OT: GOOD NEWS FOR DSonIL & DD -- loooong (of course)

YES -- I am shouting and when do I EVER post anything in a short, concise manner?!?!? :-))). After five years of not being able to work or drive or even see too well, DSonIL has been approved for government disability. The **BEST** result is that DD will no longer have to pay for health insurance for him -- to the tune of about $500.00 PER MONTH! He's had long term coverage for big stuff through his work insurance but nothing for the day to day things. He will now be on Medicare and SSI which will be a huge help. He had his court date this morning and DD phoned me as soon as they were in the car to tell me the results. In a rare occurrence, he was approved right then and there -- no further waiting for paperwork, etc. Apparently this is very rarely done but they were told that his disability was SO obvious that the judge didn't feel they should have to wait the extra time after being approved. They looked at his past work record as a registered & certified Architect for 20+ years before the stroke and then BAM, he was unable to do anything for months and months and now is quite limited. He had to get on the stand and tell the judge and the room full of folks waiting their turn that, YES, he was disabled and unable to work in his chosen field. THAT alone was a huge step for him and I am unbelievably proud of him for finally being able to admit this. It was a very long, very hard road for him to get to this point. He now wants to look into going back to school to learn new stuff and just find out what, if anything, there is out there for him to work at. He was told that even with disability, he is allowed to actually work at a job for 8 or 9 months without losing his disability. At that point, if he is able to keep working then his disability will be discontinued. THIS in itself is a god-send and I am so happy to know that AZ (at least) has implemented this policy. Not having much use of his left hand isn't too big a deal as he tries to use it as much as possible and is very, very slowly getting more use of it. His not being able to see well enough to drive also isn't a big deal as Lizard Land actually has got a fairly good public transit system -- at least from where they live. DD's job also allows for her to come as go as is needed throughout the day so she could schlepp him to/from public transpo if needed. His biggest disability -- and it's one that I don't think will ever improve much with more time -- is that he has what we call Swiss Cheese memory. He might know which bus to take but will forget which time he needs to be at the bus stop. Or vice versa -- know the time but not remember the bus. He can look at the bus schedule and 30 minutes later, he has forgotten what he read. He has used EVERY memory improving thing out there. WE bought him the Brain Age (or whatever it's called) hand held gizmo for his B-day several years ago and he still uses. It helps him remembering other things but NOT stuff related to time. This whole dysfunctional time thing is a result of having had a right brain stroke. He also is almost totally unable to "multi-task" so even if he could see, he shouldn't drive. No way could he remember to watch front, back, left & right. Half the time he forgets to look at the street light to see if he can cross the street!!! When we go to anywhere, he just wanders off, without letting us know where he's going. Now, I know this is a guy thing but he doesn't even remember walking off and leaving us! When Raechel asks why Daddy does this stuff, we just tell her that Daddy is a bit kookoo after his stroke and she accepts that. Actually, he tells her the same thing :-). When the kids at school ask her why her Dad doesn't work and is a bit weird, she tells them his brain got sick when she was just a baby and he's a little kookoo now so can't work. SHE has a better memory than he does and he actually listens to her better than he listens to the rest of us -- LOLOL! He also has problems with his social interactions. He talks incessantly -- long after any topic has been worn out and his listeners have gotten bored to death. He invades other's "personal space" and doesn't realize he is doing this. He can no longer pick up on the subtle clues we all send out that let others know they have talked too much or are too close, etc. When they are at a social gathering and he starts to act inappropriately, DD will whisper Ruby Begonia in his ear and this lets him know that he is coming on too strong. WHY he can remember this and not other, easy things is anyone's guess but it works. Anyway, he's now on disability as of right now and it will make life so much easier for the whole family on many, many levels. Also, Cheeto STILL seems drawn to him and spends a large part of his kitty day on Steven's lap. This really means a lot to Steven so I am immensely glad. He's still R's kitty when she gets home and then makes sure that Mom gets some attention when she gets home, too. All around just happy news to be able to share :-))). CiaoMeow >^;;^<

PAX, Tia Mary >^;;^< (RCTQ Queen of Kitties) Angels can't show their wings on earth but nothing was ever said about their whiskers! Visit my Photo albums at

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Tia Mary
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Reply to
Kate XXXXXX

He's been gone a long time but I used to have an attorney friend who was just dazzlingly brilliant. His 'smart' was just off the charts and yet he never quite grasped simple concepts such as one way streets. His favorite indoor sport was weaving and unraveling all it took to get disability approved for folks who had been unfairly denied. That dear fellow was a blessing to many. I know that your son-in-law's finally getting approval is a major wonderful event. So very happy for you, Mary. And yes, the kitty knows. They're smart like that too. Polly

Reply to
Polly Esther

What wonderful news! When you're facing medical issues... and money is tight -- life just isn't a whole lot of fun. Hopefully, this will relieve at least some of the financial stress... and DD & DSonIL can breathe a little easier. And this may also open other resources such as your state's vocational rehabilitative training programs (which in MI -- are available to those who qualify at no cost to the individual).

On another note... and clearly it is none of my business... the "kookoo explanation" thing bothers me. I would fear that there will come a point in time where this will bring negative attention to your DGD. If it were me -- I would encourage her to lose that label... and just tell people "my daddy's brain had a stroke and doesn't work like it is supposed to". It is clearly more accurate and doesn't cast the negative stigma that "kookoo" carries. As the mother of a son with both mental retardation and mental health diagnoses -- kookoo just isn't something I take to well -- so I may be over-reacting.

Reply to
Kate in MI

I am so very happy for your daughter and SIL. The road to getting on disability is long and bumpy and immensely frustrating. The relief they must feel has to be joyous! Wishing your dear SIL all the best. Donna

Reply to
dealer83

I'm so glad for your SIL and DD. I can tell you from personal experience, that admitting that you're worth nothing anymore is harder on the soul than anybody can ever say. And the system requires that you work hard to prove that you're worth nothing. I was approved pretty quickly once I started disability proceedings. And the biggest blessing has been Medicare, which didn't kick in for me until I'd been on disability almost two years. (I don't understand the rules, I just live with them.) Please tell your SIL for me that I think he's done a very important thing and that he has my total respect. Those of us who have worked hard sometimes have a hard time accepting disability. I hope he has good friends and something he loves to do that will get him through.

Sunny

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Sunny

Reply to
Joanna

Your DSIL and DD have had such a hard row to hoe, I am so glad to hear they are finally getting some much need help. What a huge relief it must be!

Sounds like your DSIL has a great support system with your DD and Racheal. So glad to hear that Cheeto is doing his part too. :-)

Thanks for sharing the good news! Michelle in Nevada

Reply to
Michelle C.

I suppose it's just the way my family deals with this sort of thing. My older DSis was severely physically handicapped and I grew up with having kids make fun of *me* as a result. I suppose that was just kids being mean they way they usually are. Actually Steven is, more often than not, the one who tells the kids he's a little kookoo from having had a stroke. Since he and DD volunteer in R's class as often as possible, all of the kids know him and have just sort of accepted the explanation as something that makes sense to them as First Graders -- and last year as Kindergartner's. I understand your point of view so don't worry about having expressed it. You're not over-reacting at all IMNSHO :-). If i'm going to tell you all of this stuff, then I am more than happy to hear what your opinion of it is. We have made a point of periodically talking with R about her Daddy's problem and asking her what the kids think and say, etc. Every once in a while she will talk about a kid (usually but not always someone new to the class) saying something a bit snarky. As often as not one of the other kids puts a stop to that or R just says her Daddy has a sick brain from a stroke and that puts an end to all of it. Not that any of the kids know what a stroke is, they just mostly want to know why HER Daddy doesn't go to work like everyone else's Daddy does! Leave it to kids to find the bottom line :-)! CiaoMeow >^;;^<

PAX, Tia Mary >^;;^< (RCTQ Queen of Kitties) Angels can't show their wings on earth but nothing was ever said about their whiskers! Visit my Photo albums at

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Reply to
Tia Mary

How wise and wonderful your young Raechel is. She warms our hearts. Which, of course, is not to say that she's totally prepared to deal with Cheeto. How's that going? Polly

Reply to
Polly Esther

Sooo good to hear your good news! HUGS to your SIL and DD, too! What a relief it must be for them. You wonder why some of the most important decidions take soooo doggone long! (5 years?!?!?) ME-Judy

Reply to
ME-Judy

On Wed, 6 Jan 2010 14:20:36 -0600, Tia Mary wrote (in article ): . Also, Cheeto

Cat's always seem to know just who needs them the most. Cheeto is a smart little guy.

Maureen

Reply to
Maureen Wozniak

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