“This blog, Hablemos de Berdon, is an informational and support space created by and for families affected by Berdon Syndrome. It does not replace professional medical diagnosis, treatment, or advice. Always consult your specialist doctor before making any health-related decisions.”
“We strive to share accurate and up-to-date information, but medicine is constantly evolving. We do not guarantee the completeness or current relevance of the content. The authors and collaborators are not responsible for any errors or omissions.”
“The care guides, procedures, and recommendations are shared based on personal experiences or consulted professionals. Their implementation is at your own risk. We recommend medical supervision for any intervention.”
“Family testimonials reflect their individual experiences and do not guarantee specific results. Every case of Berdon Syndrome is unique.”
“Links to third-party sites (hospitals, organizations) are provided as additional resources. We do not control or endorse their content or privacy policies.”
“Under no circumstances shall Hablemos de Berdon or its contributors be held liable for direct, indirect, or consequential damages arising from the use of the information published here.”
“All content (texts, images, infographics) is the property of the blog or used with permission. Commercial reproduction is not allowed without authorization.”
“By using this site, you accept this disclaimer. If you do not agree, we recommend that you refrain from accessing the content.”
By using this site, you acknowledge that you have read, understood, and accepted this disclaimer.
All information is intended to support—not replace—the relationship between patients, families, and healthcare professionals.
The information in this content is educational, not medical. Each case of Berdon Syndrome is different. Please consult your medical team before applying any recommendations. Read our legal disclaimer.
