Treatment Plan

Today was a big day of appointments! This morning I had my first appointment with the dermatologist at the Cancer Center. She was very nice and went over all my background infomation with me and then did a full body check for suspicious moles. She was very personable and the check was easier than I anticipated! She said I’m a pretty simple case and there are only two moles she wants me to watch. She instructed me to do monthly skin checks myself and only needs to see me every six months! After seeing Dr. Curiel, I was talked to by a health educator about sunscreen and wearing long sleeves(cue eye roll on my part) and given some sunscreen samples. I heart samples!

Danny and I took a break from the cancer center for lunch. After lunch, we met with Dr. Cranmer, my oncologist. He was FULL of information and made sure we understood his role as well as interferon and the controversy surrounding the treatment. Essentially, it’s not a super effective medication, but it does improve odds for some people and is the only treatment available. The current plan is for me to start Interferon next Wednesday, the 16th. I need to have a pulmonary function test, chest x-ray, and IV port put in before I can start. So, I have a busy few days in front of me! I will be having 20 days (4 weeks, 5 days per week) of high dose interferon followed by 11 months of 3x per week self administered (by injection) low dose interferon. Interferon is a protein the body makes naturally to fight infection. So, although I am hopefully already cancer free, Interferon will increase my immune system and help it defeat any remaining melanoma cells in my body. I am also starting an antidepressant tomorrow since 40% of patients on interferon struggle with depression and an antidepressant is considered part of the course of treatment.

In the last part of the afternoon, I took part in some “word games” as part of a study and had bloodwork drawn. At 4:30 we finally left to pick up the kids from my parents after a LONG afternoon! I’m glad to be home and have the appointments behind me. I dread beginning the treatment, but I am glad to begin putting it behind me!

Our New Routine

What’s life like as a Melanoma patient? At the moment, it’s pretty darn boring! We started a new family routine today that will carry us through my first month of interferon treatment and perhaps for awhile afterward. I’m hoping to be able take over most of the kid duty after that first intense month of treatment. At the moment the kids are going to school full days on Mondays, Tuesdays and Thursdays. Danny drops them off at 9 and my Mom is picking them up at 4. Mom takes them back to her house and then Danny picks them up on his way home from work around 5:30. I predict they will be exhausted and I am going to learn new appreciation for those evening hours with them. (Or, they’ll be grumpy and I’ll just want to put them to bed like normal!) 🙂 On Wednesdays through my first month of treatment, my Mom will have the kids for the day and is going to help me with some laundry and housework. My Dad is changing his work schedule so he can watch the kids on Fridays. Once I start treatment, Danny will drop me off at the cancer center (very close to work for him) in the mornings and then drive me home at lunchtime.

It’s been a semi-rough day emotionally. Being a stay at home mom is SO important to me and although this is for a limited time, it’s tearing out my heart to not be able to take care of the kids. Cancer has taken away a little of my identity as a mom and it’s just another reason cancer sucks. My kids couldn’t be in better hands. I just talked to Mom and Joey did well today, but Abby is struggling. She’s been showing more anger lately. We’re trying to stay consistent with discipline and grace. Both kids ask about my drain and back. Abby is a little more interested in the drain and is already asking when I can “take it off.” We watched the Arthur episode about cancer with the kids last night. We haven’t explained that Mom has cancer. They’ve probably heard me talk about it on the phone. We’ll probably talk about it more specifically this week as we adjust to our new routine. Please pray for all of us as we adjust!