Wulf Women
The Wulf Women Code of Ethics
Information is Free
Patient resources are free. The directory, guides, tools, and educational content on this platform will always be free to access. We will never paywall the information patients need to navigate their care.
We Do Not Sell Treatments
We accept no compensation in exchange for promoting medications, supplements, hormones, or medical treatments of any kind, including GLP-1s, hormonal therapies, supplements, or treatment programs.
We may partner with lifestyle brands to help fund this work. You might see us share a link to a cute dress, shampoo, or a pillow, for example. You will never see us selling you an endometriosis treatment for profit.
We will share treatments that have worked or not worked for us personally, including how and why we made those decisions. We will never profit from those recommendations.
Note: This website previously included affiliate links to supplements. Those links have been removed after careful thought about who Wulf Women wants to be and who it serves.
Partnerships and Editorial Independence
Partnerships, grants, affiliations, and collaborations of any kind do not purchase influence over our content, our directory, or our positions. No organization, donor, or partner will ever dictate what we publish.
Directory Integrity
Directory placement cannot be bought. Surgeons are listed because they meet criteria patients care about. No surgeon has ever paid to be included, and no surgeon ever will. Patient feedback will not be removed at the request of surgeons or their representatives. We are here for patients.
We Will Correct Mistakes
The people behind Wulf Women are human. There is a potential for errors on this site, no matter how careful we are. That's why you shouldn't follow Wulf Women, or any other party, blindly. Gather information, double check, and make the right decision for you.
If you see an error on this site email deb@wulfwomen.com and we will get it corrected as soon as possible.
We are not your doctor.
Wulf Women is about pulling together information and presenting it to women with endometriosis to help them make informed medical decisions for themselves.
Nothing here replaces a qualified healthcare provider.
Note from the editor
The endometriosis space online has some great information. I figured out I have endometriosis through social media when no doctor was able to diagnose me. I am grateful to the women on the internet sharing their stories.
But I also see a lot of practices in this space I disagree with, like hiding information patients need behind a paywall and promoting medications or products as solutions while profiting from selling them.
Women with endometriosis can be desperate for answers or quick solutions. This makes us vulnerable to buying or believing things that we want to be true (I know because I was one of those women). I have spent years doing the hard, unglamorous work of figuring out what actually helped my body, and I refuse to sell you a shortcut I don't believe in.
This is not an attack on every social media creator who charges for their work. Nutritionists, coaches, and educators deserve to be paid for their expertise and time. This is about something more specific: profiting from the treatments and products they are recommending to vulnerable patients.
I wrote this code of ethics because I want you to know exactly where I stand and hold me to it. If you ever see me breaking my code of conduct, please give me a swift kick in the ass, publicly. I should be held accountable like everyone else.
Xoxo, Deb