Personal stories and spoonie tips from people living with chronic pain.
The Mighty community shares surprising physical symptoms they've experienced due to Ehlers-Danlos syndrome (EDS).
People with invisible illness share what they wish emergency room staff knew about them.
These memes nail what it's like to have blood work done.
Lindsay Rodgers explains what her life with migraines is really like in honor of Migraine Awareness Month.
The Mighty's chronic illness community shares their favorite brands of leggings. Here's what they recommend.
Immie Jones, who lives with a sleep disorder, offers tips to help people improve their sleep hygiene.
Mast cells play a major role in your immune system, but when they go awry, they can cause a wide variety of symptoms and a spectrum of conditions collectively called mast cell activation syndrome.
The writer describes some of the challenges he and his wife experience because of her fibromyalgia, which causes her fatigue, pain, brain fog and depression.
The Mighty community shares things they do to cope with chronic pain, which their coworkers don't realize.
Essence Cheatom shares 10 things living with epilepsy has taught her.
The Mighty community shares photos to demonstrate what different symptoms of fibromyalgia can look like.
If your rheumatologist exhibits any of these signs, it may be time for you to find a new doctor.
Eleanor Morrissey lists the relatable thoughts she has daily as a spoonie with an autoimmune disease.
A letter for anyone with chronic illness who is hard on themselves.
The Mighty community shares the "white lies" they tell about their illness and the truth behind them.
The Mighty community shares the intrusive or "taboo" thoughts they have about chronic illness, and how these thoughts affect them.