Endometriosis Awareness Month

img_5486As March is upon us again and our thoughts turn to Spring and of new growth and warmer weather.  There are some ladies who just think about coping with what life has thrown at them.  They are the one in ten women who suffer with Endometriosis.

Endometriosis.org describes the disease as, “where tissue similar to that of the endometrial lining travels and attaches itself elsewhere in the body causing all kinds of issues, including a chronic inflammatory reaction, that may result in scar tissue. It is primarily found on the pelvic peritoneum, on the ovaries, in the recto-vaginal septum, on the bladder, and bowel.” It can then grow on other organs as well and is difficult to find.  It is debilitating often causing chronic pain and is far more than just “a heavy menstruation” as it is often thought by those who are alas ill informed.

March is for them.  Those women. In the past few years March is not just the month we have just stumbled upon.  It is what they do, in a bid to raise awareness for a debilitating condition, which is not yet recognised as a formal disability, but wreaks havoc upon the lives of women across the globe. Many are hoping that by doing so, their family, friends and employers will have an understanding of this invisible illness. One which can cause a multitude of symptoms and a world of pain.  They do not require sympathy for they are fighters and far stronger than you might think, they go through so much but they do require your understanding.

It takes a minimum of seven years to be diagnosed with this disease, but it is incurable.  It renders many women infertile and can cause unbearable pain.  Multiple operations, hormone treatments and periods of time when you could be absolutely fine, lulling you into a false sense of security and having taken seven years toll upon you, it can cause depression and the breakdown of relationships and the loss of employment. You may be pain free for months, or even years following treatments and possible surgery and then it will suddenly rear it’s ugly head again causing new symptoms which you had previously thought were unconnected, but later turn out to be.  It can affect women from puberty to menopause and sometimes further than that.

There is so much more information about this disease available now at your fingertips. From groups on Facebook set up by women who want to share experiences, research and competent medical contacts and offering support to fellow sufferers to Endometriosis Research Foundations and Charities, who enable us to find out more about the condition. They are known as “Endosisters” and are united by their illness and the need for understanding it.  Should you wish to find out more about this condition please feel free to select the link below for more facts. http://endometriosis.org/resources/articles/facts-about-endometriosis/

 

 

 

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