Dearest Friend,
I have been
trying to write this letter for some time now, but it is so hard to put into
words what I have been going through. I fear that my delay in explaining my
past behavior has worsened the strain on our friendship. But if there is one message to convey to you in
this letter, it is that I have done and always will do the best that I can. It
is just that sometimes my best falls short, and I have finally figured out why.
Last week, my doctor performed
laparoscopic surgery to explore my abdomen, and he found what he had suspected
all along—the presence of a terrible disease called endometriosis. I should have told you sooner, my dear
friend, but it has taken me a while to wrap my head around this harsh sentence
of chronic pain, infertility and many other unpleasant symptoms.
I know
you’re wondering, “What is endometriosis?” Well, all women have a lining in
their uterus that builds up and then sheds during their menstrual cycle. But for
women with endometriosis, this uterine lining escapes the uterus and attaches
to other organs, the pelvic wall and the ovaries, and can even travel as far as
the kidneys, the lungs, and even the brain. Wherever it is implanted, this
lining thickens and bleeds during the menstrual cycle, causing scar tissue,
adhesions and blood-filled cysts. This
condition is not natural and is incredibly painful. After my surgery last week,
my doctor told me “There wasn’t a place in your abdomen that didn’t contain
endometriosis. Your abdomen was filled with the disease.” Adhesions had grown
over my ovaries, causing them to stick to my pelvic wall, which made my monthly
ovulation excruciating. Parts of my urinary system were also attached to my
pelvic wall, and endometriosis was found on my bladder, which would explain my
constant need to urinate. Finally, the disease had spread to my bowels and my
intestinal tract. Now I know the cause of my horrible stomach issues for the
past 15 years!
Recovering
from surgery has been really hard, but what I think is harder is dealing with
the diagnosis of endometriosis itself.
There is no cure for this terrible disease, and because it is often dismissed
as a non life-threatening female condition, there are very few researchers
studying it despite the enormous impact it has on 1 out of every 10 women. The only real treatment is surgical excision,
but this is not a cure. There is a good chance the disease will continue to
grow and I will have to have many surgeries throughout my life to treat it.
I am
writing all of this to you in an attempt to explain what has been going on with me, and what you
have been noticing, for years. You
probably thought I was a hypochondriac. Mirriam-Webster defines hypochondria as
extreme depression of mind or spirit often centered on
imaginary physical ailments. Honestly,
until I had my surgery, I wondered if it was all in my head! I recall all of the times I had to cancel on
you at the last minute because I had my period and was in so much pain. When I was feeling well enough to meet you
for dinner, I would often have to go straight home afterwards because my
stomach was upset. I am plagued with
guilt when I think about that time I couldn’t help you move because I was
ovulating and couldn’t even stand up straight. I will never forget when I missed
your big party because my period left me so dizzy and nauseous that I couldn’t
make it out of bed. There are so many
things I missed out on because of this disease. There have been so many times I
have let you down.
I want you to know
my disease is real. My pain is real. I
know I may have come off as flaky, unreliable and even at times apathetic to
our friendship. I know I may seem high-maintenance
because wherever I go I need to have a bathroom close by, and I can only eat at
restaurants that have a menu that won’t upset my stomach. I know that being my
friend means you have to be extra flexible and understanding all the time,
which must be exhausting. Endometriosis
often leaves me exhausted, and there are many times I want to give up on
myself. But I won’t give up, because my
life is worth fighting for.
Despite how my disease has challenged me, it
has also made me a better person and in turn, a better friend. I am stronger
because of it and can be strong for you when you need it. I rely on hope and
grace to carry me through the most difficult times and can share these wisdoms
with you. I have learned to appreciate
the wonderful people in my life and hold them close. I remind myself every day of what I have to be
grateful for. If you stand by me, I will be the most loyal friend you have. I don’t sweat the small stuff. Little things
like a functioning heating pad and dairy-free ice cream make me incredibly
happy. Handling this disease and facing
all that comes with it require an excellent sense of humor. How else could a
person deal with highly invasive medical tests and ridiculous bowel symptoms? I can share all of this and more with you if
you choose to stick with me through this.
I
hope my diagnosis helps you understand my situation a little better. I
encourage you to research endometriosis for an even clearer picture of what I
am going through. I encourage you to ask questions. I promise I will talk about
it with you. I will let you know how I am feeling and why. I will be open and
honest with you at all times.
As you can see, with my new diagnosis
I need friends more than ever! Right now, I am overwhelmed with the thought of
what endometriosis means for my life and my future. Will I be able to meet
someone who will want to date me with all that comes with this disease? Will I
ever get married? Will I be able to have children? How will I manage to live
with a disease that has no cure and very few effective treatment options? These
are big questions that I don’t expect you to answer. They have no answers. What
I am hoping is that after you read this letter you will want to come over and
watch a movie with me. I have a pint of
chocolate coconut ice cream in the freezer, and seeing you would make my heart
happy.
With Love,
Your friend with endometriosis
Great post! I had no idea about endo before I met so many lovely ladies on twitter who suffer from it.
ReplyDeleteI love this. I'm with you on all of it - especially the chocolate coconut "ice cream".
ReplyDeleteYour Blogger is very good. I am very interested for this. Friendship and Lovesite I like very much
ReplyDeletePowerful. So, so powerful. I love this because other women could "steal" pieces of it in order to help them explain their endometriosis to their friends...if you were okay with it of course.
ReplyDeletecasey, this is awesome! i would love to publish it in my book by the "relationships" chapter! would you let me?
ReplyDeleteEven though our diagnosis isn't the same I related to this so much. It's hard to have "normal" relationships when you are suffering. I'm the queen of "selling out" on plans and nobody hates it more than I do.
ReplyDeleteI was fortunate enough to have two amazing children, but the rest I could have written myself. Decades of misery, finally diagnosed, but still no end, and no cure in sight. Frustrating at best.
ReplyDelete