I don't have any experience of Abraxane (Paclitaxol NAB) but Paclitaxol and I received my SBC treatment in Canada. I look for the patient handout for Abraxane from our cancer center official website and seems should seek doctor or get emergency help immediately if any heart problem.
Thank you all for your reply’s, really means a lot to me. I’m really trying to stay positive and not look at too many statistics!! xx
I cannot reply in any detail but thinking of you ❤️.
No doubt you will hear from others who can wish you well.
Angel Eyes x
Welcome to board, I haven't been on here long having been diagnosed with secondary in April to lung, liver and a couple of bones. I had my primary diagnosis in 2015 so was quite a shock to be re-diagnosed. I'm not TNBC I'm triple positive so on a different regimen to you but I think most chemos share identical side effects so I can identify with what you're going through with that.
I have kids but not as young as your daughter, it's tough isn't it? I hope you are getting plenty of support and taking things easy, I know that's easier said than done when you just want to be mum and keep things as normal as possible.
I'm sure someone with similar diagnosis will reach out to you here, as has been mentioned, weekends are quieter which is a good thing I guess as hopefully people are making the most of it with family etc....
Take care x
I agree with Shi. Lots of people read each post but don’t add a comment as they may not have any experience of their own to add. In fact I viewed your post earlier but don’t have TNBCor lymph node involvement and was therefore going to see if anyone who had the same would add their own experience. Weekends are also a very quiet time on the forum, as I’ve noticed over the years of being a member, so you may not get anyone who has the same diagnosis able to share their experiences during this time.
I do hope your treatment works well for you, with few side effects and please use the phone lines available as Shi has suggested if you need to speak to someone. Hopefully someone, in a similar position to you will respond and offer advice.
Mcclaire ❤️ Please don’t take the views tally personally, the threads are open to the world and some people use to try and get information for themselves or a friend or loved one without ever joining the threads, others might be thread members who will read your post and if they think they might be able to share their experience if the think it might help you will respond but if they don’t feel they have anything to write that must be of assistance to you will not write ❤️ Please don’t pay any attention to the numbers who view your posts ❤️Please do ring the number on here and speak to someone or see about using the someone like me option too 👭💕💕✨✨Shi xx
im new to all this, had my first round of Chemo on Tuesday and so far (3 days in) feel pretty rotten. Heartburn, shakes and bone aches to name a few side effects kicking my butt.
I was diagnosed only 2 weeks ago stage 4 BC with avid metastatic lymph node involvement but not seen on PET CT in my organs yet..
its such a scary diagnosis and I guess what
im looking for people to share some honest, realistic expectations and experiences with me. I have a 4 year old daughter and life has been going so well, we were such a happy little family and this has hit me so out of the blue and I feel completely lost.
thank you so much for any reply’s