Date
Breast Cancer Ribbon

Archive for July, 2007

My Daughter, Myself…

posted by:

My Daughter, Myself…

There’s a quote I think from the Twilight Zone movie (or maybe the series) along the lines of…What’s the scariest thing that’s ever happened to you? And then the movie or the episode tries to outdo that scariest thing in your mind by scaring you to death. I’ve been through a lot of scary things in the last few months, but none prepared me for the scare with one of my daughters… You are traveling through another dimension, a dimension not only of sight and sound …a dimension of mind…But first, about my third chemo therapy treatment…How much scarier can they get? I had it last Tuesday. I tried to explain to the doctor how I felt following the previous treatment. Doctors need actual descriptive words and phrases beyond I felt sick all over…I was sick in my head, sick in my stomach, nothing tasted right…So, the doctor decided that since the only thing we’d done differently between the first and the second treatments was the Neulasta shot following the second treatment that we would not do that again. Maybe the side effects of that enhanced the red poison side effects to do me in. He did say that I could come for hydration treatments the next two days and then the third day if I wanted to. So, everything got scheduled, and I went for the chemo treatment. Oh, who accompanied me this time?…My son, John. He was an excellent escort. He was just the right amount of low humor, very few questions, and not talking too much, but just the right amount. When he found out how easy it was, he offered to cover me for all the rest of the treatments. He was very patient afterward, turning in my prescriptions, picking up lunch, and going back to pick up the prescriptions. So, the next day I went to work; and then Joe went with me for the hydration treatment. I started to feel a little of that indescribable sick feeling, but we went and had dinner following the treatment. The next day, I went to work, felt a little more queasy, and Joe and I went for the hydration treatment. I slept through the treatment, and then I slept around the clock after we got home. The next day, it didn’t feel right to go to work…too queasy, too tired. That day I asked Joe to drive me to the Institute; I was really not feeling well. I slept around the clock again. On Saturday, the fourth day following the treatment, I slept some more. Sunday, with effort I made it to church because Jay and Shelly and the kids and Kathi and Krista were all going to be there. I barely made it through the hour. I had to have a chocolate milkshake on the way home though, and that helped. Sunday, I slept some more. One thing I hope to remember to tell the doctor next time is that throughout all of those days, I found it difficult to talk…not to think of the words or to say the words, but…to find the energy to do so. It just required too much of me to answer a question, talk on the phone, or have a conversation at all. For those of you who know me…you know that’s serious. Dottie, unable to express an opinion, give advise, or tell a story…that’s completely out of line…I hope my doctor will have some really great ideas for helping me through my next and final red poison treatment, because, honestly, this cure could kill ya….Back to the beginning of this post…About the scariest thing and my daughter, Susan. She is not only my daughter, but my best friend. Even before the cancer, we talked almost daily on the phone. We were working the same hours and on the road at the same time in the morning and after work, so we would catch up. Since the cancer, there’s barely been a day that we haven’t talked. She has been the biggest nudge about everything. She insisted I give up Sweet ‘N Low, even coming over and throwing it in the trash. She said I can’t use Cover Girl makeup any more or regular deodorant that doesn’t have a breast cancer symbol on it, or any of those glorious lotions from Bath and Body Works. I keep telling her that I already got cancer, so why can’t I continue to enjoy all those things that make me happy and smelling good. Because she’s had health issues in the past and must continue to have timely check-ups and blood work, and I think also because she worked for many years in doctors’ offices, and probably because of all the nudging, she scheduled a mammogram for herself. Here comes the scariest thing that’s ever happened part…she got a call to come back and have more pictures taken of her left breast (Susan, pardon the personal information here). Can any mother think of anything scarier than that? That was unspeakable! It couldn’t be happening! I knew by the time she was scheduled to go back for further pictures, I’d be in the throes of chemo side effects and could not even offer to go with her. What do you say to God and all the angels when you get a scare like this? Are there any other big guns left to pull out? Am I not taking the cancer hit so maybe none of them will have to? Would there be anything fair or even sane about Susan going through this, too? We don’t have the final results yet from her doctor, but from the site (although I’m sure they’re not supposed to say anything) they reported that it looked like some calcification, and her doctor would probably tell her to get checks every six months. What’s the scariest thing that’s ever happened to you?     


Mouth Sores…

posted by:

Mouth Sores…

O.K. I got ‘em. They’ve been coming on for a few days. After the first chemo treatment, I had one; and it went away. This time I have several. There are a few on the inside of my lower lip and some on my tongue. I think the ones on my tongue bother me most and hurt the most. They are like canker sores. So, if you’ve ever had one of those, you know what this feels like. I got up in the middle of the night (they were hurting) and read about them in my cancer books. There wasn’t much of anything helpful there, except to explain that they are a side effect. (Yep, got that part). Cold feels better than hot, like I need another reason to eat ice cream. I’m not complaining about the mouth sores. I’m sure I could have much worse side effects; and even these could be worse than they are. I’m really only mentioning them here to continue chronicling my experiences, at this point with chemo treatment in particular. So, about the mouth sores…for the first chemo treatment, the nurse had me chew so much ice, I could barely stand it. For the second one, the nurse grabbed what was left of my Diet Pepsi and dumped in into the cup of ice, saying that no one says it can’t be flavored ice. I remember talking about the difference in treatments and noting that time would tell if more or less ice was the key. The cancer books said that there is no agreement among doctors about whether the ice treatment is effective or not. I guess for my two cents, it seems like more ice is better than less ice in my individual case. I think the doctor sent in approval for me to get hydrated through an IV after the next chemo treatment. I hope that will help me keep from getting as sick as I did last time. I completed my first week on my new job. Laura and Anthony (her little boy) came to visit on Friday. Laura will be coming to work at Harmon, as well. What a reunion this new job has turned out to be. I met Robert (principal) and Laura the first year they began teaching. We’ve all been friends ever since, and being reunited in the work place after five years just feels right. Today, a bunch of us made it to church together; it was great…Joe, Jay, John, Kathi, Krista, and me. I haven’t seen much of John lately since he started his new job. I could tell he’s missed me though. I don’t always see a lot of Jay either because he works a lot. Periodically though, he brings home gifts from women (from his work place) who have had cancer. When I had the mastectomy, a lady sent a Susan G. Komen bag with goodies in it. I still use the soft pink pillow and the pink quilt. Another lady sent a pink journal for me to write in, and the other day I got a pink bag with all kinds of little goodies and sayings to go with them. When it’s appropriate, I will pass things on to others as well. 

 

Strong Women

posted by:

Strong Women…

I’ve been informally gathering information on strong women throughout my life. Maybe it was to provide me with a treasure trove of stories and characteristics upon which to draw when I really needed it; that seems to be now…I was born into the world with two strong women in my life. My grandmother, born in 1896 was the oldest female in her family. I can’t remember how many children there were altogether, but I do recall at least six others. When she was a teenager, her mother died; and she became mother to all those siblings. I can’t even imagine how tough things were then, but she made it through. She brought up all those children and then continued to help them, when and if they needed it and if she could, throughout their lives. My grandmother’s maiden name was Faircloth, and she was very proud of that fact. My grandmother divorced her first husband, something almost unheard of back in those days. I think she must have been very strong-willed to do that, to bring up two children on her own. Because of my grandmother’s divorce I never knew my biological grandfather or any of his family, with one exception. He remarried and had a son, and my mother and his family visited often. My mother had a special affection for her half-brother. My grandmother worked hard all of her life. She actually worked at the Teachers’ College. I don’t know what she did there, but I wouldn’t be surprised if she cleaned dorm rooms. My grandmother did provide me with the only grandfather I ever knew, her second husband; and he was dearly loved Grandpa Jack to me. Every morning, during the years that my mother and I lived with my grandmother, when I came downstairs, my grandmother greeted me with, “Good Morning, Mary Sunshine!” I didn’t know enough then to understand that life couldn’t get much better than that. My mother was the strong woman who brought me into the world. She may not have started out that way, born and brought up in a small town with a working, divorced mother; but she grew into it. Divorce seemed to become a way of life with the women in my life, because my mother divorced my father when I was three. I don’t think she had much choice, if she wanted to hold her head up in town and continue on with her life and raise her small child. When my mother and father met at 18, neither of them drank alcohol. Life was simple then. My parents got together with friends, playing cards and going to movies; no one in their crowd drank. Not too long after I was born, much to my mother’s surprise, my father came home drunk one night. He was forever changed by alcohol which became part of his life, as far as I know, until he died. Alcohol lead to philandering, and that led to my parents’ divorce. My mother worked hard all of her life. She was a telephone operator, and she took that very seriously. Back in those days, operators actually sat at a switchboard and “plugged in” calls; they made the connections from one party to another, which included all emergency calls as well. No matter what the weather was, snow six feet deep, my mother would find a way to get to work, because she felt her job was important.

After Kathi was born, we moved to upstate New York to a community where everyone worked for IBM. The family who lived across the street from us had several children and a beautiful woman who was the mom. I don’t know if strong is the way to describe her, but I’m putting her in that category anyway. With all those children and what it took in the early 1960s to get through the day with household chores, my neighbor always looked like June Cleaver; the kids all looked like Wally; and the house was spotless. I think she had to be strong to do all of that, look that good, and stay with the husband she had (enough said).

Years later, I met another woman whose qualities are in my treasure box. She, too had a large family, and I’m not sure, but perhaps an abusive husband. She didn’t talk about it. In those days, many women, including me, did not go on to college. I’m sure everyone’s reasons were different (money, family background, no expectation to do so, young love, whatever). Many women then married young, had large families, and went on with their lives in whatever directions they took. I met this particular woman through a volunteer organization. She started out as a volunteer and eventually went to work for the organization. Somehow, with all those children and the husband, she managed to get through college and become a teacher. That took a lot. The qualities of determination, perseverance, and goal-oriented come to mind. I know she later went on to become a school counselor and recently retired.

The next strong woman I met was when I went to work on the graveyard shift as a pit clerk at Caesar’s Palace. Oh, the other women there were “strong” too, but they weren’t fit to shine the shoes of this lady. I guess maybe way back in this writing I should have qualified “strong.” The strong women I’m referring to combined strength with class, respect, and goodness. Speaking in generalities, for the most part (not ALL), the pit clerks swore like truck drivers, exhibited little or no respect for anyone, and were the lowest class of women I had ever met. At least two of them were sending their 12-year old sons to live with fathers they’d never really known because they were getting too much for their mothers to handle. Anyway, Judy was a light in the darkness of that particular group of women. She, too, had married young; and she had five sons. One of her sons, in his early twenties, had been in a horrendous car accident which left him with many injuries, including being legally blind. I didn’t know her when the accident happened but met her shortly afterward. She never missed a beat. No matter what was going on in her life with those boys, she came to work. She did her job (better than the others); she put her family/personal problems aside while she was at work; and she held her head high. We worked in two other casinos together in the pit clerk business. When she had a heart attack, she worked right through it (Who does that?) Then she went home and ended up in the hospital with quadruple bypass surgery. I learned a lot from her. As far as I know, she’s still alive and kicking (although the love of her life passed on a few years ago) and probably taking care of her invalid son, now in his forties.

Over the years I’ve met a lot of strong women in the world of education. But sometimes their strength is not combined with those other qualities of class, respect, and goodness. In the world of higher education, the most important person in my life is Maria. She saw me through a difficult time in my doctoral program and provided me with the support and will to persevere. She also brought me in as co-author of a book for teachers. Maria is one of the smartest people I’ve ever known. She’s always on the cutting edge of what’s new and next in literacy. She is steadfast in her beliefs; she stands behind them, and she stands up for them.

You might guess where I’m going next with strong women…Those four daughters of mine…My oldest daughter Kathi…I suppose being first born of a large family could account for some of it, but she went way beyond those qualities. Kathi put herself through college and following graduation, at the age of 23, packed up her car and drove across country for a hotel job in Indianapolis. Did I mention guts anywhere in my description of strong women? Well, she’s gone on to have a very successful career in the hotel industry, serving as Vice President with at least two major companies…Susan also put herself through college and then packed her car and moved to Arizona (A serendipitous move since that’s where she met Kevin). Susan has had health issues, the worst of which she went through while living away from the support of her family. Susan went on to get a masters’ degree. She has worked her employment around her son, Jason, so she could always be there for him, getting him to all kinds of lessons, sports teams, and school functions…Teresa is a civil engineer. She was just recently charged with the responsibility of opening and supervising a bay area office for her firm. Teresa is always involved in many things beyond her workday, from the Society of Women Engineers to Toastmasters to training for a triathlon…Krista grew up with the title of “princess” which she most likely took delight in. She’s doing great in her career in communications, and I’m sure there’s no telling how far she will go one day. But look what happened to the princess when her mother got cancer? She’s been the strength her mother didn’t have to face up to so many new and scary experiences. Like her sisters, she is a strong woman who combines that quality with class, respect, and goodness. So, thanks to Mildred, Lavinia, two Judys, Lu, and Maria and those four women I gave birth to for providing me with examples to fall back on when I wonder how I’m going to get through the next step in this unplanned part of my life.


Recovering from the Second Chemo Treatment…

posted by:

Recovering from the Second Chemo Treatment…

It seems to be the general consensus by oncology nurses that one thing that probably caused a problem for me with the last chemo treatment was that I did not push liquids. As I wrote in my guestbook response to Danette, even driving toward the Institute makes me feel physically ill now. Just the thoughts of what goes on in that place can put your stomach and head in a tizzy. Yesterday when I went for the weekly post-chemo blood draw, I had a different nurse whom I’ve never seen before. She was very nice, very helpful. She didn’t count to three before inserting the needle into the port, but she did ask, “Are you ready?” She talked about the need to push liquids following the treatment. She said that it’s hard for everyone, with how you feel and the change in your taste. She suggested trying anything acidic next time…like lemons or limes…adding them to water. She said that works for some people. She said she’s even heard of people adding vinegar…so, basically, whatever works and helps you to down a ton of liquid, which I imagine is to dissipate the red devil poison. Also, you can go to the Institute the next day or so and have an IV of liquids. I guess next time I’ll see what the doctor has to say about the horrible experience I had last time and what his recommendations are. Probably what didn’t help me with that treatment either was that I was not working that week and felt no responsibility to leave the house, not to mention the added trauma of my first few days with NO hair, as well. Now, I am back at work; and I’m in my new position as AP at Harmon. So far, so good. Of course, Connie is going to be about the best medicine there is…she makes me laugh out loud; and I know that’s what I need right now. Getting up at four-something in the morning is not the easiest thing to do, cancer, chemo, or not. It will be good when these insane hours are over, and the district can run the air conditioners during normal work-day hours. Susan came by today to see my set-up at my new school. She said I looked great. I said I look stupid. She looked at the back of my hair (wig) and found there was a small strip sticking out through the back. So, now, Connie really does have a wig-checking job every morning to make sure there are no stray parts of the wig poking themselves out through the (fake) hair. Susan and Jason will be gone for a few days now to Iowa (Kevin’s already there) so Krista will have to double or triple her check-in phone calls to make up for all the ones I’ll be missing from Susan. Those girls check on me periodically throughout the day. What would I do without them?

When I feel sad about having thrust them into the roles they’re playing now…worrying about and caring for their mom (and all that goes with it…the procedures, the doctors’ visits, the chemo treatments, the buzzed hair, and the crying), Little ‘Ole Me reminds me to get over it… that I brought them up to be who they are; and they’re doing what they need to do. Hmmm…look who’s helping who now…I take all pep talks to heart… 

The Worst Chemo Ever…

posted by:

The Worst Chemo Ever…

 

Words cannot describe how horrible the aftermath of my second chemo treatment was…Seriously, I have no words to describe it…I had it on Tuesday. By Friday night I felt I had two choices in life…one was death (therefore, no more life like this), and the other was to be in a hospital…Why can’t I describe it? Probably, you have to be a member of the club to relate to it, because it’s not like anything else in this world that I can remember…and I’ve been around for a lot of years…Did I feel like throwing up? Yes, but I kept telling myself that I wouldn’t because I was taking anti-nausea medication. Did I want to eat? Yes, but no. Did I want to sleep? Yes, but it was short-lived and fitful at best. Did my stomach bother me? Yes, beyond any stomach flu…Did my head bother me? Yes, beyond any headache…Could I read? No. Could I watch T.V.? Yes, but I’d fall asleep before the end of any program…Could I go anywhere? No, no, no. Could I talk to anyone? Barely, it was a challenge even to answer the phone, much less, communicate beyond, “Hello.” Maybe my whole outlook on this treatment was different from the first one; and maybe that made the difference…I’ll never know. I was emotionally upset on the way to the chemo treatment…I didn’t want to do it. The first one was still fresh in my mind, and I didn’t want to feel like that again. I met Krista in the parking lot and started crying. I don’t know how my youngest child (by thirteen minutes) puts up with/has the strength to deal with her emotional, sick, basket-case mother…Somehow she does it though. Remember she’s the one who approves of crying so she just lets me and says it’s understandable. After a minute or two, we went in. We found out there would be an hour wait after the “labs” because they check your bloodwork before they go ahead with the treatment. Right away, I was not happy…as I saw that I would be getting the nurse who was not my favorite…the one who told me about the sore port cite that, “When you’re going through something like this, you have to get used to being poked and prodded.” Yeah, like I decided to have cancer and go through all these procedures and treatments; and since I made that decision, I should know that I have to be poked and prodded. Let’s see, which day did I decide that? Was it the day I found the lump? The day I heard the results of the biopsy? The day the lumpectomy wasn’t enough? The day the mastectomy wasn’t enough? The day I was told I needed eight chemo treatments, followed by radiation? I don’t remember raising my hand any of those days…you know, like all those little kids in classrooms…”Teacher, Teacher! I want to be line leader this week! See my hand? Choose me!” O.K., “Hey, Hey, Doctor! Doctor! I want to have cancer! See my hand? Choose me for the diagnosis! I want the whole nine yards! And I won’t wince or say a thing when I’m poked and prodded because I understand right now that’s part of the whole thing when I sign up!” Back to the nurse…well, first an aside…I have a few pet peeves in life, who doesn’t? One of them is at the grocery store when the clerks are talking back and forth about who’s going on break, what time they came in, what time they get off, etc. I think that’s talk for the Break Room, not at the register when I want my groceries moved along. The same goes for chemo treaters…when I got the nurse I didn’t want, someone asked her if she had brought in the treats for the day. She was unaware of them and asked where they were. Someone replied where they had been left. She responded no, but did that person want to share an omelet with her…How about me? I’m emotionally upset here, can we get on with this? She drew the blood, and Krista and I returned to the waiting room. Next, we saw the doctor. He was very encouraging. He answered my list of questions. One was whether the chemo was cumulative? Did this add on to the previous one, increasing the impact of the drug? He said that I would not feel any worse than I had last time. I felt that I could live with that… no worse, no worse, no worse…He said I would come back on Thursday for a shot to help prevent the lowering of white blood cells. Off we went to the chemo treatment room again, and the nurse I didn’t want. Now, I don’t want to say that she was confused, but I will anyway…she was CONFUSED. At one point she mentioned that I was having a two-phase treatment and that I would be back on Friday for the second part. I said no that’s not me, I have it all in one day, could she check? In the meantime another nurse had to come by once or twice to check my beeping machine. When MY nurse finally came back, I asked her about what we were doing, had she checked, and she said (somewhat flustered) that she would have to check with my doctor. Krista said we needed to ask her when she came back exactly which drugs she was giving to me. When MY nurse returned again, she mentioned some drugs called FCC or  FTT or something like that…I knew enough to know that was wrong. She went and checked. She came back with the red poison and the other bag in a large plastic bag…all the drugs had my name on a label on them. She explained that she had two patients, but now she had it right. I don’t think any of this helped my mind set, worrying about whether or not I was going to receive the right poison. Finally, she started. After that, I thought she was all right. I asked her if she was going to put on the blue smock to administer the red stuff. She said she’d been doing this for 11 years…she didn’t think any police were going to come in to see if she had the smock on, and she wasn’t going to get any on her or on me. I liked her better after that. Following the treatment, I went home; and Krista went back to work. The next day was another emotional day, as Susan and Krista came over to help me part with my hair. About the hair…you can think you’re ready to lose your hair…you can say when it starts coming out, you’re going to get it buzzed, you can have a cute wig ready, you can have all kinds of hats and scarves ready….it doesn’t make you ready to lose your hair. My hair had gradually been coming out since the Tuesday before. My goal had been to make it through my two university classes without losing my hair, and then I added the goal to make it through Teresa’s and Elliott’s visit for the 4th. The last couple of days, I had been kidding that the hair that anyone could see on my head was being held on by hairspray. So, the night of the chemo treatment and the next morning, I faced up to the hair loss and just kind of took it off. Most of the hair was loose anyway and just needed to be taken off. So, the next morning Susan and Krista came over; and Susan used the buzzer to take off what was left. What is there to say about having your hair buzzed off? Nothing, it’s also beyond words. I think Krista explained pretty well a couple of days later…Before the hair loss, I could still walk around like a normal person and pretend I didn’t have cancer. I could hide results of all the surgeries. I could hide that I was in chemo; but the fact that you have no hair is about as glaring as it gets. Can I hide it in public? Yes, I suppose I can hide it like the other things, but a wig is a wig, a hat or scarf with no hair under it is a hat or a scarf with no hair under it. Where does Joe fit in all of this? Well, I don’t have him go to chemo with me…He’s a smoker; there’s no smoking on the Institute’s campus. One time when he went with me for something else, he mistakenly parked in a valet spot. The valet guy came over and asked him to move out of the spot…then he sent Security over to tell Joe he could not even smoke in his car on campus…C-A-N-C-E-R…no smoking, makes sense…After the (at least) three horrible nights following the chemo treatment…Joe trying to sit up on the couch with me all night…I couldn’t go to bed…I don’t know why…On Saturday morning he got up and said that although I have the ca
ncer he feels like he’s dying. I’m sure he does. He sat around with someone too sick to talk (for me, can you imagine how sick that must have been?) for three days. Saturday, I suggested he go out for a few hours. He did. Susan, Jason, Krista, and Zoe (Krista’s doggie) came over to keep me company. I don’t know what Jason thought when he saw his bald-headed grandmother, but when I asked him, he said, “It’s cool.”  My thoughts over the last few days have been depressing, I know. I’ve thought about what if I just never did anything about the lump in my breast. What would have happened? No tests, no surgeries, no treatments. Would the cancer have been getting into some vital organ and hastening my death? Would I be sicker from the cancer than I am from the treatment? I honestly don’t feel that I’m going through all this for myself. I’ve said many times what a great life I’ve had, that I already had about three lives in one…I had those marvelous six children; I went through the education phase, earning a doctorate, co-authoring a book; went on to go into school administration…how could I ask for more? Do I need another life? I’m not doing this for me; I really don’t think I am. I’m doing this because some people need me to be around longer. I think Kathy, Susan, and Jay have had their mother for a very long time (they are all in their forties); I was a child when they were born. John’s had his mom for a long time as well; but Teresa and Krista at 27 need their mom a few more years…not to mention the grandchildren, those already here, and those not born yet (which people really should start making plans for). I hope this will all be worth it, that I will look back and say I survived cancer. The last few days, I don’t think there were any thoughts, or dreams, or plans that could have made how I felt worthwhile. I feel life coming back into my body today. I hope it lasts for the couple of weeks I have before I endure another chemo treatment. I hope I’ll see Teresa and Krista each exchange wedding vows someday (and John, too) and give birth to their first children. I’d love see a grandchild graduate from high school. This past week, though, I wasn’t worth the space I was taking up on this earth. I couldn’t have done a thing to help another person, to bring any joy to anyone, to solve any problem, to think any good thoughts. Yesterday was better, today’s a little better than that…maybe tomorrow will be a good day…CANCER SUCKS!

 

The Best Class Ever…

posted by:

The Best Class Ever…

 

What a delightful time I had with the best class ever that it has been my pleasure to facilitate at the university. I don’t know if I could tell from the very first night, but it didn’t take long to know that this was a special combination of people in this class. It was a 7:00 graduate class that would meet for five weeks, three consecutive nights a week. For my part, I spent the first three nights modeling what I wanted them to do the rest of the semester. Our goal was that on each night of class a group would present a research-based critical literacy strategy and an expert literacy method. There would be papers to turn in along with the strategies, and each group was to engage the class in adult-level activities, which could be modified for any age group of students. They also had readings for most classes and shared their ideas in what I call Points to Ponder. They were required to informally present a pop media share…these turned into some of our more lively discussions. They were also asked to join a professional organization, for example, International Reading Association or National Council of Teachers of English. Their final share was a professional letter to be written on their chosen topic to a chosen entity to persuade or dissuade the use or modification of a program, procedure, etc. being implemented in the educational community. Each and every presentation turned out to be useful and could be modified by teachers for students in kindergarten through middle school. Some of the students appeared to already be friends, while some friendships seemed to develop over the course. At least three of the students I have had in previous classes, and that usually provides a special bond to see them come back as experienced teachers. One of the students I actually supervised as an AP in his school for half a year. He was one of two males in the class, and I do believe they added a particular dimension to the class that would not have been there without their presence. Some people had the luck of the draw of partners for presentations; it depended on how their karma was working when they chose their seats the first night of class. Regardless, everyone seemed to work it out and make it work. My friend Lisa substituted for me on the fourth night of class, because that was the day I had the port placement; and I was advised to take it easy for the rest of the day. By that day of class, Lisa could also feel the specialness of this group. Following Lisa’s class, I did go ahead and tell them about the cancer. I really don’t want to base my relationships with individuals or groups on my cancer; but I felt that I owed them an explanation about why I wasn’t in class. I merely explained that I had kept asking doctors about whether or not I should keep my summer plans for working in the daytime and teaching at night, and all said to just keep my life the way it was. However, they had not told me about the ancillary procedures that would take up days, for example, the port placement. I added that I hoped there would be no reason to miss any more classes, and, in fact, there wasn’t. I asked them if they were aware of the hair sensitivity training Lisa was providing with her shades of red/purple. Lisa made that up saying that her colorful hair would be good preparation for when they would see me with no hair. Actually, I’m happy to report that I was able to maintain my hair throughout the course and didn’t have to turn to wigs or hats. I survived my first chemo treatment while I was teaching that class. You might remember from my chemo post that Susan came with me the second night after the chemo just to provide support and make sure that I was all right. I had good conversations with Tracie, who told me her mother was an oncology nurse. She told me that her mother said she couldn’t believe I came to class following my first chemo treatment. I took that as kudos for me. Once the students started presenting the strategies, I began sitting in the back of the classroom. I sat next to Andrew. I found him to be so articulate and with a super sense of humor. He actually got me in trouble during at least one of the presentations. That was a first for me, but it demonstrates the nature of this particular group. I wouldn’t say that the students were out of control; but, I’d say that it became their class very quickly. Once in awhile there was a curse word uttered, and on more than one occasion, when in small creative groupings, there were sexual innuendos in their reports back to the whole group. I don’t believe there was anything offensive, and certainly there was nothing indicating discrimination. On the last night of class, they reported the topics of their professional letters. I delighted in reading their letters later. In general, their letters were about NCLB and the pitfalls that we all know accompany it by now. I was amazed at the number of letters that were derogatory to Accelerated Reader. For several semesters I’ve noted positive reports from students on how great this program is to get children reading. In this class, the students were reporting the negative side of the computer generated tests that students take when they finish a book and the lack of meaningful literature discussions, etc. that are apparent when a child interacts with a computer instead of other children or a teacher. Probably, the funniest letter was Wendy’s about the number of times she has had to be fingerprinted for CCSD. She said she was actually going to mail her letter, which, of course, was not a requirement for the class. On the last night of class as I walked up to the front of the room for an announcement to get things started, I noticed a large bouquet of flowers on the table. I thought it was a prop for the next presentation. When I asked what it was, Brittney came up and explained that the flowers were for me. She said something along the lines of: “Dr. Dottie, we got these flowers for you because we love you and because we’ve been naughty.” I received hugs and well wishes from many of the students. Some were going out to celebrate the end of class. Andrew had offered to take everyone’s email and make a contact list, in case they wanted to continue sharing some of their ideas and experiences. I’ve been teaching at the university level for many years and have had more special students than I can even recall…but this particular class was beyond special, not something that I seem to be able to put into words appropriately, but I think they would get it if they were reading this. I hope it wasn’t the cancer announcement, and I don’t believe it was; but, of course, I’ll never know for sure…Anyway, my enduring thanks to the best class ever for making my summer evenings pure delight, which I’m sure was very instrumental in getting me through my first round of chemo treatment…Best of everything to each and every student in that class!