Started back to work
Hello, friends!
After 13 months of treatment I finally went back into the classroom this week. I moved from grade 7 to 5. I feel the younger students will be more forgiving when my chemobrain can't finish the sentence, " Boys and girls, don't forget to check the ------". And someone will yell out "CLOCK!" Yeah for you, here's your sticker; you got the word of the day!
Post it notes are my favorite tool - I started carrying them in my pocket with a pen. Then I hang them where I need to remember things. I think I can create a new job in my classroom - collect all of the post it papers at the end of the day!
Folks have been very kind - only a few asked how I feel. My response is always the same, " I am coming along, taking each day as I am gifted."
My radiation onco was a little concerned about the fatigue, and I must admit that I am ready to crash when I get home. The only problem I have so far is some dehydration. On day 2 I woke up at 5 am with severe head pain and nausea. I thought I would not make it to work, but it was only the second day of school; no way I could call out. After an hour of vomiting I finally felt stable enough to shower and eat toast. So off I went --- no coffee, no plan if I could not make it through the day, no idea if I made the right decision to return. After going over my Day 1 of school, I realized that I had not had even 3 glasses of water all day. It was also above 90 degrees for several days. Although I am blessed to have air conditioning in my room, I was still in and out in the heat.
I have been on Armidex for about a month, and I had already switched from taking it at night to taking it in the morning. I am not sure if that caused my "episode" or if it was the fatigue/dehydration. I guess the best I can do is monitor and chart symptoms. I can not meet to get my Survivor Plan until October 11th. Now that I am back to work, my schedule can not be as flexible. While I have plenty of PTO, getting a plan together in the beginning of a school year is no easy task.
Just thought I would share that there is life after treatment! Although I won't be at peace until I get that NED, I am grateful to be back with the children. They can make a tiring day bearable with just a smile.
Comments
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Congratulations!
Congratulations on going back to work! and for the end of treatment! I have just a mere 4 more radiation "boost" treatments to go after a long 11 month journey of hell (surgery, chemo, more surgery & radiation) and can't wait for it to end and hopefully start feeling a little better. Please make sure you are drinking more than you described above, I'm sure you are used to drinking ALOT more than that during the past 13 months of your own journey!
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way to go
way to go
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And then reality set in . . . .
Well, friends, I have been back in the classroom for 3 weeks now. I think I have adjusted my dehydration issue, but my new issue is that my eyes hurt - all day, every day. I'm not sure whether to go to my opthalmologist or wait until I see the onco for my survivorship plan (Oct. 11).
A bigger issue has been dealing with the expectations of others. While I "look great" as I keep being told, I feel most people think I can do everything I did before dx and treatment. I used to juggle nine things at a time - now I feel all the balls are in the air and I am waiting for one to zonk me in the head. How can I politely say that I can handle myself and the students in my room, but adults need to figure things out for themselves? I have been asked by others to solve their computer issues, set schedules, and assist with their lesson plans. I am wondering if I went back too soon. Fatigue and neuropathy still plague me (treatment ended in July), and being asked to meet after school hours until 4:30 is just too much. I spend my lunch in my room getting things done so I can crash when I get home.
Thanks for letting me vent . . . I'm not even sure my family gets my frustration.
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ah yes....the old "you look great...can you do this for me?" routine has reared its head. First, take a nice deep breath . Now exhale slowly. This is not your fault. People who have not gone through what you have just don't understand. You have to inform your coworkers that you cannot do the extras they are requesting. Tell them you can handle your job, your classroom, your students, and that's it. Tell them how you go home and "crash" at the end of the day. I was told if it takes a year to go through your treatment, it could take a year for you to be strong again. It is normal to want to go back to work and get back to the routine. But that routine has to be adjusted so you can continue healing. If your co workers have never had your cancer treatment they don't know the extreme exhaustion we deal with. You need to tell them now. They will be able to function without you assisting them for a while. If you don't tell them, they won't know.
I think the comment about looking great is a reflex statement for a lot of people. I had one woman tell me I was looking great on a day I had just left chemo and i'd had the "red devil" infusion. Guess i must have looked pretty spiffy all bald, sick to my stomache, blotchy with hives, teary eyes and all. I told my husband it's too bad she must be going blind.
Good luck!
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Thanks!Sasu said:ah yes....the old "you look great...can you do this for me?" routine has reared its head. First, take a nice deep breath . Now exhale slowly. This is not your fault. People who have not gone through what you have just don't understand. You have to inform your coworkers that you cannot do the extras they are requesting. Tell them you can handle your job, your classroom, your students, and that's it. Tell them how you go home and "crash" at the end of the day. I was told if it takes a year to go through your treatment, it could take a year for you to be strong again. It is normal to want to go back to work and get back to the routine. But that routine has to be adjusted so you can continue healing. If your co workers have never had your cancer treatment they don't know the extreme exhaustion we deal with. You need to tell them now. They will be able to function without you assisting them for a while. If you don't tell them, they won't know.
I think the comment about looking great is a reflex statement for a lot of people. I had one woman tell me I was looking great on a day I had just left chemo and i'd had the "red devil" infusion. Guess i must have looked pretty spiffy all bald, sick to my stomache, blotchy with hives, teary eyes and all. I told my husband it's too bad she must be going blind.
Good luck!
Thanks for the encouragement. I was really hoping I could just walk right back in and pick up where I left off. I do need to remind myself that I am still healing. Thanks for that reminder.
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Many dont get it and I hope they dont.
I understand what you mean. People don't get it and like I said, I hope they don't. I would not wish this on an enemy. I think you and Sasu are right. When people dont know what to say the dumbest words come out. They just need to say nothing or wish a cancer patient well and go on. People get tired of us being sick and it is their fear we will never become well or they are just selfish or dont get it. You have to just keep taking care of you because if you dont, you will fall on your face. Ignore them, you can be "selfish" and take care of yourself.
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