This won't be very long today, but yesterday was a bad day. 2 weeks ago I had my 6 month PT scan which came back as perfect, showing no cancer in me. That next Monday I found out that my CA 125 was elevated and the CA 125 is more sensitive to the cancer cells. A week later I had another blood test to confirm it was elevated, and that is what I found out yesterday.
It sounds as if I will be getting 1-3 chemo treatments but I do not know when they will start. My Dr. does not want to let the microscopic disease to go untreated, and truth be told neither do I. A reminder that ovarian cancer is it's own beast. Microscopic for ovarian is not the same as for some other cancers. It's still a big deal. There isn't a pill I can take. There isn't a wait and see policy because of its aggressive nature. And we know mine really wants to get me since it's trying again- so it's aggressive. I encourage you to go online and learn a little about OC. Mayo Clinic is my favorite spot.
How am I? Well, quite frankly I'm angry. I feel good. I look good. I'm taking care of me. But I cannot believe that another baseball and track season are going to be ruined because of this AGAIN!! At least it's not to the date this time. Another 6 month check failed. Another time curly hair has proven to mean there is cancer in me.
I will probably be going to a different chemo place so that I won't have to get another port put in. That is really good news for me. I hate those ports. Chris said that just these few treatments should not bother my veins and make them collapse. So probably Henry Ford Macomb is where I will go.
How is my family? I just don't know. I let them know it isn't a life or death moment but probably a way to control the cancer for the rest of my life barring God's miracle for me.
And that's what I ask you to pray for. I want to be a living miracle- even before the chemo starts and they take my blood work again... Let the number be in normal range and the cancer cells vanquished from me.
Here's to believing third time's a charm.....
Vicki
No comments:
Post a Comment