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Help us better understand PMOS experiences
We’re speaking with women who have been diagnosed with PMOS, think they may have PMOS, or are still trying to understand their symptoms. Your input will help us learn from real experiences and shape something more useful and supportive.
What is your name?
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What is your email address?
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Which best describes you?
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A
I have been diagnosed with PMOS
B
I think I may have PMOS but have not been diagnosed
C
I am currently exploring symptoms or seeking answers
D
I am supporting someone with PMOS
E
Other
Would you be open to a short user interview?
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A
Yes
B
Maybe, I’d like more information first
C
Not right now (I'm not interested in an interview)
Anything you'd like us to know before we reach out? (optional)
We'll use your details only to contact you about HerRoute user research. We won't share them with third parties, and you can ask us to delete them anytime by emailing hello@herroute.health.
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I agree to be contacted about HerRoute research.
Submit