im also having EC.. I’m having that first then packitaxel. Glad your not feeling too bad at the moment and managed to get out yesterday for a little bit. I’m thinking I’ll be going through a few box sets over the coming months too.
Take care and big hugs
Wow, it's great to be so quick between diagnosis and starting chemo so you can get this thing started, but that's a helluva lot to get your head around in a short period. Do you know what your chemo treatment regime will be yet? Not much by the way of tips yet as I'm just on day 3 after my first cycle of EC - not feeling toooooo rough - mega nausea the evening after, but had abated by the next morning, so I managed to go for a walk in the park yesterday afternoon and eat normally. Up pretty early this morning with a pretty dicky stomach, but snuggled up on the sofa with a boxset and the cat and feeling better, and hoping I can get out and about a bit today! Sending you love and strength for the next few weeks xxx
Just jumped on here as I’m starting chemo this month possibly this Friday if not the one after. I was diagnosed with TN breast cancer on the 19th July. Totally freaked out by it all so came on here for some reassurance and Support. Iv loads of amazing people around me but I’m sure you’ll all agree no one knows what your going through unless they’ve been or are going through it themselves. Iv got 6 months of chemo ahead of me 😫 Iv had some tips Already on how to get through it but any other tips would be very gratefully received.
Hi EM39, cripes, that sounds like a lot of surgeries to get through, this is such a twisty turvy journey, as treatment always seems very different to the first appointment (I was just initially expecting lumpectomy and rads). It does feel good for getting this started, so will be thinking of you next week and then it's one ticked off. Day 2 here today and whilst I couldn't get out of bed until 11.30am, I managed a shower and a walk outside in the park for an hour, as well as chatting with the inlaws who were here looking after my youngest - who knows what the next few days will unfold but I think this being less of an unknown is helpful!
Wigs wise, I felt better after my chop as it's helped me get used to myself with less hair... I haven't looked at those shops you mentioned, but I had two arrivals from annabelle's wigs today, pretty cheap acrylics but I love them https://www.annabelleswigs.co.uk - I'll try and post a photo of them in real life on here if I can figure out how to log in from my phone... I'm awaiting an NHS wig which I'll get for free (it seems very random how different hospitals work this as I've heard other folks getting a voucher towards the cost, whereas they told me any acrylic wig would be free- I'm under the care of Guys and St Thomas, and they have a wig fitting unit there who have helped me order one and then will trim it to size) - went for a more conservative one for the school run. Also got a nice turban from Rona's turbans on etsy.
Good luck and I hope you have a lovely treat filled weekend before things start next week 🙂
I'm 39 with 2 young boys (5 & 8), diagnosed in April with 8mm IDC, Grade 3, ER+ and HER2-. I had lumpectomy and sentinel nodes were clear. Three surgeries later, they couldn't clear margins, as DCIS and a little more invasive cells were found under the microscope, so I'll definitely need a mastectomy.
Meanwhile, I have had the oncotype DX test done and this came back at 21 and since I'm under 50 that's a 6.5% chemo benefit. Had appointment yesterday with oncologist and I start on Thursday 8th Aug....ahhh everything moves so quick and super scared. I due to have 6 sessions of FEC over 18 weeks - to be reviewed after 4 sessions. Wondering why I won't be having FEC-T (oncology ward manager did question this, but seems to have confirmed I've not to have the T) Anyone else just having FEC?
I'm petrified about losing hair and just realising how much it makes me look like me. ANyway, I will try cold cap but realistic that it only works for a few people (getting hair chopped on Tuesday afternoon) and wig appointments Tuesday mrn with local shops. Looking at a few sites and wigs are so pricey....anyone heard of these ones (www.sheswigs.co.uk; www.urhair.co.uk) wigs look nice and good price too compared with some human hair wigs at ££££.
Can't wait to get started on this...so I can get it over with! Totally know what you mean with the fit and healthy, so weird that all this is going on inside and we can feel completely well. I'm getting my eyebrows microbladed tonight so hope this looks natural (fingers crossed).
So glad for this support forum...we need all the info and support we can get from each other.
👍well done Becky first on ticked off 👍👍keep the fluid flowing now. If your antisickness meds don’t work ring your unit, they will tweak them till they hit on right combination. Some ladies on my oct17 thread used the travel bands for motion sickness and found these helped 👍for those not cold capping and going for the chop, hair usually starts to fall out around day 15 onwards, please think about donating your hair to little princess trust that make wigs for children and give them to them for free 👍turn it into a positive 👍💕💕✨✨Shi xx
Another newbie here - I had my first chemo this morning so just made it to the August group 🙂 Writing this slightly whoozy in my bed, as it feels like the side effects are just kicking in, currently feeling as if I have I downed an inadvisable number of gin and tonics over lunch time - head is a bit fuzzy, a little touch of nausea and everything is a wee bit slow and befuddled.
I was diagnosed in April with hormone positive lobular cancer, had a mastectomy and immediate implant reconstruction in May, and they found macromets in a node, so this was followed by full node clearance at the end of June. Luckily other nodes were clear - I was borderline for chemo and they had discussed the Optima trial (the tumour would be sent for the Prosigna test to determine likely benefit of chemo) with me before realising I was too young (to go on the trial you need to be over 40 and I'm 36), so after getting my CT scan results this Tuesday (full body scan was clear) it was full steam ahead today! I'm on accelerated EC, so 4 fortnightly doses, and then 12 weekly paclitaxel, so feels a long old slog ahead, but I'm pleased to be onto this phase and cracking on with it now, and hoping I get through without too many delays so I'm done for Christmas.
All feels a real unknown about how my body will cope at the moment - cancer aside (ha!) I'm fit and well, and I've gotta say it feels very alien to be subjecting my body to something that will make it feel ill, as aside from the obvious physical after affects of surgery and being pretty generally anxious, I've been quite 'well' through this process so far. I have two young daughters (3 and 6) so home life is hectic. Work wise, I'm a self-employed storyteller and musician running workshops and groups for families, so I've had to take a few months off already and dep out my work (I've done odd sessions when I can). I'm working on some recording and digital content whilst I'm off regular work, but I'm hoping on better days I might be able to do some sessions, but just trying to take it day by day. Finances aside, it's so frustrating to be forced away from the job I love and business I've built up, but I think I will approach things differently (in a positive way!) when I go back rather than rushing back at full pelt.
Oh, and I went for the big hair chop yesterday and am not cold capping (my raggedy mum hair wasn't really my crowning glory, and I figured I'd get very frustrated not being able to style, and a wee bit obsessive about watching for shedding, so going to embrace the wigs, scarves and bald look for a while) so will be watching my head with interest and go for the full shave. Quite enjoying my funky short 'do in the interim though!
Sorry, this was a mega post 🙂 Look forward to meet you all on here, good luck and love to everyone
Hi wolves girl ❤️Glad you’ve found the thread ok 👍just need lisaloo79 to climb on board the chemo cruise ship 🚢 as you all set sail in August ❤️❤️ Take notes at your meeting and have questions ready at each appointment. Take your temperatures regularly during chemo and drink at least 8 glasses of water a day too 👍 If your antisickness meds don’t work ring your units you should get a rapid response card so you are seen within an hour during chemo 👍 always ring your units for anything during chemo, they want to keep you safe 👍if your pee burns but no temperature ring them, it’ll be a uti and will need treating ASAP. See your dentists before starting, oral hygiene is very important during chemo. You get lots of ❤️👭on here 💕💕✨✨Shi xx
I have joined this thread as I might be starting chemo in late August or early September. I was recalled from screening at the beginning of May. To all intents it was DCIS but on histology showed a small (11mm) Grade 3 in the middle of it. I found out today that nodes were clear so am hopeful that it has all been removed. Sadly it is TNBC so only chemo and radiotherapy as treatment options but I remain positive that this will work given that it seems to have been caught early. It has been a long three months but the care I have had is excellent. Just need to get on with this now and get this thing sorted. Hope that we will be able to support each other through this challenging time. xx
I’m new here too - I was diagnosed with HER2+ breast cancer three weeks ago, and will be having neo-adjuvant chemotherapy (two cycles of EC then four of docetaxel plus Herceptin and Perjeta, I think) before surgery. I just received the date for my first chemo session today, and it will be a week today (Wed 7 August, with the pre-assessment on Mon 5 August). I am glad finally to have a date for treatment to start after days of waiting for scans/tests and results, but I am terrified at the same time! I am trying to be prepared (deep cleaning the house, freezing some home-made soups, and buying an ear thermometer plus lots of supplies to help with side effects as suggested on the forum threads), but it is all so unknown and I feel out of my depth. My job is in the health sector and involves lots of public contact, long-distance travel and working with patients in GP clinics/hospitals, so my oncologist has said I cannot work at all during treatment due to the danger of infection. This is getting me down, as I know that I will really miss my work and the feeling of being useful. I also live on my own (although luckily only 4 minutes walk from the hospital where I will have treatment), so I am worried about how I will cope with the side effects if they are really bad. I do have good help from friends and neighbours, but they all work so are not available all the time.
It would be great to link up with others who are also about to start chemo, and hopefully we can support each other and share experiences as we go through the next few weeks! I know it will be challenging, but I am sure we can do it!
Hi New here not sure how it works...I had my mastectomy in June and lymph node surgery July I was offered chemo and due to start.. in few weeks...which I’m unsure of as I was told it was my decision to take treatment
Thank you for getting in touch. I am sorry you've not yet had a response to your comment. I'm sure someone will be along shortly to continue the conversation.
Social Media Officer
This thread is for anyone due to start chemotherapy in August 2019. Others will be here soon but please come on here and introduce yourself and you can all help one another through this phase of your treatment. If you have any questions please post away on here and others in the community will watch over you whilst you are getting started. Once you are into it you'll be pretty good at helping each other. You can also ask the nurses on this forum if you have any concerns. In the meantime, the top tip is always to stay well hydrated throughout chemo, aiming for 2 litres of water per day.
Here is the BCC guide on chemo:
I finished my chemo over a year ago and doing very well again now. Here is my story which has some chemo tips on how I coped which were collectively shared from others who had gone through the same from this forum: http://lifeafterlola.com/
Best wishes xx