Wednesday, February 25, 2009

Am I asking too much? update February 25th 2009

I had a scheduled appointment to see my oncologist today at 9am. I have to actually see him face to face so he can see how I'm reacting to the new meds and chemo and tell me how I should increase the doses. I also need prescriptions from him which require an in person visit.

I got there at 8:45 for a 9am appointment. I knew I wouldn't be seen at 9 because the guy is never on time, ever. I hoped that maybe I'd be seen my 9:30.

At 9:30 there was no sign of him. I asked the front office if they knew his ETA. They didn't. I went back to wait some more.

At 9:45, I asked again what his ETA was. I was told he was on his way but two other patients were ahead of me. At this point, I got really frustrated. Each and every time I make an appointment to see this guy, I end up waiting an hour or more. I feel my time is valuable and by making an appointment I have some sort of agreement or contract with the doctor that he will be available to see me at a reasonable time.

So, I left. I still have to actually see him, but dammit, I'm not going to have my time wasted either.

I think it's time for me to find a new oncologist. Seriously.

Tuesday, February 24, 2009

Update February 24 2009

I feel much better emotionally today. I ended up going out Saturday and although it was a long night I had a good time.

I had my second series of chemo treatment yesterday, and so far so good. I'm starting to increase the dose of all my medications slowly. The dose I'm on now is really small so I know I will have to increase it in order for it to have an effect. Of course, the chance of me getting side effects goes up as I increase the dose.

This is a short update. I'll try to write again later today.

Saturday, February 21, 2009

Update February 21st 2009

I'd prefer not to write this, but I have to get this onto paper, so to speak, or into the ether, and out of my head.

For the last two days, I've been in a really weird space emotionally. Physically, I feel fine, almost normal. After being on this chemo protocol for almost two weeks, I can honestly say this is the best I've felt. Aside from some very minor side effects such as skin irritation and some joint pain, I don't feel much different then when I was off chemo.

I've been in a good place emotionally, too. Now that I'm back on a chemo regimen that I can apparently handle OK, I'm not dreading the treatments or the after effects. I know that I'm on a small dose of everything and that it will be bumped up gradually. But for right now, everything is OK. That's lifted a great weight off my back and really cleared my head up, for the most part.

Starting yesterday, though, I woke up in a weird, uncomfortable place. I'm not really sure why. I don't really feel like seeing any of my friends or going out, even though I've had offers to go out last night and tonight. I feel like I want to shut out the world, not answer my phone, and just go away.

I'm trying to fight that urge to disappear. Usually, when I feel this way, there's an identifiable reason, such as being scared of the upcoming chemo treatment. That's not really an issue for me right now, so I'm not sure why I am feeling like this. It's one of those things I go through now and again, and at least writing about it gets it out of my head.

Tuesday, February 17, 2009

Update February 17 2009

This is the second day I've been on the full chemo protocol, and all is good. I do have some side effects; particularly joint pain and skin irritation, which is normal. I am also extremely tired. The good news is that I have no stomach / bowel issues to speak of and in general I feel pretty good.

Monday, February 16, 2009

Update February 16 2009

As of this morning I am on the full chemotherapy protocol, including standostatin injections. So far, so good. No side effects as of yet. I'll keep you posted.

Wednesday, February 11, 2009

Octuplet Update February 11th 2009

First let me address how I'm feeling - I'm not feeling too bad, although I have a cold. I have had no side effects from the chemo as of now, but I haven't begun taking the full protocol yet. Hopefully things stay stable.

This morning on the news there was coverage on the single mother in Los Angeles who recently had octuplets after fertilization treatment. She already had six previous children, so she now has 14 (!). This boggles my mind. How anyone, particularly a doctor who treats women for fertilization, can allow someone to have 8 children at one time, particularly who has 6 other children? It's criminal. This woman should have had her head examined, not her tubes. Of course, we as taxpayers are going to end up supporting both the mother and the kids. This is so wrong, on so many levels. They should absolutely take her kids away from her, for their own protection. I don't care if the mother is considered fit. 14 children is too many to handle.

Tuesday, February 10, 2009

OK OK, Here's an update Update February 10th 2009

In response to the millions of requests I've had to update the blog...

I restarted chemotherapy yesterday. The entire protocol is different and the primary delivery source are pills and shots rather then infusion. I'm taking Xeloda (which is a form of 5FU in pill form) on a daily basis. On a bi-monthy basis (every two weeks) I have Avastin in chemo form. Once a month, I get Zometa, also in chemo form, for my bones. In addition I'll be taking Standostatin in shot form (once my pharmacy gets it in, that is), and Methotrexate in pill form (once a week, for my chrone's). So far, everything is good. I'm not on the full protocol yet, but I am hopeful that things will be different this time around.

So, lets repeat (there will be a test later):
Xeloda, Zometa, Avastin, Standostatin, Methotrexate. Everyone got that? Spelling counts, by the way.