A wander interview series
on record
Women on endometriosis. Firsthand. Unedited.
Most people with endometriosis have spent years being edited: interrupted, doubted, told to describe a nine as a four. On Record does the opposite. Your words stay in your own voice, uncut, and nothing ships without your approval.
“They said I just have a sore tummy and to go home, I felt so dismissed.”
How it works
Six steps, and you hold the veto at every one.
- 1
Submit your application
Fill in the form below and tell us as much or as little as you want. A real person reads every one.
- 2
We follow up by email
Any questions we have, we ask in writing first, so you can answer in your own time and change your mind at any point.
- 3
Introduction call
A conversation, not an audition. We talk through what you want to say, what is off limits, and how filming works.
- 4
We film the interview
One camera, one conversation, black and white, no scripts. We keep the hard parts in.
- 5
You approve it
You watch the edit before anyone else does. Nothing goes out until you say yes, and you can pull anything.
- 6
It goes live
Your episode publishes, and we send you the shorts and stills to share however you want.
You can stop at any step, including after filming. If you change your mind the day before it goes live, we delete the footage. That is the deal, in writing, before we ever press record.
Step 01 · your application
Tell us your story.
We are looking for the whole truth of it: the years of being disbelieved, the surgeries, the fertility, the work you lost, the people who stood by you. You do not have to be articulate or composed. You just have to be honest.
Whānau and partners can apply too. This disease is carried by more than one person.
We believe you. Nobody has to prove anything to us.