Jo's Voices is a network of people affected by cervical cancer or cervical abnormalities who can contribute their views, opinions and experiences to help develop our services, information provision and campaigning.
As a member of Jo's Voices we'll offer you opportunities to:
- share your experiences to help improve our work
- represent the views of those affected by cervical abnormalities and cervical cancer by becoming involved in our research, information provision and campaigning work
- respond to surveys about activities at Jo's Cervical Cancer Trust.
We will usually communicate with you via email and you will gain access to a page on our site with details of all the new projects that you can contribute to.
If you have limited time, the most we would ask of you is to complete online surveys as and when we have them. For those who want to get more involved there are opportunities to take part in patient focus groups which help us develop new information materials both on our website and printed leaflets.
Once you've joined you will receive our regular e-newsletter to keep you up to date with our work.
We look forward to having you on the Jo's Voices team!