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Louise64's avatar
Louise64
Member
5 years ago

6 months Post DCIS now heart failure at 57

Went for 6 month checkup at radiology oncologist - now have been diagnosed with severe heart failure and need aortic valve replacement. I can’t believe after having nothing wrong for 30 years- only 2 caesareans in 1990 and 1992 ... here I go again. Any suggestions for support groups like this one? Once again - I’m not telling anyone but my sister, daughter and school principal... I know so many worse off than me .. more surgery.. more time away from work... more frustrating than worrying. 

26 Replies

  • They don’t think so- but also have no family cardiac history. Just unlucky 👍
  • @Louise64 is the heart failure because of radiation? This was my concern when going through it, as family history of heart problems. 
  • You’re anything but boring! 😆☺️. I like your mum’s viewpoint 👌🏻, cos that’s all it really is 💟
  • Thank you. My mum would have said (she died of breast cancer and mets to spine, lungs, brain etc)..just another speed bump in life.
    Now starting another journey on another road...at least I'm not boring !
  • Sorry to hear that Louise 😢. Really unnecessary at this time. What an absolute bugger. I don’t know of any support groups, but maybe your specialist will know? 
    I wish you all the luck for the best outcome 🍀🍀
  • Oh dear, that’s disappointing. As you say, more frustrating than worrying as the ‘fix’ is a well known and successful one but it does tend to hit home. It was a Heart Condition (I always thought of it with capitals) that sent me off to a counsellor five months after bc diagnosis. I could handle the cancer but a Heart Condition??  The counsellor was a good thing overall, and I was, and still am, perfectly fine, of course. Just needed a bit of time to get rid of the capitals! Best wishes for a rapid resolution and recovery!