Hello ladies, hope you don't mind me gatecrashing your thread, but I've just read through it all and it's made me feel so much better, your all so nice and posative

I was diagnosed with triple negative BC in June, I am on my 5 of 8 cycles of chemo, these last four being Carpoplatin and paxataxil, there breaking down the paxataxil to every week, i have my last chemo on 6th January and although we shouldn't wish our lives away, I can't wait, after that it will be surgery and radiotherapy, I have three lymph nodes under my arm and two lymphs under breast, but on last scan the two under breast have cleared, I'd like to ask if any of you on paxataxil oy carboplatin have had fuzzy head, I can't explain it but fuzzy slight dizzy head, I'm at day 10, my other cycle I felt so much better by day 10, it's not really bad but just annoying as I can't drive while feeling like this. Again lovely to read all your posts and really hoping your all feeling well, xxx

Hey Davia

Of course not, welcome to our group that no ones want to join haha!  I was diagnosed in August so just had my 3rd course on Tuesday.  Not feeling too bad at the moment, fingers crossed it stays that way.  I have 1 more of EC then i go onto the carbo / paxo and paxo weekly.  Hope there are no major side affects of these.  How you doing on these drugs, just the dizzyness.  

I have in my lymph nodes too so will have to have all of them out, little worried about the opp but one day at a time eh.  I'm also waiting on my brca test, guess they will send a letter confirming yay or nay.

Yeah i could drive for a few days after my second one, felt like i was on drugs all week!

I managed the cold cap on Tuesday, but hair is thinning quite a bit so not sure if I'll carry on .

Hugs

xx

Sue I was just thinking this morning that the forum had been quiet. That sounds like bad advice to me. My oncologist in Hong Kong and my oncologist in London have both said 3 monthly check ups for two years and then annual for another 3 years. However, both did say that the 3 monthly check ups would be the blood tests and that not all doctors believe in these, that they don't give a true picture. I'm doing all treatment privately which may be why they're offering to do them. However, you should certainly be getting annual mammograms and ultrasounds. It seems crazy to me not to offer that, people I know that have been treated for bc on the NHS have definitely had annual check ups for 5 or 6 years after.

xx

Hi Sue & girls

I thought it was quiet in here, I replied on the 11th March and had no emails since, My mum went through all this last year and she doesn't get 3 month check ups, infact shes due her 1st year mammogram on Thursday.

Hope you are all ok while in isolation x

linda x

Hi Linda,

Sorry I haven't replied to you, I've been feeling pretty low lately. What with no checkups and the registrar telling me I needed more chemo. The oncologist, however, doesn't think oral chemo would be beneficial and I will still have a 20 - 30% chance of a recurrence.

Did your mum have triple negative breast cancer? The after for that is different to other types of breast cancer.

I hope you're keeping well.

Love Sue xx

Hi Claire,

I will be appealing against the decision. I was in shock when I was told no after care.

Keep well

XX

Hi Sue

Yes mum was triple negative too, she finished all treatment in sept for me to be diagnosed in Nov x

Sue are they saying none at all? Not even yearly?

Lindylu how awful. Have you both had the BRCA test?

Mum wasnt offered it as she was 67 with no family history, I have been tested and am waitihg for my results they said up to 12 weeks so am hoping they arrive sooner rather than later as if i am positive i'll be having preventative surgery with recon. My last chemo is Friday, i have a telephone appointment with my oncologist tomorrow to see if thats going to happen what with the coronavirus. I have had a good response to chemo with the lump going so if i dony have the last 1 i think they will do a lumpectomy as urgent they said then mastectomy once i get results if needed. This virus is awful so i would rather not have last 1 tbh so i can get my immune system back on track x

Hi Claire,

I don't know about yearly mammograms as it wasn't mentioned. I was really shocked that I won't be having regular scans or blood tests. I asked how I would know about recurrence and the oncologist said to wait for symptoms. By that time surely it would be too late !!. 

I'm in a terribly state about it as I was sure I would get regular checks

XX

Sue it sounds awful what you're going through, you will get a yearly mammogram or should for 5 years as thats what mum was told. I wont know what they will offer me until july time after Radiotherapy.

You would think they would do more in our 1st year as we are all worried its going to rear its ugly head again.

Sending you a big hug x

Sue it sounds awful what you're going through, you will get a yearly mammogram or should for 5 years as thats what mum was told. I wont know what they will offer me until july time after Radiotherapy.

You would think they would do more in our 1st year as we are all worried its going to rear its ugly head again.

Sending you a big hug x