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Top 10 Search Results for "iuds and endometriosis"

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IUD For Endometriosis, Adenomyosis And Fibroids. Pros And Cons.
A MyEndometriosisTeam Member asked a question 💭

If you have or have had an IUD what were the pros and cons for you ? Did it help endo symptoms ? How about fibroids ? Or adenomyosis symptoms ?
Thank you !

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A MyEndometriosisTeam Member

Same experience for me as Stephie2. On my second Mirena. No bleeding or periods except occasional rare spotting. Which is great because any bleeding is also agonizing for me. I have adenomyosis and… read more

Can I Take Co Drydomol 20mg With 20 Mg Amytriptyline ?
A MyEndometriosisTeam Member asked a question 💭
A MyEndometriosisTeam Member

Thank you x

Has Anyone Ever Tried The Newest Mini Pill, Slynd ?
A MyEndometriosisTeam Member asked a question 💭

I tried 3 IUDs and my body rejected all 3; then tried Norethrindrone and I hated it . My weight changed for the worse and it effected my mood. So I stopped . My doc told me about a newer pill called Slynd . Wondering if anyone else has had experience with this ?

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A MyEndometriosisTeam Member

You're most welcome. Incidentally, I'm not sure where you are in your endo journey. Birth control can help, but really they just mask symptoms. It's important that your doctor tell you that it doesn't… read more

Have Widespread Endometriosis
A MyEndometriosisTeam Member asked a question 💭

Hi I hope someone can help I've been to my GP he did blood test and my estrogen levels are low I'm 47 it's causing a lot of problems down below he has prescribed 10mg of vagifem weekly to help I was a bit concerned because I said to him I taught that estrogen feeds endometriosis he said it was fine because it is a low dose and I'm not taking it by mouth so it's just helping the problem below has anyone tried this before as I'm getting really depressed cause I've tried all of the creams and… read more

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A MyEndometriosisTeam Member

Yes I was talking a low estrogen pill orally, it made everything so much worse than it would have been if I was just using my progesterone implant. The implant wasn’t controlling my bleeding so we… read more

Has Anyone With Radical Autoimmune Issues Tried An IUD?
A MyEndometriosisTeam Member asked a question 💭

I have horrific autoimmune issues with my thyroid, endometriosis, and likely adenomyosis. I already have daily cramps, abnirmal bleeding, and a fever 4 days out of the week. Plus, 90% of my hair has fallen out. I'm in the ER almost monthly with awful pelvic and abdominal pain. I think an IUD could come near to quite literally killing me.

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A MyEndometriosisTeam Member

That’s good to know! Thank you!

Endometriosis Or Adenomyosis?
A MyEndometriosisTeam Member asked a question 💭

I'm 17 years old right now and have been dealing with chronic pain(abdominal and migraines) since I was 12. It started with dually migraines and then went into daily nausea. I went to every odctot possible and they couldnt figure out what it was. I have been in the ER too often to count. It went over too extreme abdominal pain more in the upper area and then in the lower area also. I was checked for gallstones through ultrasound and blood tests. I also had a CAT scan done and two upper and one… read more

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A MyEndometriosisTeam Member

Love I am dealing with chronic pain I have both I trying to figure out what can help.

Surgery And IUD
A MyEndometriosisTeam Member asked a question 💭

I am having surgery to remove the scar tissue and while I am asleep, they want to put an IUD in as well. I am super nervous about the IUD and want to know if there are side effects, and if the IUD is a good route to go.

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A MyEndometriosisTeam Member

I have had the mirena but honestly I think it al made my Endo worse.. after the mirena I had a time without hormones and ovulation was less painful I think but menstruation pain got worse. After they… read more

Experience With Skyla / Hormonal IUDs?
A MyEndometriosisTeam Member asked a question 💭

I got a laparoscopy last year and was diagnosed with stage IV endometriosis; the surgeon suspects adenomyosis, too. After the surgery, my periods and cramps were light, and my IBS went away. Four months later, I inserted the Skyla IUD. At first, I felt no different. Two months later, my IBS was back, I'd gotten a huge ovarian cyst and had to start taking another birth control pill on top of the IUD. Now, I'm experiencing cramping pains every day - something I didn't even have before my surgery… read more

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A MyEndometriosisTeam Member

Hello, I'm so sorry for the pain you have to endure because of IUD. Unfortunately, I had my mirena removed on the 30 March 2022 after using it for a year with excruciating pains. I changed my gynae… read more

Can Mirena Coil Mask Endometriosis During Laproscopy
A MyEndometriosisTeam Member asked a question 💭

Hi I have the mirena coil in place and I'm due to have a laproscopy in 2 weeks. I was just wondering if the mirena masks the endo? Does it make it harder to find endo during surgery?

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A MyEndometriosisTeam Member

I agree with MissCaitlin. I was on depo during my surgery and my doctor found tons of endo. I think it will depend on the skill of the surgeon. I hope it all goes well!

Why Do We Have To Endure An Invasive Surgery To Have A 100% Confirmed Diagnosis For Endometriosis?
A MyEndometriosisTeam Member asked a question 💭

My gynecologist told me that she is certain I have endometriosis as well as pcos, with all my symptoms fitting them perfectly. But she also informed me that it would require surgery to confirm it so that I can get the treatment needed. I can’t take time out of work or college to do the surgery and life is miserable living it in pain and sleeplessness all the time. It’s not just a matter of missing out on work or school, it’s the money too. I can’t afford to be off more than a day, and I’ve been… read more

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A MyEndometriosisTeam Member

I can't answer why but I agree that it is ridiculous and unfair. I had the discovery surgery just to get told "yes you have it" and had to have the excision surgery 3 weeks later. Such a waste.