My journey with Endometriosis began long ago when a doctor told me I had appendicitis,
which was a good trick since I no longer have an appendix. It took over a year of chronic
pain to find out what I was really suffering from. A strange disease that when you say the
name people either think you are dying or making it up. I am at a loss as to why so few
people know and understand Endometriosis since 1 in 4 women suffer with this disease.
Too many times have we heard it's all in our heads, because it is not. It is real, it is not
"just that time of the month", it is not normal, and it is time to speak out!
Endometriosis is a disease that is confusing not only to the sufferer but also to the patient.
It is defined as "the presence of tissue resembling endometrium (the lining of the uterus),
outside of that organ" by Dr. Lyle Breitkopf, M.D., author of "Coping With
Endometriosis". To put it in simple terms you might say that it's part of your body
that appear in the wrong place and causes all sorts of problems.
Endometriosis commonly has three basic characteristics. You can have one of the three or
you can end up suffering with all three. They are painful periods, pain during intercourse,
and infertility. Any way you look at it Endometriosis spells PAIN.
They really aren't sure what exactly causes Endometriosis and right now there just aren't
very many ways to fix it. There is really no cure. This is one mean disease. Not
only is it physically painful, but it is emotionally devastating for many.
Many women choose to try and become pregnant rather than go the hysterectomy route.
A lot of times this results in pure frustration because they are unable to conceive, or they
have to contend with the bitterness of being able to conceive just to find out that she can
not carry the child. I had three miscarriages before my first daughter was born and can
testify to the fact that miscarriage is just as bad as losing a child that has been born. It's
your child, you grieve, there is no way around it. Like I said Endometriosis is pure
pain.
So what do you do when you find out that you are dealing with this disease? First get all
the information you can, you can't ever learn to much. Then surround yourself with
support, because you are going to need it. Make sure your "significant other" knows that
what you are dealing with is NOT PMS. Make sure you have a good doctor-
patient relationship and if you don't, find a doctor that you can have one with, cause you
are going to need it. And make some decisions...well informed decisions.
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