May 2017 chemo starters

Thanks ladies. The chemo unit asked me to go down there and get checked over. They’re reluctant to prescribe antibiotics so got some Gelclair - I think you mentioned that Mai- and to let them know if it doesn’t improve. Was worried it was an infection so happy to be reassured.

 

Glad to hear you have more energy today Mai; it’s all too easy to think we’re fine and then end up doing too much.

 

Wolfee - I’ll try the bicarbonate too; luckily at the moment all is well down below. Long may that remain, Hope you’re veins have warmed up. Hopefully, the weather is good where you are, I’m in the south east and it’s a lovely, sunny day here.

 

treehouse - cobweb detector sounds like an excellent job, better than working from home which I’m attempting today.

 

Good luck for round 3 tomorrow Katie at least you’ve remembered to drink the water, I forgot last time and they had trouble with my veins. Was pleased to hear no injections with Paclitaxel, I won’t be sorry to see the back of those.

Has anyone noticed any nail changes yet? My cuticles have been dry and flaky for a while but I moisturizer lots. Today the cuticles seem to have disappeared completely and the nail bed underneath is purple. I was warned the nails might discolour and fall off. Aaahh! That to me would be worse than losing my hair. How do you cover your hands?
Eeeek!

Thanks Mai, I think I will get the nail polish out again I had gone them quite dark for the first couple of weeks but then swapped to a pale nail strengthener. I will use it as undercoat. The skin feels like it is pulling away and the nails don’t feel as secure, almost wobbly. ,?
My hair was never great but I always took pride in my nails. I know this sounds stupid!

How is your hand Wolfee? Did you call ??
Nails are bow dark electric blue :raised_hand:?

Hi All, they told me that some feeling in the site is normal but look out for brushing and if it swells but tenderness should go ??
I’m just digging out my nail polish now I have a black or a dark red?? I’m about to have a bath, oil my head and paint my nails.
What about our feet do we need to do toe nails also???
Xxxxx

My chemo nurse said that it’s the docetaxol that makes the nails go black so that’s when I’d need to paint them. Until then I’m using nail oil to keep them in condition. I hope the aching veins and hands get better. Oncologist appointment tomorrow before round 2 on Thursday. I hope things go well tomorrow Katie. X

That makes sense, I am due round 3 docetaxel on Monday ?

Good luck today Katie and Mjk. Hope all goes to plan and is drama free x?

Thanks treehouse. So do I x

Good luck MJK x

Good luck today Katie and MJK , thinking of you both xx

Oncologist appointment this morning. White blood cell count has fallen quite a bit but still ok for second dose tomorrow. Drinking lots. I hope today is going well Katie. X

Is this number two for you now tomorrow MKJ. I’ve just done number two Monday. It hasn’t felt much different overall apart from the 1st day with the headache and hand pain but not it’s averaging out fairly the same but perhaps a little more tired this time.
Hope all goes well for you tomorrow ill be thinking of you. X

Hi ladies, I just wanted to pop in and say hello and thank you!
I have just been diagnosed last week, all I remember are the words breast cancer, chemo and genetics so will need to ask loads of questions. I posted on a forum just diagnosed and was advised to look on this thread regarding the chemo.
I may sound like a stalker here but I have read your thread from beginning to now and it has helped me immensely understand what I have in front of me and I do not feel as scared (still am tho). I have to go for an ecg tomorrow then oncology on the 27th so I guess chemo will start next month, just as the kids finish up for summer ?

Any way well done to you all so far and keep up the fight ???
Feels like I’ve come to the end of a good book lol
Take care everyone :heart: xx

Hi Maryann, I’m glad you found us and welcome to our group we all know how you are feeling right now and it is so very scary (still is) but it really does help to talk ask your questions and have support from others who are feeling and doing the same.
We will do our best to ease your anxiety and support you and we will all get through this together.
Come and chat with us as and when you need and I promise you the days will get easier. Once you have your plan and dates set you do kind of accept it and it becomes easier once you start treatment and you know you are actively doing something to rid this horrible intruder your mind adjusts and it does get that tiny bit easier.
Wishing you the best xxxxx

Hi Marryann. I can’t remember exactly how you are feeling but you will get through this and will surprise yourself how strong you are. I’ve just had round 3 this morning and all went fine. The anticipation is much worse than the actual event in all Ive been through… (I’ve already had surgery and will have radiotherapy after chemo) stay strong and we are here if you need us xx

Omg chemo brain or what. Sorry MaryAnn. And it should say I can remember! !!!

Thank you ? yes very keen to get started, just think the longer the wait the more time it has to grow! surgery will follow the chemo as I have to get the gene test (my mum and gran both had BC) so the results of that will determine what will happen.
Glad I found you all,I have laughed and cried reading you journey’s definitely good to keep the humour ? xx

I currently awaiting the result of my genetic test too. No history but I am triple negative xx

Must be quite fun reading it in one go! Lol . These forums are definitely a good support network. You don’t feel as alone . Even though you have people around you , they don’t quite get it xx

Hi Maryann. Glad you found us. I can honestly say the waiting limbo you are in right now is the worst part.I don’t say that to make you feel bad. Just once treatment starts you feel better knowing you are fighting. I forget that our crazy conversation can be viewed by anyone. OMG we have discussed lady gardens and more. Lol. Keep asking questions and let us know when you find out what your treatment plan is. We are all here for you. ?

Hello everyone, just had 3rd round of FEC today (weeks are flying by). Bloods done yesterday WBC and neutrophils came back low, so had to wait while they did another blood test today. Came back as ok - so treatment went ahead. Isn’t the body amazing how it can regenerate itself! Oh, and the hospital and staff - they’re amazing as well!
Half way through now Katie11.