About Body Dysmorphia Australia
Our Journey
Body Dysmorphia Australia (BDA) was founded in 2017 with a vision to shed light on and combat body dysmorphism, a condition that often goes misunderstood. Our journey began as a passion project by a group of individuals who had personally experienced or witnessed the impact of this disorder. Recognizing the lack of accessible and reliable information, we set out to create a dedicated news platform focused exclusively on raising awareness and offering support.
Mission and Purpose
Our mission is to be the premier online resource for all things related to body dysmorphism in Australia. We strive to provide unbiased, accurate, and compassionate content that educates, empowers, and connects individuals affected by this condition. BDA aims to foster a community where people can share their stories, seek help, and offer support.
Filling the Information Gap
The internet is brimming with information, but when it comes to body dysmorphism, much of what exists is either misleading or outdated. We identified a critical gap in reliable, up-to-date resources tailored specifically for the Australian context. This prompted us to create a website that offers evidence-based insights, personal narratives, and practical guidance to empower individuals on their journey towards recovery.
Unbiased Information and Accuracy
At BDA, we uphold the utmost standards of journalistic integrity. Our commitment to providing unbiased information ensures that all articles and resources are based on scientific evidence and expert opinions. We employ rigorous fact-checking processes and strive for accuracy in every piece published. Our team meticulously sources information from reputable research institutions, healthcare professionals, and personal narratives to deliver content that is both reliable and sensitive.
Serving Our Community
Our target audience includes individuals struggling with body dysmorphism, their loved ones, mental health professionals, and anyone interested in learning more about this condition. BDA offers a safe space for open dialogue, encouraging users to share their experiences and engage with the content. We believe that by fostering connections and providing valuable resources, we can make a significant impact on the lives of those affected.
Engaging with Our Readers
We encourage reader engagement through comments sections, feedback forms, and social media platforms. Your input is invaluable in shaping our content and improving user experience. Whether you have a personal story to share, a question for our experts, or suggestions for future articles, we welcome your involvement.
The BDA Team
- Dr. Emma Wilson – Founder and Chief Editor, an experienced clinical psychologist with a specialization in body dysmorphism.
- Sophia Lee – Content Creator, responsible for crafting engaging articles and personal narratives.
- Michael Brown – Research Analyst, ensuring all information is fact-checked and up to date.
- Aisha Singh – Community Manager, overseeing user engagement and support.
- Lucas Davis – Web Developer, who crafted the website to be both visually appealing and user-friendly.
Our Business Model
BDA operates on a combination of ad revenue, sponsorships from mental health organizations, and user donations. We prioritize maintaining a free-to-access platform while ensuring financial sustainability through these means. By keeping our content accessible, we reach a wider audience and maximize our impact.
For any queries or collaborations, please reach out to us via our Contact Us page. Your feedback is welcome, and we look forward to connecting with you!