I have endo. My ovaries are clear, but the resulting scarring and adhesions from endo around the area blocked my right tube.
but a lesson must be lived in order to be learned.
and the clarity to see and stop this now
that is what i've earned (a.d.)
Married to DH 7 years and have three fantastic kiddos! DS 6, DD 4, and DS 2 ...... lo and behold another is on the way!
My sister had endo and was never able to have any kids. Life is so unfair. I thank God for my 11 year old son everyday.
I am 34 years old and was told in February I have endometriosis after a surgery to remove 3 of 5 fibroids discovered during a fertility test. I am worried that I would never be able to have children, my doctor suggested IVF since my insurance covers it but my husband hates the idea. (talk about stuck between a rock and hard place ) I have been researching other treatments to help with the endometriosis that has caused me to have one tube remove and the other appears to be blocked as well but the doctor didnt see the need to remove the other tube yet. During my research I came across Endovan formally Fibrovan but I am skeptical of medicines purchased on the internet. Anyone tried Endovan and successfully achieved pregnancy???? HELP I am running out on options.....
Endometriosis affects the fertility of approximately 40% of women who have been diagnosed with the disease. For many of these women, they only find out they have endometriosis when the possible causes of their infertility is being investigated. Infertility can be one of the consequences of Endometriosis. Women are not only dealing with a debilitating disease but they are also in fear of not being able to have children. The most common problems identified by laparoscopy are endometriosis and scarring. Your doctor can also detect blockages or irregularities of the fallopian tubes and uterus.
I was diagnosed with Endo when I was about 17 or 18 (I'm 27 now). I was diagnosed after chronic pain and chronic problematic periods. I had two laps and was put on depo, and told that if it got worse I would have to go up to steroids (which of course I didn't want to do!) I was feeling particularly desperate and started doing my own research. I found this book: http://www.amazon.com/Endometriosis-Key-Healing-Through-Nutrition/dp/0007133103/ref=sr_1_1?s=books&ie=UTF8&qid=1317532738&sr=1-1 which helped A LOT. I found following the diet guidelines caused a significant reduction in my symptoms. I also started to stay away from soy, processed meats, and cut back on my diary and meat products (basically in an attempt to avoid as much antibiotics, hormones etc in my food as possible). And of course, buying organic when I can. Being diagnosed with endo became a spiritual journey for me and there were a lot of spiritual, emotional and health elements that I underwent in my life. Though I do not want to make it out as though it is as simple as changing your diet, I am now hormone free, having regular periods and have not experienced any major endo symptoms in years. I do get the odd pang where it tends to pop up (my right ovary side) but often I take it as a sign to revaluate my diet, stress, exercise and being vigilante and making the necessary modifications has been enough to make the pain go away.
Now I know that endo can be described as a disease that can easily be masked. I have heard of women with minimal pain but high rates of endo and infertility, and I've heard of women who have a high rate of pain and uncomfortable symptoms while the endo remains minimal. I have not had a lap in years so I am not going to pretend I know for a fact that I am endo free or that it is not affecting my fertility (I will be ttc this spring so we shall see!). BUT what I can say for a fact is that changing my diet and exercise helped me dramatically! I never knew things like soy could cause such havoc on someone with endo, or that certain foods would reduce inflammation and pain. If you haven't looked into your diet and the connection to your endo symptoms already, I would highly recommend you give yourself the time to look into it :) I know how painful and uncomfortable this disease can be.
I've had Depo-Lupron (the menopause shot) twice. they were given a year and a half apart. It never helped with my endometriosis but did help the ovarian cysts. After I got off the shot, they started coming back. I've had 5 laser laps because of the endo and cysts. My drs have been telling me to get pregnant since I was 17 because it was going to be harder as time went on. Needless to say, I'm 22, 3 months from 23 and we've decided to start TTC just after February when this Depo-Lupron wears off and I get my first period!
|50 members and 9,181 guests|
|AlaskAnne , americanjuly , AwesomeJessica , blissor , bluefaery , buttercup , girlspn , japonica , jennajung , jul511riv , katelove , kelz251 , lilmissgiggles , LiLStar , LittleLlama , Mama2Cesca , mckittre , mearph , Milk8shake , Minuteman , MissMuffet , moominmamma , Moonrising , Mylie , MylittleTiger , NaturallyKait , N¡¢0¢0 , neemoomommy , oxford , Poddi , Ponyomum , rainydaywoman , sandiegongp , SandiMae , sarafl , Serafina33 , sofreshsoclean , spiderdust , Springshowers , stephgibbs , Tigerle , Tracy11360 , TrishWSU , usually-lurking , zebra15|
|Most users ever online was 449,755, 06-25-2014 at 12:21 PM.|