Oh my word. I am so sorry. Love to all of you.
Denise xxx
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I live in a three generational house, my father in law was diagnosed with Alzheimer's disease about 4 years ago. His memory is quite bad and in the next few years will definitely need a full-time carer. My mother-in-law was diagnosed with metastasised rectal cancer. She has had radiotherapy in the hopes to avoid a bowel obstruction. In December she was given a 6-month prognosis and subsequently is refuse to have chemotherapy. It would be in my opinion too much to ask my wife to become my full-time carer bring up three children try do a part-time job to bring income as well as being a carer for her father and possibly her mother to.
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My husband has a feeding tube. He's not using it yet but I know his hands are such that this will be an option that we will gratefully use. I encouraged him to have it done because I wanted to help him. Originally I had to cancel the operation because he wasn't having it done. My daughter told him 'dad it's not just about you'. don't know how I would have felt if I had to just watch him starve when he didn't need to. He has a bipap machine to help him breath. Great we all need help so why not use it. I'm asthmatic I use an inhaler and do what I can to help me. There's nothing that says I won't be in an accident tomorrow and end up worse off.
take what help you can and improve what you have now. Worry about the rest later. I'm sure your family would rather have you with them knowing you are trying to help yourself. Its your choice and their's too. You must talk to them. Think about what it would be like if another member of your family was in your place. Wouldn't you feel hurt?
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It is a very personal choice. That is a wonderful analogy Ellie. I've also added to my visualisation a bridge coming off that hill, aka a cure, taking us off MND mountain before we get to the bottom. Given the marvels of the Covid vaccine, I think we can ask the medical world to get cracking on that bridge now!π
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Everything ends, mountains, seas, suns and planets. Compared to that lot what are we? ππx
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I read these and don't know what the hell to say............just want you to know I am reading and with you........fgs
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Ellie, I just love the analogy of us all rolling down a hill taking different paths and journeys. Im hoping to hit a very large clump of heather.
I guess we all have very different ideas about what interventions are acceptable .Since I was diagnosed I have totally changed my mind and I am willing to accept help available but I respect anyone who doesn't want it.
I am fortunate in that I have had time to think about things and talk to people. The experience and understanding of friends on this forum is invaluable.
Love and hugs,
Debbie x
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DJW Again, death without indignity is something to which we all aspire - there is absolutely no shame in having a feeding tube or using NIV, just as there is absolutely no shame in not having a feeding tube or in not using NIV. Living where we do, we are fortunate in having the latitude to determine (most of) our treatment in a non-judgemental fashion.
Once we are diagnosed with MND, we find ourselves at the top of a hill - some of us roll down the hill without obstruction; some of us roll sideways for a bit before changing direction; some of us find big clumps of heather along our path, which holds our weight for a bit before yielding and we continue our journey. We all end up at the bottom of that hill, having come down it in our individual ways, without anyone claiming the moral high ground - as we know, MND produces no winners...
I admire your strength and resolve.
Love Ellie.
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We all do what we feel is appropriate for our individual situation - there is no right or wrong way, no rule book.
Originally posted by DJW View PostI refuse to go down the path of tube feeding or any intervention that artificially sustains my life. I feel that I will be dying with dignity
I have many life enhancing tools - feeding tube, NIV, braces, meds, carers, mobility aids, profiling bed, eyegaze tech, wetroom and a supportive family and friends - and when I die, I too will die with dignity.
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I totally respect that but if you havenβt already done so please have the discussions. These are choices that will impact not just you but your whole family.
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Currently I can no longer talk, eat or drink and I am on pump feed. I am checking out when I can no longer use my hands but my MND will kill me before that happens. Life IS what YOU make it. Just saying init? ππz
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