@spoonfulofhannah - Tumblr Blog

Hi, I’m Hannah! I became disabled in 2020. I’m extremely sick. I can’t legally drive, and I can’t have a normal job. I recently opened my own at home business to support myself because I’m home bound. I press and make them all from my own home. Here is a new shirt from me! https://www.etsy.com/listing/4325498020/hot-people-hate-fascists-leftist?ref=share_v4_lx

Made by a disabled owned home business: Little Magic Spoons! This is the perfect shirt for anyone that supports human rights and minorities!

#human rights #leftist #disabled #disability #epilepsy #pots #chronic illness #lgbtqia #autoimmune disease #hashimotos #potsawareness #dysautonomia #mecfs #politics #liberal

fibro-memes

Just a reminder that disabled people can still serve with a mobility aid

#girls with tattoos #disabled #chronic illness #girls with piercings #women with tattoos #alternative #pots #epilepsy #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #disability #selfiie #tattoos

PLEASE HELP A DISABLED PERSON

I had a fainting episode from my POTS. I have a broken nose, stitches on my nose and the inside and outside of my mouth, a concussion, a sprained neck, and an injured tooth and tailbone

My husband has to stay home with me, and we have so many bills including medical bills and medical supplies that we need to buy. If ANYONE can help, thank you so much.

#disabled #disability #pots #chronic illness #postural orthostatic tachycardia syndrome #dysautonomia #epilepsy #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #spoonie #crowdfunding #chronically ill #chronic pain

I have no one around me that understands what it’s like to be so sick. I feel like every time I voice how I feel, I’m interrogated, I’m treated like I’m insane, or it’s downplayed. I don’t want to be here anymore, and I can’t even really tell anyone that

I am not okay

#disabled #disability #epilepsy #pots #chronic illness #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #postural orthostatic tachycardia syndrome #chronic pain #chronically ill #sad thoughts

Disabled people are not obligated to do everything that a non-disabled person can do. Stop treating us as though our bodies are the same. What you do normally can be detrimental and dangerous to us.

#disabled #disability #epilepsy #pots #chronic illness #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #postural orthostatic tachycardia syndrome #seizures #actually disabled #chronically ill #chronic pain #chronic fatigue #spoonie #ambulatory wheelchair user

My book, Equanimity and Grace

#poem #booklr #trauma #childhood trauma #quoteoftheday #quotes #sad thoughts #bpd #actually bpd #cptsd #ptsd #books #poetry #writing #mental health matters #mental heath awareness #mental illness #mental health

Living with Borderline Personality Disorder (BPD) is feeling everything too much. It’s like your skin hurting to the touch all over your body. It’s not attention seeking; it’s survival. Be patient with us, and we’ll keep working on being patient with ourselves.

#mental illness #mental health #bpd #actually bpd #borderline personality disorder #bpd awareness #mental heath awareness #mental health matters

Help a disabled person 🚨

Hi, everyone. I’m Hannah! I have severe POTS, epilepsy, ME/CFS, an autoimmune disease, etc. I am desperate for some things that would make my life being disabled easier. A wheelchair ramp, a shower chair, and more. If you could please get the word out, I’d be so thankful. I made a wishlist. If anything on it doesn't make sense, ask and I'll explain. Thank you so much

Also: CA: $itsmeliz1129

Venmo: hannahliz1129

PayPal: hannahcampjohnson

Amazon.com

#disabled #disability #epilepsy #pots #chronic illness #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #postural orthostatic tachycardia syndrome #seizures #dysautonomia #chronically ill #chronic fatigue #chronic pain #spoonie

Help a disabled person 🚨

Hi, everyone. My birthday is the 29th. I’m not getting gifts or anything because of the stress from my grandfather’s cancer and my mom’s kidneys. If anyone is willing to share, I’m desperate for a wheelchair ramp for myself and help with medical bills. Thank you so much.

#disabled #disability #epilepsy #pots #chronic illness #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #postural orthostatic tachycardia syndrome #dysautonomia #wheelchair user #seizures #pots syndrome #chronically ill #spoonie

Disabled and chronically ill people are allowed to enjoy things and do things they like (if they’re able) while still being sick and disabled. Yes, even if they aren’t employed. Hope this helps.

#disabled #disability #epilepsy #pots #chronic illness #me/cfs #myalgic encephalomyelitis #autoimmune disease #hashimotos #postural orthostatic tachycardia syndrome #wheelchair user #dysautonomia #spoonie #pots syndrome #chronically ill #chronic fatigue

#disabled #chronic illness #epilepsy #pots #me/cfs #myalgic encephalomyelitis #hashimotos #postural orthostatic tachycardia syndrome #dysautonomia #autoimmune disease #disability #chronically ill #chronic fatigue

spoonfulofhannah

Help a disabled person 🚨

Hi, I’m Hannah. My birthday is in a few weeks, but I will be spending it with appointments all this month. I have two procedures (colonoscopy and endoscopy), a barium swallow test, another GI appointment, a neurology appointment, and an MRI. My copay for the MRI alone is $150. Both the endo and colonoscopy are also $150 each. All I want for my birthday is to be able to pay for it all. If possible, please share this. Thank you.

Also linking proof of my testing scheduled!

spoonfulofhannah

$60/$500

spoonfulofhannah

I had to reschedule my colonoscopy and endoscopy due to the cost. Please keep sharing this

#chronic illness #epilepsy #actually epileptic #seizures #pots #postural orthostatic tachycardia syndrome #dysautonomia #autoimmune disease #hashimotos #me/cfs #myalgic encephalomyelitis #actually disabled #disability #disabled

From my book, Equanimity and Grace by Hannah Elizabeth

#poem #disabled #chronic illness #epilepsy #pots #me/cfs #myalgic encephalomyelitis #disability #poetry #postural orthostatic tachycardia syndrome #dysautonomia #autoimmune disease #quotes #quoteoftheday #booklr #books #writing

Healthy people really don’t understand that there is a drastic difference between them resting for relaxation and chronically ill people resting because our body depends on it

#disabled #epilepsy #pots #me/cfs #autoimmune disease #hashimotos #postural orthostatic tachycardia syndrome #myalgic encephalomyelitis #pots syndrome #disability #spoonie #wheelchair user

spoonfulofhannah

Help a disabled person 🚨

Hi, I’m Hannah. My birthday is in a few weeks, but I will be spending it with appointments all this month. I have two procedures (colonoscopy and endoscopy), a barium swallow test, another GI appointment, a neurology appointment, and an MRI. My copay for the MRI alone is $150. Both the endo and colonoscopy are also $150 each. All I want for my birthday is to be able to pay for it all. If possible, please share this. Thank you.

Also linking proof of my testing scheduled!

spoonfulofhannah

$60/$500

spoonfulofhannah

No other donations unfortunately

#chronic illness #disabled #epilepsy #gastrointestinal #me/cfs #long covid #postural orthostatic tachycardia syndrome #pots #dysautonomia #autoimmune disease #hashimotos #gastroparesis #disability

I wish all chronically ill and disabled people a very “doctors listening to you” November

#disabled #chronic illness #epilepsy #seizures #me/cfs #myalgic encephalomyelitis #pots #postural orthostatic tachycardia syndrome #pots syndrome #dysautonomia #autoimmune disease #hashimotos #disability #mental health #mental illness

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