This is my first posting for 4 years - since I had a mastectomy. I have now been re-visited by the dreaded C and was diagnosed with liver mets in May of this year. I am having both Vinorelbine and Herceptin. I chose Vinorelbine because my oncologist said I would not lose my hair. But - he was wrong !! - after 2 sessions it all came out in handfuls. My onc says this is very rare - but I wonder if any other ladies have had this happen to them. I did find out that the dose they gave to me was too strong and, as well as becoming bald, I ended up in hospital with Pneumonia for a week. They have now reduced the dose - but too late for my poor hair! The very best of luck and love for all you ladies in the ‘secondaries club’.
Sorry that you have had to join this club. I am on Vinorlbine to and the first couple of session nearly killed me thankfully they have reduced it down twice now and this seems to have helped. Reguarding hair loss my hair has tinned out but is bascially its still there. Maybe you first dose was too strong. Hope your keeping well.
Know nothing about Vinorelbine I’m afraid (currently on capecitebine) but I too have liver mets, dx May 2007. Just wanted to say “welcome” to the club no-one wants to join - I’m sure you’ll find masses of support and info here.
Such a shame about your hair - does sound as if it could be as a result of the too high dose. If so presumably it might start growing back whilst you are still having the chemo. Fingers crossed.
Thank you ladies for your words of encouragement. Yes, they have almost admitted that they overdid the second session. They could not believe that I had lost a stone in weight in 10 days - but I had. They therefore went ahead and gave me the same amount as the previous session - which was obviously too much for my weight.
However, I am encouraged that there are lots of ladies on this ‘secondary’ forum who seem to be coping really well and all remaining positive. I hope I can do the same.
Oh you poor thing.
Vineralbine has been the only thing that i didn’t lose hair with. It thinned with xeloda and gem/carbo but was still there as it had come back so quick.
Regarding the overdose, the same thing happened to me 3 weeks ago on my first dose of taxol and I was so ill and it spoilt my last holiday with the children.
I lost a stone in weight on taxotere the first time round, it was the diarrhoea and lack of apetite that did that.
Nw on weekly taxol and can feel my hair is going to fall out very soon - the horrible prickly feeling on scalp.
Good luck and I’m sorry you’ve had such a bad time. My best results were on vineralbine by the way,
All the best
Kate
I have just started my second cycle of Vinorelbine and have been wondering about this apparently rare hair loss as I am losing quite a bit of hair - not loads in hands like with previous chemo but enough to think oh-that’s-quite-a-lot. I combed my hair in bathroom today and noticed a lot of hair in the sink so (ridiculously, I know) started to count the strands and realised there were too many and have come on the forums this afternoon to see if any others have lost their hair on this chemo and saw this thread.
Linda, so sorry to hear that you have lost your hair completely. I am going to hairdressers on Thursday to get my hair cut and coloured and am having second thoughts now.
I was in hospital two weeks ago after my first cycle of Vinorelbine as my WBC had dropped to 0.6 and had high temperature. I came home stuffed full of IV antibiotics and a couple of bags of blood and was feeling a lot better until I had more vinorelbine last week.
I echo JaneRA in that it is alarming that incorrect doses or too big a dose is being given.
Hello maid
Welcome to the forum …the thread u are posting to is a very old one but there are ladies that have been on the same chemo as you and hopefully will reply to you with some helpful advice.
in the meantime enjoy the forum …there are lots of interesting posts to read .
Carolyn xxx
I’m starting on Vinorebeline intablet form tomorrow. What are the worst days on this chemo? I will take it on Week 1 and 2 and get week 3 off. Oh how I hate the unknown of a new chemo!