What is something you wish people knew about living with Crohn's?
What is something you wish people knew about living with Crohn's?
Your response may be used in an article or video on The Mighty.
The Mighty is a safe, supportive community for people living with health challenges and the people who care for them.
What is something you wish people knew about living with Crohn's?
Your response may be used in an article or video on The Mighty.
The Mighty is a safe, supportive community for people living with disabilities and the people who care for them.
These past four months have been one of the worst times of my life and I'm at a point where no doctor is helpful at all. The "it's all in your head" bullshit is stronger than ever right now. From both my family members and the doctors. I can't find any doctor at all that'll take me seriously. What do I do? I'm really desperate.
#Fibromyalgia #ChronicIllness #InflammatoryBowelDiseaseIBD #IrritableBowelSyndromeIBS #ChronicPain #Anxiety #Depression #ObsessiveCompulsiveDisorder
Hi, my name is BetsyS. I'm here because I want to learn more about MCAS, Ehlers-Danlos, Dysautonomia, and IBD.
#MightyTogether #Depression #Fibromyalgia #Crohn 'sDisease
Some "To Don'ts". Which one are you taking?
#AutismSpectrum #Agoraphobia #AnorexiaNervosa #Anxiety #Addiction #BipolarDisorder #BackPain #MentalHealth #ChronicFatigueSyndrome #CeliacDisease #Cancers #ChronicIllness #InflammatoryBowelDiseaseIBD #InterstitialCystitis #ADHD #EatingDisorder #Lupus #Grief #Schizophrenia #PTSD #JointHypermobilitySyndrome #MoodDisorders #NarcissisticPersonalityDisorder
Living with a health condition like Crohn’s disease or Ulcerative Colitis can be challenging, frustrating, painful, and uncomfortable. It can also be hard to know how much to share — or how to explain something that isn’t always visible but affects every aspect of your daily life.
Maybe you use medical terms to help others understand the seriousness of it. Maybe you simplify things to avoid long explanations. Or maybe you keep it private unless you really trust someone.
What’s your approach? How do you talk about your condition with friends, coworkers, or family members — and what helps those conversations go more smoothly?
#UlcerativeColitis #CrohnsDisease #InflammatoryBowelDiseaseIBD #CheckInWithMe #ChronicIllness #Spoonie #MentalHealth
Exactly how I felt off my last appointment, but add to that extreme anxiety that made me physically sick to my stomach with the WORSE headache I ever had and feeling like screaming and crying and bundling up in a ball in my bed covers over me and just not participating in life for a bit... That's how I felt because I got diagnosed with yet ANOTHER autoimmune disorder... #autoimmunedisorders #SjogrensSyndrome #InflammatoryBowelDiseaseIBD #Gastroparesis #Gastritis #Colitis
Hi, my name is beamlakalebel. I've been diagnosed with IBD since 2018 has taught me strength and resilience. Passionate about raising awareness, breaking stigma, and supporting others facing chronic illness.
#MightyTogether #Crohn 'sDisease