After months of development, the Jnetics website became publicly available in August 2010.
Created as a resource for affected families, patient groups, healthcare professionals and the Jewish community, the website has been designed with the following objectives in mind:
- To provide a professional and accessible tool to help raise awareness about Jewish genetic disorders and new developments relating to these conditions.
- To serve as a valuable ‘signposting’ resource containing links to further information, services and support for everyone affected by Jewish genetic disorders.
- To create a communication channel between Jnetics and the public that provides information about the charity, our activities and how we can be contacted.
We view the current website as a starting point. As our activities and resources develop, we plan to expand the information included and may create specialised resource areas for different target audiences e.g. healthcare professionals and Jewish community leaders and educators.
In addition to regularly updating the content so that it remains accurate, we will periodically review and upgrade the website to ensure that it reflects the information needs and interests of its visitors.
As such, we would love to hear your feedback – please send any comments you have regarding the Jnetics website content and design to info@jnetics.org.