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Linda,

In case anyone is interested, and regarding the Olmstead Act, I'd like to
digress somewhat and give some information  and background on what we are
doing in Calif on this and other issues.  I encourage others to do the
same at the Federal and State level.

On the same day we--PAN's grassroots advocates, Greg Wasson, Northern
Calif's Grassroots Coordinator,  Maxine Krugman, acting Congressional
District Coordinator (who's is from Sacramento, Calif's capitol), AJ
Campbell, and I, Charlotte Mancuso, Congressional Dist. Coord., for the
14th district, and also Lynn Fielder--were in Sacramento at a press
conference and hearing to support separate legislation brought by State
Senator Ortiz, to allow therapeutic cloning, embryonic stem-cell
research, and explicitly, legislation to fight against U.S. Senator's
Brownbach's bill that not only totally bans therapeutic cloning, but
criminalizes any participation in it by researchers--basic scientists,
researchers applying it for curative purposes--and patients, making it a
felony punishable by up to 10 years in the slammer, and $1,000,000 fine,
and to support U.S. Senator Feinstein's bill that supports it, and U.S.
Senator Spector's bill that also supports it.

Maxine and I were also there to attend the annual California
NeuroAlliance Conference that concludes with visits to our state
representatives.  One of the top issues on the Alliance's agenda is for
Calif to do be more proactive in implementing the Olmstead decision more
fully and more quickly, and for oversight to be formed to make sure the
Olmstead initiatives are carried out.  The California NeuroAlliance,
which Maxine and I are also members of, is made up of Neurologists and
advocates throughout the State of California, representing the various
neurological disorders.  Under the auspices of the American Academy of
Neurologists (AAN), the national professional org of neurologists,
together with professional and lay advocates in Calif., have formed the
first state NeuroAlliance to take on  state health policy issues, in part
because the Association of California Neurologists was becoming more
involved with advocacy.  The CNAlliance believes that much of the health
care issues, like long-term care, access to health care, HMO policy
issues, and more, can be more effectively dealt with at the State level,
and that relying on the Federal level entirely to implement  broad health
policy issues for the entire nation is unrealistic, which I agree with.
The formation of the Alliance coincided with Gov. Gray Davis forming a
health care policy advisory board, made up of a director, and other paid
staff, and professional and lay volunteer participants from the
community.

I believe, for the most part, the account I have given above is accurate.

Regards,
Charlotte Mancuso

On Sun, 31 Mar 2002 07:34:25 -0500 Linda J Herman <[log in to unmask]>
writes:
> This report highlights federal inter-agency actions to implement
> Pres.
> Bush's  NEW FREEDOM INITIATIVE , which "calls upon the federal
> government
> to assist states and localities to swiftly implement the decision of
> the
> United States Supreme Court in Olmstead v. L.C. In that case, the
> court
> found that, under certain circumstances, the Americans with
> Disabilities
> Act (ADA) requires states to provide community-based services for
> persons
> with disabilities and holds that unjustified institutionalization of
> a
> person with a disability is discrimination under the ADA. "
>
> This initiative and the following report  look very promising --
> hopefully it will be adequately funded and implemented. The report
> identifies the supports needed by  disabled people to be able to
> live in
> the community -- Housing, Personal Assistance, Direct Care Services
> and
> Community Workers, Family Caregivers support, Employment,
> Transportation,
> Access to Technology, Legal compliance with the Olmstead decision,
> Public
> Awareness and income supports.
> Linda

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