Hello. I am new at this website. My mother was diagnosed with ALS in 1999. She had been ill for some time but it was difficult discovering what she had. I hope I can answer some questions. Mom had a feeding tube implanted late in 2000. She was choking on food and had trouble with some fluids. She was unable to talk by then, too. It seemed to be fine for about 6 months, but then she began to worsen quickly. She began to fall and began to have trouble writing. She had some trouble with the feeding tube and it had to be replaced after about a year. She was rapidly loosing weight, despite the feeding. The most important thing was that the tubes and machine be cleaned religiously.
She refused to use a ventilator. It made the end a little more difficult, but she feared she would suffer and live longer with it. I know this is going to be hard to read, but a year after the tube was put in she was in great distress. She would ask me to pray that she could go to heaven. She survived for about 16 months with the feeding tube. It did give her that chance to see her 8th grandchild, but she wished that she had not had the feeding tube.
If you have any questions you can contact me.
I hope this helps. I know what a terrible thing this is. My prayers are to you and your family. It is very difficult caring for a loved one with ALS. It is a wonderful thing you are doing for your father, but take care of yourself.
Shane K
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Originally posted by slaughter17: Hello to all. I have posted before about my father who is currently living with ALS. Or in his terms "dying with ALS." He has always said that when the time comes he will not allow anyone to prolong his life in any manner, including a vent or feeding tubes. Well, he is coming up on that point in the disease where he must start thinking about that option. He is seriously thinking about using a vent to keep him alive. I truly don't know how to feel about this. I can only tell him how I feel about it, and hope that he makes the right choice that makes him happy. I am one of his caregivers during the day and I have questionable thoughts and feelongs about it. I am not for sure how long it would prolong his life. Does anyone know? Maybe months or years? The docs say right now he only has months left. My mother is having a hard time with this whole thing in general. And she is just assuiming the worst anyway. I work for hospice, and I know it will make things harder for him and his caregivers. I guess I need to know more about having a PALS using a vent. Has anyone ever experinced an ALS patient, (or in my case a family member) who uses/ or has used a ventilator? How is the procedure done? How will he eat, a feeding tube? How long can it prolong life? I am really heart broken about this. If I was my father I would just die comfortably and happy. not prolong the inevitable.
Signed,
Frustrated and concerned family daughter |