Thank you x
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
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
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 ?
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
Hi everyone! I am 25 and have learnt i have endometrioma in my left ovarian (4cm) and high CA125 level, my doctor wants me on Visanne. I have read so many side effects and therefore i couldnt dare taking Visanne.. I am on Yasmin contraceptive pill instead. My mother told me she also had endometriosis when she was few years older than me and even with endometrioma in one ovarian, she could get pregnant and give birth to my sister.. Could you share with me if you have similar experiences… read more
I've been on visanne for 6months. Almost 4months having this spot/slight bleeding. The next day right after finishing 6months taking visanne i got slight period. I dont know if it is normal. My endo… read more
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
Love I am dealing with chronic pain I have both I trying to figure out what can help.
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
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.
My gynecologist told me that she felt a pelvic mass on a bimanual exam that suggested to her that I might have an endometrioma or more on the other side of my vaginal cuff. She also noted a polyp on the vaginal side of the cuff that might be endometriosis. Why would a transvaginal ultrasound and a CT scan find absolutely nothing, when I was in so much pain that I needed hydromorphone in the ER to control it?
Sorry you are still experiencing pain after all you’ve been through, it feels hopeless at times. Maybe the doctor who did your pelvic exam was incorrect….or maybe you have a lesion where they can’t… read more
I have been experiencing the same thing all over again. My doctor told that they removed all the endometriosis but I feel like it has come back. I mean is it possible within a year or so that it can return. I believe I had my laparoscopic surgery last year or the year before that. Experiencing pain, fatigue, painful with sex as well as periods.
On the same boat here. I had my surgery in November and now doing IVF... I was told today I have severe endometrosis again... not happy at all especially when trying to get pregnant.
Im on them now and just want to know what poeple experienced after they stopped the injections. Xx
*these are montly stomach injections for 6 months or 2x over six months. They bring on temporary menopause**
Is that Lupron that makes your body believe that you and perimenopause is that that has so many things done that I have no idea at this point. I’m just going back in time.
I can't count how many times I actually fainted today. I spent most of my day in bed with depression consuming me, but I had to be so careful every time I got up because I know I'd just fall right back onto my bed. I didn't have the strength to blow dry my hair after my shower and even showering made me short of breath and dizzy. I started bleeding lightly today, first day of my strange irregular cycle maybe? Never know if I'm just spotting, point is I'm not bleeding heavily. I've eaten exactly… read more
Pots is probably what you're experiencing or some type of dysautonomia