I must not have a high threshold for pain like other women do because everyone gets cramping and pain.
Continued with oral contraceptive (7 yrs with no break at this stage) and saw a lot of crap doctors in the following years. I also have beck pain, my butt feels like a a needle is stabbing it when I sit sometimes. He scheduled me for a sonogram 2wks later and that revealed a cyst on my left ovary about the size of a tennis ball. Also in between contractions there was relief! I am sure many of you know exactly what I mean. All I am really looking for is a diagnostic. After an MRI and another sonogram my doc set me up an appt for surgery. Truly sorry that I am not more help, but hope that you find some relief soon. Do not give up- there IS hope for a better quality of life! I’m 20 and was just told I have endometriosis. Download Here Free HealthCareMagic App to Ask a Doctor, All the information, content and live chat provided on the site is intended to be for informational purposes only, and not a substitute for professional or medical advice. Both of which have their own unique side effects, or may only provide short relief to dull the pain. Hello, i am a 15 year old girl who is living in constant pain and being this young cannot take it anymore, all the symptoms-signs of this illness. I told my parents it felt like I had been “stabbed or shot in the stomach”, but when I mentioned going to the hospital my mom said, “I’m not taking you to a doctor, you’re probably just having cramps!” (considering this was a day after my cycle that was a pretty logical conclusion to come to) The pain started around 9:00pm and persisted throughout the night. My menstrual cramps were worse than contractions. She said it sounds like I may have scar tissue from previous cysts and possibly endometriosis.
Please someone help. I feel like I’m ruining my family’s life and feel I am the crabbiest and most annoying person to be around. im 22. i had my son in 2009 then got an iud. I have a hard time just going out to shop as the pain gets pretty intense and goes down my legs, have to stop frequently and rest. I was given Lupron and Depot Pervera (not sure I’m spelling the latter one correctly).
I’m not a doctor – I only have personal knowledge of endometriosis. , my mom raised three of us while suffering from endo & so my heart goes out to you but i also want you to know that you, my mom & other moms w/endo are my True HEROINES! i feel like an old person, I am 47. The doctor explained that she had had it for about 5 years. (OMG I thought I was going crazy! I did have an ultrasound scan which turned up nothing, and it was my laparoscopy (keyhole surgery) that eventually found my endo. They got me to check in to the hospital using the covid app which was the…, Going with zero waste laparoscopy recovery this time. Or if no one believes you. However, it has lasted much longer than usual. I am 37 w 2d, FTM. I have found a acupuncturist that is very at “healing” my pain to make life easier and tolerable. Doctors suspected that I had it from as early as 18 as I had really painful periods. Nothing out of the ordinary, apparently!
Chronic pain is the largest aspect of living with endometriosis. I found a great dr who has helped with bioidentical hormone replacement, I have thyroid issues also. Listen to your body and become more educated in other options and different lifestyles. He referred me to a gynaecologist but said he was sure they would find nothing. Most of us have cramps during our periods, but women with endometriosis often have debilitating pain. Even off my period the pain remains. My doctor induced and I was expecting the worst, but I found it to be merely uncomfortable. I had made a reply on someone else’s post but here’s my entire little thing. Women with infertility might be referred to a reproductive endocrinologist or a fertility specialist. I was wondering if anyone could explain the back pain they experience plz. Yahoo forma parte de Verizon Media. Change ). 45, one child, and just been Diagnosed with Endometriosis. My lower spine felt like it was jolting. I am looking forward to a doctors appointment tomorrow to try and figure it out.
I found myself again and my life outdoors, work was fun again. Basically, almost everywhere hurts.The pelvis, left and right (now mostly right) hurt so much, the pain is sometimes burning, and sometimes really sharp like needles.
The pain is unbearable, even with 10 mg of morphine every 3-4 hours for the past 4 months. and my period are very clotty. You’ve done everything right so far!
My mom was actually thinking of taking me to the ER on Sunday, but since I had an appointment on Tuesday, I said to wait, plus I don’t think they would do anything, which hurts emotionally because it could be something very bad and they just dismiss like I just have a cold (I had acid reflux for 3 days and mild left abdominal pain a few months ago and my family doctor said that it’s because of the acid. You DO have rights & choices available to you. I’m on ovranette now and just wanted to ask did you ever get a diagnosis? My hormone levels were off which caused fatigue as well as migraines at the beginning and middle of my cycle. I don’t want to keep putting money onto surgery every couple of years to maintain a reproductive system that ill never use, but making the choice to have it removed is also very hard. The pain is often accompanied by a tugging sensation, the feeling that the area inside you is caught somehow, snagged on some unseen surface.
That’s the last time I had a period. You’ll do great!!! does this sound like endometriosis??? Often, symptoms can be controlled with medications like birth control pills or leuprolide acetate. I just dealt with the pain and one day couldn’t take it and called for pain medication. During this procedure, a thin, lighted tube will be put into a tiny abdominal incision.
No woman looks forward to “that time of the month.” Most of us deal with mood swings, bloating and cramps, which are never fun. With the second doctor.
Then I remembered what I read about natural ways to help with the pain (if it’s from hormones) and to get my period back to being regular without putting hormones in my body.
I had to go to the ER for an ultra sound and have lab work done, but they didn’t see anything so I was went home with hydrocodone and my pain at a 9 out of 10. Wow! Having experienced both, Labour pain was horrendous. I initially wanted the hysterectomy, but my doc said that was to aggressive to start with and that we should try the lapro and IUD first… so that didn’t work out to well! My thinking was 1) I’m tired of going to the doctor all the time, trying to control the pain and switching medicine around all the time and 2) why am I trying to maintain a reproductive system that I will probably never use anyway? I will deffinetly mention this to my doctor. I did the Lupron injections a few years ago, for a total of five months. I started my period around 12 & began experiencing pain & heavy bleeding around 14, often staying home from school. I know it’s really hard to not freak out at the “what ifs” scenarios of treatments, but I’d encourage you to so slowly and take each decision at your own pace. A TENS machine , a hot water bottle, painkillers, and CBD oil are among my favorite ways to manage the pain. Only you know what your body is asking for or wanting. To this day I still have trouble with my knees. ( Log Out / I’m sorry I didn’t get a chance to reply to your comment before your surgery, but we’ve been talking on Twitter, so continue to talk to me there if it’s helping at all. The dye allowed her to see affected areas that couldn’t be seen with the eye.
It radiates down into my groin and thigh and it hurts bad!! Change ), You are commenting using your Facebook account. I have been having pain in my lower right and major... View answer. Keep trying and don’t accept normality as an answer if you know something is wrong. I got my period at 8 and I had heavy horrible periods up until about the age of 15, since then I’ve had regular, light periods (every 28 days, I’d have a 2 day period) things were fine. Establishing the idea that endometriosis only hurts once a month and therefore “isn’t too bad”. I was diagnosed with endometriosis at 23, but it’s likely looking back that I had it for many years given my odd period symptoms in my teens. thank you for encouraging others to stand up for their selves. I don’t know what the right choice is, and I’ve been crying all evening trying to figure it out. I couldn’t do anything when it arrived. Endo is totally debilitating . I was sweating a lot that morning too. I know that this is not comfort to thers but everyone experience pain differently my is painful. I went in to the acute care clinic and the doctor originally was saying ingrown hair, then hernia, then ectopic pregnancy. No cure for endometriosis? I live in a very remote part of the country with a limited health service, so an advice line or something similar would be really helpful. Then, nothing until the end of June, that period lasted until August 1. Replaced my dressings today. I would highly recommend her to anyone!! The personal stories on here are amazing! I have visions of kicking him in the crotch and then telling him to work like nothing has happened (irrational, I know, but it helps:). My advice is to stay educated & most importantly, IN CONTROL of your treatments. It does this by: A common treatment for endometriosis is to prevent a women from experiencing a period by putting her on a constant stream of oral contraceptives, to “trick” her body into believing she is either pregnant or experiencing the menopause. In February or March (I don’t remember exactly) I had a normal period.
I’m going in for my first laparoscopy on Monday to see if I have endometriosis, my doctor is very helpful. The pain was similar to intense stomach diarrhea and I would get very nauseous. I am so scared as i don’t want any more operations with other probs i have had 17 in total and really can’t face anymore. Don’t give up. I’ve been in so much pain in my lower back, sharp pain like nerves being pinched. I had a great experience with the epidural so I definitely recommend that. My morning bowel movements are getting worse! I was diagnosed with endometriosis at 18 after suffering years of symptoms. I am also anemic so it makes it more challenging especially when I have a period at the end of three months as has been recommended. Just remember that contractions, unlike lots of pain, come and go AND they’re temporary and doing something. I can’t live like this anymore and the fact that this ilness can make it hard to have a child in later life makes it all worse as it breaks my heart. Looking forward to having answers and hopefully some relief soon. I welcome your comments below, and this is by far the most popular page on my website. If I were in your shoes I’d consult my new GP and contact the practice manager about making a formal complaint about it, what a horrible way to find out!
You seem to be having endometriosis. I am now 40 years old and still on the pill. I can never seem to be truly comfortable at night either and its worse at night and in the morning. I then started experiencing lower back pain with numbness in my left knee about a week before my period was due. Some endo moms I know have remarked on how easy labor was compared to endo. I recently got out of a terrible marriage (we had no children) and last year I decided I was sick and tired of trying to maintain my disease and decided to take myself off of my birth control. Diagnosed with epiploic appendicitie in November 2012 and. i am 24. was diagnosed with pcos in may 2010. i naturally conceived in dec 2011 but miscarried @ 7 weeks. Month later, still had horrible pain rated around an 8-10 so I went to another clinic and saw a different doctor, he originally said I had ovarian cysts rupturing and took my off a tri-phasic birth control from the other doctor and put me on monophasic hoping to regulating the hormones better.
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