Morning Eitaki, it was my first FEC of 3 yesterday, 3 Tax to follow, only your oncologist could explain variants. I’ve keep nausea at bay with anti sickness meds, do no wait for nausea to start, I am going to take until tomorrow, giving it 3 days, until I see how I feel naturally. I’ve been awake since 3am, the steroids I expect. Going mack to bed once house people free and dogs fed x
Hi all, I am now on day 6 following my first fec dose. Can’t say I am feeling much better than I did on day 1 really. Been feeling really cold & tired & not up to doing very much really. Is this sort of normal as expected the nausea/vomiting but not this.
I’m feeling really useless really.
Hi ladies. Sounds like we’ve all got our first one done - well done us! Think a treat is in order. I’ve also had stomach cramping type pains - Senakot did the job with the constipation, then had upset tum for a day or so and seems to have brought period on early. Picked up my wig today and bought a nice cap at the same time. Just managed a yoga session after work, trying to carry on ‘normal life’ stuff as much as possible.
Hi ladies,
I’ve been reading all of your posts (from this thread and others) and am ready to take the plunge!
I’m a 32 year old woman who was diagnosed with BC in my RB (no lymph involvement) at the end of Jan (my brother’s birthday to be precise!). I am due to start neo-adjuvant chemo tomorrow for 6 cycles. I’m due to receive 6 x FEC, with a possibility of switching to T after 3 cycles.’ “Larry” (my lump!) is 32mm, stage 1/2 and grade 2.
I was originally due to start chemo yesterday, but my onc wants me to have my MRI scan first so I’ having my MRI tomorrow at 9.30 and my chemo straight after. I was really scared when I received the letter at the weekend, but after the appointment being rescheduled, I now just want to get on with it. I am a bit of a control freak and want to know what it’s like and I think once I’ve done one I can move forward with my treatment. I’m trying to look as chemo as a friend which is going to help me out, but we’re going to fall out sometimes!! It isn’t exactly how id like to be spending my Spring/Summer, but we’ll all get through this and it’ll be like a distant memory for us! Remember we are in charge (even though the chemo/surgery dictates to us sometimes), but we will win overall!!
Now, can you all remind me of that over the next week or so when I’m not feeling as brave!!!
Hi all,
I am on day 7 of my first fec treatment & although I have been down since my diagnosis I seem to have completely crashed as low as I have ever been in my life in the past two days. I have been prescribed anti depressants which I still haven’t started yet as not sure whether I should or not even though I cannot see any light at the end of a very long tunnel. Does anyone else feel like this or is it just me?
Hi Bella, yeah I’ve been feeling really low, tearful all day long. I think it is definately the chemo having major impact on my mood. I managed to get out for a walk yesterday, did quite a bit of exercise. It helped. I’m reluctant to take antidepressants, on enough chemicals already!
Welcome new ladies, hope your first one isn’t as bad as you think it will be.
Mel51 - Your situation sounds v similar to me, I’m having neoadjuvant chemo that was delayed while I had an MRI. Mine is 35mm in right breast, ultrasound not showing any lymph node involvement but won’t know for definite until surgery.
Have swings of being upset and down, think you’d be superhuman not to and sure the chemo will impact on your mood too. Agree that walks and fresh air help a lot, and definitely prioritising spending time with friends.
Thanks for the welcome Stelwah.
Here I am on the morning of the chemo and actually feeling OK about it. I went to look at wigs yesterday and have found the perfect one, so that’s sorted for when I need it. I also ordered some fab bandanas and hats to use regardless of hairless as they’re soooo nice!
Think I’ve thought every worst case scenario is going to happen that I’ve left myself quite worn out by it, so am now ready to get on with it!
Will fill you all in later.
Hi Mel and welcome to the BCC forums
Along with the support and shared experiences here you may be interested in taking a look at the BCC ‘Younger women’ support services which include our ‘Younger women together’ weekend forums, here’s the link :
breastcancercare.org.uk/younger-women
Our helpliners are also on hand with further practical and emotional support on 0808 800 6000, lines are open weekdays 9-5 and Saturday 10-2
Take care
Lucy BCC
Yesterday was a looooong day. The chemo itself and the process was not anywhere near as bad as anticipated. However, apparently I have tricky veins (1st time I’ve even been told that!) so think I’m going to have a PICC line fitted before next round. As far as SE I didn’t each much for dinner due to the nausea, but the anti-emetics kicked in over night so I managed some sleep, but the steroids limited that!! I’m tired and a. It achy this morning, but just had a little breakfast and my steroids. One of the greatest pieces of advice I read on here is to not wait until you start to feel sick and drink plenty of fluids before, during and after the chemo and I think this is working, but I’m sure time will change that!!
Do however, have a bit of a headache he - think from trying to sleep when couldn’t and a runny nose on occasion!
For Mother-In-Law (as no internet)
Started treatment on Monday with her first lot of FEC-T chemotherapy, she is having 4 cycles 21 days apart for 1.5 hours each.
Had anti sickenss tablets for first 2 days after, and then having injections for next 5 days to help with white blood cells.
It seems to have made her more tired than she expected and changed her taste for different things, her throat and top of her mouth have become very sore, and her hands are tingling alot.
She is rubbish at asking questions and the time, so asks after, I am guessing all these things are normal, we have been using the MacMillan site alot for info, but great to see others stories too.
How long will these last?
How’s everyone doing? Day 13 for me and feeling really well, hope I haven’t just jinxed it! Haven’t lost any hair…yet!! Xxx
Hi everyone day 12 today of my first fec, like elsieoc I had pain in my lower back and pelvic area day after injection finished, really bad did not want to walk! Now much better as injections finished wednesday. Otherwise im fine no side effects, mouth ulcers or anything. Hair is ok too fingers crossed cold cap worked. Going to make the most of this week. Please ladies stay strong xx
On Day 4 of FEC1 and feeling surprisingly well. I had a little nausea on Saturaday morning, but managed to up my fluids and eat a little pineapple and a banana and the nausea soon passed. Quite tired mid-morning, so I have a little nap, and again in the afternoon if I need it. I’m trying to build all of my meals/snacks around my 5 a day and taking in plenty of fluids throughout the day. Don’t fancy anything fizzy, but do have hunger, although not really sure what I’m hungry for!! All in all, a good start, but I’m trying to take each day as it comes as you’re never sure what is around the corner!!
Need to make a decision now about the PICC line and also try and stave off the boredom - but as my friends said if I’d known these would be my only two issues at the start, I would’ve been happy and I have to agree.
Keep talking ladies and remember there’s always someone on here who is feeling the same.
Good to hear everyone is doing better. Been feeling great over past few days, enjoying the sun and working as normal. Waiting for hair loss to start - nothing yet though so hoping it’ll hang on in there as long as possible.
Just had a shower and lost more hair than I would have liked. Not a lot but wondering if it is the start 
I have thick hair so hoping it won’t be noticeable for a while and I did use cold cap. I have a wig already in preparation. My usually bald husband looks hysterical in it lol!
My FEC symptoms so far have been, vomiting for first 2 days, the next two days u was just weak and felt pathetic. Wanted to stay in bed but couldn’t get comfy, my arms were really restless which was weird. Then I just felt really tired, light headed, fuzzy head, and generally drugged. By day 6 I had to be completely back to normal and back on school runs etc. I have a 5 yr old and 16 week old so that week was hard. I’ve had a furry feeling on the roof of my mouth, dry mouth at night and a few aches and pains but I dud think it would be a lot worse. Hoping they can do something more for the sickness next time. I’m back next tues so going to make the most of this week. Don’t like the waiting game of if and when the hair is going to go. I’m only 36, how old is everyone else if you don’t mind me asking ?
Hi dh. I’m not looking forward to hair loss starting either. I didn’t use cold cap though - sounded unpleasant and extended time spent in hospital - so guessing it’s a matter of days now. I keep looking at the plug hole/pillow with trepidation, but wig and hat ready to go.
I’m 37. Already had a different cancer when I was 24 that involved surgery and radiotherapy, but chemo all new to me.
Morning…can anyone recommend a milk alternative…I have been told to avoid dairy and soya milk…is Almond milk ok to drink? Trying to plan a healthy diet…tx Donna
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Ahhaaa…found the following info …may interest others…regarding almond milk
it is free of cholesterol and saturated fat, rich in vitamins and minerals and omega fatty acids. Level of manganese, selenium, and vitamin E is quite high in almond milk. Almond milk can supply 30% of your daily calcium requirement.
It promotes growth and repair functions of the body.
Magnesium helps break down the consumed food into energy.
Vitamin E acts as an antioxidant and destroys the free radicals which cause damage to cell membranes.
Selenium improves the function of reproductive and immune systems. It promotes thyroid function.
No cholesterol, risk of heart diseases is significantly reduced.
Potassium helps maintain normal blood pressure.
Good luck ladies for your first sessions this week.
I think that the anxiety on the run up to it is worse than the reality of it. If you read the threads they all say the same - it’s all about figuring out how your body is going to cope with the chemo. Keep a good diary of how you feel and how the drugs impact on you and remember to feed that back to the onc. I used the Paxman Cold Cap and found it bearable - I took someone’s advice and took a couple or paracetamol before it went on and this seemed to help. Take lots of layers and a hoodie/hat for afterwards as you head home. I’ll persist with it as long as I can or have hair as it may be linked with a quicker re-growth, but who knows!!
Best of luck for Thursday and remember to listen to your bodies and rest (even if the steroids tell you otherwise!).
I am 32 years old by the way!