Softcore and hardcore porn from Tumblr
search invisible illness on PinDuck or ClipFuck or XXX search
submit your pics
jennakellen: To all my friends struggling with depression, anxiety, and other mental / invisible illnesses: If you got out of bed today, I am proud of you. If you got dressed, I am proud of you. If you ate a meal, I am proud of you. If you drove
crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you, have you ever seen someone get out of
depressingshitpleaseenjoy: maggiemae87: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to
starklyinaccurate: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you, have you ever seen
ms-demeanor: I made a comic about what it feels like (to me) to cope with having an invisible illness and the judgements and accusations that sometimes come with invisible illnesses. I did it in green ‘cause that’s the color of the Celiac Awareness
ahollowyear: leias: “What I didn’t realize, back when I was this twenty-five-year-old pinup for geeks in that me myself and iconic metal bikini, was that I had signed an invisible contract to stay looking the exact same way for the next thirty to
toohottoforyoutohandlle: depressingshitpleaseenjoy: maggiemae87: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m
jennytrout: mttheww: uglylilmonster: pardonmewhileipanic: thefemcritique: lestieloftus: How most people with invisible illnesses are treated by health care “professionals” The Golden Girls didn’t fuck around pls watch honestly i really
rosalindrobertson: fysw: Carrie Fisher and Gary - Star Wars: The Force Awakens Premiere at Leicester Square on December 16, 2015 in London. So, this is important. Carrie Fisher has an invisible illness and disability - severe mental illness - and she’s
nicocoer: rosalindrobertson: fysw: Carrie Fisher and Gary - Star Wars: The Force Awakens Premiere at Leicester Square on December 16, 2015 in London. So, this is important. Carrie Fisher has an invisible illness and disability - severe mental illness
thesylverlining: pardonmewhileipanic: thefemcritique: lestieloftus: How most people with invisible illnesses are treated by health care “professionals” The Golden Girls didn’t fuck around pls watch My mom actually shared this on Facebook
very true
thefemcritique: lestieloftus: How most people with invisible illnesses are treated by health care “professionals” The Golden Girls didn’t fuck around
nudityandnerdery: rosalindrobertson: fysw: Carrie Fisher and Gary - Star Wars: The Force Awakens Premiere at Leicester Square on December 16, 2015 in London. So, this is important. Carrie Fisher has an invisible illness and disability - severe mental
grayeyes-brightskies: lobotomyfail: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you,
enigmatic-nic: oneman-wolfpackk: Black girl with a Chronic Invisible illness here. The top 2 pictures are what I look like when I am having an okay day, which isn’t often. The rest are a little peek at what my life is actually like. As many of my
mttheww: uglylilmonster: pardonmewhileipanic: thefemcritique: lestieloftus: How most people with invisible illnesses are treated by health care “professionals” The Golden Girls didn’t fuck around pls watch honestly i really appreciated this
It disgusts me that even in communities of people with invisible illnesses, people still are trying to one-up each other by deciding who is and isn't disable enough to reference "The Spoon Theory." It's no one's job to judge anyone and how ill they are.
Making Invisible Illnesses VISIBLE
toxic-cupcake: jesussbabymomma: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you, have
sophygurl: ms-demeanor: I made a comic about what it feels like (to me) to cope with having an invisible illness and the judgements and accusations that sometimes come with invisible illnesses. I did it in green ‘cause that’s the color of the Celiac
fatassvegan: boo-author: starklyinaccurate: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this
toastyfoxito: bittergrapes:goldenheartedrose: Idk. I have difficulty with full gallons of milk and orange juice. This could be really great for people with dyspraxia or other disabilities that cause weak motor skills. Don’t you love it when people
selfcareafterrape: ms-demeanor: I made a comic about what it feels like (to me) to cope with having an invisible illness and the judgements and accusations that sometimes come with invisible illnesses. I did it in green ‘cause that’s the color of
Ehlers Danlos Support
chronic-illness-cat: from the amazing mevslupus.tumblr.com[picture of a cross-eyed Siamese cat’s head against a gyronny (a triangle-sectioned background) with six shades of blue. Top line of text reads: Sometimes my ‘Invisible Illness’ || Bottom
The Spoon Theory written by Christine Miserandino - But You Dont Look Sick? support for those with invisible illness or chronic illness
baberahammlincoln: I’ve been battling invisible illnesses for my entire life (seizures/asthma/hypoglycemia/allergies) and 4 years ago I began battling chronic pain along with all those issues. I’m currently diagnosed with fibromyalgia (although I
aristoteliancomplacency: One of the weirder things about chronic illnesses, and especially mental or ‘invisible’ illnesses, is that on the one hand you worry that you’re a burden to your friends and family and that you’ll either push them away
Using an old selfie for #invisible illness week. i hope that’s okay.The first time I suffered from Costochondritis, the pain was 10/10. I couldn’t think about anything except the pain. I couldn’t move, I couldn’t breathe, I couldn’t not breathe
TTC update
I have to wear a heart monitor for 2 days to capture the WPW on record. Then I have to go see my cardiologist near the end of February. If I need that ablation to correct this, my mom’s probably going to fly out. If I get the ablation and it corrects
My doctor said this WPW is rare and serious but fixable. And I was confident til I started reading the tags on tumblr for this particular heart condition😓 I’m going to trust what my doctors say but I’m quite nervous now. Fuck
I can’t go to the gym til 6 weeks past my surgery date which is still 10 days away but then I consult with a cardiologist and MIGHT need heart surgery. So that’ll mean another long recovery. But if I do have this heart surgery, it’ll probably make
I got my heart monitor in the mail today. I have to keep that phone within 10 feet of me at all times so it can send my recordings in right away. Hopefully I won’t need heart surgery but I probably might :/
I have this chronic pain condition and it doesn’t flare up a lot but when it does, it’s excruciating. The muscles around my heart and along my ribcage become inflamed and the first time it flared up, I honestly thought I was having a heart
I’m just fucking disgusted with my own body and I want to sleep but I can’t yet. I’m so incredibly frustrated with myself
I’m sick of feeling nauseous 24/7,even after positive changes in my diet. I’m sick of my constant heart palpitations;I feel like I can never get enough air. I’m sick of constantly feeling like I’m having a heart attack. I’m
Holy crap I’m exhausted as fuck. Everything is kicking my ass today and I barely have the energy to read in bed. 😓
When you have chronic pain and chronic illnesses, getting a doctor who can draw blood quickly and painlessly is like finding pure gold.
Today’s the worst flare day. I couldn’t sleep because of the pain and inflammation in my muscles and joints. I’m so fucking sick of being in pain every day.
How I feel today. My chronic pain and illnesses are really messing with me lately and I can’t make an appointment til Monday.
Before my dosage of Synthroid was upped, I was in so much pain. I had severe muscle and joint pain. I was fatigued all the time, even after 12+hrs of sleep. I had trouble waking up before 11 am or even noon. Now though, I’m doing fantastic. I get
I only managed to do a little cardio at the gym today. My joint pain flared up and it felt like my bones were being ground up so I went home early. I’m not going to quit though. I still hope losing weight and being active helps my joint pain like
thewhaleridingvulcan: vkdemon: depressingshitpleaseenjoy: maggiemae87: crohns-sucks: neecygrace: Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard.
ms-demeanor:I made a comic about what it feels like (to me) to cope with having an invisible illness and the judgements and accusations that sometimes come with invisible illnesses.I did it in green ‘cause that’s the color of the Celiac Awareness
sea-glass-siren: Mental Health Awareness Week from October 5-11 Even mermaids can have a mental illness, for a mermaid has no tears and therefore suffers so much more. I’m that one person out of every five who has an invisible illness. I’m a suicide
lupielucie: chronically—courageous: Illness isn’t always visible or obvious. Sometimes people can look healthy on the outside, but be dying on the inside. My name is Whitney, and I have battled with invisible illnesses. I have more illnesses and
thefrogman: A lot of people ask me advice on how to deal with family members who don’t understand the nature of illness. I hate to make an example of my cousin here, but this is the kind of interaction people with invisible illnesses have on a regular