Here's a recap of what has happened since the diagnosis last Monday:
- Met with Dr. Christian on Wednesday, July 25 for a full report on type of cancer and options. I have Invasive Ductal Carcinoma, 2.8 cm (which is a T2 grade of tumor). We can't "stage" the cancer until we get further information, but from the tumor size, we know I have at least Stage II cancer. If it has spread, it will be considered Stage III.
- I tested positive for both Estrogen and Progesterone Receptors (NEU2), which means that my cancer cells respond to those hormones by replicating. They will put me on a drug therapy for 5 years that will help to block the hormone receptors in the cancer cells. We are still waiting for the results of a genetic test called FISH. If this test comes back positive, I will definitely need chemotherapy. If negative, there is a chance that I won't have to go through chemo.
- The tumor was within 1mm of the extra tissue taken in the biopsy on two sides, which means that they need to go in and take more tissue (called a lumpectomy).
- They also need to do a Sentinal Node Biopsy, to see if the cancer has spread. The lymph nodes are the main filter system of the body, and will be where the cancer cells head first. They inject me with a blue dye and a small amount of radioactive material and will look for the main (or Sentinal) lymph nodes under my arm (which will turn smurf blue). They will remove those and immediately test them to see if cancer cells are present. If so, that means that the cancer has a high chance of having spread, and chemo and radiation is needed. They will then take the rest of the lymph nodes out.
- I need to have an MRI to see if there are any other areas in either breast that could be worrisome. I had the MRI on Friday, 27.
- My choices at this point are: Lumpectomy & Sentinal Note Biopsy followed by 5-7 weeks of radiation (everyday) or Mastectomy. As stated earlier, we won't know if chemo is needed until we see if the cancer has spread.
- If I have a lumpectomy, there is no guarantee that that they will get all the cancer, and the radiation will have a permanent, negative effect on the tissue of the breast.
- On the other hand: if I have a mastectomy, my chances are reduced to 1-2% recurrence and I won't need radiation. I won't have to worry as much when I go in for a mammogram (which is every 6 months.) But, I will lose my breast and be numb in my chest for the rest of my life.
So, David and I left with a lot to think about and some very big decisions to make. I must admit, I've had a few breakdowns during this time. This has all happened so quickly, and the decisions made can literally mean life or death.
After talking to my mom and sharing the results, she called me to say that Sister Dulce wanted to see me again. I made an appointment for the next day (Thursday, July 26). On the way to her ministry, I was contemplating my choices. It is very evident to me that my cancer is aggressive and not something to play around with.
I go in to see Sister and she asks me what the latest status is. I fill her in on the details and she takes my hand. She told me that she doesn't think it has spread, but we need to wait for the lymph node results to be sure. She asked me what I was considering doing. I told her i was leaning towards mastectomy. She said, "If it was me, I would go ahead and take both. I have see too many women over the years choose to take one breast, only to have a tumor show up in the other breast two weeks later." This confirmed what I felt in my gut. We talked some more and she consoled me during some of my weaker moments. She reiterated that we need to move quickly...not to let the doctors prolong action. I left there feeling much more resolute than when I entered.
So, now we wait for more test results: FISH test, MRI. We should have test results by Tuesday or Wednesday (which will help with the mastectomy decision if it shows more lesions). I am meeting with a plastic surgeon today to discuss reconstruction options. If I decide to go with the mastectomy, the plastic surgeon will be there during the Sentinal node biopsy and will take over immediately after the mastectomy.
On a lighter note: David surprised me with a visit to New Orleans Saturday and we were not allowed to discuss the "c" word during our stay. We had an incredible meal at a restaurant called "Root" (highly recommend) and had a couples massage. It was nice to detach from things for a little while.
But, back to the fight. We will be pushing hard to move forward with one of the options as quickly as possible. We want to start on the recovery side of this. The lesson in "Patience" has been a hard one, but part of the plan.
I have to say again how awed I am by the outpouring of love, prayers and support from friends and family. It is overwhelming and I am so thankful. Keep those prayers coming...they are felt!
More to come...Angie