Having a stressful day today. Had my pre chemo consultation by phone today. Went well with lots of information given about what to expect.  However, I did forget to mention about some niggling breast pain I've been having. They come and go, sometimes slightly shooting pain. Did phone breast care nurses last week, who said probably due to all the biopsies I had. They were done a few weeks ago, so wondered if pains would only start happening in the last week. So annoyed with myself, even had it written down. I know I can mention on Monday, but will now have to go through two more days of stress!!

Hi Pippin 24, I think every little niggling pain is a worry when you're in the position that we are, try not to worry hopefully the chemotherapy will start to work killing all of the harmful cancer cells,  hope everything goes well for you on Monday,   I'm anxious at the moment waiting for my PET scan results on Friday the 8th xx

Hi ladies, I had posted previously but my cancer was more advanced than they first thought so i am now joining the chemo train. I saw my oncologist for the first time yesterday, he said there's about a 4 week wait so i expect I'll be April now. I need 4 x EC and 4 x Taxel (?), and then a whole host of other things after that including more surgery, radio and tablets and infusions. Hope you are all ok x

Thanks Jolamine, so far so good. I did  have a headache all day yesterday, but that's not unusual for me. It's the reason I didn't go for the cold cap, which I think was the right decision. Finger's crossed I'll be fine once off the  anti sickness meds. Xx

Hi Greeny80, all has been fine apart from a slight headache all day yesterday. However, I am prone to headaches anyway, which is why I decided against the cold cap.  Had a lovely walk with hubby and was able to cook dinner. Good luck with your chemo on the 19th and with your wig shopping. I was really happy with my wig and have also bought a few nice hats. I got my hair cut short last week, still trying to get used to it. I'm  a bit apprehensive about it falling out though! Please let me know how you get on. Xx

Hi Annielouise, sorry to hear your cancer is more advanced than first thought. I was initially shocked how advanced mine was, as I'd only had a clear mammogram 14 months before. It sounds like your chemo is similar to mine, I'm having EC-T. 3 cycles of EC, then 4 cycles T (Docetaxel). I think there are different T options, so not sure if yours will be the same. I had my first cycle of EC on Monday and all went smoothly. So far side effects have been minimal, with just a headache all day yesterday. Hope all goes well with your chemo, always here for a chat. Xx

Hi, mine is paclitaxel, it's a whole new vocabulary isn't it! I'm glad you didn't have side effects, hope they stay away! I'm in two minds about the cold cap, it seems a but of a faff... 

I was diagnosed 11 Dec and they initially said lumpectomy and radiotherapy, stage 2. Then it emerged there were 4 lumps, so it was DIEP, then the lumps were aggressive and I had 3 infected lymph nodes, extra capsular? So now I'm stage 3 and booked for chemo etc, it was such a shock in a short space of time x

Hi Pippin

So glad you're having minimal side effects with the chemo.  I wish my ride had been the same lol.  It's been a nightmare!  But, hopefully unless they change my regime again, tomorrow is my last chemo.  I will then have surgery some time in April (what kind depends on repeat MRI scan to check the efficacy of the chemo) then 6 months of immunotherapy (Pembro).  My hair started to fall out in earnest on Day 14 after chemo.  I tend to wear scarves around the house if I have video calls, sometimes embrace the bald to let my scalp breathe and keep the wig for going "out out".  It was strange wearing a wig at first and I was very self conscious, now I'm used to it and have a little more faith that it won't just fall off lol.  I hope you continue to have minimal side effects an that your journey is a smooth one. xx

Hello,,I had Paclitaxel  first with hardly any side effects ,whilst on the EC I felt slightly different ,more chemo brain and neuropathy in my little toes and fingers .Tell them in the unit about any changes and how you are feeling . Keep on drinking plenty of water and rest when your body tells you to . 
Good luck on your journey xxx

My hair also started falling out on second treatment ,my son gave me a good shave . I felt happy wearing hats and hair grew back very quickly once treatment was over xx

Oh that's odd - I had a severe reaction to Paclitaxel so they moved me on to Doctaxel then had to stop because the neuropathy got quite severe in my fingers.  They moved me onto EC which has had fewer side effects for me except for extreme nausea for about 7-10 days after treatment (plus the usual tiredness!).  Just goes to show everyone is different and how we react is very different!  Good luck on your journey. xx

Oh bless you hun, how are you feeling after the update.

Oh bless you hun, how are you feeling after the update.