Telephone talk
We realise that not everyone is comfortable with interacting in the electronic medium. If you would rather have a telephone discussion with someone who has experienced CUP as a family member please use "Contact us" to arrange a telephone call. Because of the problems of misuse we do not publishing a contact telephone number until contact has been made.
Please note that Jo's friends does not offer medical advice – these interactions are for sharing information and offering support. (If you are someone who has experienced CUP as a patient, relative or friend and would like to help us with this service we would be very pleased to hear from you.)
If in the UK, it is sometimes possible to put you in touch with one of our medical advisers if you have a particular query with regard to a complex diagnosis.
Message board
Meeting Space
Join others affected by
CUP to share information
& gain support in a moderated forum
Thank God for this forum! I cried when I found it!
The immense relief that I have obtained so far from just reading everyone’s stories on this site is incredible. Up to this point I have felt so very alone as no one could give me any advice, nothing to read, nothing to comfort me as I flounder..
At first I was tired of answering the questions about CUP to friends and some doctors but this website has helped me realize that the world needs to know about us.