Hi ladies
I was just wondering if you can tell me when you started to feel better (improve) after your last chemo treatment?
I had 3 FEC then 3 Docitaxel (Taxotere). I am day 7 of my last chemo today.
I have been a very unlucky one in that I have suffered terribly with Docitaxel (taxotere) and I found that I was still unwell and truly down and out when my new Docitaxel was due. With the FEC I had bounced back to a certain degree but not with these ones.
I have a small holiday planned from 9/7/12 (soon) and I just wanted some feedback as to how people were feeling 3 weeks down the track of Docitaxel. I know it is hard to compare cause everyone is different but I would love some feedback please lovely ladies.
Thanks heaps and wishing you lots of warm fuzzies your way.
Mich xoxo



Comments
Hi Mich, so sorry to read that you had such a rough time with the Taxotere. I have my first Taxotere next Friday 6/7 and am dreading it. Firstly 'cos I do not know if I will have a bad reaction when they give it to me and secondly what the side effects will do to me. But, on the upside, FEC100 x 3 are behind me. I do hope and pray that you will get stronger and stronger each day in preparation for your holiday break in July. All the best, Ann
you will feel better
Hi Mich , I am pretty sure you will be feeling okay in time for your holiday, I also had Taxotere 6 treatments my last chemo was 7th may and i felt brand new after 3 weeks, telling yourself its all over and your body can renew itself now helps. Hope you feel great soon and enjoy your holiday. x
Thanks Pip for your positive thoughs, that is great, I will take them on board and run with it.
Mich xoxo
Hi Ann
Thank you for your good wishes.
Congrats on making it through your 3 FEC.
I did not get any of the ractions on the day that they talk about from the Taxotere so that was a bonus :-) I did take the Dex as instructed (probably earlier in the day than I was told because I knew how it affected me. It obviously helped.
All I can say is be prepared for the reaction and speak up in the chemo ward if feeling a big different (even in the slightest bit). Be prepared for bone and nerve pain and have pain killers on hand at home. Make sure you start Panadol every four hours the morning of your chemo and continue it the whole time you need it. Add in extra pain killers if you need on top of the Panadol. Don't let the pain set in because then it takes ages for the medications to relieve the pain.
Neulasta injections don't help with the pain either that is for sure. I give myself the injection in the afternoon and by night you can feel the pain moving through your body, it is so wierd.
I am on pain patches which the doctor reviews regularly and I also take Panadol and Endone every four hours to keep on top of pain which isn't always possible and it does flare up sometimes.
I also have very sore mouth and no taste buds (except for chocolate - I am serious hee hee) I rinse my mouth every four hours but it is still yukky.
I have other side effects but they are miniscule in the big picture.
I just keep telling myself everything is temporary but I am so worried I won't be on top of things before the holiday. Trying to pack and get organised for the holiday is also a chore at present. When I return from the holiday I will go straight in to my 7 weeks of radiotherapy down in Perth. I am hoping like crazy I will be feeling better next week and have less of a chemo brain because I can't think on things to plan and organise. I am sure it will be a wonderful holiday once I get there and I am so looking forward to it. Sometimes it is good not to plan and just let it happen.
I am defnitely getting accliamatised with the weather we are having at present in W.A.
Congrats again, well done, I hope you have a smooth journey ahead of you.
LOL
Mich xo
Hi Mich
I had to go back and have a quick look at my blogs before I answered your post. I finished chemo on Feb 23rd and was feeling good 2 weeks later when I started radiation.
Hope you are feeling great soon.
Love penny xx
Thanks Penny I will definitely keep fingers crossed I am feeling good too. Did you have a lot of issues with Taxotere, I think you did from memory??
Mich xoxo
Oh yes!
I hated taxotere! The bone pain was awful, and the sore mouth. For me FEC was a lot easier.
Hope you are doing well. Congrats on finishing chemo my friend!
Xxxx