Morning ladies...
well this is all a joy. Was doing wonderful and then got a temp 38.2. Straight in to A&E which was horrifying mostly because I know them all there.
Im a 46 year old Paramedic and I recently landed my dream job as a practioner at a Gp practice but before that I worked as a Paramedic in A&E and seeing all my colleagues yesterday when I felt so vulnerable wasn’t my best. I know it’s sounds a bit strange but I’m quite private and it was like being on parade.
So ive got 2 children in their 20’s who are awesome my son lives in Barcelona but my daughter is just up the road with her boyfriend who’s also a paramedic and a lovely husband who yes you’ve guessed it is also a Paramedic. My mum also died in an RTC, she was on her way back from her appointment where they had just told her she was over breast cancer! It’s so strange how it all works out. I do feel for you Jamesy loosing someone in Trauma is a horrible horrible thing to deal with. You sound strong but I can guess some of what you’ve been through.
My tumour is 7cm Lobular in my left breast with the twin nodes they removed showing cancer so Chemo then surgery for me. Not sure if anyone else who has still got their tumour is getting a reaction to the chemo but my boob is literally like rock and very tender, like the little b@st@rd is all angry, they did tell me there maybe a reaction.
So so I digress I am now on the ward playing the please let me go home waiting game...xx
O gosh. Stay strong. I am suffering like you and don’t know how I’ll do more of the same. I really hope you get some sleep x
Hi all,
I started my first round of EC on Friday. Friday afternoon and night were awfull. I have been really poorly all the weekend.Nausea so nearly unable to eat and in a lot of pain, with the blood buring on my veins, bruises hurting and feeling feverish even though I have no temperature. I can sleep only 2 to 3 hours at a time before my symptoms wake me up. I am supposed to have 8 rounds of chemo. I am not sure how I will survive this.
I went to A&E today, and got some pain killer and anti-sickness medication. I am now feeling better now, but really tired as I didn't manage to rest because of the side effects.
Bless you Jamesy46. Thanks for sharing. You sound very strong! I think it helps to know why we are being subjected to this x I forgot I am Her 2 - er and pr pos. Proof my brain has gone wrong. Speak soon and take care. X
I know this is out there but I really think that stress and sadness brought this all on.
Hi again, lost track of what’s going on with everyone but you all seem to be okay from what my brain can take in...it’s a bit foggy. I can’t believe that some of you are managing to get out of the house x
I’ve been in bed all day following sickness attack last night that left my shaking for ages. I’m worse it appears after the bone marrow injection I have in the evening. Is anyone else having these injections...
to prevent me being Nutrepenic.
Yes I had TAX followed straight away by Carboplatin. The thought of it again makes me panic.
What meds can you recommend to ask for. What is this EMEND I’ve heard mentioned.
best x
abit of background on me.
Im 48 with a five year old daughter and a husband. I’ve kept this low key so no one near to help apart from my lovely neighbour. I lost my Mum suddenly to brain cancer whilst pregnant and she would have been an absolute trooper with me now. My dad on the other hand is a disappointment having remarried and moved on instantly and can’t even offer to walk our dogs or help out at all. His new wife has taken everything and doesn’t allow him near us.
i had a Grade 1 17mm Cancer removed by WLE (two operations) but the tumour showed vascular invasion and cancer deposits 2.2 mil (just positive) were found in one of my two Sentinel Nodes. They’ve offered me AUX clearance but have yet to decide as I have a muscle wasting disease and mobility issues and rely on my left arm etc. I’m hoping chemo will blast my nodes. That’s why I’m having Tax and Carboplatin as opposed to FEC because of my muscles and risk to heart.
Thanks Dealdoh...so you’re clearly on breast cancer round 2! Blimey!! Hats off to you all brave ladies. Fec you’re in my thoughts xxx
I love that you ladies can make me laugh on here. So glad I wasn’t standing in that queue Rosie.
I asked about your surgery as I had a double mastectomy in November and because there was evidence of spread into left axillary nodes I had total axillary clearance on that side. I had already had total right axillary clearance following a WLE on the 16 years ago. I know lymphoedema is always a concern but you just have to adjust and be careful. Ive managed perfectly well for the last sixteen years. It is now slightly more problematical as the potential is for lymphoedema in both arms, so unless it is an emergency, blood will need to be taken from somewhere else (usually feet) and blood pressure on the leg. I have already bought a couple of lymphoedema medic alert bands, just in case for any reason I can’t warn people off!
Hi Dealdoh...yes that’s what they’ve said which is a bit of a bummer but not the end of the world!!
im guessing having it post Chemo means at least I can’t get cellulitis when my immune system bows out.
Well done Tracey on the trip out...I’m with you dealdoh on the feeling a bit fraudy especially reading Fec’s reattion. I’m wondering if it’s because I’ve started with the T and not the FEC.
Fec you’ve got a baby too bless you, bloody disease doesn’t discriminate does it...hopefully by Monday you may have settled a bit.
I just popped out to do a few bits but unfortunately my tummy is a bit rumbley shall we say which is resulting in a certain aroma...I may not feel too bad but I’m not entirely sure the same could be said for anyone in the M&S queue behind me!!! Xx
Hi Ladies
Im day 2 and so far so good. Slept well last night and while I woke with a headache it was only mild. Trying to drink loads and taking my medication like a good girl. Feeling a bit of a fraud at the moment, as I seem to have got off very lightly but waiting for the s@#*t to happen.
hugs for those who are not faring so well and Aliand thanks for the positive words as usual.
Rosie when you talk about radical do you mean mastectomy and total axillary clearance.
FEC as a friend told me, dont worry in a few days you will feel so much better, I hung onto that and believe me it was true. I'm keeping a diary of how I feel everyday, they suggested I did and I think it will be god to look back on.
I'm on different treatment to you but on day 4 I was suffering from headaches, murky brain, lethergy, and horrible constipation. Day 5 it was lifting and by day 6 I was almost back to normal. Took to about day 7 for tastes to be more normal though water is only just tasting better as of yesterday. I'm now day 11 and I'm totally back to myself, housework and taxi driver. The only thing I'm not doing is mixing with others. DH is so worried about me picking anything up as theres so much flu around and some of it isnt covered by the flu vaccine and also pneumonias that are landing healthy people in ITU. So amazon and ASOS are my best friends and I send my teenage kids or friends out to get what I need.
The other advise my friend gave me is when people offer to help use them. People want to help and feel good that they have done something for you. If you keep saying no some will stop asking. If youve people offering to do school run take it up. If people will take your daughter to play after school say yes please. Don't think you have to do this on your own you don't. And this is coming from the woman who used to bend over backward trying to do things for other people but NEVER asking for anything from anyone unless I was absolutely desperate. I'm learning.
Tracy12059 hope you got to the park, my daily walk is a lifesaver getting out and about.
There is light at the end of the tunnel with each cycle. I much less worried about my second dose. In fact I'd have it this week if I could. Get them over and done with, it's going to be a long 24 weeks !
Keep in touch girls and keep smiling xx
Hi RosieH,
thank god for my husband who is doing everything for my daughter who is 5.
real test starts for me on Monday when he goes back to work!
Let me me know how you are tomorrow x
Crikey Fec...bless you. Only day two over here.
Tracey I feel for you Mummies so much. Mine are grown although I’m only 46 and it’s hard to watch their pain.
To be looking after babies must be so so...I don’t know the word but my thoughts are with you xxx
Day 2: steroid red face
Day 3: Vomitting, stomach cramps, nauseous
Day 4: Nauseous, exhausted, pain in bones from injections...so bad!
Diet of biscuit, greek yoghurt with Manuka, soup and plain bread.
anyone else on day 4?
Hi ladies
First T down and feeling ok. Not like I want to go dancing ok but not horrific. Strange taste in my mouth and very red cheeks!! Found out yesterday all organs and bones are clear but my Sentinal nodes were positive for cancer. Apparently no change in treatment but when I have surgery it will be a radical!
However back to Chemo and one day at a time it felt awesome to get started on the treatment...hope all you other ladies are doing ok? Xxx
Ahh Jamesy that made laugh - you sound like a woman after my own heart. The nurse said it depends on the type of chemo and maybe the way it is administered by I got the impression I was good to go if I wanted to after the three days. Aaparently alcohol doesn’t react well with the antisickness stuff.
Aliand, the nurse said the injections affect the white cell producing bits of the body and mentioned the long bones and hips. I still miss the nursing but I wouldn’t go bac as it is now. I think having been a nurse has helped prepare me a bit for this. Would you say the same.?
off to bed now to try and catch up on some zzzzs. Night all - hope it is a good one x
Thanks Aliand, the cake was good, left over from my birthday on Wednesday and I’m keeping my fingers crossed. I’m not particularly worried about giving the injections (was a nurse in a previous life) just the possible aches and pains.
Sorry Jamesy. One of the chemo nurses told me no alcohol for 48hours post chemo and another nurse said no alcohol while taking the anti sickness medication (so three days I guess).
Kirstyp86 how are you feeling? x
Well first one down - yayyy. All went well and feeling ok at the moment. I have the same medication as you Fec, hope it works. My hubby made me an omelette when we got in from the hospital,and then I spoiled it by having some chocolate cake. I hope that wasnt a mistake!,trying to drink plenty but oh my I would love a glass of wine but I do know that that is a no no.
Was also given the GCSF injections, which I have to self administer for five days starting on day five. Yuk
Glad and to hear that your tooth is feeling better Aliand
onwards and upwards ladies x
Hi there, i hope you and your mum are doing ok? What is the Alice band for with the cold cap?
@Confuseddaughter wrote:
Hi everyone...
I've been bit quiet on here for a while but mum starts the second part of her journey this week so thought via me, she could be part of this. Lumpsectory done back in November, lovely Christmas now time to start!
Tomorrow she has her first dose of herceptin so it's a good few hours at the hospital tomorrow we are told for observation, then Thursday starts chemo, as she is her2+.
Bit surreal that this day we knew was coming is here... mum is having paclitaxel weekly for 12 weeks and herceptin every three weeks.
We have been following everyones great tips and support, mum has been taking the manuka honey since diagnosis. We got it from holland and barrett, the 24+ one, highest concentration, it's a bit pricey at £55 but they have a penny sale on so you get two large pots for £55 which helps and she has a spoon a day! My sister dad and I have all had a cold the last month and mums the only one who hasn't! Think we need to start taking it!
Lots of deliveries in the post this week, paxman shampoo and conditioner, hair nets for sleeping in, silk pillowcases which are meant to be better for the scalp, eyebrow stamps (!), wide comb,
@Confuseddaughter wrote:
Hi everyone...
I've been bit quiet on here for a while but mum starts the second part of her journey this week so thought via me, she could be part of this. Lumpsectory done back in November, lovely Christmas now time to start!
Tomorrow she has her first dose of herceptin so it's a good few hours at the hospital tomorrow we are told for observation, then Thursday starts chemo, as she is her2+.
Bit surreal that this day we knew was coming is here... mum is having paclitaxel weekly for 12 weeks and herceptin every three weeks.
We have been following everyones great tips and support, mum has been taking the manuka honey since diagnosis. We got it from holland and barrett, the 24+ one, highest concentration, it's a bit pricey at £55 but they have a penny sale on so you get two large pots for £55 which helps and she has a spoon a day! My sister dad and I have all had a cold the last month and mums the only one who hasn't! Think we need to start taking it!
Lots of deliveries in the post this week, paxman shampoo and conditioner, hair nets for sleeping in, silk pillowcases which are meant to be better for the scalp, eyebrow stamps (!), wide comb,Alice bands for the cold cap and have been told that whatever you do reg the cold cap, just make sure it fits right!
I know I'm not going through this myself but have been there every step with my mum and am always reading everything posted on here, it helps. Was thinking this morning, of all the emotions felt the last few months more so at the time of diagnosis, feel like they are resurfacing a bit and try to not get upset but we are ready for this now. Also will show mum the responses and comments from everyone so she knows she's not the only one! (She's not too technological!)
Thinking of you all and here's to the next few months. Reassuring knowing you are all out there going through similar experience and I think when mum goes to the ward Thursday she will see that herself.
Take care everyone and if starting, sending you hugs and support
Xxxxxx
I know I'm not going through this myself but have been there every step with my mum and am always reading everything posted on here, it helps. Was thinking this morning, of all the emotions felt the last few months more so at the time of diagnosis, feel like they are resurfacing a bit and try to not get upset but we are ready for this now. Also will show mum the responses and comments from everyone so she knows she's not the only one! (She's not too technological!)
Thinking of you all and here's to the next few months. Reassuring knowing you are all out there going through similar experience and I think when mum goes to the ward Thursday she will see that herself.
Take care everyone and if starting, sending you hugs and support
Xxxxxx
@Confuseddaughter wrote:
Hi everyone...
I've been bit quiet on here for a while but mum starts the second part of her journey this week so thought via me, she could be part of this. Lumpsectory done back in November, lovely Christmas now time to start!
Tomorrow she has her first dose of herceptin so it's a good few hours at the hospital tomorrow we are told for observation, then Thursday starts chemo, as she is her2+.
Bit surreal that this day we knew was coming is here... mum is having paclitaxel weekly for 12 weeks and herceptin every three weeks.
We have been following everyones great tips and support, mum has been taking the manuka honey since diagnosis. We got it from holland and barrett, the 24+ one, highest concentration, it's a bit pricey at £55 but they have a penny sale on so you get two large pots for £55 which helps and she has a spoon a day! My sister dad and I have all had a cold the last month and mums the only one who hasn't! Think we need to start taking it!
Lots of deliveries in the post this week, paxman shampoo and conditioner, hair nets for sleeping in, silk pillowcases which are meant to be better for the scalp, eyebrow stamps (!), wide comb,Alice bands for the cold cap and have been told that whatever you do reg the cold cap, just make sure it fits right!
I know I'm not going through this myself but have been there every step with my mum and am always reading everything posted on here, it helps. Was thinking this morning, of all the emotions felt the last few months more so at the time of diagnosis, feel like they are resurfacing a bit and try to not get upset but we are ready for this now. Also will show mum the responses and comments from everyone so she knows she's not the only one! (She's not too technological!)
Thinking of you all and here's to the next few months. Reassuring knowing you are all out there going through similar experience and I think when mum goes to the ward Thursday she will see that herself.
Take care everyone and if starting, sending you hugs and support
Xxxxxx
Xx
My meds for sickness are, Ondansetron x 3 per day, metoclopramide x3 per day and dexamethasone before the day, on the day and after. It’s calmed a bit but still feel yuk. Should I request Emend?
So sorry you are all feeling so sick it's just the pits isnt it, but it won't last I promise. My nausea lasted several days but I only vomited a day. The awful taste in my mouth coupled with the nausea gave me no appetite at all but I made myself eat small amounts. I think nutrition is really important to repair all the damage done by the chemo so I'd suggest you try to eat small amounts of healthy food, maybe soup for example. I found muller yoghurts a lifesaver as they tasted ok and the coolness and smoothness was really great. Also keep an eye on your bowels I got really constipated with the anti sickness meds - another reason to eat and drink.
My tooth is sooooooo much better today, though I'm taking regular brufen as well as the antibiotics and my temp was 37.3 this morning so I hope I'm not brewing something. Cant believe I'm not more tired actually.
I've been online looking at scarves, thinking the hair will probably go next week and I've a couple of things but want to be prepared. Not heard anything from the wig guy yet.
Time for my daily constitutional sending you all hugs xxx
I had a conversation with the doctor who gave me some other anti sickness meds. Seems to have calmed down 65% but still have tummy cramps, can anyone recommend what or if I should eat IF I get hungry. Thanks. I’m in such a state. How is everyone else today x
Hi Tracy. Finally managed to drift off at just gone five. Glad to hear your night wasn’t too bad and hope your day is the same. I’m thinking it must be that much more difficult when you are trying to deal with this AND you have a young family. At least it is just my hubby and I at home, our daughter is married and lives with her hubby and 9 month old about an hour away and our son emigrated to Canada in October of last year (😢).
i will let you know how it goes.
Fec - are the anti sickness pills helping?
Morning,
hope per you are all coping. Bad night for me... awake at 4am with vomiting and stomach cramps. Went off for a bit but now back again. Have taken my anti-sickness meds too. Xx
Morning,
hope per you are all coping. Bad night for me... awake at 4am with vomiting and stomach cramps. Went off for a bit but now back again. Have taken my anti-sickness meds too. Xx