Ann, I’m glad I managed to put your mind at ease regarding the tattoos. I’ve been telling everyone that I have 3 tattoos. Ha ha, I think they’re imagining pictures not3 small dots!
I started my radiotherapy this week and have had 2 sessions so far. I’m not finding it too tiring but my poor husband is exhausted from the driving as it’s a 5 hour round trip to the hospital everyday.
Mine is on my left breast too, so I have been doing the breath holding which isn’t too much of a problem. There’s a TV screen on the ceiling with photos to distract you too.
I’m having tablets for the bone strengthening. It’s interesting how different hospitals have slightly different treatments.
I have been shielding since my treatment started in June as I was told to from the beginning. Once the treatment is over It will be strange to go anywhere other than the hospital, doctors or dentists!
Hi Ann glad your planning went ok. I got mine tomorrow saw oncology yesterday to talk about radiotherapy, then today I had a call to say can I go tomorrow for my planning meeting. I asked them about the tattoos but my hospital dont do them any more. I'm just having all the scans and telling me how to breathe hold my breath as my cancer on left breast and it can effect your heart/lungs. So hopefully they will also give me my start date. I am only having 9 treatments that 5 one week then 3 booster the following week. Then that's me done. I have got to hv an infusion/ injection every 6 months for 3 years for my bones.x
Hi Girls, hope you are all ok, Horseylass thanks for your comments stopped me worry about my tattoo's which I had today and all fine on a bruised boob Julie, just a scratch. My radiotherapy starts 23rd and then it's just the two infusions every three weeks until August next year. I have been advised to stay shielded through all cancer treatment so I am hoping this new vaccine is good as some retail therepy would be nice. Keep smiling girls, we are on the home straight. Love Ann
fantastic news about your scan results, you go girl!
My oncologist organised my radiotherapy too. I am 6 sessions in, have 3 left. My main radiotherapy was for 5 days and I started my 4 booster sessions yesterday. Providing there is no delay on the machine I am usually in and out within 15 minutes, however I do realise that some people may be longer depending on the amount of radiation beams you need. I have no pain or discomfort, however my breast does get a little itchy when I am warm at night, but E45 lotion is sorting this.
Glad to hear you will be starting radiation soon Horseylass and if your body tells you to sleep then you sleep girl! I do 😝
Hope everyone is doing okay with their treatment and feeling okay within themselves especially with the new lockdown coming into force.
Take care ladies and stay safe!
Love ❤️ Tara xx
hope all went well for you on Tuesday!
Yes I am a Community Champion. Really enjoying the role, love being able to share my experiences of the journey we are all on and hope I can bring some peace of mind.
If we all come together we are strong 💪 this is something that will bring cancer down. Together we can get through this!
I had my operation in May and have been doing my exercises since then. I was told by the physio ( in my phone appointment) that I should carry on doing them for 6 months after my radiotherapy. I remember that it was difficult at first but does improve gradually. I do now have pretty much full mobility but my shoulder still gets stiff every now and then if I do too much.
I had my radiotherapy tattoos last week and they are no more than a scratch. They are tiny. I have one on my sternum, one below that and one under my arm. None are actually on my boob.
I start my treatment next Tuesday. If I’m like Tara I shall be falling asleep on the way home as it’s a 2 hour drive. Fortunately my husband is taking me.
Julie, so pleased that your nodes etc were all clear.
Stay safe and strong ladies, we can do this. xx
Hi Julie, exc news, well done. I am waiting for my radiology CT scan, the tattoo is aparently permanent and am a bit concerned that tattooing a bruised boob might be rather sore but will let you know. My armpit scar is still sore and has been since the op, I am still doing my exercises, I am hoping to get full mobility back, perhaps the girls that had their ops early could let us know how long they had to do the exercises for and if they got full mobility? Jab and infusion starts today for 14 treatments every 3 weeks till I think next August, lets hope covid is on the run by then. Anyway hope you all have a good week. Love aNN
Yes doing ok thank you. Results came back that markers were clear and so was the 6 nodes clear, so that was excellent news. I had a letter to say I now been referred back to oncology so not sure if its them that organise my radiotherapy appointments. I feel like iv been left to my self since OP. Was going to ring nurses today as my armpit has started to hurt more since sat. I even had to take paracetamol. Not sure if this is normal or due to excercise I'm doing, did you get this That said it no where as bad as chemo. Hope every one is getting on ok and have a good day x julie
Thanks Tara, I am waiting for my dates, jab and protein infusion starts tomorrow. Just noticed you are a community champion? Love aNN
No it wasn’t anything you said. It was half term here last week so busy, busy, busy. My life never runs slowly, always at 110 mph 😝
I hope you are feeling okay after your operation and finding the exercises a little easier to do.
Radiotherapy went well. I started last Wednesday. So far the side effects I have experienced have been a slight itchy feeling to the breast that is being treated. Nothing too bad and treated with E45 as recommended. I have definitely felt like I have more energy since being on the beta blockers and blood thinners for the blood clot on my lung and fast heart rate, however about an hour after radiation I feel really tired like I am ready for bed. Luckily you can ask for a time that suits you for radiotherapy and if it is available they will let you have it. I always ask for late afternoon. I am at a different local hospital for radiotherapy as the hospital closer to home do not do it.
Radiotherapy is like a walk in the park compared to chemo, it really is okay. well I have found anyway. I seem to be more tired now that I am getting near the end of treatment and have had swollen gums that I am receiving antibiotics for, but I think this is because my body had that much adrenaline to get me through chemo it has taken a breath of relief now and my system is a little low!
I am still very swollen fTom the steroids and are trying to move around to lose it, it’s just hard when you have been told to rest more.
Hope everyone is feeling okay and looking forward to Christmas, even with the new lockdown rules. I know I am and can’t wait to spend it with our little household bubble.
Lots of love to you all ❤️ Tara xxx
Hi girls, missing your posts, was it something I said? Butler 10 hope you had good results, Tara hope radiotherepy went well, how is everyone else doing? hopefully most of you should have finished chemo by now? Love aNN
Hi Butler10 thanks for your message, yes feeling fine but wiped out, doing my exercises but they knacker me, waiting to hear about radiology the Macmillan nurses say I am down for it and my jabs start next week. Had really good result from my op, complete pathological response, silly really but it's a bit hard to take in as all I concentrate on is the treatment, I know it is hard girls but keep biting the bullet, it is going to be worth it. Really sorry you are having such a bad time Tara but pleased it will not delay your treatment, I have not heard much about radiology re side effects etc so do fill us in if you can, hope it does not affect hair as I am getting some back. I was sent a brochure on lymphoedema which I am going to have to be really careful of because like horseylass I am a smallholder/farmer so I spend most of my time getting dirty on the veggie patch or mucking out, I get very rough hands so I am now washing my hands with Acqueous cream as it is also a soap and am buying gloves that I can work in which should help protect me.
Anyway enough of me, hoping you all have a good week. love aNN
Oh Tara, you poor thing. Thank goodness you rang the hot line. I’m pleased that it won’t affect your treatment though. Good luck with your radiotherapy this week, fingers crossed that it all goes smoothly for you.
Enjoy your day with your boys. Cold and windy here too.
Take care. xx
Glad your op’s went okay, hope you are all feeling well. I found my op a walk in the park compared to chemo.
Horseylass, I am due to start radiotherapy next week. Just waiting for the call. Have been given a machine number and had my lympadema chat yesterday.
I have had a nightmare of a week this week though and was unsure if I would be able to have radiotherapy. After a trip to A and E Monday with swelling to my hands, fingers, ankles and feet and what I thought was severe heart burn and breathlessness I was given 3 scans and a covid test over 2 days. Turns out I have a high, irregular heart rate for which I have been put on beta blockers and a blood clot on my lung. Just when I thought I would be getting better lol. I will have treatment for 6 months to prevent further clots and wait for this one to dissolve. The good news is it won’t halt my cancer treatment!
I am happy to hear everyone else seem to be coming along fine. Just if you feel different or unwell, please get checked out, don’t assume it’s just the side effects of treatment like I did. I had no temperature and it was only because the heartburn burn pain was getting worse and chemo had finished that I called the hot line. Apparently pulmonary embolisms and blood clots are common in cancer patients.
Hope you are all having a good day, weather not too good here, but making the most of relaxing with my boys with the heating blasting.
Lots of love 💕 Tara xxx
Glad your surgery went well. I too thought I had a fab sleep when I had my surgery. I was astonished how quickly I was knocked out and then what seemed like the next minute I was in recovery.
I have my radiotherapy planning scans on Monday and my tattoos! It’s a 2 hour drive each way which is the worst part. It makes for a long day. But hopefully I’ll get my dates soon for treatment. I’m having 5 days in a row and then I’ll get to ring my second bell! After that it’s surgery on my right breast to even things up. Whether I’ll get that this year or not, who knows. As it’s only cosmetic, I wonder if it will be postponed because of Covid.
I hope you are all doing well and have a good weekend
Hi Anne Yes home by 4pm. Morning was busy thou had to go and hv 2 wire markers put in, then walk the length of hospital physic dept to have a injection of radio active which was for the blue dye to go in before they started op went out like a light when I got to theatre had best sleep ever.lol. my Consultant phoned my hubby while I was in recovery and told him all gone well And that she phone me next Monday 27th. So hopefully radiotherapy next then 🤞 all done. Are you doing well.xx
Glad it went well. Iv been up for my covid test this morning so hope it comes bk ok as my OP is on Monday. Got to be in by 7.30 then at 9.30 I got to have another marker put in plus the blue dye. Then I persume I go down to theatre or back up to ward to wait my turn. Hopefully it will still be just a day job. Then hv few weeks then start the radiotherapy fingers crossed every think finished before xmas.xxx
Hello Ann, Tara and everyone,
Well done on getting through the final treatment on Wednesday. Do you expect to have some tough days now? Were you still on FEC or on Docetaxel? I’ve found Docetaxel easier to handle, round 4 was a bit grim back and forth to hospital with side effects, but round 5 was the most manageable yet, no triage trips needed.
Did you get to ring a bell? We don’t at our hospital but we do after radiotherapy in November. I’m having 2 weeks. I asked the Consultant were they still doing the condensed one week treatment at a higher dose and he says that is how radiotherapy is evolving - they used to do 5 weeks, then three, but trials in the last few years have showed that fewer sessions at a stronger dose are effective. I believe mine will be a week on the right breast and a further week more closely targeting the tumour area. It’s really only a precautionary clear up of any last cells lingering (could there be any after 6 x chemo?) and the consultant said it only offers about an extra 1% chance of cancer not recurring but I’m glad to have all the layers of treatment (tamoxifen is something like 7%).
Tara, I had my tattoos done on Monday. Felt very cool telling my 15, 13, 10 year olds their boring old Mum has tattoos but they weren’t terribly impressed 😄 It’s horrible that you had bleeding, I didn’t have more than a pin prick.
Throughout chemo I found I limited my reading on the forums and generally online, has done quite a bit to learn things early on but hadn’t the mental strength to cope with it after the treatment started. Recently I came across a sort of virtual conference bus Penny Brohn, about integrating other types of help around traditional treatments and I attended some of these sessions. They were very well run. I feel this will help me for the onward Journey to plan some of the things I know I need to improve (stress and exercise and sugar intake). Maybe some of you might like a look, I believe you can still get tickets for the recordings: https://yestolife.org.uk/event/your-life-and-cancer-2020-1/
All the best,
Hi Butler 10, thank you so much and well done for remembering, I find it hard knowing which day of the week it is let alone remembering when someone else has surgery, all went well thanks but still have a bag attached, I met a woman Lisa, just starting her journey, she had only known about her cancer for 2-3 weeks and had her masectomy that day, I recommended her to this site as I am so grateful for all of you, your stories, comments and support help so much, I hope we all keep posting here. I have radiotherapy next and then the jabs, hopefully more of you have now finished your chemo by now and are starting to feel better. Please post when you can. Love to you all aNN
Sorry for the spelling mistakes. My fingers are still swollen from the steroids and too big fir the buttons on my phone! X
sorry I have not been on fir a while, I have been well in myself, have just been trying to sort out an EHCP fir my youngest. He also has a lot of hospital appointments at the moment.
Thank you for discussing your treatment with me. It seems like most of us have more treatment to move onto after chemo, whether it be radiation or surgery. I was told if the virus was not around I would have had chemo first rather than surgery. It’s interesting to see that those ladies diagnosed slightly later have had chemo first. I wander if things will change again with the virus getting stronger again?
My radiotherapy planning went well. I had a CT scan without the cannula, which was a bonus and the tattoos were not too bad, however I did bleed quite a bit in my good side. Never felt a thing on my right side where the tumour was. Funny really because I have sensation in my nipple but could not feel the ratio being done at the side of my breast. The one in the middle of my chest was not too bad either. I should start radiotherapy on the 28th of this month. All moving quite quickly.
I have found that since finishing chemo, I am really tired. Think this may be because I tried to carry on as normal, home schooling the boys, washing, housework etc and now it is all catching up on me.
Anna, I hope your last chemo goes well tomorrow and anyone else that is due chemo too.
It will be nice to stay in touch on here even as we move on to different treatments or finish completely.
Thinking of you all ladies!
Lots of 💕 Tara xx
I had my last chemo 30th Sep ! Im still not back to normal, but getting there slowly :-).
Im booked in to see the surgeon on the 15th Oct, but still not received an appointment for MRI yet or surgery. Covid has slowed things down again at my hospital. Ive to have target therapy again on the 21 Oct to cover me until my Mastectomy and axillary node clearance.
Hope everyone is doing the best they can, and keeping safe
Its so good to hear that we have finally finished or nearly finished our chemo treatments. Way back in June it felt like we’d never get here. I had my last dose yesterday. I’m waiting for the side effects to start tomorrow when I start the injections. Thanks Tabs for mentioning the moles. I seem to have a few mainly round my middle and also more skin tags than I’ve ever had.
I think I also need a dentist appointment as my jaw aches and front teeth at the bottom.
Tara, how was the radiotherapy planning? What happened exactly? Was it scary, I’m such a wimp, is it like a CAT scan which I’ve only seen on TV. They look a bit claustrophobic. I’m having radiotherapy but haven’t had the appointments sent out yet. Hopefully I’ll be able to have the five sessions of treatment.
This awful Covid virus shows no sign of going away. I live in a area where there has been lockdown rules, so no visits from family and friends which is very lonely. I haven’t even been in a shop since before Easter! Only hospital visits and dog walks for me!
Take care everyone
Love CactusQueen 💐💕
It's really nice to hear that you're all coming to the end of chemo. Am very jealous, mine isn't due to finish until the end of November. It was meant to be mid November but I tested positive for covid in a routine test before a chemo treatment. It was a week when test results were delayed so I didn't find out for 6 days. On the plus side, I didn't have any of the usual symptoms, the achey neck I thought was chemo, and the prickly heat on the tops of my hands and feet the doctors thought was chemo too. I think that one of my teenage boys must have given it to me but it's not their fault. I've also been referred to have a mole removed as it's changed colour during chemo, which apparently is a thing so check your moles for changes and check with your GP if you find any. I'm waiting to find out if it can happen during chemo, or if I'll have to have it removed between chemo and radio. I'm meant to have the 5 days of radio and then Letrozole for 5-10 years. I was hoping to have the radio this side of Christmas as there were reports that the isotopes or whatever they use in radiotherapy may be affected by Brexit. I guess everything will take as long as it takes. I'm looking forward to having my other breast removed in Spring so that I can be symmetrical as I'd already lost my right nipple in the original mastectomy. I'm also awaiting the results of the genetic tests, but was told it can take 3 months, hopefully it will be negative so that my boys won't have to worry if they're carrying it. Anyway, I hope you're all well. It's great that we're nearly through it. Good luck everyone, Tabs
Hi Tara and everyone,
I have my final chemo next Wed, all being well. I had a couple of postponements along the way because I took a dose of the cold twice. Fingers crossed all will go ahead. The Covid rates around here are really rising, and with my 3 children at school I’ve been expecting it will come close to home at some stage.
Tara, I’m also going on to radiotherapy after chemo. Initially it was to be an intensive dose for 5 days but I believe they may have moved back to the standard 3 week programme now. I have my planning appointment on Monday. Expect to be done radio by end of November and then tamoxifen for 5+ years. I’m also waiting on results of the BRCA1/2 gene test, has anyone else had this? I have 2 first cousins and 2 aunties who have had breast cancer so this pushed me across the threshold for testing. There’s only a smallish chance of it being positive, but a positive result would mean removal of ovaries for definite and a discussion about bilateral mastectomy. We’ll cross that bridge if we come to it 😊
Take Care, everyone.
well done on your final chemo, you did it, I hope you rang that bell hard! I have not done it yet as I want my boys to be with me as they have had to get through this with me too. I will take them after radiotherapy to do it.
Had my planning appointment and tattoos done yesterday ready to start on the 28th of this month. Everything is moving quickly. This year seems to have gone do fast.
Is anyone else doing radiotherapy after chemo?, if not are you having any other type of treatment?, I would love to hear about it.
To those of you still doing chemo, not long now! Stay strong ladies, we will beat this!
Lots of love 💕 Tara xxx
I had my 6th and final chemo this morning. Yay. I got to ring the bell! 🔔
That’s done with. Now I just have to wait until November to start my radiotherapy.
I hope you are all ok? Everyone seems to have been a bit quiet for while.
Stay strong. We can beat this. xxx
Oh Tara & Jo. I’m so sorry to hear of your problems. I hope you both manage to get your last chemo sessions done as soon as possible. It does seem the more of the treatment we have the more our bodies take a hit. I suppose it’s inevitable but not nice.
I had full dental X-rays taken yesterday as I need work done before they can hive me the bone strengthening drugs. It’s one thing after another isnt it.
Stay strong girls. Fingers crossed that you get your last chemo soon.
Tara , sorry to hear of your trouble and having your lady chemo postponed 😖
ive got my last chemo tomorrow, but got to also have a scan on my arm with picc line as It’s very swollen and they think I’ve got thrombosis in it 😩
hope everyone’s doing ok x
hope everyone is doing okay. Well done to those of you that have finished chemo and good luck with your surgery/ radiotherapy.
I have my radiotherapy appointment for 30th September so will let you all know how this goes. I also should have my last chemo tomorrow all being well, however have had some little abscesses appear on my nipple scar. I called last Thursday and was told I was fine because I did not have a temperature and they are only small, however when number 2 appeared on Monday I decided to take myself up to the unit. Had swabs and had to have heart rate monitored for 2 hours as it was high. Told I can’t have treatment tomorrow if an infection. Will have to let you all know!
Hope everyone has enjoyed the sunshine over the past week. Horrible here today. I’m enjoying relaxing inside.
Love to all Tara xxx
Hi Julie, our first finisher. well done, hope the pains don't last, New Forest sounds good, only time will tell what Covid is going to throw at us, I am just looking forward to some freedom and being abe to eat anything I like. Take care all
hi Ann I had my final chemo on wed. Today got my aches and pains in legs☹
Had phone call yesterday to say my OP has been put back to 19th October. Due to my last chemo being a week later.
Also got told tok make a dentist check up, as after op and radiopharpy I got take some tablets for my bones and it can effect your jaw!!. I hv now booked me and hubby a few days away @ beginning of Oct to new forest. Fingers crossed covid dont mess it all up again. Hope all hv a good weekend
That’s great news Ann and hopefully great news for you next week Tara. I had my 5th session on Tuesday and hopefully my last one will be 6th October.
We are beating this, ladies. One step at a time but we are beating it!!
Thats fantastic news, well done You. I bet it is such a relief to be over!
Do you have any further treatment such as radiotherapy? I know you said you are having an op soon. I think you will breeze through this after chemo.
I will hopefully have my final chemo next Thursday. Never thought I would say this, but I can’t wait.
Stay strong ladies, nearly there now!
Have a lovely day.
Well girls I had my final chemo yesterday. I start 29th May, 7 infusions later and it's on the home run. Thinking of you all.
hood everyone is doing okay today. I have had a lovely day. I watched my eldest play football in the sunshine 🌞 and then after the game we had his presentation outside on the grass.
Ann, I will be sure to keep talking about my friend, your right she will live on that way. I had never met her husband but have managed to tell him a couple of stories through social media that I hope will make him smile at such a devastating time for him and her children. I also talked to my husband about it a bit lady night. He said you have to be selfish and think about yourself where cancer is concerned to ensure you best it. I told him I fully intend to never let the disease get the better of me. I hope it has given him some peace.
Hope you too goes well along with Butler. Time seems to be going so quickly!
Anna, I was told that chemo should put you through the menopause, but my not sure if I have or not as I was in the contraceptive injection and have not had a period for 7 years. I would say by the night sweats I get after chemo that it is a possibility but I just don’t know. Funny things for me are, I expected to loose weight from sickness, but thankfully from not being sick I have gained 2 stone. I also used to have dark facial hair. This happened due to medication taken for an ectopic pregnancy 13 years ago. All that fell out and it has come back as white wispy hair. I can deal with that. Also I thought my children would be horrified by how I look and I would scare them, but they have taken the attitude that if they laugh at me it’s the best way to deal with it. They will quite happily point out that I have a double chin and wonky breasts. This works for us all. Thought I would feel mortified but I really don’t. I quite agree with them.
I do hope everyone has had a nice day. Has anyone finished chemo yet. I you may have said but if not I would love to hear.
love 💕 Tara
Thank you all for your lovely messages and for posting your updates both good and bad, it is so nice to hear your news, it makes the op day less scary especially as I am sharing it with you Butler10, quite comforting to have the same date, I will also be thinking of you, glad you were able to enjoy your 60th although having any delay is a mixed blessing.
Tara, I am so sorry to hear about your friend but keep talking about her because in that way she lives on. Sounds like your hubby might be having a rough ride, in some ways it must be harder for our partners, especially if his parents are scaring him, we have womens grit and determination to keep us going and we can talk to each other, blokes aren't always good at that.
Jo77, hopefully you have some good friends and family around to help you through, that must have been really hard to bear, life can be a b..ch sometimes. When one door shuts another one always opens, I just hope you don't have to wait long for that door.
Hugs and love all round aNN
Hello Tara, Jo, Ann and all others,
good to hear how everyone is getting on, there are tough things happening in everyone’s life and home but the weeks are passing and we are getting there. I had round 4 on Wed 2nd, first Docetaxel same as many of you. It was a joy not to have nausea and vomiting for a change and I sailed through a day or two, but then got bone pain and fatigue and inflamed mouth and stomach and am just coming out the other end after two visits to oncology triage. Really good to be feeling normal again (and arguing with my boys about WiFi as usual 😤)
I was thinking about the little things on the cancer journey that have amused me in spite of it all - thought I’d share and maybe you could share yours too:
Because of being 45, they warned me that when chemo causes the ovaries to shrivel and give up for now, it may be temporary or it may be permanent. Amused to report my ovaries seem determined to stick it out til the bitter end, just got another period after round 4 😀
thank you for all your condolences. It is very sad, but I have come to learn that cancer dies not discriminate and can be very cruel. It makes me more determined to fight and never let it come back!
Jo I want to say that I am sorry that your partner has left, but I don’t know your relationship so it may be a relief that they left. No one knows what goes on behind closed doors do they? I want you to know I am here for you if you need to chat as I am sure the other ladies are too.
I have found since having my diagnosis I have become a stronger person and don’t take any messing anymore. My husband has struggled, we don’t talk about things really and he keeps saying to me that I look really well and he thought it would hit me more. I look well because I get up each day no matter how I feel inside to take Care of my children. In my mind if I get up and do it won’t beat me. My husband has even said it is making me crazy. I agree I say my point a lot more now, but that is because this is a hard fight and it is all I know how to do at the moment. Before I would pussy foot around things and say things like, dont be silly all nicy nice even when I didn’t agree. Now I just give me opinion. I am not making excuses just think I have become quite threatening to some people. We are strong women now and I don’t think they will ever go away.
My mother and father in law just keep harping on to him how their cancer was much worse than mine and I generally feel that he is panicking. To me I have been told I can be cured. This is what I fight for, but to him he seems scared that the worst could still happen. He won’t open up and dies not believe in counselling so I just leave it for now.
If you need me you know where I am. That goes to all you lovely ladies.
Have a good day. Stay positive and strong ladies. We are almost there and we have done this ourselves. It’s a great achievement.
Much love 💕 Tara xxx
Anne and Butler , wishing you all the best for your operations ,Tara ... sorry to hear of your loss .
Hope everyone else is doing ok !
Ive got 1 more treatment to go ... had paclitaxel last time safer my reaction to docetaxel, which has been fine. Although my partner left me a few weeks ago which was unexpected so am in rather a mess.
I guess we are nearing our journeys now which is a positive!
I should of had my last chemo on Thursday but it got cancelled to Wednesday now as blood was low. But hay on bright side I could enjoy my birthday . I also was given my surgery date for my OP it to is 13th October,at the rbh. So will be thinking of you to that morning. Mine is a lumpactomey and just in for the day hopefully. Have to go up to clinic the day before just to hv some blue dye put in for guidance so they no where to go and at my next ultra sound they are putting in a tiny magnetic thing lol as guidence too. At least they shouldn't get lost in my boob.xxx
Oh Tara, I’m so sorry to hear about your chemo buddy. I’m glad you are using her passing to make you more determined. I’m sure that’s what she would want but huge hugs nevertheless as it’s never easy to lose anyone.
Ann, so pleased you are nearly at the end. I too has my surgery before chemo, although I Will have to have my non cancer breast reduced to match after my radiotherapy. I too found the surgery no problem at all. One minute they were putting me to sleep and the next they were waking me up. I had very few problems afterwards apart from the drain which was just annoying really.
I have round 5 of chemo on Tuesday and then just one more after that to go before I move on to the radio. It seems like ages since we started but at the same time I can’t believe this is number 5!
Keep strong ladies, we’ve got this. xxx
wow nearly there now! Well done you.
I unlike you had my operation before the chemo. I know you are nervous because I was too. I had never had an operation before, not even had a filling on my teeth. I personally found the operation easier. I had a lovely sleep and although I had a head ache for a couple of days after, I think from dehydration, but was well after a couple of days.
You can do this Ann, I feel you are through the worst now.
I have not been posting for a while as I lost my chemo buddy on Sunday. I knew she was terminal when I met her, but her passing knocked me a bit because she seemed so well.
I am more determined than ever to beat this now and live live live.
Hope everyone is feeling okay. Nearly there now we can all do it!
Lots of love 💕 Tara xx
Hi girls, hope everyone is ok? missing seeing your posts. I've got my last chemo next Thursday and just been given my op date of 13th October, luckily not a Friday, really nervous about that. Hope to hear soon
love from aNN