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Hi again Barb,

I became a CNA in 1980 and was heading into nursing school. You have just

flashed me back to that time in my life. I jumped the following year and

got an engineering degree! I wanted a career with less heartbreak that was

not so physically taxing. I agree: good nurses aides are gold.

Anne

At 07:17 AM 9/4/2002 +0000, you wrote:

>

> >Can any one tell me about how many patients a NH nurse or aide has

> >to look after in a shift? I mean, clean, dress, feed and ETC.

> >That would be interesting.

>

>, I worked as a nurses aide for about 6 years, and then for 10

>years I worked in the nursing home in the accounting department...I

>worked on the Alzheimers wing and loved it. Why did I go to an

>office job, because of the work. You are right it is unbelivable

>what is expected of the nursing staff but especially the aids. The

>ideal number is suppose to be anywhere from 6 to 8 residents per

>aid. The reality is usually 8 to 12, because of aids calling in sick

>or time off or just being short staffed.

>

>The day shift starts the morning by making sure everybody on her list

>is up. One at a time you go in and get them up, toileted, washed up,

>teeth brushed, dressed and if they are in a wheelchair you put them

>out into the hall until someone can take them to the dinning room.

>If they are mobile you get them started in the right direction. If

>they need total care you wash them up in bed and get them dressed

>then up, if they are a two person transfer you have to find someone

>to help you...good luck on that one. O yea unless the nursing home

>has someone to come in and make the beds you are also expected to

>have the room cleaned and beds made. Showers/baths are given on a

>rotating schedule and if you are lucky you work for a home that has a

>bath team, otherwise you save your bath people for last. Okay your

>fist two hours is gone and now it is breakfast, everybody that can be

>spared is in the dinning room helping to feed the residents that need

>help. Some people are easy to feed, you deal with them first. Other

>residents have to be coaxed to eat (with one lady we use to give her

>an m & m for every bite she took). If you are a good aid you don't just

>sit there and shove food into their mouths...it is my personal

>opinion that shoving food is the reason some of the residents quit

>eating. This is all done in approximately the first 3 to 4 hours of

>the day. Some other time if you want I will talk about the other 20

>hours...it doesn't get any easier. But for all of that for the right

>people it is a very satisfying job. The evening shift has fewer

>staff as after dinner residents start going to bed and it isn't as

>hectic. The night shift (it is not refered to as graveyard shift in a

>nh) have even fewer staff as they just make rounds during the night,

>some of the residents will be wandering but mostly you answer lights,

>on every floor but the alz. floor, toilet, change, turn residents

>that can't turn themselves. By the time you compleat your rounds it

>is time to start over. " O " I forgot at the end of your shift you have

>to leave enough time to chart everything that needs to be charted for

>the day. Fun huh! Now ask yourself why do they do it, it certainly

>isn't because of the high wages. I am worn out just writing about

>it. God Bless all good nusing aids. Barb

>

>

>

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Barb, thanks for the reply. It was very detailed and interesting. I was not

trying to judge any one. I would like to say taking care of just one person can

be taxing. Just think taking care of 6-12 people! Like you said the pay is not

very good, very hard work. We will always have very good and caring nurses,

aides. Of course there will be those that just put in the time. The Aide that

helps us said she had 15 patients to care for. Also they had to turn the

bedridden patients every two hours. Not much sleep for the patient.

Thanks again,

Re: (subject changed)

>Can any one tell me about how many patients a NH nurse or aide has

>to look after in a shift? I mean, clean, dress, feed and ETC.

>That would be interesting.

, I worked as a nurses aide for about 6 years, and then for 10

years I worked in the nursing home in the accounting department...I

worked on the Alzheimers wing and loved it. Why did I go to an

office job, because of the work. You are right it is unbelivable

what is expected of the nursing staff but especially the aids. The

ideal number is suppose to be anywhere from 6 to 8 residents per

aid. The reality is usually 8 to 12, because of aids calling in sick

or time off or just being short staffed.

The day shift starts the morning by making sure everybody on her list

is up. One at a time you go in and get them up, toileted, washed up,

teeth brushed, dressed and if they are in a wheelchair you put them

out into the hall until someone can take them to the dinning room.

If they are mobile you get them started in the right direction. If

they need total care you wash them up in bed and get them dressed

then up, if they are a two person transfer you have to find someone

to help you...good luck on that one. O yea unless the nursing home

has someone to come in and make the beds you are also expected to

have the room cleaned and beds made. Showers/baths are given on a

rotating schedule and if you are lucky you work for a home that has a

bath team, otherwise you save your bath people for last. Okay your

fist two hours is gone and now it is breakfast, everybody that can be

spared is in the dinning room helping to feed the residents that need

help. Some people are easy to feed, you deal with them first. Other

residents have to be coaxed to eat (with one lady we use to give her

an m & m for every bite she took). If you are a good aid you don't just

sit there and shove food into their mouths...it is my personal

opinion that shoving food is the reason some of the residents quit

eating. This is all done in approximately the first 3 to 4 hours of

the day. Some other time if you want I will talk about the other 20

hours...it doesn't get any easier. But for all of that for the right

people it is a very satisfying job. The evening shift has fewer

staff as after dinner residents start going to bed and it isn't as

hectic. The night shift (it is not refered to as graveyard shift in a

nh) have even fewer staff as they just make rounds during the night,

some of the residents will be wandering but mostly you answer lights,

on every floor but the alz. floor, toilet, change, turn residents

that can't turn themselves. By the time you compleat your rounds it

is time to start over. " O " I forgot at the end of your shift you have

to leave enough time to chart everything that needs to be charted for

the day. Fun huh! Now ask yourself why do they do it, it certainly

isn't because of the high wages. I am worn out just writing about

it. God Bless all good nusing aids. Barb

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Barb

Thank you for asking about my dad. I did put in a post earlier that he

is being transferred back to the hospital. My only problem with that is

they can't " fix " him. Of course, as a group, we all know the LBD person

can't be fixed, just loved and cared for.

I haven't been doing real well. Have been having some strange feelings

lately...bright lights in my right eye, light headed, sick to my

stomach, migraines, hot flashes...the list goes on. I made a dr. appt.

yesterday and today had to go back for glucose screening. Showed some

low blood sugars so we are going to try to balance it with diet. Now,

tomorrow I need to call the dr. back for any further testing.

I truly appreciate your thoughts and concerns for my dad and myself. It

is wonderfully comforting to know this group exists and so many people

care.

Sandie

Des Moines, IA

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Hi Sandy. I am sorry to hear about you and your Dad. I must have missed

your post about your Dad going back. Do you think they are admitting him

due to " behavior " , or do they feel he may have some actual " medical "

concerns?

I too have suffered from light headedness, dizzy spells, and not feeling

" par " . I did notice my hemoglobin was down, so I am taking some iron which

has provided some relief. Anemia often is a problem when fatigue and light

headedness are present.

I hope the doctors fix you up and you start feeling better. Please make

sure to insist on a full blood work up, hormone work up, and they may want

to run an H-Pylori test (bacteria in the stomach, makes you feel nauseas).

Good luck and keep us posted. I will keep you on my ever growing prayer

list!

Re: Re: (subject changed)

Barb

Thank you for asking about my dad. I did put in a post earlier that he

is being transferred back to the hospital. My only problem with that is

they can't " fix " him. Of course, as a group, we all know the LBD person

can't be fixed, just loved and cared for.

I haven't been doing real well. Have been having some strange feelings

lately...bright lights in my right eye, light headed, sick to my

stomach, migraines, hot flashes...the list goes on. I made a dr. appt.

yesterday and today had to go back for glucose screening. Showed some

low blood sugars so we are going to try to balance it with diet. Now,

tomorrow I need to call the dr. back for any further testing.

I truly appreciate your thoughts and concerns for my dad and myself. It

is wonderfully comforting to know this group exists and so many people

care.

Sandie

Des Moines, IA

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Thank you for your thoughts, prayers, and concerns. The nh said my dad

was aggressive and striking out at people. Of course when I asked if he

has been taking his meds., again, no he hasn't. I just don't understand

why some people have such a terrible time giving dad his meds. My

opinion is...it is all in the approach.

So far my doctor found I have been experiencing hypoglycemia (sp). And,

since the test I have not experienced any light headed feelings. My

head is pounding, as my family is prone to migraines. I am sure stress

has something to do with how I am feeling too.

Anyway, you are such a thoughtful and caring person. I really

appreciate how you reach out to people! Thank you!

Sandie

Des Moines, IA

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Hi Sandie,

Watch that hypglycemia. Make sure you are eating small meals and snacks

frequently....and low in sugar. The worst thing you can do is fast for a

prolonged period of time and then in a quest for a boost of energy,

drink a sugary soda or have a snack high in sugar. This spikes your

sugar way up and when it goes back down, it reaches levels lower than

before you craved the energy and had the sugary snack. The danger here

is that you can faint....(and hurt yourself.) I was hypoglycemic but

have been able to keep it under control by watching sugar and eating

very small meals several times a day. Your hypoglycemia could also be

causing your headaches. I was having that problem too until I changed my

diet.

Don't forget to take care of YOU! I hope that you are feeling better!

sanclown@... wrote:

>

> Thank you for your thoughts, prayers, and concerns. The nh said my dad

> was aggressive and striking out at people. Of course when I asked if he

> has been taking his meds., again, no he hasn't. I just don't understand

> why some people have such a terrible time giving dad his meds. My

> opinion is...it is all in the approach.

>

> So far my doctor found I have been experiencing hypoglycemia (sp). And,

> since the test I have not experienced any light headed feelings. My

> head is pounding, as my family is prone to migraines. I am sure stress

> has something to do with how I am feeling too.

>

> Anyway, you are such a thoughtful and caring person. I really

> appreciate how you reach out to people! Thank you!

> Sandie

> Des Moines, IA

>

>

>

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Hi Sandie. I read an article in a medical journal detailing the effect of

stress on our bodies. It is amazing what an effect it can have. When you

are stressed, apparently one hormone is released which can actually cause

weight gain along with other more serious effects (nausea, stomach & bowel

problems, headache, muscle spasms, higher cholesterol....). The list was

huge! They say regular exercise can alleviate a lot of the stress we feel,

but I find it hard to find the time to fit it all in (working full time,

kids, bills, house....).

Well, I agree with you on approach. My SIL () is also a big

" approach " believer. I hope they try the " re-approach " method too. What do

they expect from him if they are not administering meds consistently? You

and your Dad have been through so much lately that I will be praying for a

good spell to come soon for your father.

Take care of yourself. As for my being a thoughtful person, well, what is

that saying? Takes one to know one?!!!! You take care Sandie!

RE: Re: (subject changed)

Thank you for your thoughts, prayers, and concerns. The nh said my dad

was aggressive and striking out at people. Of course when I asked if he

has been taking his meds., again, no he hasn't. I just don't understand

why some people have such a terrible time giving dad his meds. My

opinion is...it is all in the approach.

So far my doctor found I have been experiencing hypoglycemia (sp). And,

since the test I have not experienced any light headed feelings. My

head is pounding, as my family is prone to migraines. I am sure stress

has something to do with how I am feeling too.

Anyway, you are such a thoughtful and caring person. I really

appreciate how you reach out to people! Thank you!

Sandie

Des Moines, IA

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Sandie,

I agree with you regarding the medicines and approach. Mom's meds they crush

and put in applesauce. I bought in some of those individual puddings,

chocolate, for them to use too, especially when Mom maybe agitated. One of

the nurse's likes to use strawberry ice cream to mix in the meds. They also

call her by name first and then tell her they have her medicine for her, what

they have mixed in with and ask her to open up to take it. When Mom was in

the hospital they used similar methods.

I bought in the chocolate pudding because I think it mask the taste of the

meds better.

At the one NH that Mom was in for two days, they said that she wouldn't take

her meds. I think it was the way they approached her.

There has been a few times when Mom has spit her meds back out, but I think

that is to be expected with this disease!

I really think she has a bug right now too. She has been feverish, had

diarrhea once yesterday and today (to the best of my knowledge) has been

drinking a lot, not eating off and on (the 7-3 nurse told me she fed Mom one

of the puddings this morning because she wouldn't eat her breakfast. She ate

the pudding! She also drank her fluids.) The mumbling and growling wasn't

there today. She was actually able to talk fairly clear today.

I'm a little frustrated because I don't feel that the staff was as concerned

about this as they should have been. I called Mom's doctor to report what I

was seeing and he was going to follow up on it.

They have to remember that one size doesn't fit all. They are still

individuals regardless of whatever reason has them in the NH.

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Sandie,

I agree with you regarding the medicines and approach. Mom's meds they crush

and put in applesauce. I bought in some of those individual puddings,

chocolate, for them to use too, especially when Mom maybe agitated. One of

the nurse's likes to use strawberry ice cream to mix in the meds. They also

call her by name first and then tell her they have her medicine for her, what

they have mixed in with and ask her to open up to take it. When Mom was in

the hospital they used similar methods.

I bought in the chocolate pudding because I think it mask the taste of the

meds better.

At the one NH that Mom was in for two days, they said that she wouldn't take

her meds. I think it was the way they approached her.

There has been a few times when Mom has spit her meds back out, but I think

that is to be expected with this disease!

I really think she has a bug right now too. She has been feverish, had

diarrhea once yesterday and today (to the best of my knowledge) has been

drinking a lot, not eating off and on (the 7-3 nurse told me she fed Mom one

of the puddings this morning because she wouldn't eat her breakfast. She ate

the pudding! She also drank her fluids.) The mumbling and growling wasn't

there today. She was actually able to talk fairly clear today.

I'm a little frustrated because I don't feel that the staff was as concerned

about this as they should have been. I called Mom's doctor to report what I

was seeing and he was going to follow up on it.

They have to remember that one size doesn't fit all. They are still

individuals regardless of whatever reason has them in the NH.

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Sandi,

Dear dear girl, What will you face next!!!!! Have you started your search on

a new facility yet? I have heard good things about a facility in Indianola

that has a special unit for Alz. and know of two families who have used it

for Alz parents and were very happy there. I just found out that my dads

brother is there as well. He has Parkinson's. If I can be of any help let me

know. Thinking about you!!!

Debbie Curtis

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Thank you for this helpful information concerning hyperglycemia. I need

all the help I can get with this newfound health problem I am facing.

As for my dad...to the group...new news. He is still at the hospital,

(adult psychiatric unit) and when I talked to the nh yesterday, the

assistant director of nursing told me a letter is being sent to me

stating dads involuntary discharge. In other terms, the nh is giving

him 30 days to be placed elsewhere. Just spoke to the social worker at

the hospital, even they feel lied to. Anyway, in a nutshell, I am

looking for another nh for my dad to live.

Sandie

Des Moines, IA

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Thank you for this helpful information concerning hyperglycemia. I need

all the help I can get with this newfound health problem I am facing.

As for my dad...to the group...new news. He is still at the hospital,

(adult psychiatric unit) and when I talked to the nh yesterday, the

assistant director of nursing told me a letter is being sent to me

stating dads involuntary discharge. In other terms, the nh is giving

him 30 days to be placed elsewhere. Just spoke to the social worker at

the hospital, even they feel lied to. Anyway, in a nutshell, I am

looking for another nh for my dad to live.

Sandie

Des Moines, IA

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Sandie,

How devastating. I am so sorry to hear this. Did you by chance have a

" back up " facility in mind? Was he in a " dementia " unit or a " cognitively

Impaired " unit? I wish you the best in searching for a better place for

him. In a way, maybe some good could come from this? If you start

somewhere else, you can kind of train them how to do things for him now that

you know what works and what doesn't. Giving them all the " reading "

material so the new place can have a full understanding of what your Dad

has. Who know, maybe the next place will have better staff too. Extra

prayers going your way.

Keep us posted.

Re: Re: (subject changed)

Thank you for this helpful information concerning hyperglycemia. I need

all the help I can get with this newfound health problem I am facing.

As for my dad...to the group...new news. He is still at the hospital,

(adult psychiatric unit) and when I talked to the nh yesterday, the

assistant director of nursing told me a letter is being sent to me

stating dads involuntary discharge. In other terms, the nh is giving

him 30 days to be placed elsewhere. Just spoke to the social worker at

the hospital, even they feel lied to. Anyway, in a nutshell, I am

looking for another nh for my dad to live.

Sandie

Des Moines, IA

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Dad was in the Alzheimers Unit of the nh. When telling people of the

change, I word it as having liked knowing there was change coming

instead of being smacked upside the head with the news. Now that the

news has had time to settle, I agree, there has to be good coming out of

this. I am hopeful a different facility can give better care. In fact,

I learned last evening late, that the administrator, 4 one in 2 1/2 yrs,

resigned. Hmmm, makes me think there is a lot of chaos at the nh. I

really don't want my dad to go back, even if it were a choice. Thank

you for all of your kind thoughts and words. I appreciate the support.

Sandie

Des Moines, IA

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Dad was in the Alzheimers Unit of the nh. When telling people of the

change, I word it as having liked knowing there was change coming

instead of being smacked upside the head with the news. Now that the

news has had time to settle, I agree, there has to be good coming out of

this. I am hopeful a different facility can give better care. In fact,

I learned last evening late, that the administrator, 4 one in 2 1/2 yrs,

resigned. Hmmm, makes me think there is a lot of chaos at the nh. I

really don't want my dad to go back, even if it were a choice. Thank

you for all of your kind thoughts and words. I appreciate the support.

Sandie

Des Moines, IA

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Sandie, so sorry to see that NH problems continue with your dad. I hope

there is a quick solution out there. The same goes with your health issues -

the sooner resolved the better.

Cheryl

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Sandie, so sorry to see that NH problems continue with your dad. I hope

there is a quick solution out there. The same goes with your health issues -

the sooner resolved the better.

Cheryl

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Wow Sandie. The 4th administrator in 2 1/2 years???!! That speaks volumes.

You know, you would think Alzheimer's units are usually well versed in

handling patients experiencing " agitated " moments wouldn't you? Well, on to

better places! Good luck!

RE: Re: (subject changed)

Dad was in the Alzheimers Unit of the nh. When telling people of the

change, I word it as having liked knowing there was change coming

instead of being smacked upside the head with the news. Now that the

news has had time to settle, I agree, there has to be good coming out of

this. I am hopeful a different facility can give better care. In fact,

I learned last evening late, that the administrator, 4 one in 2 1/2 yrs,

resigned. Hmmm, makes me think there is a lot of chaos at the nh. I

really don't want my dad to go back, even if it were a choice. Thank

you for all of your kind thoughts and words. I appreciate the support.

Sandie

Des Moines, IA

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Wow Sandie. The 4th administrator in 2 1/2 years???!! That speaks volumes.

You know, you would think Alzheimer's units are usually well versed in

handling patients experiencing " agitated " moments wouldn't you? Well, on to

better places! Good luck!

RE: Re: (subject changed)

Dad was in the Alzheimers Unit of the nh. When telling people of the

change, I word it as having liked knowing there was change coming

instead of being smacked upside the head with the news. Now that the

news has had time to settle, I agree, there has to be good coming out of

this. I am hopeful a different facility can give better care. In fact,

I learned last evening late, that the administrator, 4 one in 2 1/2 yrs,

resigned. Hmmm, makes me think there is a lot of chaos at the nh. I

really don't want my dad to go back, even if it were a choice. Thank

you for all of your kind thoughts and words. I appreciate the support.

Sandie

Des Moines, IA

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Sandie,

I truly wish you luck in finding a sutible above your best expetations,

place for your Dad to live. I have been praying extra hard lately and it

seems to be working. I will pray extra hard for you and everyone. Shirley

_________________________________________________________________

Chat with friends online, try MSN Messenger: http://messenger.msn.com

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Thank you for the continued support and prayers. I believe my dad is in

much need of all prayers right now. This truly helps knowing many

people are praying for him.

Sandie

Des Moines, IA

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Thank you for the vitamin information.

I too will look into getting started on the vitamin E. With dad having two

brothers, one passed away from a heart attack and had some kind of dementia

and the other brother having Parkinson's. My dad has both (LBD). My odds do

not look very good. I worry about it skipping a generation in My family and

my children possibly being a target for one or both of these diseases.

Sandi,

I find it interesting that your dads brother has Parkinson's. Call me if you

need to unload to someone who understands and can lend an ear. Thinking about

you.

Debbie Curtis

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