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lpearce

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  • in reply to: Personal Tracking Device for someone who wanders #18398

    I haven’t used a tracking device, but my son’s new cell phone is an Android device and I’m using one of the many tracking programs (Preyproject) available on that platform to track him via the internet. Of course these programs are intended for tracking phones, not people, but as a rule he has his phone with him when he’s out. We went with Wind, because they are the only provider using the infrastructure that makes WIFI access possible in some TTC subway stations.

    in reply to: Fee For Service and Passport- Autism Spectrum Disorder #18372

    Further to Jennypink’s comments, I agree that it’s important to consider both what your adult child WANTS to do (in my case, what he wants to do is hang out at home, watch videos, and play videogames, with occasional breaks for fast food or the acquisition of pop) and what they NEED to do (keep physically active, learn new skills, be out in the community, help out at home, build independence, etc.). My husband and I brainstormed a list of such goals and then tried to think of things that could help our son achieve them, many of which did not involve a specific program or service so much as practical matters, like nightly walks, or planning and preparing one family meal a week, that we could support him doing within the family or with friends. That was useful when thinking about how external resources could be called upon and what role they would play in his life.

    I would also say that to aid the transition into adulthood for someone who finds transitions supremely difficult, we worked hard to try to change only a few variables at a time. For example, we were sure to retain some programs and activities he started in his teen years as well as adding new ones, rather than starting with a blank slate. We also withdrew him from school a day a week for his last two years in school, something I realize not everyone can do, with the intention to somewhat disrupt the school routine before school came to an end for him. I credit that strategy a fair bit with the fact that his post-school transition went so well.

    in reply to: Fee For Service and Passport- Autism Spectrum Disorder #18364

    I agree that it’s important to always ask for accommodations rather than waiting to have them offered to you. Even if you choose not to include your child in the SIS portion of the assessment (and I’m very glad that we did make that choice), if the travel to the local DSO office is a challenge you should definitely ask for a meeting at home.

    Oops, hit Enter accidentally. I’m interested in hearing from other families on this topic. I am not a Facebook (or other social media) user myself, but I’m wondering if my son would benefit from having a page where he could post his experiences and thoughts to share with family and friends. This is not something he particularly desires to do, or truly understands (although he manages email just fine). I’m worried about trolls and the like, but on the other hand it might offer him connections that are otherwise difficult to maintain.

    Thoughts?

    in reply to: Day & Respite Program for adults #18319

    Re: looking for day programs, not sure where you are in Scarborough but we have been very happy with the AAIMS program run out of East Metro Youth Service’s Galloway house (Kingston Road and Galloway). They have a scalable program so wait lists may not be as much of an issue.

    Further to Jennypink’s comments, Parks and Rec offers, in the east and central regions, a day program called Active8 that is free and operates two days a week. It fills up fast, though. You should definitely reach out to the Adapted and Integrated Services people at Parks and Rec for Scarborough for other ideas.

    Also, it’s important to understand that the agencies you will see exhibiting at the DSTO fair are definitely not “all the agencies”, they’re just the agencies that receive Ministry funding. Many of them are starting to offer fee-for-service programs, but their funded programs are accessible only through DSO, not directly with the agency. Be sure you clarify which services they are offering, to avoid getting all excited about a program when no-one can tell you when, or if, it will ever have a spot open for your son. Non-funded agencies can have their literature on a community table at the DSTO fair, but as Jennypink notes, the Community Participation Supports page on this site lists many of the non-funded agencies/organizations and their offerings.

    Hope this helps.

    Thanks so much, Sharon – Toronto Ride is a great resource and will be a great help for this family, particularly since it will allow them to take advantage of free Parks and Recreation day programs. And here I thought I knew everything!

    – Laurie

    in reply to: Communicating with Developmental Services Ontario #18232

    Although it is certainly true that you need to go through the DSO process to have any hope of getting funded services, so this was bad advice indeed, the service provider might have been considering the possibility that people who qualified for services under the “old” system would not qualify for them under the new standardized criteria and so would lost their slot. I believe there is some uncertainty in this area. That said, even once you’re through the DSO process, it is strongly advisable to get a copy of your adult child’s record regularly so it is as current as possible – maybe make it part of birthday activities so you don’t forget. I also suggest that you get a copy immediately following the whole DSO assessment process: this should be give to you as a matter of course, but when I went through the process some years ago this was not the practice, and my son’s record was profoundly inaccurate.

    in reply to: Learning to take pills #18166

    Thanks for the suggestions. One of the answers raised another question – knowing when he’s sick. Although verbal, even chatty, my son has a strong resistance to making declarative statements of any kind. For example, the other day he had a nose bleed, and my only clue (until he came into sight) that this was happening was him starting to talk about things that are red. Yes, it’s a never-ending game of 20 questions in our house! This means I can’t rely on him to report on how he feels – he will very occasionally complain about an obvious illness (“I don’t like it when my nose is stuffed up”, for example, or, commenting on a bout of vomiting, saying that he didn’t want to have another “long cough”) but otherwise it’s a guessing game. Basically if he doesn’t get out of bed in the morning, goes to bed unusually early, or lies down on the couch and pulls a blanket over his head, he’s sick, not that he’d admit to that. (Our family dog, who died several years ago, was a useful barometer for our son’s health, seeming to have an instinct that drew him (the dog) to stay close to our son when he (the boy) wasn’t well. Anyone encountered anything like that? The problem is, of course, that feeling sick is so subjective, but sometimes I lie awake at night worrying what would happen if he had symptoms of a serious illness that simply didn’t present in a way I could actually see….

    in reply to: Lack of funding – what are YOU doing? #18165

    Evi, I’m a parent as well, so I understand the panic and despair all too well (not that that’s much help, I know). First, and you probably already know this, be sure you tell DSO the full extent of your situation – tell them often. I don’t think there’s a lot of point in telling them in advance, no matter how obvious it is that you will be in in desperate straits upon your daughter’s graduation, but you need to tell them explicitly once that situation arises. Will money magically appear? No, but that doesn’t mean you shouldn’t keep in touch with them, being sure they know of every event and circumstance. Also, make sure your daughter is on the list for direct funding, and for person-directed planning. Request a copy of the information they are using to match your daughter to any programs that might open up at some time in the future – I found that some of the information in my son’s record was completely wrong – again, that doesn’t mean she’ll be put in a program, but if the information isn’t correct, any matches that might arise in the future won’t be appropriate.

    The only other practical advice I can share is to try to make as many connections as you can with other families – are there any other parents, for example, in your daughter’s graduating class that might be able to pool resources with you to arrange transportation, or to share the cost of a support worker? Anyone you know from any other activities you or she take part in who might be in a similar situation? Personally I think the education system is incapable of doing transition planning, but you should talk to them too, maybe they can suggest a connection you haven’t thought of.

    Sorry if this isn’t any use – I feel that one of the many ways the system fails parents is that it encourages us to remain in our individual silos rather than facilitating collaborative thinking and action. I believe Plan Toronto (now called Partners for Planning) can help build a “circle of support” in the community (I know, I can hear your eyes rolling, but desperate times call for desperate measures). Or if not that, do you have a friend who can help you brainstorm some ideas and work through some alternatives? I can’t imagine having been on the journey of raising a son with ASD on my own, but even with two of us we often find ourselves not able to think, if you’ll excuse the cliche, out of the box.

    And yes, many of us are contemplating selling our homes and moving to less expensive parts of the province, as extreme as that sounds. I’m not sure we have a choice.

    in reply to: Welcome Policy #18088

    And just a reminder for those parents whose children have crossed the threshold into official adulthood: their income, not your income, is taken into account for the Welcome Policy. If their only income is ODSP, they fit the criteria for the Welcome Policy.

    in reply to: Wanting information on how to teach Financial Literacy #18087

    This might not fall into the category of “resources”, but in working with my son, who has ASD and cognitive delays, I found the best way to teach money skills is to allow the person you are teaching to actually have money and make choices around how to spend it. My son has extremely poor math skills on paper, but once we started paying him for doing household chores (instead of an allowance) and for participating in volunteer work/school co-op, it took him very little time to figure out financial matters related to his daily life. The key is motivation – he doesn’t find money interesting, but he finds things that money can buy extremely interesting. For example, he quickly grasped that a bottle of pop cost more than a can of pop, for example. He saves his money for desired objects (particularly DVDs) and suffers the emotional pain of having to not buy something he wants right now in order to be able to buy something later. We discuss his choices, but if he makes a foolish decision with his money (we’re talking relatively small sums here, of course) then he gets to feel the pain. We’re in the habit of counting his money before he leaves the house so he can plan ahead about what he might want to buy on a particular outing (and what he’s allowed to buy – without any rules he’d be swigging a coke for breakfast), and use envelopes for him to store his savings (keeping a visual tally on the outside of the envelope so he knows how close he is to his target). I remember soon after we started this effort, we were walking to a variety store and, unprompted, he decided he had to go home and do more work because he realized he didn’t have enough money for his treat: he wasn’t happy, but I was thrilled. I was also thrilled recently when he rather wistfully commented that “buying a pineapple wasn’t a good idea” (buying certain food items that he won’t eat but likes to have is one of his quirks).

    Petra, you may have already tracked this down, but here are the guidelines for employment income:
    http://www.mcss.gov.on.ca/en/m…..kearn.aspx
    To the beset of my knowledge, volunteer work does not at all affect your ODSP: they are concerned only with paid work.

Viewing 12 posts - 1 through 12 (of 12 total)