What do bone Mets feel like?
Hi Gals I was diagnosed almost a year ago with stage 3C DCIS - (Beryl for those in the know!) Beryl was pretty busy and managed to have 13 not so darling babies (lymph nodes). So a mastectomy was on ...
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Welcome to the blog, @Majellablue - SO sorry to see you here, but it is the best place to be to ask any questions of the group & get honest answers - as we 'get it'.
I was checked late last year for persistent pain in my pelvis - and got the all clear - but am very aware of any new persistent pains as they present. :( Sadly, it is all a part of this bloody disease & a side effect of the AIs we are on.
I actually asked my Onc about the 'pain that could indicate Mets' - and she said that it is a deep seated persistent 'different' pain to 'general aches & pains' that we get from AIs ..... but advised to get anything investigated if it lasts longer than 1-2 months.
All the best for your CT on Friday - fingers & toes crossed for a good result. xx
I was checked late last year for persistent pain in my pelvis - and got the all clear - but am very aware of any new persistent pains as they present. :( Sadly, it is all a part of this bloody disease & a side effect of the AIs we are on.
I actually asked my Onc about the 'pain that could indicate Mets' - and she said that it is a deep seated persistent 'different' pain to 'general aches & pains' that we get from AIs ..... but advised to get anything investigated if it lasts longer than 1-2 months.
All the best for your CT on Friday - fingers & toes crossed for a good result. xx