Thank you for sharing your story, there are no judgments here, only unconditional love. Sending you healing pure energy and a tight hug... xxxxxx
Good luck with dose #5 today Nettinoo.
All done Daisydi, you will get through this bit now and out the other side.
Implausible yes I did go for a good walk on Sunday. It was a relief to have ‘me’ back. Horse tranquiliser drug has been so strong that I have been in tears sitting on my sofa thinking I won’t be able to complete my Macmillan Hike in July . H1 says I don’t have to and my walking buddy says we can always catch an Uber if we feel awful but I so want to get to the finish line 🤪
So it was lovely to feel light and free and walk instead of shuffle. Actually it was exhilarating!!! I am convinced my legs are stronger- no aches or pains at the end of the 16 miles. No aches or pains the next day either. I caught the bus back from Hartfield ( £6.20 😳). I am aiming to get to 20 miles before the big event. H1 will be joining me on this training.
I think this walking is becoming something of a pilgrimage dedicated to the heart.
On Sunday morning I was out and walking at 8.30 am ( so glad to have my body and brain back) that by the time I was at the start of the Worth Way the bells were ringing at St. Nicholas ( I mean peeling away) that I got all choked up. It’s like they were ringing for me 🤗
I too have experienced domestic violence x2 ( I shared this in my most recent art therapy) so it was very good to get it ‘off my chest ‘. If you are wondering it was with H1.
The second time ( about 10 years after the first incident) I called the police and H1 spent the night in a prison cell.
We have managed to forgive each other but I have not forgotten.
We had only known each other for like 40 days or so before I fell pregnant.
I was at the time teaching in Istanbul. I told H1 over the phone and he let me decide whether I wanted to keep the child ( my daughter) or not.
I continued to work at the school in Istanbul until I was 6 months pregnant and then I came over to the UK and moved in with him. We had never lived together.
H1 had been married before and his marriage had ended after 4 years ( no kids) and the lady had gone with money . When I met him back packing in Thailand I liked that he never said anything bad about her.
Anyway our first bust up was when my daughter was 11months . It was over our pet parrot ( which I had bought from the Friday ads for a Valentines gift) anyway the parrot hated females ( it loved H1 it would feed from his mouth) and it would dive bomb me when it was let out of its cage.
I used to watch him like a hawk but he never went for my daughter. One day I had had enough, rowed with H1 and stuck bully boy ( that’s what I had named him) out in his cage in the back garden. H1 went mental.
I packed and left ( back home to my parents in Greece).
The second incident was just before Christmas, I had bought tickets to take my kids ice skating in London. H1 and I had got married by this point ( we got married when my daughter was 6 and my son 3 I wanted to get married but he was a lot more reserved seeing he had been ‘burnt’ first time around) and I was teaching at a Pupil Referral Unit for children who have been permanent lay excluded from mainstream education. I had 2 awful weeks at work ( and I mean ‘flight or fight’ situations - these kids project all their ‘stuff’ on you) and I came home tired and an argument over the dinner that H1 had prepared for me ( I said something like ‘I am not eating this **bleep**’) and I cannot remember what else but I do remember being shoved outside . I could hear my daughter upset inside and I went back in got both the kids and called the police on my mobile phone because I wanted my kids to know that it is not ok to behave like this.
H1 got pepper sprayed and handcuffed and I didn’t see him for more than a week. I didn’t know what had happened to him and the police wouldn’t tell me . It was awful.
Thanks to advice from the vicar that married us I went back and retracted my statement at Crawley police station.
That was 7 years ago.
H1 doesn’t believe in counselling (I have suggested it) .
H1 found the lump in my boob.
I am working on myself and my own demons.
H1 loves all of us. I don’t think my Mum has let stuff go but she should.
Hence all the heart chakra work.
Love and forgiveness,
Edinbird if it helps, you can tell your sis etc that I've never taken anyone in with me to any of my consultant appointments.
I've never wanted to, and to be fair nobody has offered to come with me but I would have said no thanks if they did... I feel like I need to concentrate at the appts without the distraction of someone with me, and if someone else was in there with me hearing possibly bad news at the same time as I heard it, then I would be too busy worrying about them when I should be thinking about me....
My other half did take me to all my chemo appts however, but that's because I was advised I shouldn't drive myself home after them. And the hospital is in the middle of nowhere. To be honest I reckon I would have been fine as usually felt ok on actual treatment day, and I just ended up feeling guilty that I used up 6 days of his annual leave.
Especially given all he ended up doing each time was sit there playing games on his phone while I talked to the chatty lady in the next bed!
Daisydi don't worry you didn't scare me, I know all these drugs have their side effects and we need to find our own cocktails that work. I'm putting hormone regime worries firmly on the backburner for now
Morning, well the steroids have done their job and kept me awake most of the night again. Will prob have to take a sleeping tab tonight and this is going to be a long haul on steroids this time. No other probs so far but then Im not expecting them yet.
Sarah didnt mean to scare you about Letrozole. Everyone is different and some people are fine. We just have to find the drug that suits us best but make sure we dont suffer in silence. Apparently even different brands can give different effects but hey we dont have to think about that until the radiotherapy is over. One step at a time.
Edinbird good luck with the surgeon. Let us know how you get on later.
Praying for you Nettienoo. Know exactly how you feel but I did it so so can you. Take care x
Hope everyone else is ok xx
🍀🍀Good luck Nettinoo, 🍀🍀
you’ve got this 🤞.
It will be lovely to have you son with you today, even if not in the nicest situations.
Ive had a rubbish nights sleep, serves me right thinking I was coming out the other end early 🤪🤪🤪 hopefully I’ll catch up on sleep later xx
I’ll pop back later when brain has engaged
Good luck Nettie xx I’m having the kinda opposite issue whereby I’m going on my own to my surgeon appointment and I can tell my mum and sister are a bit weirded out by that. I just figure whatever needs to be done needs to be done and there’s no point disrupting anyone else’s day by it. I never went to any of my husband’s surgical appointments unless we had to travel a long way together (he used to get seen for his shoulder at National Orthapaedic Hospital in London so that was always a bit of a trek). Doesn’t help that I still feel rough though. Sat in bed with sore ears and feeling a bit strange, went to bed early as I came over dizzy and sick but then couldn’t sleep until about midnight. My legs are still aching just laid here and I’ll have to walk from work to the hospital and back. I understand that these appointments need doing and I need to get scheduled ASAP but why can’t they make them when side effects are likely to have worn off a bit more?
Oh and it’s my first day back working after the last treatment... although my boss doesn’t expect me to do much. Starting to think I should have gone sick now... I’m sure I can get through a few more days. I really want to speak to the Chief Constable and Head of Wellbeing about my experiences and see if some kind of cancer protocol can be put in place. I’m astounded still by the lack of understanding that there’s been of my treatment and how I might be feeling. It’s easy if you like if someone is diagnosed and then just goes sick but I was truly made to feel like I was strange wanting to work and my needs on chemotherapy - and this is with the DDA protection! I guess I’ll get round to that soon enough. Need to focus on getting out of bed first.
Will let you know what the surgery decision is later xx
Nettie all the very best for today.... both for the chemo and with oh so gently agony aunting your son a little!
My 2 older boys are coming up to the same age as yours and I know that they are both adamant in not wanting kids. Luckily (for them, not for my grandchild prospects!) their respective girlfriends seem to be in agreement for now. But if that were to change I could see it causing trouble in paradise, for sure
Totally understand why you are dreading the side effect stage of this next chemo btw, I've been the same since my hospital trip, and I didn't even have sepsis! I've been so determined not to end up back at the hellhole hospital that I pretty much took chances I shouldn't have last time around and refused to go in even though i couldn't get my telp down under 38 for ages. I got away with it, but with hindsight that was silly of me. Ignoring the high temp and just heading to bed and hoping for the best was daft.
But this cycle, I'm delighted to say that I seem (fingers crossed and touch all the wood!!) to have got through the danger zone without even having to lie to myself! I had one spike at 37.7 yesterday but half an hour later that had gone back down to 37.0. Result!
So here's hoping that you also get a hospital free cycle this time, boy do you deserve it!!!
Daisydi I love the photo a fitting souvenir of your last chemo. And as Nettie says, if it was turning your ears to icicles then it must have been freezing your follicles too
Not so in love with your words of wisdom about Letrazole (sp?) though! There was me all pleased with my "post menopausal" diagnosis as the doc had told me that letrazole was easier side effect wise than tamoxifen.... but it sounds like it still ain't a walk in the park (literally!!)
I guess I will try whatever they give me and if it really doesn't work for me then we either try something else or I weigh up the risk/benefit of continuing to take the drugs..... will worry about that later, got rads to get through first
Hope everyone has as good as a day as possible, despite the lousy weather x
Just realised we are approaching 5,000 posts girls. I reckon we’ll get there in the next day or two. How fabulously chatty are we? Xxx
Daisydi, big hugs for getting to the end of this absolutely Barrying 💩 stage of treatment my darling. I’m sure if that cold cap was freezing your ears off it would have been doing it’s job in protecting those hair follicles. Great news about the doc too. I am hoping things will be different for you this time as far as side effects as he seems to be trying to cover everything. I bet you wanted to hug him for giving you a bit of hope in that department. Such a shame not all drs are like that.
Implausible so sorry you have been suffering so much the last couple of days honey. Sounds like you are starting to improve a bit now if you managed to get clean. The days when you can’t even be bothered to have a wash/brush teeth or peep out from under the duvet are just awful aren’t they? I think you are right about PTSD and cancer treatment though. Our previous army life has obviously made us very aware of it. My cousin has been treated for years since being injured by a roadside land mine in Iraq but thankfully doing well now and sings in the Invicta choir amongst other things. I have watched my husband like a hawk over the years for signs as he was in N.Ireland for a bit and Gulf War. Thankfully, he seems to have been able to cope.
Cancer treatment is a prolonged period of extreme stress and anxiety and there will be people who need help with PTSD afterwards. I hope that help is there for us all if we need it.
I have been awake since 5am worrying about chemo 5 this afternoon. I want to have it and get it out of the way but the thought of what the outcome will be this time terrifies me to be honest. I don’t think I can stand one more day lying in a hospital bed feeling dire and the ensuing delay of next cycle etc.The fact is that I felt like this pre chemo 4 and yes I did end up in hospital again but it was only 2 days and it wasn’t sepsis this time so I am trying to hold onto that.
We all need this rain to Barry off don’t we? It’s not helping with low mood issues.
My youngest turned up here just before midnight straight from his boat in Norway and wants to take me to treatment today bless him. It will be nice to have him “captive” with me for a few hours so we can have a good catch up. (That’s if I can manage a conversation as the FEC going in makes my head really fuzzy and I often go into my own little world.) My Tom is having relationship issues so I think that’s why he’s come straight here rather than to his girlfriend in London. It’s the age old thing, after 7 years together, she wants commitment, babies (totally understandable) and he isn’t ready yet.Not sure he ever will be as he is 31! Kids eh? You think when they grow up and leave home you won’t worry so much but you seem to end up worrying even more!
Anyway, I’ll shut up now and start getting on with the day. I’ll update later just to let you know mission accomplished.
Love you all, each and every one of you. I would never have got this far without your support you beauts. 😘😘😘.
My sister thought it was funny that I was trying to tuck my towel into my cold cap as my ears were freezing off and couldnt resist taking a picture! My very last chemo ...
Oh and good luck for tomorrow Nettienoo. x Nearly there.
Maryln I think I will be on Anastrazole too. It is reassuring to read that the December girls are coping ok. My friend is on it too and she doesn't really have any problems. She was on Letrozole but couldnt walk after 2 days so they stopped that immediately. And she is very very fit so I was dreading that one.
Must go and wash all this stuff off my hair for the last time and hope it stays put!
Daisy our posts crossed there
Sounds like you have had a mixed day for sure. You could have done without that cold cap palaver giving you extra stress! But hopefully the other model they used is just as effective. Your hair has taken no prisoners throughout this whole thing, it ain't going to give up now.
And I really hope that the new regime of drugs from the nice doc help you have an easier ride through the final set of side effects. Glad they have taken you seriously.
As for the scan results, docs are so good at saying something that sounds super worrying, then saying it is nothing to worry about, and then walking off leaving you worrying regardless! I wish they would try a little harder to fully explain and reassure....
Now get plenty of rest and drink lots of water and think non itchy thoughts!!! Xxx
Last time I posted properly on Saturday morning it looks like I was in good spirits and planning on getting some art done etc.
Yeah that didn't happen!
I've felt like utter death for the past couple of days, pretty much unable to do anything other than fall in and out of sleep, and feel very sorry for myself.
But.... maybe.....hopefully....touch wood I'm starting to come through that now. I just now had a shower at least.... baby steps
I used my special shampoo bar for the first time that is supposed to encourage faster and thicker hair regrowth. I'll let you know if anything sprouts! It has a slightly minty herbal smell but nothing too strong and it has left my little fuzzy stubble nice and soft.
Rosina it looks like you walked a marathon yesterday from the step count I saw pop up on your Facebook! So if that was 10 days post T I should be fit to run a 10k by this Friday. Will hold you to that
Right....catch up time....
Seaside.... those Google photos and "Facebook memories" and the like are a nightmare aren't they! Talk about rubbing it in.... I don't want to be reminded of how healthy looking I was a year ago, thank you very much! I'm kind of dreading this coming October when it will remind me how I happily hiked up the hill to the Hollywood sign, all suntanned and full of energy and hair. It was a hard hike but so much fun and I wonder if I will ever be able to do something like that again :/
Really feel for you (and Edinbird) with all those work related worries hanging over you Feels like we should all be eligible for some kind of free pass at the moment. No extra worries allowed. The BC is enough!
Absolutely love the photo of you and your daughter at Race For Life. 2 peas!!!!
Susie I hope that your weather isn't as horrid as ours right now. It isn't great Dibley walking conditions out there today.
Oh and thanks to all for congratulating my young oik on his job. Yes it is the same kid who lost the weight and got new clothes. Next time he wants new gear he can buy his own now
MBJ/Daisydi/Susie B ... you are definitely not alone in a little overthinking getting you down. Or just in general wondering how best to navigate the future without it being too dominated by the big trauma we've been through, worried about recurrence etc., not feeling able to make plans,...
I've had counselling in the past for PTSD, related to the domestic violence issues from my marriage. And to be honest I can't see how this isn't kind of similar... big long drawn out unpleasant experience with the fear that at any point going forward it could raise its ugly head again. And various potential triggers to bring up those fears or flash backs.... I think we are all going to have to work hard to get those feelings under control.
But having done the work and recovery before, albeit from a different situation, I can at least assure you all that it won't be on your mind all day every day forever. The happy in between days where you don't dwell on the past and/or the scary future get more common as you go on. The days when you just enjoy the present. Those are the best days. May we have many, many of those ones!
My son's counsellor just happens to be a breast cancer survivor herself (total coincidence). In fact that was what prompted her to retrain from accountancy into therapy. He said that she told him that the first time you go in for your post treatment check ups / mammogram etc it is terrifying because you are CERTAIN it has come back. The second time you are nervous. But by the third and fourth it is much less scary.
Anyway, I'm rambling. Just to say, I hear and share your worries and down days. I've spent the last couple of days almost torturing myself reading multiple accounts of women who say that they are still suffering from extreme fatigue and various other unpleasant side effects years after treatment ended. Why do I do this? It is like I am seeking out my worst fears and validating them in some kind of self fulfilling prophecy. Of course if I go looking for horror stories I will find them....
I rebalanced this rather flawed research by reading the last few pages of the August 2018 chemo starters thread here on the BCC forum - I felt a bit nosey doing so! But I am glad I did. Because those ladies are only 6 months or so ahead of us but 1) a couple of them are doing the Race for Life this month! And 2) they are all dyeing their hair It is all so encouraging.... just to see them starting to go back to work and see their energy levels picking up. That'll be us in a few months
MBJ it is interesting to see you say about feeling abandoned by the docs and nurses, I think I felt like that as soon as my surgery was done in January! I haven't heard a peep from my BCN since before chemo started. And have only seen the onco once since early Feb. I did see the chemo nurses every 3 weeks obviously but only in a very practical way while they were administering treatment. Nobody has asked how I am, or anything. Whereas after diagnosis and building up to surgery they seemed more interested in how I was coping.
I read on the other threads about people having Macmillan nurses come to appointments with them, being offered all sorts of support.... I feel a little left out, got to say! I found the maggies centre and got on the LGFB course on my own after seeing it mentioned on here. You'd have thought my medical peeps might have said about it, otherwise without this forum I'd be none the wiser..... And then there are all the scans and extra check ups that a lot of you have had that I have never been offered. Anyway, never mind, I've coped ok I guess. But my point being, I can see why, if you have actually had good support throughout, you would be nervous of it going away! Without you lovely lot I would have felt very alone indeed throughout this whole process.
And how long now till the cruise? Is it this Friday, this week? Exciting!!!!
Edinbird I hope today has been a better day for you. I also hope that your surgeon and onco can give you reassurance at your meetings this week on the effectiveness of the chemo treatment to date and next steps. You will feel so much happier once the lump is gone, I promise. It feels like a ticking time bomb when it is still lurking in there. Before my surgery I was *convinced* I could feel it growing day by day. Daft because of course it wouldn't have been that noticeable, but our brains are idiots
It must be particularly scary being on a big forum where some members have passed away hopefully still a small percentage? But even so it would still cause a bit of a gulp.
I'm reading this book of roughly drawn newspaper style comic strips at the moment.... I can recommend it, it is harsh and to the point but also funny!
I didn't realise until after I bought it and was half way through, however, that the author didn't survive her BC.... makes it more poignant but also so very sad, and also not something I am really over keen to dwell on right now!
And you must be so fed up of everything deciding to break at once around the house!!! Let your hub take the brunt of worry about that stuff, if you can. You have enough going on!
Totally hear you re not being able to take comfort in nice food. My taste buds are worse than ever on this final round of T everything I try to eat leaves me feeling like my mouth is lined with clay, or grease. It is disgusting. I didnt bother to eat at all yesterday. Today my son bought me a cheese and onion pasty home. That was a mistake. Bleurrghhh. After that I managed an apple turnover which was ok during but had a nasty after taste. That will have to do.
Daisydi, how did it go today? Sorry you had to go into your last session still feeling so rough but it is done now. One more lot of the nasty side effects to get past and then it is all up and up.
Ocean, I live for your photography posts I really do, thank you so much for all that wonderful colour!!! I swear you should have an exhibition or bring out a book.
Really glad that you are coping with the weekly Taxol. If the worst side effect if Haribo addiction I think you have done well
6 weeks of rads sounds like an awful lot though I've not heard of anyone here having more than 4 weeks. Is it worth pushing back on that a bit?
Its fab you ended up able to keep your daughter over in France for so long. And that the son you were worried about isn't fretting too hard. Waiting to tell them face to face paid off there I think although it must have been so difficult for you.
Rosina love your photos too!
Nettie I hope you enjoy your vegetarian experiment. I've been veggie since I was 15 so i can't remember what life was like before! I have done the odd vegan phase here and there but I always relapse as I love cheese too much. That said they do have much better vegan cheese nowadays.
PS I'm glad your washing machine was only messing with you!
Seaside I've been heavy on the mental downer this cycle so far too.... as you can probably tell by this even-more-rambly-than-usual post. Do you think it is because it is the last one and now we start on another phase of the great unknown?
But as you say, nobody else who isn't going through this can really get it. :/
Glad we have each other!!!
Ok that's more than enough of me blathering on!
Night all x
PS Marlyn, where's our fish and chips (or veggie equivalent)??? Chop chop!!!
Well I'm home and done. Feel very strange. Dont feel like celebrating last chemo. Just cant get my head around it at the moment. Had a bit of a meltdown today as my cold cap machine was broken and I had to use an older one with a different style of cap. I have worked so so hard to keep my hair and I will be devastated if it all goes on this last cycle. Made such a fuss but there was nothing they could do. Did see a dr for a review before my treatment and he has really upped my doses of everything and prescribed new stuff so hopefully I wont suffer too much with my usual side effects. Wish they had done this last time. He was a very nice dr and explained loads of stuff to me. He even managed to show me my nuclear medicine bone scan which had been bothering me. I have arthritis in my shoulders, neck, knee and feet and thats before I start taking hormone tablets for 10 years! Told me that my tumour markers were still 4.8 apparently normal is 5 and this is to see whether there is still cancer in the body. It has gone up from 4.1 last time but he says its ok under 5. I didnt even know about this before. Something else to worry about now. I have been prescribed huge amounts of steroids for about 8 days, then stuff to help with tummy issues as steroids can irritate gut which I didnt know about and then anti fungal tablets for 8 days which hopefully wtill stop the burning, itching and swelling in my armpits and down below. Please god hope it works.
Sorry some of you are feeling so anxious. Just seems the norm for us at the moment but we are all here for each other and I will try my best to help all of you along the way just as you try to help me.
Love to every single one of you xxxxxxxxxxxxxxxxxxxxx
Susie, I totally get how you're feeling. It's so rubbish having to deal with uncertainty all the time. Marlyn is spot on by saying that we are good at covering what we're feeling on the inside and that this tends to attract all the unhelpful comments from people.
So far this cycle, I haven't fared too badly with physical effects but mentally I am really struggling. I am constantly worried about work and what will happen when I return. I just generally feel low and like nothing makes sense anymore. I am truly grateful I've got you ladies to chat to as I don't think anyone else understands.
Sending you a big hug 💕
i think your mood reflects how we're all feeling, this is our safe place to say what we want....no one can understand what truly goes through our minds....one resident has just said to me " keep smiling "! .......yes, I'm very good at that but behind that smile is a wide range of emotions.....I do make allowances for people with their off the cuff remarks but one day I do fear what I'm actually thinking will come spilling out, I just hope it's not to one of my residents! This morning one of the ladies asked me when I'm putting on a fish and chip lunch ( before bc it was monthly) boy I had to control myself!
Thanks for all the photos today Ocean21 and Rosina. I certainly need something to cheer me up. After starting yesterday feeling anxious by the evening it turned into feeling pretty low, not bad enough to define as depressed, and have felt the same most of the day so far. I think lots of different things have popped into my thoughts or things have happened at the same time leading to a bit of an overload. Not so long ago, just before diagnosis an insurance policy linked to our endowment mortgage had matured and due to an earlier inheritance from my Mother-in-law we had previously paid off our mortgage. Upshot of this was that we could use the money as we wanted so we were discussing how much to put away for retirement, spend on house, treat ourselves (short luxury breaks to London and Aix, the timing of which was dictated by Gremlin not us), and that kind of stuff. We were also thinking about our 45th wedding anniversary having celebrated our 40th in style last September. I haven't talked about those plans since because although I know this bc will be sorted I really don't know what the future has in store. Not knowing yet if I'm HER2 positive, triple negative or even a mix of the two definitely isn't helping. Booking next years holiday was a huge achievement for me. Then I'll also be waiting to see if I'm all clear after surgery. If so I'll have 2 more rounds of FEC, not clear and it'll be 2 rounds of TC. Will explain more on that when I get the results after surgery. Then there was the small matter of having my wedding ring cut off. It needed doing but I wanted it cut off and enlarged on my terms not Barrying bc. I won't have my ring resized until all my treatment is finished. Then there's the conundrum which some of you have talked about, how do you know chemo is doing its job after surgery. The oncologists replies don't seem to be particularly encouraging. And added to all this, if I get one more email from my mum asking "How are things?" - her way of asking how I am with the bc - I'll scream. I ignored the last one I received on Friday as we'd replied to her emails last Sat, Sun and Monday. Then on top of all of this there'll be the worry of annual mammograms, 3 monthly checks for lymphodeama by their machine and it just seems never ending. As some if you have said it's difficult when people say things will soon be over, you'll soon be back to normal, etc. I for one know that things will never be 'normal'. In time no doubt there will be a normal but a new and very different one. Sorry if this makes for depressing reading but I really do need to offload and put things in writing. Funnily enough I do feel a bit brighter, shame the weather isn't 🌫🌪🌨☔. Thanks everyone for listening, so to speak or reading this post. Will read the rest of today's posts and catch up later today or tomorrow hopefully in a better mood. Love to you all❤❤❤❤❤❤❤❤
last one woop! Woop!well done girl side effects will soon be gone - well done ❤️❤️❤️👍
Edinbird, you are doing so well coping with these household problems on top of everything else (even though you probably think you aren’t). They are the kind of things that in normal life are a minor inconvenience but during chemo break us very easily. I thought my washing machine had broken last week when I was feeling grotty and was in floods of tears. Turned out the child lock had accidentally been turned on!!!!! Felt a bit silly and slunk off to bed. 🥺 xxx
Thinking of you Daisydi xxx
Ocean, thank you for the update and more gorgeous photos. Poppies are so beautiful but then so are all the other plants/flowers. It was interesting what you were saying about your vegan son. My youngest has been vegan for about 3 months now. He was constantly suffering with dry patches on his skin and symptoms of IBS. Tests have not shown anything so he decided to try a vegan diet. His skin and stomach problems have improved dramatically already. I was very dubious when he first told me but I know he will have done the necessary research to ensure he has the rift nutrition. He is a great cook anyway and has steered clear of processed food for a while so I think he has found the transition fairly smooth. He wants me to try going vegetarian (not trying to make me a vegan as I think I would really struggle). I will certainly be considering it in the future but whilst chemo is ongoing I just need to be enable to eat what I fancy rather than not eat! X
just wanted to pop in to wish you well today love, we're all there with you....virtually cheerleading you as you walk out the unit xxxxxx
Good luck Daisy xx
The flowers are all amazing Ocean. I’m stuck in bed again. A bit self enforced... waiting on the plumber coming as I desperately need to wash my hair so I can’t do it and then they turn up and need to turn stuff off. Legs are still a bit sore but much better. Need to get up and try for shopping later to prove I can manage to get to the surgeon appointment tomorrow. I think I’ll be ok. It’s sunny outside and the rest of the week looks miserable but not much I can do right now.
Save myself some money anyway since need to pay the plumber, and alarm people who can’t come until Thursday... now the smoke alarm has started making noises too that should just be a battery but I’m sick of everything breaking!!! It was somehow ok when it was just me broken!
I’d cheer myself up with some nice food if there was such a thing... maybe by the end of the week if I’m lucky! Might brave the kitchen for toast and run up to bed if the plumber makes an entrance
Morning lovely ones.
Fantastic ,those of you who have finished chemo , we’ll get there those of us who haven’t quite finished.
I’ve got a session tomorrow and then another two before I’m finished.. You may remember I’ve been having Taxol weekly. It’s worked out well very few side effects although I must say it’s dented my appetite and practically everything I eat either has no taste or is far too sweet. Bizarrely, I can eat Haribos until the cows come home. Have to will myself to walk past them when we go shopping 😅.
Sonia28 was super happy to read that your lung is clear. Was holding my breath scrolling through to see what happened.
Edinbird hope that you’re doing well. Sounds like you need to search out some triple negative forums that are more in keeping with your positive mindset.
Susieb hope your anxiety is getting more under your control. It can be really debilitating. I didn’t have hot flushes or night sweats during menopause but out of nowhere I’d have awful panic attacks. Me being me i kept them to myself, very hard, but goodness me they were awful. Dr Jiang my Chinese medicine doctor and acupuncturist was a gem, treatment from her really helped immensely.
Marlyn, sorry to read about your sore boob. I had my first meeting with the radiologist last week. He said that before treatment I must use any creams , butters or lotions or the boob itself as they act as a barrier to the rays. He’s given me a prescription for cream that they want me to use on it. Got it from the chemist so it’s there waiting even though I don’t start with the rads until the end of July. I have to wait 4 weeks post chemo before they start treatment. Was a bit down when he told me the number of sessions I have to have. Far more than you.
I’m down for between 5& 6 weeks of treatment. He said that they decided at their team meeting to give me a little extra because I had one node involved.
Ive more or less accepted it now as 6 weeks was what was down on the protocol treatment sheet that the oncologist gave me. I was upset because I’m sure the surgeon told me I’d need a couple of weeks so that’s what I’ve always had in my head.
To be honest , although I’ve been p* ssed off at it , I know we’re all different but, reading your updates i seem to have had a very simple treatment protocol to what you guys have experienced. Apart from the injection that I needed the day after treatment with EC and some nausea meds I haven’t had anything else. A couple of weeks ago I was prescribed something as the nails on my fingers and toes became really tender. They’ve lowered my Taxol dose and it’s not so bad now. Still got dark shadows on most of my nails but I’m told that will work itself out when I’m done with chemo.
As I anticipated a short course of rads I thought everything would be finished before my eldest son arrives with my grandchildren at the end of August but I won’t have so we’ll have to work around it. Can’t wait to see them.
My daughter is still here. It’s lovely. She’s going back on Sunday, I’ll miss her loads but she’s got an interview with M&S so she has to go back.My youngest rang yesterday and it gladdened my heart to see he’s not fretting about me . They’re all obviously concerned but they see up close how I’m doing and that reassured them.
My daughter has me trying all these vegan recipes.My youngest has been trying a vegan diet as a friend of his said it helped his eczema. My boy has had it seemingly for ever , now he’s plagued with it on his hands, it’s even on his palms. He’s always struggled with dairy products so I used to but that lacto free milk when he lived at home. Now he’s cut out dairy altogether it seems to have made a big difference to the eczema.
Inspired by his needs while he was over , me and my girl have been a vegan cuisine kick. Our biggest success has been meringues. Chick pea water ( aquafaba) ,icing sugar a bit of lemon juice and vanilla whizz it up and voila .. they take an age to cook though, however I’m very impressed. Never been interested in food chemistry but aquafaba seems to have a myriad of uses so Id be fascinated to learn what properties it has that make it so useful.
Anyway, bank holiday over here today . Staying around the house loads to do for gite , aiming to list it as available from this coming weekend providing engineer coming fro. Orange doesn’t find any issues getting WiFi access. It can be a huge problem in rural areas and we’re no exception.
Right my beauties, pics for you. Poppies have been out in force.
I am enjoying the TOAST podcasts .
This one is about walking the South Downs.
I think that's the problem Sonia. We are all such strong women and just expect to get over it all quickly but it seems to knock the strongest the hardest. We will be fine x
Daisy, I didn’t recover the last time, note the 2 days of tests in hospital. I’m glad it is the end of chemo, as not sure I would be able to
continue. Fingers crossed for you tomorrow, and be kind to yourself don’t expect too much
( finding that hard myself) my body and mind are not quite working together, but hopefully it we will be all on the road to recovery very soon.
Sorry for being quiet
Feeling a little rough and mainly dozing in and out
But I'm ok and not in the hospital yet, that's the main thing. In fact after creeping up and up all day I just took temp and it has gone back down to 37.0 which is great news as it was flirting with the dange zone this afternoon
Heading back uo to bed now. Catch up properly tomorrow.
Hi everyone, Seaside that is such a beautiful photo of you and your daughter. Such lovely smiles. Edinbird its good that you have faith in your oncologist. Ive only seen mine twice and to be honest I dont really like him but I suppose its the nature of the job. Just had to use the mobility scooter again as I have no energy, really sore knees, feet and toes. Doesnt bode well for the last one tomorrow, who knows what joys it will bring. The worst thing is that I have also had 8 steroids today and I should be buzzing and I am just not! Glad you feel better Rosina. Hope you are alright Implausible. A white t shirt was not a good idea today. I am covered in black flies. Not a good look. Love to all xx
I’ve got oncologist on Friday. He was very positive at the last scan. He’s the clinical director so I can’t complain and will absolutely be guided by what he says.
Yes whatever is there is coming out!! Scans show the lump is very isolated from an otherwise healthy breast although the nipple issues and skin thickening do concern me. Dunno how many lymph nodes they’ll want to take. Not long to wait to find out.
This came up on my Facebook and it made me laugh... not that it was remotely funny what we have been through or at the time but I guess we can smile now 😆 we are all still here and kicking its arse so...
No more hospital dashes please!!! 🤞
sorry to read your day is kak, I hope you manage some sleep tonight.......it's rough enough feeling so lousy....but add no sleep to the mix....oh boy!
I have a friend who is triple neg, she's doing ok but does constantly worry, I read up on it for a better understanding, naively I thought breast cancer was one diagnosis....until I had it....then I realised there were different types....does your onco give you much feed back on how it's all going? I mean, if there's not much shrinkage they can still remove it right? Xxxx
Well done to Mini Sar! I think a lot of us are feeling like pap when it’s so quiet you can sense it...
Third day predominantly in bed. Aches are far less severe but I get so dizzy if I stand for more than about 5 seconds. When I’m laid down I’m fine so I’m particularly frustrated.
And it is husband’s birthday today 😕 I only even managed to write his card this morning! He wanted an iPad but changed his mind so he doesn’t have a present 😔
Feel bad for feeling so bad. Went on my triple negative forums to ask about response to chemo with my lump not shrinking much. Less because I’m worried but more because I knew I’d get people telling me they had similar experiences and I’m normal. People keep dying on these forums too. It’s just unfortunate there’s no pattern it’s just the way of my type of cancer. Our recurrence rate is more Barry than others. I’m not down about that it’s random. Sitting in bed watching TV stinks!!
Well done Seaside Sar to your daughter for doing the Race for Life this morning. Georgeous photo of the pair of you too☺. My son is due to run the Race in Taunton next month with a couple of friends.
Glad I'm not the only one to hit low points every now and again. It almost makes me feel normal. I woke up this morning very much on edge/anxious and have ended up taking a full dose today of my meds for anxiety☹. Apart from the upcoming surgery I don't think just passing the 6 month point since diagnosis has helped, especially as there is still so much to go through. And yes, my poor hubby gets the brunt of my meltdowns. It all gets a bit too much sometimes and knowing that things will never be as carefree as they once were doesn't help either. This Barrying bc is💩.
Anyway less of my ranting, today hasn't been too bad. It's stayed dry and me and Dibley had a lovely walk while hubby did some work in the garden.
Enjoy the rest if the day. Love to you all❤❤❤❤
Congrats to your daughter Seasidesar.
I feel like I am back to ‘normal’ at last, 11 days after being ‘dosed ‘. Head is much clearer 🤗
Hi Seaside Sar
Well done to your daughter for running in the race for Life. I have just come home from singing with the Rock Choir for the Llanelli Race for Lifeh in not so sunny Wales. But at least it was dry. Wonderful to see so many people running for a cause so close to our hearts.
It's dry and sunny here today which is a good job because my daughter ran the Race for Life this morning. So proud of her and will admit to feeling a bit choked up when I saw everyone gathering at the start line.
Good to hear the news about your son, Sarah. Massive congrats to him!
Sonia, I hope your rads are all done in time for your trip away. It is frustrating not being able to plan ahead but fingers crossed for you.
Glad to hear you're feeling a bit better today, Daisy. I went into super grump and depression mode yesterday evening. Poor hubby as ever got the brunt of it. It's just hard at times facing the reality of what we're going through.
Hope everyone else is having a good day.
Loads of love
I was not trying to emphasis having dark thoughts as such. But to highlight the fact that it's absolutely normal for us to feel anxious sometimes. All the literature talks about it. We and our nearest and dearest can't expect things to be as they were before BC but my aim was to show that we all need to find our new normal whatever that may be. Campaigner, champion, volunteer or just quietly picking up the reins of our life. Like me sailing off on my cruise on Friday, looking forward to it now but still a bit scary as it will be the first time away since my diagnosis. Reading about life after treatment is helping me realise what I am feeling. It's strange to feel a bit abandoned by the nurses and Dr"s after being closely monitored for months. Not that I want to need them or become dependent on their support, but it is taken away very suddenly. Like your safety net has been wiped away.
But obviously I am well and out and about doing stuff, but it is still early days and there is still healing to do.
Afternoon all, just popped in to say huge congratulations to your son Sarah. What a star x Hopefully that has made you feel a bit better.
Nettie is it you and me on for Monday then? I'm not so miserable today but a bit grumpy!
Edinbird sounds like you had a bit of a hard night. Hope you're feeling better.
Rosina, Seaside, Sonia and Deano hope you are all ok and not suffering too much and Maryln hope you are enjoying your weekend off.
MJB glad I'm not the only one having dark thoughts but I suppose it is expected isn't it? Trouble is because I am not doing very much I have too much thinking time. Hopefully it will get better with time.
Ocean hope you are ok and nearly finishing your chemo? Susie hope you are ok. Not long to wait now.
I would love to write a big long post to reply to everyone but I cant remember what has been said and I cant scroll down. Sorry if I have missed anyone out. Its start of the roids tomorrow so at least I will have a healthy glow.
Love to all xx
Implausible, I’m made up for your son. Especially as he thought he hadn’t got it. Well done. 👏👏👏👏👏. Xx