My Cancer Journey

It has been over two years since I started this journey, and I have now taken Anastrozole (Arimidex), an aromatase inhibitor (AI), for a little over one year. This particular drug is given to post-menopausal women whose cancer feeds off hormones. Many believe that women no longer produce estrogen after they have gone through menopause. This is not true. Our bodies do not produce as much, but we all have an enzyme called a romatase in our fat tissue that converts other hormones in the body into estrogen. The AI blocks the production of estrogen.  Pre-menopausal women are given hormone blockers like Tamoxifen which prevents estrogen from binding to cancer cells. AIs and hormone blockers have side effects ranging from severe to minor; most are somewhere in between. The most common side effects are hot flashes, weakness, joint pain or stiffness, bone pain, osteoporosis, brain fog, edema, sore throat, cough, headache, depression, insomnia, high blood pressure, nausea, vomiting, ski...

Eleven weeks after my last infusion of Kadcyla my body still seems to think I am receiving treatments. Some of the side effects still occur about the same time they did when I was getting treatments. They are not as severe, and do not last as long, but they happen almost like clockwork. My energy level is pretty much back to how it was pre-cancer. Sleeping has never been one of my superpowers, but it got worse when I started getting the infusions. It is sometimes difficult to fall asleep, and sleeping beyond 6:30 in the morning is late for me. Even though I try hard, my body very rarely lets me nap.  The brain fog is almost gone. It feels terrific to be almost back to my normal self. Not having so much brain fog so nice, but it also means my obnoxious self comes out more frequently. Now Craig must deal with me not agreeing with him all the time again. On the good side, I am better able to control my temper. It is easier to keep myself from getting angry and frustrated. The migraine...

Friday, February 2, I had a pre surgery check to make sure I was healthy enough for the upcoming surgery. They take your vitals and blood. The port-a-cath is very convenient in that the person drawing your blood does not need to find a good vein. That day I found out that phlebotomists are not trained to access a vein through a port, so she needed to draw my blood through a vein in my arm. All the tests looked good, so I got the okay for the lumpectomy (partial mastectomy).   The following day I was able to start using adult toothpaste. My mouth was no longer sensitive! More news - I was excited to have hair growing on my head again, but that was not the only place it had started growing. There was still no hair on my legs or armpits. That was fantastic! However, a few hairs that had been growing in a couple of moles on my face were back. Even though I had the moles removed many years ago :( I would have preferred my eyelashes and brows were back instead :/   Thursday, Februar...

On Thursday, January 10, I had two tests, an echocardiogram to make sure my heart had not been affected adversely by the Herceptin, and an MRI to see how well the tumors had reacted to the chemotherapy.    My heart looked good. It did not seem it was affected at all. Great news! I was, however, concerned about the MRI. The contrast (color) they put into my system to get a better picture, made me nauseous last time. Not to the point where I vomited, but I did not want to take a chance that would happen.    First, I thought to put Vick’s Mentholatum in my nostrils as the nausea was brought on by a chemical “smell,” but the smell did not enter through the nose, but from inside my body. Therefore, I did not think it would be possible to block the smell. Instead, I brought one of my anti-nausea pills, the sublingual (melt-in-your-mouth) Zofran. I took that right before the MRI and it worked great. No nausea!   The other concern was that the tumors had not shrunk enou...