Guest guest Posted October 24, 2004 Report Share Posted October 24, 2004 Hi- Even though I do understand the emotional devastation you are feeling, I would suggest that you try with all your might not to let LBD take you down with it. Please try to look at the positive side of this, he is still with you. I do understand that you feel it best that he takes his last breath, yet once they are gone there is no more wishing. I know of the struggles and overwhelming pain this leaves us with, yet once our loved ones are gone, we cannot look into their eyes again and feel that bond we have always known. Please know you are being prayed for, and I am sure not only by me, but my many members of this group. There is such power in prayer. Revel in the strength you have, even if you have to dig deep to find it. My thoughts and prayers are with you this evening. Hugs- Sandie Des Moines, IA -- husband has LBD, now in nursing home I am so depressed and feel very helpless seeing my husband like this. I'm overwhelmed with sadness. He is now in a nursing home again after 6 months of hospitals due to broken hip. I had him home and it only lasted for 5 days before he fell and dislocated the hip again. I see him almost every day and feel so very sorry that his/our life has come to this. I know that there is nothing more that I can do for him. I just needed to talk to someone tonight. I pray everyday that he will just never wake up again but then it just never happens. If this continues I don't know how I'll ever manage to stay sane. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 24, 2004 Report Share Posted October 24, 2004 Pondme, I was a caregiver for my Mom who passed away in 02. So I can not relate what it means to lose a husband. I know I felt much as you do. I expect to take care of Mom until she died and when she finally consented to live with me, I really thought I had no more than a year and I would lose her.. Well, 4 years later she finally passed away. I do think the hardest part is knowing the end results of this disease and having no idea when it will end. Unfortunately you probably will stay sane and the stress will build up. Part of that stress I had was related to my thinking I knew this should be over and it was not and I had more and more problems to cope with. One of the things I did not do for for myself as much as I could have was to find a way to get some help for myself. And in the end no matter how much I did, there remained some guilt over the question of did I do enough. I would encourage you to find a support group (in person as well as here) of any kind you find helpful and go learn there are a lot of others out here doing the same thing you are doing. Do not let the disease dicate your life. (Yeah, I can say that now.) It was so hard to do at the time. You do know we have a spouse support group. Maybe they will be able to share things with more credibility. I really know when it got really bad I found a SW from the Alzheimers Association where Mom went to day care and just unloaded. Sometimes that was enough. Just knowing I was not alone took some stress off and helped me think more creatively. You are able to spend time with the long good by that some do not have. Let yourself do that. I am think of you and sending you a Big Hug and wish I could be there to help in some way. Donna R Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2004 Report Share Posted October 25, 2004 hello, my name is sharon m my husband and i caregive for my 70year old father. i understand your pain, and wish i could ease it, but you have foudn the right place for companionship, where you can vent, scream, yell, cry, laugh, share stories or whatever you wish. some of us are taking care of relatives others are taking care of spouses or signifcant other , but we all are in this together and are here for you, , since we are al scattered around the country and even the world, there isnt very often whe you dont get a response back fiarly quickly, try to keep the faith, and feel the hugs we are sending you sharon m a smile a day keeps the meanies away!!! laughter is a breath of fresh air! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2004 Report Share Posted October 25, 2004 Hi, I am very sorry to hear of your husband's condition. I am glad that you have reached out to us in your time of need. I know you are overcome by all that you have been through with your husband. Being a caregiver of a LO with so many needs is not an easy task. It is hard watching our LO's become but a shell of the person they were. Know that you have done the best that you could for your husband and that you are not alone in this. My husband has LBD. I believe he is in the beginning of the end stage. It is very hard to watch him struggle with this disease and to see him degress more and more. All that are involved with this disease struggle. It is very important that you take some time for yourself and focus on other things that you enjoy like; being with a friend, reading a book or a hobby. I know it's easier said than done, but your husband is in good hands and it sounds like you could use some time for you and your health. This is a turning point in your life and your health is very important too. Please take care of yourself. My thoughts and prayers are with you.......Jan C. in California --- pondme wrote: > > I am so depressed and feel very helpless seeing my > husband like > this. I'm overwhelmed with sadness. He is now in a > nursing home > again after 6 months of hospitals due to broken hip. > I had him home > and it only lasted for 5 days before he fell and > dislocated the hip > again. I see him almost every day and feel so very > sorry that > his/our life has come to this. I know that there is > nothing more > that I can do for him. I just needed to talk to > someone tonight. I > pray everyday that he will just never wake up again > but then it just > never happens. If this continues I don't know how > I'll ever manage > to stay sane. > > > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2004 Report Share Posted October 25, 2004 Hi, I am very sorry to hear of your husband's condition. I am glad that you have reached out to us in your time of need. I know you are overcome by all that you have been through with your husband. Being a caregiver of a LO with so many needs is not an easy task. It is hard watching our LO's become but a shell of the person they were. Know that you have done the best that you could for your husband and that you are not alone in this. My husband has LBD. I believe he is in the beginning of the end stage. It is very hard to watch him struggle with this disease and to see him degress more and more. All that are involved with this disease struggle. It is very important that you take some time for yourself and focus on other things that you enjoy like; being with a friend, reading a book or a hobby. I know it's easier said than done, but your husband is in good hands and it sounds like you could use some time for you and your health. This is a turning point in your life and your health is very important too. Please take care of yourself. My thoughts and prayers are with you.......Jan C. in California --- pondme wrote: > > I am so depressed and feel very helpless seeing my > husband like > this. I'm overwhelmed with sadness. He is now in a > nursing home > again after 6 months of hospitals due to broken hip. > I had him home > and it only lasted for 5 days before he fell and > dislocated the hip > again. I see him almost every day and feel so very > sorry that > his/our life has come to this. I know that there is > nothing more > that I can do for him. I just needed to talk to > someone tonight. I > pray everyday that he will just never wake up again > but then it just > never happens. If this continues I don't know how > I'll ever manage > to stay sane. > > > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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