June 2007 Chemo

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  • honeygirl
    honeygirl Member Posts: 1,718
    edited June 2007
    Hi galnok , No , I'm not taking any steroids. I have been feeling anxious and took a xanax and did sleep better last night. Thanks. No nausea so far today! Also no headache as of yet. I thought maybe it might be due to a herniated disk problem I have been dealing with since April. I am taking nurotin and it has improved a great deal(pain in neck and arm) since then. Well , hope all is well with everyone.
    Cheryl , that really sucks. Migraines suck!
    I have no suggestions for your child. But you are deffinately in my prayers. Take care.
  • carrie59
    carrie59 Member Posts: 6
    edited June 2007
    Hi Everyone,

    Well I had my first TC treatment yesterday and all seems to be going well. My biggest thing is how tired I feel. I am pushing the liquids so I was up quite a bit through the night to go to the bathroom plus I haven't had a full nights sleep since the surgery on April 30. At least I don't seem to be nauseaous or anything I guess the meds are working on that. Its good to have that first one over with so now I know what to expect. I want to thank everyone for all the tips that I have read not only on this site but some of the other discussion boards. I am taking them all to heart and trying to do everything to help myself through this with as little side effects as possible. I think that if my husband sees that I can get through this he may calm down a bit. I think he is worse than I am right now. Any hints on how to calm spouses down. Well I am going to rest now so take care everyone. Have a great weekend.
  • SusieSwan
    SusieSwan Member Posts: 111
    edited June 2007
    So many posts to catch up on! I got some bad news on Thursday, my Dad, went in for an angio and ended up being sent to another hospital to have bypass surgery yesterday so it has been so stressful. I feel bad for my Mom having to worry about both of us. Dad is recovering well, ended up with a quad bypass. Doctor said it was a life-saving procedure because these are the blockages that people just drop over dead from with no warning or symptoms. So, I decided that we BOTH had life-saving procedures this year

    Cheryl, I've suffered from migraines for years. The only nice thing about vomiting is after that point, you know you're on the downward slide, at least that is the way it was for me.

    Glad everyone that is starting chemo without too many issues. Bummer to think this is my last "normal" feeling weekend for the Summer.

    Hope everyone had a great weekend!
    Susan
  • DebbieK
    DebbieK Member Posts: 116
    edited June 2007
    Yes, Susan, I have been lamenting my last normal weekend for the summer as well. It is so hard to predict how the summer will play out with all the treatments ongoing. I am 4 1/2 weeks out of my mastectomy and reduction surgery and starting to feel normal again. At least starting chemo gets me one more step along this journey. I am so glad to be done with surgery unless I decide to have a reconstruction after all the treatment and rads.

    Cheryl, I can't believe the day you had trying to get your PET! Like you didn't have enough on your plate already! I think your idea of getting your hair cut before it comes out on its own is a good one. Hopefully if your son can deal with it in stages it will help him accept it better. I feel to fortunate to have grown children and just me and my husband at home to deal with all of this.

    Well, I better get going and enjoy this weekend. Take care everyone!

    Debbie
  • kath11
    kath11 Member Posts: 102
    edited June 2007
    Good morning everyone,

    Susie, I'm so sorry to hear about your dad, but my dad had the same surgery, quad bypass, and he recovered so well. He was like a new man. I hope your dad does the same.

    Has anyone had dreams about the chemo? Last night I dreamt that I was receiving chemo in my living room and my husband was trying to help me and the drugs kept leaking onto my favorite chair and burning it! My first treatment is Monday, so I guess my anxiety is finding its way into my dreams as well.

    But all in all I'm just ready to get on with it. Thanks to all of you ahead of me preparing me for what is to come. Each experience will be a little different but it truly helps to hear what everyone else is experiencing.

    I hope you all have a great weekend. I'm going wig shopping today!

    xoxo
    Kathleen
  • lastminuteD
    lastminuteD Member Posts: 333
    edited June 2007
    Hi all!

    Thought I'd check in for day 2! Actually I should start with the end of day 1 - got a migraine - I believe it's from the cytoxin - took a relpax, went to bed around 5 or so - called for dinner around 7:30 - went down around 9:30!! but feeling better by then. Ate, brushed/rinsed teeth - back to bed!! Today has been fine. Took the emend, went shopping with my daughter, took a little nap and doing a little of this and a little of that.

    so far, so good. Hope everyone is enjoying their weekend.

    Good luck Monday Debbie - let them know you've only had your port since Tuesday - they'll probably ask you anyway.

    Dawn
    12/05 IDC er+/pr+ her2+ stage 1
    3/07 IDC er-/pr- her2+ stage 2
  • DebbieK
    DebbieK Member Posts: 116
    edited June 2007
    Thanks for the good wishes, Dawn. I plan on telling them all of my stats just to be sure everything goes well on Monday.

    By the way, a few days ago I ordered a cheap wig online. I picked out a color I thought was similar to mine and a short style since my regular hair is short. Well, it came today and I put it on. I thought it looked ok for a cheap wig; but my husband and my daughter had a fit! They didn't like the style or the color...who knew? Anyway, back in the box it went, and they studied the catalog and picked out what they are sure will look a lot better. We will see how well they did! I really don't plan on wearing it much anyway, but thought it would be good to have one if I need it. I much prefer the turban hats and scarves. I ordered on line because I just couldn't get interested and energetic enough to go try on a bunch of them.

    No doubt about it, this bc trip leads us into strange and mysterious circumstances. Never thought I would buy a wig! My 6--year old grandson kept asking when I would take my pill so my hair would fall out! We've been telling him my medicine was going to make me bald, and I guess he thought I was just going to take a pill.

    Gotta go run errands. Take care,
    Debbie
  • tos
    tos Member Posts: 376
    edited June 2007

    Susan, I'm so glad your father is ok! What a scare but so glad everything worked out ok.

  • TerryNY
    TerryNY Member Posts: 603
    edited June 2007
    Checking in again and hopefully can keep up now that the wedding is over and guests are gone!
    I see a lot of new names, welcome to all!
    I hope the ones getting ports inserted soon do well. I've had mine for almost two weeks and it feels so much better since I removed the bandage on Friday. Before that, my dr had recommended covering it with saran wrap and duct tape to shower (I was told it had to remain dry)....what a site to behold. I'm sure my husband was laughing hysterically after helping me tape up....at least he had the courtesy to wait until after he left the room...LOL
    Anyway, it's barely noticeable now except for a light pressure in my neck. The incision site is healing nicely too. So, to all of those waiting for your ports, it isn't that bad and trust me, I was being a huge baby about this!!
    I start my first chemo tomorrow at 9 AM, I'm pushing fluids today and plan on making a chart for my pills. My brain is on vacation for the summer I think and don't want to risk missing a dose. I've got a few books packed and plan on snacks and drinks too.
    Last week I purchased Biotene toothpaste and mouthwash just-in-case. The tips on the board have been immensely helpful.
    I know someone else is starting tomorrow, Debbie?, I wish you well! (I'm having a hard time keeping names and facts straight and will apologize now for future mistakes. ;-) )
    I look forward to posting and reading about everyone's experiences, what a great group!
  • DebbieK
    DebbieK Member Posts: 116
    edited June 2007
    Hi All,

    Terry, I will be thinking about you tomorrow when I also go in for my first chemo. I too am pushing fluids today and will continue to try to do so over the next few days.

    I am amazed at the different direction we get from our doctors. No one said to me to protect my port incision from water. I took a shower the second day after surgery with the clear tape on it from the procedure. After my shower I removed the tape because it was really irritating my skin. In my next shower I actually washed the area with just the little strip of tape on the wound and then yesterday (4 days out of surgery) I removed that tape! Everything looks and feels fine. I will admit I am always anxious to get all surgery stuff off as soon as possible. So far, no problems.

    I can't even imagine dealing with a wedding and house guests during this time. My daughter got married last summer, and it was a very challenging few weeks what with arrangements and houseguests and all. You are doing great, Terry, to have come through all that plus your bc procedues!

    All for now. Take care, Debbie
  • SusieSwan
    SusieSwan Member Posts: 111
    edited June 2007
    Debbie K - Same thing here..doctor said to leave it on for a week but I did have some bleeding and it wasn't sticking well and started irritating me so I took it off last night (3 days after insertion) and it's healing fine. I really thought the port area would stick out more and up higher on my chest but because I'm a little chesty, you can't even see it..you can feel it but not see it.

    Dad is doing pretty good today...wow, what a scare. My Dad has always been so strong and he was sooo upset when I told him I had cancer and this just threw him for a loop. But, he was up walking today. I'm amazed how quckly they have you up after open heart surgery.

    I also had my MUGA scan Friday and that was no problem...I don't have the results yet but they said they would call if there was a problem. They did have to find a BIG vein as they use a large needle but fortunately, my tech was really skilled and got it right away.

    I'm going tomorrow for my wig fitting from a gal that has a hair salon in a nearby town. She is a b.c. survivor herself and started this business due to her online ordering of wigs when she had chemo. She said she hated everyone she ordered and found the fits challenging and there were some tips she never got until afterwards. She is a breath of fresh air and I'm hoping I'll find one! I'll probably do mostly scarves for summer but will like hair for working or a night out!

    Susan
  • Charlie451
    Charlie451 Member Posts: 69
    edited June 2007
    Hi All,
    I had my port installed last Tuesday. It really feels strange and I have two "dracula marks" around may neck and collarbone area. I am getting used to it slowly. I have been trying to figure out, besides drinking lots of fluids, what nutritional support to get for chemo. I guess so much depends on what you can actually keep down. My onc says just take a multivitamin. I meant to ask if you can take antioxidants ( vit A,E,etc.) but was too overwhelmed by the pace of events to get more specific. I have read on the rad thread and in other areas that antioxidants may interfere with therapy. I have list of questions for the onc tomorrow but if any of you have ideas about this please write in.
    I am really glad to lots of positive stuff from you all about experiences so far - ports and first treatments. Let's hang in there and stay informed.
    Linda
  • kath11
    kath11 Member Posts: 102
    edited June 2007
    Hi Everyone,

    Terry and Debbie, I'll be starting my chemo tomorrow as well. I'm drinking so much water I think I may float away. I'm also packing a bag to bring along, with the ipod, books and maybe some knitting. I'm a little fearful of not having a port, but I'm sure I'll get through tomorrow just fine. I'll be thinking of you both and hope your day goes well. Were either of you given Emend to take an hour before treatment? Those were my instructions. Should help with the nausea.

    Linda, I've been confused about vitamins and supplements as well. My husband bought me some protein powder to add to smoothies, but it's made with soy and I think I read somewhere to avoid soy during chemo. Hopefully, I will learn more tomorrow about what we can have and what we need to avoid.

    I'm feeling really great today, and so happy to get the show on the road. I hope you all had a great weekend.

    xoxo
    Kathleen
  • DebbieK
    DebbieK Member Posts: 116
    edited June 2007
    I did a little research on the net today about taking antioxidants while on chemo. It was hard to understand but the gist of it seemed to be that the antioxidants help protect the body's cells from the toxicity in the chemo. The assumption is that if it protects the good cells it may also be protecting the cancer cells so the advice of most onc. drs. is not to take antioxidants while on chemo. I didn't have time to do a lot of looking, but thought I would share what I did get.

    I have been drinking water all day as well. We'll see how we do tomorrow and check in tomorrow night.

    See ya later, Debbie
  • allgone
    allgone Member Posts: 16
    edited June 2007
    Hi everyone,

    Susieswan, I am so glad your father is doing well!! Adding the stress from your fathers surgery with what you are going through is alot. As I found out my son has to go for another surgery (this is number 4) in the middle of my chemo. Since he is only 5yrs old I can only imagine the stress we will be going through.

    I am going to look at more wigs tomorrow, and I think I will start to drink my water tomorrow (I can't stand water) hopefully by Thursday (1st chemo day) I should be able to drink the 8+ glasses without feeling sick!!

    I'm glad to hear that there hasn't been too many issues with the girls that already started. (I am begining to get a little scared and anxious...not a good combo)It always feels comforting to read how everyone else is doing, it seems to make me forget a little that I will be going through it by the end of the week. Anyway time for bed...


    Keep smiling
  • TerryNY
    TerryNY Member Posts: 603
    edited June 2007
    Good luck to Kathleen and Debbie today, I'll be thinking of you while I'm hooked up too. Hope it all goes smoothly for everyone.
    Kathleen, I too have Emend to take this AM, in fact I need to take it in about 10 minutes...think I should pop a xanax too. I'm getting a tad nervous.
    Susan, I hope your father continues to do well!
    Ok, ladies, let's get this show on the road!
  • SusieSwan
    SusieSwan Member Posts: 111
    edited June 2007
    Allgone, what kind of surgery is son having if I may ask? Hopefully your hubby is really helpful! That's another big struggle of mine (as well as most Moms/Wives) is that I'm always the caretaker and I make the household run as efficiently as it does. If I'm not feeling well, it doesn't seem to bother anyone else that the garbage is overflowing, dishes are in the sink, shoes on the floor, dog hair on the carpet, etc.,...

    Kathleen, Debbie & TerryNY, I'm thinking of you guys today and hoping it all goes very well.

    My port site is still bruised and very tender..I sure hope it settles down before Thursday.

    Susan
  • lastminuteD
    lastminuteD Member Posts: 333
    edited June 2007
    Checking in to let you all know how yesterday - day 3 - went. I had a lot of trouble sleeping Saturday night - not sure why and had weird dreams. Took my last emend pill, went to church Sunday morning, DH took me to breakfast and then I went to bed for several hours. Rest of the day pretty normal but didn't sleep well again last night. Got up this am and did the treadmill for 20 minutes and am at work today (desk job). So far, so good. No clue what to eat but trying a little of this and a little of that and that's working out.

    My kids are older than some of yours - 16, 20 & 24 right now. I can't imagine how hard it would be with little ones. My blessings to those of you going through this with little ones.

    Hoping to keep up with the treadmill since I've heard it will help a lot. Next treatment will be the 21st.

    Good luck today Kathleen, Debbie & TerryNY.

    Hugs to all,
    Dawn
    12/05 IDC er+/pr+ her2+ stage 1
    3/07 IDC er-/pr- her2+ stage 2
  • TerryNY
    TerryNY Member Posts: 603
    edited June 2007
    I am back and it went so much better than I anticipated, that's the hardest part, the unknown.
    I'm glad the onc dr pushed the port for me, I was against it all the way but I can see his wisdom now.
    The nurses were great and explained each procedure before starting. The adriamycin gave me a slight metallic taste in my mouth but not too bad. If that's the worst side effect I'll be a happy camper.
    I'm already peeing in color! LOL
    Kathleen and Debbie, I hope your first treatment goes as smoothly as mine. And thanks to everyone for the good wishes sent my way, they are truly appreciated.
    Dawn, I agree with you, I can't imagine dealing with this with younger kids. Mine are 24, 20 and 18 and have been a big help throughout the ordeal. My hat is tipped to those raising youngins and dealing with BC.
    Susan, I totally understand your Captain of the House comments, I am the same way. But I figure this is a temporary situation and most things can wait....if I can stand it! I hope your port settles for you too, make sure you tell the nurse that you are tender. They sprayed mine, lightly, with a numbing spray and I didn't feel a thing.
    I go for my Neulasta shot on Wed. And I'm having an MRI done today because I'm having drainage from my nipple from the orginal lumpectomy done in March.
    Allgone, I wish the best for your son.
    Hope everyone is having a great Monday!
  • allgone
    allgone Member Posts: 16
    edited June 2007
    Hi evryone,

    Susieswan, my son was born with hypospadias. He has also had a couple of hernia surgeries. So this is going to be surgery #4 for the hypospadias repair, and the 3rd surgery for hernias. (the hospital for Sick Children in Toronto has been GREAT and they will do more then 1 procedure at the same time if they can do so safely)
    Terry, Thanks for your good wishes.

    Telling my son about the chemo was alot easier then I thought it would be. My husband, my son, and me sat on the bed to talk (I didn't want any distractions toys, tv. ect.) I told my son I was going to have "Super Hero Mommy Medicine" and this was going to make sure that the cancer was gone. But only Mommies can take this medicine...boys, girls, daddies can't. I told him I might get a tummy ache and throw up, and I might be really tired but "that's o.k." I will get better when I stop taking it. Then I told him my hair was going to fall out, and I patted the top of my head. Without missing a beat he looked at me and then his father (who has lost some hair on the top of his head) and said "you are going to look like Daddy" I thought it was so funny I gave him a big kiss. My husband is sitting there going "I have hair here" my son said "but not on the top" I told my son when all my hair falls out he can rub my head and kiss it better. He asked me all weekend "when is your hair going to grow out" I told him about "pretend mommy hair" that I will wear when we go out. (he didn't understand WIG) children really are quite accepting. He seemed fine with everything...we will see when it starts.

    My thoughts are with everyone starting today!!

    Terry, I can't imagine peeing in color...I guess I will be experiencing it first hand on Thursday!! And If the side effects that you have had (metallic taste and pretty color pee) is the worst I hope I am just like you!!

    Keep smiling
  • burquie
    burquie Member Posts: 129
    edited June 2007
    Hello Ladies;
    I'm glad to hear that those who have started their chemo are doing well thus far.....keep up the good work girls!!! I know we can all do this!
    I had my PET/CT scan this morning; now just have to wait and pray that they are both a-okay. I go for my port next Tuesday and hopefully that will be uneventful.
    As some of you have mentioned, I too am "captain of our ship" I keep things running smoothly around here. We also care for my 81 yr old father, who just did a stint in the hospital (came home this am) for pneumonia. He has COPD and is diabetic. Luckily I have a supportive husband and 2 teenage sons; and also 1 older brother and sister (I'm from a family of 8) who have stepped up to the plate to give us a hand with my Dad!
    Hope everyone continues to feel good (as good as we can anyways). Thanks for being here!
    Bonnie
  • Terrilee2
    Terrilee2 Member Posts: 13
    edited June 2007
    Hi to all of the stong women in our June group!

    I am now into day 12 post 1 tx. I have felt wonderful these last 5 days!!! I want you to know that we will have days of normalsy this summer!!! I have been the "Queen" of "this will be the last time" moments leading up to chemo, and want to say that every day we endure, and we live, and we love, and we make it!!! One more day.... My Hair started falling out today... I got a little bit weepy, then pulled myself up by the straps and got on with living! I am so proud of all of us!!!
    I would love to plan a survivor party for all of us a year from now... doesn't that sound like a good thing?

    Peace to you all,
    Terri
  • bomber410
    bomber410 Member Posts: 564
    edited June 2007
    Hi everyone, it sounds like we are fully underway. I'm impressed with everyone's strength and positive attitude. I'm 4 days out from my first chemo treatment and cannot complain of anything but a bit of fatigue but just slows me down to other people's 100%. I bet you all see the same thing when you think about it. Just compare how you operate normally to others and when you slow down it is a challenge for you but you are still moving mountains compared to the average Joe.

    I have experienced no mouth blisters, no nausea, no bone/joint pain from the Neulasta (my worst fear) and no insomnia (Tylenol PM every night). I did experience the constipation but I have uncooperative bowels. The sennakat is a miracle pill and supposedly natural. It doesn't have to be all bad. I realize the next treatment may be different but probably best not to compare from one treatment to the next.

    Monday chemo ladies, did you find there was enough steady activity that it wasn't really possible to listen to the iPod or get into a book? At least when I got the Adriamycin, it was in those big tubes that the nurse had to hand inject into the infusion set up. The cytoxin was probably the best lull with it taking 90 minutes. And did you find how nice everyone is? I'm already thinking about what gift or goodies to bring in.

    Terri, I so appreciate you offering up what's happening with you right now. The hair coming out in clumps has to be a bit freaky. When are you going to zip it or is it done aleady? :-)

    Allgone, how sweet the way you handled the situation with your son. I suspect he's a pretty resilient child given what he's been through. And you and hubby are too. That's why you'll do so well.

    I don't know about others but I had the chemo and Neulasta shot on the same day. I was handed one script for the Compazine to take for 72 hours. Otherwise, I'm taking nothing more than the Tyl. PM and the Sennakat. Pretty exciting. :-)

    My treat for me is that I was able to run/walk for 50 minutes tonight. It was heaven. I found the right bra/camisole combination that holds me tight but doesn't rub on the port area. I too was told no shower for 48 hours and then keep area covered with new bandage after each shower for next 48 hours. BTW I make sure I get extra of those bandages like the clear tape that sits over the gauze from the doc. They just count up a stack that should cover the number of days.

    It'll be great to hear from Terry, Debbie and Kathleen. Hope your day was 'uneventful'. :-)

    Cheers,
    Debbie C.
  • DebbieK
    DebbieK Member Posts: 116
    edited June 2007
    Hello to All,
    I am so enjoying reading all of the posts tonight! Terry, I too found the treatment to be easier than I thought it would. I didn't even get the metal taste! The nurses were so great, and all went smoothly. I go in for neulasta tomorrow. They put an anti nausea med in the iv that will last for 3 days plus gave me additional meds to take by mouth if necessary. They also gave me a steriod. So tonight I am doing well. The nurse said the 3rd day is the day I will want to stay in bed but she told me to get up every couple hours and do a little something and I will feel better sooner than if I stay in bed all day. I will try to follow her instructions and see how it goes. I agree the fear of the unknown was worse than just getting on with it.

    The treatment room had lots of people in it so there was lots to watch. My husb. and I did a little reading and visiting but the time went fast. At noon he walked over to the Subway and got us sandwiches, yum! All in all a good day.

    Allgone, such a relief that your son accepted all the information with a positive attitude. Kids are so amazing, and it is obvious that you and your hubby help him to react so positively.

    I am hungry for dinner so I am going to sign off. Take care everyone!

    Debbie
  • bomber410
    bomber410 Member Posts: 564
    edited June 2007
    Debbie, you sound great! And you are right about the action. When I got settled in for my treatment, there was a guy snoring to beat the band. Apparently, his treatment is truly an all day process. They start him early and he's the last to leave. Makes me count my blessings.

    Did anyone else have sandwiches and soup brought up around lunch time? What a deal?

    Have a good night.

    Debbie C.
  • GracieM2007
    GracieM2007 Member Posts: 1,564
    edited June 2007
    Hello, everyone. I finally got my start date. June 18th, four rounds of AC, every two weeks, then four rounds of Taxol, every two weeks, then five years of arimidex. My PET came back clean YEA!!! Hubby and I went and had banana splits for a celebration.

    Am so glad ot hear that everyone who has already started chemo is doing well, and hope that we all get through this with very few side effects, and that we kick cancers rear.

    Guess we all have to be the warriors we were born to be.

    Will keep each of you in my prayers as we go through this, and as we each face our own set of problems along the way. You all ROCK!!!!

    Blessings,

    Gracie
  • DebbieK
    DebbieK Member Posts: 116
    edited June 2007
    Congratulations, Gracie on your test results! That is wonderful news. You will get your first treatment the same day as my second one. If you are like me, you are anxious to get on with it. Try not to worry too much before the 18th. I'll be thinking about you. We will all make it through this together.

    We June gals are going to kick some cancer butt this summer!

    Debbie
  • litig8or
    litig8or Member Posts: 54
    edited June 2007
    I have my chemo and Nuelasta on the same day too. And it does give me joint pain, which I didn't realize that was the cause until I read other posts. Days 4 and 5 seems to be my worst--after tx #1, I was able to attend all of my son's graduation parties and luncheon and such.
    Tx #2 is Wednesday, so we will see how that goes. I have heard that some women have the same pattern after each tx, and in some it builds up and the tiredness gets worse--I hope I'ts the former for me and everyone else!
    Meanwile, my 21 month is asleep upstairs and my 17 year old (yes, I typed that correctly) registers for college tomorrow. What a life we live!

    And for you just undergoing tx #1 his week, my thoughts and prayers are with you! We are STRONG!
  • kath11
    kath11 Member Posts: 102
    edited June 2007
    Hi Everyone,

    So many great posts and updates! It's 8 p.m. on the West Coast and my treatment (#1) was at 9 a.m. I'm feeling really good. I have a slight headache, but not nauseous. I was home by 10:45 and yes, Debbie C., there was no time for an ipod or books! Just lots of information from a wonderful nurse. I don't have a port and I didn't feel a thing. I know that will become more difficult with time, but so far so good.

    When I got home I walked my dog with a friend for about 45 minutes and then hung out with my daughter who just came home from college. We're watching all the Ocean's 11 movies to get ready for the new one. But can we go to the movie theater? I forgot to ask that question today. My husband made dinner, but I'm just eating small snacks every two hours instead of any one meal. Between all the mini meals and water I'm drinking I feel like I've had plenty.

    I guess everyone is different. I go for my Neulasta shot tomorrow. The nurse recommended I take a Claritin tomorrow and for two days following which should help with the bone pain.

    I feel so fortunate that my children are 18 and 20. I know it must be difficult to care for little ones, keep the house running and still be able to take care of yourself. I admire all of you with little the ones and/or parents you are caring for.

    So it's one down, seven to go! To those of you waiting to start your first treatment, it's a huge relief once it's underway! Now I'm sure I can do this, we all can do this, and I think a gathering of our June 2007 chemo group is definitely a must in the future!

    xoxo
    Kathleen
  • SusieSwan
    SusieSwan Member Posts: 111
    edited June 2007
    Good Morning Ladies!

    So happy to hear everyone is doing well!

    Kathleen, I'm hoping my dogs will be my trainers as well and keep me moving!

    Gracie, that is awesome news on a clean PET and way to celebrate...you're a gal after my own heart!

    Debbie K, my husband was already asking when we're going to have lunch since my appointment is at 12:30, ha, ha. Since this will be my first treatment, I'm just hesitant about eating very much right before. I would love to be being infused and send him out for lunch!

    For those of you that are getting your Neulasta shots on the day of treatment, that is encouraging, since I am driving 2 hours one way for my treatments, I was wondering about that Neulasta and if I would have to drive all the way back the next day for the shot.

    I went and picked out a wig last night and was pleasantly surprised. The gal that I went to is a breast cancer survivor herself (9 years, yeah!) and is a beautician. She started the wig service because of the lack of options she had when she went through chemo. This girl is a doll and was so helpful. The wig is picked out is actually nicer than my own hair and wasn't as awful in the fit or the look as I had anticipated. so, that will be in next week and she'll style it more to my liking. My husband says to just go ahead and buzz the hair while I'm there but I should still be a week out with hair so I think I want that week :-)

    Have a great day girls,
    Susan

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