Replying to @brea.powers Severe Ulcerative Colitis. Most people have never heard of ulcerative colitis until it changes someone’s life. Ulcerative colitis is an autoimmune disease where your immune system attacks your colon, causing bleeding, severe pain, diarrhea, fatigue, and inflammation. And for many Black women, the battle starts long before the diagnosis. 👩🏾🤎 Our pain is too often dismissed, our symptoms blamed on stress, and we’re frequently diagnosed later than we should be. There is
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Replying to @brea.powers Severe Ulcerative Colitis. Most people have never heard of ulcerative colitis until it changes someone’s life. Ulcerative colitis is an autoimmune disease where your immune system attacks your colon, causing bleeding, severe pain, diarrhea, fatigue, and inflammation. And for many Black women, the battle starts long before the diagnosis. 👩🏾🤎 Our pain is too often dismissed, our symptoms blamed on stress, and we’re frequently diagnosed later than we should be. There is
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Find a positive in everything….😜#colitis #autoimmunedisease #trend | autoimmune disease
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sind eure Symptome wegen der Hitze schlimmer?😢💩 Ich hab mit meinem Stoma zum Glück keine Probleme bei den Temperaturen 🙏🏻🙏🏻 #stomanaund #colitis #bauchschmerzen #künstlicherdarmausgang #reizdarm
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How often does your mind get a chance to rest and recover while living with Ulcerative Colitis? Mental overload isn't just having a lot of stressful things on your plate. It's when your mind rarely gets a chance to quiet down. It's the overthinking. The rumination.The feeling of overwhelm from everything you're juggling and trying to manage. It's carrying the weight of past experiences or unresolved trauma. It's the constant mental effort to stay on top of your responsibilities, manage the detai
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Most people don’t realize how much Ulcerative Colitis can take over every part of your life. The urgency. The pain. Always needing to know where the nearest bathroom is. Canceling plans. Feeling isolated and betrayed in your own body. My name is Dr. Kelli, and I’ve lived with moderate to severe UC for nearly 20 years. I’ve been through the roller coaster. Countless medications that didn’t work… or stopped working over time. Side effects that were absolutely miserable. The exhausting cycle of fla
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