2005 ROCK-TOBER CHEMO GIRLS

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  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    I just ordered one from www.paulayoung.com. Lots of cute styles and colors. And, you can return it if you don't like it. I measured my head to know the exact size and then ordered 5 different styles. I plan on keeping the one I like best and returning the others. The ones I chose are real similiar to my current hairdo, because I just kind of want to look like me! Good luck to you!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005

    Okay, you may laugh buuuuuut...you can buy disposable face masks at any pharmacy or even the first aid depts. at food stores. I am going to have some on hand (I start chemo on Oct. 26th) just in case. I laugh when I think about the looks on the faces of my family or friends when I answer the door wearing one!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    Ladies,
    My doctor wants to know if I want to be part of a study that would use mammosite radiation to irradiate only my lumpectomy section. If you have had any experience with this, please let me know. I need your input right away!!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    Hi Laura,
    You're probably right about the number of infusions. I will only get 4, spaced between 3 weeks. I believe I will get Adrymiacin and Cytoxin. Then I rest for a month, followed by 6 weeks of radiation.
    The study nurse called me today, though, asking if I want to be part of a study where I may be able to get my radiation in 5 to 10 days! I am trying to find out as much as I can about it.
    I have a 2 year old Scottie named Angus. He always has this pensive look about him. He rarely barks, rarely wags his tail. He loves strangers that he meets during our daily walks.
    Good luck to you too!
  • TracySeattle
    TracySeattle Member Posts: 690
    edited October 2005

    Jane - I had my chemo class this past Monday. A lot of it I already knew by being here and reading books. It was good to see where they actually give the treatments,etc. The antibiotics really helped the infection, I felt much better this morning. I have rescheduled Wig shopping for Monday afternoon!

  • AnnaM
    AnnaM Member Posts: 1,387
    edited October 2005

    Thank you, Calico. I saw two oncologists yesterday and they said A/C x 4, followed by T x 4. They both wanted receptor testing done on the positive nodes, I wish the final pathology report would get done. They differed on two points: one was for dose-dense, the other against. Also, one wants PET (?) scan, the other CT with contrast and bone scan. I just don't know how to choose the right course here. It's all so new to me. I will start chemo in 3 weeks, and now I guess I should start thinking about wigs and stuff. I feel so hopeless.

  • oldsambvca
    oldsambvca Member Posts: 22
    edited October 2005
    Had my first AC on Tuesday . . . knocked me right on my butt! Zapped every bit of energy I had. Went to work for about 2 hours on Wednesday, not at all on Thursday. Hubby drove me in today and I brought a blanket for napping. Fortunately, the nausea has not been an issue - meds are working well.

    Hope all is well with everyone. Hang in there!
  • ake
    ake Member Posts: 684
    edited October 2005
    Amina,

    I had a PET scan and CT scan with contrast...not a big deal...it was just more tests to know exactly what was going on in my body. It was definitely scary to wait for the test results, but so worth it to know that there is nothing bad inside me right now. All these tests are anxiety-provoking, but there's such a peace of mind afterwards.

    I don't know about dose dense vs. not...I start my chemo next week and it is dose dense...8 cycles every other week. I heard from other women that sometimes dose dense is better...it's more aggressive (and what's wrong with that?) and it's over quicker.

    I felt hopeless a lot too...I know what works for me is to find the things that I can control. Like the whole thing with wigs...I'm shaving my head with my husband a week after the 1st chemo treatment because I refuse to go through the worrying about the hair falling out. I just can't go through that psychologically, so I'm doing it first. I bought my wigs last week because I want to be prepared before chemo starts. Find little things that you can control and you will maybe not feel so hopeless. Even with the path report (it's god you're waiting for the receptor stuff)...I bugged my surgeon every day until she finally gave it to me.

    The waiting is the worst...once everything is known, you will feel hopefully better. I felt a calm once everything was known and treatment was decided and things were scheduled. And trust me, I've been anything but calm since diagnosis!

    Hang in there!!!
    Amy
  • AnnaM
    AnnaM Member Posts: 1,387
    edited October 2005
    Amy: Thank you so much. I will look for the little things I can control. I like the thought of shaving my head; I will plan to do that. I have never liked my hair and now I think it's so beautiful all of a sudden. Just like I never gave a second thought to my breasts and now I miss them so bad. Gosh, were they beautiful! I know I will grow accustomed to what I have now, but everything feels so horribly numb and heavy, and the backs of my arms hurt when anyoune touches me. It just came so fast! I haven't had time to catch up.

    Where did you get your wigs? It looks like you are near me; I live in Leesburg, VA.
  • kapensy
    kapensy Member Posts: 21
    edited October 2005
    I had first chemo one week ago and had dull headache for several days (even a little today). I didn't call my nurse, but if you are at all concerned about anything, ever, during your treatment, you should call. There is absolutely NO stupid questions during this! My cousin and daughter are nurses, so I have extra support and they tell me to call about anything I'm uncomfortable with, even if it seems dumb. And my chemo nurse is a friend from high school and she said the same thing. So if you are concerned about the headaches - call. You don't need the stress of worrying about it. That will just cause more problems! :-)

    Good luck!!! God Bless!!
  • TracySeattle
    TracySeattle Member Posts: 690
    edited October 2005

    For those of you looking for wigs. I just called the American Cancer Society in my area so that they could recommend wig stores--which they did, but they also told me that the American Cancer Society provides free wigs to cancer patients. Some are used (cleaned & styled) and some are new. You just have to make an appointment to go there and they will show you what they have. I figure I will combine it with my wig shopping on Monday....

  • TracySeattle
    TracySeattle Member Posts: 690
    edited October 2005
    Sherryhaire - I can't find hip-hats.com. Is there more to the web address? I really want to see those hats! :-)

    Thanks!
  • gzl3mx
    gzl3mx Member Posts: 1
    edited October 2005
    Hi everyone,
    I'm not sure if I'll be starting chemo in Oct or Nov. I had 6 tumors ranging from 1mm-7mm on my right side. I opted for a bilat done 9/19. My appt with my onc. is for Oct 18 and I guess I'll find out then what is instore. I had no node involvement and the tumors were a combo of invasive and DCIS. I had found the lump on my own and neither the mamm or ultrasound could ID the tumors. I'm so tired and I feel like I've not even started.
  • ake
    ake Member Posts: 684
    edited October 2005
    Amina...I went to Crown Wigs in old town (they have a website...www.crownwigs.com i think). go on a saturday and have the woman, grace, help you...she totally gets it and is amazing. it's on king street and s. washington....let me know if you have any questions!

    -Amy
  • ruths2
    ruths2 Member Posts: 78
    edited October 2005
    I had my first AC last Friday, Nulasta on Saturday and today when I went for followup blood work my white count was really low (1.8 when normal range is 4.5-10.5). They said no work or public places until it comes back up. Is this common? I have been feeling really good and had no "symptoms" to indicate this.

    I cried more about being told I couldn't go to work today than anything so far. Hopefully the Nulasta will do its job before my treament next Friday (dose dense, every two weeks). I'm trying hard to "stat in the moment" on this.

    Ruth
  • Calico
    Calico Member Posts: 1,108
    edited October 2005
    Welcome to this board!!

    Good thing for breast self exams!!! You find this a great place to be! Remember, one day at the time , it is hard.

    It helped me a lot to be on this board as well as read through the entire www.breastcancer.org site as well.

    Ruths,

    they told me it could go down even more, lucky me not yet....just be extra careful

    Hope everybody continues to have a great day!!

    God Bless
  • sherryhaire
    sherryhaire Member Posts: 192
    edited October 2005

    Tracey just type Hip Hats it should come up it is really neat

  • TracySeattle
    TracySeattle Member Posts: 690
    edited October 2005

    I found Hip Hats! Thanks! I got a wig today! My husband and I stopped off at a wig shop on our way home from work. I tried on several, but bought the very first one that I walked right into the shop and picked. My husband really likes it. It is short with some volume. My hair won't have that much volume when I get it cut short, but the transition should still be kind of transparaent to most people. I will probably get one more wig, maybe when I go shopping with my friend on Monday.

  • LNRN
    LNRN Member Posts: 2
    edited October 2005

    I am either starting chemo in October or November. I don't know the type yet. Any suggestions for wigs etc in the San Diego area?

  • TracySeattle
    TracySeattle Member Posts: 690
    edited October 2005
    Just in case you would like to see the wig I bought today, check it out at: http://www.wigdeals.com/product.php/39088/125/

    Mine is the "Mason"

    I also found out today that about 80% of women wear the "Average" cap size in case that helps anyone ordering online.
  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    I just happened to buy a wig today and I am from San Diego!!
    I went to a place called S.D. Beauty Lab. They gave me a 20% discount when I told them about my upcoming chemo. The place is on Clairemont Mesa Blvd. in the complex where Soup Plantation is. 7051 Clairemont Mesa Bl. #304 B. They had me sit down and helped me try on the ones that I liked. I ended up with a short bob the same color of my hair.
    I hear there's a huge place in Mission Valley across from Target (where Montgomery Ward used to be).
    Good luck to you and hope to hear from you again!!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    Hi there again,
    I decided not to be part of the study that only irradiates a section of the breast in a fraction of the time. I found out that it was not the Mammosite type I've heard good things about. This one does not have a lot of stats to speak of yet. I think I'm going conventional with the radiation.

    I found out today that I do my Muga scan on Monday and my first infusion is Thursday the 13th (YIKES!!!!!) from 12 noon to around 2 PM. I want to bolt! Give me a good reason not to!!!! I am so scared. I think the chemo nurse noticed how anxious I was. She added Ativan to her list of drugs to add to my IV.
    We will get through this, won't we? Well, we'll just have to!
  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    Sherry,
    I'm so glad to hear you are doing quite well after your first infusion. I hope I respond the same way to my first (next week - oh no!). Take good care of yourself.
  • ake
    ake Member Posts: 684
    edited October 2005
    Brenda,

    I start on the 13th too...we're not bolting...we're going to do our first treatment, so we can say we have one down. The waiting is the worst, don't you think? I just want to start already, so I can know...hmmm...this is what it's like to have chemo.

    I have Ativan as part of my cocktail too...I think my doctor told me it actually helps prevent the naseua (as well as calm us down!) My infusion starts at 1:30, so about the same time as yours. Just think...this time next week, we'll be already through 2 days of having chemo!

    -Amy
  • tressie
    tressie Member Posts: 1
    edited October 2005
    Brenda
    I will be starting chemo next week also. Hope you do well. I stand on Isaiah 41:10. My plan of attack is to quote this verse thru everyone of my treatment. When Jesus makes a promise he keeps it. Good luck and I will lift you up in my prayers.
    Tressie
  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2005
    Amy and Tressie,
    Thank you. I feel better knowing we will be doing it together. My husband will be with me, but I will visualize us ladies holding hands and getting through this.
  • AnnaM
    AnnaM Member Posts: 1,387
    edited October 2005

    Thank you, Amy, I will check out Crown Wigs in Alexandria. Does anyone have any tips for someone who is starting chemo in two to three weeks? What else can I do to help myself be adult about all of this?

  • sherryhaire
    sherryhaire Member Posts: 192
    edited October 2005
    Brenda--
    Make sure they do your infusion slowly, had headache for 2 days afterwards Onc nurse said they will slow down drip next time
  • Nickinnn
    Nickinnn Member Posts: 2
    edited October 2005
    I started my chemo on July 26th. Just wanted to let all of you know its not that bad. I was so scared. I have now just finished 4 rounds of A/C and had my first taxol yesterday. Don't listen to the horror stories. I didnt have any real side effects to the A/C. No nausea,no mouth sores. It was totally doable. In fact I went back to work full time. I think the hardest thing for my was the fatigue. Figured out that was because my red bloods cells dropped after the third A/C. Then got a shot of procrit and that took care of the fatigue. My onc told me most people do not have bad side effects so Im wishing you all the best of luck.

    Hang in there - you can do it.
  • LMeszaros
    LMeszaros Member Posts: 1
    edited October 2005
    I am joining the October ladies! I will start 4 rounds of AC every 3 weeks on Monday then onto herceptin (we hope). I have IDC ER-/PR+ Her2+++, clear nodes. I had a bilateral mastectomy September 12th. I am 35 years old with 4 year old triplets and a 1 1/2 year old. I have already cut my long hair to a very short pixie style and bought a couple of cute wigs and hats. I had my port placed last week. I have been a trooper until the last couple of days, now I just want to stay in the bed and cry all day. I hope that passes. It is driving my husband crazy. He tried to take me to a nice dinner last night and I was a mess. I love the support here. It's the only place that someone understands me.

    Lisa
    Naples, Florida

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