I’ve been feeling pretty overwhelmed lately. Getting on the same page with my son’s new
supported-living provider has been a challenge, though things may be starting
to improve. My son keeps skipping out on
his IDS program because it’s not meeting his needs and we’re waiting for DDA to
offer any solutions. And the D.C. Office
of the Chief Financial Officer, for the third time this year, has misplaced my
son’s monthly check – this time, lost it for good. You know it: every day there’s some obstacle
or headache standing in the way of the real work of improving the lives of
those we care about.
So it helped me to lift my head above my day-to-day problems
on November 12 and attend one of the DDS briefings about the legislation that’s
been introduced into the D.C. council.
This bill, the “Citizens with Intellectual Disabilities Civil Rights
Restoration Act,” addresses one of the major hurdles in the way of moving D.C.
into the 21st century of disability rights - namely the practice of
commitment. At this point, please look
to the right and read my posts under the label “Past Reforms” (especially “35
Years and Counting” and “Where We’ve Come From”) so you’ll know what I’m
talking about, and also take a look at the page “Acronyms You Should Know.” Now you’ve done that, please keep reading!
About 1/3 of the people receiving services from DDA under the
I/DD waiver still have to be “committed” by the D.C. courts in order to get
those services. We are the ONLY place
in the country where this is still true, and I’ll admit that I find that
horrifying. When my son was found
eligible to receive services, I was terrified he would have to be “committed”
and that a lawyer would step in between him and us to decide what supports he
needed. Coming from that perspective, it
was helpful to me to sit in the Shaw library and hear from people whose family
members are under commitment: it made me
more understanding even though it hasn’t changed my mind. There are people who still remember when the only
way to get D.C. to keep people with disabilities safe was for the court to be
watching over the government’s shoulder.
A huge amount has changed since that time, but it’s not hard to
understand why some people like a system they know, especially if they happen
to have a lawyer they like. For people
in that position, the bill allows people under commitment to continue if that
is what they, or a trusted person, decide they should do.
And on the subject of “trusted person,” the bill also
proposes an alternative to court-appointed guardianship, in the form of a Supported
Decision Making (SDM) agreement to allow the person with a disability to
formally designate someone who can help her/him make important decisions. Supported decision making is an essential
concept, and I also believe everything needs to be done to avoid guardianship
where possible. I’m going to be taking a
very close look at the bill, though, to make sure the proposed SDM agreement
doesn’t have unintended consequences where a different legal alternative to
guardianship, the power of attorney, is concerned. Both are needed.
Erin Leveton (erin.leveton@dc.gov)
said the bill will soon be posted on the DDS website and that a joint hearing by
the council’s Health and Human Services and Judiciary committees will soon be
scheduled, probably in January. I’ll do
my best to keep folks informed about the timing, but between now and then,
there are a couple of other important things to mark on the calendar. The report to the council on what it would
take to expand eligibility for services to all people with developmental
disabilities will be submitted on December
1, and DDS has also promised to post that report on its website. And the next meeting of the Supporting
Families Community of Practice will take place on December 14.
Speaking personally, I’m hoping that some of the challenges
we’ve been facing will smooth out over the holiday season so that we and our
son will see fewer obstacles and more person-centered solutions by the time the
New Year rolls around.
Laura: I would like to discuss the upcoming hearing re: Bill 21-0385...hearing scheduled 1/27/2016. I don't like the term committment but a lot of individuals don't have support like we give our young adults. I have a problem trusting the system to do the right thing. There are some great case managers that my son has had but his current person is the absolute best and cares. These case managers can only do but so much and have a load that almost requires attention 24 hours a day and that is impossible. I feel individuals need to have legal representation and definitely for those who can't communicate. It should not be left in the hands of DDS. I do agree that all individuals should have the same services. If the courts don't oversee these agencies and/or service providers what happens. Furthermore, why has this informtion not been circulated to everyone via mail, email, service providers etc regarding this hearing. I found out through lawyers. This needs to be circulated to the media.
ReplyDeleteHi, this is Erin Leveton, Program Manager of the State Office of Disability Administration at DDS. I am happy to discuss the bill and answer any questions you may have about it. You can reach me at erin.leveton@dc.gov or (202) 730-1754. Sorry for the late reply -- I am just seeing this, since Carol cross-referenced it in her post today.
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