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“Because the body’s nerves are constantly firing they never get a rest, so when they get triggered by “smaller” things, they will hurt more than a “regular” person.” Please Don't Confuse My
#ChronicPain With 'Low Pain Tolerance' https://buff.ly/30VZsR1#chronicillness#cpp -
“In all my years as a doctor treating patients with
#chronicillness, I never saw a patient who enjoyed feeling ill. I saw the opposite, patients who were once very active, desperately trying to find answers and treatment for their overwhelming symptoms.” https://buff.ly/2KmZOtW -
If you have a
#chronicillness you will definitely understand how this feels.. Getting the energy to go for a shower. Having a shower. Having to lay down or nap after a shower because it was so exhausting and used up all of your energy. -
"I have come to realize that the words I say out loud and in my head end up defining me. " Thoughts on self-identity with
#chronicillness . | Those Are Fighting Words! Metaphors Make Meaning by@klclark525 http://bit.ly/2SaoPur#Fibromyalgia -
tears the minute I got home. PLEASE to all my fellow
#chronicillness warriors out there: if TMS is recommended to you, please be sure you are well enough to attend the sessions—don’t be sold on the idea that you might feel too sick/weak now but the TMS will make these 3/Prikaži ovu nit -
Getting a massage later today for my broken down immunosuppressed ass


Self care party of 1 
#ChronicIllness#Neurosarcoidosis#StopSarcoidosis#DepressionIsReal#Anxiety pic.twitter.com/uatndjVcj8 -
Serious and funny truth about
#chronicillness here https://twitter.com/FibroBloggers/status/1224393381486505985 …
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When the weather changes every inch of the body knows before the meteorologist. It is a war of body and mind. Depression, pain, multiple illness symptoms, and extreme tiredness is the everyday war battling behind a mask every chronic warrior faces.
#Fibromyalgia#chronicillness -
My illness may be invisible. I am not.
#chronicillness#invisibleillness -
I also currently cant do any of this because a) money b) chronic pain and fatigue and c) I'm too tired to do anything but unbelievably bored because I cant do anything
#chronicillness#MECFS Oh and d) I dont have the space for all that stuffPrikaži ovu nit -
I am an educated biochemist from one of the best universities but I can't help in the fight against ME/CFS. Just laying in the dark. I want to help, give my skills to research teams to end this devastating illness. :(
#MECFS#chronicillness#MEaction -
Waking up when you have POTS be like...
#chronicillness#potsawarenesshttps://twitter.com/erikacostell/status/1224321048646160384 … -
You don't look disabled You don't look ill Old people get arthritis We all get tired I'm in pain too You can't show weakness Many are worse off I swear by Glucosamine You can't give in
#AbleismInFourWords#chronicpain#chronicillness#Behcets#AVN#Neutropenia#arthritis -
#ChronicIllness really be like that, especially in winter! pic.twitter.com/s7ikfgQwXH
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My Mother is my hero. Dealing with a child with a cold is a lot. I will never know how she made with a chronically ill child. She’s entitled to any imperfections people may dislike about her.
#chronicillness#parenting -
#ChronicIllness life: In tonight's adventure, I'm lying in bed, about to watch my beloved fiancé in The Curse of the Midas Box. Suddenly, I feel the eminent need of the trash can. You know what I mean. I dive for it; the remote to my fire stick goes flying & shatters. pic.twitter.com/G4mkHdMEQW
Prikaži ovu nit -
Relationship Status Update!
#chronicpain#chronicillness#invisibleillness#spooniepic.twitter.com/vHHIJeVTdp
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#disabled &#chronicillness friends, similar to my "Have you tried...?" thread, what comment do you receive from ableds that drives you up the wall? What's the phrase they all think they are completely unique in sharing w/ you? Give me your worst, weirdest, & most annoying!Prikaži ovu nit -
“It can be easy to become lost within chronic illness itself and begin to see that it is all we are. And so becomes a wave of grief and loss. The loss of yourself. The loss of that which defines you, as well, you.” https://www.brainlesionandme.com/identity-crisis-am-i-defined-by-chronic-illness/ … via
@serenebutterfly#chronicillness -
Dear
#pwME, we are looking for someone with a blog about M.E. / Chronic Illness that would be prepared to blog about#MEawarenesshour. We would love to hear from you if you feel you can help.#ME#MECFS#MyalgicE#ChronicIllness#InvisibleIllness#blog#Awareness#MEawarenesshour
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