Wow, it's been awhile. And in standard form, I've been away from blogging for a nice long stretch. It's not that I haven't thought about it, I think about writing all of the time. It's just that, well.... just see the name of my blog. If it's not one thing, it's another.
Instead of writing one loooong blog about my whole life story the last six months, I'll just start with one event and write other blog posts about the others. I'll spare your eyes and my fingers the torture of doing it all at once.
Let's start by saying that I've had, er, let's say... female troubles my whole teenage through adult life. These troubles are characterized by more pain than I could possibly describe without electrifying the chair you sit in. And maybe install spikey things. Maybe then.
I have a family history of Endometriosis, and have been told I have cysts on my ovaries. Lovely things, these cysts. I've had them burst, sending me to the emergency room begging to be run over by a truck. Repeatedly. Until the pain stops.
A few months back I started having pain on my left ovary-ish side. Nothing bad. Just enough to make me go "huh.". Over the course of several weeks, the pain got worse. I finally broke down and went to the doctor, who immediately ordered all sorts of tests. Let's just say I knew it was bad when the brusque and Brumhilda-like ultrasound technician suddenly turned kind and sympathetic after taking the images she needed. All 40,000 of them.
Come to find out, it wasn't what *was* wrong with me, it was what *wasn't*. The ultrasound showed that I had two very large chocolate cysts on my left ovary. Blood and other tests showed markers for cancer, and extensive precancer of the cervix. (There's a name for this, couldn't tell you what it was at the moment) The doctor also strongly suspected rampant Endometriosis.
I was scheduled for my pre-op appointment about two weeks after my last test. To make a long story short, I ended up in surgery much earlier. The pain was too much, and even hard core pain-killers stopped having any effect. ( And this coming from the person who goes unconscious when she takes benedryl.)
After the surgery, the doctor came in to see me. The conversation went something like this:
Doctor: "How are you feeling?"
Me: "Mmrfflflap" (patient note- Those little morphine push button thingies are THE BOMB)
Doctor: "O.K. good. (I'm guessing he understood Morphinish.) Well, the surgery went good. The cysts were very very large and I can see now why you were in so much pain. (Thank you Captain Obvious!) You also had extensive Endometriosis. It wasn't the worst case I've ever seen in my career, buuuuut..... it what pretty far up there. I'm very confident we were able to remove everything. (Note: by everything, he also meant ovaries, tubes, uterus and cervix. Yep, I was gutted like a fish!)
I know women often feel like they are missing something when they have full hysterectomies. I've read more information about it than is probably healthy, and most of what I read said to expect to go through the mourning process for this. I can't say this has been the case for me at all. After having so much pain for most of my life due to what I now know was Endometriosis, and the other problems I have had, I can truly say I am SO relieved!
Yes, I have to take hormones for about the next 20 years. But the knowledge that the problem was identified and addressed gives me so much relief and peace of mind. The recovery has been long, and my stomach muscles may never be the same. (Not that I was running around in bikinis before this!) But it has all been worth it.
I will have to continue to be checked once yearly because of the type and extent of the precancer areas that were removed. The moral of this story is: Get your yearly checkups! These cells would not have been found had we not been testing for an unrelated condition. I have not been good about getting mine done every year, and this may have had a catastrophic ending had the cysts not forced me to the doctor.
EVERY. YEAR. Schedule yours now! Do it for your kids, do it for your loved ones, do it for YOURSELF!

Instead of writing one loooong blog about my whole life story the last six months, I'll just start with one event and write other blog posts about the others. I'll spare your eyes and my fingers the torture of doing it all at once.
Let's start by saying that I've had, er, let's say... female troubles my whole teenage through adult life. These troubles are characterized by more pain than I could possibly describe without electrifying the chair you sit in. And maybe install spikey things. Maybe then.
I have a family history of Endometriosis, and have been told I have cysts on my ovaries. Lovely things, these cysts. I've had them burst, sending me to the emergency room begging to be run over by a truck. Repeatedly. Until the pain stops.
A few months back I started having pain on my left ovary-ish side. Nothing bad. Just enough to make me go "huh.". Over the course of several weeks, the pain got worse. I finally broke down and went to the doctor, who immediately ordered all sorts of tests. Let's just say I knew it was bad when the brusque and Brumhilda-like ultrasound technician suddenly turned kind and sympathetic after taking the images she needed. All 40,000 of them.
Come to find out, it wasn't what *was* wrong with me, it was what *wasn't*. The ultrasound showed that I had two very large chocolate cysts on my left ovary. Blood and other tests showed markers for cancer, and extensive precancer of the cervix. (There's a name for this, couldn't tell you what it was at the moment) The doctor also strongly suspected rampant Endometriosis.
I was scheduled for my pre-op appointment about two weeks after my last test. To make a long story short, I ended up in surgery much earlier. The pain was too much, and even hard core pain-killers stopped having any effect. ( And this coming from the person who goes unconscious when she takes benedryl.)
After the surgery, the doctor came in to see me. The conversation went something like this:
Doctor: "How are you feeling?"
Me: "Mmrfflflap" (patient note- Those little morphine push button thingies are THE BOMB)
Doctor: "O.K. good. (I'm guessing he understood Morphinish.) Well, the surgery went good. The cysts were very very large and I can see now why you were in so much pain. (Thank you Captain Obvious!) You also had extensive Endometriosis. It wasn't the worst case I've ever seen in my career, buuuuut..... it what pretty far up there. I'm very confident we were able to remove everything. (Note: by everything, he also meant ovaries, tubes, uterus and cervix. Yep, I was gutted like a fish!)
I know women often feel like they are missing something when they have full hysterectomies. I've read more information about it than is probably healthy, and most of what I read said to expect to go through the mourning process for this. I can't say this has been the case for me at all. After having so much pain for most of my life due to what I now know was Endometriosis, and the other problems I have had, I can truly say I am SO relieved!
Yes, I have to take hormones for about the next 20 years. But the knowledge that the problem was identified and addressed gives me so much relief and peace of mind. The recovery has been long, and my stomach muscles may never be the same. (Not that I was running around in bikinis before this!) But it has all been worth it.
I will have to continue to be checked once yearly because of the type and extent of the precancer areas that were removed. The moral of this story is: Get your yearly checkups! These cells would not have been found had we not been testing for an unrelated condition. I have not been good about getting mine done every year, and this may have had a catastrophic ending had the cysts not forced me to the doctor.
EVERY. YEAR. Schedule yours now! Do it for your kids, do it for your loved ones, do it for YOURSELF!





