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Ray is back in the nursing home now


swilkinson

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Ray is back in his nursing home again. He didn't get out of bed today as the head nurse wanted the physio to sign off on his suitability to be back in his wheelchair self-propelling again. As the conclusion at the end of his hospital stay was that he had had a bad seizure, or maybe a series of seizures he should not have to be signed off, after all there shouldn't be any significant changes to his cognition as there would be had he had a stroke - should there?

 

I found the days long in the hospital as I sat beside his bed for five or six hours each day. I like to be there to act as his interpreter. Ray cannot answer questions easily, it may take him two or three minutes to answer a simple question, if it involves thinking back more than a few hours he is not able to answer it at all. So it is easier if I am there to be his memory aid.

 

I am glad Ray is back at the nursing home but will be sad if this latest event has taken more away from him. For instance if he is not able to go in the wheelchair, or if he is not considered suitable to eat in the dining room now. It is small things like that that add to his life, being able to be where people are, where the acivities are going on, being able to join in. I put myself in his shoes and that ability to go on with some sort of life is what I would want for me.

 

A lot of people have asked me if I am getting used to being alone now Ray is in a nursing home. You call that a SNF and it is officially an Aged Care Facility here but you all know what I mean.

 

The answer is "no" - I am not getting used to being alone. Just as Ray, like everyone who goes into full-time care, wants to "go home", I want and NEED him to be here. However I do know that the Ray I would want home is not the Ray that is in a nursing home needing three people to get him showered and changed but the Ray from some years ago who could walk, converse, laugh at a joke, and generally enjoy life.I put him into the NH because of all the changes and difficulty of one person handling him and that will not change with time.

 

I know we all to some extent live in denial. I too have thought "this will never happen to us". I am posting this in the hope that some of you will look ahead and see that some day you may be in the same position I am in and in some ways prepare for it and others may see how fortunate they are not to be in the same position as yet and be thankful for the companionship they can still enjoy with their partner/loved one.

 

I guess as the time stretches out I will get used to the routine of going to the nursing home and back, fitting in life around the visits to Ray. I know that he will eventually settle down and remember little from the many years he lived here with me. I try not to be sad about that.

 

I know in order to keep friends now I need to alter my lifestyle. For so many years it has been "Ray and his carer/wife Sue". Now it is just Sue here and Ray in a nursing home so I need to learn to relate in a different way. Maybe I need to change my mindset and find some new things to do or return to old hobbies I dropped because I took up Ray's care. It scares me sometimes that this living without my husband of 43 years is the way it is going to be for a long time into the future. I guess it is this sense of "aloneness" that makes it so difficult to accept.

 

Here on my piece of the lovely Central Cost we have a lot of nursing home complexes, in some cases accompanied by self-care and hostel type residentials. There are a lot of people like me still living in a home once full of family and friends and buzzing with life. I am not unique, just new to being one of this vast number of mostly separated women facing changes in their lives. Does this thought scare me? Not really, just reminds me that life evolves and somehow we all have to live with that.

 

So Ray is back in the nursing home and the visiting there will hopefully become routine for me. It will be do some chores, visit Ray, come home and have some late lunch, do some chores, dinner and whatever the evening brings. I guess it can be a good life. As long as I can ensure it is not a sad and lonely one I should be okay.

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Sue, When Dick first moved into the nursing home I too blogged with the hope that it would help someone someday. At that time it was very hard to find support from others who had gone through the same struggles and I think it is still true. I hope your message reaches many. You have a good sense of what your mindset should be. Of course we both know that time is what it takes to adjust to each change stroke and dementia brings to our lives. When Dick left the house I still had a couple children living at home. As of a couple weeks ago the youngest moved out so I am learning the role of living alone with you. Mostly it is good but there is times when that ache still comes back longing for what we once had. I find that my cats bring a lot of comfort just from the companionship they give. Of course they are a big responsibility but not as much work as dogs. If you like animals bringing a rescued animal into your home just might help. Then I keep busy with building contacts outside my home. Since we moved here just after Dick's strokes, I have had not chance to build a social network so I am starting from the ground up. Yes, time will help bring a nomalacy to our lives again. It is nice to have some encouragement in the interim though.

Ruth

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Sue, Even though I know that someday, I will be in the same position you are in now, visiting Dan in a nursing home. I was so close to it earlier this year that I came to accept it for what it is. However, I know that in some ways I am still in denial. I know how difficult it is for you, it's hard sitting by their bed for hours and then coming home to an empty house. It can and will be a good life for you, it will take time to get used to it all.

 

Thank you for sharing your thoughts and feelings with all of us.

 

Hugs, Mary Jo

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My situation is much different but then again similar. I am the stroke survivor and Jerry passed away Oct. 23, 2011, of lung cancer. It was a shock as he was in great condition and it was diagnosed just 3 months & 3 weeks before he passed. I am the one who is alone now, although I am fortunate enough to have a caregiver to help me out 8 hours a day. I stumble through the rest of the day myself and so far it's just okay. My caregiver drives me to therapy, does grocery shopping laundry, changes my bed and other things I'm unable to do. I feel I'll be improved enough to drive sooner or later and I am not looking forward to the real alone I'll be sometime soon. I'm scared and sad and miss Jerry so much. Sue you are a wonderful inspiration; I'm glad you have family around. We had no children and my sisters live in different states. My friends have helped immensely but I do isolate by necessity. I always pray for all the stroke survivors and caregivers and I will keep doing that. God Bless you all. He is how I survive each day. God is my refuge. Leah

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