Hello from a new member of the family

Today I joined the army of people sitting around different waiting areas, carrying my belongings and my "gown" as we went through the various tests to find out if we had breast cancer. Some were, like me, totally new to the routine, others were at various stages in the journey and one lady was given the great news that she was still clear of her cancer five years since her treatment ended. 

I already suspected that my symptoms of strange lump, pain and puckering were caused by the big C, so I wasn't surprised when the lovely consultant showed me the first ultra sound scan with its big black area where there should have been breast tissue, saying it was pretty definitely cancer, and proceeded to tell me what would happen next. 

What did happen over the next two hours was quite unpleasant and painful and I now have a 12 day wait to find out exactly what we are looking at regarding type of cancer and treatment. Strangely enough I have no feelings of fear for the future, although twenty years ago I had a scare that saw me fearful and tearful, now I'm an old dear I'm just cheesed off that I will have quite a lot more unpleasantness to face. I'm one of those boring people who don't often get ill, so when I do I'm the patient from hell, or so my daughter tells me. I admit to being grumpy if I'm ill for more than two days. 

I have read a lot of the posts, here, during my wait to go for the tests, feeling like an outsider looking in, but now I'm in, too!   I suspect future posts from me will be less upbeat, but I would like to record my experiences here, and to share others' experiences, too.

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  • Hi,

    I am new to the group and BC. I was diagnosed in July. I had  a partial mastectomy with reconstruction 2 weeks ago. Yesterday I went back for the results only to be told that my margins weren’t all clear and I have to go back in on Friday for another op to remove more tissue. I’m also waiting for results of Oncotype test so decide what my treatment plan is. I haven’t been frightened or fazed by anything so far but yesterday I came away really *** off! My wound has just healed and now they are going to re open it. But hey ho. I’m 48 and like you have always been healthy and am crap at being ill. I do hope you don’t become down beat x

  • Hi Cazrosie - I am currently being offered a lumpectomy (assume same as partial mastectomy) or a mastectomy + reconstruction for a 3.5cm globular tumour. With the lumpectomy they indicated I would go from a B to an A cupsize so offered me a breast reduction on the good side. Size is important to me so I would rather go for a reconstruction to get symetry and also avoid touching the good breast? Are you happy to tell me about your situation? Did you have the same type of cancer? How much of the breast did they have to take? What type of reconstruction did you have (via liposuction or LIDAP)? Di they do the reconstruction at the same time or later after radiotherapy? I am sorry your margins were not clear - did you go for a further lumpectomy? - they suggested that this may well be the case with me due to the globular cancer type that I have. Were you - are you happy with your results? I do hope all went well with you after this post - best wishes Karen

  • Hi Karen,

    Firstly I'm sorry you have joined this club but hopefully the support you can get from this group will help. So I also had a 3.5cm lobular tumour. My boobs were only a B cup too, so not huge. I would say my reconstructed boob is smaller but think it's only really me that notices. Boob tubes are harder to wear these days as tend to fall down on the smaller side :laugh:

    I would say they took away a third of my breast in surgery, then used a LIDAP at the time of the surgery to reconstruct. I managed to keep my nipple.  I do have a huge scar and at the time looked like I'd been in a fight with a shark but it has faded really well and I'm actually really proud of my scar. It runs from under my boob, around my side and onto my back. When my margins weren't clear, it was along the bottom section so they just took the remaining breast tissue away, in that area, in another op. I was never in over night and recovered pretty quickly.

    2 years down the line, my scar has faded, my breast is not the same shape as it ever was but I'm not that worried. It does have numb areas and you get the sensation of pins and needles when you press it and tingles in your back area! I do have to ask them to be more gentle on that side when I go for my mammograms. But I'm still alive and as far as I am aware, I am now cancer free! So I am grateful for that and can live with a slightly odd shaped breast! Feel free to message me if you want to chat more

    Caroline x

  • Hi Caroline,

    I'm still here (though not stalking), reading your last post/s. From the beginning till now, I have been in awe of your trio. Everytime I read, it gives me hope.

    Christine, Sam, are you cancer free too?

    Much love to all xxx :love:

    Vee xxx

  • Hi Carosie - thanks for your reply - so glad you are happy with your result. I don't know if I am a bit de- sensitised - I haven't felt that I am likely to die - so I guess I have been quite focused on getting the most pleasing visual outcome - over the number of ops/duraction to achieve it. Interesting that you had a lumpectomy with plastic surgery - I was not offered this option - and was told that it wasn't possible - it's not until I read literature that I realised it was - and that I think it is just not available at my centre. I have asked for a 2nd opinion at a different centre that does both - so I get fuller info? do you know of any reasons why someone would not qualify for this? Did you consider having lipofilling rather than LIDAP? If not was this because of how much you had to have removed? Interesting that you had plastic surgery at time of lumpectomy - I wondered whether this would be delayed due to needing radiotherapy and that radiotherapy can shrink your tissues - not sure if they over compensate on size to allow for shrinking? Did you have radiotherapy? If so did you get shrinkage? Also did you get any appearances/colour changes in skin or tissue? do you always get a scar with LIDAP - or does it depend on how much they take? Do you ever wish you had taken a different path. So kind of you to offer your info - I am very grateful - best wishes Karen

  • Hi Karen,

    So, just to double check we are talking about the same procedure. I had what is called a Latissimus Dorsi Flap. This is where they flap a piece of tissue/muscle over from your back. I think most lobular breast cancer results in having to have a mastectomy. My surgeon specialised in the surgery I had so she didn't really give me a choice.  They did it at the same time as my breast surgery as it involves flapping a piece of muscle/tissue over from your back, into the breast. I did have radiotherapy but it didn't seem to affect it. It looks like a normal breast but not as rounded. My nipple is slightly pulled in too. My scar is pretty large as it is a major operation but I was very good at putting bio oil on, which has meant it has faded massively. 
    And like you - I didn't really think I was likely to die from my cancer at the time I was having treatment. But I found after everything had finished, then my brain started to process it and I did struggle for quite a few months as normality has changed.

    I think it would maybe depend if you have a surgeon who is confident at doing this type of surgery. I was warned that if they couldn't get my margins clear then I would need a mastectomy but to be honest, I wasn't worried about losing the breast. 
    x

     

  • Vee, I love the fact you are stalking really :laugh::wink:

  • Hi girls, our number is increasing, I see!

    i did write one of my usual long missives a couple of days ago, taking the best part of half an hour, or even more, then I tried to correct a typo, everything turned blue and when I tried to get it back to normal it disappeared and nothing I tried could get it back!

    This is an abridged version. 

    Welcome back Superwoman, I'm glad you are back with us, still live. Why were your legs so bruised? I know nothing of the surgery you've been through except what you have told us, which is very little, and I have been in awe of your retelling the stories with so much humour. 
    Caroline, I knew you would be able to give more information to Vee, than I could, and Sam can add to that. I see you have another follower needing your information and advice, I know you will be able to help her. 
     I'm also glad that you have come through your period of adjustment post treatment and sound very positive again. I bet your family are glad to have you back!  Is your niece still with you? How is she doing?

    Vee, reading your other posts I can see you belong to this group. You are treating your present situation with exactly the right amount of bloody mindedness and disrespect that the disease requires.  Good on yer! I hope things start moving come the 14th.  The waiting for action is the worst part of this condition.

    Hi Karen, hope you are getting all the info you need to help make your decisions about treatment.

    To the other ladies and lurkers :) all good wishes.

    Now I have a painting to get back to!

    lots of love,

    Christine xxx

     

  • Hello lovelies!!

    Christine - Ahh yes, and yep we are growing (loving the 'we' sound) steadily. I know I belong in this group, I just needed one of you to acknowledge it! My prayers have not gone unnoticed x

    Caroline - you won't need a restraining order, but you may just regret that stalking bit. I got me a shiny brand new set of BC buddies who all think the same. (sorry for making you sound like false teeth!). :laugh:

    Sam - Even though we will gradually return to our lives pre cancer days, I will always have time for you all my lovelies. You have answered some of my initial worries, but I still have a few things to ask, when I start my treatment. (you don't get off that easy). 

    Karen - I'm not sure how to approach things as yet, but I'm sure we will share a word or two about our experiences along the way. Although, the ladies here are exceptional and on point, so I probably won't bring anything new to the table. (I'm here for the beer really).

    Im only like this cos I've not started my treatment and not sure of how it will affect me, so I'm getting it "all out there" now. Treatment might just bring me down a few pegs eh? Who knows, it might, I say MIGHT make me worse than I freakin well am now! (Oh Lord help us do I hear?)

    Who needs an apple a day to keep the Dr away when I have the power of 3/4/5/6 and counting eh? 

    Serve yourselves right. That's what you get for being so nice and understanding :laugh:

    Anyhoo, take care lovelies x

    Big hugs and much love xxx :love:

    Vee (unleashed) x

  • Hi again Vee,

    Yep am still cancer free.  Just trying to get blood tests organised to see if I can stop one of the longer term treatments that I have (zolodex to dry up my ovaries)...will I officially have shrunken ovaries or not I wonder???

    You're the part of the bestest group on this site now you know!  Well done to you, pity its all down to us having blummin (andf I'd swear if I could) cancer!!

    I'm the sort of person who isn't generally afraid of anything ( well only of cleaning and hard work) but I did find, as I generally do, that information is POWER!!  I did all I could (within reason as you could drive yourself mad) to find out what I could from others who had gone through what I was due to do so, but also bore in mind that we are all individual and therefore react differently. What is is they say plan for the worst and expect the best? I remained optimistic throughout and therefore everything was fine...well, that's my logic anyway and I'm sticking with it, flawed though it may be.

    Being called nice and understanding is certainly a first for me, thanks (I think??).

    Sam x

Reply
  • Hi again Vee,

    Yep am still cancer free.  Just trying to get blood tests organised to see if I can stop one of the longer term treatments that I have (zolodex to dry up my ovaries)...will I officially have shrunken ovaries or not I wonder???

    You're the part of the bestest group on this site now you know!  Well done to you, pity its all down to us having blummin (andf I'd swear if I could) cancer!!

    I'm the sort of person who isn't generally afraid of anything ( well only of cleaning and hard work) but I did find, as I generally do, that information is POWER!!  I did all I could (within reason as you could drive yourself mad) to find out what I could from others who had gone through what I was due to do so, but also bore in mind that we are all individual and therefore react differently. What is is they say plan for the worst and expect the best? I remained optimistic throughout and therefore everything was fine...well, that's my logic anyway and I'm sticking with it, flawed though it may be.

    Being called nice and understanding is certainly a first for me, thanks (I think??).

    Sam x

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