My mum was diagnosed last week along with metastasis in her lungs. A stent was fitted Friday to help with the jaundice and itching. Mum didn't want to know how serious it is or how long she may have but as an only child and single I needed to know what I may be facing in terms of care etc so I could be prepared. I saw a specialist nurse Friday who explained the stent would hopefully give her 'a few months' and I know from what I've read that it might not be many.
The nurse also told me they wouldn't be offering her any treatment. She said chemotherapy is often not as effective in the elderly and side effects can out way benefits. This came as a shock as I thought they would offer something. Mum is bright in herself, no pain, feeling pretty well now the stent is in and raring to get home which should hopefully be later today. Two months ago she was digging drainage ditches in her garden, I can't help but feel she's just being written off because of her age. I'm sitting listening to her talking about plans for when she gets home and next year whilst knowing they aren't going to treat her and she may not have much time and at some point she is going to ask me about treatment and what am I going to say?
We lost my dad two years ago after five years of cancer treatment for three different cancers that she nursed him through, it's so unfair on her. I'm angry, upset, frightened, lonely and finding it hard to accept that they aren't going to try anything to help her. Sorry this is long winded but just trying to decide if I should ask for a second opinion or even approach a private cancer specialist, has anyone experienced anything similar with an elderly parent being offered no treatment?
Thank you
Hi…My Mum was 90 and had oesophageal cancer.The local hospital tried the same.I contacted the PA of the top consultant at the local specialist cancer hospital, got her an appointment.She was given oral chemotherapy with no side effects. She died about 10 months later, not from cancer, rather MRSA she picked up during a visit to the local hospital.Get a second opinion and push.If you are in the South, insist on going to the Royal Marsden. You have to battle.I am having to do this daily as my husband has PC. Good Luck.
Thank you so much for your reply, it makes me so angry when people are seemingly written off because of there age, it should always be on the individual not just their age. I will push for a second opinion and wish you and your husband all the best
Please push them.With Mum it was some years ago, but the hospital had basically put her on the Liverpool pathway.At the hospital where she picked up the MRSA, which of course wasn’t put on her death certificate, they wanted to put a DNR on her file. They discovered that they were dealing with the wrong person I.e. me.Fortunately there was a very ethical young doctor ( from the EU), who told me that my Mum had a blood infection (MRSA)… she only went in with a UTI as the GP wouldn’t agree to District Nurses giving daily IV antibiotics at home.The young Dr said that she was dying and we should take her home to die in dignity in the arms of her family.This is what happened she passed peacefully.
The McMillan nurse should give you support.But we had one, who told us a pack of BS when my husband was diagnosed.She was not qualified to pronounce the diagnosis, which she communicated and which was totally wrong!
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