In blissful ignorance this time last year. Went on to enjoy Jan, Feb & March and then it bit me on the bum in April. The rest they say, is history.
Claire xx
This time last year - just trying to get my head round my dad's death from cancer in September and my father-in-law's death in October and looking forward to 2008 being a better year! BC bit me in May.
Here's hoping 2009 will be a better year for all of us
Mal
This time last year - looking forward to Christmas, looking forward to friends popping in, looking forward to wearing a new black dress to dinner with friends, looking forward to a sunny holiday in Barbados with my best friend.........Oh and had a job! Bit me in July too Kat.
xx
This time last year I was in blissful ignorance. A friend in Oz had emailed me a link to www.nbcc.org.au and their questionnaire to assess my risk of BC. ( my Mum died of BC )
I was low risk and thrilled.
But there is no hiding and it sat up and bit me July this year.
Same Ozzy friend jumped on plane and we had an unusual summer!!
Kat xx
nbcc.org.au great site.
Last year was essentially 'normal', planning and packing for Christmas away at Granny's house in the forest. After diagnosis in July this year, surgery 12 Sep that revealed a 14cm DIC and invasive cancer and 27/35 affected lymph nodes we will be staying here for Christmas. The side effects of chemo and persistent spiking temp means I want to be near our local centre. Only 2 more Tax to go, then 3 weeks rads, then 5 years Tamoxifen...
Looking forward to finishing this treatment and getting onto Tamoxifen in 2009 to try and get a new sense of normality
Tanya x
this time last year i still has my dear sis with me ,although she had been really ill with heart problems we wernt to know that jan would bring bad news re a cancer spread diognosos and then her death im march ,also my bro in law who was diognosed last christmas died on the same day .im fighting liver mets and lymphodemia in arm is giving me gip ,now going to see consultant tomoz re right side ,dont know if ill be posting next year but my god i intend to fight with all my ,might !! hers to 2009 hopefully it will bring better times for all .lynn x
This time last year I had been dx but was thinking it would mean a few weeks off. I was on a Uni course and thought I could manage to stay on that with 3 weeks off for rads........surgery was 27th Dec and after that they discovered it was grade 3 so I have done all the chemo, dropped out of Uni, to some extent dropped out of life.
The worst thing was telling my Mum. Even telling my kids paled in relation to that. The best thing was that I now know without doubt who my friends are, and who was not to be relied upon.
I recommenced the course this September (by the skin of my teeth!) and am working more or less normal hours again. Very tired but some hair peeping out of my scarves and taking Tamoxifen without too many ill effects. For me, this Christmas can only be better than the nightmare of last year.
Good luck to all of you
Louise x
This time last year I was making up for the bad xmas I had the previous year , having just finished treatment and thinking my end was nigh 😞 I had a ball of a time, and intend to have the same this year. Life takes on a whole new meaning when you have been on this cancer journey.
Merry Christmas girls, I wish you all the best for the future whatever stage of the journey you are at
Marge
This time last year I was ringing my GP after finding a lump (turned out to be a cyst but they found the lump in the other breast...I didnt even know it was there!!! which still scares the pants off me) had mammogram and biopsy 17th Dec and DX christmas eve.
We have put up our christmas tree today and have just been all organised and made a christmas card speadsheet on my new laptop, its been a roller coaster year even though prognosis is good and ploughing my way through the 5 years tamoxifen/zoladex combo. I dont post too often these days but do pop in and have a read now and then. Thank you to everyone who kept me sane.
Good luck to all and heres hoping the next year is better than the last for all of us.
Love and luck to all. S x
This time last year I was bald, but happy, after the usual mastectomy, chemo and rads, and although prognosis not brilliant ( large grade3 triple neg ) I was determined 2008 would be better. Could it be worse? We booked a holiday, theatre trips, Katie Melua tickets, and signed up for Ribbon Walk. Had to cancel everything after developing severe back problems and spent the year unable to sit, stand or walk! Thankfully no return of cancer, but at least 2007 was spent vaguely fighting something. This I can't fight. Having 3rd op tomorrow, so with a bit of luck 2009 will be cancer-free and pain free!! I am not going to book anything in advance ever again, but do everything on the spur of the moment!
A year ago I was being discharged after having lung biopsies done, the lining of the lung re-attatached , and several pints of fluid drained! This was a bolt out of the blue. I'd had 12 cancer free years from the primamry diagnosis, and had just begun to think that I was perhaps going to be one of the lucky ones with no further problems-as if!
This year, I have just been discharged from hospital-Hickman Line became infected, so was in for 6 days. With next to no immune system due to the chemo, it was pretty hairy to discover that I didn't repond to antibiotics, and it was only after several days when the " restricted access" antibiotics were administered, that I started to respond.
In the past year, my hormone status has changed from er-, to strongly er+, and yet I didn't respond to hormone treatment. I had limited success with combined taxotere/herceptin, and when on herceptin alone, the short period of stability (2 months) was soon over, and the tumours progressed further. We'd had such high hopes that herceptin alone would have held things at bay, for a while at least, so it's failure to do so has been a bitter blow. I re-started chemo (capecitibine), a few weeks ago, and am now on my second cycle.
Overall I still feel well, deriving huge pleasure from life, and able to do most of what I used to do. I'm so grateful that it was found when it was, as I'd had no symtoms-it was picked up simply through a chance comment to my gastroenterologist, who prudently decided further investigations were wise. Thank goodness he did, as the mets to the pleura he found have now spread to the liver and bone, so tough times ahead. It's hard to find the balance between trying to stay optimistic that we'll find a therapy which will be beneficial to me, and expecting too much-made that mistake with herceptin!
This time last year I was living in ignorant bliss, had been to my GP with my breast lump. Age 30 and no family history - no worries right? January 08 was a catalogue of hospital appointments. January 29th diagnosed, Feb 18th my Dad dies. Feb 27th my Dad's funeral, Feb 29th Mastectomy. Chemo finished Aug 29th, Rads finished Oct 22nd. Now what? Can't wait for 2008 to end!
This time last year I had lost all of my hair and just had my 3rd dose of Chemo,I was feeling dreadfull and was wondering if I could go through the next 6 months.
It was a long journey.
But here I am today with a good growth of hair and feeling better,roll on 2012 when this Arimidex ends.
Good Luck everyone and have a good Christmas if you can
Jackie xxx
This time last year I had decided to move back from Birmingham to Stoke... had found myself a great boyfriend and a great job... now I'm having radio after a lot of chemo... boyf and job are still there but its all very very different!
But even with everything... bc included, I'm alot happy now than I ever was in Birmingham... and realise that you can't take everything for granted and know just how much support I have around me... you think you have friends but you never know until you've been through all of this
Erin xxx
My 19 year old daughter was travelling in Oz,My 22 year old son was giving me a hard time and I was wearing a wig.Now my daughter is home and applying to do nursing, my son is in London,working ,happy and a lovely girlfriend,and I have a short grey crop--- need a hair cut !!!
This time last year I was happily preparing for a skiing holiday & x-mas, this year I'm preparing for my first chemo (on Monday) but also still preparing for my skiing holiday (on Saturday) and still looking forward to x-mas as I wont let it rule/ruin my life and have learnt to make the most of fun times with friends & family.
Good luck and best wishes to you all.
xxx
A year ago I was unpacking from moving house, which I am also doing this year again but a lot more slowly (but this time bought) ... last year was writing Xmas cards and this year am writing fewer to the people I really want to stay in touch with... cos friends are what make a big difference to this merry-go-round... last year was not 'in remission' because I hate and loathe that expression, but this year have had secondary diag in May and am coming to terms with that, but living life to the full (with a few more rests in between!)
a year ago had just had my mastectomy and expander implants .....this year the usual emotional roller coaster now waiting for a bone scan but i am still here and am maxing it up xxxxx
A year ago I was looking forward to Dec 12th when I had my 18th and last herceptin so ending my hospital visits of every three weeks.
So it was a very happy end to 18 months treatment.
Good luck to others still going through it. It does end one day.
This time last year I was unleashed from my tutor and allowed out on solo patrol in my new career, my husband was starting a new job, the kids were all ticking along nicely for a change and after a rough time over the previous 3 to 4 years for the family caused by deaths, family rows, children leaving home (some), marriage difficulties we were hoping for to a "quiet, uneventful" year ahead (for once). We got 9 months without anything major happening for once and everything improving, marriage, son being selected for prestigeous college, daughter sorting her life, husband and self getting to grips with new jobs and doing well in them. 18 August this year BC dx, mx, now going through chemo wondering whether I can and will get back to that "quiet, uneventful" life or whether there is ever such a thing as a "quiet, uneventful life".
This time last year I had just finished radiotherapy after 6 months of chemo. And preparing to fly to the USA for two weeks with OH and son for a longed for break as we had to canx our summer holiday due to my diagnose
Still coming to terms with finding out I had secondaries only a month after my primary diagnose. And now waiting to find out if its gone walkabout again and settled in my chest
Looking forward to Christmas with OH and son -every extra day I have with them is so precious
Jools
A year ago for me was pretty stressful sorting out my friends estate who had died in a car accident. I thought by the time January came I could put 2007 to bed and get on with my life and start my new photography business, alas not. It all started in April I woke up one morning and bingo a large lump was sticking out of my chest I went to see various Doc's and on the 7th May diagnosed with lobular BC 25mm alien in situ! I could not believe it I am 39yrs old I have been fit and healthy all my life, I don't smoke or drink, wow I sound boring!
Anyway I have had 6 lots of chemo which was hell, a mastectomy and node sampling and now waiting for my rads to start which will be on the 3rd Dec, just found a small lump below my scar last week so I now have to get this new lump looked at, I have shed some tears again this week praying that it has not come back so soon. I just want to get on and enjoy living again with my 10 year old son and Hubby.
Best wishes to all.
Gilly x
This time last year I was in Viet Nam, having travelled through Thailand and Cambodia. Life was good, celebrated my son's second Birthday in December, and cancer was something that happened to other people. July this year I found a lump while I was on a family vacation, and whammy, two weeks later it's a mastectomy and sorry love, your prognosis is poor. Life, however, goes on, currently having chemo and looking forward to rads and Herceptin.
This time last year I was on holiday in Fuerteventura we had a super time.
I didn`t know what an oncologist was ...yes really!!..chemotherapy and radiotherapy I heard other people talking about but knew very little about and lymphoedema ..whats that?
Two months later I felt a huge lump in my breast and went my G.P who told me not to worry it was nothing and gave me a10 day course of antibiotics, my lump was still there 10 days later and guess what, she told me not to worry it was nothing serious and gave me anther 10 days antibiotics!!!.
As we were going on holiday I went to see her before we went and got more antibiotics to take with me!!! when we got home I went to see her again and guess what. she gave me more antibiotics, but finally referred me to the breast clinic telling me not to worry they would drain it!!
I have, as we all have, learned so much over the last nine months, I am off to Tenerife on Thursday and hope to goodness next year will be a better one but have learned to take just one day at a time!!
By the way now my treatment is over we have finally put a letter of complaint to the surgery manager and feel better for it!
Take care,
Janx
This time last year......had found lump in left breast on 6th November but was in the middle of my period so waited a month just in case in was hormonal-it wasn't! Then developed swelling under left arm and knew I had cancer.Went to see GP on 21st December..........and the rest is history!
Alli.
This time last year I was half way through 30 rads and about to start Herceptin. A rota of people from my village were taking me into hospital each day (and not all the ones that I might have expected to be helpful, I must say). After chemo I was bald but had a lovely wig.
Now I finish herceptin tomorrow and I have hair longer than I did before. I am trying a new style now that it is curly but as it came back grey, it is now a rather nice strawberry blonde courtesy of my brilliant hairdresser! I have a very different lifestyle, having decided to reduce from full time to part time work so that I can spend more time doing exercise as I was told to lose weight. I have lost nearly 2 stones and feel much better for it but need to lose as much again. I have also taken up watercolour painting and I love it.
Arimidex makes me ache dreadfully so that is a constant reminder of what I have experienced since diagnosis on Friday 13 April last year and I also have osteoporosis, but I feel so much better than this time last year. I am realistic about what the future may hold, but at the moment, things are pretty good.
All the best
Anne
Suffering from Jet lag after the best holiday of my life, then wham 4 weeks later told I had breast cancer how things can change in a few weeks.
Debra
I was deep in chemo I was on EC at the time and not doing too bad on it, if I say so myself. No hair, of course but a very good wig. The general good responses you get at the outset had faded a bit, but people where kind enough to remember me and from September to Christmas there where flowers of some sort in the house. I did do some internet research but like you Magsi I wasn't brave enough to write something myself until after Christmas. I was beginning to realise who really were going to be good friends to me.
What an interesting thread - and what a year.
A year ago I was living the Expat life, out in the Middle East with my husband and three children (then 13, 10 and 8). We had a tough January, as my father collapsed and died totally unexpectedly from a massive heart attack, and then 12 days later my father-in-law died from a brain tumour. After all the turmoil and upheaval, we treated the family to a holiday in South Africa, and began to come to terms with what had happened - little did we know..
In June this year I felt a strange hardness in my breast, a bit like mastitis, but as you've guessed was actually 2.5cm of lobular tumour. What I hadn't felt was the other 6cm one hiding in there too. I've been back in the UK since 1st July, living alone in our "holiday" home whilst undergoing treatment - 4 cycles EC and 2 (out of 4) taxotere, with mastectomy planned for January. My husband is coping manfully with breadwinning and being a single parent nearly 4,000 miles away, but thankfully they will all be back for 4 weeks at Christmas - can't wait.
Like many of you, a year ago I had just started on the bc rollercoaster.
The cyst I had found turned out to be just that but the ultrasound on 31st October showed up two suspicious areas, then the usual array of tests with results on 7th November being inconclusive and results on 14th showing the need for a lumpectomy on 27th (my birthday) and finally a mastectomy on Dec 14th.
This time last year I hadn't discovered this site as we were in the middle of changing from dial up to broadband and were without a connection for several weeks. When I did log on early in Dec. I saw the word cancer, closed it down and didn't venture on until after the mastectomy. Finally at the end of December I once again logged on and am so glad I did. The information and support on here has been amazing, as have the people and the friends I have made.
M x
This time last year I was in blissful ignorance - Bc was diagnosed in February. My dad was still alive and I had spiky hair and still had a figure. Maybe the cancer was there already as certain warning signs appeared before diagnosis if look back on it. I am less tired now and this time last year i think the bc was probably brewing or about to appear.
This time last year i was so happy that the breast lumps i was feeling were fibrocystic changes. Wanted to get on with my life as had been really low since my husband left me and my 3 boys the previous year. One of my sons started going off the rails and was in lots of trouble with police just got his court case past thot was time for things to start looking up for us all. Went for my Mammogram after his court case was recalled 2 weeks later now i am waiting for the results of my core biopsy because my mammogram showed a shadow which turned out to be a small lump (that i cannot feel) and fna showed abdormal cells. My doc chasing up resullts am at the waiting game stage just hope that 2009 is a better year and no BC hanging over me!!
A year ago I was tired, and had an itchy nipple!!! I lost my Mum suddenly in january my boss resigned I took on the section - still felt tired and was diagnosed in march - triple neg with local node involvement (stage 3C). I have been through chemo and radio - not operable so no surgery. I am not as tired as I was prior to diagnosis, and i am overwhelmed by the amount of wonderful people you find when going through this type of c**p, at the hosiptal and on sites such as this. A year ago i did not expect to be a Granny - especially at the age of 44 but my son is due to become a father on or about 11th December he comes back from Afghanistan for three weeks on 4 December in time for the happy event. There are always things to make us feel sad but i have learnt that you appreciate the positives and the special moments so much more - not something I really did a year ago. It has been a long year and one in which I feel I have aged a hundred years but somehow I have got through it
Helen
This time last year I was celebrating my daughter's second birthday, and my three month old son's Christening.
I had no idea that my life would be now on this hideous rollercoaster, that is breast cancer.
In Feb, I was diagnosed with advanced (15cm x 10cm) IBC, and have since had 2 x FEC, 4 x tax, 11 x Her, a mastectomy & 20 rads ... roll on 2009, as I don't want a repeat of 2008, & what do I wish for ... lots more birthdays to share with my children.
A year ago I was having treatment for breast cancer. I am still having treatment for breast cancer. In a year's time there won't be any treatments left but I'll still have breast cancer, or maybe I'll be dead. It doesn't get better..it gets worse...!
Jane
Ayear ago I was one year from op and had just had first NED followups.I was still very tired and hadnt much hair but there was a glimmer of light at the end of me tunnel.xx
Cannot remember. It seems so long ago. In blissful ignorance and thought I had a future. Dont know anything anymore. Fearful of the future and just finished taxotere. Never again!
I had been diagnosed on November 2nd and was waiting for my mastectomy on December 5th. Also I was trying together with my mum to sort through my brother's estate as he had died suddenly that July. Looking back I don't know how I got through it! But you do at the time..now after chemo and rads I've not had the best couple of months, it all seemed to hit me, but feeling better in myself this month. My birthday present in March was losing my hair! On Christmas Day I walked my dog, with difficulty, as arm was still weak, to my brother's grave and sobbed, and hoped I wouldn't be in there this year...but I am doing well.
Best wishes to all, a good thread,
Liz x
This time last year I was packing my hopsital bag in preparation for an operation ............on my foot (which had been broken in 2005 and operated on in 2006 but failed) I was feeling sorry for myself having to go through it all again.And dreading another Christmas in Plaster up to my knee and not able to weightbear.
Still, I thought once it was fixed I could get back to normal,Ha ha! I returned to work fulltime mid June after a phased return and had my Breast Clinic appt on 30th June.
Swiftly followed by Mastectomy and recon and now just Tamoxifen and depression!
At least I can cook Christmas dinner this year,it was impossible on crutches/wheelchair!
Lets hope next year is better (although I am bit scared to hope!)
Dot
xx
A year ago I was feeling discouraged because a bone scan had shown some progression of my hip met (I have bone mets but no other secondary spread) and I had been put on IV Zometa, the strongest "bishbosh" for bones. This year's bone scans have been better news and I am now on tablets (Bondronat) instead of the IV.
A bit discouraged tho, because I've regained some weight, after losing 2 stone after dx in 2006. Can't put all the blame on my Femara, it's up to me what I eat... aarrgghh!
And looking forward to a better family Christmas than the previous two.
Best wishes to all!
October last year I'd just come back from a manic week in Florida (5 theme parks in one week?!) including swimming with dolphins. It was absolutely brilliant. About this time last year I'd just found the lump in my breast, actually it was a "ridge", it was huge and I didn't want to know, so I put it to the back of my mind and got on with everything else for a few months.
The last 9 months have been something else! At the end of February it turned out within the "ridge" there was a lump 45mm (yeah, that's huge too huh?!). I knew I was in trouble after the mammogram when the radiographer wished me good luck!
After the first op, Mother's Day was really bad, as I had to tell my teenage children and my parents the day before that I had grade 3 cancer. My birthday present this year was my last taxotere. I don't want anybody to give me THAT again thanks! I've made friends through this website, both locally and further afield, which is an unexpected bonus. I used loads of information I got on here to ensure I got the right tamoxifen - and I'm actually LOSING weight (not a lot, just a few pounds) rather than gaining it!
Really interesting idea this thread Lanterna - it's quite a thought to look back over the last year.and realise how quickly it has passed, even though it seemed to go on forever whilst in the midst of it.
It's almost exactly a year to the day: the mammo that caught something wrong. I was happily chatting with the radiographer about digital imaging (something I have to know about for work), and she said "These are really good images..."
And then stopped. I knew straight away something was up, and she knew that I knew etc. And the cancer rollercoaster started at that moment.
What were you doing a year ago? Were you already on that rollercoaster, or wondering if something was wrong, or facing the end of treatment? And how are you now, looking back on the last 12 months?