August 2013 Chemo Sisters

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  • SewStrong
    SewStrong Member Posts: 399
    edited August 2013

    Oh yeah, and I groomed the schnauzer and cut my husband's hair all by 6: 30 pm. We just got back from our hill climbing and my hair is dripping sweat. I have two more hours before I wanted to go to sleep, so I'll have to think up things to do. I could vacuup the staircases. No. I think I'll pass. Oh yeah, and I almost forgot, I wrote a volume for an encyclopedia for breast cancer today. God bless all of you. I'll give my first after chemo report when I get home if I don't have a massive headache or something. I promise this is my last post today.

  • Martie1228
    Martie1228 Member Posts: 73
    edited August 2013

    Sharon, Could you come visit me?!?! I don't do HALF of what you do when you're NOT on steroids!!! Praying that you'll rest tonight and your first treatment will be better than you anticipated! The Ativan really does help. ;)

  • SewStrong
    SewStrong Member Posts: 399
    edited August 2013

    You are so beautiful, Marty. I will come. I'm glad there's another southerner on here. I feel like my accent sticks out sometimes. It seems that everyone else is from New York, California, New Zealand, Texas, New Jersey. Well, I welcome y'all's company.  I am doing well tonight. I probably won't sleep much because I'm still hyped up. I don't feel nervous. I just could paint the house. That's a good thing except it's brick and doesn't get painted. Think I'll get a prescription for sterhoids afterwards so I can get my spring cleaning done. I have done everything by the book so I hope you're right. If I have a bad experience, then we'll know all of that preparation wasn't even necessary. Or maybe it was. Maybe I would have a really severe reaction and have to be hospitalized. That would be awful. The hospital is about 1 mile from where I will be, so I guess I don't have anything to worry about. I still have to wipe my kitchen counters, but I will have time in the morning. I wanted to bleach them since I had raw chicken out. I used dish soap to wash it off, but I don't trust that after chemo. I am going to be extremely careful. I'll be 69 in November, so I don't want to push my luck. I'm a healthy 68 year old with cancer!!! I had better go brush my teeth and get myself close to my bed so I can fall in. My husband is in bed watching TV. I have a wonderful husband. I hope you have someone who cares for you and will help you through. It looks like you are on your second go-round. I can't imagine. I have triple negative, and it recurs quickly. That's why I demanded the most aggressive treatment I could get. There is no 5-year pill for triple negative. Mine is the most aggressive, but the tumor was 6mm, but it was IDC, so it could have gotten into the bloodstream. Here I go again. Sorry. My typing teacher taught us to type with paper over the keys so I am sitting here in the dark. It's a good thing sometimes, but when someone had to read my books, it must be taxing. Thanks for the



  • LisaSp
    LisaSp Member Posts: 253
    edited August 2013

    Sharonanne: Wow you impress me. Come clean my house!



    What a dynamo. I'd say your husband is lucky to have you!

  • SewStrong
    SewStrong Member Posts: 399
    edited August 2013

    Here it is 11:30 pm and I'm not the least bit sleepy. I took two benedryl at 11, but I don't know if that is powerful enough to cut through these steroids. I promisesd I wouldn't write any more, but I must have lied, because here  am. I cleaned the drip pans on the stove, washed a sink-full of dishes because the dishwasher is full, ironed several blouises so I can snatch them out of my closet, found something to wear tomorrow, did two more loads of laundry, scoured the kitchen sinks with bleach and both bathroom sinks with scrubbing bubbles. Do you'll think I'm kidding? I haven't worked this hard since the wedding July 12 this summer. It needed it because after the wedding my husband and I crashed for a month. Now here we go again. I'm really not drunk. I just sound that way. I don't drink, unless my friends on the beach talk me into a margarita. I'm going to bed and see what happens. I may be up sweeping the yard with a whisk broom. What's in that stuff, anyway? I really am sorry I wrote so much today. Those times I was writing were my rest periods. God bless you all. I'm shutting this contraption down so I won't be tempted to write again. I heard someone say, "Finally!" Steroid Sharon I've been spelling that word incorrectly. Thought so, so I looked it up.

    Martie, I can't even spell your name right when I see it on your avitar. Sorry

  • LizzieWhiteLoper
    LizzieWhiteLoper Member Posts: 1
    edited August 2013

    Hi team august chemo sisters. What a relief and surprise to find a group going through EXACTLY my symptoms and questions. I am on herceptin, taxotere and perjeta. So far my worst symptom has been extreme exhaustion. Luckily I have been giving several meds for nausea as this was the one I was dreading. My biggest advice is stay hydrated! Helps everything :) for anxiety I was getting before biopsy, dr consult and procedures I was given Xanax. It works and even helped constipation a little. Tomorrow is my 2nd time. Can't sleep but I will be there. I had plans before this hit me. I'm 45, I want to be brave and get well. I wish the same for all of you.

    My GP and dentist gave me a bunch of tips for private and painfully side effects.

    1. Fluoride after brushing, do not rinse. Helps sores and dry mouth

    2. Desitin for privates rashes, works in one minute!

    3. Hair fell out end of third week just as they said. I got a pixie cut to keep what I have!

    Question for you all out there...what do you do when you feel super anxious like your body limps want to jump around?

    I hate it.

    Well good night sisters. Feel better very soon. <3</p>

  • gavinsgrandma
    gavinsgrandma Member Posts: 407
    edited August 2013

    Lizzywhite, good luck tomorrow on your treatment, I hope all goes well, I have joined the ranks of non sleeping sisters tonight😕

    Sharonanne, you got this lady, you will do great and keep us posted.I pray for minimal SE'S for everyone having treatment tomorrow.



    Shary🍁

  • Gashgold
    Gashgold Member Posts: 58
    edited August 2013

    9.14 pm Monday - just about to drift off to sleep after a blurry, fuzzy day at school, thinking specially of you all starting your day of chemo. SharonAnne, where can I get a dose of those steroids? I could sure do with the energy : )

    Welcome LizzyWhite...hope your anxiety settles...I just walk miles and pace when I'm inside. The day I was diagnosed I literally could not sit in the chair.



    I've become obsessed with googling turtle cake! Trying to find the perfect from scratch recipe for when I'll let myself eat cake again. The sugar substitute debate- at least sugar is sugar. I've never trusted that other stuff, just try not to go overboard on the real thing.

    My chemo nurse said no point in trying to find why we got breast cancer. We just make ourselves feel bad and guilty when we shouldn't. She sees everyone and all sorts. At the moment, she and her colleagues think golf causes cancer because there has been a run of golfers through chemo.

    Shary, hope you catch some of my sleepiness!

    Night, all. Kia kaha ( be strong)

  • SewStrong
    SewStrong Member Posts: 399
    edited August 2013

    LIZZIE, I am so glad you're here this morning. I am the one who wrote volumes of text yesterday because TODAY is my first chemo! I promise not to hog the boards every day. I had taken 2 steroid tablets and it hyped me up so much I worked myself ragged yesterday.  What is good about thati s that these women don't mind. They're all here to encourage you and hold you up as they have me. You will meet all kinds of personalities, some of whom you'll click more than others because of common interests, but everyone's story is amazing and you will find comfort here. I was up at 4 this morning after going to sleep around 12. We're leaving at 9:30 EST to head to Northern Kentucky, where my doctors are located. You and I are on similar schedules, perhaps. I will go every 3 weeks for chemo, then 5-7 weeks for radiation. I have triple negative breast cancer. We'll all go through the mill for the very same reason...to eraticate every last cancer cell from our bodies. You are welcome here.  Thanks for the tips. I will buy Desitin today. I used it on my babies. Can we buy fluoride over the counter? Sharon

    Shary, I slept from 12 to 4, so I was one of them last night, too. Thanks for the encouragement. If it hadn't been for this board, I would not be as confident heading to my first chem as I feel this morning. I am still a little high from the steroids, and today, they will give me more!!!!!On Tuesday, I have to take them one more time!!I really hope you have a good day with no pain and nausea.

    Gashgold, I'll have to talk to my doctor for you. I'd be put in jail if I sent you some. I'm not sure if they would give me chemo there. Uh Oh. My husband is in trouble. He's an avid golfer. Is it lung cancer that golfers are coming down with? I know that the golf courses here use sprays to control weeds. That isn't sounding good to me. He's been a golfer all of his life and we go to Florida where he plays and I walk the beaches.  Next, I guess we'll hear that beach foam causes cancer. Well, maybe that's why I'm here. Have a good day. I declare that you are going to feel fantastic today, well, tonight, I mean. You're going to bed and we're getting up. I hope you can sleep and wake tomorrow feeling fantastic. I leave in 3 hours for the chemo. I'll picture you fast asleep with sweet dreams dancing in your head. When I get the recipe from my neighbor, I can send it to you. It can't get any better than hers. Sharon

    Everyone, Declare yourselves a good day. I declare myself a good first chemo. They will find the vein in one poke, I will not have an allergic reaction, and I will finish up with no headache or nausea. Is that asking too much?



  • steelerfan
    steelerfan Member Posts: 8
    edited August 2013

    RhodyMMM, I live in east Tennessee but have been a die hard Steelers fan since Bradshaw played! I saw them play when I was about 8 and was Steelers hooked. I still have my pennant from that game hanging on my wall above my tv! Go Steelers!!!

  • LisaSp
    LisaSp Member Posts: 253
    edited August 2013

    Sharonanne:You'll do well and so will I, I just know it. For everyone Biotene toothpaste and Biotene mouthwash is the way to go. My mouth got really dry after the first tx so this was my routine: brush four to five times a day (also the tongue) and rinse with the mouthwash. Also every night before bed, used the Biotene gel (diff product). All at Walmart!



    Welcome Lizzie! Just realized we both have chemo today like Sharonanne. We'll all have to see where we're at later and compare notes.



    Today is my baby's first day of 7th grade and my 2nd tx. Busy day. Didn't sleep well and am up too early.



    I am declaring its going to be a great day!

  • Martie1228
    Martie1228 Member Posts: 73
    edited August 2013

    SharonAnne: Praying for you this morning (and will be throughout the day) that God will give you grace, strength, and peace. What chemo are you getting? BTW, I loved all your steroid-driven notes yesterday! (I think I'm going to ask for some from my MO! I have some closets that need cleaning out!) And yes, I do have a wonderful husband of 34+ years, one son and his wife who live in town, another daughter and son that come in quite often from Clarksville, TN and Frederick, MD, respectively, quite often (with grandkids in tow. :) ), an awesome church family, and lots of wonderful friends! My kids insist that i have to stick around 30 more years to watch their kids grow up! I'm all for it!!! Where in Kentucky are you? I just may have to pop up and visit some time!



    For those who shaved their heads ahead of time, what does it look like when your hair actually falls out? My head is itching like crazy today (day 13).



  • Martie1228
    Martie1228 Member Posts: 73
    edited August 2013

    Where do you live, Steelerfan? I am in East TN as well.

  • carolpr56
    carolpr56 Member Posts: 241
    edited August 2013

    Good morning! Blessings to all having infusions today - especially you first ices, Sherry, and Lizzy your second. Someone, is it Rhodymartha is tomorrow! Gof bless us all with in eventful infusions and manageable side effects!



    I still fight this bloody headache, but the rash is much better and I'm going to work. No telling what the WBCs are doing, but the bone aches tell me the meds are working, right?



    I was so blessed yesterday - my oldest came over with his fiancée (I call her the DIL anyway), and she took my DD and did the grocery shopping and the DS took the DH to the hardware store. then they cooked, while I supervised my recipes ; ). It was a good evening, and I'd been antsy for company for 4 days!



    Hoping to have a "good" week 3, as week 2 did not end up that way : (

  • carolpr56
    carolpr56 Member Posts: 241
    edited August 2013

    Gashgold, I'm sure you've already googled recipes, but her are 2 that look authentic: one uses a Betty Crocker mix, and the other is a scratch cake.





    http://www.cafelatte.com/turtle_cake.pdf



    http://www.bettycrocker.com/recipes/chocolate-turtle-cake/20fb6793-6b6c-4dd2-82f1-96787d229b50



    Enjoy!

  • SewStrong
    SewStrong Member Posts: 399
    edited August 2013

    Lisa, I bought biotene mouthwash, t oothpaste, and that gel you put in your mouth at night. I also made up salt water and soda to gargle. It's healing. I have a slight sore throat this morning. Hope nothing is brewing because the waiting is definitely the hardest. I'll be picturing your little pink tips doing your chemo. You might scare the nurses into thinking all of the chemo is going to your hair.

    Carol, sounds like you have a great future DIL.

    Lisa, Lizzy, and little old me: We will declare that our chemos today will be awesome. Is that possible? No headache, but if it's nausea over headache, I'll take a migraine.

    Martie, I have triple negative breast cancer so there is no targeting medication for it like for the positive kind, where women take a pill for 5 years to help keep it from recurring. I am going to be on taxotere and cytoxin. The strength will be increased with each infusion. I live in Northern Kentucky. On the map, where that little bump is located at the northern-most tip, I live at the very bottom of that on the west side. I'm 36 miles south of Cincinnati, Ohio. It can't be that far if we meet in the middle sometime, now can it. Thanks for your encouragement. I'm glad you have a good support team. I do, as well. How blessed can we be. \

    God bless all of you for getting me to this level of confidence. Effexor helps too of and so does my DH. He's doing the rest the laundry and tidying up the kitchen. Wait. I haven't eaten yet. I have to go. It's oatmeal and blueberries for me.

  • LisaSp
    LisaSp Member Posts: 253
    edited August 2013

    Ladies: Here I am at chemo. Seriously! Almost half way through Taxotere. No reactions. My MO liked the cap I'm wearing. Only thing I can say is wow is it cold in here!



    The MO was pleased again how well hydrated I am. Oh the nurse said no flu shot probably until chemo is done and the MO said that on my regimen (TC x 4) the SEs wouldn't get worse with the exception of fatigue.



    I am thinking good thoughts and feeling peaceful. Hope everything is going well for everyone getting tx today!

  • gavinsgrandma
    gavinsgrandma Member Posts: 407
    edited August 2013

    Lisa, that is great that no SE'S are popping up as you have your Tx, good luck and you are in my prayers for a smooth easy go round.

    Sharonanne, thinking about you lady, let us know how you are doing.

    I used the biotene spray after surgey and the rinse after my 1st Tx and I never got one sore in my mouth😄I did get a sore throat and ears but that went away as soon as MO started me on antibiotics for my low WBC. Hope every one has a very blessed day and oh yea I ordered 4 cute skull caps the other day and I am excited for them to get her, owing to the fact that after treatment # 2 this week I expect to be shaving my head probably next weekend or shortly there after. I guess 25 yrs of doing hair will come in handy for that😛



    Shary🍁

  • raynaj
    raynaj Member Posts: 236
    edited August 2013

    Sharon Good luck today, I hope everything goes well for you and you have very little SE's. Will be thinking of you today.

    Love, Rayna

  • raynaj
    raynaj Member Posts: 236
    edited August 2013

    Carol; Thank you so much for the special thought, Yes they did come along I figured I wasn't going to miss out on the beautiful day God had given me so I went along and stayed away from them (infection). But I think I have decided that I don't want to spend too much time with this woman, we stopped for a shore lunch and everyone got off the boat except me, (I had to stay out of the sun)everyone at one point made a point of asking if I was doing okay or came on the boat to visit me, except her, Nothing. Unfortunately I have noticed that a lot of woman in my life are ignoring me and I cant figure out why, you would think they would be the sympathetic ones. Oh well, I don't need people like that in my life. I have a lot of very caring people who mean the world to me.



    Sharon: You made me laugh out loud at the thought of you moving away from your husband, if you know, he got a 4 hour one. lol Also, that is sweet that you have been together from high school, here's to another 30 years together. Good luck today

  • raynaj
    raynaj Member Posts: 236
    edited August 2013

    Welcome Lizzie: I know what you mean about you limbs jumping around, I get like that for 5 days and cannot sleep even when so exhausted, my whole body won't let me stay in one position for very long so sleep is impossible you have to get up and move. someone told me to take my steroid night pill earlier in the evening but that doesn't help me because I can't sleep no matter what time of day. I was going to ask the onco for a sleeping pill but I might not because I don't need to be anymore tired and still not be able to sleep. Sorry wish I had some advice but if anyone has any I could use some too.

    Love, Rayna

  • gavinsgrandma
    gavinsgrandma Member Posts: 407
    edited August 2013

    Rayna, I find I very interesting how women do stay away, not sure what that is all about? In fact I thought to myself the next time I see someone I know that has not called or anything and they say " oh I have been thinking so much about you " I just might say" And yet you haven't called? Don't know but this whole cancer thing is really frustrating and anoying. Hope you are feeling well and have a good day.



    Shary🍁

  • tonya845
    tonya845 Member Posts: 25
    edited August 2013

    Hi Ladies, I had my 1st chemo tx on 8/21, i was okay till later, i was soooo nauseous and weak. We did end up going caming for the weekend, i just slept alot. I got my first neupgen shot today, my husband gets to do the other 6 for me, not sure how I feel about that yet, lol. I'm just feeling weak, fuzzy head feeling and acid reflux is really annoying. I just want one day where i actually feel okay, will that ever happen?? Getting my head shaved this friday with my sister who is my biggest support system. Also need to tell my boys what's going on, but not sure how to tell them, anyone have advice? thanks :)

  • raynaj
    raynaj Member Posts: 236
    edited August 2013

    Gavinsgrandma: You too, heh? That maybe should be a topic of discussion. I know the first time I read somewhere that breast cancer is a very lonely disease, I did't quite get it but I do now, it can be soooo lonely.



    Everyone Else: Have the woman in your life treated you differently since you have been diagnosed?

  • carolpr56
    carolpr56 Member Posts: 241
    edited August 2013

    Most of the women i work with and go to church with have and am otherwise been friends with have been Incredibly supportive. There are some who have surprised me, though. In one case, i know she just does not know what to do, but even the day she called me to invite us to their pool party, and I said i was sick in bed (not 20 feet from their pool) - i had to tell HER it was ok, to not worry about disturbing me with their noise and she was all surprised. SAID she had fruit for me, then it was 5 days later before she CALLED to say she had it, offering to bring it over as an afterthought. That said, some women are insensitive and some just don't have any sense!

    Good thing none of US is like that ; ))))

    Rayna, no surprise this woman didn't even come over! it's all about her. Hope she had a good time on Your boat. I am SO glad you went! Good for YOU! lets pray for no nasty germs...

    Lisa - yay! fingers crossed for no SE's. you know from us what to expect if it happens!

    Tonya, your boys look small. How about showing them pics of other BC ladies with no hair, say that's going to happen to YOU, too, cuz you're having the same medicine. They will no doubt think you are very cool. I suggest you might even offer them buzz cuts as well, and they can say "this is for my mom who's got breast cancer." Make it a part of regular discussion - the new normal for the whole family. It won't hurt them, it will make them stronger and more sensitive to people who are sick or "look funny".  Will your husband buzz cut too? Make a party around it! pink ribbon tshirts for everyone, etc.

    I'm a lemonade from lemons kind of a gal, ya know!

    Work is going well. I keep thinking about Sharonanne, hope all is going perfectly for her along with Lisa. I bet shes making multiple potty trips with all that hydration and is the belle of the infusion room, going around visiting with everyone as she zoooms on her steroids! A fun picture...

  • TanyaF
    TanyaF Member Posts: 54
    edited August 2013

    I am lucky to have some supportive ladies in my life. My little sis even buzz cut her hair, had it dyed pink, and then had a ribbon shaved in! She works in a salon so different hair is OK to have.

    SE kept me down over the weekend. Kept the nausea down with meds, but still had some stomach pains. I was pretty light headed on Saturday plus TIRED! Kept mouth issues at bay, but still had the annoyance going on all weekend. I also had bone pain yesterday.

    Today is much better. Some parts of mouth go numb every now and then. Head is great!

    Hope everyone doing treatment today is feeling well!!

  • raynaj
    raynaj Member Posts: 236
    edited August 2013

    Tonya: Yes you will feel better eventually, I know with my first treatment, I didn't feel better until about Day 12, the exhaustion was so utterly complete that I couldn't even hold my kindle to read, not that I could read anyways because I couldn't concentrate on anything for more that 3 minutes, I would reread a paragraph 20 times before I would put my book down. Walking was difficult and would take me 20 steps to equal what before I would walk in 5 steps.

    About your children, I don't know how old they are but if you are sick and have been going to doctors, I'm sure they know something is up already. Please tell them right away, let them know you have Cancer (use the word) and that you are doing everything you can to get better but that you will have to get a little sick first. Depending on their age just word things differently, If they ask the dreaded question "Will you die'? I said to my son that people do die from cancer but I am going to do whatever I have to, to make sure that doesn't happen.

    I know its hard and I made the mistake of not telling my 11 year old son as soon as I found out and wanted to wait until I had biopsies, and knew for sure but that was a HUGE mistake. There were people coming over with flowers and food and hushed conversations, (that was enough for him to know something was going on) plus I had made a list of questions to ask the surgeon and he decided to clean for me one day and found the list) When I finally asked him if he felt things had be different around the house he said Yes and then I asked him if he thought he knew what was going on and he said "Do you have cancer?" I told him yes and asked why he didn't come to me when he found the note and he said "I thought you would be mad at me" (OOOH, my poor baby) I had to explain that I was only waiting so he wouldn't have to worried if it turned out to be nothing. Now at this point he felt we were keeping things from him or that it was none of his business and that we were lying to him. What is he going to believe now?

    I tell him everything now, there is nothing I won't tell him and I reassured him that I wouldn't exclude him anymore no matter what was involved.

    This did a bit of damage too because ever since he has been having panic attacks and seperation anxiety and I know most of it is over the fact that his Mom has cancer but I can't help thinking if I had done this differently he may have adjusted to the news better than he did.

    Be truthful, this affects the whole family and they need to know and they aren't stupid they know more than we ever give them credit for.

    I knew the day I was going to have the talk with him and I'd get ready to say something and get chocked up so I'd wait and then I just knew when the timing was right and I was in control so I wouldn't start bawling and scare him, I was very calm and didn't shed a single tear, which I think helped. I told him I was scared, they have to know we are not invincible to such things as fear.

    I hope I helped or shed some light on the subject for you, if you want more information or want to talk more about it Private Message me, I'd be happy to help.

    Love, Rayna

  • Shalimar630
    Shalimar630 Member Posts: 100
    edited August 2013

    Well, I spent the morning in the ER, getting fluids, which I had lost all day yesterday. I tried to keep the fluid intake going. Thought I was feeling better, but right before bed I also started having low back spasms. Don't think that is associated with chemo is it? So I also got treated for that as well, but it was a rather miserable night.

    On other women.. I am rather surprised at the ones who have stayed in touch and those who don't. One who I thought was one of my closest friends, I have only heard from twice this summer, and at the end of each visit, she always says to keep her informed. I'm rather hurt that she can't make that effort. We also have close relatives living on the same street, which I have never heard from. If we have a family function, they ask how I'm doing, but otherwise, nothing. I find this so odd. It the situation were reversed, I would be over there often offering to help. I guess some people's comfort levels are just completely different.

    Is there anyone here who is from the West Coast? I think I saw someone else from Oregon, but not many more from around this area...

    We are supposed to go camping this next weekend in Astoria. Big Family reunion which happens each year. At least we will be outside instead of confined inside where germs may be. Looking forward to it. My daughter and two gkids from Philly will be arriving on Tues!!

    Also, where I work they try to get everyone to get a flu shot. I called my MO office and they said I should get one. Now I just saw the post about another MO saying not to get it. And we wonder why we are so confused...

    A bonus today was they did lab work while I was there and it looked good...

    Special thoughts to all who had/have an infusion this week. Will send positive vibes your way for very minimal SE.

  • LisaSp
    LisaSp Member Posts: 253
    edited August 2013

    Hello all! Back from chemo 2. I am so definitely jazzed on the steroids forgive me in advance for long and/or multiple posts.



    I just started on SE meds which my MO gives on a schedule before nausea starts. Took steroid, Zofran and Ativan and. Pepcid AC because I could feel sore throat starting. I plan to take Pepcid everyday now throughout chemo as recommended by the nurse. Also started taking Colace. (stool softener) three times a day.



    Had new SE oh boy. Weakness in legs so I put in a call to MO to see if this is a concern. Still going for a walk later.



    The tx itself was very uneventful and took 2 hours. Side effect meds first then Taxotere then Cytoxan and at the end heparin to flush the port. I used lidocaine cream on the port 2 hours before put Saran Wrap over it; it did not hurt w the needle at all. Have to say I love the port.



    Discovered I have a birthmark I didn't know about! On the back of my neck and scalp is a irregular red mark the size of an Oreo. It's a 'stork bite'! Since I have never not had hair even as an infant no one knew. Well makeup would cover if I want bald is beautiful looks. Maybe I should have a henna tattoo there reading "stupid cancer" in fancy writing to cover it. :)

  • Martie1228
    Martie1228 Member Posts: 73
    edited August 2013

    Tanya: I heard someone tell their children that the medicine they give you for cancer is very strong, like a superhero. When the superhero (chemo) battles the bad guys (cancer), the city is pretty much destroyed and takes a little time to rebuild. My son used this with my 4-yo grandson to explain Mimi's cancer. (Needless to say, he's now colored me a boxful of superhero pictures. The Teenage Mutant Ninja Turtles are working hard to save me! ;) )

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