Endometriosis is a chronic painful disease which occurs when endometrial tissue grows as lesions outside the uterus, mainly in the area of the ovaries and fallopian tubes, but can also affect the intestinal tract. The condition results in chronic pelvic pain, painful menstrual periods and pain during intercourse.
Ihas been a poorly understood illness for years incapacitates and affects the productivity and lifestyle of millions of women around the world. Just in the United States alone, endometriosis affects nearly six million teen and adult women at a cost of approximately $1.6 billion annually.
Many women who have endometriosis report having high levels of stress due to trying to deal with the painful symptoms that affects their everyday lives – work, personal relationships and family. There is currently a new study that is investigating the relationship between stress and the painful symptoms of the disease. This will be the first time a study has been done that offers evidence of the negative consequences of stress in the progression of endometriosis, most likely through an effect on the immune system.
The study was conducted on seven female rats who were induced with endometriosis. Half were subjected to stressful swim tests for ten consecutive days, a chronic and stressful situation the animals could not control.
According to the senior researcher for the study, Dr. Appleyardm the study conclusion was:
“These findings contribute to our understanding of how stress may affect the severity of endometriosis. We think there is likely a connection with the immune system because of the observed levels of mast cells in the colon and the increased levels of inflammatory cells in the peritoneum of the affected rats, since this has also been observed in patients with endometriosis. The results offer a jumping off point to help identify stress-management interventions that will help those women who are affected by the disease.
Alysse says
Hi my name is Alysse and for 8 years I have been dealing with endometriosis, IC, and cronic bladder infections. I am only 21 years old and due to having these diseases I was forced into home schooling in high school. Now I am still struggling in order to find help with my pain. My doctor finally set up an appointment with me to see a pain specialist, the only medication I have ever been on that took my pain away to a level I could deal with is oxycontin. However, the pain specialist still has to determine whether or not I am a good candidate for pain treatment. Which I think is almost rediculous for someone like me who have been in pain for the majority of their lives. Sometimes it is nice to hear from people who struggle with some of the things I do because it makes me feel like I am not alone on my quest in living a life that is actually worth living.