Date
Breast Cancer Ribbon

Will I Glow in the Dark by Christmas?

posted by:
dottie

Will I Glow in the Dark by Christmas?

One week of radiation under my belt…well, not exactly under my belt, if you know what I mean. A few weeks ago I had an appointment with my radiation oncologist. I didn’t like him at first, but by the end of the visit, I thought he was all right. I probably didn’t like him because he brought up all bad memories. He started from the beginning…so you found a lump in your breast? And then he ran through everything…the number of lymph nodes involved…all the gory details that I haven’t thought about in a long time. Doctors like to tell you stories about other patients. Dr. Dean said that there’s almost no reason to take time off work while you’re undergoing radiation. He highlighted this with a story about two cocktail waitresses, both from the old Desert Inn. First, he treated a young gal in her twenties. She went through radiation without needing to take even a day off. Then an older gal [I think he said in her seventies...must have been well preserved] came to him for treatment. She wanted a note to get her off work. He said he couldn’t do it, that it would be age discrimination if she couldn’t work, but the young one could. Point well taken…radiation’s no big deal. This week I started my treatments on Monday. I go early in the morning before I go to work. I was a little nervous and apprehensive the first day. The two girls set me up, drew all over my chest; and Dr. Dean came in for a moment or two. The treatment itself only takes minutes. They said the first day is longer than most days because of the first-day prep. They’ve been right so far. I’ve gotten to work quickly every day. Thank goodness that I’m getting my treatments near home and school. Here’s how it works. I can’t wear my earrings or necklace; and I don’t want to wear my wig, pressing it down on the table, etc. There’s a tiny little dressing room, if you could call it that. There’s no mirror, so here’s what I do. I carry my jewelry and wig and leave them in the car. When I’m finished with the treatment and go to my car, right in the parking lot I change my hat up for the wig. I hope for the best as to how the back of it looks since I can’t tell. Once I get in traffic, I try to decide if I have enough time at each light to get an earring on and maybe put the back on it at the next light. Somehow, I’m almost together by the time I get to school. On the second day when I went into the dressing room, I noticed that the transparent shoe hangar on the wall had my last name on one of the pockets. I told the girls (technicians)…just what I always wanted…my own private, labeled holder for my medical gown. Also, on the second day, I asked about deodorant under that arm and/or lotions. They asked if they had given me the handout on skin care the day before, which they hadn’t. This answered some of my questions. During the day on Monday, I had what looked like marker all the way up on my neck. One or two people mentioned it to me, but I just said that I’d lost control of a marker…that seemed quite believable to teachers. On Tuesday, I mentioned the marker all over my chest to Tina, and she said alcohol would take it off. On the way home, I bought alcohol; but it was tough going to get the marker off. The next day I asked the technicians about that; and, once again, they had forgotten to give me something…little pads that take it off. They said it’s actually paint. Lying on the table for the first treatment, I was thinking…Oh, please let this be a good day for these girls (technicians). I remember thinking that when I used to go to the hairdresser…let this be a good day for her…you don’t want to be there on the day she’s had a fight with her significant other or her dog was run over. Can you imagine the difference between a bad hair cut, from which you can quickly recover, and the possibilities of radiating the wrong section of your body, for example, your heart or other vital organ? It puts a bad haircut into perspective. On Tuesday while lying on the table, one of the girls, out of the blue, mentioned that this was Mike, a whatever technician who would be checking on my skin each Tuesday. There’s no time for modesty while you’re completely exposed to whoever walks in. You might as well just get past it, because there’s little you can do about it. Most of the time I just keep my eyes closed, so I don’t know who’s in the room; and I don’t much care. I just want to get through the treatment and go on with my day. I mostly just try to say decades of the rosary while I’m lying there. Oh, it’s not all that comfortable. You lie on a completely flat table, but they do put something under your knees. There’s a sort of head-rest, and I have to turn my head to the right to avoid the rays shining on my left side. Both of my arms are above my head, and there are two grips to hold on to. My elbows are flat. The first day, I hardly thought I could keep my arms in that position much longer; but since then, it’s been faster and more tolerable. Thankfully, someone gives you an arm to grasp so you can pull yourself up when you’re done. I’d be there for the duration without help. Another patient comes in around the same time I do, and we talk when we can. It’s only for a minute or two because I get called in; and when I’m done, she’s on her way in. She told me she’s 73. I would never have believed it. She looks great for her age. She said her daughter got breast cancer first, and she was going back and forth to California to help her; and she got cancer herself. See? there are much worse scenarios than mine. Will I glow in the dark by Christmas? I hope so; I’m working hard on it. That’s a question I posed to Patti the other day. She was standing up on a chair in the testing cupboard that’s outside my office. I couldn’t see her so I didn’t know she was in a precarious position. I just called it out to her. She said she almost fell off the chair, but she got down and came and gave me a hug. By the way, about hugs…my hugger, Lety, left Harmon and went to work in a middle school. Now, I’m back to hug training again. Superna, who’s transferring from the library to the office, is definitely going to be a hugger. Also, there’s Patti and JoAnn and Sherrie and Tara. I’m noticing a couple of other possibilities so I’m still working on the hugging thing and adding members to the club. The holiday season seems to soften up even the most tense, so random hugs are easier to come by at this time of the year. I saw Donna again this week, and that’s always great for me because she’s such a solid survivor. She looks great, and she says eventually this all becomes memories. Won’t that be great when I have to read back through this blog, if I will ever care to, just to remember what cancer treatments were like? I haven’t yet told about my first Herceptin treatment so I’ll get to that next time. In the mean time, if you see a lady with reddish, blondish hair or no hair but a hat that says “Bad Hair Day” tearing through “Tarjay” or a mall; and she appears to radiate glow-in-the-dark markings and Xes on her chest, just say, “Happy Holidays” because that’s me!

4 Responses to “Will I Glow in the Dark by Christmas?”

  1. Krista says:

    Mom, I have to tell you something… you have always been glowing… I just think that everything you are going through shows how much you do.

    Oh how I hope that I am as strong as you someday.

  2. Kim Y says:

    Dottie
    it was so nice to talk with you today. I wish we could talk for hours. since you’re feeling better, we need to go for drinks after the Christmas (I’m sssooo tired of saying ‘holidays’!) break. we’ll get a bunch of us and come down your way so you can taste the vanilla rum properly. Hope you have a wonderful time with your family. we still miss you a bunch at goolsby. thanks for the hugs today…..

  3. Bonnie says:

    Dr. Dean was – is my radiation oncologist (I still see him every six months.) I had 37 treatments total. I never glowed – still don’t. Radiation is a snap after chemo. The inconvenience of undressing, getting zapped, then going about your work gets a little old, but it’s over quickly. The only side effects for me were a sunburn on the affected area, some pretty significantly dry skin, and a shrunken breast – about one full size smaller than my unaffected one. I am no longer MANDT certified as I was cautioned that radiation can cause bone weakness in the affected rib areas and I don’t intend to have a rib broken by a flying elbow any more. The worst of the treatments should be over, Dottie, and I would suggest NOT reading your blogs later. Reading them myself has brought back many, many memories – none good. Oh, they have certainly helped me empathize what you’re going through, but this experience is one that you will be glad to let fade into a comfortable recognition of a journey, not chosen, but endured. The tears will come. Mine never came at once, rather before every checkup with the doctors, before and for days after every mammogram, before and after family gatherings, and now, thinking of my 14 year old dog who was diagnosed with lung cancer 6 months ago, and who is now only days away from having to be “put down”. I’m glad I wasn’t put down, but I’m really getting tired of the “c” word showing up so often. A word that was at one time so foreign to me. Oh, for the chance of naivity (sp) again! Marge Conner was my cancer coach and her comment was always, “Stay positive! Cancer hates positivity”. Easier said than done, but I think she’s right. This is a little long – reading your blog today caught me in a bit of a mood – but I’m proud of you for your spirit, and your candidness in your blogs.

  4. Dr. Dottie says:

    Bonnie,
    It’s always inspiring to hear from you. I feel that you are right about not looking back later at this experience. I’m sure it will be something to leave in the past…once it’s finally past. I’m in for 25 radiation treatments; and, as of today, the score is 15-down, 10-to go. So far it’s worked out well to have two of the weeks fall over the holiday season. It hasn’t been great getting up early to go for 7:30, but other than that the best part is mentally ticking each one off as you complete it. You’re right about the “c” word showing up everywhere now. It seems as though there’s hardly a family left untouched by it. I know sometimes my blog entries may give the impression that I’m not staying positive. I think that the writing of the blog allows me to express some of my innermost painful thoughts that I do not verbalize to anyone. On the whole though, I am really positive and believe attitude helps! I’m sure it will be scary when I go for that first mammogram and for everyone thereafter. Right now, I’m just glad that 2007 has come to an end. It seems as though the official, final ending of this atrocious year gives me additional hope and positive feelings with the beginning of a whole new year. Thank you for your response, and please continue to stay in touch.
    Dottie