Hello there

Just joined this evening. Been looking up my results on the web and just messing up everything in my head. Was supposed to be a straight forward Grade 2 invasive cancer, have lumpectomy, a wee bit of radiotherapy and hormone tablets for 5 years. On result day, 3 weeks after my lumpectomy, my breast care nurse phoned to say they had clear margins, 15mm size but grade 3 and 1 out of 3 lymph nodes affected. I'm awaiting a phone call from the oncologist to discuss options. Options include chemo now since lymph node positive. I have invasive ducal Carcinoma with DCIS, ER pos, PR pos and HER 2 neg. anyone similar here? I want the best treatment available as I have 2 Autistic children, my son is 14 and my daughter is 22. She has taken a years break from Uni where she is studying Biomedical Science due to anxiety, depression and eating disorder. She's having a lot of treatments, hope she can rejoin uni this September. 

  • Hello Hazel 

    I was diagnosed in October 2019. I was like you are tonight blown away by the shock of it. Felt SO alone and terrified. Hard to put it into words actually. Just isolated despite having really good support. It just feels as if the world had gone away.  (I can see the current situation re. Covid only serves to  complicate things even more as well) 

    Can I just say I used the MacMillan nurses a lot during the early days. They help so much. They are informed and supportive because they absolutely ‘get’ what we are going through. Truly they are the best resource when you are reeling from a diagnosis. 

    My tumour was ductal too and grade 2 (although initially it was thought to be grade 1)  My lymph nodes were clear fortunately. the ER and PR were both positive as are yours. HR2 Negative.  

    I am writing a response because I wanted  to tell you that from that awful scary and threatening October day I have had the tumour removed and had 15 sessions of radiotherapy  and had few side affects. Supposed to take hormone tablets for 5 years now but I doubt I will. Won’t go into that, it’s just I have a big resistance to taking them. It’s me!!

    Hold on tight.  It IS a roller coaster but the day I was told  and the next couple of weeks for me were the hardest  of all,  it felt as if the end of the world had come. It hadn’t. 

    Emotionally I have the odd day of course when I feel threatened but mostly I am able to get on with life and feel grateful for the NHS. It’s a gradual acceptance of this is where I am, and once you get a treatment plan in place, you will see more clearly this is where I am going. It takes you to a different place. A kinder gentler place  

    No nothing is ever quite the same,  but you have a kind of peace come over you. You feel back in control of your life, well more or less. As I say I have my moments.  

    Please take care. Talk a lot about it. Talk to trusted friends.  I found my partner (although lovely) could only see me as a strong warrior when at times I was  falling apart inside. 

    This forum is great too. Everyone on hear ‘gets It’. We are all in it together although travelling along different parallels.  

    Google?? Well I found it terrified me much more than it helped. I don’t do it at all now. A lot of the posts are not correct either. Your breast care nurses are the best reference place.

    I wish you much good fortune and health. 

    Go well

    Kebbs x 

     

  • Hello Hazel62

    Ive just been reading your post and I've benn diagnosed very similar to you and I was wondering did you have the chemo? I was hoping to avoid it but because of the lymph nodes being positive I'm not sure now. I go for lumpectomy in August but the consultant has said Chemo would be needed but he'll know more after he's taken the lymph's out. I hope you're on well on your way to recovery now and got through the covid situation with continued treatment Txx