Starting Chemo in December 2013
Comments
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haha barb, I'll ask them that tomorrow! No more playing tic tac toe on my chest...Barb says so!
Sounds like I have more drawings than anyone else...I'm special? Or they are bored
I also realized how important eyelashes are...not just to make your eyes look pretty. They keep stuff out. Was walking yesterday and kept getting stuff in my eyes and you know how you are supposed to pull the top lid over the bottom to get it out..well I couldn't without eyelashes. It was so weird when I tried to do it and oh yea that's right, no eyelashes. Had to rub it and let it tear out. Little stubbles for eyelashes coming in. This hair regrowth progression is so weird
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bare with me here:(. I usually would post this on my FB page but I just can't. I need some feedback and help. Trigger warning- Here we go:
My 6 year old asked my sister today where my dad's body was. She told her the funeral home, but that his spirit was in heaven. She gets that- Catholic school girl. She then said: I think I need to say goodbye to his body. My sister said you will have to talk to your mom. I wasn't planning on them going up the aisle completely. She then says: paw paw is dead. My sister said yes it is sad Ellison. She replied: and my mom is going to be next.
What! Someone has scared her and we are trying to make it better. When I told her paw paw was now an angel, she said: but paw paw didn't have cancer. Wth! Who is saying this sh@)(; to my little girl. My heart is breaking. I told her the doctor said I was going to be fine and please try not to worry. I think once my hair comes back she will think that I am better. I guess I do look so sick to her:(
My ultrasound today showed the node did shrink but the dr said by millimeters. That annoyed me. I asked my RO why tinge middle node in the chest wall chain was positive but the others not. Didn't make sense to me that they could skip. He said they don't. Which means it was or is in the others. Really bad day. Praying tomorrow when I see RO again he says screw the u/a dr. He did say it didn't matter that his plan would stay the same regardless. He feels like he will get them. I just read how people are cancer free starting rads and I am not and my daughter is freaking me out. Probably overly sensitive bc of my dad but ugh!!! I am usually upbeat so I apologize for all the downer stuff lately! PleAse pray I kick off next week on a positive note. Right now I suck:(
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Jodi, it is possible that she has overheard people discussing cancer or that someone in school may have experienced a family member with cancer. It is a good thing that she is having this conversation. Sounds like she is just trying to make sense of it all. We find it confusing as adults and talking does help. Or typing!!
You have my prayers! Prayers for strength, peace of mind and heart, healing and courage. If I have missed something, let me know and I will add it!
Radiation - I have marker all over me. There is tape covering it all. Both sides and chest, no tattoos. I look like someone let loose a preschooler with a sharpie! I have lines, circles and X's to mark where the boluses go, where I line up on the table and where I line up with the vac lock. A couple different colors too.
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jodi, sorry you are having such a hard time right now. When it comes to our kids, I think we are super-sensitive. At least I know I am. I'm sure she doesn't understand it all right now...
No need to apologize. Prayers coming your way!
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Jodi- I'm so sorry this is happening. I hate that cancer affects the entire family not just the patient. My 9 year old cries at least one night a week. It breaks my heart.
How old is Ellison again? Depending on her developmental age, it is normal for children to ask about mom or dad dying when they experience a death in the family. Not sure if knowing that helps or not. I'm sure a cancer diagnosis of a parent makes it even more complicated for the child.
Does MDA have any programs your kiddos can attend while y'all are down there for rads? It has helped my girls some to have the counseling through Wonders and Worries.
I am going to tell you that you don't suck. Cancer sucks but not you. Vent and rant away.
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Jodi, I am so sorry you are having to go through all of this. I don't know if it really even changes based on the childs age. My 18 year old daughter brought home her english papers the other day and she is going into English in college and Creative Writing so she is a very well written, smart girl. I was looking through some of the things she had written, and one was about me and getting diagnosed with cancer and how scared she was of losing me. She had never expressed this to me at all. I cried when reading it and asked her if i could keep it....i also asked her why she had never told me how scared she really was and she just said she didn't want to worry me with any more. Ugh. I felt horrible.
I have marker all over my chest. They draw on me every day! I have clear tape over one area where they don't want me to lose those marks. I met with RO yesterday and he said everything was going well. I have no idea what to ask him as far as questions......I seriously don't know if i even have cancer in me still and if the radiation is just to kill anything that may be lingering. I am assuming so? I am hoping the chemo got everything it needed to get? the surgery also? Maybe I am just scared to ask the questions i need to ask........
Today will be my 7th treatment.....my skin is still holding up great, but know all good things usually come to an end! ha! Tomorrow is my daughters open house for her HS graduation and graduation is on Saturday. I CAN"T WAIT TILL ITS ALL OVER!!!! This momma is exhausted!
Have a great day everybody!
Michelle
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Michelle,
I got a great analogy on radiation. She said to think of it as cooking raw chicken in your kitchen.....You wipe down the counter to clean it up and remove the remnants....but you follow it with the Lysol to be sure all the bacteria is gone.
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Today will be rad #8. My skin is holding up fine, but I am losing range of motion even with my PT exercises each day. RO gave me different exercises to do and if it no improvement or worsening by Monday, it is back to PT and adding muscle relaxer to prevent permanent disability. UGH.....Happy I brought it up, did not realize what a big deal it was.
Michelle - enjoy the festivities!! Congrats to your daughter! It is an exciting time!!
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Robin, why do you think you are losing ROM? Does it have something to do with radiation and skin tightening? My L hand goes numb with the position I am in for radaition but I had some carpal tunnel, cubital tunnel (ulnar nerve compression at elbow) issues before but managed it conservatively and it was not constant. Now seems more consistent and at night is worse. My arm or hand is not swollen and I have good ROM. I have been doing some stretches and nerve glides.Will see how this goes with the overhead position. They only did 2 positions with me yesterday (the machine moved in 2 positions, one "shooting" from the R side and one from the L side I think-Ill take more note today)
Jodi, You DO NOT SUCK! youve had so much on your plate recently that it is normal to have a bad day.. or a few, just go with it. You are usually upbeat as you say and you will get back there. Take care of yourself and your kids. You are beautiful and strong. Express yourself as much as you want here. It is a safe place. One of my moto's has been "every tear you shed makes room for strength to enter" so we have to have those down days in order to get to the strong days
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Helloooo to all !!
my goodness just trying to catch up on posts.
DJJ - yes it was me with the freaking fuzz face, and I went and had it threaded, ba bye.. there is still some there but nothing like what it was.
I have to say my skin is starting to feel the effects of the rads, my boob just looks tanned its a little itchy but my armpit is a different story, its sore just feels chaffed but still annoying and totally manageable. I have 10 treatments left, getting there.
I am glued to twitter and the TV and my phone with the shit show unfolding in my home province about an hour and a half away from home, in Moncton NB, 3 RCMP officers dead, 2 wounded, still hunting for the bastard that did this, I have family in moncton and my brother is on the search for him as he is a police official. I am just sick about this, I cant believe this has happened.
My hubby and kids are flying up this weekend to Toronto to spend the week with me I cant wait, there is so much here for us to see and do.
DJJ - you can do it with the tattoo, I just got another one before I came to Toronto in honour of my brother that I lost in January. Its all script I will post a pic, I love it.
Jody - I am sorry for these challenges you are facing with your dad, and your daughter. My condolences to you and your family.
I am going out for dinner tonite with a very old friend from my hometown, I am excited to see him and catch up he lives here now.
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Jbokland - Congrats!!!
Kimie - I have been following some of that via your FB. Truly frightening.
Lisa - RO feels it is the scar tissue that is tightening. I had cording issues after surgery and it appears that those issues are returning. Make sure you speak with RO about any/all issues no matter how "small" you may think they are. I thought mine was small and debated mentioning it. Learned my lesson with the scar tissue scare a couple weeks ago. May not always be as minor as we think.
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lyrics from one his favourite songs...Ramble on Led Zeppelin... his birthdate his signature and his death...:( man I miss him.... alot
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kimie- that is beautiful
Jbokland - congrats!!
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jb, congrats. Another chemo treatment bites the dust! Yea!
Kimie, have a good weekend with your husband and kids. I'm really worried about skin problems as I am fair and my skin burns easily. A woman in the summer rads 2014 forum from New Zealand is going to be using mepitel film to prevent skin issues from rads. I forget her name but she attached an article from a study. It's so much better to prevent than treat once there is a problem. I'm going to bring the article to my RO next week.
http://www.ncbi.nlm.nih.gov/pubmed/24486117
Robin, good luck with the arm rom. I'm interested to know how you make out with it. Would they redo your rad position? I have this form I lay in that was custom molded around my upper body so that I'm in the exact same position each time, but it's kind of uncomfortable. But it's only for a short time. The machine is only in 2 positions and for 18-20 seconds each. I count each time when I hear the buzz of the machine start. So only 40 seconds of actual treatment time!
I also asked about all my markings and if they were all necessary. She said she could remove a few so I don't look like a drawing from a preschooler who was let loose.
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Jbokland, WOHOOO!!!!!
Kimmie, love the tattoo!
Robin, I'm sorry. I've had enough of the crap time you've had through this. I'm flipping off cancer for you!
I've done 4 treatments and my armpit is already sore from where the lymph nodes were removed. Not bad just a little tender. RO said it was common and take IB. 26 more to go.
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DJJ - cancer sucks....who knew?!?
I'm okay, have a game plan! It could be worse...
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had to share! The local BC foundation donated this bell for other patients to ring when they complete chemo. My chemo suite is very mundane, busy place. I call it the chemo factory. All of these friends showed up to surprise me! Man we shook up that place!! What a way to End my chemo!!!
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JB amazing! I actually donated a bell and a framed poem that goes with it to my facility as they did not have one. I haven't seen where they put it up yet. I thought maybe they'd call me when they put it up but haven't heard from them yet. We/they didn't have one and I wanted other pts to celebrate with "the ringing of the bell, three times well..."
Robin, I ordered a color me your way book. I've loved your pictures. What do you do with them when they are done? Have you framed them?
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Jbokland - The bell and the turnout from your friends is amazing!
Lisa - I still have them in the books. I am thinking about framing them, but think I will wait until I have more finished. Then I can choose wisely!!
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jbokland - love that bell. What awesome friends you have.
Lisa- where did you find the bell and poem? My facility didn't have one either. What a great thing to donate!!
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Robin- I feel some lessening of ROM too. Haven't mentioned it to RO but I guess I should at next doctor day. It is slight but I can tell a difference I feel tighter. I'm also having some irritation / discomfort in the under arm area but it's slight and tolerable. Doc says if it gets worse he will give me lidocaine cream.
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holli, I found a nice bell on eBay but it wasn't mounted on anything so they'd have to mount it to a plack or just to the wall. The poem I copied from an online site and printed on nice paper and put it in a frame. I included a letter about where the tradition originated. It was at mds hospital by a army general who treated for cancer and wanted some thing to commemorate the end of treatment so came up with this idea and poem
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lisaj514- thank you. It will come. You're about a month behind me, chemo wise. Mine started off the same....white/blonde barely visible soft fuzz. It's still soft chemo hair. But it continues to get darker along with my brows. This is me about a month ago. My hair was light and my brows were drawn on. This is my youngest in the pic with me. He's almost 1 1/2.
I'm 37.
I'm impatient too. I understand. If these other drugs don't mess with my hair, I figure I should have chemo curls by my birthday, the end of September.
I've started a new regimen because my path report came back with a sub-type of metaplastic breast cancer and also with a possibility of mets. Metaplastic is for sure and it is very rare, very aggressive and has a high recurrence rate and a low 5 yr survival rate. As for the possibility of mets, my onc doesn't agree. We're going to do a PET scan as soon as chemo is done.
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DJJ- I also get asked if I did this on purpose. lol Some women assume that I have cancer and pray for me. I also get told I have a perfect shaped head. Guess I never would have known otherwise! Great picture! You will be there soon! I'd say within a week or 2 I went from some lashes to being able to apply mascara. I agree about the tattoos. Ouch!!
RHGSR- thank you. I am 37. Doctors are so strange. My onc had originally told me I'm "cured" but everything I've read online is that you're not actually considered cured until you make it to 5 years without a recurrence.
Lisaj- very cute! I actually liked the white stage. I was so excited just to have hair. lol I decided to be cute and try to put a clip in it on Easter and it stuck! Haha!! My Easter pictures are funny. lol. I had a hard time staying still during the rad sim. And I had no idea that the position my hands were in has to be the same exact way each time. I had all the markers too. I couldn't even see the little tattoos when she was done. I have 4 dot tattoos. 3 on the right, above, below and outside of boob and one on my left side. I didn't have to keep the markings though. ??
RobinLK- I LOVE that scene!! Every time I think of that song, it reminds me of that movie. To the window, to the wall!!
Keepthefaith- I have peach fuzz in my face and forehead too. I wonder if it will slow??
Jbokland- congrats on your last chemo!!
Charusa- congrats on a good path report! I am also numb on my underarm where my nodes were removed. Feels weird to put on deodorant.
Jodi- I'm so sorry for your loss. I'm glad you chose to go to the hospital. Hugs! I'm sorry to hear about your daughter. The hardest part of all this is thinking of what it's doing to my boys.
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Cenri- I'm am also 37 (until today after 1pm :0). I have 3 children my youngest is 2. I was breast feeding him when I found what I thought was a clogged milk duct.
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Cenri--You look fantastic!
RHG- Very heartbreaking to hear your discovery.....I am often reminded the perspective when I hear the stories of you moms out there with little ones.
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Hi ladies - Got my Mac back last night. I hate typing on my iPad. I've been reading up on your posts and just wanted you all to know that you all are an awesome bunch of ladies.
Jodi - You're in my thoughts and prayers today.
Michelle - Have fun with graduation. Love your fb pics.
Robin - There is something very zin about looking at your pics that you color, thanks for sharing. I went to the PT every week during rads. Rads does make your arm stiff and the cording worse, having the PT massage my arm and back for drainage kept everything manageable.
Jbokland - Congrats on finishing chemo.
Hoping for minimal SEs for you all going through rads.
Kim
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Happy birthday Hollie! Pardon the spelling if incorrect. I think I may have "chemo brain." Perhaps you have heard of it!
Cenri - you do look amazing! Your little one is a cutie patootie! Prayers for a clear petscan. I am happy your MO is staying on top of all this. Sucks that you have to wait for answers again.
Kim - welcome back to laptop land. I will get on the PT wagon again! Thank you for the info! Even when it is a small thing, and you wouldn't wish it on anyone, it is still nice to know we are not alone! Thank you on the pictures, it feels very zen when I am doing them. I love brain centered activities and they help in that respect!
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Well, two fingernails have bitten the dust. Luckily the new nail has grown halfway, so I have half fingernails on 2 fingers. C'mon, the rest of the nails can hold on!!!
Supplements during rads - from the nurse yesterday - do not take multivitamin or ACE during rads. Antioxidants that you eat (blueberries, etc.) are fine. So are Vit D and Biotin. Thought I'd share since this was news to me.
I did not start rads after all yesterday. Another day of simulation/films. And you cannot start on a Friday, so first rads is Monday.
My hair is coming in really dark. My dad and grandmother both had wavy black hair - I always wished that I would get it. Real black Irish. Maybe this is my chance!!
JBokland, congrats on finishing chemo! whoop! whoop!
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