Starting Chemo in April 2014

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  • Blueberry4
    Blueberry4 Member Posts: 98
    edited April 2014

    Sunshine, I'm sorry you are having a rough time.  I hope it gets better soon.  A good cry often helps to reset my balance and helps me to move forward.

    Nana and Holly, great hair ladies.  Really.  I'm getting nervous about my cut tomorrow, but you all look so cute I am trying to approach it with some excitement.  Thank you, Holly, for the link to the hair donation site.  I'm going to use them.  

    Also, Holly, the high oncotype thing is a tough one.  It worries me, but my MO ensures me that with chemo we high oncotype ladies can lower our recurrence risk significantly.  I hope this thought helps me cope in the next six months.

  • SharonDe
    SharonDe Member Posts: 222
    edited April 2014

    All the pixies are very cute!

    Welcome to the April thread, MameMe. Sounds like you have had a lot happening in a short time.  Hoping the side effects from the Taxol are not too bad.  I see you are from Maine - hope the snow is gone. We spend the summer half of the year in Maine, but will be delayed getting there this year.

  • Longislandl8y
    Longislandl8y Member Posts: 145
    edited April 2014

    Nana & Holly, your cuts are adorable! You just might want to keep the hair short like that after it grows back!

    Mameme - welcome.  You will find lots of support and good humor here which is great medicine.

    I have one good week left before my next treatment and am hoping the weather cooperates so I can get my garden beds cleaned up!  It's a beautiful day in New York today and spring is finally here, so hallelujah! It's a bummer not be able to get any sun which I normally love during the transition seasons but I suppose there is always autumn to look forward to for that!

    Wishing everyone here a good day - little to no SEs and good energy! xo

  • HollyHope
    HollyHope Member Posts: 46
    edited April 2014

    Good luck with the cut Blueberry.  I would love to see a picture!

    It's wonderful to hear you are feeling well LongIsland - enjoy your day!  I'm right there with you, with my next treatment being a week from today.  The biggest issue right now is the pain/discomfort from my left TE.  Wondering if any of you other ladies with them are also experiencing that.

  • JanetP1507
    JanetP1507 Member Posts: 46
    edited April 2014

    Hello Ladies,

    Sunshine, I hope you are feeling better! This afternoon I have a lymph node biopsy and I'm hoping to have time after to stop by the oncology resource center to check out wigs and scarves etc. Then my blood draw on Wednesday afternoon, then chemo #1 on Thursday morning. You ladies have all give me a lot of hope and inspiration already, thank you!!

  • lilyrose53
    lilyrose53 Member Posts: 216
    edited April 2014

    Hi all,

    Made it through a rough weekend.  Not looking forward to that again.  Saw my BS this am- he tested my port and it worked perfectly!  So he cancelled my test at the hospital and called my MO.  I am feeling better today, so ran a few errands with DH.  

    Cold- thanks for the encouragement - I really needed it!

    Hugs to all,  lilyrose

  • chknfeet
    chknfeet Member Posts: 29
    edited April 2014

    Hello all!  I just received my 4/30 start date so guess I just skated by to join the club!  It stinks we have to meet this way, but also so glad this board exists.  I honestly had no clue what to expect and just browsing this board has been so helpful and somewhat put my mind at ease.

  • Kazzy115
    Kazzy115 Member Posts: 122
    edited April 2014

    Welcome chknfeet!  I thought I'd fall into April but I now start May 1st.  Like you, so grateful to all for sharing the good,the bad and the ugly!   It does take some of the feAr out of it, comfort seeing women moving forward and laughing and giving encouragement to others despite what they and their families are undergoing. 

    Hope everyone is getting some spring weather.  Chicago was fantastic yesterday.  Amazing what a lift it brings!

  • Mompv
    Mompv Member Posts: 110
    edited April 2014

    Hi all. Been lurking here. I thought I would be starting chemo this month but looks like end of May. I just got my pathology back and it's triple neg. I have elected surgery first, I was given the option. Still going for my short haircut Saturday. I think it will be easier to deal with after surgery, besides it will get me used to hardly any hair. 

    It's funny how life just changes in an instant. 

    Thank you all for sharing your experiences. 

    I am feeling a bit blue tonight so I am going to just read and veg out!

  • linda505
    linda505 Member Posts: 847
    edited April 2014

    Mompv - big cyber hugs your way!!  It is so hard to deal with all this stuff - I have good days and bad days - and  sometimes I just cry and I don't even know what I am crying about.  Sometimes I feel so alone as no one around me really understands how I feel - then I come in here and read a post from someone having the same feelings and then I know I am not alone and you are not alone.  Let us know what your surgery will be and join the Month of surgery thread - it was priceless to me to be able to talk about my surgery with people going through the same thing.  

  • Mompv
    Mompv Member Posts: 110
    edited April 2014

    Thank you Linda. I have just made the mistake if looking up the prognosis for triple neg. Good thing my DH is going out  of town the rest of this week. I can just have a  good cry about all this and not cause him more stress than he is feeling right now. He has admitted he is so afraid of losing me. I am afraid at this point!!

    Thank you for the hugs!

  • MakeLemonade
    MakeLemonade Member Posts: 153
    edited April 2014

    Went wig shopping before my BS appt .... Don't think I will rock the pixie :-(. Will probably go with a short bob and the gal at the cancer store said she would come in and shave my head when I feel like it is coming out.  Going to think about it ... Not getting haircut until Saturday.  Have to admit I was disappointed that the short ones really didn't do anything for me. Oh well, it isn't forever!

  • linda505
    linda505 Member Posts: 847
    edited April 2014

    Mompv - don't spend time googling prognosis - so much that is out there is out of date as so much is being done and added everyday to help us fight this disease - join the triple negative forum and talk to those that have and are walking in your shoes.  The triple positive women have helped me alot with learning the latest and greatest and have give me comfort.

    Makelemonade - My real hair looks ok short with the pixie but the pixie wigs look horrible on me lol.  I got a longer wig.  The girl who cut my hair this weekend did it for free.  I told her what I wanted and that I wanted it short short short and she was like you sure you want to go that short?  I told her why and then she told me she lost her mom to lung cancer three years ago - her mom was only 41 and never smoked a day in her life.  When I went to pay my bill - she told me her mom wanted her to cut my hair for free.  It was so sweet and we both cried.  I gave her a hug and said - Your mom sent this hug.

  • LovieLovie
    LovieLovie Member Posts: 68
    edited April 2014

    Mompv-  you are not a statistic you are a fighter!  I am also triple negative and not to make anyone else feel bad, but triple negatives tend to respond better to chemo according to my MO.  Please stay off Dr. Google, much of that info is outdated and frightening.  There is a TNBC thread on here with some awesome gals that focus on what works for them and you should visit too.  I do understand the need to cry. Everything feels uncertain in the beginning and then you realize that life is not that bad, just different. 

    Hey Everyone...Please remember to plan at least one fun thing to do each week that you can look forward to.  You need it for your mental health!  And, if you want to have some fun with people who ask what they can do to help you tell them you'd like to schedule a foot massage from them.  No need to lose your sense of humor.  

    Do something that makes you giggle too, mine was eating a little jar of baby food (fruit). I don't know why, it just did. You'll get some great looks from your teenagers.  When your hair comes back in and you have a different style then you did the last 10 yrs+ somehow that becomes cool too.  See, something to look forward to. 

    Soft hugs to all


  • SharonDe
    SharonDe Member Posts: 222
    edited April 2014

    Mompv - Linda gave great advice.  It's hard to stop googling, but it's the best thing. I know it's hard, but I wish you some peace in these next few days.

    Linda - that's a sweet story about the young lady who cut your hair.

    MakeLemonade - it may also be hard to really see how you might be with a short wig until your hair is gone.  I tried one on and looked like a wild ferret got stuck on my head ...

  • shellbell1963
    shellbell1963 Member Posts: 39
    edited April 2014

    Ladies

    I start my chemo in the morning and have been crying all day. I really am so stressed about this. I am taking TCH. I am 51 and had a lumpectomy on March 12 and my tumor was 1.3 cm with 0/3 lymph nodes. My cancer was the three positives. My sil just told me she went into anaphylactic shock from the t of the chemo. That isn't helping me deal with this too well. I tried Ativan for anxiety and it made it worse. I have a very unsympathetic husband who is like why are you in such a crabby and horrible mood tonight. Well duh why would I be. I seriously want to cancel this and say the hell with it. I can't take the stress. Sorry I am beyond stressed.

  • JanetP1507
    JanetP1507 Member Posts: 46
    edited April 2014

    Shellbell,

    I am so sorry!!! I would like to smack your hubby Anaphylactic shock is very rare from what I was told. Do you have someone to go with you tomorrow?? I'm sure once you get the first one out of the way you'll feel so much better! Please try to hang in there, we're all here for you and everything will be ok :) I'm really nervous about my first chemo on Thursday as well.

    Mompv--I've had a few meltdowns myself, it's perfectly normal. And don't google stuff, it will just scare you!! Everyone is different and everyone responds differently to treatment, LovieLove is right, you are NOT a statistic!! 

    The resource center directed me to a salon that will shave my head for free so I think I'm going to go ahead and do that this weekend, the idea of my hair falling in clumps is just horrifying to me, LOL! I've already ordered a couple of pretty "chemo scarves"  that will be here Thursday. Also, I live in Tucson, AZ and it's already in the 90s here, I think wigs will just be too hot in the summer when we are into triple digits. I'll try to post a pic this weekend with one of my scarves :) 

    Hang in there ladies, WE CAN DO THIS!!!!!

  • LovebeingNana
    LovebeingNana Member Posts: 134
    edited April 2014

    Shellbell I was really scared about the Taxotere too. I have so many allergies I thought sure I would have trouble with that too. But I didn't. The nurses take it very slow with that drug and they told me that can reverse the reaction immediately if need be. They have everything they need ready to go just in case. I am so sorry you are not getting the support you need…I know how hard this is. Try to take it one day at a time…sometimes I have to take it one minute at a time. You can do this. Hugs.

    Mompv - I too can get so scared about certain aspects of what I am facing….but it helps me to remember that a lot of those statistics involve many different scenarios and I can't really compare. I am sorry you are feeling so blue….I get it though. Hugs to you.

    Today is day 5 and I am sick of being sick. Had a good little cry tonight. Headaches are better but still there. Everything kind of aches. I did work for about 6 hours today and over my lunch break I went with a friend for her mammogram. She is a mammogram-phobe and is over 3 years overdue, yet she has a grandma and 4 aunts who breast cancer! We got it done! 

  • LovieLovie
    LovieLovie Member Posts: 68
    edited April 2014

    Shellbell- a virtual slap for sil & hubby ( tho, not promoting violence other than to make you feel better).  This is the time to surround yourself with positive people.  You will get that here!  You have every right to fear the unknown.  We all do.  Just think, by this time tomorrow you can check one session off your list.  The chemo nurses will monitor you very carefully.  Make sure you have a small meal a couple of hours before chemo so you don't have an empty tummy.  Think of tomorrow as 'liquid Pac Man' and its going to make you well.   

  • lilyrose53
    lilyrose53 Member Posts: 216
    edited April 2014

    Mompv - sorry you find yourself joining here.  I too, am TN.  Did the same as you- googled and scared the stuffing out of myself!  Stay away from google.  There are plenty of us TN's on here.  Also the triplenegativebreastcancer foundation is a great place for info.  My BS and MO have been very positive influences on my outlook.  Some days are just harder than others.  Let yourself cry.  The women on here will support you every step of the way.

    Shellbell- again, sorry to welcome you here.  But you will find some amazing friends on here!  I had my first chemo last week, and that's when it really hit me.  I felt good after my surgery, so somehow I guess I was in denial.  I don't know how ANYONE can get a diagnosis of cancer and NOT feel crabby or stressed!  You can always come here to vent.  We understand.  

    Hugs to you!  lilyrose

  • Lakegirl1
    Lakegirl1 Member Posts: 316
    edited April 2014

    I am so sorry ..please know there is no need to apologize here!!!  As one of my friends who is also a survivor tells me when I start toward the "dark" place...don't invite trouble.  If it hasn't happened to you, you don't know if it ever will. Chemo scares the #>^% out of me! please excuse  my language.  I just try to keep thinking about all the reasons why I continue down this path we didn't chose.  All I do to kick its a55, I do for my 6 & 8 yo daughters.  That is what grounds me...

    Also...talk to your doc, if that med didn't work, there are others!!!  You don't have to feel this bad...

    Many hugs and prayers!!!  

  • ColdInCanada
    ColdInCanada Member Posts: 95
    edited April 2014

    Good Evening Ladies! I took my LAST dose of antibiotics this morning and they are finally starting to wear off, so I actually feel ALMOST NORMAL. Three days of almost normal before the next dose of chemo? I will TAKE IT!  I'm not at all excited about Round 2 on Friday, but I'm trying to focus on the next 3 SE-free days. Thinking I might take a little trip to Michaels and get my craft on. :)

    Holly & Nana: You look so YOUNG with your new cuts! Don't you just love how the pixie cut takes weight off your head and years off your face and offers up some SASS to go with it? ;)

    lillyrose: I am so happy to hear you're feeling better. :)

    mompv: Linda gives great advice. One of the first and best words of wisdom someone gave me after I was diagnosed was "Stay OFF the internet." There is just so much outdated and misinformation out there. Dr. Google isn't a very good doctor, I'm afraid, and he just causes more anxiety.

    blueberry: I can not wait to see your new cut! Sending courage for you tomorrow - I know how hard the initial cut can be. You'll look gorgeous- I know it!

    linda: LOVE the story about the girl who cut your hair. Thanks so much for sharing - it makes me feel better somehow to hear about wonderful things like that. :)

    shellbell: I am so sorry you have to be here. But this group of ladies is amazing, and we are all here for you. We've all been there with the crying and raging and wailing and gnashing of teeth. Chemo is scary. I was super nervous, and it turned out my first chemo treatment was super-duper boring. And that's all. Just boring. I'm told that severe allergic reactions are rare, but the oncology nurses are very, VERY prepared for anything that might happen. And they'll go slowly and monitor ANY reactions at all. Bring a funny book or trashy magazine along. Or buy yourself an ipad with your husband's credit card (Take THAT honey! HA!), and load it up with ridiculous games to keep you occupied. For me that was the hardest part of Chemo Day - finding things to keep me amused while I just SAT there for hours. I'll be thinking of you tomorrow and sending prayers your way. 

    Oh, and P.S. Make sure you all have a sleep hat for when your hair falls out. It gets COLD at night. I don't know how bald boys do this in Winter...  

  • Sunshine36
    Sunshine36 Member Posts: 88
    edited April 2014

    I have to say, you ladies are all so amazing.  I feel so connected to you all, just knowing we are all battling the same enemy and dealing with the same struggles (chemo especially because ive only had one round so far and I feel like it's already kicking my butt :(

    Even though ive had a sampling of a few trademark side effects,  at this point the constipation last week (thankfully resolved!!!) And mouth sores have been by far the worst. Going into round 2 next week I am going go try to be as proactive as possible to combat both of those. 

    Ohhh and i have to share this super yummy and healthy snack .... 

    - Chocolate ensure, ice, 1 cup chocolates fiber one cereal - blend that baby in the blender and it is a fiber and nutrient packed milkshake!! 

    Hugs to all

    Jen ;-)

  • LovebeingNana
    LovebeingNana Member Posts: 134
    edited April 2014

    I agree Sunshine…it is so hard for people to understand what we are going through, this group is like a port in the storm. Biotene mouth wash (and toothpaste) has really helped my mouth so no sores yet. Headaches have been my biggest issue. 

    I will say after the last 3 days (my worst days) I was really wondering how I am going to add more to this. I decided this morning I have to stop thinking ahead and just stay in today and work through what is on my plate today. It is so overwhelming to think about doing this 3 more times!! I can't go there. :(

  • lilyrose53
    lilyrose53 Member Posts: 216
    edited April 2014

    Hi All,

    I'm trying to feel positive today.  I am not having any awful SE's right now, except for a slight headache.  I will be alone this week, which scares me a bit.  But I will push on through with the help of my animals.  :) 

    Nana - I'm with you.  I can't even think about going through this again.  I have three more rounds of DD A/C, then on to 12 of Taxol.  ugh.  I'm already dragging.

    Sunshine - I have had the lovely constipation issue too.  All the nurses seemed to be worried about the opposite!  :)  Thanks for the tip on the yummy chocolate drink.  I am usually a chocoholic, but this past week I haven't been able to enjoy any food.  The only thing that goes down w/o trouble are those little red potatoes, boiled and completely plain.

    I am determined to enjoy this week, as I have NO scheduled Dr appointments or chemo!  Yay!

    Hugs to all,  lilyrose

  • HollyHope
    HollyHope Member Posts: 46
    edited April 2014

    Welcome Mompv!!  Linda is so right - everyone here really does understand what you're going through and we're all here to support each other. This thread has already been a huge help to me.  I have my good days and bad and also just cry for no reason.  I know it's normal...just hard sometimes for the people around us to understand as they just feel helpless.

    And Linda - your haircut story is the sweetest!! There are angels all around us.

    Sharon - your wild ferret comment made me laugh!  I found that a lot of the wigs I tried on had WAY too much going on with the hair in my face and just too much of it!

    Shellbell - sending positive thoughts your way and hoping it isn't as big of a deal as you thought.  Same for you on Thursday Janet.  I found the whole day to be very uneventful other than being sleepy.  The next 4-6 days were a little fluish feeling for me and then I snapped back to normal.  I pray it is goes smoothly for you both and hoping you are about to turn a corner too Nana!

    Cold - I am so glad to hear your feeling better!!  Enjoy your SE free days and hopefully round 2 is better now that you know what to expect.

    Well today is the day!!  I'm shedding so tonight after work my sister in law is going to buzz my head along with my son (10), daughter (7), niece (7) and nephew (4).  My kids were so excited about it this morning, so how could I not be excited along with them.  I've started to notice that without nose hairs I'm getting a drippy nose.  I'll be needing the warmth of my wig and scarfs as it's only now getting into the 60's and 70's here in WI.  My blood work from yesterday showed an increase in my white cells so - yay - I don't feel as vulnerable to infection!  When the nurse called to tell me I also told her about my mouth sores and she ordered me up the Magic Mouthwash and I have to say it's nice.  A lot better than the baking soda/salt wash I was doing and it really helped with the pain.  Have you tried that yet Jen?  

    Hugs to all my new friends and wishing you all something to smile about today!

    Holly 

  • Sunshine36
    Sunshine36 Member Posts: 88
    edited April 2014

    Holly - yes magic mouthwash!! Love it!!! My script says I can only use every 4 hrs , but sometimes do it a bit sooner. Love the tingling and numbinh

  • SharonDe
    SharonDe Member Posts: 222
    edited April 2014

    Hope everyone is doing well today.  I had a pre-chemo dental checkup and cleaning today.  They gave me a tube of "MI Paste Plus" to put on my teeth every night - it looks like it's primarily fluoride.  Guess I will need to check to make sure it's ok to use it.

    1st tx is Thursday.  I start the dexamethasone steroid tomorrow.  Thanks to all of your posts, I'm not so nervous about the actual chemo, but anxious about SEs.  Thanks for the tip on the drink, Sunshine.

  • ColdInCanada
    ColdInCanada Member Posts: 95
    edited April 2014

    Good Morning everyone! I woke up this morning with a clear head and very little antibiotic-induced nausea. Yay for feeling normal-ish! :)

    Holly: Please, please, PUH-LEEZE post a picture of your newly shaved head? I am so excited for you - I can not tell you how liberating it all was. Colder, but liberating. ;)

    Jenn: I am so sorry to hear about the mouth sores. That is the ONE SE I didn't get, but it was one I feared. I used Biotene mouthwash right from the start, and I'm a bit of a toothbrushing nut, so maybe that helped? Thanks so much for the chocolate shake recipe. My Mother-in-law is here to help out with Round 2.  She's a retired homecare nurse, and she showed up with a couple of cases of Ensure, and told me I was going to drink them ALL so that I don't "waste away" during chemo. I'm going to share your recipe with her and I bet she gets all excited about keeping my calories and protein up AND fighting constipation at the SAME TIME. :D Isn't it funny what gets us all excited nowadays? HA!

    Shellbell: I hope all is going well for you today! Keep us posted if you feel up to it. *hugs*

    Janet & Sharon: I'll be thinking of you on Thursday - already sending prayers your way! 

    Nana & Lily: I hear you about wondering how I'm going to put myself through this FIVE MORE TIMES. Ugh. I'm trying to just enjoy the good days when they come, and to let the supportive people around me help me through the bad days. I keep reminding myself that even though I will lose most of this summer, I WILL be around to enjoy a healthy, happy 2014 Christmas with my family - it gives me something to look forward to. :)

    Lily: I love your comment about not having any Dr's appointments or chemo this week. Today I am taking my daughter to her violin lesson, and I am SO EXCITED to be going out somewhere that is NOT MEDICALLY-RELATED! Again, the things that get us excited, right? :D

    chknfeet: Welcome! Sorry we have to meet with this, but you'll find lots of support on this board as we navigate this whole chemo thing together.

    Wishing you all a SE-Free day! 

    Nita

  • Blueberry4
    Blueberry4 Member Posts: 98
    edited April 2014

    Hello from the chemo suite! Today was my first day of AC and thanks to you all I was not nearly as nervous as I would have been. It's all gone smoothly, nothing hurt, but I did use my emla. I had blankets and pillows and snacks. I hope all the other first timers today did okay. 

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