Who me ?

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  • justtrina
    justtrina Member Posts: 110
    edited March 2015

    Hi Keitha

    I managed to get a wig that look like it could be my own hair it looks so good my husband want me to get my hair cut like it when it grows back... but I find it uncomfortable... I would recommend you wait till you are a 'nude nutt' before looking...and if you can do a 'look good.. feel good' workshop and try different styles. At the workshop I went to I tried a red wig.. felt great and I loved the way I looked but because I already had a wig didn't get it... I did however try a turban/head cover called a 'Byron Bay'... soooooooo comfortable.  I now wear it all the time. So it's worth trying different things...

    good luck and have fun trying...

    Trina

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    That's a wonderful story ! And definitely something to keep you going Coco, how lovely.

    All of my friends and colleagues have wanted to know and be kept up to speed with what's happening and where I am so I have been filling them in. Last night I was at work talking to 2 colleagues about starting chemo on Tuesday, and both of them said "You are not alone, you have us, we are with you all the way whatever you need". One of them is a young man whose dad has bladder cancer, so his love and concern is deep and meaningful - and I love them all for it. I'm so fortunate.

    I had a few good sleeps this week, but the last 2 nights have been dire. My mind just won't rest - waiting. I know that once I have one treatment down it will be easier cos I will KNOW what to expect. And there will be only 5 to go after that too- bonus !

    One of my friends gave me a cute little black feathery hat, very chic. And several have promised to knit beanies. I am going to a LGFB workshop in a couple of weeks, I wanted to be ready. I am pretty hopeless with makeup so hints will be more than welcome, and if they have wigs to try that will be good too.

    Keep on keeping on girls.

    love

    Keitha

  • justtrina
    justtrina Member Posts: 110
    edited March 2015

    Hi Coco

    I to am a teacher and I love it. It was the hardest thing to accept that I wouldn't be returning to work whilst I go through my treatment... although I'm hoping to return just for the last two weeks of term 4. I teach high school so I told my students. There were lots of tears and hugs and a couple even offerrred to sit with me during Chemo (the school is not far from where I'm being treated).. Kids are fantastic... Teaching is one of this things I miss most.

    Trina

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    I'm struggling to fight the butterflies tonight. It's so easy to tell myself to keep positive, but as Tuesday draws closer the dread is creeping in. Part of me wants it to be here NOW, to get it over with so I the unknown becomes known. Part of me - like all of us - wants this all to be some kind of nightmare that isn't happening.

    :(

    Start my steroids in the morning. It's all too real.

    Keitha

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    I'm struggling to fight the butterflies tonight. It's so easy to tell myself to keep positive, but as Tuesday draws closer the dread is creeping in. Part of me wants it to be here NOW, to get it over with so I the unknown becomes known. Part of me - like all of us - wants this all to be some kind of nightmare that isn't happening.

    :(

    Start my steroids in the morning. It's all too real.

    Keitha

  • TonyaM
    TonyaM Member Posts: 2,836
    edited March 2015

    Your school sounds fantastic coco.What great ideas to raise money for breast cancer but have fun at the same time.I'm glad you are having time off for your treatments-one less stress to worry about if you are feeling crook. On the wig conversation;-I bought a very expensive human hair wig and I hardly wore it. It was good to have for special occasions but I could only wear it for several hours before it drove me nuts.It was hot and itchy and what's more,I felt self conscious that peolpe could tell it was a wig(silly ,I know).Chemo may bring on the dreaded menopause hot flushes and THAT makes a wig unbearable.On the upside,it's winter which makes  head gear  more tolerable.As soon as spring hit,my wig was put away.If you go for a human hair wig then you have to wash it and maintain the style -more fuss than your own hair! In hindsight,I probably would have gone for a good,but cheap acrylic one just to have on hand.I mostly wore cute caps and cotton bandanas from www.headcovers.org cos my scalp got so irritated with other headstuff.Good luck girls.

                                                         Tonya xx

  • coco
    coco Member Posts: 18
    edited March 2015

    Thanks Justrina, I have year 2 so it was quite difficult telling them. I sent a letter to my parents but I thought  it would be unfair for them to have to tell the children what was in my letter so I told them three minutes to three on Friday afternoon what they would find out from their parents. We all cried, it was heart wrenching, but I also told them we would have a celebration day and I would come and visit them which they liked. I miss them very much but needed time for me and to prepare mentally for what lies ahead. Hopefully I will go back before the end of term 4, but we will just have to wait and see.

    Best wishes,

    Sue (coco)

  • coco
    coco Member Posts: 18
    edited March 2015

    Hi Magicmum,

    Can certainly understand your nerves. I feel like I am in high school again waiting to get my rubella needle and constantly going to the end of the line  and now I find the line is finally at the end and I am next to get my bilateral masectomy. There is no more time, but in some ways that is such a good thing, cause this period of my life is in limbo and is stretching out endlessly. At this stage the type of cancer I have has not been defined other than to be invasive, So I don't know how concerned to be, crazy I know cause cancer is cancer and I should be concerned but should I be overly worried or just slightly concerned? So far on my journey my diagnosis has gone from bad to worse, so I am kind of expecting this to continue, but I would love it if after surgery they say well two rounds of chemo and that should do the trick and you can go about living your life the way you planned again.

    I really want to know about the unknown. Good luck with all that you are dealing with my thoughts and prayers are with you. Lots of love Sue

  • coco
    coco Member Posts: 18
    edited March 2015

    Hi Magicmum,

    Can certainly understand your nerves. I feel like I am in high school again waiting to get my rubella needle and constantly going to the end of the line  and now I find the line is finally at the end and I am next to get my bilateral masectomy. There is no more time, but in some ways that is such a good thing, cause this period of my life is in limbo and is stretching out endlessly. At this stage the type of cancer I have has not been defined other than to be invasive, So I don't know how concerned to be, crazy I know cause cancer is cancer and I should be concerned but should I be overly worried or just slightly concerned? So far on my journey my diagnosis has gone from bad to worse, so I am kind of expecting this to continue, but I would love it if after surgery they say well two rounds of chemo and that should do the trick and you can go about living your life the way you planned again.

    I really want to know about the unknown. Good luck with all that you are dealing with my thoughts and prayers are with you. Lots of love Sue

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    Oh sweetie, I feel so bad being a misery guts when my surgery paled into comparison. I hope it all goes so well for you, and that they find you have no nodes involved, or minimal - and that you get a HER2 negative. It IS the unknown thing for us, it's so hard.When I'm feeling sensible I know that it's pointless over-worrying - it is what it is, and worrying won;t stop it or fix it. You just get the best advice, follow it and then hope for the best. Worrying causes stress and stress can be a danger all on its own.

    We'll get there together, we'll hang on together. In a year, in 5 years, in 10 years we'll laugh and wonder why we were worried. And we'll be able to help others where we are now.

    Breathe.

    Have a look on the Net for the chillout song by Ze Frank - it really helps.

    Chin up girl, we can do it.

    love and hugs

    Keitha

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    Oh sweetie, I feel so bad being a misery guts when my surgery paled into comparison. I hope it all goes so well for you, and that they find you have no nodes involved, or minimal - and that you get a HER2 negative. It IS the unknown thing for us, it's so hard.When I'm feeling sensible I know that it's pointless over-worrying - it is what it is, and worrying won;t stop it or fix it. You just get the best advice, follow it and then hope for the best. Worrying causes stress and stress can be a danger all on its own.

    We'll get there together, we'll hang on together. In a year, in 5 years, in 10 years we'll laugh and wonder why we were worried. And we'll be able to help others where we are now.

    Breathe.

    Have a look on the Net for the chillout song by Ze Frank - it really helps.

    Chin up girl, we can do it.

    love and hugs

    Keitha

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    Oh sweetie, I feel so bad being a misery guts when my surgery paled into comparison. I hope it all goes so well for you, and that they find you have no nodes involved, or minimal - and that you get a HER2 negative. It IS the unknown thing for us, it's so hard.When I'm feeling sensible I know that it's pointless over-worrying - it is what it is, and worrying won;t stop it or fix it. You just get the best advice, follow it and then hope for the best. Worrying causes stress and stress can be a danger all on its own.

    We'll get there together, we'll hang on together. In a year, in 5 years, in 10 years we'll laugh and wonder why we were worried. And we'll be able to help others where we are now.

    Breathe.

    Have a look on the Net for the chillout song by Ze Frank - it really helps.

    Chin up girl, we can do it.

    love and hugs

    Keitha

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    Exactly the sort of feedbakc I was looking for - I hate it when my head gets itchy from wooly hats so it sounds like I'd be the same with a wig ! I'm glad it;s winter as I won;t mind the hats and scarves, and I will try a wig just in case I need something for work.

    I love headcovers.org - some really nice ones !

    Thanks !

    Keitha

  • magicmum
    magicmum Member Posts: 285
    edited March 2015

    Just home from Chemo #1. All went smoothly. No bad effects at time of infusion even from the Taxotere, the sister watched me closely for 15 mins and was very pleased. Aside from the cold icy fingers and eating 3 cups of ice chips I spent a relatively pleasant day with some other lovely ladies in a beautiful room with big windows surrounded by a pretty garden. Morning and afternoon tea, a nice lunch and my husband sat with me and made me laugh.

    Maybe I'll keep on being lucky and have minimal side effects all through ? That would be good.

    Anyway, I'm GLAD today went by so well and the unknown is not to be feared now. Ahhhhh.

    Keep on keeping on girls.

    Keitha

  • coco
    coco Member Posts: 18
    edited March 2015

    So glad to hear all went well for you Keitha, I have one day left until my surgery and have so many things I need to do tomorrow. Can't believe that in 48 hours everything will be different, but happy to start treating it all at last.

    I had a migraine today probably due to the stress of everything. Feeling a bit washed out but luckily I was able to take strong medication and sleep it off. Keep posting updates Keitha I love finding out where you are at, it is somewhere I know I will be soon.

    Take care, best wishes and lots of love,

    Sue