One Year Ago

I am at the Mayo Clinic for surgery today. I’m sitting in pre-op and was on Facebook when this post showed up in my memories.

I have been specifically looking for this post for some time and after pouring through my CaringBridge page several times I still could not find this post.

God must have known that the timing wasn’t right until today.

As I wrote the above, the nurse came to get me for surgery. The next part, before the reposting of last year’s CaringBridge post, I’m writing at 2:00am after my hourly vitals…

I was battling with coming down here, tired of procedures and travel. What was to be an outpatient surgery has become an overnight stay due to pain issues. We finally have it under control and I will be released today (Thursday).

July 6, 2015

Just spent over an hour with the oncologist. Lots of information and I almost felt sorry for the resident he had with him today as the kid looked more lost than I did! lol

Today was a big talk about numbers and recurrence and the like. With no further treatment, my five year disease free survival rate is 50%. That means if I stopped everything right now, I have a 50% chance that over the next five years, the cancer would return. To decrease the chances of it coming back we have options. Best case scenario, with every current, relevant, and available treatment brings me close to a 20% chance that over the next 5 years the cancer will return. This doesn’t mean that if it doesn’t come back in the next five years that I am considered safe or free; just a little better off.

Thankfully with breast cancer research being so aggressive, who knows what will be available in the next five years to increase my odds even more. When people ask me I honestly tell them that my prayer is to make it through Carson’s graduation. Honestly I am beyond blessed to make it through each day; the boys’ gradutaion would just be icing on the cake.

I spoke with the funeral director back home when I was there last week. He shares my same twisted sense of humor so it was nice to have a sit down chat with him. We discussed a few things (like the fact that if I am laid in a casket my feet MUST be crossed!). We talked about transporting my body across the border and he agreed it would be cheaper to cremate me here and ship me home in the mail.

Anyway, back to reality and what it means for my immediate future.

I am cleared to restart the drug Herceptin which I will take for a total of 52 weeks. I have completed 12 weeks so far. This will be an injection (through my port) every three weeks until the 52 weeks are complete.I will be meeting with radiation oncology to start radiation. Likely five or six weeks of daily radiation. Right now they are booked out until July 27 for the diagnostic/referal of radiation oncology. My medical oncologist is working to get me slipped in sooner.I will begin another drug which will help to prevent recurrance. I will take this drug every day for five or ten years.I will also begin an ovary supressing drug that will be an injection every month. This is decrease the amount of estrogen available for my cancer to feed off of.

I was hoping I would hear the words ‘remission’ but of course those words did not (nor will they ever) come. I will never be in remission from this beast. I am officially in a life long battle for my life. I almost felt sorry for the doctor explaining this reality to me…he looked heartbroken. I told him it was ok, I expected that and that I just needed to hear the words.

I will forever have cancer, I will be considered cancer free when I move from this life to eternity. It’s really tough to be sad when thinking about eternity. I will be healed, I will have no more treatments, I will no longer be at war, I will  see my four babies who have passed before me, I will see my grandfathers again. A lady who recently passed due to cancer put it wonderfully. She wasn’t afraid to die, she just didn’t want to. She felt like a little girl at a party and Dad was there to pick her up and she was crying because she didn’t want to leave.

When the Lord calls me home, that’s how it will be; like my Father is picking me up from the hockey rink and I know he’s taking me to A & W which will be amazing and fun, but I’m no where near ready to get off the ice. My kids are on the ice…

So we will continue to be thankful for everyday. I will continue to shout from the rooftops how amazing God is and how great this life he has given me. I am not afraid to fight. I am not afraid to die. I am confident that His plan is best. That my children will be held through the loving embrace of those who love them.

Psalm 23 A psalm of David.

1 The Lord is my shepherd;
I have all that I need.
2 He lets me rest in green meadows;
he leads me beside peaceful streams.
3     He renews my strength.
He guides me along right paths,
bringing honor to his name.
4 Even when I walk
through the darkest valley,
I will not be afraid,
for you are close beside me.
Your rod and your staff
protect and comfort me.
5 You prepare a feast for me
in the presence of my enemies.
You honor me by anointing my head with oil.
My cup overflows with blessings.
6 Surely your goodness and unfailing love will pursue me
all the days of my life,
and I will live in the house of the Lord forever.

Kinda tough to be upset when that’s my courage, my strength, my peace.

Once again, God’s promises comfort me. Once again I am reminded what a blessed life I’ve been granted. Once again I know God is good and I am given the opportunity to share His good news.

My cancer status is considered N.E.D. (No Evidence of Disease). This does not mean I Ann cancer free, only that there is no sign of the cancer at this point. NED is good.

 

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