E’s Ovarian Cancer Journey

As you may know, September is Ovarian Cancer Awareness Month. Jenny and I have written before about why this is an important cause for our family – we lost my mom to the disease nearly 25 years ago. The cause took on another meaning for us at the beginning of this year, though, when our friend Elizabeth was diagnosed. We’re honored to have Elizabeth as a guest poster today, to share the journey she is on. I find her incredibly inspiring, and I know you will too.
— Emily

**********************

When I started blogging four years ago, I never dreamt I’d be a *guest blogger* some day.  We were beginning the process of adopting our son from China and I figured blogging would be a great way to keep family, and a few friends, in the loop.  Mostly because I’m lazy and didn’t feel like giving updates fifteen different times.  So my blog, EEK… I have a blog, was born.  (EEK are my initials.  I thought it was terribly creative at the time.  Now I wish I could have a re-do.)

Steve, Olivia, Quinn, Turner, and Elizabeth

What started as an *adoption blog* became a pretty typical mommy blog.  It morphed into a grief blog as I lost my mom fifteen months ago.  And then in January, it turned into something I NEVER wanted it to be… a coping with Cancer blog.  And here I am today, a *guest blogger* because I am currently surviving Ovarian Cancer.

Last winter I went to visit my family doctor because of some crazy bloating (lovely, I know).  I’m talking; the* I looked pregnant* kind of bloating.  I no sooner had the word *bloated* out of my mouth and my doc had a diagnosis out of his mouth, Irritable Bowel Syndrome.  We had a good chuckle over this *old lady diagnosis.*

He asked if I was stressed.  Three kids four and under, the holiday season and the recent death of my mother.  Stress?  Check!  Drink more water, exercise and take fiber pills.  If it didn’t get better, I was to see him again after the New Year.

Over Christmas I gained 10 lbs in two weeks.  I was a faithful attendee of Weight Watcher meetings and knew FOR SURE I wasn’t simply overdoing it on the cookies.  When I went back he gave me a lecture about changing metabolisms; blah blah blah.  I was irritated but thankful when he sent me for a CT scan.  His nurse called me the evening of my scan.  The doc wanted to see me the next morning.  She had no other information.  I was smart enough to know that when a doc wants to see you immediately, it is NOT good news.

The events of the next week are a complete blur and yet deeply etched in my mind’s eye.  “The good news is all of your major organs look good.  Blood work shows healthy function of all of them.  BUT there are some masses on your ovaries that I am very concerned about.  I’m not going to use the *C* word, but I am going to set you up with a really great oncologist.”

That was Tuesday, by Friday morning; I was on the operating table with a full hysterectomy and a diagnosis of Stage 3 Ovarian Cancer.  They would give me a few weeks to recover from surgery, which also included the removal of a small part of my intestines and a fatty flap (which has a fancy name that I can’t remember) in my abdomen, and then I would begin six rounds of intense chemotherapy.

The questions, the fears, the anger, the despair that followed were intense.  What would we do with our three kids during intense chemo?  Would I survive this?  What would I look like bald?  What if I couldn’t tolerate the chemo?  What if it didn’t work?  I had panic attacks.  I couldn’t sleep at night.  I cried a lot.

Yet in the midst of it all, what held me up, what got me through was/is my faith that God is in control.  He provided so many things in that season.  In fact, He used many of YOU to do so.  Mommin’ It Up and several other bloggy friends held a fund raiser so that we could afford to hire a part time nanny to help us out.  Without her help (and those of you who gave) I honestly don’t know what we would have done.

E in May 2011

Chemo was a rough road.  Being bald is no fun.  Not having energy to do the things as a mommy I normally do was humbling.  Asking for help is NOT my strong suit, but I learned how to do so quickly.  My kids are comfortable with the word Cancer.  They are sensitive to people who are different.  Cancer is not a death sentence at our house.  They know how to pray.  They see that God is a healer and a comforter.

Friends, true friends, are those who sit with you during chemo. They pray for you, non-stop.  They make you meals.  They take your kids.  They do fund raisers for you.  They send money when they don’t know you just because they can imagine what it would be like to be in your shoes.

I had a CT scan two weeks ago and have once again been declared Cancer-free.  I am thankful for that.

E at her Cancer-Free party in July 2011

My hair is growing back.  My energy is 100%.  In most ways, life has returned to normal.  I’m still trying to figure out what Cancer has/is teaching me.  What it’s teaching our family.  What it might want to teach you.  Honestly, I don’t know.  I do know that God is going to use it.  I just don’t want to miss it.

Post to Twitter

Digest THIS. Or diagnose it for me.

Today after school, I am taking Joshua to the doctor for a mysterious stomach ailment.  It has his stomach in knots and my blood pressure DANGEROUSLY HIGH.   High blood pressure with a side of RAGE.

What’s happening is, Joshua is at least once a day, feeling “sick” DURING a meal.  So he eats some, feels sick, wants to go lay down or try to puke, never does puke, and usually within 10 minutes or so can finish at least some of the meal.

The foods involved are totally random.  The times of day are totally random.  I don’t think he’s faking it, but we’ve been battling this off and on for two months, and I am the one who’s really sick – SICK OF IT.  I am beyond frustrated.

He never throws up, hasn’t had any weird bowel issues, just says he feels sick and wants to lay down, or just stop eating for awhile. He even went to the clinic one day at school during lunch, and lunch is his 2nd favorite part of the day (after recess of course).

This all started back in July – he did throw up in July two separate times after CHUGGING chocolate milk at restaurants, so I think maybe that psychologically damaged him and now he’s terrified of getting sick so he is worrying about it so much that he is making himself feel bad.

We’ve taken him off dairy and it hasn’t seemed to have made any difference.

Bobby doesn’t get home til 7 pm, so the kids have already eaten dinner by then. I am tired of doing dinner by myself for years anyways, I ALWAYS have to struggle to get Sophie to eat, and now THIS – it’s making me apoplectic. Joshua thinks I am mad at him, which is probably making his whole psychosomatic stomach problem worse. I am not mad at him, but I am BEYOND frustrated and I can’t really hold that in anymore.  I can barely hold ANY frustration in by dinner time, which again, I might add, I do by myself five nights a week, outnumbered three to one.

So, how about it, readers? Diagnose my kid for me. That way you can save me a $30 copay at the pediatrician’s office.  And though you probably can’t save my kid from intense counseling and therapy because his mom is so mean, the extra $30 could at least go toward those future therapy bills.  You have until 4:10 PM, Eastern time to figure this one out for me. GO!

Post to Twitter

I like to Xoom and I like to Dance!

As Emily told you last month, we are spreading our coolness around the midwest by working with Verizon Wireless’ Midwest Moms.  What up!?  I was rather excited at the beginning of September when Emily handed custody of the Motorola Xoom tablet we are reviewing as part of the program.  I had never used a tablet before and I was intrigued.  After two weeks with the Xoom, my whole family is lovin’ it!  Here are my favorite ways I’ve used the Xoom so far:

1) In the car – Emily shared with you how the Xoom helped make her family’s road trip successful.  Well my family had a similar experience on our way home from Virginia after Labor Day.  Having the Xoom in the car was awwwweee-some! Not only because the fast 3G Verizon service made using the internet and listening to Pandora possible, but because since the Xoom can also be used as a Wi-Fi hotspot, we could use more than one device at the same time! Yee-haa! It was pretty sweet.

2) In a waiting room.  Oh, Lord, do I do a lot of waiting on my children.  This week I used the Xoom to get me through the waiting times at Sophie’s HOUR-LONG gymnastics lesson, her OT session, and Joshua’s swimming lessons.  I can do biz-niss on the Xoom, instead of just waiting!   Anything I would do on my laptop, I can do on the Xoom.  Pay bills, blog, Facebook stalk people, tweet, play games, etc.  And it’s so nice and portable! It fits easily in my purse.

3) At home.  Last week the kids and I hosted a Yo Gabba Gabba party, and I took the opportunity to test out the Xoom as a video camera.  I LOVED using it to record the kids and their *sweet* dancey dance moves!  It is awesome taking video on the big screen, and it was so easy, I gotta tell you I am much more likely to grab the Xoom and take video with it than I am to dig out the video camera.  And, as you can see from the videos below, the Xoom’s video quality is great!  (You should really watch the videos. Joshua’s is only 12 seconds long and features the stylings of Cortney’s son Evan and the cool detachment of Celia’s son Will.  Sophie’s is 37 seconds long.  37 seconds of ADORABLE!)


I love the Xoom! So I’m linking up to Things I Love Thursday at the Diaper Diaries. Head over there to check out what others in the blogosphere are lovin’.

___________________

Verizon Wireless hooked us up with a Motorola Xoom and 6-months of service.

Post to Twitter