Fwd: [RD] ACB SCHOLARSHIPS AVAILABLE TO BLIND STUDENTS..

2007-09-30 23:24:45

ACB SCHOLARSHIPS AVAILABLE TO BLIND STUDENTS
The American Council of the Blind will present more than 30 scholarships
and
awards to outstanding blind students in 2004. All legally blind persons
admitted to academic and vocational training programs at the
post-secondary
level for the 2004-05 school year are encouraged to apply for one of
these
scholarships. A cumulative grade point average of 3.3 is generally
required, but extenuating circumstances may be considered for certain
scholarships.
Applications and additional information will be mailed to all members of
The National Alliance of Blind Students and to those who call the
national
office to request a copy. Both the information and application are also
available on our web site at www.acb.org. Applications may be completed
on
line, but supporting documentation must be submitted in hard copy print
to
Terry Pacheco in the ACB national office no later than March 1, 2004. If
You have additional questions, please call Terry at (202) 467-5081 ext.
19.
Leading scholarship candidates will be interviewed by telephone in
April.
The ACB scholarship winners will be notified no later than May 31, 2004.
Scholarships will be presented at the 43rd annual national convention of
The American Council of the Blind to be held July 3-10, 2004, in
Birmingham,
Ala. Scholarship winners are expected to be present at the convention if
they have reached their 18th birthday. Generally, ACB will cover all
reasonable costs connected with convention attendance.
Former leaders in and near the ACB community who have been memorialized
by
generous benefactors include Delbert Aman, Dr. S. Bradley Burson,
William
G.Corey, Dr. Mae Davidow, Nicholas S. DiCaprio, Eunice Fiorito, John
Hebner,
Grant M. Mack, Alma Murphey, Floyd Qualls, and Arnold Sadler. Special
Thanks should also be extended to those who remembered Kellie Cannon and
Duane Buckley in such fitting manners. The Ross N. and Patricia Pangere
Foundation scholarships are also given as a way of giving back to the
community.
ACB also administers scholarship programs for our affiliates in
Colorado,
Maine, Maryland, Massachusetts, and Oregon.
We are hopeful that Kurzweil Foundation will continue its annual gift of
The Kurzweil 1000 software to our winners.
This is our second year presenting Freedom Scientific Awards to several
of
our scholarship winners. These awards are for up to $2,000 in
merchandise
from the company.
Note: Potential candidates will be considered for other scholarships not
Yet verified, if available.

LARGEST funding INITIATIVE LAUNCHED to Speed Nervous System Repair Strategies in

2007-09-30 12:40:11

LARGEST funding INITIATIVE LAUNCHED to Speed Nervous System Repair Strategies in MS

[INS: :INS] http://www.nationalmssociety.org/Research-2004Jan30.asp[INS: :INS]

January 30, 2004[INS: :INS]

The National Multiple Sclerosis Society has launched a new initiative to speed research on nervous system repair and protection in MS, a disease that attacks the brain and spinal cord. The Society has invited proposals from research teams to compete for grants of up to $5.5 million each to pave the way for clinical testing of repair and protection strategies in people with MS.

âThe pace of research in nervous system repair is accelerating dramatically,â comments Stephen C. Reingold, PhD, the Societyâs Vice President of Research Programs. âWith this initiative, we are aiming to have in place non-invasive tools that can determine the clinical success of any of several promising repair techniques that may be tested in the future to protect and restore nerve function in persons with MS.â

These are the largest grants ever offered by any agency for tissue protection and repair in MS, and potentially the most expensive single grants in the 58-year history of the National MS Society. The Society funds more MS research, offers more services for people with MS, and provides more professional education programs than any other MS organization in the world.

To compete for âTranslational Research Partnerships on Nervous System Repair and Protection in MSâ awards, researchers will have to assemble interdisciplinary teams and forge innovative strategies to:
* develop new disease models to screen repair and protection techniques;
* apply advanced MRI and other non-invasive monitoring tools to detect repair; and
* design human clinical trials.

Letters of intent are due to the National MS Society by April 19, 2004. Details about the program are available on the Societyâs Web site at: http://www.nationalmssociety.org/Research-RepairRFP.asp. Invited proposals will be reviewed in the spring 2005 and the winning team or teams will launch their projects in summer 2005.

Funds for research awards are provided in large part by contributors to the nationwide network of local chapters of the National MS Society, which also provide programs in communities across the U.S.[INS: :INS]

[DEL: [DEL: Newly Discovered Protein May Contribute to Tissue Damage in MS :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: May 24, 2002 :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: Isobel Scarisbrick, Ph.D. (Mayo Clinic, Rochester, MN) and colleagues have found that a newly discovered :DEL] :DEL] [INS: [DEL: [DEL: enzyme :DEL] :DEL] :INS] [DEL: [DEL: protein â myelencephalon-specific protease (MSP) â is dramatically increased in the brain tissue of people with multiple sclerosis, particularly where the myelin coating that insulates nerve fibers is under active attack from the immune system ( :DEL] :DEL] [DEL: [DEL: Brain :DEL] :DEL] [DEL: [DEL: , June 2002). :DEL] :DEL] [DEL: [DEL: If further research can confirm the role of this protein, these findings may lead to the development of therapies that inhibit MSP to block tissue damage in MS. :DEL] :DEL] [INS: [DEL: [DEL: The current study was funded in part by two :DEL] :DEL] [INS: [DEL: [DEL: (TWO???) :DEL] :DEL] [INS: [DEL: [DEL: National MS Society Pilot Research Awards, a grant program that supports investigation of unique or novel ideas with the potential to open significant new are
as of research on MS. :DEL] :DEL] :INS] :INS] :INS]

[DEL: [DEL: :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: When functioning normally, MSP contributes to proper function of myelin-making cells. When overly active, however, this protein may facilitate entry of immune cells into the brain, contribute to tissue destruction, and may harm myelin-making cells. :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: Since Dr. Scarisbrickâs team discovered MSP in 1997, they have developed probes and other tools to determine its role in myelin loss :DEL] :DEL] [DEL: [DEL: . :DEL] :DEL] [INS: [DEL: [DEL: â¦..needs some more punchy conclusion⦠:DEL] :DEL] :INS] [DEL: [DEL: :DEL] :DEL] [DEL: [DEL: The current study was funded in part by two National MS Society Pilot Research Awards, a grant program that :DEL] :DEL] [DEL: [DEL: supports investigation of unique or novel ideas with the potential to open significant new areas of research on MS. :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: :DEL] :DEL] [DEL: [DEL: :DEL] :DEL]

[DEL: [DEL: -- :DEL] :DEL] [DEL: [DEL: Research Programs Department :DEL] :DEL]

[INLINE]

FAQs Glossary

Purposeful

2007-09-30 11:48:09

Adapted from The Daily Motivator

Friday, February 6, 2004

Purposeful

When things become difficult, remember why you started them in the first place. A compelling reason can keep you going even if there is nothing else to sustain your efforts.

In dealing with the challenges that come your way it can be easy to lose sight of the purpose behind your efforts. Take the time to reaffirm your commitment to this purpose, and you gain renewed strength to meet the many challenges.

The energy needed for discipline, commitment and effectiveness for creativity comes from following a meaningful, compelling purpose. Remember why, for it helps you to determine how, and to put that strategy into action.

Remember why, and you can find the strength to persist. Remember why, and you will figure out a way to get the resources that you need.

You are at your best when following a noble and meaningful purpose. All that you are can be brought to bear when the reason is solidly connected to who you are.

Remember why, and you will have what it takes to get it done.

-- Ralph Marston

[INLINE]

~Joyce [INLINE]
I don't get headaches; I just give them.

Fwd: [lowdosenaltrexone] New MS research shows remarkable findings

2007-09-30 07:40:26

In a message dated 02/05/2004 5:33:24 PM Eastern Standard Time, lvlail_lvle@... writes:

Public release date: 5-Feb-2004
[ Print This Article | Close This Window ]
Contact: Christine Zeindler
christine.zeindler@...
514-934-1934
McGill University

New MS research shows remarkable findings

Montreal, February 5, 2004 - New research findings from the Research Institute of the McGill University Health Center (MUHC) provide hope for patients with multiple sclerosis (MS), one of the most common and devastating diseases of the nervous system. These findings, published in today in Neuron, characterize an enzyme that plays a central role in the onset and progress of MS.

" We have identified a key enzyme that triggers MS-like disease in an animal model," says MUHC neuroscientist and Professor of Medicine at McGill University, Dr. Sam David. "We also show that blocking this enzyme has a remarkable effect in preventing disease and relapses."

MS, an autoimmune disease of the nervous system, affects approximately 35,000 young adults in Canada. It is twice as prevalent in females. MS is an inflammatory disease in which the body's own immune system attacks the insulating membranes surrounding nerve fibers. This damage results in loss of sensations and paralysis. Although genetic, infectious or environmental factors are thought to induce MS, the exact cause of the disease is still not known.

Dr. David with his Ph.D. student Athena Kalyvas showed in a mouse model of MS that the amount of the enzyme, phospholipase A2 (cPLA2), is increased in spinal cord lesions. They further demonstrated that treatment with a chemical inhibitor of this enzyme results in a marked reduction in the onset and severity of the disease.

"This discovery suggests that the cPLA2 enzyme may be an excellent target for the development of drugs to treat MS, " concluded Dr. David.

###

This work was supported by funds from the Multiple Sclerosis Society of Canada.

For Information contact:
MUHC Public Relations and Communications:
Christine Zeindler
Communications Coordinator (Research)
(514) 934-1934 ext. 36419
pager: (514) 406-1577

The MS Skiathon for Multiple Sclerosis

2007-09-29 18:29:36

Attention News Editors:

The MS Skiathon for Multiple Sclerosis: A Major Challenge for a Good Cause!

MONTREAL, Feb. 5 /CNW Telbec/ - Next Friday, February 20, ski buffs and
others who enjoy a challenge are invited to Mont Chantecler, in Sainte-Adèle,
for the second annual MS Skiathon for the Multiple Sclerosis Society of Canada
(Quebec Division). The event will be presided over by Honorary Chair Bernard
Trottier, a well-known sports personality. Jean-Luc Brassard, freestyle ski
champion, will also be present and has accepted to act as spokesperson for the
event.

http://www.newswire.ca/en/releases/archive/February2004/05/c6878.html
[INLINE]

~Joyce [INLINE]
Make yourself at home; clean my kitchen!

...identified a key factor in multiple sclerosis,

2007-09-29 12:15:26

Enzyme find could fight MS
Experiments conducted at McGill. Neuroscientist finds that blocking substance controls onset, progression of disease in mice

CHARLIE FIDELMAN
The Gazette
Thursday, February 05, 2004

Montreal researchers have identified a key factor in multiple sclerosis, a devastating disease of the nervous system.

http://www.canada.com/montreal/story.asp?id=15560076-742E-4E7E-A9A0-67447668250A

~Joyce
Make yourself at home; clean my kitchen!

Fwd: [DGV] Bush Backs Away from Support of Money-Follows-the-Person

2007-09-29 10:06:20

In a message dated 02/05/2004 10:44:06 AM Eastern Standard Time, dgeditor@... writes:

Bush Backs Away from Support of Money-Follows-the-Person"
The President's Budget is out and the Administration has
backed down on funding commitment to Money Following the
Individual Rebalancing Initiative. President Bush's FY 2005
budget has no funding for Money Following the Individual
Rebalancing Initiative in FY 2005 and instead of the $1.75
billion that was in the proposed 2004 budget, incentive
funding has been reduced 70% to only $500 million for FYs
2006-2009. This is a major pull back from the President's
rhetoric about a major commitment to changing the
institutional bias.
S. 1394 (Money Follows the Person bill introduced in the
Senate) remains as it was before, as does MiCASSA.
We still need hearings to push for these bills and to
continue discussion of how to solve the institutional bias
in our long term care services. Congress ultimately
decides the budget, as well as passing laws, and we can
make the changes we want if we keep up the pressure.
******** Push for a Hearing! *************
MiCASSA and the Money Follows the Person Act
need our help to get heard in the Senate.
Senator Tom Harkin (D-IA), along with Senators Gordon Smith
(R-WA) and Arlen Specter (R-PA), sent a bipartisan letter
to Senate Finance Committee Chairman Charles Grassley (R-
IA) and Ranking Democrat Max Baucus (D-MT) calling for a
hearing on the institutional bias in the Medicaid program.
Medicaid requires that states provide nursing home care,
but leaves it up to states to choose if they will or will
not offer home and community based services, and how much
they will offer.
"Many people with disabilities and older Americans who rely
on Medicaid are denied any choice about their living
arrangements. They have to leave their homes and
neighborhoods and say goodbye to friends and families,"
Harkin wrote. "This forced segregation violates American
values of fairness and inclusion."
There are several bills to address this inequity, with bi-
partisan support, which are pending before the Finance
Committee.
* The Medicaid Community Attendant Services and Supports
Act (MiCASSA), S. 971, co-sponsored by Senators Harkin,
Specter and others, would require states to provide
community based attendant services to individuals with
disabilities and older Americans. Both bills are needed to
fully address the lack of choice in the current Medicaid
program.
* The Money Follows the Person Act, S. 1394, co-sponsored
with Senators Harkin, Smith, Specter and others, would give
states additional resources to provide home and community-
based services to individuals choosing to leave a nursing
home or institution.
"People with disabilities and older Americans have waited
too long for Congress to address this grave injustice,"
said Harkin. "We need to shed light on this problem and
enact legislation this year."
Contact these Senators today and urge to them to have a
hearing on MiCASSA, Money Follows the Person and the
institutional bias in the Medicaid program.
(Senator Grassley is the Chair of the Senate Finance
Committee, Senator Baccus is the top democrat on the
Committee.)
The Honorable Charles E. Grassley
United States Senate
135 Hart Senate Office Building
Washington, D.C. 20510-1501
Phone: 202-224-3744
Fax: 202-224-6020
http://grassley.senate.gov/webform.htm
The Honorable Max Baucus
United States Senate
511 Hart Senate Office Building
Washington, D.C. 20510-2602
Phone: 202-224-2651
Fax: 202-224-4700
http://baucus.senate.gov/emailmax.html
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Fwd: [lowdosenaltrexone] New Pants

2007-09-29 01:46:13

In a message dated 02/05/2004 12:18:06 PM Eastern Standard Time, penrose@... writes:

Wearable Devices Add Strength

[INLINE]

[INLINE] [INLINE]
By Huang, Gregory T
Source: Technology Review
Originally Published:20040201.
AT NAGASAKI UNIVERSITY IN Nagasaki-City, Japan, mechanical engineer Shunji Moromugi straps on a pair of what he calls "power pants" and gets to work. Holding a 16-kilogram barbell on his shoulders, he does 90 squats in 90 seconds without breaking a sweat. That's because the pants contain computerized sensors that detect what his legs are doing-deep knee bends-and tube-like artificial muscles, mounted on both sides of the knee, that expand and contract with flows of compressed air. The artificial muscles are attached to a steel brace that spans the thigh and calf; when they lengthen, they extend Moromugi's knee and help him stand more easily.
These power pants might just be the closest thing yet to a realization of longheld visions of mechanical systems that improve the mobility of the elderly and disabled or boost the strength of soldiers and rescue workers. Where previous wearable robots proved cumbersome and hard to control, this latest version-a collaboration between Nagasaki University, the University of Electro-Communications in Tokyo, Japan, and the University of California, Irvine-is smarter and more practical. Robotics experts say it's an important step toward building machines that people will actually use. "This is novel because it's sensing over the entire soft-tissue interface of the body," says Ephrahim Garcia, a mechanical and aerospace engineer at Cornell University and a former program manager at the U.S. Defense Advanced Research Projects Agency. "You need intense amounts of computation to pull it off," he adds.
Indeed, the system's tiny sensors are distributed over the legs and hips to measure signals that muscles give off when they contract. Every few milliseconds, strain gauges and ultrasonic disk-shaped sensors in cuffs around the user's legs measure the stiffness and density of the underlying tissues and communicate wirelessly with a computer that makes sense of the signals-predicting the user's intended movements on the basis of experimental data and mathematical models. Then, like a diligent weight-room spotter, the computer controls the artificial muscles. "We're trying to reduce fatigue and eventually help disabled people," says Maria Feng, a civil engineer at UC Irvine and a collaborator on the project.
The robotic pants are being tested at Nagasaki University for use as a physical-therapy tool for patients confined to bed. The researchers are also testing a mechanical glove that allows a user to pick up a coffee cup just by tensing muscles in his or her upper arm-important for, say, a person who has lost fine motor control due to a spinal injury or cerebral palsy. In the next two years, says Feng, the researchers will work out the remaining bugs and begin widespread testing of the devices in clinics and with patients.
If all goes well, such human-assist machines might hit the market in five to ten years. That's because dozens of robotics researchers are working on related projects, with tens of millions of dollars of funding from DARPA alone. At the University of California, Berkeley, mechanical engineers have built robotic "exoskeletons" that connect to people's legs to help them balance, walk, and run with less effort. The researchers are currently developing a prototype lower-body suit, powered by rocket fuel, that could allow soldiers to move more easily over uneven terrain while carrying heavy equipment.
So who will be the first to actually use such devices? The consensus among the researchers is that physical therapy and rehabilitation will be the initial commercial applications. But that will require streamlining the technology to make it as safe and reliable as possible. It's still too early to say whether the real impact will be felt on the battlefield or in the home. But if the research and development is successful-and wearable robots prove to be good for your health-they may become fashionable to boot.
(C) 2004 Technology Review. via ProQuest Information and Learning Company; All Rights Reserved
Back to Top

My return to chatting soon

2007-09-28 19:21:30

I just wanted to let folks know I wil be returning
to chatting soon on AOL or my own site is still
unclear . . . . I am returning!
Jayne

Into practice

2007-09-28 16:40:56

Adapted from The Daily Motivator

Thursday, February 5, 2004

Into practice

The true priorities in your life are the ones you actually put into practice. The beliefs, values, and commitments that are sincerely yours are the ones that are evidenced by your actions.

You can talk all day about what you are going to do or about the things that are truly important to you. What really makes a difference is not what you say you will do but rather what you actually do.

Your thoughts, ideas and beliefs are given life by your actions. Your values, commitments and priorities are made real and given meaning when you put them into practice.

The person you become depends not on who you wish to become, not on who you would like to become or not on who you hope to become. The person you become depends on what you do with every moment that you live.

These moments are yours to spend and fashion as you please. In fact, there is one right now that you can immediately begin to use.

Exactly what values, goals, ambitions and priorities are you willing to put into practice? This is the person you will be.

-- Ralph Marston

[INLINE]
~Joyce [INLINE]
Make yourself at home; clean my kitchen!

Adulterated Medical Devices Seized

2007-09-28 07:53:20

FDA Talk Paper

T04-03
February 4, 2004

Media Inquiries: 301-827-6242
Consumer Inquiries: 888-INFO-FDA

Adulterated Medical Devices Seized

At the request of the Food and Drug Administration (FDA), the U.S. District Court for the Northern District of Ohio issued a seizure warrant on February 3, 2004, for seizure of various neonatal chemistry and isoelectric focusing diagnostic kits at PerkinElmer Life Sciences, Inc., (PerkinElmer) in Norton, Ohio. The test kits are used to screen for several genetic diseases in newborns and hemoglobin and central nervous system diseases in adults, such as sickle cell anemia and multiple sclerosis. The U.S. Marshals Service executed the seizure warrant on February 4, 2004.

http://www.fda.gov/bbs/topics/ANSWERS/2004/ANS01278.html

~Joyce
I have taken a vow of poverty. To annoy me please send money.

Fwd: [RD] Anyone want to go to France this summer for a Disability Studies co...

2007-09-28 03:14:56

In a message dated 02/04/2004 8:03:00 AM Eastern Standard Time, tcarroll@... writes:

Begin forwarded message:

Reminder - "Challengers' MS Support Group Mtg

2007-09-28 03:08:32

We would like to remind you of this upcoming event.
"Challengers' MS Support Group Mtg
Date: Wednesday, February 4, 2004
Time: 11:30AM - 2:00PM EST (GMT-05:00)
This MS Support Group meets every other Wednesday in the
basement of St. William the Abbot RC church at 2000 Jackson Ave
in Seaford, NY

Life's Lessoms

2007-09-27 12:43:57

Adapted from The Daily Motivator

Wednesday, February 4, 2004

Life's lessons

You have the chance to learn something valuable today. Whether the day is frenzied, peaceful, stressful or relaxing there is much you can learn from the living of it.

Some people let life's lessons slip by unnoticed. Others take them to heart eagerly and often. Life offers its lessons to all, and life richly rewards those who accept and appreciate them.

You could complain that something doesn't work, or you could learn to make it work. You can allow the setbacks to discourage you, or you can let the setbacks teach you how to get ahead.

From every experience there is a lesson. From every person, situation, success and especially from every disappointment there is something to be learned.

Learn all you can from those lessons. Master life's lessons, and you will surely master life.

-- Ralph Marston

[INLINE]

~Joyce [INLINE]
I have taken a vow of poverty. To annoy me please send money.

Fwd: [RD] Medicare Power Wheelchair Rules change!

2007-09-27 11:16:09

In a message dated 02/03/2004 4:41:05 PM Eastern Standard Time, tcarroll@... writes:

Begin forwarded message:
Subject: Medicare Power Wheelchair Rules change!
Response to Fraud Opens Way to CHANGE
New Medicare power wheelchair policy
Headline News 18 Dec 2003
DMERCs Issue Power Wheelchair Policy Clarification
BALTIMORE--Following the 10-point initiative called Operation Wheeler
Dealer
by the Centers for Medicare and Medicaid Services/Office of Inspector
General
to curb fraud and abuse of the Medicare power wheelchair benefit, last
week
the four DMERCs announced a clarification of the local medical review
policy
for power wheelchairs and the adoption of "a consistent approach" to
medical
review of power wheelchair claims.
In bulletins issued from all four DMERC regions, the following
clarification
was given: "If a patient can only bear weight to transfer from a bed to
a
chair or wheelchair, the patient is
considered nonambulatory. However, if the patient is able to walk either
without any assistance or with the assistance of an ambulatory aid,
such as a
walker, the power wheelchair is denied as not medically necessary. If
the
patient is nonambulatory and qualifies for a wheelchair, a power
wheelchair is
covered only if the patient is unable to self-propel a manual wheelchair
within their home. Medicare coverage of durable medical equipment is
limited
to items that are necessary for use within the home. Although a power
wheelchair may be useful to allow the beneficiary to move extended
distances,
especially outside the home, Medicare statute and national policy do not
currently provide coverage solely for those uses."
"It's much more than a clarification; it's actually a change in policy,"
responded Sharon Hildebrant, executive director of the Rehab and
Assistive
Technology Council at Alexandria, Va.-based American Association for
Homecare.
Such strict interpretation and medical review would drastically change a
national policy that, until now, has based medical need on a patient's
ability
to perform daily living activities within the home.
**********************************
Susan Barnhill, Disability Advocate
916 372-4006, fax 372-4044
1675 Union Square Road
West Sacramento, CA 95691
Editorial Consultant for DREES'
http://www.station504.com
Past President & New World Newsletter Editor
for CDR (Californians for Disability Rights).
www.disabilityrights-cdr.org,

Fwd: [RD] True Majority

2007-09-27 09:20:44

Read and go to the site...........Informational and interesting ...Don't forget to join.

Cabbie

A weeks ago we sent around a link to this little animation we made, which
explains the federal budget using, well, Oreo cookies. The response has been
fantastic. So much so, at first, that many folks didn't get through. We quickly
upgraded the gizmos, and now 300,000 people have watched the piece. Thousands
of TrueMajority members forwarded the e-mail to their friends, and 25,000 new
people have joined our movement in the last two weeks.
Those are just the kind of friend-to-friend connections we need to get rid of
the insanity in Washington.
Now President Bush has submitted his budget proposal for the new year. Once
again, it's heavy on the guns (including useless cold war weapons and new
nukes) and weak on the things we really need-such as schools, health care, and
help for the world's poorest. If you haven't seen the Oreo animation yet, check
it out. And please pass this e-mail on to friends and family so they can see
this great introduction to the values of TrueMajority.
www.TrueMajority.org/oreo
Thanks for spreading the word,

Re: [MS_Community] Were you born March - June?

2007-09-27 01:15:42

I read the year was dx'ed that MS is an illness of
those born nder Gemini. s a emini my blood ran cold on
reading this.
Jayne

name=abcnewscom_83x20.gif

Assembly Resolution Seeks Additional Federal Heating Funds for New York State

2007-09-26 15:50:21

Assembly Resolution Seeks Additional Federal Heating Funds

Assembly Speaker Sheldon Silver and Energy Committee Chair Paul Tonko announced the Assembly's passage of a resolution calling on President George W. Bush and the United States Congress to provide additional federal funds for the low-income Home Energy Assistance Program (HEAP).

"A sharp rise in the price of home heating oil combined with this winter's record-low temperatures have resulted in tremendous financial hardship for seniors and low-income New Yorkers and a spike in HEAP applications," said Silver. "We urge the federal government to increase funding for HEAP and expand the programs eligibility. Each day, senior citizens on fixed incomes and working families are being forced to choose between whether to purchase prescription drugs and food or heat their homes."

"This winter's frigid temperatures and the extraordinarily high price of heating oil, natural gas and propane will stretch the budgets of energy consumers across this state," said Tonko. "The Home Energy Assistance Program, which is a lifeline for cash-strapped senior citizens and working families, must be adequately funded to provide benefits for all those in need."

Silver and Tonko noted that the harsh winter weather has increased the state's consumption of home heating fuels by 20 to 40 percent, putting additional strain on senior citizens and working family budgets and forcing them to absorb the cost of increased natural gas, propane and heating oil prices that are at an all time high.

With much of the winter yet to come and the number of HEAP applications growing, the Assembly resolution (K.1432) urges the president and congress to provide additional federal funds to HEAP, which currently benefits more than 700,000 New Yorkers. The resolution also asks Washington to raise the program's income eligibility levels so that more individuals and families can qualify for the federal energy assistance program.

"By increasing funds to HEAP and expanding the eligibility levels, the federal government will be providing more New Yorkers with the assistance they will desperately need to get through these very difficult weather and economic conditions. Federal action is needed immediately so those struggling to make ends meet can afford to heat their homes," said Silver.

Were you born March - June?

2007-09-26 10:20:24

Disease in Season

Does Your Birth Month Affect Your Health?

By Marc Lallanilla
ABCNEWS.com
Feb. 3 You may dismiss astrology as a harmless pseudo-science, but your birthday could have more importance than you think. Some scientists now believe the month in which you were born may predispose you to certain illnesses.

http://abcnews.go.com/sections/Living/US/disease_month_040203-1.html

~Joyce
Kindness is a language that the blind can see and the deaf can hear.

'Miracle workers'

2007-09-26 01:23:34

'Miracle workers'

Lindsay McReynolds
Herald-Citizen Staff
Two months ago, 68-year-old Raymond Rodgers couldn't walk or talk -- he had had a "mild" stroke that left him confined to a wheelchair. It took three nurses just to get the Cookevillian out of bed. But two weeks ago, Rodgers returned to his home, not only talking but also walking with a walker and working toward walking with a cane.

http://www.herald-citizen.com/NF/omf.wnm/herald/features_story.html?[rkey=0029280+[cr=gdn

[INLINE]

~Joyce [INLINE]
Kindness is a language that the blind can see and the deaf can hear.

Fwd: [lowdosenaltrexone] Multiple Sclerosis Research Group, UT

2007-09-25 21:13:40

In a message dated 02/03/2004 11:28:24 AM Eastern Standard Time, cowsarus@... writes:

Check out the drug, Fampridine below.

UNIVERSITY OF TEXAS

MULTIPLE SCLEROSIS RESEARCH GROUP NEWSLETTER

THIS EDITION OF OUR NEWSLETTER presents information on new studies which will soon be enrolling patients on Copaxone^® with relapse, a trial of an antibody against white blood cells, and two ongoing trials using antibiotics in the treatment of RRMS and dose-responses measurements of ingested IFN-alpha.

THE ANTI-ADHESION ANTIBODY TRIAL is a phase II study of Antegren^® (Natalizumab, an antibody that blocks cell migration into the brain) with Copaxone^® in RRMS. The primary aim of this double-blind, randomized, placebo-controlled, parallel group clinical trial study is to determine whether adding Antegren to the standard regimen of Copaxone^®, when compared with adding placebo, is safe and well-tolerated. A secondary objective is to see if the combined therapy could be more effective as measured by new active lesions on cranial MRI scans. In this study active lesions are gadolinium-enhancing lesions and new/enlarging T2 lesions. Subjects will receive IV Antegren^® or placebo every 4 weeks in addition to Copaxone^® daily for up to 20 weeks and undergo monthly MRI scans. Biogen sponsors this clinical trial.

ANTIBIOTIC THERAPY FOR CHLAMYDIA. Many infectious agents have been suggested to play a role in the etiology of MS. Dr. Sriram at Vanderbilt University has presented evidence that Chlamydia pneumoniae can often be identified in the spinal fluid of MS patients. We are enrolling patients in a placebo-controlled trial to test whether antibiotic therapy effective against chlamydia can reduce MS disease activity. Patients should have relapsing-remitting disease with mild disability and not on interferon, glatiramer or other immunosuppressive therapy. This study is supported by the NMSS.

FAMPRIDINE (4-aminopyridine) is an orally active drug that may be useful for reducing the severity of some MS symptoms such as fatigue, weakness, or limited endurance. We will be participating in a study to test the safety and usefulness of a sustained release form of this drug. Subjects need to be able to walk 25 feet without resting, and should not have had a recent exacerbation. Acorda Therapeutics sponsors this trial.

INGESTED IFN-ALPHA may decrease new MRI gadolinium lesions. Initial results suggest that doses lower than 10,000 IU may show the best effect. We are seeking 17 MS patients to examine blood before and after swallowing 100, 300, 1,000, 3,000 and 10,000 units IFN-alpha. Patients will come to the Clinical Research Center in the morning, swallow IFN and have blood drawn 4 hours later once per week for 5 weeks. This information will be important in deciding the doses for the next MRI/MS clinical trial.

We appreciate your help in referring patients to our Multiple Sclerosis Research Group. Your efforts allow MS patients the opportunity to be involved in cutting edge clinical trials. You should know that these trials are fully supported by various sponsors. There is no charge to your patients, unless a brief pre-screening evaluation is required in our regular clinic.

If you have or know of patients that might wish to participate in any of the clinical trials outlined above, please call Robert Boudreaux at 713-500-7135.

Jerry S. Wolinsky, MD, Director The University of Texas

Staley A. Brod, MD Health Science Center at Houston

J. William Lindsey, MD Department of Neurology

Judy Booth, RN 6431 Fannin, MSB #7.044

Myrna Koh, RN Houston, Texas 77030

Lucie Lambert, Assistant Phone: 713-500-7135

Fax: 713-500-7041

Focus on abundance

2007-09-25 16:48:14

Adapted from The Daily Motivator

Tuesday, February 3, 2004

Focus on abundance

Abundance is a state of mind. See the world through eyes of abundance, and you bring that abundance surely to life.

If you live in fear of scarcity, your very actions will serve to create that scarcity. Let abundance color your thoughts and your moments.

There are positive possibilities in every direction. Choose the ones that best fulfill who you are. Bring life to the highest of your possibilities with richness and passion. Dive into the abundance that is waiting to be lived.

The problems and challenges may seem big until you compare them to the positive possibilities. Lack and limitation may seem real until you experience the reality of true abundance.

Focus your thoughts, moments, actions, and days on the abundance that is surely there. The more of it you know and experience the more there will be.

-- Ralph Marston

[INLINE]
~Joyce
Kindness is a language that the blind can see and the deaf can hear.

Fwd: [RD] Student Activism Scholarship.......

2007-09-25 12:09:11

In a message dated 02/03/2004 11:33:27 AM Eastern Standard Time, tcarroll@... writes:

Begin forwarded message:
Student Activism Scholarship
Please distribute widely:
Attention student activists: Information about the Davis-Putter
Scholarship
Fund, the application process, and the students we support, can be
found
at:
www.davisputter.org
The Davis-Putter Scholarship Fund provides grants to students actively
working for peace and justice. These need-based scholarships are
awarded
to those able to do academic work at the university level and who are
part of the progressive movement on the campus and in the community.
Early recipients worked for civil rights, against McCarthyism, and for
peace in Vietnam. Recent grantees have been active in the struggle
against racism, sexism, homophobia, and other forms of oppression;
building the movement for economic justice; and creating peace through
international anti-imperialist solidarity.

Antisense Therapeutics Presents Preliminary ATL1102 Phase I Results At Neuroscie

2007-09-25 03:31:30

Want to send this story to another AOL member? Click on the heart at the top of this window.
Antisense Therapeutics Presents Preliminary ATL1102 Phase I Results At Neurosciences Conference
VICTORIA, Australia, Feb. 2 /PRNewswire/ -- Antisense Therapeutics Limited (ASX: ANP), a biopharmaceutical company today announced that preliminary data from its Phase I human clinical trials on ATL1102, Antisense Therapeutics' second generation antisense drug for multiple sclerosis (MS), was presented at the Australian Neuroscience Society Scientific Conference in Melbourne on January 30.
Dosing is completed in both single and multiple dose Phase I trials. The aims of the Phase I trials are to obtain information on the pharmacokinetic behavior of ATL1102 in humans and to assess the safety and tolerability of increasing dose levels of ATL1102.
Blood and other biological samples are being collected from every individual to measure safety parameters and the blood level concentrations of the delivered drug and safety parameters over prolonged periods of time (lasting several months after dosing). Laboratory analyses and collection of the biological samples are still continuing and full and final results are expected to be reported mid-year.
Preliminary indications from the data collected and analysed so far are favorable for both safety and pharmacokinetics.
These indications provide Antisense Therapeutics with the confidence to begin planning the Phase IIa clinical trials in MS patients with the selection of appropriate dose levels and dosing regimens. At present, study designs for the Phase IIa clinical trial are being discussed with potential clinical trialists and contract organizations.
Once final reports are received for the Phase I trial and the results are assessed as satisfactory, the Company will make an application for the Phase IIa patient trial.
Regulatory agency approval and commencement of the Phase IIa trial are targeted for the second half of 2004.
A copy of the PowerPoint presentation made to the Australian Neurosciences Conference is available on the Antisense Therapeutics website www.antisense.com.au.
Multiple Sclerosis (MS) is a life-long chronic, incurable disease that progressively destroys the central nervous system. It is commonly diagnosed between the ages of 20 and 40 years. MS affects about 350,000 people in the US where the estimated cost of the disease is more than US$2.5 billion. Although current treatments are unable to slow disease progression, the aims of therapy are to reduce the duration, frequency and severity of attacks.
ATL1102 is a drug under development by Antisense Therapeutics, which aims to prevent the synthesis of a protein called VLA-4 known to play a part in both the onset and progression of MS.
Antisense Therapeutics Limited is an Australian publicly listed biopharmaceutical drug discovery and development company (ASX: ANP). ANP's mission is to create, develop and commercialize novel antisense pharmaceuticals for large unmet markets. Its two most advanced projects target Multiple Sclerosis (ATL1102), and Psoriasis (ATL1101). ANP plans to commercialize its pipeline via licensing/collaboration agreements with major biotechnology and pharmaceutical companies. The Company's major shareholders include Circadian Technologies Limited (ASX: CIR), Isis Pharmaceuticals Inc (Nasdaq:ISIS), Queensland Investment Corporation and the Murdoch Childrens Research Institute. Further details are available on the Antisense Therapeutics website: www.antisense.com.au
SOURCE Antisense Therapeutics Limited
CO: Antisense Therapeutics Limited
ST: Australia
SU: SVY TDS
Web site: http://www.antisense.com.au
http://www.prnewswire.com
02/02/2004 13:05 EST

How To Virtually Eliminate Your Risk Of Rheumatoid Arthritis or MS

2007-09-25 03:21:21

How To Virtually Eliminate Your Risk Of Rheumatoid Arthritis or MS

Researchers have found women who eat a diet rich in vitamin D may reduce their chances of developing rheumatoid arthritis (RA) and multiple sclerosis (MS). Two studies involving women have shown proof of the vitamin's benefits.

The RA study followed 29,368 women aged 55 to 69 years, and the MS study looked at more than 185,000 women. The participants were given questionnaires to fill out about their dietary habits and vitamin D intake at the beginning of each study, and researchers followed up with the women every four years for up to 20 years. They discovered that women were 30 percent less likely to develop RA, and 40 percent less likely to develop MS, when taking the recommended daily amount or more of vitamin D.

Out of 100 people worldwide, one or two will develop RA and around 0.04 percent have MS. Both of these conditions are thought to occur when the bodyâs immune system turns against itself. Researchers suggest that vitamin D may work by calming overactive immune cells.

Responding to this study, vitamin D experts advise future researchers studying vitamin D levels to administer a blood test to read the levels more accurately, and cautioned that this study did not use the best way to determine vitamin D levels in the participants.

Neurology January, 2004 13;62(1):60-5

Arthritis & Rheumatism January, 2004;50(1):72-7

Fwd: Register by 2/6 for the NY Primary

2007-09-24 21:33:07

for the New Yorkers in the Community

Robinson was diagnosed with primary progressive Multiple Sclerosis

2007-09-24 07:14:25

New novelist weaves words through adversity

By Perry Flippin
February 2, 2004

Doug Robinson, once a globetrotting adventurer with a flair for action romances, writes stories that leave readers wanting more.

http://www.gosanangelo.com/sast/news_columnists/article/0,1897,SAST_4955_2623040,00.html

[INLINE]

~Joyce
Incontinence hotline; can you hold, please?

Fwd: [MS_Community] Genetic information from a simple blood test

2007-09-24 06:13:52

In a message dated 02/02/2004 1:19:14 PM Eastern Standard Time, saynotomeat@... writes:

Detecting Changes in Multiple Sclerosis

MONDAY, Feb. 2 (HealthDayNews) -- Genetic information from a simple blood test may help doctors detect changes in people with multiple sclerosis (MS) and improve diagnosis and treatment for these patients.

Genetic information from a simple blood test

2007-09-23 23:14:12

Detecting Changes in Multiple Sclerosis

MONDAY, Feb. 2 (HealthDayNews) -- Genetic information from a simple blood test may help doctors detect changes in people with multiple sclerosis (MS) and improve diagnosis and treatment for these patients.

Less than perfect

2007-09-23 17:52:58

Adapted from The Daily Motivator

Monday, February 2, 2004

Less than perfect

Things will never be perfect. Sometimes they will never even be close, yet this is no reason to hide away from life or no reason to curse your predicament. On the contrary it is every reason to rise up and go forth with renewed determination.

If you wait for conditions to be perfect, you will never get much done. If you refuse to go ahead unless you can be guaranteed of a sure thing, you will never get very far.

It is great to aim toward perfection, but in order to arrive at perfection you must cross through a lot of imperfections. To get everything just right you must be willing to deal with things going wrong.

Take this day and moment with all its flaws, and make the very most of it. Rather than complaining about what you do not have or where you would rather be you can make full use of where you are and of what you do have.

Aim toward perfection while also accepting the reality of what is, and excellence will surely result.

-- Ralph Marston

[INLINE]
~Joyce
Incontinence hotline; can you hold, please?

Reminder - Glenda's birthday!

2007-09-23 17:21:20

We would like to remind you of this upcoming event.
Glenda's birthday!
Date: Monday, February 2, 2004
Time: All Day
She is Bumblegeek@...

Reminder - Joyce's birthday!

2007-09-23 05:26:30

We would like to remind you of this upcoming event.
Joyce's birthday!
Date: Monday, February 2, 2004
Time: All Day
Joyce's email addy is
jfromsnell@...

Re: [MS_Community] LONG-TERM CARE The Ticking Bomb

2007-09-23 03:14:38

Thank you for this, Carol!
Jayne

=== message truncated ===

Largest brain repair initiative in MS

2007-09-22 12:04:42

Largest brain repair initiative in MS will speed strategies to restore nerve function

The National Multiple Sclerosis Society has launched a new initiative to speed research on nervous system repair and protection in MS, a disease that attacks the brain and spinal cord. The Society has invited proposals from research teams to compete for grants of up to $5.5 million each to pave the way for clinical testing of repair and protection strategies in people with MS.

http://www.eurekalert.org/pub_releases/2004-01/nmss-lbr012904.php

~Joyce
Silence is acceptance!

Update on MiCASSA

2007-09-22 11:51:54

Update on MiCASSAhttp://www.adapt.org/casa/update.htm

The House and Senate have adjourned until January 20th 2004 and Congress has returned to their districts for the end of the year recess. This is the perfect time for you to visit both of your Senators and your Representative about MiCASSA and giving folks Real Choice in long term care.

Give them a call and make an appointment to talk with them about this important legislation.

We must call for their support of MiCASSA!

* Contact your Senators and Representatives NOW and ask them to support MiCASSA (S. 971 /HR 2032) and the Money Follows the Person S. 1394.
* Get them to become a co-sponsor of both bills
* and to call for hearings for MiCASSA by March 2004!

Can't get an appointment? Visit with their staff person.

Keep your eyes and ears open! They often hold town meetings, public forums and the like to meet with Constituents (that's a fancy word for you!) to talk about issues.

Sometimes they go to public events or come to meetings. Invite them to your Christmas party, or an event in early January.

Be creative, have fun but please -- make contact over the Winter recess and let them know you want their support for MiCASSA and Money Follows the Person.

LONG-TERM CARE The Ticking Bomb

2007-09-22 08:33:34

Introduction
⢠The Promise of Coverage
⢠States that Stand Out

LONG-TERM CARE

The Ticking Bomb

Diagnosis: Long-term care threatens to bankrupt Medicaid and the states that pay for it. The best hope for a cure lies in cutting down on the need for institutional care.

[INLINE] ith the population aging, states are struggling to balance the relentless need for nursing home care, increased demands for home and community-based services and a way to fund it all. Further compounding the problem is another Medicaid population in need of expensive long-term care services: younger disabled adults unable to live independently without assistance.

The cost for long-term care for the elderly and disabled who qualify for Medicaid is enormous. Traditionally, the bulk of those services is provided by nursing homes, and increasingly, the greater proportion of people in those nursing homes are Medicaid patients. In the past few years, the federal-state Medicaid partnership has been the primary payment source for over 60 percent of all nursing home patients. The state share of that tab was $21 billion in 2002.
February cover

As the demand for non-institutional care grows, many state Medicaid programs have expanded home and community-based care. All totaled, the Medicaid program spent $16.4 billion in 2002 for home and community-based care; states paid about $8 billion of that bill.

That translates into a heavy load for each state. On average, long-term care eats up 35 percent of state Medicaid budgets. Among those above the average is North Dakota, where long-term care accounts for 60 percent of the stateâs Medicaid budget. Four other states that are also well above the average are Connecticut, Kansas, South Dakota and Wisconsin, where long-term care is more than 50 percent of Medicaid costs.

As fiscally challenging as long-term care expenditures are now, the pressure on states will intensify. The aging of the population is inexorable. One hundred years ago, only one in four Americans lived past 65. Today, three in four do, thanks in part to advances in medical science. Medical advances have also helped many younger people injured in accidents or afflicted with devastating illnesses recover, even though many of them remain physically disabled and unable to live independently or without assistance in basic personal care.

Given the fiscal and demographic pressures, itâs not surprising that Mike Lewis, chief financial officer of the Alabama Medicaid Agency, wonders âhow the system will sustain itself.â

CASE HISTORY

Before the 1970s, the elderly or disabled generally had one alternative to living with family, and that was to take up residence in a nursing home. A societal shift began about 30 years ago with a move to de-institutionalize the developmentally disabled. This was accompanied by an active independent-living movement on the part of people with physical disabilities and a similar push from advocates for the elderly to seek alternatives to nursing homes. âAll three groups struggled against the cultural beliefs of the time, which were that if you had a disability, you were broken and somebody needed to fix you and that needed to be a health care worker,â says Lee Bezanson, of Boston College.

The Shift Toward Home
Data for this graphic

The movement toward de-institutionalization got a big boost from a 1999 Supreme Court decision, Olmstead v. L.C. The court ruled that, based on the Americans with Disabilities Act, unjustified institutionalization is a form of discrimination. As long as an individual wanted transfer to the community and was judged to be qualified for community living, the state should work to move him to a less restrictive setting.

The court acknowledged that this might not be immediately possible if the move required âa fundamental alterationâ of a stateâs programs â a sizable limitation that is being tested in courts around the country. Nonetheless, the ruling has been âa catalyst decision,â says Sara Rosenbaum, chair of the Department of Health Policy at George Washington University Medical Center. âThe law didnât simply prohibit certain conduct,â she says. âIt imposed an affirmative requirement among states to start redirecting their public expenditures to get community integration to happen at a reasonable pace.â

The federal government is pushing this prescription. Its Centers for Medicare and Medicaid Services, known as CMS, set up a resource network for states to share their experiences with alternative forms of services and by 2000 began awarding âreal systems change grants.â These provide seed money for states to experiment with fundamental alterations in the delivery of services. In 2001, President George W. Bush issued an executive order requiring federal agencies to âpromote community living for persons with disabilities,â and two years later the administration launched a five-year program called âMoney Follows the Person.â It enables an individual in an institution to take the money provided for his or her care in that setting and use it to live in the community instead.

Budget Roller Coaster

Data for this graphic

As the demand for alternative-care options emerged, Medicaid began issuing waivers that permit the states to use federal matching funds to finance home or community-based care for patients who would otherwise qualify for nursing-home care. While the cost of that care cannot exceed that of care in a nursing home, Medicaid waivers provide substantial freedom for states to design their own systems.

In addition to those eligible for nursing home care, however, there are elderly and disabled people who qualify for Medicaid and require ongoing assistance , but require a lower level of assistance than a nursing home provides. All states offer home health services, largely medical in nature, but they are often very limited. About 30 states provide some level of personal care, which is not medical but includes help with basic personal activities: dressing, bathing, eating, using the bathroom, shopping or managing medicines. There also are state-financed services that can help prevent the need for more expensive institutional care.

COMPLICATIONS

Logic suggests that keeping Medicaid patients out of institutions and in their communities would drive down program costs. In Arkansas, for example, the cost of caring for a person through home and community-based services available through the stateâs Elder Choices waiver program â homemaker services, a personal emergency response system, adult day care and a respite program for family caregivers â is a third as much as placing that person in a nursing home. In Vermont, it costs $25,000 a year to provide care to someone at home and $50,000 in a nursing home.

The Long-Term Care Tab
Data for this graphic

But the long-term care fiscal ledger is more complicated than that. Individuals who use non-institutional care are often a different patient base than those who enter nursing homes. An analysis by the University of Michigan found that 45 percent of state Medicaid patients receiving waiver-funded home-care services were at the lower end of the spectrum in terms of the acuity of their personal and health needs, whereas only 8 percent of nursing home residents were at that same level.

When Michigan expanded its Medicaid waiver for home care, the state went from paying for 2,000 days a year of home care to 3 million days a year. âBut we didnât see a 3 million-day decline in nursing home use. It was flat,â says Paul Reinhart, Michiganâs Medicaid director. When the state put a lid on home-care enrollment, demand for nursing home placement did not, as one would expect, increase. âItâs decoupled,â Reinhart says. âNursing home utilization doesnât decline unless there is some forceful front-end mechanism that really constrains enrollment in nursing homes.â

Funny Figures
To control long-term care spending, states need to tamp down their nursing home bill, but lowering those costs isnât as simple as, say, capping nursing home enrollment for Medicaid patients. To start with, nursing home finances are similar to those of an airline. It costs a lot to fly a Boeing 747 from New York to Los Angeles, but the costs are about the same whether the plane is full of bi-coastal fliers or has only three people on board. The airline still needs fuel, pilots, flight attendants and, of course, the 747. The same applies to nursing homes. Cutting down on the population of any individual home doesnât save much money. The facility still has to spend a set amount of money â on utilities, on the mortgage, on the medical infrastructure â to keep operating, whether the home is full of patients or nearly empty.

As a result, simple reductions in nursing home populations donât substantially lower a nursing homeâs costs â or the price states have to pay for Medicaid patients living in the facility. For instance, when the number of patients in Kansas nursing homes dropped by 13 percent between 1996 and 2001, the per-person bill for Medicaid patients doubled. And in Idaho, when the nursing facility population declined by 7 percent during the same time period, the bill for the stateâs patients increased by 39 percent.

Itâs only when many beds in a nursing home are closed â or the facility is shut down altogether â that Medicaid can realize savings on its nursing home bills. But almost any state action to control nursing home costs â whether itâs by limiting the number of beds that can be built or operated or other means â runs smack into powerful state-level nursing home lobbyists. They have proven themselves adept at pressuring legislatures to increase rates and keep up the count of nursing home beds. Theyâve also been effective in fighting attempts to siphon off long-term care resources for other service options. One convincing argument for legislators, many of whom have a nursing home in their district: Nursing homes are good for local economies and provide jobs.

âThe business interests in the nursing home sector are very powerful,â says Barbara Edwards, Medicaid director in Ohio, where 83.5 percent of the stateâs Medicaid budget goes to institutional care. Nursing home reimbursement is set by statute, and the facilities are guaranteed rate adjustments. âChange is inevitable,â she says, âbut it will be a slow change becasue so much revenue is tied up in bricks and mortar.â

In Louisiana last winter, the stateâs executive branch proposed diverting some nursing home residents into home and community programs â a potential blow to an industry in which 7,000 beds in the state are currently empty. The reason behind the proposal was simple. âThe demand for nursing home care is declining. And yet we have this vast institutional network that we continue to support,â says David Hood, secretary of the Louisiana Department of Health and Hospitals. Nonetheless, the proposal went nowhere, and the lobbyistsâ role in fighting it off was clear.

REMEDIES

Limiting Supply
Gaining control over the supply of nursing home beds is clearly one key to taming the cost of long-term care. States can use certificate-of-need programs to restrict the building or purchase of new medical facilities or equipment, nursing homes included. But many states have abandoned the certificate-of-need approach, and that limits their ability to cap nursing home supply. A case in point is Utah. After it eliminated certificates of need in the 1980s, a number of new nursing homes opened and occupancy rates slipped to 84 percent by the mid-1980s. In 1989, when the state placed a moratorium on accepting new nursing home providers for Medicaid, the old providers kept adding beds. Occupancy is now at 75 percent. âWe are hugely over-bedded,â says John Williams, the stateâs long-term care director.

Rooms to Spare

Data for this graphic

Oregon and Vermont, on the other hand, have both been quite effective at controlling the growth of nursing homes through certificates of need. Oregon has used more than the blunt hammer of regulation. The state initially sweetened the pot with incentives for nursing home operators to develop alternative services, such as assisted-living facilities. These are apartment-like complexes that provide living quarters in individual apartments but also make available basic non-nursing services â personal care, meals, transportation and the like. This less expensive form of long-term care did get overbuilt, however, and there is now a moratorium on new construction. The stateâs success in shifting people away from nursing home care has resulted in low occupancy levels as well.

A critical element in developing Oregonâs approach was the work legislators did on the stateâs Nurse Practice Act. In many states, such laws restrict the performance of a variety of patient-care tasks to nurses. Oregon embraced the concept of teaching and transferring skills to other individuals who could then perform them at lower cost. The newly trained personnel also helped address another issue, the shortage of nurses, particularly in the field of long-term care.

The changes dovetailed well with Oregonâs overall attitude toward long-term care, which is to build a home and community services infrastructure for people who can afford to pay their own way as well as for those dependent on Medicaid.

Thanks to its tough line on limiting nursing home beds, Oregon was able to divert spending on nursing facilities to home and community care. Today, the state devotes a significantly higher proportion of its long-term care budget to home and community programs than any other state. In so doing, its overall long-term care costs are well below the national average: $604 per capita compared with the U.S. average of $996 per capita.

Vermont is on a similar course. As the state began to realize savings from limiting nursing home beds, it put the unspent money in a trust fund. That fund was then used to provide seed money to develop community programs. âWe made smart investments,â says Patrick Flood, commissioner of aging. âThe more you build the system, the more people can go to it, and the fewer people go to nursing homes.â According to a 2002 AARP report, the percentage of long-term care dollars that Vermont spent in nursing homes dropped from 55.4 percent in 1996 to 44.1 percent in 2001. But itâs still using nursing homes efficiently. The occupancy rate is 90.6 percent, compared to the U.S. average of 82.5 percent.

Leveling Care
Several states have been able to hold down long-term care costs by making sure that the nursing home option is reserved only for those whose needs cannot be met safely in less restrictive â and less expensive â ways. This is only possible, of course, if a wide range of alternatives is available. But the approach starts with, in effect, a system of triage.

Maine, for instance, created a uniform assessment system in 1995 that is carried out by an independent agency. The agency oversees admissions for both private- and public-pay nursing home stays.

Arizona has a particularly unusual system, one that has helped that state achieve an enviable record: Its nursing-home population is 1.1 percent of residents who are 65 or older â well below the U.S. average of 3.7 percent.

To accomplish this, the state starts with individual screening to see if an applicant for care qualifies for long-term services. Those who do are then assigned to a managed care organization that receives a pre-set payment for every individual under its care â a blended rate corresponding to nursing home costs and home-based costs that is generally similar for every individual for whom it provides care. The MCO â five of the seven that cater to the elderly and disabled long-term community are county run â helps its patients select the setting thatâs right for them, but there is a clear incentive to keep people in their homes as long as those services can be offered at less cost than a nursing home.

Whatâs to stop managed care officials from overutilizing low-cost options? âIf the program contractors donât ensure that they have the right amount and type of services for those people living in home and community-based settings, they will experience more acute care and more emergency room utilization later on,â says Alan Schafer, program manager for Arizonaâs long-term care system. In Arizonaâs model, those cost increases will be born by the managed care organization, not shifted to some other group.

Arizona isnât just trusting to fiscal pain to assure that care is appropriate. The state has established a number of quality-assurance mechanisms to make sure that people are getting good services and that they are being placed in a program that provides the proper level of care.

Another creative but simple approach to determining who gets what kind of care is the way Vermont handles its waiting list for home and community-based services. Instead of admitting people on a first-come, first-served basis, the state sets priorities: Those in the greatest need â the ones most likely to end up in a nursing home if they have to wait for services â are pushed to the front of the list.

In an effort to expand on that idea, Vermont is currently asking CMS to approve a waiver that will allow the state to divide the people who qualify for long-term care into two groups: a higher need group and a lower need group. Those with the most acute needs would have a choice: They would be entitled to either home and community-based care or nursing home care, depending on what would be the most appropriate level of care for them. After that population is taken care of, the money that remains would be spent on those in the lower-need group.

Cash and Counseling
The approach that may have the greatest promise for national overhaul of long-term care is called âCash and Counseling.â Since 1996, it has been jointly funded by the Robert Wood Johnson Foundation and the federal government.

The idea is to give people who need long-term care â the frail elderly, the disabled â the choice of using cash to purchase the personal care, equipment, remodeling or other services that they need to keep them living at home safely. Instead of using an agency, the recipients (or a responsible family member on their behalf) are put in charge of hiring and firing employees and arranging for care by the individuals they choose.

To help people make their plans and choices, a counselor or consultant helps them establish a budget that will meet their needs. The adviser also stays in contact with each client to make sure that all is going well. A bookkeeping service is offered for people who want help in administrative and financial tasks, such as paying employment taxes.

The program has been implemented in Arkansas, Florida and New Jersey, with a total of 6,700 individuals. Results are being closely watched.

The first set of evaluations centered on Arkansas, since it was the first to get the program up and running. Arkansas won an A for its efforts. There were no instances of fraud or abuse â one of the big fears officials have when control shifts from a bureaucracy to an individual. Since 1998, when the program started, only four people out of the 3,000 who have enrolled were shifted out of the program because of problems in the way they were handling their own services.

The differences Cash and Counseling makes are clear. When outcomes for those in a control group in the old system were compared to those in the new program, the disparities were âgigantic,â according to Kevin J. Mahoney, national program director for Cash and Counseling Demonstration and Evaluation. In Arkansas, there was a 20-point difference in the levels of customer satisfaction. Whatâs more, people who had control over their own employees had equal or fewer health problems, and there was a major reduction in unmet needs.

The program also appeared to provide a solution to the longstanding problem of worker shortages and to providing help in difficult-to-reach rural areas. Since participants were able to hire neighbors or even family members to help them, they had a much easier time finding people to work at difficult hours, such as early morning or weekends. âAccess improved markedly,â says Mahoney.

This approach was such a notable success in Florida that the legislature unanimously passed a bill making consumer-directed care a permanent option in state programs. In May 2002, CMS came out with model âindependence-plus waivers,â which provide a template for states to set up programs that are similar to Cash and Counseling. Meanwhile, the Robert Wood Johnson Foundation and its federal government partner are expanding their specific Cash and Counseling program to an additional 10 states.

PROGNOSIS

Regardless of the remedies states try, long-term care is going to grow more expensive. Simple demographics, coupled with advances in medical care, dictate that. The number of elderly people residing alone without living children or siblings is expected to reach 1.2 million in 2020 â up from about 600,000 just a decade ago. Some of them will qualify for public programs, and the number of younger people available to pay that bill is declining as a percentage of the population.

The quality of services in nursing homes and in the community is improving â even as those improvements boost costs. And that is likely to continue, as will the pressure for states to deliver more and better services. The power of older Americans as a voting and lobbying group is well known to politicians, and their concerns are not easily ignored.

So, are the states stuck with an inexorably growing budget item for long-term care? Possibly, although state associations are working on the issue. The National Governors Association has argued for a shift in funding responsibilities to the feds for years, but the emphasis is now greater than before. The new chair of the NGA, Idaho Governor Dirk Kempthorne, has announced that making changes in the long-term care system in this country is his number one initiative.

A greater reason for guarded optimism lies in state efforts to encourage citizens to take individual responsibility â expressed, for example, by bolstering familiesâ capacity to take care of one another and by encouraging more affluent citizens to buy insurance to cover long-term care costs.

What appears to be missing from the equation is appropriate education of the American people about the horrific financial burdens that await them. Just as many self-interested Americans finally realized that they could not have a comfortable retirement based exclusively on Social Security income, states would be well advised to encourage a similar awakening regarding long-term care. Only 15 percent of Americans polled by AARP were able to make a remotely accurate guess as to the cost of long-term care; most were totally confused about whether Medicare would pay for their long-term needs. As an AARP report concludes, Americans âknow less about long-term care than they think â and than they should.â

⢠Introduction
⢠The Promise of Coverage
⢠States that Stand Out

Copyright © 2004, Congressional Quarterly, Inc. Reproduction without the written permission of the publisher is prohibited. Governing, City & State and Governing.com are registered trademarks of Congressional Quarterly, Inc.

[USEMAP]

Top patient-rated MS treatments

2007-09-21 21:02:05

Hi,
I thought everyone might like to see the latest Top 10 list of patient-rate=
d MS
treatments from RemedyFind. A little background. Remedyfind is a non-comm=
ercial
and unbiased site (not sponsored by any drug companies etc.) where individu=
als can
rate the effectiveness of the treatments they have used for specific health=
concerns,
including Multiple Sclerosis.
Obviously this Top 10 list has to be taken with a "grain of salt", especial=
ly as MS is
such a complex and unpredictable illness. We are all different, and what w=
orks for
one person won't necessarily work for another, but my hope is that certain =
trends
might show themselves over time (and after hundreds or thousands of patient=
ratings). We'll have to see about that, but at least in the meantime I thi=
nk it is helpful
to hear other patient accounts of what has worked, or not worked, for them.=
Please share your opinions on what has - or hasn't - worked for you. You ca=
n choose
from dozens of treatments to rate, from meds to nutritional supplements to =
alternative / complimentary and psychological therapies. Or suggest somethi=
ng I've
missed. The site is free and you can be as anonymous as you would like yo=
u choose
your own member name and your contact information is not shared with anyone=
. Here
is the address of the Remedyfind MS section -
http://www.remedyfind.com/hc-Multiple-Sclerosis.asp
All the best,
Brett Hodges
Founder / Editor
Oh, MS Community is listed on this page and you can rate it for its helpful=
ness (it is
one of the "brand" selections) - Emotional Support: Online Discussion Group=
s
http://www.remedyfind.com/rem.asp?ID=5418
Top patient-rated MS treatments
(As of February 1, 2004. The first number is the averaged rating (0 = poor=
est; 10 =
best). The number in parenthesis is the number of ratings the treatment ha=
s
received.)
ReVia etc. (Naltrexone - low dose) 9 (37)
Emotional Support: Family / Friends 8.9 (26)
Marijuana (Cannabis Sativa / Indica) 8.7 (28)
Copaxone (Glatiramer acetate) 7.5 (54)
Neurontin etc. (Gabapentin) 7.2 (42)
Rebif (Interferon beta-1a) 7 (34)
Provigil etc. (Modafinil) 7 (22)
Solu-Medrol etc. (I.V. Methylprednisolone) 6.4 (24)
Avonex (Interferon beta-1a) 6 (42)
Betaseron etc. (Interferon beta-1b) 5.8 (52)

What matters most

2007-09-21 17:58:11

Adapted from The Daily Motivator

Sunday, February 1, 2004

What matters most

Before you put a lot of time and energy into being frustrated or annoyed, worried or angry about something, ask yourself this: will it make any difference one way or the other five years from now?

Rather than turning a minor inconvenience into a major issue, take a moment to put it into perspective. If it won't matter a few days or weeks from now, is it really worth getting upset about? Why focus on the petty, insignificant things that take your time and energy away from what is truly important? Life is too precious to waste even a few moments because in each of those moments there is priceless opportunity.

Imagine what you could do today that would indeed make a positive difference five, ten or twenty years from now! Think of how you can spend the moments you have right now so that you can always look back on them with satisfaction and being thankful for the choices you made.

Live this day like the special time that it is. Keep reminding yourself to focus on what matters most, and let everything else flow quietly on by. In doing so you will be creating value that will stay with you always.

-- Ralph Marston

[INLINE]
~Joyce
Silence is acceptance!

Fw: [jjworld] Diary of a wheelchair-riding wild woman!

2007-09-21 15:11:59

-----Forwarded Message-----
From: Jooly's Joint <jooly@...
Sent: Feb 1, 2004 5:34 AM

Re: [MS_Community] Arizona to be center of MS research

2007-09-21 07:46:07

Yes Jayne
THis is very interesting.
Spent the day food shopping in this cold! We were out of food.
Mom called to say that my step father Pete found a condo for us, Could
we come down to see it next Saturday. People are interested in it.
Someone bid on it for 100 grand. Oh please!
im going to call back Take care. Carol

Fwd: [RD] Self-Settled Income Supplemental Needs Trust Outline.............

2007-09-20 21:04:21

In a message dated 01/30/2004 1:02:37 AM Eastern Standard Time, tcarroll@... writes:

Self-Settled Income Supplemental Needs Trust Outline
Stephanie T. Seiffert, Esq.
Woods Oviatt Gilman LLP
700 Crossroads Building
2 State Street
Rochester, New York 14614
A Self-Settled Income Supplemental Needs Trust is an important planning
tool that can possibly save, for a qualified individual, the assets
necessary to maintain a comfortable lifestyle while at the same time,
qualify for Medicaid benefits.
I. Who is a qualified individual?
A. Under the age of 65*
B. Currently receiving Social Security Disability (SSD) benefits (not
SSI)**
C. Wishes to qualify for Medicaid benefits
D. Has more income or resources than Medicaid will allow to qualify
for benefits
E. Has an individual who can act as Trustee
II. How does it work?
A. Assets The trust assets will include all of the beneficiaryâs
assets and income in excess of the Medicaid level, once the person
qualifies for Medicaid. Currently, as of 2002, this means that any
resources in excess of $3,800 or income over $654.00 per month would be
placed in the trust. Since the trust language generically describes
the trust property, there will be no need to amend the trust as the
income received by the beneficiary changes, as long as any amount over
the Medicaid level ($654.00) is placed into the trust on a monthly
basis.
B. Trustee The trustee is the person, appointed by the beneficiary,
who has the power to make deposits and withdrawals from the trust
account. The trustee may set up the trust account at any bank or
financial institution that he or she chooses.
* Please note that income and assets may only be contributed to the
trust until the beneficiary reaches the age of 65. After that, the
assets already in the trust may still be used, but the beneficiary is
legally unable to continue to contribute to the trust principal.
** The same type of trust may be used to protect resources such as
retroactive benefits or proceeds of lawsuits for SSI recipients, but it
may not be used to protect excess income to make someone SSI eligible.
It is the Trusteeâs responsibility to make sure that the deposit of
the income over the Medicaid level, known as the "spenddown amount," is
placed in the trust account every month. Annually, upon
re-certification, it is the trusteeâs responsibility to provide a
simple account to the appropriate caseworker at the Department of
Social Services to prove the proper amount was deposited into the trust
account every month. The best way to ensure the account is accurate is
to save the monthly statements from the trust account and copies of
cancelled checks.
C. Access Once the income has been added to the trust, it is no
longer considered part of the beneficiaryâs property. Therefore, DSS
cannot consider either that income or the trust account as available to
the beneficiary. The "spenddown" amount is essentially zero. This is
the reason the income can be saved and yet the individual can still
qualify for Medicaid benefits. However, since the trust account is
titled in the name of the trust for the benefit of the individual, it
is impossible for the individual to have direct access to the account.
Instead, the trustee must be the person to write checks out of the
account directly to creditors and for any other payments for the
beneficiary.
III. What can the trust assets be used for?
Basically, anything that would make the individual more comfortable.
According to Article "V" of the trust agreement, the Trustee has the
discretion to pay "income and/or principal to insure that the
Beneficiary enjoysâ¦education, vocational training, hobbies, vacations,
modes of transportation, entertainment and any other needs and/or
comforts the Beneficiary may require to maximize the Beneficiaryâs
life." Clearly, the trust assets can be used for virtually anything
that the would enhance the life of the beneficiary.
IV. How do you establish a Self Settled Supplemental Needs Trust?

First, it is necessary to draft the trust for the beneficiary and the
trustee to review. In
order to complete the trust, your attorney will need the full names
and addresses of both
the beneficiary and the Trustee, and the beneficiaryâs Social Security
number.
Next, someone will need to establish the trust for the beneficiary.
There are two ways to
do this. Since the statutes governing the operation of these trusts
were originally intended to assist disabled minors, the regulations
state that the trust must be established by a guardian, parent or a
grandparent of the beneficiary, or if such individuals are not
available, the beneficiary must obtain approval from the Surrogateâs
Court. The parent or grandparent need not be involved in any aspect of
the trustâs operation consenting to the establishment of the trust.
If a guardian, parent or grandparent is not available, it will be
necessary to petition the court for approval to establish the trust.
This is not a lengthy process and will not necessitate a court
appearance by the beneficiary. The petition will explain the
disability of the proposed beneficiary and state that there is a need
for the trust to be established. It will also outline the financial
status of the beneficiary. It is important that all of the information
is presented accurately. In addition, the attorney will submit an
affidavit to attest to the veracity of the beneficiaryâs petition. The
court will then review the petition and sign a decree indicating that
it is permissible to establish the trust.
Two waivers are also necessary for a consent for a court to establish
the trust. One waiver must be signed by trustee stating that he or she
agrees to his or her appointment as Trustee. The second waiver will be
signed by Monroe County Department of Law agreeing to the establishment
of the trust. These waivers are standard and it is not typically a
problem to obtain them.
Once all of the paperwork is in order, the trustee must open an account
in the name of the trust for the benefit of the beneficiary at a bank
or financial institution. This is done by taking the courtâs decree (if
needed) along with a signed and notarized copy of the trust agreement
to the bank. As stated above, it will be the trusteeâs responsibility
to ensure that the "spenddown" amount is properly deposited into the
trust every month. Failure to do so could result in the loss of
Medicaid benefits for the beneficiary for the month the correct
"spenddown" amount was not deposited into the trust. Again, the
correct "spenddown" amount will be any income received by the
beneficiary over the current Medicaid limit of $654.00.
V. Cost
The cost of establishing this kind of trust depends on the method used
to establish the trust. If it is necessary to petition the court in
order to setup the trust, the cost will be
approximately $1,250.00 which includes a $165.00 filing fee. On the
other hand, if a petition is not necessary, the charge will be closer
to $750.00. These quotes are subject to change and will be discussed
at the first meeting. Usually it is possible to agree upon a fee
payment schedule to start after the trust is funded.

Attached to this outline is a Self-Settled Supplemental Needs Trust
Application that must be accurately completed in order to draft the
Supplemental Needs Trust.

Fwd: [MS_Community] Fill life

2007-09-20 19:51:48

Adapted from The Daily Motivator

Saturday, January 31, 2004

Fill life

Fill the world around you with beauty, and there will be no place left for darkness. Let your spirit be filled with joy, and there will be no room available for anxiety.

Fill your body with nutritious food, and there will be no room for toxic junk. Fill your heart with love, and there will be no place left for hatred.

Fill your actions with real, meaningful purpose, and there will be no room for doubt or insecurity. Fill your moments with goodness, and there will be no place for resentment.

Fill your relationships with kindness and sincerity, and then there will be no room left for discord. Fill your mind with positive thoughts, and there will be no space left for dismay. Fill your days with passion and meaning, and there will be no room for regret. The more good, positive, loving, productive and effective things with which you fill your life the less room there will be for the undesirable things.

Fill your life and world with the best that you can give.

-- Ralph Marston

[INLINE]

~Joyce [INLINE]
Dedication is doing the best with your life rather than settling for what is only good.

A support group for people with ms & their friends & relations. We try & keep informed of developments in ms research & stay abreast of legislative issues that may effect us.

Federal Action on Medicaid Needed Now

2007-09-20 16:25:39

In a message dated 01/30/2004 2:21:56 AM Eastern Standard Time, jayneadler@... writes:

-----Forwarded Message-----
From: F