Guest guest Posted April 4, 2006 Report Share Posted April 4, 2006 This whole entry is wonderful. And very well written. When I found out that my friend/loved one, oh I'll just call him '' was sicker than we both imagined (yet is it really known, this condition is tricky in a way, or maybe it's his and my denial.) Well, anyway, when I realized that we may not have as much time together as I have thought I wrote a list of simple little things that I wanted us to do together; play cards, read a book together, go bowling, slow dance, make a list of his favorite songs with an explanation and I'd burn them on a CD, and take MORE pictures. I would sent him " care packages " , jokes, small treats, CD's of music that brought him to my mind, articles, when he lived farther, he has since moved closer so I take him things or send them home with him. But this past month I have felt a sense of pulling away from both of us and get weepy when I think about him, I'm not sure what's going on. (Oh hell, sure I do...) Tracey In a message dated 4/4/2006 12:39:26 A.M. Eastern Standard Time, no_reply writes: There are things that you can do to help your loved ones through these trouble times. I've listed some of them before and others have added to it. Keep their days happy and exciting by doing little things like lighting a candle on the table when you eat. Take walks and notice the creation. Give them a back massage with lotion after a warm bath. Talk to them about old memories and the good times of life together. Let them know how you feel inside, the goods and bads about the illness and that you plan to always be there for them. Focus on what is special and important to them and put your wants and needs as secondary all the time. Taking care and time for yourself is one of them. If you become worn out, than your partner who needs you will know and respond to it. The positive outlook is that we are here today, living and breathing and being with one another...the negative is that we will be alone without them. Enjoy one day at a time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 4, 2006 Report Share Posted April 4, 2006 That was a beautiful essay. Do you know if anyone in this group has primary liver cancer from the cirrhosis, I am afraid my Grandfather now has that, he has had a " lesion " in his liver since last summer (that I know of), it was 1cm and had not grown as of Nov., he was again in the hospital twice in the last two months, from hepatic encephalopathy. The last time when we got to the ER they did an ultrasound on his liver right away and didn't say much, then the next day they did an MRI, I asked my Grandmom if they thought he had liver cancer and she said it was " a possibility, " so the next day they sent him home, I asked her what the results of the MRI were, and she said " oh, they never even mentioned it, " now I know they don't give you an MRI and then " not mention " the results, so I am assuming he has liver cancer. He seems to be getting sicker quickly, I just wanted to know if anyone can tell me what happens next. Coping Caregiving of someone with cirrhosis is a difficult job. Some may think it is easy...then they never had to go through this. Watching someone who is ill, especially someone very close to you, is difficult. Caregivers feel like they need to do more to help... they may spend hours researching material on the disease to see if there is any remedy or care they should give that they are not giving now... At times they feel totally helpless even if they are doing the most they can do. It is draining emotionally, physically, and mentally. Emotionally cause they are scared of loosing someone so dear to them and feeling like they become responsible for it if they don't try hard enough. Physically, cause things that were once handled by two people is now handled by one and not everything may be understood how to handle it. Mentally cause they want so much to find a miracle cure to prevent the ineviable. They also become so stressed at the fact they may fail in taking proper care and left some stone unturned that will come from out of no where later on when it is too late. The one who is cared for feels like a burden to those around who are helping them. They may feel jealous of them since they are able to do the things they are no longer able to do and have health and something to look forward to. The disease engulfs their whole world and they feel like they are walking through an never ending nightmare and that things may only get worse, and may get worse faster than expected. It is like living on the end of life and death is one step away. The only way they survive is if they avoid that last step at least for a little while. Depression is common place for both of the people above. Still now, when I look at my loved one, even after the transplant... I wonder how much longer we will have together. With all the complications and now taking drugs that have side effects that must be taken to live...we found out that they can cause things that really will only give us a short times period again to be together unless our bodies are strong enough to fight it all off. The feeling of loneliness is there, the feeling of losing control over life situations is there, the fear of being alone, many things can make a person depressed beyond compare. This is why I state to live one day at a time. Forget the pass except the fond memories and don't look directly at the future ....look toward the future with hopes in your heart. Live for today, Live for those who love, give your mind to the important things in life like having those loved ones around you. With the time you have left together...think of building fond memories the best you can, things that will last the rest of your life and into the future. What can you do today to make this come about? There was a list made up of things to do to help others without them knowing. Like parking farther away from the store and walking so someone else can have the front spaces. Another one is putting a coin in the meter for someone whose time is running out to park. Taking shopping carts clear back to the store and a few others with it to save someone else the trouble. There are things that you can do to help your loved ones through these trouble times. I've listed some of them before and others have added to it. Keep their days happy and exciting by doing little things like lighting a candle on the table when you eat. Take walks and notice the creation. Give them a back massage with lotion after a warm bath. Talk to them about old memories and the good times of life together. Let them know how you feel inside, the goods and bads about the illness and that you plan to always be there for them. Focus on what is special and important to them and put your wants and needs as secondary all the time. Taking care and time for yourself is one of them. If you become worn out, than your partner who needs you will know and respond to it. The positive outlook is that we are here today, living and breathing and being with one another...the negative is that we will be alone without them. Enjoy one day at a time. Quote Link to comment Share on other sites More sharing options...
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