Third infusion

I had my third infusion this morning. It was free of incident, as usual. The doctors were interested in my mild symptoms of peripheral numbness, but they thought it was very minor and did not change my Abraxane dosage. I'm pretty tired now (9:20pm), but I didn't sleep well last night and I find the infustion days stressful, even though they are pretty dull and slow. I still can't tell if the drugs make me tired, or all the surrounding angst makes me tired.

I am definitely losing my hair now. They told me to expect it around week three, so maybe this is a bit early. I noticed yesterday that a lot of hair came out in the shower. Single strands, but quite a few of them. Now when I run my hand through my hair, if I apply any friction at all I pull out multiple strands of hair. I can feel them pulling out of my scalp, but the roots have died so they come out very gently. I didn't think this would be a big deal for me. It is, after all, a tiny blip in the big deal scheme of things compared with having cancer. But it is not making me happy.

Oh well. I have quite a few cool new hats so I'm ready for the bald head (I guess). I bought a number for myself to make sure I was prepared. Friends have also given me several really cool hats. I'll post pictures when I start wearing them.

Our walk after chemotherapy

Here are some photos Margaret took on our walk in Golden Gate Park after chemotherapy this week.
















This is our new dog, Mia, waiting for us to come in through the gate.



And here's Lucky Boy.

Photos below...

I added the photos in the posts below just to give a recent view of Alex and Rebecca. Joseph took these snapshots a few weeks ago on the first day of school. The last one is from two years ago when, on a backpacking trip in the Grand Canyon, Joseph and Alex ran into John McCain camping with his son...

Alex's first day of middle school

Rebecca's first day of sophomore year

John McCain encounter - Grand Canyon 2006

First update via Blog

This blog is experimental. I have updated a number of people about my diagnosis (metastasized melanoma) and my treatment (chemo) via email, but I inevitably leave someone important off the list, or feel that I am spamming people who don't feel comfortable telling me they'll just ask if they want to know something about me. 

So, I'm going to see if blogging my updates works better. I'll send the URL out to folks, update the site periodically, and see if this turns out to be a good way keep people who want to know the latest up to date.

The latest, latest as of today (9/20) is that my second treatment this past Tuesday was uneventful. I still feel very well. I didn't get too tired. My hair has not begun to fall out yet. But I think I have beginning symptoms of numbness in my fingers and toes (mild enough that I'm not 100% sure it isn't my mind playing tricks on me). This is a symptom of neuropathy, which is a pretty common side effect of Abraxane (my chemo drug). I'll tell the doctors about it this week and we'll see if I skip a week of Abraxane, or if they reduce the dose. I think it will be one or the other. TTFN.