Showing posts with label Breast Cancer. Show all posts
Showing posts with label Breast Cancer. Show all posts

Monday, November 9, 2015

MONDAY'S MUSINGS—HUNKERING DOWN FOR THE LONG HAUL




I’ve learned much, the past couple of months, about the battle against cancer.

For one thing, it’s not a battle, it’s a war and wars are won by winning a series of battles.

Mobilizing for war is arduous especially while defending against an unexpected attack. It takes clear thought to the goals and what will be lost if one doesn’t win. There’s the cost of fighting a war, mentally, physically, psychologically and monetarily.  One leaves behind ‘normal’ life and has to focus everything on fighting and winning the war. It becomes the daily existence. One has to channel funds into getting the best weapons and equipment, assembling a strong motivated fighting force, and have a good knowledge base of the enemy and its goals. Not an easy task. The initial euphoria after an attack often wears thin and so keeping the reasons and goals for fighting the war to begin with, needs to be kept to the forefront of everyone’s mind. Then it’s hunkering down for the long haul and fighting to win.


Somewhere along the line I lost sight of parts of that mobilization process. I was unexpectedly attacked and I mustered up what was needed initially. Mindset, support group, funds to deal with travel and tests. I was armed but it was only the first of the battles that needed to be faced and although there were skirmish victories my mind lost sight of the long haul. And it’s daunting.


I think one of the problems is I’ve had several surgeries in my life. Usually, after a surgery for a particular thing, the mind then faces the healing process (like rebuilding after a war). In this instance, the removal of the tumor was successful. Pathology indicated that all was clean in the breast. Lymph nodes all clear. My mind leaped right past the concept of war and focused on the battle won and onto healing...wrong. It was only the initial battle. Yes, I won that series of battles but the war was by no means won.


This trip to CTCA was very intense. I had a list of questions and one of those questions had to do with further treatment. See, everything was healing. Pathology showed all clear, so why did I need chemo or herceptin? I brought my page of questions forward and got back several pages of answers and much more information for the war beyond this initial series of battles.


We went back to the preliminary findings and again defined the cancer I’m facing—Her2 positive, grade II, stage II—highly invasive and consequently fast growing and with a penchant for stray cells to migrate to other places and basically homestead. Without proper treatment this cancer will come back and even more aggressive than it was initially. I was given a clearer picture of what it takes to conquer this particular type of cancer and what weapons I will need to win the war
 

Scary stuff.


Countries gearing up for war can divert resources from existing assets and/or increase taxes to fund it. I have no one to tax and only a limited amount of funds to divert and yet there is no question that if I want to live and win this war, I have to go forward. On the plus side I do have very good insurance. On the negative side the co-pays are going to hurt financially. Then there is travel, daily food, and lodging that must be taken care of over the next eighteen months. This war is going to be expensive.


Just like soldiers and civilians in a war, I want normal life back. Well, that’s not going to happen for awhile. There is much in between the victory in these initial battles and eradicating the threat and demolishing the enemy. All the wishing in the world isn’t going to make this cancer go away as quickly as I want it to.


All I can do is have courage and move forward, keep my spirits up, and focus on demolishing the enemy. To do that I have to hunker down for the long haul. 

And it will be a long haul.  

Monday, October 12, 2015

MONDAY'S MUSINGS: LEFT TURN INTO THE TWILIGHT ZONE





I know many of you have wondered where I’ve been and why I haven’t been posting.  I had every intention of posting after Labor Day and doing my normal blog with guests and all. Unfortunately, my life took a left turn into the twilight zone.  I cancelled my guests for September and October.


I was diagnosed with breast cancer, invasive ductal carcinoma (IDC), on September 2nd. Welcome to the sisterhood I never wanted to be a part of.  My life ceased to resemble anything normal after that.

Cancer.

It’s such a scary word when you hear someone has it and even more so when you find out you have it. Even with the cure rates, which are good if you catch it early enough, there is still an adjustment time of dealing with the word and its meaning. I can tell you that I had to face that basement of fear before I could do anything. Or tell anyone other than my husband.

I found a lump the third Wednesday in August. Being one who is very aware of her body I knew something was wrong inside but not exactly what. I had been pondering over what it could be. In fact I dreamed I had cancer several days before I found the lump. I think my subconscious mind was scanning and analyzing what was going on inside. It’s done it before and has been rather accurate when it does. 

My husband confirmed that no, it wasn’t my imagination, there was a lump. He was half asleep at the time and I assure you after he checked, at my request, he no longer was drowsy.  “Oh my God, there’s a lump here. You need to get this checked out.”

“I will. I’m going in Tuesday for a mammogram.” I kept it cool and easy when inside I was anything but calm. My heart was pounding. I didn’t even try to downplay it by saying it’s probably nothing because I suddenly knew, for a certainty, it was something.

I had my mammogram August 25th and sure enough, there it was as clear as daylight. I always look at the scans when I have them done and I watch the techs. The tech’s wide eyed look was the only reaction she showed. If I hadn’t been watching her closely I wouldn’t have even noticed. She looked up at me and said, ‘you knew there was a growth, didn’t you?”   
Sure did and I had gotten to know it quite well in 6 days.

I told my sisters, first, because they are incredible women and I knew I needed them on my team. By this time I had already walked right through fear and assemble my battle gear and got my mind into battle mode. I knew I was gearing for the battle of my life. I needed, as any who fight cancer, a strong support team so I could kick ass. I had and have no intention of taking any prisoners or being taken.
   
I saw my doctor two days after the mammogram and had a biopsy on the first of September and the confirmation by the second. It was at least 1.8 centimeters by 2 centimeters. The doctor wasn’t sure whether it was still stage 1 or in the beginning of stage two. It ended up being stage 2, grade 2 and HER2 positive which is a protein based and not hormone based and it wasn’t there two years ago.

Although my local breast center was good I opted to go to Cancer Treatment Centers of America and the Midwestern facility in Zion, just outside of Chicago, for treatment. One of the considering factors was that particular center has been awarded Breast Cancer center of excellence. Not many breast centers achieve that distinction and there are only about 50 in the United States.

It’s been 18 days today since the tumor was removed. I still tire easily and don't have as much stamina but I'm healing and in pretty good spirits, over all. Just taking it slow and steady. 

Pathology reports are good. It hadn’t yet spread to the lymph nodes and is nowhere else in my body, yay. I go in for my first infusion of chemo November 6th. At this point I will be receiving 4 cycles of chemo and perjeta and then a year of herceptin. I have no idea how I will react to all that and it differs from person to person. I’m a bit of a weeny contemplating it. I can honestly say, I wish I didn’t have to do this part and of course I can say no, but I don’t want to have to face this again so yes, I will throw back my shoulders and lift my chin and do it.

I do reserve the right to be to whine, be wimpy, and weak now and then. 

The cure rate for this cancer is excellent and I’ve met and spoken with many who have been cancer free for 5 years, several who are celebrating 10 years and two fabulous ladies that marked year 13 and 15. Very encouraging.

Life doesn’t come with guarantees. We all die at some point or another but as Gandalf says, in the Lord of the Rings, …All we have to decide is what to do with the time that is given us.” 
I don’t choose to waste that time or live in fear.


“A day may come when the courage of men fails… but it is not THIS day.”
– Aragorn


I’m not sure what my posting schedule will be the rest of this year. I'd like to try Monday Musings, at least, depending on how I feel. We’ll see.