sorry if this has been covered in this thread already
can anyone help with a vinegar taste?
i am 9yrs down the line since 1st DX & have had many different chemos over the years
and i remember this happening before but i cant remember what i did to help myself?
my food tastes fine when i am eating it, everything tastes as it should,
but around half n hour after i get a horrible vinegar taste.
the chemo i am on this time is kadcyla
kimi x
Hi team. I'm just wondering if anyone has any suggestions on foods to help Increase white blood count. I've just bought some wheat grass powder, has anyone got any suggestions or advice? Thanks hbunny
Hi sugar, contacted the help line yesterday and saw an oncologist within an hour. They weren't worried about the lymphodema in the ankle, and that is definitely better this am, however were concerned about swelling in forearm, which was caused by a leak of chemo drugs into the surrounding tissue which could cause problems and will need to keep an eye on it for ulceration. It does however look a little better this am (she says holding her breath), but will see what happens over the next few days, hopefully got away with it! Now day 5 cycle 2 fec100 + tax (3x each) and one third there!
Just a bit anxious now about what happens for cycle 3-6 to prevent a recurrance.
Hope you are doing well sugar. Positive hugs. Hbunny
Hi all, sorry to butt I to your thread, I've just popped over from the July thread to see if anyone has any tips. I'm doing fec100 + tax (3of each) and now day 3 of fec 2. I have suffered with phalbitis since day 1 cycle 1 but last night saw lymphodema pop up in my arm and ankle (r). Anyone know what causes this side effect or any tips to help. Currently walking around in a compression sock and tuby grip and massaging regularly.
Ps, will have to get the smoothly maker out I bought a couple of years ago and never used, thanks for reminding me. Love to all going through crap right now, happy to say I haven't been sick yet but the side effects are different this time round, probably due to changes to anti sick meds.
Thanks for any suggestions offered. Hbunny xx
Hi Louise, Thank you for taking the time to reply, it is most appreciated. Yes, I am on FEC too.I will take your advice on the fruit - probably not doing this as much as I should but Im definately drinking - one day soon Im sure Rose Wine will be back on the agenda! But for now fruit juices and water!!
Well done on only having 2 more to go, go for it girl and as for everyone sending you my good wishes and happy healthy life from now on, for the future.
I do enjoy this website, but probably I shouldnt write on it when feeling down and would prefer to spirit other friends on this website with joys of encouragement. xx
I know I too thought the 1st dose was awful but now am thinking that maybe with each dose it gets worst. 2nd dose was 6 days ago with 1st dose of Herceptin and only just feeling human. I couldnt quite believe I could feel that ill and still be alive! I had to give myself a stern telling off each time! Hang on in as I am trying to do, when we hit rock bottom the only way is up!
I thought my 1st treatment was hell and kept a diary for the oncologist and he changed the sickness treatment after, but just had 2nd and again, sorry to say that was hell too, its now day 5 after treatment and still feeling very sick, got given Metoclopramide by the hospital but they are not working, I also started to loose hair and Im not sleeping - as I live on my own unfortunately the days are long and not sure if I can get through another 4 treatments - really need a kick up the xxx! I took 1/2 sleeping tablet one night but it made me buckle and I couldnt stop myself falling so hurt knee and wrist - so a bit down in the dumps. Please let me know any tips to get me through months.
Angel77 said:
hi all . i had my second chemo TC-H on 2 july and have lost most of my hair so today im going to shave it all off . the main thing i struggle with is the gcsf injections and loose of taste .. anybody got any tips to quench my thirst ? x hope your all doing ok . i have 2 chemos left to go x.
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Hi Angel77. Good to see that you are manging well. It's amazing how we just get on with the treatment an side effects once we begin the journey. Was the 2nd cycle any easier, the same SEs,or worse.
I am struggling with the gcsf also but mine in the flatulence and bloatedness that i don't know what todowith myself senario. Anyway today I danced and it worked. No discomfort after a while a felt much happier.
The lost of taste also happen for me but my body seems to crave the food that I can actually taste so listen to what it tells you and eat what you crave.I feel like a pregnat mother with these cravings 🙂
Don't know about the thirst. i set my alarm to drink water every hour during the day and so far so good.Have you tried sucking the pineapple lollies?
Keepwell
Sugar8
smileyvery-happy:Hi all
Just had my first FEC-T treatment yesterday, so far, so good! Had a bit of a 'fuzzy' head all day, but apart from that, tickety boo!
Lots of handy tips on here to keep me going as any needs arise, thank you for taking the time to share 🙂
Hey Queen Bee i had that experience with my 1st fec and then it turned into feeling like i had been hit over neck and back of a head with a metal pole !!! I rang hos and they said take pain killers,it helped and never had it since.they seemed to be pretty familiar with it but did say to ring back if pain meds didnt work ...hot water bottle help alot.
Hey Queen Bee i had that experience with my 1st fec and then it turned into feeling like i had been hit over neck and back of a head with a metal pole !!! I rang hos and they said take pain killers,it helped and never had it since.they seemed to be pretty familiar with it but did say to ring back if pain meds didnt work ...hot water bottle help alot.
Hi Ruth, I make my own icypoles at home with water and lemon or lime juice, but you could use cordial. I take them to hospital in a chilly bag and store them in the chemo ward freezer and then my husband runs back and forth as required!
The best tip I have come across is to suck ice or icypoles during chemo - it protects the lining of your mouth and prevents the loss of taste too! Same theory as cold cap - reduced bloodflow so less exposure to chemo drugs. I didn't know about this trick for my first cycle and had a sensitive mouth and lost my sense of taste for a couple of weeks, but it did come back for the final week of my three week cycle. Next time I ate 6 icypoles during chemo with fab results, didn't get a sore throat either which I had had first cycle. Can't recommend this enough, life is bleak enough going through this ordeal without losing the pleasure of food.
Hi Lakeslover,
Thanks for the tips regarding food and what drinks to try.I also didnt know that about the free prescriptions. Good idea re taking things in to amuse yourself with, as I have been told to expect to be there for 4 hours each session, as I have opted to try the cold cap. Whether it will work on me I have no idea, but I am having my hair cropped short today anyway.
I think I will go onto Amazon now to download some books on my kindle 🙂
xx Ruth xx
Hi Louise3721,
I am also about to start Fec on 29th April. I am giving the cold cap a whirl first, as I am told it has a 60% success rate with people who use it not getting hairloss. However, I am having my hair cropped before the treatment begins.
Although my lump was 8mm, I am having chemo as 10 of my lymph nodes were affected.So I am about to have a Fec session every 3 weeks for 3 months, then another drug weekly for 3 months, follwed by radiotherapy and then a hormone tablet for 5 years. So much onformation to take in ! I am having a bone scan this Thursday and I have also opted to have a portacath inserted under sedation this Fridaym before my treatment begins.
I was also advised to buy body moisturizer, hair moisturizer ( if using cold cap), mouthwash/bonjela and a digital thermometer. I hope this helps Good Luck xx Ruth xx
Hi Everyone,
I am about to embark on 6 months of chemotherapy ( seeing the chemo nurses today for the first time ). I have scrolled back to pick up on some of your tips and wondered if there are any basic just starting xhemo tips for a newbie? Thanks xx Ruth xx
my top tips would be-
or the couple of days every cycle where my mouth was too sensitive even for mild toothpaste - brush gently with bicarbonate of soda instead of toothpaste.
I had horrible acid reflux / heartburn, and I found drinking hazelnut or almond alpro, both of which are v alkaline, to soothe all the passage of my acidic gullet and relieve the acid for a while. Personally I found it more effective than the medical alternatives, and of course it had no side effects and is quite nice!
Good luck everyone x
Thanks June unfortunately i am at work and cannot call so thought i would ask on here
Hello Scattyfox
Welcome to the forums.
As well as the support you will receive on the forums we also have a free helpline where you can talk things through with a member of staff who are there to offer emotional support as well as practical information. The free phone number is 0808 800 6000 and the lines are open Monday to Friday 9.00 to 5.00 and Saturday 10.00 to 2.00.
Best wishes
June, moderator
Hi ladies i will be starting my first chemo session in a few weeks once this wound has healed. Have you any tips as to what i should take with me on the day
thank you