Monday, December 31, 2012

Happy to be Alive!

Three years ago today, I received the scariest and most devastating news that I’ve ever heard. My oncologist called me with results regarding a CAT scan I’d had a few weeks earlier. I was in a wheelchair because of all the pain in my leg. It was cold and rainy that afternoon, and I remember it so well because we were having a new front door installed (we had to get it done before the end of ’09 so we would qualify for a special home improvement tax break lol). Anyway, my oncologist’s nurse called me around 12:30 that afternoon and said they wanted to talk to me in person. I told her that we would try our best, but we were having a new door put in and it might take awhile. So she made the appointment for 3:30 and the Champion guys were done by around 2. I knew the news was bad. I started crying and praying as soon as I hung up the phone, begging God to give me strength to handle whatever the doc had to say. I was in so much pain that I couldn’t take the two steps down into our garage to get in the car, so I scooted down the steps on my butt. John wheeled me in my chair for the rest of it.

When we got to the doctor’s office, they took us back almost immediately, and my doctor came in to the exam room to deliver the news. He started with “unfortunately…” and put his hand on my shoulder. I just took a deep breath and listened as he told me and John about how the chemo wasn’t working and the CAT scan had detected several lesions on my liver. Me and John just looked at each other, stunned. I was too scared and too surprised to cry. I was just so sure that the chemo was working. My doctor ordered an x-ray on my leg to see if the radiation had helped at all, and to ensure I didn’t have a fracture, so I could start physical therapy. Over in the Radiology department at the hospital, it was dead. After all, it was 4:00 PM on New Year’s Eve. While everyone was off making big party plans, me and John sat alone in the waiting area, quietly wiping tears, trying to hold it together. The x-ray technician had to lift me out of my wheelchair and hold me on the table because I literally could not move my lower body. He told me to hang in there and as long as I didn’t have disease in my liver, I would be fine. “You will do great as long as it’s not in your liver; anywhere but your liver…” he said. Then I told him that I had found out an hour earlier that it was in my liver. He said, “Oh, well you will still be fine, I just know it.” He was embarrassed for putting his foot in his mouth, and I was kind to him. He didn’t mean it badly. In addition to that, he had been carrying my 150 pound ass all over the exam room, so I had to cut him a little slack. On the way home, I said something like, “well this is it, this is how I’m going to die…” but John never accepted that. He just told me I was going to make it. I think he said it 2-3 times during the ride home. Maybe he was trying to convince himself.

When we got home, all I wanted was to watch something mindless and funny on television, and have a double cheeseburger from Burger King. I was afraid to eat onion rings because they always give me indigestion, and I knew that my mind would trick me into thinking those tumors on my liver were the cause. After we ate, I had to call my sister because I knew she would be wondering what was going on. She had been at work all day and I was off (I was working from home, but had vacation time that day). John went into the office bedroom because he couldn’t stand to hear the conversation between me and Cat.  As soon as I heard her voice I started crying really hard and she knew. We cried together and she agreed to break the news to our parents. I just couldn’t do it. I wasn’t even sure how I would be able to look at my parents without crying, much less be able to tell them the awful news. After me and Cat got off the phone, I cried really hard for about a half hour, then I called for John to come back into the living room so we could watch something funny. We flipped channels and found “Paul Blart - Mall Cop” on one of the movie channels. Normally, movies like that don’t do much for me, but it was just what both of us needed. We laughed throughout the whole movie. I was still scared and worried, but for an hour and a half, it was nice to laugh and think about something else.

Today, three years later, my life is so different. I’ve had lots of ups and downs since then. But today, I’m up walking around – no scooting down steps on my butt LOL. I’m working in the office instead of at home, propped up in bed. As of October 24, my liver is still clear of tumors (next scan is at the end of January). I spent this afternoon cuddling on the couch with my pup, helping John install a window sill in one on our bathrooms, and eating a great homemade Indian meal that John made after he finished the window work. Now we are watching the Twilight Zone marathon on the Sci Fi channel and my mind is much more at ease. I still get really scared, but three years ago, I didn’t think I would live to see another New Years Eve, much less three more New Year’s Eves!! To be honest, this post is hard to write, because thinking about how things were three years ago still scares me to death. Sometimes it’s hard to believe it even happened. It’s like something you read in a book or see in a movie.  But I need to think of how awful things were, so when I have a self pity moment,  I’ll remember  how great my life really is now.

Thursday, December 27, 2012

Merry Christmas and Happy New Year!

My last entry was angry and full of self pity. In moments of weakness, it's easy to forget how blessed I really am. I experienced some really nice blessings during the holiday weekend. My Christmas with John and my family was wonderful. I'm thrilled that I'm here to celebrate another holiday and that my body feels strong enough to enjoy two of my favorite things: shopping and baking! We also went to the Christmas Eve candlelight service at church and it was so nice.
 
I went back to work yesterday after having a few days off. I learned that one of my contacts at our headquarters office died suddenly over the weekend. I never got to meet her face to face, but we spoke on the phone and emailed frequently regarding work projects. In fact, I just talked to her last week. I knew that she had been sick and recently had surgery, although she was back to work and recovering. Hearing this news made me very sad, and her family is in my prayers. But it also reminded me that none of us is guaranteed tomorrow. Three years ago, I could barely celebrate Christmas because I was in so much pain. It was all I could do to put on my wig and makeup and pretend to feel good so I wouldn't disappoint or scare my niece and nephew. Now, I'm working in the office every day, going to church, shopping, cooking/baking, and hosting my family at my house for the holidays. I'm so thankful for all of these things.
 
One of my Facebook friends posted something really cool and I’m going to do it in 2013. On January 1, you take an empty jar or container, and put in little notes about good things that happen throughout the year. Then on New Year’s Eve, you empty it and read all the little notes. I think that sounds really awesome. I’m going to make sure to date each note that I write too. What a wonderful way to truly count your blessings!

Sunday, December 9, 2012

Another Weak Moment...

Day in and day out, I try to maintain a positive attitude. Every day is a gift and I’m thankful to be alive. People ask me how I am and I always say that I’m good and can’t complain. But right now at this very moment, I’m pissed off. I don’t really know what brought it on. I’ve had a great day today. I woke up with minimal pain. Me and my husband went to church and heard beautiful music and a great sermon. We enjoyed a tasty Japanese lunch with my parents.

I guess I just started thinking about things in my life and how some people complain about stupid stuff and I just get tired of it. I hate that I’ve been bald for 3 years. I hate that I have pain every day. I hate that I dated so many stupid people before finally meeting the true love of my life, and now I’m going to die and leave him here alone. I hate being on a cane because no matter how much makeup I wear and how much money I’ve spent on a quality wig, I still look like a sick person. I hate that my toenails never grow and what I do have are so damaged by the chemo that I’m too ashamed to let John see them. I hate that I have two pink lines across my chest instead of two breasts, which by the way, were really pretty at one time. I hate that I have to go to the doctor every few weeks and worry every time about what he’s going to say. I’m so tired of hearing “this is good news but…” or “unfortunately…”  I hate that I have hot flashes that make my face blazing red all the time. I hate that I’m so self conscious that I push my friends away and avoid most social situations. I hate reading articles about celebrities or pseudo celebrities like those stupid housewives of whatever city talk about a “very scary” breast surgery for a BENIGN tumor. Really? You are scared because you “almost” had breast cancer? Give me a break. I would give my right arm to have had an “almost breast cancer” scare. I hate it when people talk about how tired they are of being sick, when they’ve been sick for a week with a cold. I hate that I can’t help my husband with housework or go grocery shopping by myself. I hate seeing disabled people that don’t work and I’m working full time. I hate the show Bridezillas, but I hate even more that I’ve been sitting here for two hours watching it!

Well, now that I have all of that out of my system, I feel better. I think it’s normal and human to have pity parties and get mad sometimes. I’m thankful that it doesn’t happen often and usually happens in private. John is painting one of our bathrooms so he doesn’t even know that I had a “moment.” I like to cry in private because I’m the world’s ugliest cryer lol. I love my life and I want to live to be 80, but I have moments of fear, anger, frustration, sadness, and pain.  It just gets to me and I have to release it.  Okay, I’m done. Uplifting and happier blog entries are coming soon. :o)

Thursday, November 15, 2012

It's Time to Shave, Yes It's Time to Shave!

I'm in a wild mood this morning, haha. I'm thinking of the stupid Brady Bunch kids singing the "Time to Change" song - you know the episode where Peter's voice changes right before a big talent show. So I'm singing to myself about it being time to shave my head. Right on schedule, a few weeks after my first chemo, my head hair is coming out in huge chunks. I bought a new wig last weekend, so I'm ready for the hair loss! I don't really mind looking freakish as my hair falls out, but what is most annoying is the trail of hair that I leave all over the house. That's why it's important to just shave your head when you start losing hair. Little things like towel drying your hair after a shower or turning over in bed in the middle of the night pull out bunches of hair. We will have to wash sheets, blankets, and towels this weekend haha!

Wednesday, October 31, 2012

Scan Update

Well, as of yesterday, I’m back in chemo. I got scanned on 10/24 and got results yesterday. My organs are great, which is a huge relief. However, some of the spots in my lumbar/sacrum area have grown a little. So my oncologist wants to be aggressive so the spots don’t grow more or spread to any of my organs.  Yesterday, I started on Abraxane, which is in the Taxol family (the chemo that I was on forever and ever LOL) and Xgeva to strengthen my bones. The Abraxane is a thirty minute intravenous treatment that goes in through my port every three weeks. The Xgeva will be given through a shot in my arm once a month.  The doctor has also ordered a Neulasta shot once a month to keep my white blood cell count up. I’ve never had bad counts, but he doesn’t want me to start having them now.

To be totally honest, I’m disappointed. I’m so thankful for healthy organs and the news could have been so much worse. But I’m just now at the point to where I’m comfortable without my wig and my eyelashes have been coming in so nicely. The nurses in the infusion room told me that my hair may just thin a little bit, but I’m not getting my hopes up about that. I lost my hair with the first round of chemo drugs, and stayed hairless during the Taxol treatments. So I wouldn’t be surprised if I lost it all again. There are benefits to losing my hair though: no shaving under my arms, no shaving my legs, and no Nairing my face – yes you get lots of facial hair when you go through menopause haha! I’d rather be bald and have my tumors shrinking than to be full of cancer with long beautiful hair. There is more to life than a head full of hair and long lashes. :o)

So I’m going to keep working, keep exercising, and keep pushing. That has worked for me for the past three years, so I’m not stopping now! My medical leave for the hip replacement ends tomorrow so the routine at my job will be great therapy. I have a lot to be thankful for at my job. The benefits have paid for all of these crazy chemo drugs and I make good money. If I didn’t have a job with great benefits, I would really struggle paying for my treatment. The last thing I want is to be a financial burden to my husband. I know he would be glad to help me but holding on to a little of my independence is important. I also work on a great team with a fabulous boss. My co-workers are also my friends and they have been so understanding about me working from home on chemo days. My boss is super flexible and kind about my appointments and work load. A lot of people can’t say that. I remember sitting in treatment one day last year, and a patient was on her cell phone fighting with her insurance company about coverage.  I’m so blessed!

Thursday, October 11, 2012

Hip Update


I had a follow-up appointment with the surgeon today, and I got a great report! In fact, he released me. I don’t have to go back until next August. I’ll be on a cane for awhile since I’m building all new muscles. I’m going to do something I rarely do on Facebook or in the blog: post a picture! I thought it was really cool to see the “before” and “after” versions of my hip. The image on the left is the new hip. The image on the right shows the old rod and the screw that moved through my weak hip ball. I'm really not sure how long I walked around with the old hardware out of place, but it was very uncomfortable. I'm so thankful for modern medicine and miracle surgeries! I feel sooo much better now! Although I already wrote this in another post, I have to write it again - the bone fragments removed during surgery had NO cancer. It's a miracle!


Tuesday, October 2, 2012

Breast Cancer Awareness Month

I’m a little embarrassed to write this, but I promised myself I would always be honest in my blogs, even when it makes me look bad.

Before I was diagnosed with BC, I used to roll my eyes a little when it came to breast cancer awareness, particularly breast cancer awareness month. It just seemed to me like most of the advocates were the ones that had teeny tiny tumors and they caught it so early that they didn’t even need chemo. So why were they being so damn dramatic about it and acting like they knew everything about cancer? Well, now I get it. Finding BC early is so important. If I had been more aware of my body and been doing self exams, maybe I would have caught mine before the tumor grew to six centimeters. And while I’m being honest, I knew that I should have been doing self exams. My OB/GYN preached self exams from my very first visit to him in my mid-twenties. I just laughed it off. I also donated to BC charities and read literature about BC. So I knew that anyone could get it and age didn’t matter. Somehow though, I still felt immune. I went through a short hypochondriac phase in my early twenties because I had a thyroid cancer scare. I have underactive thyroid disease and it turns out that I had some lumps on my thyroid gland. The doc increased my synthroid dose and the lumps shrank. A needle biopsy also proved that they were benign. However, after that scare, for about two years, I got every ache and pain checked.  I even went through a period when I thought I had lupus. Then one day, a specialist laughed at me and I was mortified. I promised myself that I would never be a crazy hypochondriac again. I still went for my yearly checkups so I could get synthroid refills and saw my OB/GYN once a year.  I took pride in never complaining about health stuff, and bragged about being healthy. I was determined not to revert back to being a crazy hypochondriac. Unfortunately, that was my downfall when it came to finding my breast lump. I only waited a few weeks, but as aggressive as my tumor turned out to be, I should have run to my doctor – literally. Hindsight is 20/20 I suppose.
Since it’s October, everyone will see billboards, commercials, internet articles, Facebook posts, etc regarding breast cancer awareness. I’m sure many people will think, “damn, enough already!” But please take my word for it – be aware of your body. Don’t be afraid or ashamed to look at yourself in the mirror and examine yourself. I used to say, “well I’ll start doing that when I’m 40…” But breast cancer does not discriminate. It can strike anyone, any age, men and women. I have no family history of breast cancer and I was never sick a day in my life (unless you count chicken pox and the occasional cold/flu). I didn’t meet any of the criteria or “warning signs.”  If you find a lump, RUN to your doctor. I don’t want anyone to go through what I’ve been through over the past three years.