Hello all,
Before I get into my post, I’d want to note it contains content about my mums end of life care. I do not want to worry or upset anyone so my post is more for those who are either end of life themselves, or have supported a loved one at this stage.
If you are a family member, I kindly ask that you do not share information of how long end of life care has been or was.
The next part contains my questions.
Unfortunately my mums cancer has stopped responding to treatment. Her oncology team are now working with our wonderful hospice team to manage mums symptoms.
One symptom they are struggling to control is nausea, vomiting and trapped wind.
Medication used has included Cyclizine, Metoclopramide and Levomepromazine. A syringe driver was used for a little while before being swapped out for tablets but the nausea and vomiting has returned.
We think mum is stuck in a cycle where she feels nausea, doesn’t want to eat, takes medication which irritates her tummy, creates wind and then she vomits. We are trying to break the cycle and the lack of food is making her very weak.
She is on a mix of other medications including pain relief, antidepressants, laxido and buscopan.
Does anyone have any similar experiences? If yes, was there something specific that worked? The hospice has said they just need to get the medication balanced and it will improve but it’s just taking time and is distressing seeing mum so unwell.
Thank you in advance x