How can I get rid of my community aids?

Page 2 of 2 [ 24 posts ]  Go to page Previous  1, 2

somanyspoons
Veteran
Veteran

Joined: 3 Jun 2016
Age: 49
Gender: Male
Posts: 995

26 Nov 2016, 11:13 am

K_Kelly wrote:
What exactly do I tell the case manager? What do I need to bring up? I'm afraid of not being able to address all my needs and wants because I just have trouble expressing them verbally, or even in writing sometimes.

I do live in the US, and I am not in school anymore.


So those are really good questions. I do suggest writing things down and giving them to the people in charge. It is too hard to verbalize something in the moment, in my experience. It's especially hard when you are anxious.

Why not use wrongplant to help you put into words what your concerns are? Lots of people here would be happy to help you.

Here are some words you can use. Feel free to change them if you need to:

I don't know why the aids are taking me out of the house. I understand that my parents think I should get out more, but I don't think I should be getting out for no reason at all. I want to be independent and to live on my own someday. But I don't want to be doing things with community aids that don't work on these goals.

Here are things that I am interested in learning to do with my community aids:
1)
2)
3)

I also need my aids to be trained better in recognizing sensory overload and helping me when it starts. They are not being helpful and it is causing me increased anxiety. Every aid who comes to my house needs to understand autism and triggers, and right now, I'm not seeing evidence that this is so. Here are the things they have done that triggered my anxiety:

1)
2)
3)


So, I have no idea what you would want to write under 1,2 +3. That's just a model. If you want, you can just talk about your complaints here and we can help you organize your thoughts. But you should also be able to just send a complaint email to the case manager and have them help you figure out what kind of help you need.



Campin_Cat
Veteran
Veteran

User avatar

Joined: 6 May 2014
Age: 63
Gender: Female
Posts: 25,953
Location: Baltimore, Maryland, U.S.A.

26 Nov 2016, 9:18 pm

somanyspoons and Campin_Cat wrote:
OK. I worked in this field for 20 years. That's really bad advice.

Okay, I've LIVED "in this field" (meaning, as a client), for over the last 18 years----and, surely, you realize the way a professional experiences this field, is quite different from the way a client, experiences this field. Also, I really think the way one professional relates to another (or, TELLS another how they relate to a client), is quite different from the way they relate to a client.

Your case manager is not the enemy. This isn't high school. You aren't tattling. It is normal to talk to the case manager. This is what it is to be a grown up. The case manager is in charge of training and dispatching the aids. Its is up to them to make sure that they are doing their jobs -not you

I never even came CLOSE to suggesting a case manager is an enemy----and, it IS "tattling", where I come-from. If, at the times I've had caseworkers / managers (and, the times that I've dealt with them, in regard to MY client, as a Home Health Aide), if I would've gone over a caseworker's head to the case manager, I would've REALLY paid for it!! The only time I would, PERSONALLY, even THINK of speaking directly to a case manager, is if I was in an IEP meeting (or, whatever that plan's called), and the caseworker(s) was hearing what I was saying, at the same time, I was saying it (and, not getting it second-hand, where it can misconstrued); OR, only AFTER I've talked to the caseworker(s), to no avail.

It IS up-to-me, as a client, where I come-from, to make-sure they're doing their job, in regard to my needs being met----AND, when I have a client, I make-sure that what they want, is related to the caseworker (which, is how it was PREFERRED, where I am, because they only want to make-time for my "concise translation" of what the client wants, because the clients do so much hemming and hawing, and changing their mind). I, and many others, "in the system" (as a client), don't have alot of trust for alot of medical / psychological / whatever professionals, because they're all-the-time making decisions based-on what they've read in a BOOK----or, because most clients seem-to want certain things, so they just mark EVERYBODY down, for the same things. It has not been a rare thing, to have to work, really hard, to get a professional to listen to a client (OR, a Home Health Aide). IMO, one's well-being should NEVER be left, SOLELY, up to a caseworker / manager, and that a client should have a say, as much as a client is capable of saying.


What Cat is suggesting would be continuing to argue with people who have no power to change anything. Aids simply carry out orders. They do not make the goals you are working on. They do not get to decide if you go out or why. Further more, since they are the ones who are going to be interacting with you every day, you really don't want to be arguing with them at all. Trust that your case manager has seen this dozen of times. They deal with these kinds of issues every day. He or she will not be shocked and you are not going to seen as some kind of traitor for talking to them.

How can one "continue to argue", when, as-far-as-WE-know, K_Kelly has never even spoken to them, regarding his desires (let-alone, "argue"----and, who said anything about arguing, anyway; my suggestions, were for TALKING).

As for Aides "simply carry out orders": What I was suggesting to him----and, at least, PART of what he seemed to be saying----was that the Aides don't seem to be taking his feelings into consideration (like, in the way they talk to / treat him). I AGREE that a case manager makes the decisions, in what he DOES (like, whether or not he goes into the community, and what he does in the community), but that's not what I was addressing.

Also, again, case managers are NOT to be trusted, IMO, just willy-nilly (at least, not until a rapport has been established----and, IMO, that has not yet occurred with K_Kelly as he has been, seemingly, letting everybody else make decisions, FOR him)----and, your saying that they have "seen this dozen of times", is one of the reasons, WHY. IMO, case managers need to give MORE consideration, to the INDIVIDUAL----and, NOT, as I said before, just treat everybody the same (ESPECIALLY, if not all of their clients are ASDers).



Wow, somanyspoons, I don't think I've ever seen you, seemingly, not properly read / misconstrue a post (mine or anybody's), so badly----nor, post a, seemingly, purely, emotionally-driven response.




_________________
White female; age 59; diagnosed Aspie.
I use caps for emphasis----I'm NOT angry or shouting. I use caps like others use italics, underline, or bold.
"What we know is a drop; what we don't know, is an ocean." (Sir Isaac Newton)


somanyspoons
Veteran
Veteran

Joined: 3 Jun 2016
Age: 49
Gender: Male
Posts: 995

26 Nov 2016, 9:31 pm

Well, I can't really read you're response because that way of breaking up the post and responding piece by piece is not accessible to me. I can't process it. Also, the bold purple makes my eyes swim.

If you want to get an emotional response from me, a great way is to tell a younger person to do something that I see as destructive. I do get really emotional about that.

He's just starting out. Putting him in a position to get in conflicts with his caregivers seems mean to me, although I don't think you really meant it to be that way. The affect is the same. You have to talk to the people in power, and that is not the community-aid.



Campin_Cat
Veteran
Veteran

User avatar

Joined: 6 May 2014
Age: 63
Gender: Female
Posts: 25,953
Location: Baltimore, Maryland, U.S.A.

26 Nov 2016, 11:39 pm

^^ It has NOT been destructive, in my experience----I would never, in a million years, make the suggestions I have made, if they had been destructive, in my experience.

It would NOT, IMO, put him in a situation to get into conflicts with his caregivers----again, going-by my experiences; so, it certainly was NOT a mean thing to suggest to him.

Also, since I have HAD community aides (as you call them), and BEEN a community aide, they ARE in a position of power, when it comes-to the consideration of his feelings (again, the way they talk to / treat him). You seem insistent on ignoring that that's what I said I was addressing. Do you really think that if someone told their "community aide" that they wanted them to consider their feelings, more, that the Aide would say: "Wait, I need to get direction / a decision from my boss, on that"?

Now, unfortunately, K_Kelly is probably going to feel even more confused than ever, and have to start from scratch, figuring-out what to do, because, for some reason, you seem to have taken offense to my posts (aside from seeing my suggestions, as being destructive for him), and made terribly matter-of-fact statements regarding things that I wrote, that you don't seem to have read, well.




_________________
White female; age 59; diagnosed Aspie.
I use caps for emphasis----I'm NOT angry or shouting. I use caps like others use italics, underline, or bold.
"What we know is a drop; what we don't know, is an ocean." (Sir Isaac Newton)


Campin_Cat
Veteran
Veteran

User avatar

Joined: 6 May 2014
Age: 63
Gender: Female
Posts: 25,953
Location: Baltimore, Maryland, U.S.A.

27 Nov 2016, 12:47 am

I just re-read through this thread, and now I'm thinking that you took offense to me telling K_Kelly that I would NOT suggest going to his case manager, INTIALLY; and, I'm thinking that you didn't like that, because it was in disagreement with what YOU told him he should do. If that's why you responded to me the way you you did, all I've got to say, is: "Wow".

(Funny thing IS, I didn't even know that you had told him that----I wondered where he got "case manager", from. When I clicked on the tab, that was this thread, it opened to his post where he was asking what he should say to his case manager, so I figured I had read everything, up-to that point.)






_________________
White female; age 59; diagnosed Aspie.
I use caps for emphasis----I'm NOT angry or shouting. I use caps like others use italics, underline, or bold.
"What we know is a drop; what we don't know, is an ocean." (Sir Isaac Newton)


BeaArthur
Veteran
Veteran

Joined: 11 Aug 2015
Posts: 5,798

27 Nov 2016, 11:43 am

Let's not derail this thread on a personal argument between two older autistics on who gave the best advice. Campin Cat and spoons, if you want to stand you ground and defend your position, PLEASE do it via PM so k_kelley doesn't have to get anxious about it.

I used to work in community mental health and I was BOTH the case manager and the aid. Any place k_kelley wants to start asserting his wishes should be acceptable.


_________________
A finger in every pie.


Zane
Deinonychus
Deinonychus

User avatar

Joined: 12 Apr 2008
Age: 38
Gender: Male
Posts: 347
Location: Tempe, Arizona

27 Nov 2016, 3:59 pm

Just be Honest. It is after all true to yourself.

I hated all of mine (aides) growing up and all of the classes which were supposed to teach m life skills.

Otherwise you will have to prove to them that you are able to function w/o their help and that is not easy.

Hope this helps.


_________________
"The world is dying; time to suit up"


Campin_Cat
Veteran
Veteran

User avatar

Joined: 6 May 2014
Age: 63
Gender: Female
Posts: 25,953
Location: Baltimore, Maryland, U.S.A.

28 Nov 2016, 9:47 am

BeaArthur wrote:
Any place k_kelley wants to start asserting his wishes should be acceptable.

It is very difficult for me to understand anyone who thinks going-over somebody's head, is okay. I certainly wouldn't like it, no matter my position in a company (I would MUCH rather someone told me to my face, what I was doing wrong, so I could correct it BEFORE the boss found-out)----and, I would think any ASDer would be able to relate, considering we're so often discounted / disregarded in, even, "regular" situations (let-alone, in a work situation).




_________________
White female; age 59; diagnosed Aspie.
I use caps for emphasis----I'm NOT angry or shouting. I use caps like others use italics, underline, or bold.
"What we know is a drop; what we don't know, is an ocean." (Sir Isaac Newton)