hello, 36 and finished treatment today!

I had my last radiotherapy session earlier today. Its been a huge rollercoaster through diagnosis in March, my WLE and SNB operation in april, chemotherapy from end of april to august, and radiotherapy from september to october. Just another 4 years 11 months of tamoxifen to go now hopefully!

I dont feel hugely elated, but i dont feel low either, a bit inbetweeny really, and tearful, though tears are so part of life now i dont really notice them much.

But I do feel relieved and am very glad i am at this end of the treatment, and that i found my lump when i did as otherwise i could have had a great 2010 but it would all have been waiting for me.

I know that the convalescence period will have its challenges, but i thought it was worth posting about where I am today. Its been hard but I have got through it and everyone keeps saying how proud they are of me. And to be honest, they are right, I have done brilliantly and i am very proud of myself too today.

Thanks everyone for your continued support,

Vickie

Hello & Well Done Vickie. We shared the summer from hell and come out the other side. Be proud of having dealt with everything so well. Hopefully, we will never ever have to do this again and see our boys grow up. Big Hug. Tina

Congratsulations Vickie.
At the beginning it seems like one long rollercoaster, with the finish of one treatment heralding the start of another. With tamoxifen started you are done with all the beginnings so that is definetly something to celebrate. It’s a hard road and I was elated last week when my onc talked about starting rads before xmas to finish in the new year. His comment “you can have your life back then” seems very apt for us all and reading your post today made me feel glad I went and got things checked when I did.
Here’s to a happy, healthy and treatment free 2011
Ali.
x

You’ve done it and you helped others do it. Of course you should be proud of yourself. Those other Yummy Mummies have got nothing on you. Dxx

Well done Vickie. You have every right to be proud! I hope you can get your life back now and soon 2010 will be just a distant memory.
Love on ya
Debs
x

God i hope so! Have taken the anti-cancer diet approach today, hot chocolate, huge piece blackcurrant cheesecake, pizza and sparkling wine!bit of halloween store cupboard chocolate thrown in too for good measure.

Well done, you really should be proud, and it is great to post and give hope to oehters at the start of their own journey
And I love the diet! Did you actually eat in that order - I am really impressed!
Sarah

yes but with a three hour gap between the cheesecake and pizza!

Vicki Well done you have done so well and been so supportive of others on this forum too.Hope you can get some semblance of your life back you have been so brave I wish you and the men in your life well ,both the little ones and the OH Can I come and have cup cakes too or pizza and cheesecake if you like.This has been a b****r of a year but roll on Nov etc. Hugs and love Jackie

HURRAY! What a year but you’ve done it, and Yes we should all be proud of ourselves! A big cheers to this forum as we have been able to support each other through good and bad times with people who really understand!
Heres looking forward to 2011!

Well done Vicky and many congratulations to you on finishing your treatments, you should definately feel very proud of yourself, hope you have a great celebration lined up as you deserve it pet.
Lots of love to you and heres to a happy and healthy 2011 .
Well done
Linda xx

vicki,

you are an absolute star and so glad the treatment is over for you. Concentrate on your kids and oh and enjoy ! Cupcakes in Manchester with you and tartan trolley girl would be great !

K x

Big congtrats vickie :slight_smile: Damn rightu should be proud of yourself. All the very best for the future you deserve it
tina x

Vick,
That is so brilliant, you should be proud, it’s bloody fantastic.
Joxx

Hi Vickie

well done and congrats its great you have now finished RADS and can now start looking forward without having to worry about hospital appts etc…

I know ‘it’ will never leave you as such, but its a great milestone to get past

take care xxx

Well done for getting through all this i still remember your first post. It was very touching. It’s good to know your finished.

Wishing you lots of love for the future.

Jaynexxxx

Congrats on getting through. This has been an annus horribillis for me too having finished active treatment last month. Your posts have been supportive to others throughout and I wish you well in the future. xxx

i think we have all done, and are doing, really well in a horrible year.

Now my problem today is…what do i do? Are there any doctors/nurses out there who would like to see me as am at bit of a loose end!

Congrats Vickie, A huge step forward

Love Nell xx

Hi again everyone,

Jayne, your post made me have a look back at my first post and i have copied and pasted it below. I have come such a long way since then, so wanted to put it on to let any people who are earlier on in the treatment process than me know that it does get better.

Vickie

tors says on 26 Mar 2010 22:03

Hello, 36 and diagnosed early March 2010

Hi everyone,

I was diagnosed with invasive ductal breast cancer earlier this month. It feels like I am living through hell and have had the sh** kicked out of me. I have cried a lot. I feel like my friends are the luckiest people on earth as they are still living the carefree life I was living up til 4 weeks ago when I found my lump. Thats the new me, jealous of my own best friends.

I found a lump in my left breast when I was examining myself on a Saturday night, and was given an appointment at the local breast clinic the following monday. I cannot fault my GP and the breast clinic staff so far.Supportive and lots of information. That day I had a mammogram, an ultra sound, a fine needle biopsy and then got the results the same day and was told “it is cancer”. My husband was with me . I had to lie down on the bed as i nearly fainted. I had to go home and tell my mum and sister. They were minding my two little boys who are just 2 and 4. Seeing my mum and sister’s faces crumple when they saw my face was awful. thank God for my husband being with me. Suddenly I totally depended on him, having whinged about him for years like we all do. I think I quite like him again now!

That night I was beyond shock. The absolute worst bit was when I went to bed. Previously I had always looked forward to bedtime, especially as sleep is at a premium with young children. But the second the light went off I started panicking and breathing too fast and had to have all the windows open. My lips and fingers went tingly and it took my husband ages to calm me down. there wasn’t much sleep to be had that night.

The next morning I was back at hospital and sobbed silently through the ultra sound guided core needle biopsy, although I was still aware enough not to move whilst sobbing in case she slipped and hurt me! The sound of the needle thing clicking was awful and I certainly couldnt watch ( though my husband did), and I hummed throughout to keep calm, so must have seemed mad. But it really didn’t hurt as the local was great.My breast was black and blue after though. The thing that really got me was that the last ultra sounds I had had were to see my little babies when I was pregnant and now it was because apparently I have breast cancer. And after a year of my persuading and convincing, my husband and I had finally been trying for a new baby and I had been expecting to have ultra sounds at this time for pregnancy again, not for this bag of rubbish. Thank god that I didn’t get pregnant though, it is hard enough wiht just my body to take into account.

I saw my breast cancer nurse again after the core needle biopsy and totally collapsed. I was convinced that this was cancer from somewhere else which had spread to my breast, so my body was already riddled. She reassured me this was extremely unlikely but who believes statistics now as we all know that someone has to fall foul of them, and as has already been proved, I am already on the sh** unlucky list…

Waiting for my biopsy results was horrific. The wait in the clinic waiting room was genuine torture. The tumour ( which is a word I really really really cannot believe applies to me) seems 15 by 11mm, and the results indicate its a grade 2, but only “vaguely” oestrogen positive ( 4 out of 8 if that means anything?).There “is no reason to believe that it has spread to the lymph nodes” but who knows? And when did lymph nodes become so important in my life? I don#t think I had ever even said the term a month ago.

So now I am waiting. I have my lumpectomy on Monday. When i first heard that I had the dreaded cancer, I told them to take the top half of my body off. At the next appointment I downscaled to a double mastectomy, then a mastectomy and finally have agreed that a lumpectomy is the way to go. I have to have a wire put in via ultrasound to mark the place before the op, and am having sentinel node biposy so need to go to the nuclear medicine department at a different hospital first. Nuclear medicine! Wow, am going to be glowing from that, with a blue breast, blue wee, blue poo and blue contact lenses from the dye! I will be like an avatar, if only they could stretch me to make me taller and skinnier too! although I did lose half a stone in a week through total inability to eat at first.

So onward and upward. I am terrified about getting worse news after the op, as i am slightly more able to cope with the status quo now than I was before. I feel that this is totally unfair, I am a good girl , never smoked, never ever taken drugs, hardly drink , not overweight, breast fed both babies for 7 or 8 months until they got top and bottom teeth they could bite with.

Have just realised how much I have written, hope I haven’t sent anyone to sleep and well done for reading this long if you have! Think I feel a bit better for telling people what has happened to me, although feel as though am preaching to to the converted, coals to newcastle etc!

xxx