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What are the Public perceptions: how effective are the services for endometriosis on the Isle of Man?


Thriving Student
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For my Public Health Degree I have created this questionnaire around Endometriosis and the public’s perceptions on the services offered for it on the Isle of Man.

Open to all to fill out and is completely confidential.

I would appreciate honest answers.

Thank you 

 

https://docs.google.com/forms/d/e/1FAIpQLScFtVj3SIYjMoZexNZ9NilluX4Th4qdKl6-RMJA9XMCdXPJhg/viewform?usp=pp_url&entry.345984952=Under+20

 

 

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As a male, I'm afraid I have no personal insight to offer, but I wish you well for any positive change you can encourage for women suffering from this awful condition. I have a relative in the UK whose life was ruined for many years of what should have been her prime by endometriosis that triggered spontaneously shortly after a pregnancy in her mid 20s. The extreme physical pain also brought her to the very edge of despair mentally, and she went through several rounds of intrusive treatment with varying degrees of efficacy. She later developed other conditions that might have been related. Good luck in shining a light on the disease. It deserves far more attention.

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