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I’ve been diagnosed with Grade 2 invasive ductal cancer, HER2+, due to start chemo then surgery for a mastectomy (unsure if it’s 1 or both at the moment). I’m so worried that I won’t be able to take care of my 9 month old little one...we have a hugely supportive family thankfully but I’m so unsure how it’s all going to affect me (I haven’t really known anyone with cancer to ask). Just hoping for a bit of advice really... I was due to return to work after maternity but now everything is so up in the air...
sorry you have had to find us here, but we are all here to support you too.
I know it all seems like you are just one stop from the funeral home at this point, but honestly, you will be fine. I suspect you may have been told to stop breast feeding if you were still, that's quite hard, but it is obviously necessary.
The time between diagnosis and starting treatment gets very stressful, but once you get started, you will find things much easier to deal with. With your family help you will get through the treatment and will be up to running around with your little one before you know it.
I was diagnosed over 6 years ago and I'm still here, so there is lots of hope.
I am not medically qualified, please consult your doctor or undertake your own research.
This is my second time around and I must say much much older than you.
I have found that actually giving people the chance to do things: pick up medicine/ dry cleaning, vacuuming, shopping, cooking a meal etc helps everyone. They feel they have really helped - and they have- and you get a rest from it all. A bit like the early days of motherhood, let them help.
If you choose how they are helping you this might help. A rota of taking you or the baby out. They will love it, so will you and your little one will be smothered in love
Leolady56 aka Lndsay
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Life is like a boxing match, defeat is declared not when you fall .....
But when you refuse to stand up again .......
So, I get knocked down but I get up again. x
Hello Daisy, I am so sorry you're in the midst of the pre-treatment limbo land which is when I felt most overwhelmed. It all seemed so daunting and long. I am far from a veteran and just at the beginning of my journey (one chemo cycle down, 7 to go before mastectomy, radiotherapy and Tamoxifen or similar for 10 years) and my children are now young adults, but I wanted to echo others' thoughts and also tell you about a remarkable woman I met a week ago at the hospital. She has four children under 7 and is doing the same treatment for a triple negative cancer diagnosed when she was pregnant with her now beautiful baby. She was beyond generous to me when I was in my nervous pre-chemo assessment state and she talked to me about what helped her. She said that she accepted every ounce of help offered and had to get used to the fact that it may not always mean things were done as she would do them, but it made life overall better for everyone just to let people in and help her. She also said that the kids were therapeutic (not always!) as it meant she had another focus and a reason to get dressed and keep on keeping on. Finally, she was really open about her fears, worries and emotions. Not with everyone, but with those she loved and trusted and on whom she could rely. After all, this is rubbish right? None of us wants it and we all have a host of feelings and emotions to manage on top of everything else. A safe, supportive outlet for those emotions and someone to walk alongside us when we feel/express them are transformative.
I am trying to take it as much as I can one step at a time - breaking down the long path that lies ahead and not getting bogged down in it all because it becomes too overwhelming. I don't always succeed, but I do find that if I can take a deep breath, maybe indulge in a cry or go for a walk, I can regroup a bit and come back to now. I will be thinking of you lots and hope you return to the group whenever you want to or feel ready. We are all cheering you on. xx
I'm Sam age 34
I have the same cancer and diagnosis as you,I'm having my 3rd cycle out of 6 Thursday...my chemo is TCHP that's targeted therapy also as I'm also HER2 positive,it says very tiring for me but everyone's body is different,I won't lie I do struggle some days..but rest when you can is the best thing to do xx
Thankyou everyone, he keeps me very busy so daytimes are good as all of my energy is focused on him. I just hope I will be able to keep doing some of our regular activities once treatment has started... Hopefully after my first Oncology visit tomorrow everything will be a bit clearer.
Hope your treatments go well Sam and Anna (and anyone else who has treatment coming up too) X
I am new to this site and apologise as I am not up to speed with all the termology. I was diagnosed in September with Her2 positive early stage breast cancer Grade 2. I have just had my 4th of 6th chemo TCHP. I have experienced the tiredness but have also been able to function inbetween. Everyone is different (I have finally learned this). The best advice I can give is rest and sleep (if you can) when your body tells you. I did try to fight it at first as I wanted to carry on as normal. I agree the worse bit was waiting to start treatment as you just want to be doing something. I found everything overwhelming as I am sure everyone does. Sending you best wishes for your treatment x
Thanks for you reply Vivvy1970 - my first chemo session of 6 is done, thankfully husband has a few days off work so I can rest up if I need too, just waiting to see what the next few days bring - taking each day as it comes but finally glad that things are on the move to fix this
Hi Daisy sorry I haven't been on here for a while. I know what you mean about getting things on the move to fix it. That is exactly how I felt when I had my first chemo. I have just had my fifth.I have tried to approach this with a positive attitude and got my last one on 9th Jan as long as my bloods are ok.. Hope your first chemo went well. Take care and have a good rest and good christmas x
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