Body Vs Mind

Body Vs Mind

Body vs Mind

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More Posts from Spoonful-from-the-honey-pots and Others

Queer, undiagnosed, disabled, homeless artist still trying my best to be happy

After my PTSD was triggered I could no longer live with my childhood abuser. The stress caused me to get ill. I moved out so I wouldn't have to live with them. I'm Now temporarily living at with my girlfriend's now. My condition has been getting worse. I can't walk without a can. My lab results keep coming back normal, but I suspect I have pots.

ENOUGH WITH THIS SAD SHIT THOUGH

After several months of taking a social media break, I'm back! I want a community, a place to show my art, and maybe even make a business.

This is me, this is my art ٩(๑`^´๑)۶

Queer, Undiagnosed, Disabled, Homeless Artist Still Trying My Best To Be Happy
Queer, Undiagnosed, Disabled, Homeless Artist Still Trying My Best To Be Happy
Queer, Undiagnosed, Disabled, Homeless Artist Still Trying My Best To Be Happy
Queer, Undiagnosed, Disabled, Homeless Artist Still Trying My Best To Be Happy

If you like my art, or are another chronically ill baddie, feel free to follow it even dm me (^_-)-☆


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Things my disability has made me more grateful for:

My support system. I have been around some, let's just say, very mean people in my life. I've curriated a chosen family I couldn't be happier with. With special thanks to my girlfriend and her family for giving me a temporary place to live and taking care of me

Self care. Before while I did take care of my body, I didn't take it as seriously as I should. When I had to use the restroom, shower, brush my teeth, drink water, eat I didn't always attend to my needs. Now a days, even though they are way harder to do, I put in extra effort. Because I deserve it

My art. I have a lot of self esteem issues with my art, and even have shut downs on occasions from a piece not being “perfect.” But at the end of the day, when it’s just me in bed, with my art book, and my markers, I can forget about being disabled. I can fully put effort into something I love and have worked so hard on. And my efforts pay off. I can tell my art is improving

No, I am not I am not glamorizing being chronically ill and disabled. This is the best way I’ve learned to accept and cope with it though


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I am NOT cured, I repeat I AM NOT CURED 😭😭

Guys.. I was able to take a short walk and go up the stairs easier. I think I might be cured from chronic illness 🤭

gentle check in for my fellow POTSies. does your body feel:

heavy

weak

shakey

sweaty

or generally overwhelmed?

if yes, here's a little reminder to hydrate, get in some electrolytes, take ur meds if you forgot, and adjust your positioning if you can! sit down, lay down, stretch your legs, elevate your legs, etc. if you've been in one position too long, you may find a little bit of movement to help.

i know for me even sitting upright too long can exhaust me and i dont realize until im out of sitting up spoons. i just did that today now, after some wandering around the house, im having my Horizontal Time (bed). after this i'll likely take a 5 minute walk.

there's no shame in needing rest. there's no shame in needing a break from something to go stretch or get water/food. there's no shame in only being able to do very light exercise. it's okay to listen to your body and do whatever is best for you!

Signs you're getting better that are NOT symptomatic | Chronic Illness Addition

You're adapting: Instead of pushing yourself past your limits, you learn ways to make your life with chronic illness just a little easier. It could be sitting while you beush your teeth, or opting for a bath instead of s shower.

You stop telling yourseld you "aren't disabled enough:" Maybe you're an ambulatory wheel chair user or you don't always need a cane to walk around. Stop telling yourself that just because your chronic Illness differs from day to day, means you aren't disabled enough. Go buy that cane or walker and use it when you need to. You don't need anyone's permission. You don't need to prove anything to anyone

You've learned to ask for help: I know we all want to be independent and not rely on other people for help. But even able body people need help from time to time. Our body function differently, and it's okay to need extra help than the average person. You're not a burden.

You priorities your mental health: Mental health is extremely important especially when dealing with chronic illness. You may be grieving your old body or experiencing jealousy. This is all normal. Ways that have healped my mental health tremendously are making a gratitude list to remind me what I'm grateful for, creating a schedule, and minimizing the time on my phone.

Please feel free to add to the list


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Say it with me! Wheelchairs aren’t sad! Mobility aids aren’t sad! Mobility aids are instruments of freedom!

Psst… HEY

If you are also queer, disabled, and/or have chronic pain, and wanna see art and other content about it, then feel free to follow my youtube ;))

I've been making shorts, and hopefully filming a full video when I have the energy!

One of my videos (´ . .̫ . `)


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Happy Birthday To Meee!!!!! Introducing My Walker Named Susie, Throne On Wheels

Happy birthday to meee!!!!! Introducing my walker named Susie, throne on wheels

THANK YOU TO EVERYONE WHO DONATED TO MY GO FUND ME TO GET MY WALKER


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spoonful-from-the-honey-pots - Chronically cute
Chronically cute

Tired, disabled, queer artist

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