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Information about the hiv patient association

What is the Hiv patient association about?
The Hiv Vereniging stands for unconditional equality of people living with HIV in the Netherlands, in any situation, at any time. People with HIV are central to everything the association does. The association is for and by people with HIV and their loved ones. We offer support and contact, so that you can take control. We tirelessly denounce subjects such as discrimination and the emancipation of people with HIV. In addition, it is important that people can be free in their own way of life, and for this we provide objective information. By connecting different groups within the association, we are strong in promoting collective and individual interests.
Information and support
On hivvereniging.nl you will find information and tips about themes like hiv-care, healthy living, work and money. Actual information about hiv you will read on our blog: verenigingsblog

Our advocates discuss the problems you encounter in the medical, social and legal fields. With the aim of solving these and preventing recurrence.

Do you have questions, topics or problems you would like to discuss with someone? Please contact our Service Point. Trained experience experts offer a listening ear and think along with you.

We can be reached by phone on Monday, Tuesday and Thursday from 2 p.m. - 10 p.m. on 020 - 689 25 77.

Would you rather contact us by e-mail? Then send us a message with your question.

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Looking for a meeting?
Check out the agenda here
Volunteers organise activities throughout the country. Join us for lunch, dinner or café evening for informal exchange or take part in informative meetings.
Do you need a one-on-one conversation with an experienced expert? Based on your questions, we will link you to a peer-counselor. In two to five conversations you will be helped to find your own path.

You can also participate in the workshopreeks ‘Positief leven. A number of informative meetings in a fixed group of five to ten people. The mutual exchange of experiences and way of looking at living with HIV is often self-reinforcing.