January clinic visit

Serenity had her monthly appointment at the clinic on the 20th. I was anxious to learn what her ANC was because of her previous dentist appointment. Fortunately, it was 2.8 which is pretty high for a cancer kid. So high, in fact, that they decided to bump her chemo up to 75%. She was on 100% chemo for months originally, so it makes me a teensy bit nervous when they have her on less than a full dose. (Her ANC should ideally fall within a certain range, so the chemo is adjusted based on her ANC. Too little and she’s not getting enough to fight the cancer; too much and her counts will crash. It’s a delicate balance.)

The clinic was super busy when we were there. Our provider told me that there were 6 new cases that day! It’s always a weird feeling to see newly diagnosed families in the waiting room. I hear the things they say and a part of me wants to interrupt and tell them what they’re really in for for the next 2-3 years. Instead I keep my mouth shut and mind my own business. 😉

Serenity had her lumbar puncture after our clinic visit. For the first time the medicine the anesthesiologist gave her didn’t put her to sleep immediately, which unnerved me. After a few seconds he drew it back through her line and pushed it again. This time it made her sleepy, but she was still sitting up and looking at me, and she started to cry. Usually she falls asleep instantly. He gave her another small dose and she continued to cry and call out for me as I laid her down on the bed. He put the oxygen mask on her face and she was writhing around on the bed and crying softly. It was the saddest thing. At that point they asked me to leave so they could start her procedure, so I did, but it was hard. I knew she was too out of it to know what was happening, and would be asleep in a few more seconds, but it was hard to leave her there calling for me. 🙁 She did great through the procedure and woke up quickly afterward, still calling for me. We had an incident when Indigo broke her jaw a few months ago and kept waking up through the anesthesia, despite the fact that they kept increasing her dose. I was afraid that Serenity would wake up during her lumbar puncture (spinal tap) and maybe she did. These kids go through so much and just take it all in stride. It makes me proud of her, and in awe, and breaks my heart all at the same time.

After her lumbar puncture, where they put chemo into her spinal column and draw out some fluid to test for blasts, Serenity was soon back to normal although a little subdued. She’d been fasting all day for her procedure and it was funny to hear her talk about all the different things she suddenly wanted to eat.

We went back up to the clinic for her vincristine in her port, and then home. I was supposed to start her back on dexamethasone, which helps the vincristine cross the blood barrier, and I forgot! I didn’t remember for 2 days, and I am just kicking myself for that. They even reminded me at the clinic. Every once in a while we make a mistake on her medications – and while I know that it happens, and it’s even factored into the 2-3 year treatment protocol – there is always a small part of me that knows that if she were to relapse, I would always hold myself responsible.

This week we’ve been dealing with a VERY emotional and clingy Steroid Girl. Serenity gets hysterical very quickly on steroids and stops speaking in words we can understand. She throws herself on the floor and screams unintelligibly while Phil and I rally around trying to guess what she is upset about. This week has been harder than most. I’m sure it’s not helped by the fact that she doesn’t feel well. The kids have all come down with a horrible cough and cold as well. Phil and I are teetering on the brink of becoming sick and I just don’t know what we’ll do if it happens. I’m so exhausted and worn out just trying to take care of everybody that I can’t get sick myself.

Please pray for Avalon

Avalon is an amazing and very brave 6 year old. She underwent 2 years of treatment for leukemia and is in remission. Avalon has brain, GI, neurologic, and musculo-skeletal damage from the treatment and continues to amaze and inspire family and friends alike.

Avalon’s mother has been a huge support to parents of children with ALL. Her emails and words of advice and encouragement have helped me more times than I can count. I consider her a friend and my heart is breaking for what Avalon and her family are going through right now.

Serenity insists that we include several cancer warriors in our prayers every night. If one is forgotten – which only happens when someone other than Serenity is saying the prayer – we start over. Avalon is one of those warriors. Right now Avalon needs all the prayers she can get. Please take a moment to visit her website and keep her family in your thoughts and prayers.

http://www.caringbridge.org/visit/avalonhavan

Dentist

Serenity had a dentist appointment today. She was scheduled for a cleaning next month but yesterday the receptionist called and said they could fit her in today.

It wasn’t until we were there at the appointment that I remembered that her oncologist wants her to have prophylactic antibiotics a few hours before her appointment. I’ve forgotten in the past and they’ve always had us just hurry up and take some as soon as I remembered.

So I called the oncology department, a little embarrassed that I’d forgotten. The person I spoke with chastised me because she was supposed to get a CBC ahead of time in order to make sure her ANC is above 500. I’ve never done this before! I really think I would have remembered. I mentioned that we’d never done it before and I don’t think he believed me. He said they always want them to have a CBC ahead of time. He did agree to call in a prescription, but I wonder now what her ANC is and if everything will be alright.

We have an appointment next week for her monthly vincristine, and she’ll have another lumbar puncture with methotrexate injected into her spine.

No news

No news is good news. 🙂 I expected Serenity to get exposed to something over the holiday weekend, but she has been feeling great. A few days ago she had horrible dark circles under her eyes; it usually happens when she is about to get sick. But she’s looking better now and acting like her adorable sweet self.

Today was the last day we have health insurance. We’ve applied for Medicaid, so hopefully that will cover us until Phil’s able to find work. It’s funny to me that in some ways we’ll now have better insurance – no co-pays for prescriptions and hospital stays. Medicaid won’t cover home health visits so we’ll have to make more frequent trips up to Primary Children’s.

I think she will have another CBC sometime this week to see if her ANC has risen at all.