Chronically.Corey

Chronically ill and trying to raise enough to work less before my ME/CFS takes me out… HEDS & co.♿️ https://coreycreates27.etsy.com Cashapp: ChronicallyCorey

[chronicallycorey]

Help me work less hours at my ft job so I don’t worsen my baseline anymore #MECFS

ETSY: https://coreycreates27.etsy.com

Cashapp: ChronicallyCorey

[chronicallycorey]

https://coreycreates27.etsy.com

[chronicallycorey]

https://coreycreates27.etsy.com

Everything is free shipping and factored into pricing, appreciate u all🫶🙏💕

[chronicallycorey]

https://coreycreates27.etsy.com

Everything is free shipping that’s factored into the pricing of the items, Appreciate u all🫶💕♿️

[shyyycatsblog]

I am seriously desperate for help right now. Please donate anything you can. I am begging everyone to reblog this, whether you can donate or not, please don't let this flop. I need your guys help more than words can express. I need help with my phone bill as well as getting some toilet paper and other necessities. In total I need $125 but anything and I genuinely mean anything helps. Please reblog if you can't donate, it means so so much to me 🥺🙏

pp

vmo

cshapp

$0/$125

[shyyycatsblog]

$67/125

Sadly I had to use some of the funds to get my pain meds, so my goal is set back a little bit, but I'm still trying to remain hopeful 🥹💜

[shyyycatsblog]

Please help me reach my goal, I'm so close but so far still 😞 PLEASE reblog if you can't help, I'm so serious guys please help me

[shyyycatsblog]

$97/$125 🥹💜 Im getting so close to my goal now

[shyyycatsblog]

I'm so close to my goal guys, please help me reach it 🥺🙏

[shyyycatsblog]

PLEASE HELP i need $28 left!!!!!!

[shyyycatsblog]

I actually need the full thing all over again bc of how long it took, the total has raised and I'm so broke I can't afford to live rn. Nothing is working out.

[chronicallycorey]

https://coreycreates27.etsy.com

If u r interested in this keychain⬆️

[chronicallycorey]

Made another ME/CFS keychain, posted on my Etsy, FREE SHIPPING, help me work less hours!🫶💕♿️

[fibro-memes]

[chronicallycorey]

https://coreycreates27.etsy.com i appreciate everyone that’s already bought from me🫶💕

[chronicallycorey]

Anything helps even a repost Thankyou all🫶🙏💕

[chronicallycorey]

I have mild to moderate MECFS, and still working a FT damaging my health even more. You can help by supporting my Etsy or just sharing so I can hopefully cut back on hours 🫶💕

EVERYTHING FREE SHIPPING!

Use code: Bday21 to get 20% off your order

https://coreycreates27.etsy.com

[chronicallycorey]

I have mild to moderate MECFS, and still working a FT damaging my health even more. You can help by supporting my Etsy or just sharing so I can hopefully cut back on hours 🫶💕

https://coreycreates27.etsy.com

[chronicallycorey]

I have mild to moderate MECFS, and still working a FT damaging my health even more. You can help by supporting my Etsy or just sharing so I can hopefully cut back on hours 🫶💕

https://coreycreates27.etsy.com

[chronicallycorey]

it’s getting to the point where several days out the week I have to go to the bathroom multiple time during my shift to through up. Or go in the vaccine room to lay down with my legs above my head. Anything helps, sending love🫶💕

[chronicallycorey]

#mecfs #plankforme #plank4me #

[sacredrelicoflove]

May is myalgic encephalomyelitis awareness month!

This disease can be devastating and affects millions of people around the world. For months, I was confined to bed in a dark, silent room. Any amount of light would pierce my eyes and head with a staggering migraine. Any sound physically hurt to the point of tears. I couldn't sit up for more than thirty seconds or my heart rate would easily climb into the 180s. I lost the ability to bathe myself, to walk more than a few feet, to carry out any tasks of independent living, even the ability to cry as the exertion would cause a crash into worsening symptoms. My constant pain level was unbearable enough that nearly drove me to ending my life. This is the reality of living with severe ME, and it's nowhere near as severe as this illness gets.

Those who are at the most severe stages cannot speak, move, or open their eyes. They are often tube or TPN fed because the action of chewing is too much for their bodies to bear. This condition has taken so many lives, some of which I have known and watched die in slow motion. Onchologists have likened the quality of life of those with this disease to end stage terminal cancer.

The plank4ME challenge was created to raise awareness for this disorder. The idea is to hold a plank for as long as possible to feel a fraction of what it is like for someone with MECFS to lay flat in bed "resting". Research for this disease is drastically underfunded and so no strides in care have been made in many years. Even with millions of us missing from life and confined to dark beds, there is still no treatment, and no cure.

Please, consider donating to the Open Medicine Foundation at the link below to aid us in our search for the cure. Because no one deserves to live in a dark room.

https://openmedicinefoundation.crowdchange.co/54040

[chronicallycorey]

Trying to raise money to cut back on hours at my FT job before MECFS ends me!!! Everything in shop is 20% off with promo code: Bday21

Because it’s my 21st birthday this week! Shop link is attached! Everything FREE SHIPPING!

https://coreycreates27.etsy.com