I’m a hospice nurse. Eat what you fancy as and when you feel up to it. You’re eating for pleasure now, not for nutritional input. Soft foods are popular with our patients, e.g. soup, fish pie, mashed potatoes, soft stews, ice cream is very popular as it is cooling to the mouth, custard, chocolate pudding etc. Ice chips for comfort.
As others have mentioned, the appetite decreases towards end of life so do not worry if you do not want to eat. Try to maintain fluid intake if you are able; again drink for pleasure but if you do want to incorporate some nutritional aspects then there are supplements available like Fortisps. We make our own supplement including full fat milk, milk powder, nesquik and cream/ice cream. Supplements are nutritionally balanced, ours is designed to get fats in for energy so geared less for our very end of life patients but many still enjoy it. Broths also. OXO/marmite with hot water are reasonably popular.
Please do not stress about eating. Families become very distressed when they see their loved ones going without food and drink. It’s normal but hard for relatives to witness. If your family starts discussing IV or subcutaneous fluids, be warned that these are rarely recommended for end of life and can cause fluid overload because the body cannot cope. Medical professionals not in specialised palliative care can sometimes make unwise decisions because their instincts are to preserve life. Go with your gut instinct and needs before agreeing to something you feel is not in your best interests.
Make sure palliative care are involved somewhere in your care; pall consultant, MacMillan nurses, community pall team, community nursing, local hospice at home team if available near you. Also make sure you have anticipatory medications/just in case medications prescribed and at home; at a minimum this should include pain meds, e.g. morphine or oxycodone, something for terminal agitation like midazolam and something for respiratory secretions e.g. glycopyrronium/hyoscine butylbromide. Different trusts/ICBs have their own formulary so they may prescribe different drugs but you need an analgesic, something for agitation and for secretions. These should be injectables and should also include other drugs prescribed dependent on your diagnosis. This is where the community pall team are good, they can guide GPs in the right direction.
Discuss your needs and wants with your loved ones. They may not want to talk about it but it really does help. Wills, burial/cremation, funeral directors, details of bank accounts, what bills you pay etc.
Above all this is time to be selfish. Now is all about what you need to die with some form of peace. All the best xxx