Starting chemo in March 2023

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Hello

ive had a recent diagnosis, just last week, HER2+ Ductal stage 3. Been for ultrasound, biopsy, MRI, have another biopsy coming, but expect to start chemo around the 21st March. 

feeling sad/ angry/ confused most the time at the moment. It’s going to be a rubbish 36th birthday present as I could be starting on or close to 24th which is my birthday. Also have a 14month old, who I’m so worried I just won’t be able to enjoy the way I should for such a crucial part of his growth, and that’s getting me down. 

 Any other soon-to-be-starters? 

Any one have any advice on what to buy/ bring to chemo treatment sessions? 

  • One positive my hair has started growing back

  • Hi Angie463, sorry to hear of your diagnosis. With your indigestion if you speak with your BCN or oncologist they should be able to give you something for it. I had lansaprozle which helped me. It got rid of my indigestion and the strange sensation in the back of my throat too. 
    Wishing you all the best for your journey.

    Hugs from cuffcake x x x x x

  • I too was given lanzoprazole from cycle 1 of chemo. 

  • Hi Dolphinstar, i found the side reflects different on Docetaxel. I don’t think it was any easier really I still had nausea and tiredness. Nausea was helped by the anti sickness meds. My worst days were days 5 to 10 when I was on filgrastim. After that I was ok. My fingernails did get sore but used Polybalm to help and so far all is good. Once bonus was my hair started to grow back. 
    Everyone is different and some do say they got on better with Docetaxel. I didn’t have any allergic reactions to it and that was always my biggest worry. Keep up with the fluids and a good healthy diet. Exercise helps too even when you don’t feel like doing much. 
    Wishing you all the best for your journey.

    Hugs from cuffcake x x x x x

  • Interestingly I have had pegfilgrastim injections throughout my chemo which has been one jab 24 hours after chemo and that's it. I did ask after my neutropenia if i should have more jabs having seen people on here having more but he said no.

  • Hi F1 petrolhead, that’s interesting. My oncologist told me peg was ok with EC, but on Docetaxel filgrastim would work better. I have no idea but one trusts ones medical team. I guess it something that each team have different opinions on and have found what works best for them throughout peoples treatments.

    Hugs from cuffcake x x x x x 

  • I had a filigrastim jab when I had neutropenia. Apparently the peg is a more slow acting jab and the filigrastim is instant. Like you say different oncologists different opinions

  • Thanks cuffcake, that's feels slightly reassuring. As you say everyone is different. I jave just read some horror stories! 

  • This reads like my week! 1st  Docetaxel was Monday, I really can’t be bothered to shift all week but awake at 6am due to birds chirping & steroids! 
    Also booked for LGFB on Wednesday so hoping for a boost Blush

    Hope you are feeling a little more enthusiastic now the weather is turning, I did sit outside to read the paper this morning…. that’s progress for me!

    got a fabulous gift from Little Lifts yesterday, check out the website- it’s free to anyone currently having chemo or radiotherapy 

    so impressed that I’ve donated forwards, hope it brings the same gooey feeling to another person on this crap bus trip!

    taste is crap, marmite on crumpets, ritz crackers, ginger ale & black cherry yogurts  are my current staple foods Pig Will worry about my weight another time Wink

    but we made it, another week done 

    well done to us all Champagne glassFingers crossed tone3Kissing heart