Welcome to the June BC Chemotherapy Discussion.
Looks like summer has finally arrived - All we need now are a few Swifts & Swallows.
This thread is for all of you good folks going through chemotherapy to browse through, ask questions, answer questions and be there for each other in a way only you all know how.
If you want to find this post quickly, you can hit the 'Save In My Favourites' button - See discussion tools box on the right >
If you need any extra tips, our Chemo Tips Page is something you may find very helpful, and if you find a tip which helped you just reply to share with others who are also going through chemo. One top tip, ask about parking at the hospital where you are being treated; for some Cancer patients parking is either free or heavily discounted - So it's worth asking about.
Macmillan produce this Healthy Eating booklet if you have any diet concerns MAC13612_Healthyeating.pdf
If you need to refer back a month here is a link to The May Discussion which will be being locked to replies soon.
Remember, you're never alone, you have us! while going through this tough part of your runaway mine cart ride.
Don't forget all cancer patients are entitled to a 5 Year Prescription Fee Exemption Card from your GP for meds to help with any side effects.
Fingers crossed for minimal side effects and maximum impact, G n' J
I’m having my 2nd dose on Wednesday. Yes Sandra I was given injections for 7 days. Didn’t like doing them and they made me feel a bit dizzy. I decided to brave the shave today. My hair was coming out in clumps which was really upsetting and very messy. Feel so much better now.
Take care all Mags X
Hi,
Had the filgrastim injections when I was on the docetaxel. I was prescribed x5 doses and took them on first night after chemo however this was too much for me got terrible leg pains and stomach . Next time discussed with oncologist only took x3 injections took them 3 days after chemo which was a lot better and my bloods ok.
With the FEC don’t normally get fgrastim but due to Covid getting this now. To take on day 14.
I just discussed all my side effects with the oncologist in the chemo unit. She was so helpful and understanding and was able to help me adjust my meds for what was best for me. I also reduced my steroids gradually as that helped also.
Good luck everyone and take care. My motto don’t ask you won’t get. This chemo is hard core xxxx
Hi
I was given filgrastim injections which started 4 days after my first round of chemo and lasted for 5 days. Apprehensive at doing the first one but found it ok after that.
Strange how we all are given different meds but I suppose it's down to our individual treatments.
Good luck to all having chemo this week
Linda xx
Hi they only gave me one injection to do the day after my chemo and said I will have another one to take after every chemo thereafter I've only got to have 4 thank goodness. ( my husband done mine )
Yes second that good luck to all having chemo this week.
Hi
I've got my onco test results today (27) and chemo is recommended. I've found lots of useful info= thanks for the links.
I'm meeting the oncologists next Monday (22 June) to discuss my treatment plan.
I realise treatments are individually tailored but wonder if anyone has NOT lost their hair?
I had a rash on my face and head it was my first dose of docetaxel after having 4 rounds of ec I was worried because my temperature went up aa well even though I didn't feel poorly did ring RAPID RESPONSE they told me to have antihistamine to calm it down it did help just waiting now to see if the 2nd round affects me the same
Poor you,
On my second dose of docetaxel I got about 25 spots/boils all over my bottom and legs. Got oral antibiotics and antibiotic cream which helped. When I got my 3rd dose just got a few spots and zapped the cream straight on them so was nothing like the 2bd dude. Hopefully you won’t get the rash again if you take the anti histamine earlier. Good luck xxx
Hi I’m due my 5th round of EC Chemo on Tuesday and still have shoulder length hair - all be it very fine and thin with a couple of small bald patches. If I wear a cap you wouldn’t know I was having chemo. I used the cold cap for first 3 sessions, but not the 4th. I was told it would all be gone by my 5th treatment but it’s hanging on in there! Good Luck -
I hope the anti histamines have kicked in and cooling your rash.
take care
Sandra
x
Hi I hope the antihistamine as helped. My rash is only on the cheekbones and I have more boils and white heads, the antihistamine, antibiotic they gave me as calmed it a bit...when I seen the nurse yesterday she gave me some dermo cream which seems to help too.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
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