Did your doctor take your endometriosis pains seriously?

@Lulubeans I took a long time for me to get a diagnosis as well. My gyno originally thought I had a hormonal imbalance or just a bad period but after several visits and my breaking down in tears in her office trying to describe the pain, she finally referred me to a specialist. I had some trouble getting some people in my family to understand what I was going through as well, they thought I was just being dramatic.

@Lulubeans @Mina145 Hello Lulubeans and Mina145, thank you both for creating and participating in this discussion. I'm sorry to hear that you don't feel like you were taken seriously by your doctors. Let me tag som other members who can also weigh in on this topic.

Hello members, I hope you don't mind that I've tagged you. How has your experience been with your doctors? Do you feel that your doctor took you seriously? Did he or she really listen to you? Were you misdiagnosed or diagnosed late because of it? Feel free to share here!
@Ice ice baby‍ @CARNAS‍ @Mandyuk82‍ @Kastur87‍ @Sunshine56‍ @Cherryorchid1101‍ @Coco382014‍ @Luckyvibe‍ @chezzles‍ @Cairine2010 ‍ @fionaneli‍ @Maryuk86‍ @lucybundle‍ @sangor10‍ @Bartongilbey‍ @katrinaj87‍ 

Take care,
Courtney 

I was going up and down to the doctors/hospital for a number of years before I was taken seriously. They kept telling me that the pain was in my head. I did get a diagnosis eventually when my husband pushed for them to do the laparoscopy.

This makes me so sad reading all of this. I just went through a nightmare experience trying to get a diagnosis for my teenage daughter, and to know that this happens what sounds like regularly is both relieving (to know that it wasn't just us) but also so saddening. My daughter had been having pains for a few years and I admit that at the beginning I thought she was exaggerating her normal period cramps (which now in hindsight I feel so awful about not taking her seriously myself as her mother). Finally in the last year it got to the point where she could barely get out of bed, so we looked for help. Our GP was useless and we had to really press the gynaecologist and call several times to convince her to even consider looking at endometriosis. 

@CJames Yes, unfortunately it seems like it's status quo... I don't know if  anything is being done to change things.

To everyone who’s commented, including the OP, I am researching this for my dissertation.

Please get in touch if you are interested, or see my newly posted survey in the thread. :)

Not at all my doctor fobbed me off many times I've been fobbed off by many doctors in my surgery I even changed doctors and he told me it was severe period pain

Hi everyone, just bringing back this important thread in case you missed it!

This discussion on how doctors respon, or don’t respond, to endometriosis pain is sadly still incredibly relevant. Many members shared stories of being dismissed, misdiagnosed, or told their pain was “just a bad period.” If that’s something you’ve lived through, this could be a good place to reflect or connect with others who’ve experienced the same.

💬 Have your doctors taken your symptoms seriously?

📋 Did it take a long time to get diagnosed?

🤝 Or have you found a provider who really listens?

@Corinnesmith31 @Maggs62 @becky1970 @Nispa1 @pixieb @snow.white @tinkerjack1912 @twecolynne @archybald1 @Natasha11 @Fibromates @mcintam @TitchK @Bartongilbey @sangor10 @meme23 @Maryuk86 @fionaneli @Luckyvibe @Coco382014 @Sunshine56 @CARNAS @Iceicebaby @queenie85 @Brunette @rogue_1990 @Mysti75 @nikki77 @Mblyth @Louise84 @Tracy-mack @slousa @esw048 @Traceyaa @Spoonie_51 @Sarabox @Gina40 @Zoe0505 @Dayannapr @bendenning @topi34 @Rrgfeeg @HVID55 @CandiceT @Pennylein64 @imanusardi @Jempin @Emily7798 @JackieVR @marhan20 @Claire @Kimbad1990

If you’ve joined more recently or just never saw this thread, now’s the perfect time to jump in. Let’s make sure no one feels alone in this!

Take care,

Somya from the Carenity team 🌼