Patient information
Once you have provided your expression of content for SHM to use your data for research purposes through your treating doctor/ physician, you will next be informed about what happens with your data and about your right to withdraw your expression of consent. You can read about what you have been informed of in the information letter.
For the information letter for a child, see Childeren with HIV.
Our brochure explains what happens to patients' data once they have been collected by SHM and how the data eventually help to further improve HIV care in the Netherlands.
If you have any questions after reading the information, you can send us an e-mail.
Information sheet for new participants
Brochure 'From diagnosis to optimal treatment: every patient counts'
Additional information
On the following pages you can read more about how the data is collected and what happens for the monitoring of children with HIV.
