Welcome to May BC Chemotherapy Discussion.
With it's promises of warmer, sunnier days, fresh greenery and opening flowers
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 April Thread 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.
Happy Pole Dancing everyone (Maypole that is) Fingers crossed for no curved balls with all that is going on around us.
G n' J
Jostar A girl who had chemo at the same time as me recommended black nail polish. I asked my nurse and she said it did make a difference. Between one thing and another I didn’t get round to doing it and ended up with four ridges across my nails. As each ridge is growing to the tip of my finger it’s splitting and I have to cut them down. I would say it’s worth trying the nail polish! x
They told me UV light can increase risk of nail damage so the idea is wear the darkest nail varnish possible to block it from reaching nail. I've had last chemo and nails have been ok but just started to feel a bit like after you've trapped them on something so hope I'm not going to have problem right at the end .
Hiya,
Re: NAILS....
First off steri strip on a roll is much cheaper than the pre-cut packaged ones, just cut off the size you need if they start getting wobbly.
Most use some form of cuticle nail gel or cream solution like Evonail etc to stop them becoming too brittle, keep nails fairly short to avoid them splitting at the top
As for nail varnish - some chemo types are more UV sensitive than others but as a general rule of thumb if you wish to use nail varnish to help protect them... There are some water based nail varnish brands too.
The darker colour the better (black, dark blue, dark red) You can put a layer of a lighter colour on first if you want to go black, as 24/7 use of black can stain the nail slightly after time.
Make sure you only use Acetone / Solvent Free nail varnish remover - Acetone is a strong solvent and will dry your nails out and make them very brittle at this time.
There are loads of messages here that mention nails if you type that into the groups search bar
Finger Nail care is also a good protection against lymphoedema risk, especially if you have had a lymph-node clearance.
Take care, G n' J
Hi
Thank you for the tip I m 8 day of first chemo I tried black ( oncologist) mentioned the benefits but hated it so have water based dark red
my nails are short anyway, I also read that Sally Hansen nail strengthner is good.
Going to find out about Finger Nail
stay safe and take care
mimi121
Hi. I've had lots of different chemos but seem to struggle with vomiting/heaving on the 3 weekly ones. Pretty much every time I've ended up in hospital on an iv. Does any one have any tips or ideas? Next round of carboplatin this week. I think hubby would prefer them to admit me straight from chemo and keep me for the night!!
Hi,
I primed myself with crystallized ginger,taking it for a day or two before chemo and for quite a few days after about three or four times a day..If you are taking the metoclopramide they give you start taking them the day before treatment or ask for one of the stronger ones they can give you.I had no nausea or vomiting.Make sure to stay hydrated,a couple of sips only little and often may help.
Good luckx
I'm really sorry to hear that, what an ordeal.
What does your oncologist say or have they tried everything they think they might work for now?
Hi
Due to start chemo either next week or the following week. I have an appointment with my Oncologist on Thursday. Has anyone tried the cold cap and was it successful? I am going to give it a go but have chosen a wig just in case.
Hope everyone that is currently going through chemotherapy is coping ok.
Brst wishes
Linda x
Hi Linda, I tried the cold cap but after the second time my hair fell out so it didn’t work for me. A girl I met during chemo also tried it and it was very successful for her. Definitely try, you could be one of the ones it works for!
Good luck with the chemo when it starts!! x
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