Chemo May 2013

Options
24567103

Comments

  • lpc
    lpc Member Posts: 303
    edited May 2013

    Ljaeger I have only had one fill so far. I usually just use a bra bs gave me with pocket for stuffing. Not pretty but is comfortable. Wig I chose no longer made so just went to pick another...not easy to find one I like.



    Hubby has been wonderful as have kids. I am used to being in control.

    Learning slowly to give up control and lean on others.

  • okiecountrygal
    okiecountrygal Member Posts: 25
    edited May 2013

    I'm 44.  Just came back from the lovely chemo education class.  I'm not sure on the 6 chemo sessions but if I can handle them, then the way I look at it that will be more fight against the cancer.  Just dreading all the changes.  The onco nurse told me yesterday that I need to not dread treatment but look at it as this is what I'm going to do so that I can beat this thing.  It is hard not to dread it tho.  Especially the unknown.

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited May 2013

    LJaeger,

    I will be having my chemo at MKMG in Northern Westchester hospital.



    The women from look good feel better had 3 bins of wigs.

    They were able to find something similar to my very light blond hair.

    I was a little unhappy about the length...as it is my old shoulder length hair, and I've already gone short, so it is not "realistic" To walk out the door with long! However, I am not going to say no to something...I just don't know if I will use it. It will be HOT out soon and I am one of those people that is warm in the winter and burning up in the summer!



    I had seen some videos on headscarves and need to practice, in fact I just wrapped my head and am sitting here with one on. My kids like it.



    I had found some nice scarves in target. Was sooooo glad I took them to the fitting room to wrap my head because what looked good in my hands look horrid on my head! I did get some that looked good on, but originally I had ruled them out, go figure! I also popped into goodwill today to see if they had any scarves and I scored TWO for $5. I even tried them on, and was VERY happy with them.



    There is an organization that will mail you a FREE headscarf. You can check them out at www.goodwishesscarves.org. Or call them at 888-778-5998. They had a nice selection. It says up to two weeks before they ship, but I got mine fairly quickly.



    I can't speak in regards to those with fills, I don't have them, I hope in time the pain decreases for you. I am sure there must be a board for that, there seems to be a board for everything!



    Pat

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Hello Everyone, I guess I am a lucky part of this group as well. I start my chemo T/C X4 tomorrow morning (5/2)! I cannot lie I want to get this started so it will be over! But I can imagine myself having a panic attack before they put in the needle! My Hubby will be with me all the way, He is the best! I got my hair cut short yesterday to try to prepare for what is coming. My onc said my eyebrows will more than likely stick around! Yea.. Anyone else hear that? That is something right!

    TE ladies, I am petite only 5'2" and slim, my fills got increasingly more painful as they went but for only about 3 days. I had three and am done. My PS said it was because the TE's are up against my breast bone and my ribs that they were painful. I have very little pain now and have good range of motion. It was worth it....No more underwires, I can just wear a Cami and am good to go. 

    I hope Chemo goes well for everyone...I did not get a port so I hope my veins hold up....The pre steroid regime is giving me the jitters big time.. guess I will not sleep alot tonightCry Thanks to all who posted, I see many of you will be with me tomorrow as we start out first dose.  Good luck to everyone and hope for very limited SE's.  BTW anyone getting Neulasta the next day? They told me to take Claritin before I get the shot....weird.

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Rose57 My MO said that I would be tired but would not need help caring for myself. Hope that helps you feel better. I guess we will all see...Good Luck and remember you are not alone...

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited May 2013

    Gully,

    I have read on the board here that Claritin was used in a study to see if it prevented bone pain from the Neulasta shot. Apparently it does. Unfortunately my onc does not put it into her regiment, but I will be (she said I could do it if I wanted). She said the bone pain is rare and not bad. I'm thinking there is no way in heck I want to find out how bad it is should I be e one to get it!

    From what I have read on the boards take it the morning of the Neulasta shot and for 6 or 7 more days after.



    There are plenty of other hints that are on the boards my onc doesn't do. One is ice chips during taxotere...I checked with the nurses today and there are ice chips where I am having chemo, so I don't have to being my own...I will be doing that too!



    Wishing you all the best.

    Pat

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Thanks Pat! I will be sure to do that. Just called him up.....My MO said he has been suggesing patients take it for a long time. He swears it works and that the bone pain, especially in the hips and long bones of the legs where blood cells are made, will feel like an overextended water balloon as blood cells that are made build up and can be quite painfull until the cells gradually get out into the blood steream and relieve the pressure. He said I should not suffer if we can stop it.Cool

    I am stopping at Duncan Donuts in the AM and getting the largest fruit smoothie with crushed ice that I can....MO said it can help ward off mouth sores... I asked about Ice on the hands, or feet to prevent peripheral neuropathy...he said no, because the cancer cells can come back on the scalp, hands, or feet as well and that if we are going to do this we will do it the best way we can to avoid recurrance.

    Also, anyone land in Chemo because of an Oncotype DX score of 19, one digit higher than the low risk group, what a terrible decision to make for everyone with this score including me...just knew it would be me that landed at that schore... I am 46 and considered young still for BC...he said because of my age and fitness before BC that we should hit it with both barrells and do the Chemo lite, not sure if there is such a thing! I have twins at home still so I want to be around for many more years....so I said yes to the posion!

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited May 2013

    Thanks Gully,

    I like the idea of the fruit smoothie. I was thinking of going to 7-11 for a cherry icee, but realized that people might be getting the "A" in their treatment, I've heard it referred to as the red devil, and I didn't want to seem insensitive!



    My onco wouldn't do the oncotype score, she said regardless of the outcome she would recommend the chemo due to the pathology of one of my tumors. So I don't know where I would have scored, but knowing my luck it would have npbeen a 19 like you! Lol



    I am 47, and would like to be here to watch my kids grow up, youngest is 10. So I "don't mind" the chemo....if that is something one can say!



    Pat

  • JennaJMU
    JennaJMU Member Posts: 97
    edited May 2013

    I'm doing dose dense because I'm part of a study and this is the regimen and also because I'm 33 so I'm getting hit with the heavy stuff! Yuck!

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Thanks! for all the replies. I will be thinking about you tomorrow and feel less alone in all of this scary s$#%. At least when we are finished we will know that we have done everything we can to ward off recurrance and stay around to see out kids grow up! My twins are 14 and they are worth it and so am I!!! And so are you!!! There are no clear answers, but I can tell you after my decision was made I felt better.  If it comes back I will not be able to kick myself for not doing the chemo and possibly living because of it. I wanted no regrets. Lets talk tomorrow and see how things went for everyone. I heard the Taxotere is worse for side effects than Cytoxin, will let you know. Hugs to everyone!!!

  • lpc
    lpc Member Posts: 303
    edited May 2013

    Good morning May 2nd girls. May we all sail thru today with ease and grace. Hope out ses are few and anxieties lessen. Good luck to all!

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Good Morning May 2nd ladies! I hope you slept well, I got about 5 hours. Packing my kindle, cooking magazines, blanket, nausea meds, just in case and a fleece blanket and last but not least my Gauardian Angel key chain. Good luck everyone! Hugs!!!! Signing off....Time to jump in with both feet!

  • Rose57
    Rose57 Member Posts: 11
    edited May 2013

    Hi Ladies,

    I just wanted to wish you good luck today! I was suppose tp be joining you today but when I went in for education on Tuesday they had changed my start date to yesterday; whic was fine except my son couldn'tget home to go with me!  Anyway I just wanted to let you know it was not a terrible experience no side effects with the Taxotere only a minor fuzzy head (kind of like a blocked sinus)the last few minutes of cytoxin.  The nurses were such great people so on top the their game!  Afterwards we went and had a nice lunch then to the surgeons to have my new best friend Eleanor checked out that was what I decided to call my port since it was an amazing experience not to have to be poked! Would never have made it through without her.  So far very few side effects being wired from the decodran and not being able to sleep that was expected.  Also the dry mouth has started and a few chills.  They told me I would be good until Friday so looking forward to a good day,

    Good luck to day and stay POSITVE!

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Thanks for the note Rose57! Maybe I can work my way out of my forming panic attack now! Hoping I can post a positive note later today. Infusion starts at 8:45! 

  • JennaJMU
    JennaJMU Member Posts: 97
    edited May 2013

    Good luck to all of us today! Gully, I'm in the middle of a panic attack too! I'm already so nauseous from nerves, maybe I won't notice the chemo effect...

  • Jen987
    Jen987 Member Posts: 145
    edited May 2013

    Sending good thoughts to all the girls having their first cocktail at the "chemo bar" today. Drink lots of water and rest when you feel you need it. Rinse your mouth out with 1/4 tsp. Salt, 1/4 tsp. Baking soda and 1c. Warm water a few times a day to avoid sores. Take your meds to stay ahead of the nausea. Go for walks if you can to keep things moving.



    You can do this. Stay strong.

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Jenna, LOL! Me too. Maybe we could ask for some of that Happy Juice they give you before surgery! 

  • LJaeger
    LJaeger Member Posts: 58
    edited May 2013

    Good luck today, Lpc and Gully! I know you will manage well, and what a great idea to have a nice lunch afterwards, Rose! We certainly deserve a treat for going through this.



    Jenna - I'm 31. Sounds like I may be a candidate for dense dose too.



    All in all it seems like all of us here are strong healthy women, and they are going hit us hard with this chemo. But we will make it through.



    I am amazed at all the mothers here who have young ones at home. They certainly prove the best reason to fight like there is no tomorrow, but I can't imagine having to be a caretaker for someone else right now. Cheers to our partners who will hopefully step up with strength.

  • LJaeger
    LJaeger Member Posts: 58
    edited May 2013

    Wow, I reread back to the beginning of this thread, and so many ladies are starting chemo today. I didn't quite remember that! So good luck to all! You can do it.

  • Ukkate
    Ukkate Member Posts: 292
    edited May 2013

    Good luck ladies today - I will be thinking of you!!!

    I'm 42 I was diagnosed 3 days before my 42nd birthday and my kids are 13, 11 and 6 and I work full time and DJ on the weekends. I've already had a gig and have 2 more before I start chemo!! Wishing you all an easy day with very few side effects xxxxx

  • lpc
    lpc Member Posts: 303
    edited May 2013

    To quote tom petty...the waiting is the hardest part. Waiting for bloodwork to come back before real stuff can begin. Thank God for xanax kindle fire and hubby!

  • debbiema
    debbiema Member Posts: 34
    edited May 2013

    So glad to see this thread started.  Im starting my chemo t/c x4 on May 15th!  I'm 44 and have two kids 10 & 7.  I'm nervous but just like others very anxious to get this started. The sooner it gets started, the sooner this leg of the journey will be over.  Going to cut my hair in a couple weeks, which I think will be the most traumatic!  I have long hair and so need to get passed the vanity or lack thereof that's to come!  I live in West Chester, PA and am going to U of PA hospital. Anyone else out there???  Keep in touch ladies and continue to stay strong.  We will all get through this!!!

  • JennaJMU
    JennaJMU Member Posts: 97
    edited May 2013

    I'm being infused right now! Made it through the red devil, now getting my Cytoxan infusion! Little bit of sinus pressure with that but no big deal. So far it's a lot better than I thought! KNOCK ON WOOD!!

  • lpc
    lpc Member Posts: 303
    edited May 2013

    The red river about to flow.

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited May 2013

    Debbiema, I cut my hair from shoulder length to short, "pixie" cut. I almost cried, and I am not "vain"...I am a wash and go person, no fuss no muss. First time I picked up my daughter from school I guess no one recognized me? And I know there were a few that did...the silence was deafening. It hurt.

    Anyhow, went to a look good feel better program from the American Cancer Society and they give free wigs. Got one, but is is shoulder length....which is ironic, as I now have a pixie cut. So now everyone will know it is a wig.

    Can honestly say I don't know I will wear it, as I am always hot and summer is coming quickly.....

    Anyhow, I share this as you might want to try out short to see how it is before you go bald (if anticipating that). Or you might want to find a wig you like and try cutting your hair to that style....then no one would be the wiser if you shaved your head and wore the wig. Me, I'm ready to go find wigs in different colors and drive the family crazy! Lol



    Wishing all the patients today the best. I will be joining you on Monday. You are the role models for us all! God Bless!



    Pat

  • dbc4506
    dbc4506 Member Posts: 1
    edited May 2013

    I don't know How to help my 92 year old Mom.  She had Modified radical masectomy last month and seemed to be doing well.  Then at first appt. with the Oncologist yesterday he slams us (Mom, my sister and I) with how she had 7 lymph nodes of 8 with cancer too.  Dr. would really prefer to do Chemo too, as part of treatment.  ( A treatment every 3 or 4 weeks with a total of 4 to 6 treatments?) but my sister and I fear it would just make for a horrible quality if life.

    The Dr. did back off and say he could go forward without chemo very quickly when I questioned him about illness, her possible endurance, etc. as I am her health Care proxy.  But now I wonder if I am limiting my own Mother's longevity.  She has some short term memory issues and seems overwhelmed by all this, so I fear pressing for a bad solution.  But I also fear we'd stress her so hard physically that she would prematurely lose even more brain function.

    Is there anybody out there who has gone through this that can offer a layman's experienced advice?  My brother in law endured chemo at the end of his life and told me he would never agree to go through that again.  I just don't know where to have a common sense sort of dialogue to help with me and Mom's dilema.

  • Pattysmiles
    Pattysmiles Member Posts: 954
    edited May 2013

    Dbc, I am so sorry you have to deal with this.



    Has your mom ever spoken about her wishes in the past?



    My dad was hospitalized after cardiac surgery, he had always made it perfectly clear through tout his life that he never wanted life saving measures. He thought it was a huge waste of money that would be better spent by living relatives! (And we aren't well off) He received typical care.

    He was better, released from the hospital and relapsed within a month. This time there was nothing he would allow, as they spoke of possibly dialysis might help him.



    It was very tough to follow his wishes...what if dialysis worked? And then another surgery for his heart? My dad heard the doctor talking to us, opened his eyes, stared at each of us and told us "NO GUILT, this is what I want". He was 72 when he died two days later. I have no guilt as I know he had his wishes followed.



    These decisions are so difficult to make. Even knowing his decision I had wavered, but in the end followed his wishes.(I was his proxy)



    If your mom has never made her wishes clear perhaps you need to sit down and weigh the pros and cons of the situation, without putting in any emotion (I know, easier said than done). List the choices on two pieces of paper with pro and con columns. Treatment vs. no treatment. You might even want to go back to the doctor without your mom there to discuss this. Do they say how many years treatment might extend her life! What about the side effects at that age? Have your sister do her own pros/cons papers as well. Then compare notes to see where you stand.

    There are so many factors that need to be take into consideration...when you see it written on paper it might jump out and make perfect sense.



    My prayers are with you at this difficult time. There will never be an easy decision to make. Don't involve the whole family in the decision making as there is always bound to be a loud mouth that "knows better"...my twin that lived out of town was one of them.



    Pat

  • Gully
    Gully Member Posts: 268
    edited May 2013

    Ok Ladies,,,looks like things are going well for everyone so far. My appoint was at 845 walked right in, did vitals, inserted the port in my arm, infused the Happy juice, a bit of steroid, then taxotere for 1 hour and Cytotax 30. Everyone was supernice and my MO came back to chat a bit. Out the door at 11. My hubby and I did go out to lunch after and it was quite nice. Feeling sleeping from the Happy juice (IV Ativan) think I will take a nap before the twins get home from school. I hope everyone else who started today had a good experience. It was alot better than I pictured it would be.Cool Time will tell now with the SE's

  • LJaeger
    LJaeger Member Posts: 58
    edited May 2013

    Lpc, Jenna, and Gully - you are amazing! You're going to be done with your first round today. 

  • debbiema
    debbiema Member Posts: 34
    edited May 2013

    Thanks Pat!  Very good advice!  I'm going to get my haircut (thought about a pixie cut too), but will have my wig in hand!  This way it's not too noticable, however, I think (or at least hope) when I am at that point that I won't give a sh*&! what other people think!  I believe the trauma will be more for others than myself. I keep reminding myself that this is all temporary!!

    Gully - so glad to hear how well your appointment went.  I look forward to getting to that point!  Please keep me posted!  You must be relieved that round one is officially complete!

Categories