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Re: Kathy

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Peg,

My mom also has some parkinson like symptoms. She has a shuffling gait at

times, and her hand shakes but not all the time.We will find out more next dr.'s

visit as she will also see the physiotherapist who will observe her walk. It is

funny how sometimes she walks quite fast even without her walker (last time it

was when she was in hallucination mode), but when she seemed more mentally

stable she is slower than a turtle even with her walker. The worst part is, as

I slow down so she can catch up to me, it seems to signal her to slow down as

well, sometimes she has actually stopped and I have had to ask her what are you

doing? I find that if I guide her a bit with the walker, she does a bit better

and I don't feel like I am leading her in some cruel race to the finish line.

Kath

Welcome Kathy

>

>

>

> Hi Kathy,

>

> Was just reading your post in LBDcaregivers and saw that you are

from Ontario as well. I live in Stoney Creek, just outside

Hamilton. My mother was diagnosed with LBD about 3 years ago though

symptoms date further back than that. She too was moved to a

retirement home since she was still able to care for herself and was

mobile. She spent a short time in the hospital and we moved here

from there to the retirement home. From day one, she was resistent

to moving there and wanted to be in her own home insisting that she

could take care of herself. We knew this would not be possible for

her own safety. We always told her that she had to be there for her

own safety and that nurses were always available when she needed them.

>

> We brought things from her home to make her room more habitable

but she always told us that we shouldn't bring things there because

she wasn't staying, so we just gradually brought things in for her.

With her home, we began to clean out things she had hoarded for so

long and got rid of things slowly, hoping that one day she would be

able to " visit " her home and most everything would appear the same to

her.

>

> I hope that you can keep your mother close to you because I know

that frequent visits make quite a bit of difference to them.

Fortunately, the only thing that mom found good in this home were the

meals........Being an excellent cook herself, she congratulated them

on their meals and claimed the chef was excellent. At least we knew

she enjoyed the food even though her appetite had greatly

diminished. I understand what you are saying about the Taj Mahal,

but be assured that she is at least getting her meds when needed. I

know that was a problem when mom lived alone. Routine, at least kept

the hallucinations down with consistent dosages by the nurses.

>

> My mom too had limited vision which prevented her from doing so

much. She would only attend craft sessions if we took her and that

was not always possible. The volunteer that ran the program always

found things that she could do with her limited eyesite. It really

helped when a nurse of someone else would come to get her as she

tended to isolate herself in her room. The dining room was mainly

where her socialization came though she had been quite social before

this. She always said.......all those old people do is talk about

each other.........lol..........and here she was at 85 (or course,

not one of those old people).

>

> Kathy, I am so sorry to hear about the operation and resultant

fall with your mother. I know what you are going through.......have

been there!! Hopefully, time will help with that.

>

> Just be there for your mother, knowing that the home will keep

her safe. Don't feel guilty, as I did, because her condition

requires someone there constantly for her. My mom was in the

retirement home for 6 months, and never adapted to being there. She

passed away on Oct. 28th from a bowel obstruction and complications

from that. Just be there, love her, and keep on top of all

medications they give her. People in this group know so much about

medications, and what works for one, doesn't for another. During the

last 2 days in the hospital, my mom told us all the she was in her

own house and I am sure that was a good thought for her...........

>

>

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> ---------------------------------

> Post your free ad now! Yahoo! Canada Personals

>

>

>

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  • 6 years later...

************************

I am also looking into having her tested regarding her test-taking

ability; it's

abysmal! She'd be a straight A student if not for her test grades.

************************

Debbie, are her tests timed? Just curious. Josh used to have a

meltdown if he was timed. Yet, if he wasn't, he would do fine, and

most often would literally do it in half the time allowed. Just the

idea of being timed would send him into a tailspin.

BJ

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No, she doesn't have a 504 plan. I talked to the psych about it today and we

will go further with it when we are in the therapists office next week.

It is interesting what you said about having the assignments done, but not

wanting to walk past the contamination. Also, what you said about her wanting to

handle it on her own.

I think Joei may have some contamination issues and other things starting up.

The problem is, she is not communicating well with me. Nor is she communicating

with the doctors. Everytime the psych would ask her questions today she would

say things were fine or good. GRRRRRRRRRRRR So I have to chime in with my

observations. It would be nice if the darn kid would back me  up though!

We have had some good successes lately, but I also have that " gut " feeling that

we are in for a real doozy here soon. Somethings brewing, I just can't put my

finger on it yet. I'm going to get some time alone with the therapist next week

to see if I can't get some help from her in learning to get Joei to communicate

better. Joei is a stubborn girl and very closeminded as well. lol It does not

make advocating for her very easy.

________________________________

To:

Sent: Wednesday, January 14, 2009 6:22:25 AM

Subject: Kathy

Sorry you had such a bad night with Joie; aren't kids hard enough without having

to deal with OCD, for goodness sake?!

I sympathize with you on the missed assignment scenario; last semester,

missed so many assignments and here's the kicker; she had them done, but

wouldn't turn them in! Why, you might ask? Because she couldn't bring herself to

walk past all the other students (and their contaminated shoes) to put her work

in the turn-in basket on the teacher's desk. Of course, the teachers did not

tell me of the missed assignments, I only found out because we have online

access to our school, so I can look up the kids grades and homework anytime. So

I constantly found myself backtracking and basically trying to save her butt by

asking the teachers to let her turn in her homework late to get at least some

credit! We did finally get all the teachers on board letting her turn in stuff

before or after class or even moving her desk close to the turn-in basket! She

has a 504 plan, but it took some prodding to get all the teachers to actively

put it into play. Part of

the problem is , at 14 and a half, wants to be independent and handle

this " on her own " ; sometimes she resists the accommodations and doesn't want to

admit she needs them.

I am also looking into having her tested regarding her test-taking ability; it's

abysmal! She'd be a straight A student if not for her test grades.

I forget, does Joie have a 504 plan? If not, I would highly recommend it. And if

she does, perhaps another meeting with all her teachers with your concerns

outlined might help.

Thinking of you!

Debbie

http://twochinadoll s.blogspot. com

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