Thank you x
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 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'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.
Looking for some guidance about dos and donts that can help to make pain less. What should I avoid? What should I eat more of?
Gluten. Red meat. Dairy. Sugar. High processed foods. Alcohol. Caffeine. Smoking. can all make endo worse 😞
I have 2 endometriomas on my left ovary. I was scheduled to have them removed next week but the hospital cancelled my surgery due to the guidelines for the Coronovirus right now. Since my surgery is postponed I’m taking this time to do a lot of research. I’m learning excision is the best method. I’m wondering how likely they are to return or for more to develop if I’m not on anything after the surgery? My doctor said if I don’t suppress the hormones it will grow back but I thought if they were… read more
Consider looking in different states, if you find one that takes insurance it might be more doable even with the cost of travel
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.
Hi ladies. I hope that you're all coping well with your endo & that you're feeling peaceful (although probably unlikely). I'm wondering, I have a Youtube channel & am wanting to put up a video about what endo is & to share my journey with endo (to promote awareness of this condition, as well as to get us talking & sharing). What I'd like to know is if any of you would happen to have any advice or interesting tips that I could include in the video for those who may be watching? This could… read more
Hi ShaylaNicole
I can't wait to see it! I hope you are feeling good today ❤️
I have to say, I have had significant improvements in just one week after going off Visanne and switching to a natural,… read more
I am 38 and have the worst of the worst symptoms, pain, heavy bleeding, depression ect. I just started the mini pill to help ease theses symptoms. I am missing work and life. Several yrs ago I tried it and bled and cramped for 2 months. I am desperate and trying it again. I have migraine with aura so I can't tolerate reg BC at all.
I'm on it for 2 weeks now. 37 myself. Desogestrel. It has made my thoracic symptoms worse. It stopped my period but in spotting now. Also feel very down. Lap will happen Nov 30th for me. I was hoping… read more
I feel like I am going crazy. I have asked my doctors again and again to check if I have an autoimmune disease but no one takes me seriously. Well, I got bloodwork done and of course I test positive for autoimmune antibodies. But wouldn't it make sense for people with endo to have positive autoimmune antibodies? Think about it. We have uterine tissue growing in places it doesn't belong. Can't your body recognize that as foreign and start attacking it? Obviously, I'm not a doctor but it just… read more
Yep women with endimetriosis have it high.