Showing posts with label ovarian cancer. Show all posts
Showing posts with label ovarian cancer. Show all posts

Friday, February 21, 2014

A Year Ago today - the first time I found out I was cancer free

A year ago today (on Friday the 15th), I found out I was cancer free...then I rolled over and went back to sleep.  Sounds pretty anti-climatic but there was a reason for it.  That morning, I had an CT scan with contrast, which means drinking that terrible tasting drink and then getting injected with dye to light everything up.  The early morning appointment, the waiting and the stress of it all left me feeling exhausted.  I was glad I'd taken the day off from work. I didn't want to get my hopes up or stress about it, so when we got home Mike and I turned on Netflix and hit the couch.

Due to the wonders of technology, the CT was emailed to the oncologist's office and my awesome NP Lisa checked it out right away.  In the middle of my snooze, I got a text from her - "CTs just came across my desk.  You are a clean machine."  I was thrilled but not quite ready to believe it.  I had a follow up appointment for Wednesday the 20th and I wanted to wait until then to really look at things and move forward.

So I rolled over and went back to sleep, content that all the difficult times had paid off and that there was good news and health on the horizon!





Saturday, January 25, 2014

A Year Ago Today - Impossible to Believe


Its been a year since my last chemo session.  The anniversary would have been sometime last week...the 22nd or 23rd. I think its a pretty good thing that I can't remember the exact date.  It seems so long ago and just yesterday all at the same time.  It's very true that "it always seems impossible until its done" but in this case, it feels impossible that it actually is done.

My fourth and last chemo was a surreal event.  At this point, it was old hat.  Blood test a week before, a weigh in when I get there, consultation with Lisa the NP and Heidi my oncologist, and then into the chair.  After hoping the needle went into the port correctly and getting all settled, the saline and benadryl dripping from the first bag making me feel warm and dizzy and I quickly fall to sleep. My husband and my mother take turns sitting next to me, talking, dozing, trying to read.  Women come in and out, some with short chemo sessions, some with longer ones.  I looked around at all of them, taking them in, looking at who they are and what they were going through, wondering what their stories were.  I couldn't believe that I'd come to this day, where the journey "ends" or at least the treatment does.


A couple of hours passed, the bags dripped out, the tubes were taken out, a bandage placed on port and the words "Congratulations you're done."  I wanted to celebrate but it felt so wrong. Being around so many women who were so sick, some will be on chemo for the rest of their lives, some will not live much longer, it felt rude to celebrate, to be the one who leaves "cured."
It also felt strange to be free and out of treatment.  Chemo is not fun and not something to look forward to, but it at least felt like something was happening.  I wanted to attack the cancer, kill it and keep it away.  How do I know it is staying away if I'm not at the office every month, getting tests, getting treatments? What does a life that doesn't revolve around doctors' offices and strategy sessions look like?  Is keeping cancer away something I can do on my own? What happens next?

In the last year I've tried to focus on health, family and happiness.  I do things that make me happy.  I sleep when I want to. I run and exercise and try to eat healthy. I focus more on family and friends and less on work.  I am learning more about cancer and advocacy.  People have opened up to me about their fears and medical issues and I've referred more women than I would have believed to my doctor.  I've celebrated when they find out its not cancer and I've felt their heartbreak when they've found out it is.

I've gone through a journey that seemed impossible until it was over.  Now I know its never over, that it sits on the minds and hearts of the people I love, advises my decisions in work and play, and brings people into my life that I never imagined.  I don't know exactly what the next days or years will bring.  I hoping and working toward health, happiness and enjoying the journey.


Friday, January 10, 2014

Sometimes You Have to Be Your Own Hero


Recently, my husband and a close friend had a long discussion about how glad they were that they married strong women.  Having wives that would stand up for themselves meant that they still had wives to come home to. Both of us had gone through medical emergencies where we had to convince the people treating us to take us seriously.  It would have been years before I'd be diagnosis and the prognosis would be much worse.  My friend would probably not be vacationing with us this summer if she hadn't advocated for herself. 

It looks like I haven't told the full story of the knock-down, drag-out fight I had with a midwife to get an ultrasound at my first doctor's visit (but I will).  But I have written about not having to be like Angelina to take control of your health and even talked a bit about it on a local newpaper's blog. I want to share more of my story with you but also share the stories of so many other people who stood up for themselves, acted as their own heroes.  It may be medical but it could also be standing up for yourself in a relationship, at a job, or within your family.  If you have those stories, please share them me kqdemars <at> gmail.com and come back here to read what I have in store for you.  

Everyday people are realizing that "Sometimes you have to be your own hero."  Have you? Please share.

Tuesday, October 29, 2013

Teal Tuesday - Pink and Teal - its all too real

Happy Teal Tuesday my friends!  I've been a little quiet on the teal front as this month belongs to pink and pink is rather close to my heart.  Cancer is no stranger to my family on both sides.  So far, I have three breast cancer survivors and one angel in in my family tree.  That makes us all "previvors" , the risk of cancer is all too real to my family.  See, we have a lot of girls on my mothers side.  She is one of 5 sisters, 6 out of 10 grandchildren are women, and we are currently at 3 for 4 girls in the great grandchildren department.  We knot that its just not our amazing good looks that we share.  The genes we share are strong, but not stronger than our love for each other.  So this #Teal Tuesday goes out to this crew:

The winners of the most people in the photo booth contest:



These Sisters:


This Crew:







This Team:



These Aunts:





This Angel:



And these two who started it all:








Sunday, October 6, 2013

Healthy Sunday: Ovarian Cancer 5K Team Kelly - Picture Time!!!




Sunday September 15th, an incrediable group of people got together to run or walk to raise awareness and research money for Ovarian Cancer.  I feel so special and amazed that they all came together as a team for me.  My family was there, as were some of my best friends and their families and their friends.  It truly shows how cancer affects everyone.  To think that it wasn't just my friends and family, but their friends and family as well that were praying for me, cheering me on and supporting the ones I love was incrediable to see first hand.  Wearing our Team Kelly shirts, we walked, ran and laughed our way through the day.   

The day started at Albany's Washington Park where we ran into my oncologist and nurse practitioner, got to see all of the other awesome teams as well as teal swag, information tables and crafts. 

There aren't a lot of people who hang out in the 13 minute  mile zone, but my friends Thom and Joe ran alongside me      keeping time for me and cheering me on.  We finished in about 38 minutes which was good for me but very slow for them.  I totally love them for that. 

Afterward we went to Starbucks and then Across the Street Pub and I got to hang out and bask in the awesomeness of these incrediable people. We talked and laugh and at the end of it all left feeling satisfied, accomplished and loved.  

Tuesday, September 24, 2013

Teal Tuesday: Running Out of Teal

I am only a few months into #TealTuesday and I have come to the realization that I just don't have enough #teal.  Tuesdays roll around and I try to remember when the last time was that I wore a certain shirt or sweater.  I scour the sale racks to find more teal to add to my wardrobe and sometimes try to pass off other colors as teal....


more like aqua blue...

 I show you another picture of my hands...

or feet...

 or cake...

yyuuummm....cake.

But back to the topic at hand.  I've found a way to solve the lack of teal clothing by accessorizing and today I want to share my new FAVORITE teal accessory.  A while back I showed you the teal bling ring I bought from Holly at Expression Rings of Hope.  I've worn it to all kinds of occasions and I never get sick of that extra sparkle (and those little reflections on the roof of my car as I drive home from work).   

Well Holly's friend Jill saw my post and reached out to me about the awesome matching JILLry she has:

  
I noticed Jill's beautiful necklaces before as Jill and Holly often team up with matching rings and necklaces. Jill also donations a portion of her sales to charity. A portion of the awareness necklaces always gets donated to the specific charity they represent and she has a charity of the month for all the other sales.  That is incredibly generous and a lot to keep track of!  When I told her I would put her necklace on my wishlist, she offered to send me one as a gift!

I quickly picked out the Ovarian Cancer Awareness Necklace and was so excited when it came in the mail. 



(sorry for the terrible cellphone pictures)
The necklace very delicate looking, the perfect size to add some sparkle without overtaking my neck line.  I was also happy that it was long enough for my big old neck:



And that it matches fabulously with my bling ring


Thank you Jill for the awesome gift and for all you do to add some sparkle and awareness to so many great causes!  

You can LIKE Jill on Facebook:  https://www.facebook.com/HandmadeJILLry
and order from her Etsy Site:  http://www.etsy.com/shop/handmadejillry#

Disclaimer:  I was given the necklace by Jill as a gift. I am happy to write about it because I LOVE it.  All opinions are my own.  

Monday, September 23, 2013

A Year Ago Today: Lisa Called

During my cancer journey,  I was hesitant to let too many people know before I had all of the facts.  Since I let everyone know I was planning on Joining the Survivors Club, there have been many questions.  In this "A Year Ago Today" Series, I will attempt to answer those questions and also work out what the hell happened this last year in my own head, heart and soul.  Thanks for reading and if you have any questions, feel free to ask.

Hopefully, everyone who is sick has some medical professional that they can trust implicitly.  I was luckier than most because this person was also part of the family. Just about a year before, Lisa had been at my wedding, little did she or I know that less than a year later, my file would come across her desk.  As soon as she got it, she called me.  I was at work that day and didn't have her number in my phone.  Once I heard the words, "Kelly, this is Lisa, why didn't you call me?" I rushed into our Legislative Chambers, shut the door, and the flood gates opened.  I always knew Lisa worked with women with cancer, but before all of this happened, women's cancer to me was only Breast Cancer.  Since I didn't have breast cancer, I didn't call her.  Turns out, she doesn't work with breast cancer patients but with gynecological cancer patients. She quickly broke everything down for me.  She had read the file the OB-GYN sent over.  She thought everything looked good, they would have have to take out some lymph-nodes in order to prevent any type of spreading but that could be done laparoscopically.  I told her that I didn't realize that she worked in the practice that I was referred to or that I would have.  She told me she was taking over, that she had a new young doctor she thought would be a good match for me and that we would change my appointment to a day they were both in the Albany office.  I can't remember much else of what we said, I just agreed to what she wanted to do and trusted that she had a plan.  

I called my mother immediately when I got off the phone.  We both couldn't believe that we hadn't thought of Lisa.  Since she knew Lisa as well as I did, she totally understood why I would be so relieved and put so much trust in Lisa.  We both felt amazing about this. Lisa calling eased a lot of the fears I was hiding from others and hearing her voice and her words of encouragement gave me a huge amount of hope and confidence in the next step of treatment.

A year ago today, Lisa called and said she was taking over and I turned my trust over to her completely.  That is a decision I have never regretted.  

Tuesday, September 17, 2013

Teal Tuesday - Winner Winner!!

As you may remember, Friday September 9th was National #WearTeal Day and we had quite the turn out around the internet for this important day.  I had promised a little give away to anyone who posted a picture of themselves wearing teal.  I received pictures through my personal facebook and email, so I created an album on KQ Demars.  Pretty much everyone who sent a picture was related to me (except Karen) but I appreciate the support.  A few people at work rocked some teal as well, but they move too fast to get pictures of!  You can like me on facebook and check out the album here  

Here are the pictures : 


And here is the winner:

Michele Tolpa!  Congratulations!  You'll get your "Teal Prize Pack" as soon as you get your butt back home!

And of course, we can't forget the real reason behind the Teal Tuesday movement.  Here are the signs and symptoms of Ovarian Cancer again.  If you have these symptoms persistently for two weeks or more or a major change, go see your doctor!

Source

Monday, September 9, 2013

The Return to Health: Compression Socks

I've joined the club...what club you ask?  The club of runners with brightly colored knee socks.  You know you've seen them, usually bright green or pink, like the 80's meets Catholic School Uniform.  Yup, I've joined the compression sock club...and these aren't your Grandma's compression socks.


The reason why is that I was having a hard time seeing my knees.  Yes, my knees.  I'd find by the end of the day my legs were so swollen that my knee caps seemed to disappear.  My oncologist warned this could happen and I was definitely on the look out.  After breaking down into tears upon trying on shorts for the summer, I decided to do a little something about it.  I was worried about Lymphedema so I emailed a high school friend who is currently a Physical Therapist specializing in Lymhedema.

From Cancer.Net:

Lymphedema is swelling, caused by the buildup of lymph in the tissues. Lymph is the fluid that carries immune cells (mostly lymphocytes) throughout the body. It is similar to a "highway" for your immune system. Tiny, bean-shaped organs called lymph nodes make lymph and filter bacteria and other harmful substances. They can be compared to "rest stops" for your immune cells. When the lymph nodes are removed, there is a backup of lymph into the surrounding tissues. Lymphedema can be very uncomfortable and sometimes painful. It can also delay the healing of wounds and raise the risk of infection near the swelling.

During my 2nd surgery, lymph nodes in my groin and upper stomach were removed to help prevent the spread of cancer.  My friend quickly wrote back to me with a lot of information and advice.  From what she said about Lymphedema and some of my research, I came to the conclusion that I might be overreacting a bit (me...never!). Many cancer survivors suffer from painful Lymphedema that is much worse than what I am currently experiencing. It would be good to take some preventative steps against the swelling that was occurring.

The minute I put on the compression socks, I could feel the difference.  I bought them after a long day of wedding dress shopping with my sister and the relief was immediate.  I wear them to run as they are supposed to fight fatigue and speed up muscle recovery.  But I also throw them on after a long day on my feet, especially if I'm not wearing the most supportive of shoes. I got these from Dick's Sporting Goods, they only had pink but I see on the website that I am going to have to order the Teal!

I am glad to say that for the most part, the tree trunk knees are gone.  Hopefully through more fitness and exercise, I can love my legs again!    

Side Note:  I will be rocking these socks THIS SUNDAY at the 12th Annual Caring Together Ovarian Cancer 5K run / walk in Albany's Washington Park.  If you'd like to make a donation or join "Team Kelly" check it out here:  https://www.firstgiving.com/fundraiser/KQD/12th-annual-teal-ribbon-runwalk


Tuesday, September 3, 2013

Teal Tuesday CONTEST - Wear Teal This Friday!



It's #TealTuesday and I'm not wearing teal.  Except for my normal teal bracelet and teal toes, I am currently teal-less.  How could I commit a crime against Teal Power on the very first Tuesday of Ovarian Cancer Awareness Month?  Because this week, we are shaking things up a bit and wearing Teal on Friday!





That's right, Friday September 6th is National Wear Teal Day! Check back here on Friday and post you and your friends wearing Teal for National Wear Teal Day or post your photo on my facebook page https://www.facebook.com/KQDemars

I'll choose a winner at random to win a fabulous TEAL prize!


Wednesday, August 28, 2013

A Year Ago Today: I Found Out I Had Cancer (Part 2)

During my cancer journey,  I was hesitant to let too many people know before I had all of the facts.  Since I let everyone know I was planning on Joining the Survivors Club, there have been many questions.  In this "A Year Ago Today" Series, I will attempt to answer those questions and also work out what the hell happened this last year in my own head, heart and soul.  Thanks for reading and if you have any questions, feel free to ask.

A few days ago, I revealed and reflected on  how I was feeling a year ago when I first found out I had cancer.  In order to keep the reading amount somewhat manageable, I decided to break it up into two parts.  I left off at the whole "I found out I had cancer, got ice cream and went back to work" part.

My head was swimming and I was feeling a bit numb.  Mike drove us over to TCBY and I tried to focus on what I would get there.  I'd had been trying to eat better (I'm always trying to eat better, really) and so I pictured some kind of vanilla ice cream with lots of fruit.  Once we sat outside to dig into our ice cream, Mike commented, "After that news, I'm not surprised to see all that chocolate."  Vanilla...fruit...I just found out I had cancer...who was I kidding.

As we ate our ice cream, we finally found ourselves able to form coherent sentences.  We went over what the doctor had said - found it early, got it all out, stage 1a, no chemo, just a follow up with an oncologist.  We could handle that.   We would do everything he told us to do, get the CAT scan, wait until Friday for the report, go see the oncologist.  Figure it all out before telling the world.  After all, if a person had cancer and didn't know it, does it even count?  If a person had cancer and didn't need chemo, are they even a survivor?  If a tree falls in the forest....you get the picture.

Mike and I have always seen ourselves as a team.  We try to handle everything with the best attitude that we can, move through the bad and focus on the good.  That is what we decided to do that day.  Move through the bad and focus on the good.  From what the doctor said, the bad was behind us.  When we finished our ice cream and our conversation, I decided to go back to work.  I could use the distraction, I would have to ask for some time off later in the week for the CAT scan and the people I work with are my friends.

I am not sure if going back to work was the right decision.  I felt like if I didn't go back, everyone would worry.  However, when I did go back, I think I shocked them.  I walked into my boss' office and one of my co-workers was sitting there with him.  Seeing me, they figured it had gone well and that it was safe to ask how it went.  I hadn't really thought about how I would answer that question.  I panicked a bit and then did the simplest thing there was to do, I told them the truth. I focused a lot on the "I will be fine part" reassuring them as much as I was reassuring myself.  I would need a few days off for some follow up appointments but all in all, it wouldn't take up too much time.  Mike and I would just do what they told us to do and then move forward, everything would be fine.  They both responded that they were sorry to hear that and they knew I would be just fine (really what else do you say?).  Then I got up and went back to my desk, getting a whole lot accomplished with my new found nervous energy.

To this day, I wonder what it was like to be on the other side of that conversation.  I did my best to coat it as positively as I could, but they must of wondered what I was thinking, why I was back there, if I really would be okay.  The conversation had to happen at some point, so I am hoping that getting it over with right away, as opposed to going home or lying, was a good solution.

 Finding out I had cancer was a complicated situation.  So I kept it simple whenever possible: keep moving forward, keep going for ice cream (we had a lot of fro-yo during this experience!) and when possible do whats normal.

Tuesday, August 27, 2013

Teal Tuesday - Some Wedding Dress Shopping

A couple of weekends we went wedding dress shopping for my fabulous sister! Even though she hasn't made a final decision in that department quite yet, we did stumble upon an awesome sale on some TEAL bling at Charming Charlies.  50% of off clearance prices???  Don't mind if I do.....


Yup, that's a teal clutch, teal sunglasses, a teal ring, teal and pink bracelet (for September and October) and TEAL FLAMINGO EARRINGS!

Yup, Teal Flamingo Earrings.  It's the small stuff people.

Now back to wedding dress shopping.  She won't be wearing this dress, but I had to show you how cute she is anyway.




And now I know what I'm making for the bridal shower:


The resemblance is uncanny, really.

And of course, we can't forget the real reason behind the Teal Tuesday movement.  Here are the signs and symptoms of Ovarian Cancer again.  If you have these symptoms persistently for two weeks or more or a major change, go see your doctor!

Can you name any symptom of ovarian cancer?
Source 


Monday, August 26, 2013

A Year Ago Today: I Found Out I Had Cancer (Part 1)

During my cancer journey,  I was hesitant to let too many people know before I had all of the facts.  Since I let everyone know I was planning on Joining the Survivors Club, there have been many questions.  In this "A Year Ago Today" Series, I will attempt to answer those questions and also work out what the hell happened this last year in my own head, heart and soul.  Thanks for reading and if you have any questions, feel free to ask.

The short story: A year ago today I found out I had cancer, got some ice cream, and then went back to work.

The long story:

A year ago today, I went in for my follow up appointment to Surgery #1.  As I wrote about last time, my doctor typically did follow ups 4 weeks post-op.  Since he scheduled this one for 2 weeks, I had a feeling I wasn't going to like what I was going to hear.  I went to work that morning, Mike picked me up at the office and we drove to my 11:30 appointment in Schenectady.

When I got there, I was taken straight back to the doctor's personal office.  No exam room to sit waiting in, just a desk and a few chairs.  The doctor pulled his chair around to the front of the desk.  He spoke quietly and slowly, oh so very slowly.  He summarized our short history together, from diagnosis to surgery going step by step through the whole thing.  As he slowly worked his way up to what he actually wanted to say my heart was racing and my bones ached with nerves. In my head I was screaming, "Say it, just say it.  I know you're going to say it, just get it over with." I knew what was coming, how could I not? It was just taking so damn long.

The overly kind doctor took my hand, he looked me in the eyes, he said something like the bad news is you have cancer, the good news is, we caught it early.  He diagnosed it as stage 1a, that it was contained and that he got it all out.  He told me stories of his patients who had gone through the same things, how they were healthy, fertile and still alive 20 or more years later.  He assured me his tears were only a match to mine, that it wasn't that I had a terrible diagnosis, it was that he hated to see his patients cry.  He said, "You will be fine, you will do well. Very well."  Over and over.  "You will be fine. You will do well."

With legs that were not my own, I walked back out of the office and to the receptionist.  I handed her the paper with boxes checked and scientific terms scribbled out in the Doctor's terrible handwriting.  There were tests to schedule and appointments to be made.  She looked at the paper, she looked at me.  Her eyes reflected the sadness and fear that must have been in my own.  She filled out another paper for me to take to the scheduling nurse. She wrote that I would need a CT scan and a follow up appointment with an oncologist.  She filled that out and then wrote across the bottom, in all caps just like this:


And that was when shit started feeling real.  It was the first time I really saw and felt the words.  I took my paper back to the scheduling nurse and got the CT scheduled and was told my information would be passed on to the oncologist's office for them to set up an appointment.

We left the office, back outside into a beautiful sunny day, passing by people who weren't in the medical arts building to hear they had cancer.  I looked at them as I walked out, wondering what their news would be, what they were there for.  Was it just a routine visit?  Were they going to hear great news? Would they, too, hear bad news?  How was the world still moving and people still going on with their days?  What would my days start to look like?

Mike and I got back in the car and just sat there, staring straight ahead, wondering what to do.  There was so much to do and so little we could do all at the same time.  He wanted to me to tell him what I needed.  I wanted to fast forward through all of it, so that it was a day I was looking back on, not going through.  But I had to go through it, I had to feel it, I had to make a decision.  So I made the easiest decision I could.  I told him there was a new TCBY and I wanted to go have some ice cream.  Then, I did what was comfortable, routine and familiar.  I went back to work for the rest of the day.

Tuesday, August 13, 2013

Teal Tuesday - A Little Salsa?

Well it is Teal Tuesday again.  Last week's post got booted due to the awesome teal cake my coworker and his daughter.  Here is that picture one more time in case you want to drool again!



Today's Teal Tuesday outfit I bought in case I ever find myself salsa dancing.  I love the flouncy top and it is super comfortable.  Best of all, it was on sale at Target!  Maxi dresses two for $22!  Doesn't get any better than that.



 And of course, we can't forget the real reason behind the Teal Tuesday movement.  Here are the signs and symptoms of Ovarian Cancer again.  If you have these symptoms persistently for two weeks or more or a major change, go see your doctor!

Can you name any symptom of ovarian cancer?
Source 





Monday, August 12, 2013

A Year Ago Today: Surgery #1

During my cancer journey,  I was hesitant to let too many people know before I had all of the facts.  Since I let everyone know I was planning on Joining the Survivors Club, there have been many questions.  In this "A Year Ago Today" Series, I will attempt to answer those questions and also work out what the hell happened this last year in my own head, heart and soul.  Thanks for reading and if you have any questions, feel free to ask.

This post will be a little longer because I didn't start it in June, when I first started experiencing symptom.

A year ago today, I went in for surgery to remove a 10cm cyst from my left ovary.  I had been experiencing a lot of strange symptoms, most of all a frequency, pain, and urgency of urination that seemed like a UTI on steroids.  After a little urging (fighting, crying, and insisting) the midwife in my GYN practice agreed to an ultra sound.  After the cyst was found, I was referred to the doctor in the practice who assured me this was routine and necessary for fertility and overall health. He explained that cysts are a natural part of the ovulation cycle and than some do not burst when they release an egg or grow larger due to fluid build up or other abnormalities.  He assured me was too young to be concerned with cancer.  I'd also known  many people who had problems with cysts, whether it be getting them removed or having them burst.  I figured if it would help the whole fertility thing along and make me feel better, I was all for it. 

Read more here 


When it came time to have the surgery, I was extremely nervous.  It was honestly the first really big medical procedure I'd ever had.  There was the uncertainty of how I would feel after, what it would be like to be under anesthesia, what they would find. The doctor told me he would do his best to keep both ovaries in tact, but would have to take the left one out if it looked questionable.  I tried to play it off like it was no big deal, but I honestly wondered how I would feel about having a piece of me missing.

I had a laparoscopic surgery that was supposed to last about an hour. Check in went smoothly and it was no surprise that it took the nursing supervisor to come in and do the IV once my veins decided to hide.  I felt incredibly comforted by the anesthesiologist.  Once they start talking about the different drugs and what they will do to keep you asleep, everything started to feel real and I got very nervous.  She was confident, competent, and really distracted me by telling stories and keeping me calm.  My doctor introduced me to the doctor who would be assisting him and before I knew it, I was wheeled into surgery.

What was supposed to take an hour ended up taking much more (probably 3-5 hours).  I learned later that the doctor found abnormal looking cells during the surgery and called in a oncologist to consult with him.  They decided to freeze a sample and send it to the lab.  It was also decided to remove my left ovary as it was was just swallowed up by the tumor/cyst. My doctor kept my family informed through it all and when I woke up I was in a patient room as recovery was full.

Right after I woke up, I was too tired and drugged to care what happened in the surgery.  I remember waking up, talking to my family then quickly falling back to sleep.  I had never felt so tired.  The goal of the nurses was for me to be able to stand, walk, go to the bathroom unassisted and to return home that night.  I remember begging them to let me stay, I just wanted to sleep and sleep and sleep.  Walking to the bathroom was such a major production that I just could not imagine all of the steps of getting out of the hospital, into the car, drive 30 minutes, get into the house and into my bed.  It honestly felt like they were asking me to climb Everest.

With the help of my super nurse sister, my superhusband, and the hospital nurses assuring me I did not want to sleep there all night, I made it home around 8pm.  I believe I slept most of the night and spent the next few days recovering.  My surgery was on a Tuesday and I was back to work on Monday.

The doctor scheduled the follow up appointment for two weeks from the surgery.  Pre-surgery he told me it would be scheduled for four weeks post-op.  I had a nagging feeling that something was just not right, and this change in schedule reaffirmed that feeling.