Returning to the Classroom After Mastectomy

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Magister105
Magister105 Member Posts: 73

I'm not sure this is the right forum, because although I am moving beyond my surgery, I am just starting chemo this week. Forgive me if I am misplaced! I was hoping for some advice about returning to my classroom tomorrow. I have had a bilateral mastectomy with TEs. I told my students I would be out for surgery following Christmas, but did not tell them I had cancer. I believe, however, that has gotten "out". I absolutely LOVE teaching and I love my kids. I teach high school, so I think my appearance will be a shock to them (I was a double D before and am a washboard now), I have lost weight, and I will be wearing a wig. I am thinking I should be brief, honest, but not too much information. I don't want to scare them, but I think I need to be honest. I don't want my classroom to be about ME. It's always been about them, and it's vital I keep it that way.

Any suggestions, ideas, comments are welcome!! And thank you.

Comments

  • kimt
    kimt Member Posts: 40
    edited February 2010

    Hi Magister!

    My situation is a little bit different because I teach at a university, so I don't have the same students from semester to semester, but when I started this semester, I opted not to wear my wig so I look nothing like my picture that's posted in various places on our web site!  I too don't want my class to be all about me, but on the other hand, I've always been pretty "real" with my students and used real life examples where appropriate to the topic, so I started off by telling them that I had been in treatment for bc over the last year, including chemo, which explained the hair, and I didn't anticipate it having any impact on the class but you never know, so I thought they should know. 

    I also had only had 2 fillings in my TEs, so I wore a bra with inserts.  But, like you, I was a D before and am taking this opportunity to go WAY smaller!  Anyway, you can get the inserts with stuffing so as you get more fills and get bigger, you just take more stuffing out.  this way, you are not always changing sizes!  I think if you're honest and brief, they'll be fine.

     I've also volunteered in my son's kindergarten class and started out wearng a wig and then switched to a scarf when it got to hot and now just a hat.  They asked what happened to my hair and I told them.  they're curious and want to see my hair, and one told me I look like a boy, but then basically, they act normally. 

     the most important thing is to do whatever makes you most comfortable.  that's why I opted to start without the wig because I thought it would bother me more than my GI Jane look.  But i might have done it differently if I were going through chemo (I did mine in summer when i was already off), not sure.  I think if you take it all in stride, they will too.

    they're lucky to have a teacher who want sto make it "all about them" - too many don't!

  • Magister105
    Magister105 Member Posts: 73
    edited February 2010

    Kimt:

    You've made me feel so much better already! I like the way you handled your situation. I think a good classroom relationship is based on simple respect and honesty, so I want to have both of those for/with my students. Thank you so much!

  • ruthbru
    ruthbru Member Posts: 57,235
    edited February 2010

    I teach at the middle school level. I told my students very factually and calmly. They will handle it how they see you handling it. I would do chemo on Fridays, and felt good enough to be back in the classroom on Mondays, so didn't miss that much school. I did wear a wig the whole time, as I think MS kids like things to be 'normal', and me with no hair or a hat or something would have been distracting (plus I did NOT look cute with no hair Frown). Interestingly, I did chemo the spring of one year, so the new kids I had the next year assumed that the 'hair' on my head was mine, and were pretty shocked by the short curly hairstyle (my real hair) that I was suddenly sporting that December. One very 'hip' girl said, "WHAT did you do to your hair?" I rolled my eyes and said, "Don't even ask!" But I felt a real closeness with the kids I worked with the treatment spring, and I also felt like I could be a good example of how to deal with adversity and how to cope when things are tough. Plus, kids are pretty self centered; so if you don't focus on you, but on them, they tend not to dwell on your (or anybody else's) problems, and it was very good for me to keep teaching because I also HAD to focus on other things other than my own crappy situation. Best of luck, because you are thinking it all out, you will do fine! Ruth

  • iodine
    iodine Member Posts: 4,289
    edited February 2010

    Since I'm not a teacher, but a nurse who has been on the boards for a while and met and talked with many a great teacher, I admire your courage to return to the classroom (all of you!) during tretment.

    I remember one teacher in specific who had temp. tats that changed each week to meet her whims.  Another had a closet full of hats that even included Viking horns,  LOL, and she wore them to her moods. 

    I know you don't want it about you, and I understand that, but as a parent, I hope you will share with your students.  So much that we as humans need to learn is not in books, but is in our communication with other humans and their lives.  Thank you for being a teacher and bringing such great examples for the next leaders of our country.

    As far as when to be in the "moving on" section?  Any time!  To me, it's a process, not a timeframe.  Hopefully, we all can begin moving on in some manner from the time we are diagnosed.  We will all be at different stages of treatment and moving on.

  • Maggie66
    Maggie66 Member Posts: 180
    edited February 2010

    Love your question and the advice! I teach 5th grade and was diagnosed right before school started. I've been in and out of the classroom for surgeries and have been very straightforward with parents and also with kids, yet with a little less detail. I think kids know when you're hiding something and that seems scarier than the truth. I also think humor has its place. For my recent reconstruction surgery, I told the kids I'd have "T-Rex" arms for a bit, as my PS had suggested I try to keep my arms at my sides for a while. Laughing seems to cut the tension for everyone. Something that saved me when I went back to school after my DMX was lying down for 15 minutes during morning recess. The librarian set up some pillows for me in the story corner and I listened to some meditation tapes. I never fell asleep, but just being quiet and off my feet helped a lot. Good luck! I'll be thinking of you! Maggie

  • ruthbru
    ruthbru Member Posts: 57,235
    edited February 2010

    Magister, thought about you all day and hope all went well......

  • Magister105
    Magister105 Member Posts: 73
    edited February 2010

    THANK YOU for all of your support and advice! I felt so much better after reading your responses. It was a great day. Physically tiring, but so healing to my spirit. My kids were so excited that I was back, and they told me they loved my new hair style! I was just frank with them and told them it wasn't my hair, and they were even more impressed. One of my girls came up to me and said, "Can I touch it?" Of course I said yes, and she did, and said "That is so cool!" So we were able to laugh about it. I told them very briefly what was happening and why I would be in and out occasionally over the next three months, that my prognosis was good, and that I'd need them to be a little patient with me if I wasn't always my usual chipper self. They were great. Immediately went into complaining about all the work I kept sending them to do in my absence. Pure teenagers. I knew that all would be well, and things could go back to normal! Today was a nice gift after 7 weeks of recovery. Thanks again!

  • hymil
    hymil Member Posts: 826
    edited February 2010

    Magister, You are an inspiration and the thread has really touched me, all the lovely replies :)

    I shouldn't really be in the moving-on zone yet, I only got out of hospital last week but it's so good to see people moving and doing okay further ahead on the road

    Your pupils are so fortunate to have you:  a fair minority of them - mainly but not uniquely the girls - may get this disease later in life, before then some of their moms and aunties will be affected, and the energy you are pouring out now to get through the day, showing them that it's do'able, is going to make such a huge difference and help them to cope with those hard days ahead. Being back at work so soon shows us its do'able too - thankyou!

  • ruthbru
    ruthbru Member Posts: 57,235
    edited February 2010
    So glad! Just getting it out there is the hardest day; it sounds like you handled it perfectly, the kids did well, and now they can revert to being goofy teenagers (in otherwords, back to normal Smile). If you want any 'chemo and the classroom' tips, let me know. Keep us 'posted'. Ruth
  • iodine
    iodine Member Posts: 4,289
    edited February 2010

    So glad it was a good day, Mags.  I just noticed that you are just down the road from me.  It just dawned on me that you have TEENS. OMG.   You have a great deal more courage than I !!

    Hymil, so glad to see you here!  It's always a good think to ck out what we can look forward to: getting thru this and Moving On.

  • suemed8749
    suemed8749 Member Posts: 1,151
    edited February 2010

    Hi Magistar! So nice to meet you - I'm also a high school teacher who had unilateral mast and chemo two years ago. I have some seniors this year who went through it with me two years ago, and we have a special bond.

    They were so great through it all - like your kids, they loved my wig and were amazingly supportive of me. My seniors made a Relay for Life team and I still have the poster of pictures they gave me afterwards. Since I had a unilateral, I wore big clothes with the surgical cami and a soft prosthesis for awhile, and I just know that one of the major things on their minds was "which one?????" although they were all polite enough not to ask Smile.

    Mine, too, used to turn it around to them - complained about the subs. Gotta love teenagers!

  • kimt
    kimt Member Posts: 40
    edited February 2010

    So glad it went well, Magister!  Hope you have a great week! 

  • robinlbe
    robinlbe Member Posts: 585
    edited February 2010

    Magister....You're in my January MX group....You've made the jump back to school before I have.

    But I teach elementary music K-5, and am on my feet all day long, lugging instruments, moving chairs, and carting stuff back and forth.....My BS told me eight weeks off...and I am so glad.

    I had been out a couple of different times before Christmas due to the other two surgeries, so I had already had to tell my students about my diagnosis, and I had prepared them for my absence after Christmas (my BMX was 1/6/10).   I won't be having chemo or rads, so that made it easier on them, but they were all very sensitive and caring.  I even rec'd handmade "get well" cards from one class of 5th graders a couple of weeks ago.

    I didn't dwell on the diagnosis, but I felt it was only fair that they knew....and I won't dwell on it when I return either.  But, being as they were "stuck" with a sub for so many weeks (their words, not mine), I felt they needed to know the why behind my absence.

    Magister, Cleo (Linda) from our Jan. MX group teaches middle school went back to work this week, too!!  Congrats to you, both!!   blessings...robin

  • zoegr
    zoegr Member Posts: 113
    edited February 2010

    Magister,

    I know exactly how you feel. I have the same concerns. Actually i'm a dance teacher and i haven't start my lessons yet after the surgery. I had unilateral mastectomy with implant-expander reconstruction. My left breast right now is half size of the left, but i found a way to make them look similar. I took an old bra, cut the left side and sew some fabric on the back side and stuffed it. No one could tell the difference. So i fixed the boob problem.

    My other problem is the hair (i will start chemo soon). I will definitely wear a wig, but i'm sure everyone will know that something is wrong. So right now i feel so insecure. I don't even know if i will be able to teach dance during chemo. Because i don't know how bad i will feel with all the side effects.

  • bennetts1
    bennetts1 Member Posts: 440
    edited February 2010

    Magister,  I too, teach high school.  I took chemo while teaching in 2008.  I did not wear a wig because I could not stand wearing wigs, but instead wore scarves.  My students always commented on my scarves and how they matched my outfits.  You will find that by continuing teaching, the students will help you get through your treatments.  In turn, you will be a true inspiration to your students!

  • lassie11
    lassie11 Member Posts: 1,500
    edited February 2010

    As a retired teacher and chemo graduate, I am in awe of anyone trying to teach while going through chemo. Getting through chemo was a full time job on its own for me, especially the first week after each chemo infusion. Mine were three weeks apart, six times.  Maybe being a bit older was part of it, but I had no where near the energy needed to do my teaching job. My concern for you is that you would be subject to all the yukky germs that students share. If you can cope with teaching through chemo, kudos to you. If you feel like you need more time off, be kind to yourself and take it.

  • ruthbru
    ruthbru Member Posts: 57,235
    edited February 2010

    I had 4 dose dense AC's two weeks apart. I had the neulasta shots so my white blood cells would kick in right away and I didn't really feel that I had to worry so much about getting infections etc.. I also washed my hands like crazy (bringing my own soap from home, as I could only stand the smell of coconut scented soaps; wierd). I felt all HYPER, so sitting around my house would have driven me crazy. I did skip a few after school meetings, or ducked out of them early. (I kept my principal in the loop with what was going on medically and he was wonderful). Zoegr, there are some great wigs out there; mine was so cute and natural that no one knew I was wearing one unless I told them. A friend I hadn't seen for awhile, but who knew I as going through chemo, said, "Well, at least you didn't lose your hair.' Ha! Maybe have some of your better/older dance students be your 'assistants' if you don't feel so hot; they would probably be very happy to have the opportunity to help out. Of course, if you are deathly ill, then you have to stay home, but I think the more normal of a schedule you can keep, the better off you'll be, mentally for sure and maybe even physically. Good Luck All!!!! Ruth

  • comingtoterms
    comingtoterms Member Posts: 421
    edited February 2010

    Hi Magister,

    I am a teacher at an Alternative High School.  Unfortunately, my students were in the room when the Radiologist decided to call my classroom phone and blurt out that I had BC - I pretty much lost it and my kids were worried sick about me.  Long story short, I was very open from that point on about what was going on with me medically. 

     I teach teen moms and allowed them to be part of my journey - I wouldn't  change that for the world.  I worked until the day before my March 2009 MS and was in and out for visits throughout chemo.  The rest of the population I work with is not the most hygiene conscious, and "my girls" are very needy, so I knew it was in my best interest to take the time away.  There was no way I could take care of myself and them at the same time. 

    There were lots of tears and a lovely "bon voyage" party when I left and I was overcome by the support and strength I received from so many of the students in my school for the remainder of the school year.  These are kids who are neglected and abused, and who still found it in themselves to be compassionate towards me.  I think it was a powerful life lesson.  I returned in September with no hair or eyebrows, but I was welcomed back with open arms.  It is amazing what young people are capable of when given the opportunity.   Best of luck to you!  Tammy

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