Starting chemo in October

Hi All
just walked along cliffs and back along prom then up steep hill to the hotel and I made it!!! Shattered now so sitting in hotel lounge having a drink lovely :slight_smile:

With my sister and family and not content with one sister coughing all over Xmas, this one spent last night chucking up so am hoping that my paranoid approach of hand sanitising and wiping every surface with antibacterial wipes saves me from any gremlins. I got strange looks this morning wearing gloves to serve myself breakfast to avoid touching serving tongs handled by the great unwashed!

Ribby it’s great thinking about getting lines out - I can’t wait to get rid of my port as it has niggled from day one, I haven’t had a date for rads yet either and I have FEC 6 on 8th jan - must ask Onc on Friday. We really are nearly through this girls…

hope you all are able to celebrate the new year somehow and here is to a healthier 2013 xxx

hi pumpkins,
went to see onc on friday, she was worried about my still having cough and asked loads of questions about my health before all of this and she wants me to have a more detailed ct scan has she says may have scaring on my lungs. no 5 fec tomoz.
glad everyone seems to be feeling better
hope everyone as a better new year

big hugs xx

Hi all

Just to say thanks to all who wished me a good weekend, had a great time, it was nice to spend some time alone with my husband.

Back home now, started the steroids this morning before first T tomorrow, having hot flushes galore think it is a side effect of the steroids.

Hope you all have a good new year, not sure what mine will be like just have to wait and see.

Gail xx

Hi all you wonderful pumpkins!! - you are all doing so well - we all seem to be having the same problems with Tax - it seems a bit of a wicked one - tredness, aches and mouths!!! - be care about takinf Diclofenic if you hav emouth problems as it does have mouth ulcersas one of its SE as I found out when I had my hip replecement in January!! ( just got over all that when I found my lump in June!!) - we are all getting to the end now - I’ve 2 more tax to go then 3 weeks of radio - good luck to the shrinking tumours - that is such good news - I managed Christmas ok too – even had a chinese with friends on Christmas EVe and took grandaughter to the Crib service at church - Sat was great too - family party for 22!1 - I didn’t do much ofthe clearing up though!! - think the alcohol might have had something to do with that!!! - off to a meal with friends we always spend New Year with tonight - red bull all day will keep me awke!!!
So here’s to you all you lovely pumpkins - we have survived all that 2012 has thrown at us so we can really DO 2013 in style!!! - Happy New Year to you all - Janice

Gail, just a quickie to wish you well with first T today!!

Janice, glad you’ve had such a good Christmas!

Love to all other Pumpkins! Xxx

Hello to all the pumpkins. I am new to this thread. Feel I need to be able to ā€˜chat’ to other ladies going through the same thing. Only people who have been on this road know how hard it is at times and family and friends do not always want to hear all the details.
Well I spent Christmas in hospital on iv antibiotics, discharged on the 28th. I had my Christmas dinner last Saturday and my family stayed an extra day to share it with me.
My last FEC of 4 has been cancelled for this week, so will now be going on Mon 8th.
I will be starting taxol and herceptin three weeks after.
It will be lovely to join you all on this rocky road.
Happy New Year to you all
xx

Hello Pumpkins

I’m not good at posting and was writing to wish you all a Happy New Year…hopefully healthier than this year, when my message disappeared from the box!

It may show up or could be lost forever…who knows with my computer skills.

I just want to thank you all for sharing the good and the not so good experiences with people like me, who read but don’t write so often.

I’m on day 4 of FEC 4 with 2 to go…feeling frail and missing out on the parties, but had lots of visitors-bug free this morning and this afternoon so I can’t complain.

Ribby -I’ve loved hearing about your adventures with EXBF, Princess, chemo nightmares and positive encouragement to all… I too extend sympathy to those on TAC.

Little Bear you are so good at seeing The Silver Linings and giving such encouragement to everyone (yes I have looked at your site) . I just hope all those in-laws help! Normally I have a house- full of relatives and friends for our Christmas meal and this year it was just the four of us, husband, grown up son who is still living at home and daughter who has left home…but we have her back for Christmas.

This year I made Christmas cakes for relatives when I was in a good phase then ran out of enthusiasm…then the others rallied and did all the decorations, made the meal, including setting the table…AND did all the clearing up and dish washer filling and emptying …and I was in the best place chemo wise. So that was another silver lining, a stress free Christmas for me with enough sparkle- the family really did me proud!

Roanaid , I thought of you and your extra eyebrows recently when we had some logs delivered:

I’m a retired teacher and while I’m in the being FECed part of my life (a fitting description don’t you think) I tend to wear my ā€˜twosie’, furry fleece top and micro-fleece bottoms, all topped by a horrid sleep cap that the wig shop persuaded me to buy, while I have my breakfast…before I am showered and smothered in white gloop.

This is how I was dressed when I handed the cheque to the helpful, not so young man who had tipped the said logs in the awkward corner I had asked him to put themā€¦ā€œOh so you are my old teacher!ā€ It must be 24 years since I saw him…wouldn’t you think he could have forgotten me in that time!

Great to hear that treatments are doing what they should Catzooo…and others.

Funny how we measure this journey-I have worked out that my, hard fought for, PICC line should be coming out in about 6 weeks after my last FECing on 8th February. Gradually I see a small flicker of light at the end of my chemo tunnel!

I pushed for a PICC through BUPA …who then sent a letter to say they wouldn’t pay the Ā£1000+ hospital bill. This was after I had gone an extra 120 mile round trip to a different hospital to have it fitted-it was a mistake, BUPA had authorised everything …but I had a sleepless night over that one! My oncologist had arranged for a Hickman to be fitted but the PICC seemed to be a better option for my remaining four FEC s after my veins refused to cooperate with the cannula.

I don’t know what advice and choices others were given about the effects of FEC on the veins and choices…if I hadn’t had a friend in the know I would have had a much more invasive procedure than I needed…the PICC was painless to fit and although it makes me feel like a patient it has made blood tests and chemo so much easier…alas not blood pressure readings which seem to hurt the leg more than the arm!

Yes there are still the side effects to bear…currently I seem to be putting weight on at an alarming rate, knowing that I’m not alone on that one is helpful too…but flatulence is my newie …husband talks about renaming our house Trumpton.

Good to hear that people are travelling and holidaying I’m 60 in April and have decided to celebrate that with a big family and friends gathering in the Lake District and a shopping and fun trip to London with posh hotel and show with long suffering husband.

However I’m envious of those of you who have had big family gatherings and trips away- Jayne your gloves story made me smile; I escaped hospital but after the first FEC ing I had neutropenia so I’ve had to be extra careful

Welcome to susanmary…sorry you are having a glitch…hopefully you will get comfort from The Wonderful Pumpkins…bless you all, too numerous to mention, I am addicted to the site so please keep posting.

Found a new tip that helped me today-dunk your toothbrush in hot water to soften the bristles; after that I did some electric toothbrushing!

Not my usual Hogmanay treat but chemo reaches the parts that nothing else can touch.

Good wishes for 2013, keep positive…

Happy New Year Pumpkins!

Have had a lovely relaxed christmas, plenty of eating and drinking, and even made it to a school reunion last night! Caught up with girls I haven’t seen for twenty years, fascinating and lovely, and think 2013’s resolutions might include making more an effort socially, it 's definitely good for you.

I am finding Tax SEs harder to cope with, haven’t managed to shake the exhaustion for the final week before next dose like I did with FEC. Also, my skin just seems to be falling off at the moment! Patches on my hands, face and feet, sore nail beds and finger tips, and cold sore that just won’t budge. Like Andie, I’ve had raw bleeding skin down below too, though thankfully that’s healing now. Oh, and bleeding piles, this time caused by diarrhoea not constipation like FEC!

Due next dose on Thurs, and it looks like my second dose of Herceptin will be postponed because the hospital haven’t managed to organise an echo for me. Should have had it before first Herceptin, but was told not to worry and they’d make sure it was done before second. Still not done, so they are now sYing I can’t have second dose, so that’s going to prolong the whole thing by a month at the end. GRRR! I know it’s not important in the whole scheme of things, but it just bloody irritates me when I keep being told some doctor or another hasn’t read the whole page and has forgotten to do something!

well, it’s not for much longer is it folks? in a matter of weeks many of us will be emerging from our final treatments, delighted that this will be the last time we feel quite this rubbish. I will not be sorry to see the back of 2012…and whatever you’ve got, 2013, I’m ready for you! Raising my glass (of G n T) to all pumpkins!

Happy New year pumpkins xx

Happy New Year Pumpkins - we are getting there. We ARE doing it. We Will get through this gastly time.
Witchy - you made me smile & laugh at calling it FEC ing - you are soooo right :wink:
Fifi - totally get the bleeding piles too - Oh how we would never have thought we would be putting such things on the web!!! lol :slight_smile:
SusanMary - Glad you have joined, I have been a late joiner too, but have found the open honestness of everyone extremely refreshing and helpful. You are right, as much as our loved ones want to understand they just cant. A dear friend came with me today for my blood test (I have a portacath so need to have bloods done at the chemo suite) She was ā€˜humbled’ by the ward. Its a place we have all now become so familiar and I forget others are clueless to the realiites.
Gail - hope you are ok after 2nd T.
I’ve got 2nd T on Wed - they are reducing my dose due to SEs. my hands look like they have been dipped in acid & are falling apart… But a lady today said her first T was the worst, so fingers crossed its the same for us all.
I raise my glass of Chablis to all you Pumpkins
Andie xx

Happy New Year Pumpkins!!

Here’s to the 2013 we sooooo deserve!!!

Welcome to new Pumpkins.

More personal posts tomorrow, off to welcome the New Year with fizzle water now!!! Xx

AndiJ - it was my first T today and I’m really suffering with hot flushes and sweats galore, did you have the same?

Gail65 Yes I had flush after flush hardly had time to get over one then another came and through the night it was horrid but they eased after a while hope yours do too :frowning:

Happy New Year Pumpkins :slight_smile: Hi to all new Pumpkins, be so glad to get this treastment over. I have Tac no 5 on Thursday. Im finding it so much harder than the Fec, I am armed with senna and lactulose and intend taking it the day before this time as suggested by oncologist. It took me a lot longer to feel ok and still my legs ache. I have been making the most of my good days had some friends from work viisting and a good friend came for tea. Have a chilling day today blood test tomorrow and then off for chemo again good news being only one left after that 3 weeks of radiotheraphy cant be half as grim as the chemo. Been making friends with my wig went out for dinner wearing it on Sunday and a trip into town yesterday Oh to have our own hair back :slight_smile: and eylashes!
Take Care everyone thinking about you all xxxx

HAPPY NEW YEAR PUMPKINS!!
Welcome new Pumpkins… glad u find this site helpful & reassuring. Hopefully amusing too! :wink:
Last nite was a weird one. Didnt feel like celebrating so was in bed for 11! Watched Jools HOlland & watched the fireworks on telly & from the neighbours. Found it more a time for reflecting than celebrating…
Had busy few days, really enjoyed the Panto with Princess (although she was rather embarrassed when i got up gangnam styling in the aisle - btw, there were a few adults not just me!!). Took her to the pics yesterday - really appreciating 1-1 time with her. I think its so easy to forget about the quality time in everyday life…
Chilling day today. Nana & Grandad took Princess for a walk on the prom - brrrrr!!! I had to wait in for DN so unfortunately couldnt join them (phew!).
Pre-chemo for #5 on Thursday - oncologist at 3, then seeing psychologist at 4. Sounds good on paper, but the timekeeping of the Unit is horrendous so expecting to be there at least 3 hours! Cant believe #5 is approaching. In a way i feel quite positive about it, just want it out of the way tbh… Just hoping it goes as #4 did as regards minimal shaking during administeration.
Well, just wanted to pop on here & say im wishing all Pumpkins a happier, positive 2013… Keep it up ladies… XXX

Happy New Year Pumpkins!
I managed to stay awake to see the NY in but only because I’d slept for 30 of the previous 36 hours! Today is the first day I’ve got dressed since going to the hospital last friday. The SE of the T faded out by Saturday and then I got hit with a viral infection! My DH had it as well so it’s been very quiet here, do wonder if I’m borderline neutropenic but my temperature hasn’t gone over 37.5 so I’m staying put.
Just used my favourite xmas present - a Burt’s Bees Hand and foot care kit and then topped it with a pair of hand knit slipper socks, I’m determined that my feet are not going to cause me any more problems!

Wishing you all a happy and healthy 2013
Nonni

Happy New Year Pumpkins and welcome to our new friends.

I managed to stay the distance at the NYE party last night, we were on a 3 day break with my sister and her family and my mum in Bournemouth, we have done this for the last 6 years and it was booked prior to dx so decided to go anyway and hope I survived. Interestingly I was fine but Sis and OH both have had a shivery stomach bug so I am really hoping my mad sanitising has paid off but the next few days will tell. Due to their poor health, we came home early today and OH is now back in bed…

I stayed up until 1.30am, managed a dance, then couldn’t sleep as I was so wired - now slobbing on the sofa with my lovely slanket (xmas present) and catching up with everyone’s news.

I am glad you had a good time in Bournemouth Gail, the weather was dreadful but the break was nice.
Ribby, I am so pleased you have had some quality mother and daughter time and I hope no 5 is bearable. I had a giggle at your gangnam comment, my daughter videoed my sister and I trying to do it last night, we even got my Mum up to have a go!
Kirsite, it is great to catch up wtih friends, a real spirit lifter.

I hope all of you having T have more manageable side effects with your second dose, it does sound tougher than FEC.

Take care everyone

Jayne x

Happy New Year all pumpkins. I had a lovely christmas day and boxing day and for a moment felt perfectly normal as i forgot about all the side effects for a moment. I had 5th session of chemo on 27th Dec which was the 2nd T. Havent felt as bad as last time but very tired with a little bone ache but this time i seem to have got oral thrush as well as in other places. Not very pleasant but just have to keep thinking only 1 more to go and then this part will be over. My feet seem to have peeled all over aswell. Im glad some of you managed to have a good new year. Thats excellent. I did manage to stay up and even tried a glass of baileys just before midnight but it tasted disgusting so gave up and will have a drink to see in the new year once my taste comes back and my tongue is back to its normal size. We are all getting there with the treatment and heres hoping we can all have a better 2013 than we did 2012. Take care everyone and good luck for all of you going for your next session of chemo xxx

Hi all
Just wanted to wish all the pumpkins a very happy new year!!!
Stayed up to see 2013 in but felt very flat and not in the mood for partying at all still lets hope 2013 is a better year than 2012 and look forwards to finishing all this pesky treatment!
Feeling ok post tax 1 in fact i seem (touch wood) to got off fairly lightly compared to some of you. Have a feeling no 2 may hit me a lot harder!!
Lots of love and happy new year xx

Happy New Year to you all, I too felt kinda flat at ā€˜the bells’, I’d got a bottle of champagne but I did’nt feel like celebrating. I said to my husband I’d like to open it once I get over the SEs on my last chemo at the end of Jan. That will feel like the new year to me.