I think this book is a good place to start getting a primer on endometriosis, but I also think that a lot of Dr. Seckin's biases and opinions really show through the work. I have delved into information on endometriosis since being diagnosed, and some things in this book were really at odds with what I've heard and read from other researchers, like heavy periods and migraines being symptoms of endometriosis or the reflux menstruation theory. I know there's a lot about endometriosis that is yet t...

2 stars I have been told to read this book many times for my endometriosis but I generally have used up to date scientific journals and a few more up to date books for my endo reading.However, I am currently in a desperate position and so I thought I would give it a read.Here are my problems with the book:- Retrograde menstruation been dismissed now and is definitely NOT the cause of endometriosis.- There were too many constant case studies. I wanted information on my illness and how I can treat...

2.5. I think I would have found this book a lot more useful a year ago, when I wasn't sure if I had endometriosis and before all the research I've already done. It is very much a beginner's introduction to endometriosis. There were some good parts, but most often I was frustrated and annoyed.The good:- Dr. Seckin validates the pain of endometriosis and how it impacts every part of your life. That's important.- He is passionate about advocating for awareness, education, and more research. Also im...

I think this book is in really accessible language for patients, and does place incredible importance on excisional surgery that is timely; which is super hard to come by in Canada. So a little stressful, but super informational for patients and family!

In this book Doctor Seckin explains everythingggg about this disease and answers questions I've had for years despite seeing many "specialists" and reading a bazillion thingies on the internet about endo.It is evident throughout the whole book that he really cares about women who are suffering from this and wants to help them despite the fact this was not what he saw himself doing as a doctor originally. He saw the horrors and how endo ruins lives and out of the kindness of his heart made it his...

Wow! This is a must read for anyone with Endometriosis!

I have several chronic conditions of which endo is one. Out of all the books I have read about any of them, this one is outstanding. They all explain a fair amount of scientific information, and some do better than others, but this one is written by a physician in such a relatable and clear way that I flew through it and find myself ready now to ask my own doctor a lot more questions about my condition and what we should be doing that we are not.

I was diagnosed with endometriosis last month, after 8 years of pain and multiple doctors and gynecologists. I found out about Seckin and this book through the Endometriosis Foundation of America. It explains a lot more than the doctor that did my surgery has yet to. The pictures and diagrams are helpful, and everything is explained in very digestible terms. I’d recommend to anyone who thinks or knows that they have endometriosis, and to friends, family, and caregivers of anyone with endo. Secki...

As a woman with endometriosis, I love the education here and the passion of the EFA. However, it felt to me a lot like fear-mongering and “do had better take care of this as soon as possible and the right way or your life will be horrible.”There’s very little mention of: everyone woman is different and that’s not much highlighted.After reading many other books on endo and other gynecological conditions, I was disappointed.

A quick, easy primer on endometriosis. The book draws heavily from anecdotes of women who spent years being ignored/dismissed/misdiagnosed by their doctors, and while it’s nice to be reassured you’re not alone/crazy, after the third repetitive story (out of very, very many) I want it to be less “can you believe no one believes this?!” and more about the actual disease. That being said, I’ve read a lot about endometriosis but still learnt some things about its occurrence and treatment through thi...

I have one question after reading this book. How the hell is it possible that standard medical training doesn’t routinely include information about endometriosis? It’s 2016, folks! Long past time to ditch the sexist medical models that birthed all that “hysteria” nonsense. As someone who struggles with endometriosis and associated chronic pain, it is impossible to adequately express the frustration and hopelessness that accompanies being told that your pain is “in your head,” that “there’s noth

This book is a must read for anyone who is suffering from Endometriosis! Finally concise information that proves you are not alone and that the pain is not all I your head.

I give it 2 stars because it promotes endometriosis research and education. However, on the whole I abhorred the book. I read it fully through because there is little information out there and this was only 1 of 2 books at our libraries on the subject, but I rolled my eyes so many times I thought they'd stick.The author is very, very proud, and it shows. My recap to my husband was, "Here's my background story; Padma; I'm a great doctor because; I got an award because; this is why my way is bette...

Easy to read, though at times hard to accept, this is a personalized guide into a condition few in the medical community pay attention to: endometriosis. Please pick up this short book, compiled of antidotal evidence accompanied by medical knowledge, to learn more about women's health and the possible side-effects in your own life.

A very informative read about Endometriosis! Here are some things you should know:Endometriosis is actually cells that grow on, around, and sometimes in your organs. It causes a women extreme pain and heavy bleeding. It can also cause GI issues! To get it taken out, do NOT get a laser surgery! It causes more scar tissue and hardens the Endo! To have a successful outcome you must have a deep excision surgery! Endometriosis is not a new thing, but it is a newly discovered immune disease! If you th...

I cried at times while reading this. Why do doctors throw pain meds and birth control at us instead of actually trying to fix us? Because this disease is highly misunderstood. I appreciated this book greatly and will continue researching so I can advocate for myself and make informed decisions. We need more educated and specialized doctors like Dr. Seckin.

i’m putting this aside for the time being, only because it’s starting to cause me anxiety. it keeps saying to get tested and treated, but i can’t get the confirmation surgery until after i meet with my gynecologist at the end of this month. i don’t know when we’ll be able to do the confirmation surgery and this book is honestly just making me scared it’s going to get so much worse in that time. i think i’ll pick it back up when i have the confirmation.

This is the most accurate *description* of endometriosis I have ever read - painfully so. I wish everyone could read this book and have a better understanding of this disease.The book talks about treatment options - no surprises for the recommendations, and they are spot on - but I do wish it would go a little more in depth on how to decide which is best, and what they entail. For example, diet is listed as a treatment, but the book only contains a perfunctory food list with "bad" foods and "goo...

A good beginner’s guide for someone suffering from endometriosis or suspecting, as well as family members or friends who aren’t sure exactly what it is. Much of it is told from patients stories and histories, which may be helpful and comforting to someone feeling alone in their journey. It also includes a helpful guide about how to go to doctors appointments and what questions to ask in regards to endo, and emphasizes finding the right doctor. It is to be noted that this is from 2016 and researc...

As someone that is in the process of being diagnosed with this disease, this book gave me hope. I would highly recommend it to anyone who has, thinks they have, or has someone in their life with endometriosis. Worth every moment spent with it, and I am already going over it again prepping for my next doctor's appointment.