As humans, we’re hardwired for connection. Belonging to a community makes us feel safe and helps us thrive. But so often, living with inflammatory bowel disease (IBD) can make you feel physically and emotionally isolated. Not only can it be hard to do things you loved before your diagnosis, but it can also feel like no one understands what it’s like. Until now. Our mission is to cultivate a space powered by the IBD community and empowered by each other. From one-to-one chats to conversation forums, we make connecting easy. This is a safe place to find and receive advice, to seek and offer support, and to discover the authentic stories of members, just like you. Bezzy IBD is a free online platform bringing new meaning to the word “community.” Our aim is to create an experience where: - everyone feels seen, valued, and understood - everyone’s story matters - shared vulnerability is the name of the game Bezzy IBD is a place where you are more than your IBD. It’s a place where, finally, you belong. HOW IT WORKS Social-first Content Like all of your favorite social networks, we’ve designed an activity feed to connect you with other members living with IBD. We pride ourselves on making Bezzy IBD a safe and secure space where you can join live discussions, connect one-to-one, and read the latest articles and personal stories. Live Chats Need to vent? Get advice? Share what’s on your mind? Hop into a daily live chat to join the conversation. They’re often led by our amazing Community Guide, but you can also expect to chat with other advocates and experts, too. Forums From treatments to symptoms to daily living, IBD changes everything. Whatever you're feeling on any given day, there's a forum where you can connect and share directly with others. 1:1 Messaging Let us connect you with a new member from our community every day. We’ll recommend members to you based on your treatment plan, lifestyle interests, and needs. Browse member profiles and request to connect with anyone from our community with members listed as “Online Now.” Discover Articles and Stories We believe that shared experiences empower the kind of belonging that can help people not only survive—but thrive—with IBD. Our stories offer perspectives and tips from people who know what it’s like. Get handpicked wellness and member stories delivered to you each week. Connect Safely Anytime, Anywhere We take thoughtful steps to build safety, security, and privacy into our platform and foster an environment where members feel safe sharing their personal experiences. Check and send messages, see who’s online, and get notified when a new message comes in—so you’ll never miss a thing. ABOUT HEALTHLINE Healthline Media is the top ranked health publisher and number 44 on Comscore’s Top 100 Property rankings. Across all of its properties, Healthline Media each month publishes up to 1,000 scientifically accurate yet reader-friendly articles authored by more than 120 writers and reviewed by more than 100 doctors, clinicians, nutritionists, and other experts. The company’s repository contains more than 70,000 articles, each updated with current protocol. More than 200 million people worldwide and 86 million people in the U.S. visit Healthline’s sites each month, according to Google Analytics and Comscore, respectively.
Buggy
I haven’t been able to “like” any posts since the most recent update. I also have not received any in app notifications. -~-~ -~-~ -~-~ -~-~ -~-~ -~-~ -~-~ -~-~ -~-~ I love the idea of the app. It seems less regulated than it used to be. I see a lot of IBS comments; these are different conditions which is a big misunderstanding. These used to get a gentle reminder that this is an IBD group app. I would like if there was a user clause about spamming. I’ve seen a lot of posts constantly promoting the same “dr product line” when it’s not applicable to the original user’s comment.
Bad advice with no moderation
Lots of people giving bad medical advice and wrong information with nobody monitoring this. Just one example: somebody told someone who didn’t want another scope right away that doctors won’t give you one unless it’s been two years since your last. Not only is that wrong, it makes no sense at all. Why aren’t you people monitoring this??? Someone is going to end up in the hospital or worse listening to clueless people
Good helps sufferers find each other
Symptom request - please add constipation as an option, it is rare but does happen and it’d be good if people who suffer could find each other
So happy I’ve found a community
I’m so so happy I’ve finally found my community I’m 28 living with CD and I live in a small town and it gotten very lonely and isolated, I emailed my doctor and he referred me to the website and it’s there I found this beautiful app it has changed my life by having a community
Wonderful Forum
So informative! I love knowing I’m not alone in this. I have support and a community who understands exactly how I feel.
Germany not listed as a country
Can’t sign up
Amazing
Awesome app for people coming together on this journey ❤️
- Small updates and bug fixes
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