Trans people need to wait 3 years before they receive medical and psychiatric help in the Netherlands. During this time, they receive little to no communication from the Amsterdam UMC. They need to look up all medical information, events, and community themselves. In my interviews with trans patients I've learned that the lack of communication towards the patients makes the AUMC feel uncaring and antagonistic. Information is often outdated, wrong, too technical or too surface level, not applicable to the Dutch care track, or made with ill intent by transphobes. This can be isolating, depressing, and can make the AUMC feel cold and impersonal. My goal was to create a service that alleviates all of these issues, without taking time and budget away from medical professionals.
I learned from my interviews that finding community and going to events helped; that patients feel much more comfortable if trans people are the ones helping; and that they need help finding therapists with low waiting times. I chose to develop a concept for a mailing list to be sent to patients in order to create the feeling of the hospital reaching out to the patient, while not demanding any time from the understaffed healthcare professionals.
The mailing list features:
During this project I stayed in contact with the AUMC's 'project team for patient information in trans healthcare', who found my work very valuable, and used my insights for their work. I've recently spoken to them again and they said they were going to use my insights in their pitch to management for an information system.