Friday, May 25, 2012

Short but Sweet :)





Oh happy day! 

We all know the words to this song...

Oh happy day, Oh happy day
When Jesus washed
Oh when he washed
He washed my sins away
He tought me how
to watch, fight and pray
fight and pray

Oh happy day, Oh happy day
When Jesus washed
Oh when he washed
He washed my sins away
We´ll live rejoicing
ev´ry day, ev´ry day
Oh happy day, Oh happy day
When Jesus washed
Oh when he washed
He washed my sins away

Yes, We all know the words to that song. In my head I am singing the Sister Act version. It is a happy day. 

I went to my oncologist yesterday. Things are promising. Although I have not had a complete scan yet, it appears that my treatment is working! The lymph nodes in my neck and the largest one in my arm pit feel visibly smaller. YAY! So, I will take the endless hot flashes, headache, nausea and tiredness if it means that we are killing this cancer!

I will have a complete PET and CT scan in July. But for now I will lean on this hope! All the fightin' and prayin' is working! Just like Jesus taught me!


The LORD is my strength and my shield; My heart trusted in Him, and I am helped;Therefore my heart greatly rejoices,And with my song I will praise Him. Psalm 28

Thank you Lord, Thank you Jesus, thank you everyone who is praying and fighting with me! Let's keep it up!



Tuesday, May 22, 2012

Keep on keepin' on!

Well it has been a few weeks since I last posted. Nothing has happened and so much has happened all at the same time. I'm still here. I am still hanging in there. I have a few more cuts on me. I like to think of them as war wounds. Since this is a battle I am fighting.


I know it has been awhile, 42 days to be exact, since I have written anything. I don’t really know why. There is a lot going on in my head, but I just haven’t been able to get it all out. And although I haven’t written anything here, I have been able to talk it out and vent with some dear friends. But I think too, I needed time to just be in my head. I needed the time to retreat into myself and just think about all that is going on. I needed “me” time.

I needed time to think. Cancer is overwhelming. And it is not just the fact that I have a disease in my body that I could potentially have for a very long time, but everything that goes along with it is overwhelming too…..the good and the bad. It is such an emotional roller coaster of everything. The actual disease, scheduling doctor appointments, going to said appts, surgery, infusion, recovery, being present for my kids, trying to just keep moving on in a normal way, the outreach and support from others, answering every one’s questions and educating them on my decisions, taking well meant advice, going on with life, going to sports games, paying bills, new bills, and really just figuring it all out. It is overwhelming just writing it all.

I know I have a lot of support. That is very evident. But when I go to the doctor and sit in that room, or when they poke me for the hundredth time, or when I am talking to the lady from the utilities trying to explain why the bill will be late, it is just me. I know that usually someone (Nick) has been physically with me. But it is still me and my cancer. This damn cancer that has changed my life. I can get mad about it. I can retreat into myself and wallow for a bit. BUT, I also know that it is what it is. Then, I snap out of it, and remember that the support of friends and having God on my side is all I need. But, I still have to remind myself of that.

I am a giver not a taker. I am the one who takes the meals and runs the race. So, having everyone do so much for me lately is hard for me. I am very grateful. Because honestly everything that has been done…the walk, raffle, auction, zumbathon, pampered chef parties, reunions, meals, etc. has truly helped me and my family. And for that I am truly appreciative. It really is still hard to believe that it is being done for me, but I have learned to accept the help and I am trying to feel worthy.
So where am I now in my treatment? Well, I am doing a hormone therapy right now. (Not hormone replacement) I had surgery April 11th to remove my ovaries. Why? To stop the flow of estrogen in my body. My cancer is fed by estrogen, so we are starving this cancer. I have had three chemo infusions. I take a daily dose of a heavy drug called Tykerb(lapatanib). And I also take Femara (letrozole). Another drug to stop the production of estrogen in my body. I’m going this route right now to try and get the cancer out of my lymph system and chest wall. Hormone therapy tends to cause fewer and less severe side effects than traditional chemotherapy. But it is not without side effects. I am very TIRED. My energy level drains quickly in the evening. I visit the bathroom a lot for various reasons. I don’t sleep well. I have hot flashes galore. I have headaches and sometimes blurry vision. And on and on. Luckily,(and my rainbow)I have escaped the awful side effects for now. I still have my hair. Although, I do notice more on my hair brush, and I do not have the horrible rash that the Tykerb can give you. But I am not counting it out yet. Other therapies such as radiation and other chemotherapies are not ruled out. We are just going this route for now. A surgery for mastectomy is about a year away. So I get to carry these melons around for a bit longer. I am in this for the long haul.
I have learned a lot these last few months. I am learning more about the different types of cancer and just how individual cancer can be. This is more than I ever thought I would know about breast cancer. Yes, it is overwhelming, and I really do know that I am not going it alone. I am still in awe of all the support that is there. But, if I don’t tend to write all that much, it just means I am thinking. 

So for now I am going to just keep on keepin’ on. 


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