they might not work for you, or they might be out of your reach because your doctor won’t prescribe them or your insurance won’t cover them.
If you do find a medication or treatment that works for you, it might only alleviate some of your symptoms and restore part of your function. It might come with unpleasant side effects that interfere with your life in new ways.
Chronic illnesses are complex, and treating one is never as simple as getting a diagnosis and being prescribed a pill that fixes everything (or even helps).
Shoutout to everyone who can go do things sometimes but spend the next week recovering.
Shoutout to everyone who looks healthy but isn’t.
Shoutout to everyone who has put up with the “why aren’t you better” b.s.
You’re still here. You’re alive. And I’m proud of you.