ironbark

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  • in reply to: Morphine Nightmares #41945
    ironbark
    Member

    Hi Lainy,

    Morphine while it’s a good drug also has the side effects that you have discribed. Haloparidol can work well, but in some people it also has the reverse effect and can make some people even more agitated, so be aware of that too.

    Ask your medical team about a narcotic skin patch or a syringe driver with a different narcotic in it. He can still be given some top up pain relief and an anti-anxiety medication like lorazapam if needed.

    Poor Teddy must be very frightened, and this would be scaring you too.

    A regular dose of Grandchildren’s hugs always works well for me, so I can understand why Teddy would look forward to them.

    Don’t be too hard on yourself either, it’s not a bad habit, it’s advocacy. You are fighting for the best outcome for Teddy, so it’s worth it. You go girl!!

    in reply to: Tomorrow…we will know. #43046
    ironbark
    Member

    Hi Beth,
    My Dad had almost mirrored symptoms to Dave and it turned out that he had an infection. They have given him some kickin’ antibiotics and have inserted a drain to get rid of the bile, and he isn’t great but he is slowly getting some relief.
    Hopefully you will receive some similar news. We always expect what we fear the most, sometimes we are right but sometimes we’re not.
    Keep your chin up, we’re all praying for good news for you both.

    in reply to: She is in his hands now #43072
    ironbark
    Member

    That was beautiful. I’m sorry to hear that Debbie has passed, but she sounds like an amazing selfless lady who was partnered with a wonderful caring man.
    Our thoughts are with you and your family.

    in reply to: Coping with everything #43069
    ironbark
    Member

    Thanks Lainey,
    You sound like a real honey yourself.
    She is a bit of a control freak, and usually I just inwardly smile to myself and accept that that is just how she is. However this time I guess I’m just too emotional and not removed enough to see the amusing side of it.

    I agree that in the case of someone who is very unwell, as I assume Teddy is from your other postings, it is neccesary to take control and that this is done with the person’s best interests at heart.
    I’m finding it difficult to cope with the controls in place because they seem to be more about her than Dad, and because Dad doesn’t get any say.

    Honey is a good idea, but I must say that I am very much a ‘honey’ type of person anyway. When Dad was first diagnosed I was extremely supportive to her, I prepared meals so that she didn’t have to cook when she asked, I ran errands for her, and I sat down with her while she cried and I thanked her for loving and caring for my Dad.

    Her favourite word at the moment seems to be ‘I’, she had a huge hissy fit in the middle of the ward one day because she had to walk ‘miles’ to get to the motel that she is staying in. Concerned about where she was staying and her having to trudge so far every day, my husband and I offered to drive her there. It turned out that she was staying accross the road from the hospital, and it was actually further to walk to the car park to get the car that we would have used to drive her there.

    I understand that she is emotional, and that this would be very difficult for her. I also understand that as the daughter and not the wife, I don’t have the right to barge in and take over. I have no intention of doing that anyway, but I’m a daughter first and a nurse second, and the main person I am concerned about is my Dad. All of these theatrics are causing him stress that he can do without.

    As for the wrong information, as I said I’m not really sure that she is giving me that deliberately. If she is then I will not keep the fork in the drawer, even though I may dip it in honey first. I think (and hope) that it more than likely that she is misunderstanding the information that she is hearing from the doctors.
    The day I was there when the doctors arrived I didn’t say a word, just listened. After they had left I found that there were a few questions that Dad had that I could answer, and I was also able to write down some questions for him to ask for his own benifit during their next round.
    That is the sort of thing I think I could be useful for. I certainly don’t profess to know much about this or any other type of cancer, it isn’t my specialty.

    Her behaviour is just making a bad situation worse for everyone, even herself. But she really seems to crave the ‘poor me’ role. This and the rush to cash in on every bit of government money that she can get her hands on is driving me mad. Don’t get me wrong, I understand that govt subsidies are there to be used in these circumstances, and they are rightly entitled to access them, but it just seemed as though the money grab became more important than the reason it was needed at times, which I found very sad.

    I simply don’t trust the information that I’m being fed at the moment, and this is adding to my already fragile emotional state. My sons are a great help, they just want me to shout at her.
    I still prefer the fork….. that’s the nasty side of me coming out…

    in reply to: Bilirubin and ascites questions again… #42613
    ironbark
    Member

    I hear what you’re saying about the emotions Emily,

    I returned to work after having four weeks off, and Dad’s diagnosis came two days before my planned annual leave. I went back to work on Monday, and tried to keep myself occupied enough that I didn’t think, but when I walked through the door on Tuesday I just broke down into a blubbering mess. I have been given another three and a half weeks off, which will cover Dad’s surgery and some recovery time, and can extend if I need to.

    I am very lucky in one way that I work at a major hospital (not the one that Dad is in though), and my colleagues are aware of Dad’s diagnosis – partly because he came into the emergency department over the weekend and needed to be transferred to the specialist hospital, and partly because I’ve told them. My workmates are extremely supportive, but I find that when they try to be kind and are nice to me I immediately cry, so avoiding that contact would have been much easier.
    My husband has a mental illness and hasn’t been as much support as I’ve needed due to his own issues.

    Like you my Dad is my world. My mother left when I was six years old and Dad brought me up. We’ve been through some really difficult times together, and his second wife was the bitch from hell. Dad has a son to his second wife, who has schitzophrenia, so he also has issues to deal with.

    My husband and I have three adult sons, who are wonderful, but I see my role as their mother to be one of support for them, not for them to support me – even though they do.

    I’m off to get some counselling on Saturday. I just feel that I need someone to vent to, and to get some strategies to manage my feelings a bit, because I’ve never felt like this before.
    You just feel as though someone keeps pulling the rug out from under you, only to replace it and then rip it out again.

    It would probably be a safe thing to avoid anything that made me cry, or upset me, but I think in the long run that would be a mistake. I have given myself permission to grieve.
    That doesn’t mean that I have given up hope, or that I have written Dad off. What it means is that I have accepted that it’s Ok to feel this way and that it is normal to feel this screwed up when something this stressful happens.
    I have also recognised that I need to look after myself before I can do justice to caring for my father.

    It’s very hard to find positives in a diagnosis like this, but for our own sanity we need to look for them. Eg. Dad was able to eat half his ice cream today, he’s drained over a litre of bile – better out than in, I’ve got time off work so that I can spend some quality time with him when it matters.

    Keep on posting Emily, we might not have ALL the answers but we DO understand where you’re coming from.
    Take care
    Lesley

    in reply to: My Dad, Tony has passed #42586
    ironbark
    Member

    Michelle, I don’t know your father Tony’s full story as I have only just joined this forum after my own father’s diagnosis a couple of weeks ago. But I wish you well and empathise with the loss of such an important person in your life.
    Take care of yourself.
    Lesley x

    in reply to: Colon swollen cant pass stool right #40522
    ironbark
    Member

    Hi there Mr J,
    Ask your doctor if a steroid might help to reduce some of the inflammation in your bowel – it may not be an appropriate treatment for you, but asking doesn’t hurt.

    It reminds me of the old story where the different parts of the body had a discussion over which was the most important, and the end part was that it was the a*hole (sorry about that). What I’m trying to relate is that if your bowel isn’t working properly then it affects everything else in the body, so it becomes extremely important to you.

    You’ll probably need to see a combination of people to help with your case, and doctors are only part of the picture. Get a referral to a dietician for example, who can advise you on a diet that will provide you with the nutrition that you need while not overtaxing your bowel, and an Occupational Therapist may be able to assist with issues around continence and regularity, and even pad supply if you need them.

    I hope this issue resolves soon for you Mr J, look after yourself.
    Lesley

    in reply to: Bilirubin and ascites questions again… #42611
    ironbark
    Member

    Hi there,
    I’m also a devistated daughter who is just starting the cc journey with my Dad.

    I have noticed many of your posts seem to be desperately seeking some sort of reassurance that Mum is going to recover and get better. I don’t know your Mum’s individual case, so can’t comment either way, but I do wonder what support you have outside this forum.

    As with any medical condition there are some predicatble paths that a disease will take, and then there are the directions that are different in each case. Your Mother’s medical team will be best placed to answer the questions about the individual case that pertain to Mum.

    The previous posts are correct by pointing out that chemo when bile levels in the blood are too high would not be a good move, but try not to get too focussed on the numbers, that is the doctors job.
    Don’t make the mistake of missing out on good quality time with your Mum because you are becoming too focussed on this. Ask heaps of questions for sure, offer suggestions yes, but above all take care of yourself so that you can be there for Mum when she needs you.

    I’m going off for some counselling in a couple of days, I don’t know if it will work, I know it wont cure my Dad, but I’m hoping that it will give me the strength to cope with another week of this torture.

    Hugs to you
    Lesley

    in reply to: Hello I’m new #42622
    ironbark
    Member

    How does this work, am I supposed to move on to another page now that I have introduced myself, or do I keep waffling on this one?
    I’ve never been a part of any sort of forum, so don’t know how they work. It’s a great idea though, support groups are fantastic.
    Lesley

    in reply to: Hello I’m new #42619
    ironbark
    Member

    Thank you to everyone who has replied to my post. You are a great source of inspiration and support, and I shall be sure to visit often.
    Hugs to all
    Lesley x

    in reply to: Hello I’m new #42614
    ironbark
    Member

    Just in case anyone wondered, as I noticed most were in the USA or Canada, I’m from Australia.

Viewing 11 posts - 16 through 26 (of 26 total)