Showing posts with label supported apartment. Show all posts
Showing posts with label supported apartment. Show all posts

Tuesday, March 12, 2019

ADVOCACY FOR YOUR CHILD’S TRANSITION TO ADULTHOOD


I used to be funnier. I began this blog a few years after my son was diagnosed, when I’d begun to see the positives in neurodiversity and learned to navigate the school system a bit. 
I had the mental and emotional space, as well as the knowledge, to bust out my sense of humor, mostly when laughing at myself or the many ridiculous aspects of bureaucracy. I sometimes even found it in me to take certain aspects of ignorance and some of our challenges a little more lightly. 

I’ve said this here a few times, but I’ll say it again: For me, this transition-to-adulthood phase is the most terrifying part of our journey so far. 

When my son was a child, I could shelter him, protect him; now he’s headed out into a world that isn’t always suited to those with different ways of thinking and being, never mind people with tender hearts. 


And I haven’t found the funny in it yet. Basically, I’m back here, like, all the time. 


Figure I — My Overactive Extrapolator–Catastrophizer Gland

Still, I want to offer this community some really important information that should have been way easier for me to figure out…but was not. 

Between the harried high school case managers and the various overloaded  agencies, not to mention the lack of communication among all these institutions, there was so much I just didn’t know.

Fellow parents were really my lifesavers here, and I was fortunate to find a few real parent “experts” along the way who laid things out for me in a lifesaving way. If you don’t have anybody like that, this information might be very valuable; and even if you do, there may be supplemental aspects. 

This list is necessarily incomplete, and I plan to write more about this huge topic as I learn more. For now, here’s what I know — hope it’s helpful. Questions welcome (as comments or PMs):

1. Designated Agencies
These are organizations selected by the state to manage certain aspects of public health. If it deems you or your child eligible for its programs (in our case, Adult Developmental Services), your local designated agency will guide you through the process of figuring out what is available to best suit your situation. 

Above all, this agency will help apply for and then administer your or your child’s State Medicaid Waiver. 

Sometimes the language is a bit different (“service agency”), but you can pretty much google your state, “disability," and “designated agency,” now that you know what a designated agency IS (I had no idea for way, way too long). 

2. State Medicaid Waiver
The State Medicaid Waiver provides funds for key services, such as a supported apartment, and help with educational, personal, and employment matters. 

When your case manager at your designated agency initiates the waiver process, they’ll create budget lines for housing, employment, and other kinds of assistance, such as education (including aspects of supported college programs).  

3. Vocational Rehabilitation
Vocational Rehabilitation is a federal-state program that promotes employment readiness for a wide array of people facing challenges, especially people with disabilities. It also helps them find and retain jobs.

Voc Rehab can apparently provide expert help with applying for SSI (see below), too. 

4. Supplemental Security Income
Supplemental security income, or SSI, is a federally determined and dispensed monthly sum that is meant to cover the expenses of people with certain medical issues, disabilities and mental health challenges.

You can apply for SSI 30 days before the age of 18, and need to call a month before that to set up your appointment. The application leans toward medical disabilities, so work with Voc Rehab to optimize your or your child’s application 

5. College Support Programs
There are many programs offered by colleges themselves and others — private and state-run — offering group living and academic support. A lot of these options are super expensive; some even add support costs on top of college costs to the tune of so.much.money. 

If financing higher education, never mind additional supports, is a concern for you or your family, investigate state-run college programs for people with disabilities — some are free or close to it!

6. Guardianship And Independence
Independence exists on a continuum. People with developmental differences may benefit from scaffolding at the outset of — or throughout — their adulthood journeys. Options here range from limited assistance with money management (known as a “representative payee”) to various forms of limited guardianship to full guardianship.

Because I’ve vowed to presume competence, I’m trying to prepare myself to face potentially devastating choices involving risk, respect, trust and safety in this arena. But at least I’m educating myself and my son about our options.  

7. Able Now Account
This type of bank account allows you or your child to deposit funds that will not count against you/them in determining eligibility for various benefits, such as EBT, Medicaid, SSI, and the State Medicaid Waiver. 


It’s still early days here, so we haven’t navigated all of these processes (and I know there are more things to figure out: I’m looking at you, health insurance). I'm not even sure which will be appropriate — I’m just glad to know they exist. 

And now so do you. Good luck!!

Thanks and love,
Full Spectrum Mama



Welcome to Voices of Special Needs Blog Hop -- a monthly gathering of posts from special needs bloggers hosted by The Sensory Spectrum and The Mommy Evolution. Click on the links below to read stories from other bloggers about having a special needs kiddo -- from Sensory Processing Disorder to ADHD, from Autism to Dyslexia! Want to join in on next month's Voices of Special Needs Hop? Click here!


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Tuesday, September 11, 2018

BOBBY



Dear Persons,

I know Bobby because my brother-in-law used to do respite care with him. 

He often brought him to brunch at our house on Sundays. Bobby was eternally grateful for the food I cooked. He would play with my son, games most kids his age would have scoffed at. 

Bobby would hug us so tight when he left.  He had a sweet side for sure.

Bobby’s not his real name.

Bobby must be in his early twenties by now.

He’s sitting on his front porch most days when I drive by on my way to town. 

He’s trying to quit smoking.

He’s gaining weight.

Sometimes I see him in town with a “helper.” I say “Hi” and check in on whether he’s quit smoking yet.

I never see him with anyone else.

My daughter—when she sees me tear up when we drive past him—says, “Mom, that’s not going to happen to [G], he has you and he has me and you’re a good mom.”

Bobby’s mom is probably a good mom too. (Or his parent/guardian[s] is [are] good, in their own way[s].)



Do any parents not love their kids and want the best for them?

Is every life not a worthwhile life?

What can young adults DO in this small town with few young people and fewer opportunities?…And if they are on the spectrum? 

Bobby’s on the spectrum.

Even in bigger cities, with more opportunities, more diversity—are human beings with differences getting lost in the mix? I’m betting they are.

What are the components of a decent life? From my perspective, they would include community (however that is defined, in a way that makes sense for each individual), meaningful work or some sort of activity that contributes, health, the freedom and opportunity to pursue one’s interests and goals.

From my perspective, Bobby’s life seems terribly lonely and sad. 

But it’s unfair to make assumptions about someone else’s life.  And maybe he wouldn’t agree.

I think he deserves better.

Maybe he wouldn’t agree. There are certainly many things I don’t know about Bobby’s life.

I do know that I don’t want a life like his for my son.

Maybe my son wouldn’t agree.



Soon, the time will come for that conversation. I will help him in any way I can to make his dreams come true, but at a certain point* he will become more and more—or even entirely—responsible for his own life. 

I hope he’s seen and understood enough of the world by then to make healthy, positive, proactive choices, both in terms of how he wants to live and as far as what he needs to do to live that life.

Love,
Full Spectrum Mama


* When will that be, dear fellow parents of children with differences? A tough question, with as many answers as there are children…




 
Welcome to Voices of Special Needs Blog Hop -- a monthly gathering of posts from special needs bloggers hosted by The Sensory Spectrum and The Mommy Evolution. Click on the links below to read stories from other bloggers about having a special needs kiddo -- from Sensory Processing Disorder to ADHD, from Autism to Dyslexia! Want to join in on next month's Voices of Special Needs Hop? Click here!