April 2013 Chemo Group

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BeHereNow
BeHereNow Member Posts: 222

I didn't see a thread started for April 2013. Let me know if I missed it!



I begin chemo on April 1st. I've been telling myself it's no big deal. Then I got my wig prescription yesterday and it all became real.



We've got a challenging time ahead, but we have each other, and we will help each other stay strong.



My current, favorite saying:



"The absence of fear is not courage; the absence of fear is some kind of brain damage. Courage is the capacity to go ahead in spite of the fear, or in spite of the pain." ~ M. Scott Peck

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  • Moderators
    Moderators Member Posts: 25,912
    edited March 2013

    Thanks for starting the April thread Katie!

    Just stopping in to provide some more helpful links, starting with the main Breastcancer.org site's section on Chemotherapy, including what to expect, types of chemo meds, and side effect management.

    There are some really helpful key threads here in the Chemo forum too!

    Great tips and practical advice on the following discussion board threads:

    Also, Last Month's Chemo thread might be informative!

    Hope you find this helpful!

    --Your Mods

  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    Thanks, Moderators! You rock :D

  • tksteele
    tksteele Member Posts: 7
    edited March 2013

    Hi Katie,

    I start chemo 4/1/13 and I have to say it's scary. I have all kinds of feelings about this. But it is one day at a time.

    My sister is going with me this week to get a wig. I was told by a friend to shave my head myself or have someone do it for me. That way I have control and not the cancer.  I'm not sure how this will go. 

    I have been reading the other threads and they have been very helpful on what to stock up on and other advice.

    I had my port surgery yesterday and it went well. Everything seems to be a wirlwind of info and speeding right along. It's very scary. I would like things to slow down a  little.

    I am starting back at the YMCA next month. I like the yoga class and the walls are closing in on me here at home. 

    I have good and bad moments. I started a journal a friend that had cancer said this really helped her.

    Keep in touch.

  • Deyla7641
    Deyla7641 Member Posts: 98
    edited March 2013

    Hi everyone! This is going to be my second time through chemo. I did neoadjuvent ACT first time around last July. I start Ixempra coupled with Xeloda April 1st. Some April fools huh? Wishing everyone the best of luck! Deyla

  • Jen987
    Jen987 Member Posts: 145
    edited March 2013

    I start chemo April 1st also. I wish everyone well.

  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    Wow--we all start April 1st!



    Tksteele- my sister and I are going wig shopping on Saturday. I signed up for yoga for BC patients. I know it will help. The emotions are overwhelming at times, and I am very nervous. I'm glad I'll have some friends here to help me!



    Della- you've been through a lot! I wish you good luck, as well.



    Jen- welcome. Here's to an easy time for all of us!



    I bought 2 CDs today -- guided imagery for chemo patients. I'll report back about those.



    Goodnight, all!

  • kobrien
    kobrien Member Posts: 82
    edited March 2013

    I don't have an exact start date- but have my chemo teaching on 3/26 and will get my start date then.

    I have stage 2 IDC- multifocal with micrometastises to my sentinel node.

    I had a L masectomy with TE on 2/27.

    I am very scared of doing chemo.

    Kerri

  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    I am going to a chemo class today. I feel scared, too!



    Hopefully this will be a lot easier than we fear. One moment at a time!



    I am trying to get myself to start journaling to help with my emotions. There is research that shows that writing out what you're thinking and feeling about something actually improves your health. So I want do it!



    XO to all!

  • Jen987
    Jen987 Member Posts: 145
    edited March 2013

    I cut my hair really short today so when it falls out it won't be so traumatizing. It took 6 minutes to style it. So far I like it.



    I go get my port put in on Monday. Another battle wound.



    Katie: How was chemo class? I haven't gone yet.



  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    They cancelled it! I will get a private session this week. I'm a bit disappointed!



    I got a wig today. On April 16th, I go back and they'll cut my hair and use it to make a fringe under a hat.



    So I won't be getting a short haircut before that. Oh well, that would have been kind of fun!



    I'm glad you like your new 'do!

  • Sunday1856
    Sunday1856 Member Posts: 19
    edited March 2013

    Thanks to all of you for being out there and willing to share your experience. I was diagnosed in 1998 with DCIS and had a double mastectomy and am now diagnosed again with a cancerous lump on my chest wall.  I had a lumpectomy and the margins were clear.  My chemo begins on April 3rd with port placement later this week.  I am HER2 positive and will have 6 chemo treatment and Herceptin over an 18 week period.  Once the chemo is done, I will continue with the Herception infusions every 3 weeks until April 2014. After that it will be 5 weeks of radiation.   I am really struggling with the thought of losing my hair and do plan to take control and shave before it starts falling out.  I will be wig shopping this week.

     Again, thanks for being there and will look forward to future posts.

  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    Hi Sunday1856! I'm sorry to hear about your new diagnosis, but I'm glad you're here for support. Keep us posted on your progress.



    I'll report back after my chemo "training" tomorrow. Take care

  • tksteele
    tksteele Member Posts: 7
    edited March 2013

    Hi everyone, 

    Well I did it, I shaved my hair off. I have a wig, it's not the best but it will do for now. I will order another one next week.

    While I have the energy I am going to fix and freeze as many vegan meals as I can and put in my freezer. I have alot to do this week before I start chemo on April 1. Im sure you all do. It seems overwhelming at times. So I just take one day at a time and breath. 

    Keep calm and Fight on!

  • Deyla7641
    Deyla7641 Member Posts: 98
    edited March 2013

    Good for you tksteele! This is going to be my second time though chemo so i'm just gonna shave my head too before it starts to fall out on its own. Good luck with your treatment! I'm starting April 1st as well. Deyla

  • Sunday1856
    Sunday1856 Member Posts: 19
    edited March 2013

    I will look forward to hearing about your class.  This is really overwhelming!  So much info to take in and no way to know how our bodies will react.  Also, I am single and have a wonderful group of friends and family for support, but am so afraid of being a burden to them.  Appreciate this site so much!!

  • Sunday1856
    Sunday1856 Member Posts: 19
    edited March 2013

    Good for you!!  Any advice about purchasing a wig.  Also did you completely shave your head?

  • sarilda
    sarilda Member Posts: 4
    edited March 2013

    Hey everyone,

    (very new to the site and the forums)

    Guess I am part of the April club too.  I start chemo on April 4th. My teaching appointment is the day before.  I bought a wig (will be picking it up tomorrow). I cut my hair shorter, and will probably shave it a few days.  I know they say it is about controlling, and that is true, but it is also about not having clumps of hair all around your house. Smile

    Chemo scares me more than the surgery did (I had mastectomy/sentinal node dissection with reconstruction in February).  I will have 4 sessions two weeks apart, followed by 12 sessions 1 week apart, and Herceptin every 3 weeks for a year. Possibly also Tamoxifan in there somewhere too

    I had my port implanted on 3/21. I am still healing from that.  There are some really weird sensations from it.

    I wish courage and strength to everyone on this ride.  Together we can help each other through.

    Sarilda

  • indenial
    indenial Member Posts: 504
    edited March 2013

    I am starting April 10. Only doing 4 rounds so I'm not getting a port as long as my veins hold up. (A little worried because all the good veins were in my off-limits arm!) 

    Had my chemo teaching a week or two ago. It was an hour+ long session with the Nurse Navigator, listening to all the horrible side effects and how to deal with them and stuff. It actually wasn't too bad, and I felt really prepared with all the reading I'd done, so I didn't have many questions. I also got a tour of the infusion floor... not crazy about it, so dismal! Glad I'll only be going there 4 times. :) 

    Sunday1856 - I hear you about being a burden to friends & family! I have zero family support (aside from my husband and my young son), but I do have a small but amazing group of friends. However, they are all going through really serious struggles of their own. It's hard to accept help from them and even harder to actually reach out for it. I'm not sure how that will go during chemo. Guess I'm hoping to be one of the lucky ones who are able to work right through ("work" in my case means parenting my intense son without help, I'm a stay-at-home/homeschooling mom). People from my church have also offered to bring meals but I have some food restrictions & feel like it may be asking too much of them. I don't know...

    I have been trying to decide when to shave my head and I think I'll do it immediately after my first treatment. I don't want to give it a chance to fall out on its own. I'm almost tempted to shave it before the first round just in case I'm too sick to do it after, but I just don't think I have the guts to do it!

    Next thing I want to work on is deep-cleaning the house (hard right now since I'm still recovering from my BMX) and freezing some meals. 

  • indenial
    indenial Member Posts: 504
    edited March 2013

    Just wanted to share that I just received a beautiful scarf from http://goodwishesscarves.org/ They'll provide you a free wrap & there are some gorgeous choices! Money is really tight in my house so it was very much appreciated. I'm not getting a wig and I'm actually excited to wear this scarf!

    Also, there is a site called http://www.chemoangels.net/ where you can sign up to have 2 volunteers send you notes throughout chemo. I'm sure we can all use all the support we can get! 

    Look Good, Feel Better is another free program where you can get help with makeup, wigs, etc. and I think they give you a free makeup kit. I haven't gone (I'm not really into makeup) but thought others might be interested. http://lookgoodfeelbetter.org/

    Anyone else find some good resources?

  • kirklandgal
    kirklandgal Member Posts: 63
    edited March 2013

    Looks like I am joining the April chemo group.  I will be starting chemo on April 3 - only 9 days away.  It's all very scary but I think it will help to have others to go through it with!

  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    Hi all, and welcome to those who have just joined us! I am so glad I'm not alone, but sorry we all have breast cancer.



    My chemo class was great. It was just me, my husband, and the RN. The nurse covered all the side effects and how to prepare and/or deal with them. Most of what he covered, I knew. But there were some surprises I'd like to share. And please chek with your doc for any medical things you want to try!



    1. Some people prefer getting a really short cut rather than shaving their head completely. Apparently the wig can be less itchy and uncomfortable if you have a little bit of hair and no stubble.



    2. Saltwater rinse after each meal and at bedtime can help keep mouth sores away (and no baking soda is needed--research shows salt water works just as well.



    3. To avoid bone pain with neulasta, take Claritin the day of the shot and the day after.



    I went to a wig store and tried a lot of them on. The American Cancer Society in your area may have free wigs. My insurance covered about 2/3 the cost of my wig.



    Also, I'm going back to the wig shop for my haircut, because they are going to take my hair and attach it to a band I can wear under a hat -- they called it a fringe. And it will be made of my win hair!



    More later :)

  • Skigirl72
    Skigirl72 Member Posts: 478
    edited March 2013

    Hi ladies I just wanted to jump in and give you some encouragement!

    I just finished 4 rounds of AC (every three weeks) and I start Taxol on April 1st. I didn't have nausea/vomting with AC. I took the meds just as they said and I was not sick. Some side effects are unavoidable. I lost my taste buds for a few days, my hair started to fall out at day 14. I had a few solid headaches. I had a few days of fatigue.  All of it was managable. I went back to work the week of the 3rd treatment. Just part time but I did well. The docs and nurses are really good at keeping the side effects managable.

    This is doable. There are so many things I learned from the others on the Jan chemo 2013 thread. Use eachothers knowledge, experiences, ask LOTS of questions on here. I'm just going to give you the things that were a must for me...

    Stay hydrated- I drink 3 liters of water a day. Dont let yourself get dehydrated.

    Take a stool softner- I added colace to my pills on the day before treatment and until the day after I stopped the nausea meds. Constipation is a nasty one.

    Rest- Get lots of rest. Ask your MO for something to help you sleep. I took Ativan. Worked like a charm.

    Neulesta shot- A lot of the ladies in the Jan thread reported possible bone pain with the neulesta shot. They took Claritin to ward off the pain. It worked for most of them. I am not sure of the dosage or timing but I'm sure it can be Googled. I didn't have to get that shot.

    Anyway, like I said earlier, this is doable. You will have bad days and good days. I chose to celebrate the good ones and accept the bad ones. Before you know it you will be looking back on this and it will be a distant memory.

    Good luck to all of you. You will get through this and be on the other side before you know it. I couldn't have done it without the others on the Jan thread.

    I wish you all happy days!


  • erinm216
    erinm216 Member Posts: 126
    edited March 2013

    Hi All,

    Add me to the list of the April Chemo ClubFrown

    Not happy about it all and and am completely overwhelmed. 

    But hey, this to shall pass right?

  • Sunday1856
    Sunday1856 Member Posts: 19
    edited March 2013

    Isn't it amazing how important it is for us to feel in control and to remain independent?  Sending hugs your way.  Keep in touch!

  • Sunday1856
    Sunday1856 Member Posts: 19
    edited March 2013

    Thanks so much for the tips and encouragement!  I am consumed by the need for information and greatly appreciate your message.

  • BeHereNow
    BeHereNow Member Posts: 222
    edited March 2013

    Skigirl72--thank you so much! The encouragement is really calming to me :D



    Welcome erinm216!

  • AllieM
    AllieM Member Posts: 44
    edited March 2013

    Hi all,

    Going for my "chemo class" tomorrow. I'll probably be starting next week but not sure. I really appreciate all the pointers people have shared. It really does help to feel you have some degree of control - however slight.  Good luck everybody!!

  • tlbradyful
    tlbradyful Member Posts: 134
    edited March 2013

    I start TAC chemo on 4/4. My doctor suggested Claritin 2 days before shot and three days after (includes day of shot), so 5 days total. I haven't tried it yet, but will let you know next week.

  • tlbradyful
    tlbradyful Member Posts: 134
    edited March 2013

    I'm going the April Club too. I have had so much advice it is almost overwhelming. It is nice to hear from those who have been right here. I will be having TAC once every 3 weeks, 6 doses.

    I cut my hair really short to help adjust to seeing myself without my normal hair. So far, it's still sad. I bought a wig that I am reasonably ok with and got a free one from American Cancer. It is beautiful real human hair and it is one length so your hairdresser can cut it into your old style. I will use it for special occasions only because you have to style it like your own hair. It is donated by Pantene.

    I attend the Look Good Feel Better seminar and it was a helpful reminder of how bacteria spreads through makeup and showed me how to draw on eyebrows and put on a wig. It was worth it. There were lots of free samples of products I haven't tried, but found interesting. It was also nice to meet women at the same stage as I am.

    Well, here we go. I'm pulling for you all.

  • kobrien
    kobrien Member Posts: 82
    edited March 2013

    I had my chemo class today with the nurse practitioner. She was helpful. I start my chemo April 15th and am very scared..

    I've been reluctant to do chemo from the get go, but I know that doing it will only give me the best possible outcome in the long run.

    I emailed my MO yesterday because I had a few questions- she went out of her way, came to the office where I was having chemo class and sat down and spoke to my husband and I again. She had a meeting to go to- but didn't rush me and didn't leave until I felt comfortable that my questions were answered.

    I feel very happy with my breast surgeon, plastic surgeon ( he's my favorite! ) and my oncologist.. I'm feeling a little better about doing the chemo.. And having all of you on here to talk to helps ALOT!

    Kerri

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