This discussion has been locked.
You can no longer post new replies to this discussion. If you have a question you can start a new discussion

**AUGUST CHEMOTHERAPY CHAT 2019**

FormerMember
FormerMember
  • 393 replies
  • 287 subscribers
  • 413165 views

Hello lovely people, and Welcome to the August's Chemotherapy Chat! 

This thread is for all of you soldiers, going through chemotherapy to take a look at, ask questions, answer questions and be there for one another in a way only you guys know how. 

If you want to find this post quickly, you can hit the 'Save In My Favourites' button. 

For all of those of you going through chemotherapy, you are superstars. You are amazing, and you are fighting each and every day, you are my heroes. If you need any extra tips, our Chemo Tips Page is something you may find very helpful, and something that you may find you would like to share with others who are also going through chemo. One top tip, ask about parking at the hospital you are being treated at; for some Cancer patients parking is either free or discounted (big discount!) So it's worth asking about. 

To get a sense of how the thread works, here is a link to July's chat which will be being locked from replies soon, but have a read anyway if you'd like to. 

Remember, you're never alone, you have us! And, just try to focus on what your chemotherapy is doing. Its hopefully kicking your cancers butt. 

I hope you are coping with me doing these! And I hope all of you are doing as well as you can do while going through this tough part of your journies. 

Happy August Everyone, 

Lots of love, hugs, light and healing to each and every one of you. 

Alex xxx

  • FormerMember
    FormerMember

    I'm in!!! 

    Started cycle 16 of this chemo yesterday, and the oncologist told me the other day that I am his longest ever patient on this drug! My body/cancer obviously responds well to it, even though I'm on 50% of the proper dose due to severe side effects at higher doses. 

    Fingers crossed that I can push the boundaries for another few months at least!!! Grinning

    Good luck to everybody continuing or starting chemo this month - may the gods of side effects and efficacy be kind to you all! 

  • I'm in too.

    Day 18 of first round of EC, with 4xEC (3 left) and 4xT planned.

    Started shedding hair on day 16, and more each day despite cold capping, though not sure hair was wet enough,  and realistic about how EC is ther one with worst success rate for it. 

    Off to get a PICC line this afternoon which I'm dreading.  More radiation  as is in their fluoroscopy room (6 months background on top of the 10 years background from staging scans). It's ironic that treatment for cancer involves procedures and drugs that can cause it:/)  I'm not sure how I'll cope with it,  but the nurse struggled to insert the catheter for my first chemo with three attempts, so with that every three weeks as well as the blood tests etc. I know that it's to help me. 

    How is everyone else doing?

    “Remember to look up at the stars and not down at your feet.  Stephen Hawking,
  • FormerMember
    FormerMember

    I’m in! 2 x EC done and first (of 4)  Docetaxel (Taxotere) completed yesterday. Just 7 days of injecting myself now to officially be able to claim half way through Thumbsup tone1

    good luck to all, I hope the side affects are manageable for you all and you have more good days than bad.

    Ruby X

  • Hi Ruby,

    Congratulations on being half way through! I hope that you don't mind,  but can i ask why you had 2 rounds of EC instead of 3 or 4? I'm thinking of only doing the EC, and there seem so many combinations of cycles and drugs! X

    “Remember to look up at the stars and not down at your feet.  Stephen Hawking,
  • FormerMember
    FormerMember in reply to Londonmumof2

    Hi Londonmumof2

    Interesting question and one I’ve been asking myself, everyone I meet or talk to seems to be on a different regime to me. I genuinely have no idea, I am positive for EC and HER, I dont know if that’s the reason or if it’s because I was borderline for surgery first then chemo.  They decided chemo first, appears to be the right call, after 2 x EC tumour is down from 4 cm and hard to 3 cm and soft, it makes it almost worth the challenges! 

    Surgery is planned for Nov then radiotherapy Fingers crossed tone1

    Hope this helps 

    Ruby x

  • London......you'll be so pleased you agreed to the PICC and if anyone else having chemo this month or waiting to start is offered a port( take this if available) or a PICC take it! Don't  be afraid of the fitting. Mine ( a port) was inserted under general anaesthetic but removed with a local at the end. It makes having the chemo drugs so simple and painless.

    Last year I had to have  intravenous antibiotics to deal with sepsis and like chemo drugs these can block your veins. I had eight sites in 2 days because my veins are visibly non existent and the nurses couldn't find one which would support the drug.So I do know exactly how painful chemo can be for some of you and can compare it to my chemo through the port with no discomfort. Eventually I was given a picc line for the antibiotics by an anesthetist....What a difference.

    Hope your picc goes in easily this afternoon.

    Love Karen

    1. I
  • FormerMember
    FormerMember in reply to Lacomtekp

    I'm in for August and due 3rd FEC tomorrow....neutrophils were down again on Tuesday night (on my 3rd admission to hospital this cycle!)..and had my bloods done again this morning. I've had oncology nurses phone me yesterday and today, and an oncology doc just off the phone to discuss what's been going on this cycle...fainted, constant lightheadedness and shakes, legs like jelly...probable anxiety element to how I'm feeling now and not coping well at all....Ms. Strong, Brave and Independent is no longer! Sorry this sounds so negative x

  • Oh Fee!

    No wonder you're feeling anxious when your bloods are down and you're so dizzy:(

    Are they going to delay thr chemo this week? It doesn't sound like your body is ready for ther next one yet.  Did your oncologist mention doing ther dose? A lot of hospitals don't give the "F' part anymore due to side effects and consider ther EC fine.  Could you ask about that? It might help,  and at least reduce the worry about having exactly the same drugs as made you ill. X

    “Remember to look up at the stars and not down at your feet.  Stephen Hawking,
  • Thank you Lacomtekp, it doesn't feel good on my way now for the 3pm appointment,  but hopefully it will be 

    Feeling a bit negative this afternoon as I head off for it.  On the6r plus side I had a bath and washed my hair today, and chunks of hair didn't fall out (this time!) 

    “Remember to look up at the stars and not down at your feet.  Stephen Hawking,
  • FormerMember
    FormerMember in reply to Londonmumof2

    Hi 

    I am so glad that I had a PICC line from the start. It has made it so much easier for bloods and treatment. I hardly notice its there. I got some PICC line covers online so it's not as noticeable.

    I am on D14 after my second EC. Despite cold capping, my hair is coming out and is noticeably thinner. I am glad I had it cut short at the start of my journey. Not ready for a buzz cut yet.  I will carry on with the cold cap in the hope that it can be saved. 

    Lets hope that August is kind to us all x