NYTimes.com Article: Bush Pushes Plan to Curb Medicare Appeals

2006-12-31 22:53:23

This article from NYTimes.com
has been sent to you by jayneadler@....
Thought this would b of interest.
jayneadler@...
Bush Pushes Plan to Curb Medicare Appeals
March 16, 2003
By ROBERT PEAR
The changes would make it more difficult for beneficiaries
to appeal the denial of benefits like home health care.
http://www.nytimes.com/2003/03/16/politics/16HEAL.html?ex=1048921598&ei=1&en=175\
b28da4ee1fb93
HOW TO ADVERTISE

Woman, 56, could be forced into OAP home

2006-12-31 13:13:44

Woman, 56, could be forced into OAP home
March 17, 2003 07:00
By Katy Edwards and Jonathan Barnes
A DISABLED woman fears she might have to leave her husband and move into an old
people's home at the
age of 56 because of a shortage of carers in the county.
Wheelchair-bound Heather Atkinson, who suffers from multiple sclerosis, said she
could not bear the
forced separation from Alby, her spouse of 27 years.
She has already spent more than two months in rest homes around Ipswich after
her husband was forced
to admit he could no longer look after his wife at their cottage in Nacton.
Mr Atkinson, 62, a former painter and decorator, of Felixstowe Road, has chronic
back problems and
has had intensive surgery to remove tumours from his aorta and liver.
He can no longer help his wife get up in the morning and wash and dry herself -
but she cannot face
returning to a home and cannot understand why care is not available.
Mrs Atkinson said: "I can't face going back to a home, I was so miserable. I was
in two different
old people's homes and a home for very disabled young people who couldn't really
speak.
"I missed Alby desperately, but I had to go in to preserve his sanity. He's not
getting any younger,
he can't go on doing all these things for me.
"I used to have two girls who came in each week. Now they say that because of
where I live, I can't
get any care. I like it here looking at the trees and the birds. The retirement
homes were
surrounded by concrete. It felt like being in prison."
Her husband added: "I don't want her to go back in a home. I saw how unhappy she
was. I want us to
live together."
A friend is currently helping Mrs Atkinson in the mornings, but it is not a
permanent arrangement.
She would be willing to pay her contribution towards a carer, bur she cannot
afford private rates.
Jack Thain, chairman of the Suffolk Pensioners' Association, said: "It is not a
very nice situation
and I feel deeply sorry for them.
"They should be together, that's emphatic. If it comes to the point where it is
impossible to keep
them together, she should not been placed too far away. I will be asking some
questions about this."
He added: "I know there are a lack of carers in certain areas and we are looking
into this
situation. Lots of people rely on this service and it is very worrying if they
are missing out."
John Gummer, the Conservative MP for Suffolk Coastal, said he would taking up
the case of Mrs
Atkinson's care.
"This is a very real problem throughout my constituency and throughout the whole
of Suffolk. There
is a lack of home carers - and one of the problems is many of those who do this
job, and do it well,
find that the money the council is prepared to pay is not sufficient to cover
their expenses.
"I have had a particular case this last fortnight where a home carer has been
driven by very low pay
to go for another job to make ends meet."
He added: "This is a very sad state of affairs and is particularly true in parts
of my constituency.
It is particularly a problem in the more rural areas.
"The council has a responsibility to enable people to remain in their own homes
for as long as
possible and if people are not helped to stay in their own homes and forced into
residential
accommodation, that is immensely more expensive."
A spokesman for Suffolk County Council said there was a shortage of carers in
some parts of the
county and it was often difficult to recruit care staff in more rural areas.
He added an emergency response team would provide a short-term solution to Mrs
Atkinson's situation.
"We are sorry for the delay in being able to offer care to Mrs Atkinson, but
hope we will now be
able to resolve the situation with her," said the spokesman.
"We have been working to find suitable care in this area now for some time and
we are hopeful that a
carer for the area can be found from some recent job applications."

Nutrition - from Chris Fincham

2006-12-31 10:15:34

Feeding hope: nutrition plays key role in HIV/AIDS care
FAO/WHO publish new manual for people living with HIV/AIDS
25 February 2003 | GENEVA/ROME -- A good diet is one of the simplest
means of helping people live with HIV/AIDS and may even help delay the
progression of the deadly virus, two UN agencies said today.
A new manual published jointly by the Food and Agriculture
Organization (FAO) and the World Health Organization (WHO) recognizes
the relationship between infection and nutrition and offers simple
dietary suggestions for the estimated 42 million people living with
HIV/AIDS. (It offers practical solutions for people trying to balance
their diets in settings around the world)
By bolstering the immune system and boosting energy levels, balanced
nutrition can help the body fight back against the ravages of the
disease and by maintaining body weight it can support drug treatments
and prevent malnutrition.
“The relationship between HIV/AIDS and malnutrition is a
particularly extreme example of the vicious cycle of immune
dysfunction, infectious disease and malnutrition,” said Dr David
Nabarro, WHO Executive Director for Sustainable Development and
Healthy Environments.
“The nutritional aspect of HIV/AIDS has been ignored for a long
time. The attention was always focused on drugs,” said William
Clay of FAO’s Food and Nutrition division, “The message
was always: ‘Take two tablets after meals’. But they
forgot about the meals.”
Almost 95 percent of people with HIV/AIDS live in developing countries
where healthcare, resources and drugs are scarce. For them a balanced
diet is a positive way of responding to the illness.
“Food isn’t a magic bullet. It won’t stop people
dying of AIDS,” Clay said, “But it can help them live
longer, more comfortable and more productive lives.”
Dr Graeme Clugston, Director of WHO’s Department for Nutrition
in health and Development, confirmed the need to pay special attention
to the role of nutrition on HIV/AIDS and HIV/AIDS on nutrition
“The effect of HIV on nutrition begins early in the course of
the disease, even before an individual may be aware that he or she is
infected with the virus.”
THE AIDS EQUATION
Widespread AIDS often occurs when a whole range of social and economic
circumstances – hunger, food insecurity, desperate poverty and
social breakdown – collide with the presence of the human
immunity suppressing virus (HIV) in the population. Such circumstances
may force people, especially young men and women, into high-risk
activities like prostitution in order to feed themselves and their
families.
When HIV/AIDS strikes a family member the effect ricochets through the
lives of the entire household. With the food-producer ill, the family
risks becoming malnourished and therefore more susceptible to
infection.
AIDS has a devastating effect on a person’s nutritional
wellbeing:
Despite blunt appetites and difficulties in eating, people living with
HIV/AIDS should eat considerably more food to fight the illness and
make up for weight loss. As part of a balanced diet someone affected
by HIV/AIDS needs more protein to rebuild muscle tissue, more
energy-rich foods for weight gain, immune system-boosting vitamins and
minerals and water to combat dehydration.
FOOD TO CARE
The FAO/WHO manual offers households caring for a family member with
AIDS inexpensive, locally available remedies for the symptoms linked
to the disease. Herbs and spices can stimulate a sluggish appetite or
digestion and may have other beneficial effects. Cinnamon can be
brewed into a tea to calm chesty coughs, for example, and mint leaves
can be used as a gargle.
By encouraging good nutritional habits FAO and WHO hope the manual
will improve the diet, health and resistance to infection of the
entire family.
Designed to be used by carers, health-workers, community groups and
non-governmental organizations, the manual includes:
It focuses on ways of easing the symptoms of HIV/AIDS – lack of
appetite, tiredness, soreness of mouth – by suggesting recipes
for soups, teas and stews using fruit and vegetables – guava,
papaya and baobab for example – that grow in the rural areas of
the developing world hardest hit by the AIDS epidemic.
“We hope this guide will be a building block, that it will be
adapted by AIDS-affected communities and that it will make people
aware of the vital role played by nutrition for someone living with
HIV or AIDS,” said Clay.
SPREADING THE WORD
To ensure that the benefits which can be derived from proper nutrition
reach people living with HIV/AIDS, FAO and WHO are also developing
training courses and educational materials for health workers and care
providers. This week, the second field testing of this course is
occurring in South Africa and it is envisaged that the course will be
published as a complete package with overheads and trainers' and
participants' guide in September 2003.
“Nutrition counselling and support is an essential component of
care for the HIV-infected person and it is particularly important in
resource-constrained settings where malnutrition and food insecurity
are endemic,” said Ms Randa Saadeh, the WHO Technical Officer
responsible for the training and educational programmes.
Concurrently, WHO is also developing norms and standards for
nutritional intake for people living with HIV/AIDS. The relationship
between HIV/AIDS and malnutrition presents a classic example of the
vicious cycle of immune dysfunction, infectious disease and
malnutrition. However, current knowledge is limited. WHO is therefore
organizing an expert consultation to review and provide guidance on
nutrient and dietary requirements for PLWHA, and to develop a research
agenda to determine the impact of improved nutrition on HIV prevention
and rate of progression from HIV to AIDS, and the frequency and
severity of opportunistic infections; and to develop/promote food
technologies which can benefit HIV-affected populations.
“We hope that, with this new information, we can assist
governments and organizations in drafting guidelines on nutritional
care and support for PLWHA and in developing food/nutrition
interventions for HIV-affected populations,” added Saadeh.
The Manual on Nutritional Care and Support for People Living with
HIV/AIDS (PLWHA) entitled Living Well with HIV/AIDS is available from
FAO.
For more information, journalists may contact:
Stephanie Holmes, FAO Media Office, Tel: (+39) 06 57056350; email:
stephanie.holmes@...
Or visit the FAO website: FAO website
Mr Gregory Hartl, Communications Adviser for Sustainable Development
and Healthy Environments, WHO, Geneva. Telephone (+41 22) 791 4458;
Fax (+41 22) 791 4858; Email: hartlg@...
For more information on training courses and educational material,
please contact:
Ms Randa Saadeh, Nutrition for Health and Development, WHO, Telephone
(+41 22) 791 3315; email saadejr@... ; or
Mr William D. Clay, Chief, Nutrition Programmes Service, FAO,
Telephone (+39) 0657054152; email william.clay@...
Post a follow-up to this message

Roger MacDougall's story (brief version with picture) This is the only article in this thread

2006-12-31 02:32:05

From: Kip King (wodi007@...)
Subject: Roger MacDougall's story (brief version with picture) This is the only
article in this thread
View: Original FormatNewsgroups: alt.support.mult-sclerosis
Date: 2003-03-16 21:02:22 PST
http://www.wheeltonhealthcare.com/RM.htm

MULTIPLE SCLEROSIS: FLOWER BULBS IN TOWN SQUARES FOR RESEARCH

2006-12-30 16:11:49

MULTIPLE SCLEROSIS: FLOWER BULBS IN TOWN SQUARES FOR RESEARCH
(AGI) - Rome, Italy, Mar 15 - Flowers in exchange for research. "Flowersintown"
is coming back into
Italian city centres. This is the show of solidarity in support of scientific
research on multiple
sclerosis, supported by AISM, the Italian Association for Multiple Sclerosis and
by its Foundation
(FISM).
In fact, in 2,000 Italian squares Dutch arum lily bulbs for different coloured
flowers (red, pink,
yellow and orange) will be handed to people who make a contribution for research
into the disease.
Massimo Giletti is the person in the advert for "Flowersintown" this year.
Multiple Sclerosis is a serious pathology affecting the central nervous system
and it is still not
known what causes it. It affects three million people around the world, 400,000
of whom are in
Europe. 50,000 of them are in Italy and there are 1,800 new cases, especially
among young adults
between 20 and 30 years old. Sardinia, where one in 700 has MS, is the most
affected.
Women are more likely to get it than men, double the number of women compared to
the number of men.
The most effective treatment is interferon together with beta 1B which reduces
relapses and
remissions, the frequency and the intensity of the attacks, slowing down the
disability's
progression. Professor Mario Alberto Battaglia, president of AISM and FISM said,
"The objective in
2003 is to raise at least a million euro for research and for bursaries". (AGI)
151509 MAR 03
COPYRIGHTS 2002-2003 AGI S.p.A.

MS group gets grant

2006-12-30 12:51:41

MS group gets grant
The Curry General Hospital Multiple Sclerosis Support Group received $1,000 in
grant funding
recently from Teva Neuroscience, makers of the medication Copaxone.
The group plans to use the money to implement upcoming activities that will be
offered free or at a
minimal cost to MS patients, their families and caretakers. Activities might
include t'ai chi or
yoga, cooking lessons, pottery, aquatic workouts, shopping trips and dining out.
Comments are sought from all Curry County MS patients and their caretakers
interested in
participating in any group activities. The support group meets at 10 a.m. every
second Thursday in
the hospital conference room. Meetings feature informative speakers, medical
staff and other
educational programs.
For more information, those interested can call Pat and Jack Oden in Brookings
at (541) 469-9864; in
Gold Beach, Lois Collum at 247-0880; or the Curry General Hospital community
relations office,
247-3187.

Wednesday, March 19, 2003 at 8:00 p.m. ET in the MSWorld chat room!!

2006-12-30 04:15:47

Mark your calendars for our special guest speaker chat with Dr. Karl F.
Gross!
Wednesday, March 19, 2003 at 8:00 p.m. ET in the MSWorld chat room!!
Berlex Laboratories is sponsoring Dr. Karl F. Gross, as our guest speaker
Wednesday, March 19 at 8 PM ET in the MSWorld room. Dr. Gross is a
retired Neurologist and has Multiple Sclerosis. He was born and educated
in Vienna, Austria and now resides in Colorado. He not only is a
Neurologist,
he walks in our shoes as an MS patient himself. You won't want to miss
him, so make plans to attend.
Please join us at MSWorld to chat with Dr. Gross! This will be a great
chat!
Click on this link to chat with Dr. Gross!! http://msworld.chatspace.com/
AOL users click <a href="http://msworld.chatspace.com/"
If you haven't registered in ChatSpace here are instructions on how to
register. Please get registered before the chat. We recommend using
Internet Explorer with ChatSpace. The newer browsers usually work
better with Java. If you are on AOL and your AOL browser doesn't work
correctly, use Internet Explorer 5.5 or 6 and that should solve any
problems you might be having. It is accessed by going to this link.
http://msworld.chatspace.com/
AOL users click <a href="http://msworld.chatspace.com"
Warm regards,
Sandra Smithey
Host Coordinator
Technical Advisor
Transcript Coordinator
MSWorld, Inc.
http://www.msworld.org/
AOL users click <a href="http://www.msworld.org/"

Simple lifestyle changes may reduce the cancer burden, IOM suggests fr. MS Watch website

2006-12-29 20:12:31

Simple lifestyle changes may reduce the cancer burden, IOM suggests
03/14/2003
According to a report from the Institute of Medicine, breaking certain unhealthy
habits or visiting the doctor more often may reduce the risk of death from
cancer by one-third.
The lifestyle changes, though difficult to make, could prevent approximately
100,000 new cancer cases and 60,000 deaths each year.
âMuch of the burden of cancer in the United States can be traced to modifiable
health behaviors that increase oneâs risk of disease,â the report states.
The IOM said the biggest cuts would come in lung cancer and colon cancer.
For example, if people did not smoke, lung cancer would be uncommon. Cases of
the disease were minimal before cigarettes became popular.
Other health behaviors that people are reluctant to change, such as diet and
physical activity, are key to lessening the cancer burden. The American Cancer
Society and other groups focused on cancer prevention have recommended a diet
based on plant food, such as fruits and vegetables, and whole grains.
Another pertinent factor for cancer prevention is early detection through
screening, such as colonoscopy.
âThe fundamental tenet of screening for cancer is that finding the disease
before symptoms develop enables detection at a less advanced state and that
instituting treatment at that time leads ultimately to improved health
outcomes,â the report stated.
As a way of decreasing harmful habits, the institute also recommended stricter
enforcement of tobacco laws. The report said tobacco taxes are the single most
effective method for reducing the demand for tobacco.
The full report can be found on the Institute of Medicineâs Web site at
http://www.iom.edu.
COPAXONE® (glatiramer acetate injection) Product Information
© 2002, Teva Neuroscience, In

NIH.gov Assistive devices

2006-12-29 18:36:37

Message: 10
Date: Sat, 15 Mar 2003 09:37:15 -0500
From: Catherine Alfieri <calfieri@...
Subject: NIH.gov: Assistive Devices
This link from the National Institute of Health has information on assistive
devices for all sorts of conditions.
http://www.nlm.nih.gov/medlineplus/assistivedevices.html
Catherine Alfieri
7 Summer Tree
Pittsford, NY 14534
585-586-1682
Founder

OT: "Win Without War" vigil

2006-12-29 15:48:32

For more information about how to make this happen in your community
and to join with millions of others around the globe, go to
http://www.globalvigil.org
It's time for the world to come together in this moment of darkness
and rekindle the light of reason -- and of hope. It's time to renew
our commitment to building a positive world for our children.
With your help, we will see the first candlelight vigil to sweep
around the globe on the evening of March 16th. Together, we will
lead the nations of the world away from an unnecessary war and
toward a peaceful and prosperous future.
This is a key moment in history. Be a part of it. Go to:
http://www.globalvigil.org
Thank you,
-Wes Boyd, MoveOn.org
Tom Andrews, Win Without War
Tuesday March 11, 2003

Exploring potential of mind, body connection

2006-12-29 02:46:05

This Story has been sent to you by : Jayne@...
Exploring potential of mind, body connection
The idea that the mind affects the body goes back to the ancient Greeks. Hippocrates, a physician who's known as the father of medicine, had the idea that thoughts produce certain reactions in the body.
The full article will be available on the Web for a limited time:
http://www.ohio.com/mld/ohio/news/5364008.htm

(c) 2003 Beacon Journal and wire service sources. All Rights Reserved.

adding NYS assembly link

2006-12-28 22:59:05

http://www.assembly.ny.usa/mem

Carol Newsom, photographer, dies at 56

2006-12-28 16:44:59

Carol Newsom, who captured many of the most important tennis matches
of the last three decades with the lens of her camera, and who was a
Holliston, Massachusetts, resident, died yesterday [? March 13, 2003
?] at MetroWest Medical Center in Framingham, Massachusetts, at the
age of 56.
The cause was breast cancer, a disease she fought for three years,
while still managing to attend matches at Wimbledon, the French and US
Opens, as well as other prominent tournaments.
"She scheduled her chemo appointments around the tournaments to
maintain her schedule," said her husband, David Newsom.
Mrs. Newsom also battled multiple sclerosis for the last 12 years,
keeping it at bay with medications that affected her vision but not
her eye for a good picture.
A freelance photographer who had specialized in tennis since 1974, she
sold images to many publications (including the Globe) and
international wire services.
Born Carol Lee Natelson in Boston in 1946, she graduated from Girls
Latin School and then Boston University, in 1968, majoring in
mathematics.
A math teacher at Milton High School, she became intrigued by tennis
and in 1974 began contributing to a local publication, Tennis New
England.
Two years later, she was named tournament photographer at the Longwood
Club in Brookline.
She gained international recognition in 1980, when she became the
first female photographer issued a pass to work in the game's sanctum,
Wimbledon's Centre Court.
At the time, Billie Jean King and Rosie Casals were the pioneers
leading the formation of the women's pro tour.
"Carol was a pioneer, too," Casals said from her Palm Springs home,
"and it meant a lot to have her around."
"Carol wasn't only an excellent photographer, but she was always
encouraging and helpful to me and Billie Jean in our early days,"
Casals said.
Mrs. Newsom was the official tour photographer of that women's tour,
sponsored by Virginia Slims.
Mrs. Newsom, stocky, dark-haired, often burdened with a load of camera
equipment, was never too busy to spare a smile and advice for people
on the way up. At the last US Open, she told people: "I have two jobs
- pictures and fighting [the cancer]. It's a good fight."
She described her work as "always looking for a wow! with my camera."
She found many.
Since 1980 she covered the French Open, Wimbledon, and the US Open
annually, and was planning on being in Paris in June. Instead she will
be lauded that month in Newport, R.I., inducted into the New England
Tennis Hall of Fame. When her selection was announced recently, she
said, "I'm grateful, but I can't be there. I have an appointment in
Paris."

VA Fact Sheet on Telemedicine

2006-12-28 13:45:56

VA Fact Sheet on Telemedicine
(EXCERPT) Telehealth, Telemedicine and VA Medicine WASHINGTON (March
12, 2003) -- Operating the nation's largest health care system, the
Department of Veterans Affairs (VA) uses a wide variety of
communication and information technologies to ensure excellence in the
health care it delivers to the nation's veterans.
The term "telehealth" applies to technology used to provide clinical
care, patient education, professional education and hospital
administration when those providing services and those receiving them
are separated by distance. "Telemedicine" generally refers to
physicians providing services at a distance. VA considers telemedicine
part of the wider spectrum of "telehealth" services given by many
types of caregivers.
Telehealth helps VA meet a growing need to give care in
non-institutional settings to elderly veterans who have chronic
conditions and transportation problems getting to treatment.
Telehealth technologies make it possible not only to move care to
primary and ambulatory treatment sites but to extend it into the home,
helping patients maintain independent lives and avoid unnecessary
hospitalization and long-term care. Telehealth will also help VA make
the best use of its physical facilities as it allocates resources to
care for more veterans.
Advantages of Telehealth to Veteran Patients Information technology in
health care can ensure that all data related to a patient's conditions
are current and available to medical providers exactly when needed.
Timely access to health information improves care and reduces the risk
of medical errors. The Institute of Medicine has recognized VA's
leadership role in this area.
Telehealth electronic information and communications sometimes involve
high-resolution images and sound through live video. An example of
this is providing veterans in remote, rural areas prompt access to
expert advice from a cardiologist. Sometimes it involves simply
transmitting text records and digital images, as can happen in
remotely assessing patients with diabetes for possible
diabetes-related eye disease. Because telehealth moves information,
rather than people, it can be more efficient and less expensive than
traditional care and provide expert advice when a patient needs it.
Improving access to care, and permitting more frequent monitoring of
patients and their health status, are the features of telehealth that
produce high-quality care and satisfaction among patients.
As impressive as the technology is, the key to telehealth success is
the way it helps in coordinating patient care. Successful home
telehealth that matches a patient's needs to
technology that the caregiver or patient can manage also reduces
clinic visits. As a veteran ages, the need for services is frequently
determined by expert advice on appropriate treatment of chronic
conditions. Making this advice available in the home is convenient and
can expedite or defer hospital admission. The philosophy of care
coordinators using telehealth is "the right care for the veteran
patient in the right place and at the right time."
Telehealth makes it possible to exchange routine clinical data and
visual assessments among medical facilities locally, regionally and
nationally. There are parts of the country where distance and weather
are a barrier to care. Telehealth brings care to the patient and
avoids the cost and inconvenience of travel. Telepharmacy, a component
of telehealth, makes medications authorized at hospitals rapidly
available to veterans in VA community clinics. Telehealth permits a
northern "snowbird" veteran receiving care at home through telehealth
to continue a care regimen in Florida in the winter.
Examples of Telehealth in Use In VA's Sunshine Healthcare Network,
including most of Florida, south Georgia and Puerto Rico medical
facilities, about 1,500 patients receive telehealth care in their
homes. Many of them use handheld messaging devices to report their
vital signs and other medical information to hospital staff monitoring
the reports daily. Staff sends patients reminders, tips and feedback
on their progress. VA patients in Colorado, Utah, Wyoming, central
Texas, New York State, Georgia and Indianapolis use this device and
others. Many of the patients have congestive heart failure, high blood
pressure, pulmonary disease, diabetes or depression.
Many VA medical centers use an interactive voice-response system to
take questions from patients and leave phone messages for them
automatically about appointment scheduling and prescriptions. The
system permits clinicians to pose questions to patients and have their
responses recorded, becoming progress notes. Results of the calls are
forwarded to a telemedicine computer so local clinicians can follow
up.
Clinicians providing telehealth care in the Sunshine network and other
locations studied their patients' outcomes. They found improvements in
blood glucose levels, blood pressure and mental health, along with
fewer emergency room visits, days of hospitalization, clinic visits
and less extended care.
The National Cancer Institute has funded a study by the VA Sunshine
network and the University of Florida to evaluate whether telehealth
can deliver more effective care to cancer patients in their homes.
Already, VA's Puget Sound Healthcare Center (Seattle/Tacoma, Wash.)
telehealth program allows cancer patients to be treated through
teleconferences at other VA centers in the Northwest closer to home.
Patients' cases are presented to multi-disciplinary teams of
physicians at Seattle in a single session.
Home telehealth technologies used in VA locations range from the most
expensive - a telemonitor to examine a wound, for example - to the
least costly - a telephone. In between are personal computers and
videophones. Some patients receive a Polaroid camera, take photos of
their wound and mail them to the hospital every week.
In 2000, VA completed 18 telemedicine demonstration projects to
improve access and quality of three kinds of care: geriatrics and
extended care, mental health and organ transplant follow-up services.
Among the successful results: The Iron Mountain, Mich., VA Medical
Center collaborated with Milwaukee VA hospital psychiatrists to
provide mental health services at a Marquette, Mich., community clinic
through videoconferences.
In that project and in the Richmond, Va., telehealth transplant
program, no-show rates among patients declined because patients didn't
have to travel the greater distance to the medical center.
Also in 2000, VA facilities conducted 13 demonstration projects in the
homes of veterans who had suffered spinal cord injuries. Most of the
telehealth care came through weekly, real-time monitoring of skin
ulcers or surgical wounds using mounted or handheld cameras connected
to videophones answered at hospital nurse stations. VA also provided
the computer videophones in patients' homes. VA coordinators provided
in-home training in wound care and rehabilitation to patients,
caregivers and local homecare agency staff. They visited in person and
made referrals to VA's spinal cord injury centers to prevent
complications. Supplementing traditional care, the telehome care
visits reduced the need for readmissions to the centers for chronic
conditions, yet increased patients' access to specialist care.
Recently, the Grace Hopper Government Technology Leadership Award went
to a federal health care access partnership in Alaska in which VA
participates. Several agencies created a telehealth network to serve
the most isolated Alaskans. The network enables health aides in rural
areas to send images and information over the Internet to physicians
who provide diagnoses and treatment options. About 400 cases are
handled each month.
New Initiatives - The Future VA is establishing two centers to give
veteran patients nationwide access to advice from experts in the care
of multiple sclerosis. With telemedicine, a veteran who is seen at a
VA clinic or medical center anywhere in the country can have a
consultation with a specialist in MS. A network of MS experts is being
coordinated by the Baltimore VA Medical Center, the Portland (Ore.)
VAMC and the Seattle VAMC. (The last two collaborate as one MS
center.) Similarly, seven VA Parkinson's disease centers specialize in
treatment, education and research related to that neurological
condition. They are developing a telehealth network to extend care to
veterans nationwide.
VA is working with experts in diabetes care to create a telehealth
network to detect retinopathy, a disease of the retina of the eye
prevalent in diabetic patients. Preventing diabetes-related blindness
ranks as a major VA priority.
Four other VA regional networks plan to duplicate the success of the
Sunshine Network's telehealth programs with home-based primary and
mental health care.
VA will soon distribute "toolkits" to its medical facilities for home
telehealth and mental health to connect those who are considering
introducing telehealth with a network of practitioners. The kits
contain resource materials, including templates and guides to best
practices being used.
VA will continue to work with the Joint Commission on Accreditation of
Healthcare Organizations to ensure the quality of its telehealth
services. A joint activity underway will develop ways to credential
professionals who provide telehealth care. Since telehealth provides
clinical services at multiple sites where medical staff may not know
the qualifications and professional privileges of others,
credentialing can be important both to caregivers and patients.
The role of telehealth in meeting medical needs during natural or
manmade disasters figures into VA's planning for future uses.
Other challenges in the future include developing large information
networks that will support compatible hardware and software systems,
deciding whether to standardize treatment approaches and equipment and
developing standard procedure coding for workload credit. VA is
working to give patients access to an electronic patient-held record.
That achievement will be an important part of the partnership between
VA, its care providers and its patients.
VA's telehealth expertise makes it an industry leader. VA officials
foresee a time when the home can become the preferred place of
treatment, where a multimedia patient record, technology and a system
for making medical decisions will help coordinate better access and
the best possible care of veterans who increasingly accept
telecommunications in their lives.
http://www.va.gov/opa/pressrel/opalist_listserv.cfm

More on Curry

2006-12-28 04:49:17

Which ever way you look at Turmeric it looks good. Got a couple of plants
growing here now they look
much like Ginger.
All the best
John

Re: Campath

2006-12-27 18:32:16

Hi
I've just had my first month's check up after Campath treatment. The
neurologist treating me, who is also the UK based organiser of the
trial, suggested that they were struggling to find eligible
participants. I'm unsure if this only affects the UK, or also the US
centres as well.
The full details of the trial criteria (with US contact details) can
be found at:
http://www.ilexonc.com/CAMMS223.htm
The criteria are fairly strict, and only relatively newly diagnosed
patients are eligible.
UK contact details can be found on Paul Jone's website
http://www.mult-sclerosis.org
or by emailing me.
My experience of the drug can also be found on Paul's website.
If you're relatively newly diagnosed, it's definitely worth
considering as an alternative to the ABCs.
Rgds
David

National MS Awareness Month

2006-12-27 18:04:06

Sorry to be late in announcing this but I can give you a number to
call the March 13 & 20th live internet chats.
The one on the 13th is with Dr. Breiterman & the one on the 20th
is with Dr. Guthrie. Call toll free 1-888-673-6287
Jayne

FDA approves skin patch for treatment of overactive bladder

2006-12-27 11:05:49

FDA approves skin patch for treatment of overactive bladder
03/11/2003
The Food and Drug Administration granted approval for Watson Pharmaceuticals
Inc. to market its oxybutynin transdermal system Oxytrol as a treatment for
overactive bladder.
The skin patch, which is applied to the abdomen, hip or buttock twice weekly, is
the first treatment of its kind to receive FDA approval for the treatment of
overactive bladder with symptoms of urge urinary incontinence, urgency and
frequency.
The transdermal delivery system delivers a fixed dose of the active ingredient
oxybutynin through the skin into the bloodstream, providing relief of overactive
bladder symptoms for up to four days and bypassing the initial metabolism in the
liver and gastrointestinal tract that occurs with oral medications.
According to a company press release, clinical trials involving more than 1,000
subjects at 50 U.S. centers have shown the oxybutynin patch to provide effective
control of the symptoms of overactive bladder for three to four days and to be
well tolerated. The most common side effects associated with use of the patch
were application site reactions.

March is National MS Education Awareness Month

2006-12-27 05:29:02

March is National MS Education Awareness Month
03/11/2003
The Multiple Sclerosis Foundation has scheduled events throughout March to
promote National MS Education Awareness Month.
Activities include moderated Internet chats with MS specialists, the release of
new publications about MS that can be ordered online or by phone and, at various
locations throughout the country, âMS Family Days,â which combine fun
activities and a complimentary lunch with an educational program for patients
with MS.
A key feature of this monthâs activities is to educate âfamily members of
those with MS to increase their understanding of the challenges their loved ones
face,â the foundation said.
For more information about National MS Education and Awareness Month, visit
www.msfocus.org/nmseam.htm.

Re: [MS_Community] I have osteoporosis

2006-12-26 23:34:42

Carol,

Her name was Elizabeth Smart. Make sure you still get lots of exercise if possible.

Love

Bernie

I have osteoporosis

2006-12-26 21:04:59

This should not be of a surprise to me as I am small boned and thin.
My doc said Im in the early stages. Up untill 1994 , I walked alot in my
job.
If it was not for Jayne', I probBLY would not even know about
osteoporsis , Thank you Jayne.
The forward you sent me ,Jayne, about people feeling stressed about the
impending war, boy I could relate! Is any one else feeling stress? Ive
got to stop watching CNN & the Fox station, The news is not all
bad,,,for a change, The little girl that was missing for a year was
found, I cant even remeber her name. Ive only heard it 100 times!
I am ready for spring!
carol

MS sufferer in bid to save local post office

2006-12-26 14:31:50

MS sufferer in bid to save local post office
by Billy Youngson
A DISABLED Stuartfield woman has backed calls to secure a future for rural post
offices.
Multiple sclerosis sufferer Elaine Rebecca says her community will break down if
changes in the
child benefit system see post offices shut up shop.
Already Maud postmaster Allison Taylor has raised fears she could lose staff due
to new benefit
procedures. Allowances are set to be paid directly into bank accounts - instead
of collected at the
post office.
Mrs Rebecca, of 2 Knock Street, says less-able people in rural communities will
become victims of
the change.
She said: "The post office is an integral part of this community for everyone of
every age.
"Without it, the whole community would be at a lose. It is a primary service. It
would be like
someone saying we couldn't have water out here.
The housebound mother relies on husband, Douglas, to collect her disability
allowance every week. He
faces a 15-minute round trip to Mintlaw if the post service is taken away from
Stuartfield.
He said: "I have a car and it is just a little more of a hindrance for me if I
had to do that. But
there are elderly people who would be left in a much worse position than we are.
"They want to be independent but this would prevent them from doing that. They
would be forced to
get others to make time to help them do something they could easily do if the
post office remains
open.
"To an elderly person Mintlaw may as well be Aberdeen or a 100 miles away."
He added: "And children use the post office for their accounts. They may moan
about having to walk
up there but at least they can do that."
If it closes they won't be able to go to Mintlaw without someone to drive them,
Mr Rebecca says.
"Children don't have the money to be paying for buses back and forth to
Mintlaw."
His wife Elaine has been battling her illness for almost 13 years, with her
condition deteriorating
in the last 12 months.
She said: "I am set for an operation which will ease my situation. I won't be as
housebound as I am.
"I would love to be able to go to the post office and get my allowance for
myself but I am getting
ever more worried that I won't be able to that.
Her husband added: "People look for the basic services, like the post office,
when they are going to
buy a home.
"They will turn away from Stuartfield, and many other communities, if the post
office is taken away
from us."
Banff and Buchan MSP Stewart Stevenson has thrown his weight behind the
campaign.
Last week he tabled a parliamentary motion calling for a level playing field for
post offices.
He said: "This is an issue of vital importance to rural communities such as
Banff and Buchan.
"The banks have mainly deserted our rural communities and by choosing a post
office card account,
local people can help ensure the survival of their local post office."

Single Pill May One Day Treat M-S

2006-12-26 01:40:55

Single Pill May One Day Treat M-S
U. C. L. A. researchers believe they've come up with an alternative to shots in
the treatment of
multiple sclerosis and it could be something as simple as a once-a-day pill.
MS is an autoimmune disease which means the body destroys it's own tissues.
Estriol, a chemical
women develop during pregnancy, might help MS sufferers. Researchers say a pill
form is showing
promise.
U.C.L.A. neurologist, Dr. Rhonda Voskuhl says, "We followed the MRI of their
brain for six months
before treatment and six months during treatment. What we found was the number
and volume of lesions
in the brain went down significantly." So far the human trials on the pill
showed an 80 percent
reduction in brain lesions in MS patients.

Re: Fwd: [RD] WWW.HELPINGPATIENTS.ORG ...........

2006-12-25 21:41:50

I've adde this to our links,
Jayne

OT: :) Mature person's alphabet

2006-12-25 15:02:44

MATURE PERSON'S ALPHABET A for arthritis, B for bad back, C is for chest pains. Perhaps cardiac? D is for dental decay and decline, E is for eyesight--can't read that top line. F is for fissures and fluid retention G is for gas (which I'd rather not mention H high blood pressure (I'd rather have low) I for incisions with scars you can show. J is for joints, that now fail to flex L for libido--what happened to sex? Wait! I forgot about K! K is for my knees that crack when they're bent (Please forgive me, my Memory ain't worth a cent) N for neurosis, pinched nerves and stiff neck O is for osteo- and all bones that crack P for prescriptions, I have quite a few Give me another pill; I'll be good as new! Q is for queasiness. Fatal or flu? R is for reflux--one meal turns into two S is for sleepless nights, counting my fears T for tinnitus--I hear bells in my ears U is for urinary: difficulties with flow V is for vertigo, that's "dizzy", you know. W is worry, now what's going 'round? X is
for X ray--and what might be found. Y for another year I've left behind Z is for zest that I still have my mind, Have survived all the symptoms my body's deployed, And kept twenty-six doctors gainfully employed!!! -- Debbie Campbell

OT: :) HMO cost cutting

2006-12-25 12:05:40

This is long but I found it a hoot. Hope you enjoy! Irene

MS treatment costs "expensive but decrease over time"

2006-12-25 08:32:09

MS treatment costs "expensive but decrease over time"
Tuesday, March 11, 2003
LONDON
By Health Newswire reporters
The cost of disease-modifying drug treatments for multiple sclerosis (MS) is
high, but decreases
with prolonged treatment up to 20 years, according to a recent UK study.
MS costs decrease over time
A team of researchers from universities in Sheffield, Leicester and York says
the cost per
quality-adjusted life year is unlikely to be less than £40,000.
Dr Jim Chilcott and colleagues evaluated the cost effectiveness of four drugs -
three interferon
betas and glatiramer acetate - currently licensed for the treatment of relapsing
remitting and
secondary progressive MS in the UK.
They assessed the effect of each drug compared with conventional management
(including symptom
control, physiotherapy and psychiatric support) over 20 years using the best
available evidence.
Reporting in the British Medical Journal, the team found that the cost of each
year of life saved or
prolonged by using any of the four drugs ranged from £42,000 to £98,000.
The main determinants of cost effectiveness were the price of the drugs,
different discount rates,
the progression of patients after stopping treatment and the time horizon.
Dr Chilcott's team cautions, however, that there is "substantial uncertainty"
surrounding these cost
estimates.
"This uncertainty could be reduced by conducting research on the true magnitude
of the effect of
these drugs, the progression of patients after stopping treatment, the costs of
care and the quality
of life of the patients," the researchers conclude.
In an accompanying commentary, Professor David Miller, a clinical neurologist
from the Institute of
Neurology and the National Hospital for Neurology and Neurosurgery in London,
says research is
needed to identify those who will benefit most from disease-modifying
treatments.
He notes that the Department of Health has introduced a risk-sharing scheme for
providing these
treatments in the NHS. He says that although the scheme would need substantial
investment, it is
hard to see a realistic alternative.
Reference: Chilcott et al, British Medical Journal 2003;326:522-525
© HMG Worldwide 2003
http://www.health-news.co.uk/

On Nettles from Michael

2006-12-24 22:24:05

And if I can put in a short word in favour... nettles aren't just go for
you, but also plain-old *good*.
If you can get nettle tips fresh (hard to do if you live in a city or in dry
country,) they're great as pot greens too... steamed briefly - just enough
to wilt them thoroughly (this defangs the stingers) and get them good and
hot - and with wee a bit of lemon-pepper and salt... maybe a little butter
or oil too if you like.
Green tea? Why not get a tea-ball and then buy tin boxes of that
cheap-as-dirt (and totally yummy) jasmine tea they serve in chinese
restaurants? It's about $3 for the equaivalent of 1000 teabags in
Vancouver's Chinatown... surely it's available elsewhere for similar prices.
Maybe drink it while supping on a side of steamed nettles. :-)
Bon appetit.
((U))
M

Effort for uninsured takes on steam

2006-12-24 17:26:03

Effort for uninsured takes on steam
By DONNA CALLEA and MATT GRIMISON
Staff Writers
Last updated: Mar 10, 10:27 PM
DAYTONA BEACH -- Advocates rallied for universal health care outside City Hall
on Monday as hospital
officials from around the state warned legislators in Tallahassee that cutting
health-care funds for
the needy could have dire consequences.
The state Medicaid cuts proposed by Gov. Jeb Bush include an estimated $5.52
million in Volusia
County and $162,000 in Flagler County, and would lead to heavier tax burdens on
local governments,
increased costs to patients and elimination of some costly procedures, according
to the hospital
officials.
For Montye Conlan, 49, who has multiple sclerosis, the cuts would mean losing
the care and
medication that keeps her disease from progressing. The Ormond-by-the-Sea
resident, who spoke at the
City Hall rally kicking off the national Cover the Uninsured Week, faces losing
her coverage under a
state program for the medically needy. As of May 1, if the cuts go through, she
would be required to
pay $410 out of her $860 monthly disability income to remain in the Medicaid
program.
"I would have to sell my house," she said.
Unless ways can be found to make sure no one is forced to do without health-care
coverage, it could
cost the country its economic health and the well being of its citizens and
workforce, said Dr.
Alvin Smith at the Daytona Beach rally.
"We need an organized system," Smith, 71, told the small gathering at the local
Cover the Uninsured
rally. Although he didn't use the words national health care, Smith, a former
president of the
Florida Medical Association, said a solution must be found to ensure that
"health care is a right in
America."
Both nationwide and locally, the health care system "is in danger of
deteriorating and becoming
second rate," Smith said. Cover the Uninsured is aimed at bringing attention to
the more than 41
million Americans who have no health insurance. A 2000 survey found nearly
53,000 Volusia County
residents younger than 65 had no health insurance. Although Volusia County has a
better "safety net"
than many places for the uninsured, the proposed state Medicaid cuts would put
serious holes in that
net by reducing reimbursement rates at area hospitals and reducing Medicaid
co-payments for
emergency care, said John E. Evans, a spokesman for Halifax Medical Center.
In Tallahassee, Tony Carvalho, senior vice president of the Florida Hospital
Association lobbying
group, said: "Hospitals won't close their doors, but we would have to identify
services that
hospitals offer to eliminate."
Reducing Medicaid allocations also dovetails with skyrocketing medical
malpractice insurance rates.
Halifax's trauma center surgeons recently announced they will stop doing
emergency surgery unless
the Legislature takes action on the malpractice issue. Evans also noted that it
may also be
difficult to get obstetricians to deliver babies or radiologists to read
mammograms in the future.
Lawmakers said they don't know what programs they would not fund to find the
$270 million the
Medicaid reduction would cost statewide, but they said it must be a priority
during budget
negotiations.
"We have to decide what's most important," said Rep. Sandra Murman, R-Tampa.
"You don't want to be
in the mode of crisis management in hospitals."
But Murman said raising taxes is not an option for herself and other
Republicans.
The nonpartisan Cover the Uninsured Week effort is being chaired nationally by
former presidents
Gerald Ford and Jimmy Carter, and sponsored by various foundations and
organizations.
Locally, efforts are being spearheaded by the Volusia Health Alliance, a group
that includes
representatives of the area's five hospitals, the Volusia County Health
Department, the United Way,
The Chamber-Daytona Beach/Halifax Area and the Community Health Action
Information Network.
donna.callea at news-jrnl dor com
matt.grimison at news-jrnl dor com
For The Uninsured
Area events slated for Cover the Uninsured Week include:
· A panel discussion ant 6:30 tonight at the Museum of Arts and Sciences, 1040
Museum Blvd., Daytona
Beach
· A rally at 10 a.m. Wednesday at Deltona City Hall.
· A forum at 1:30 p.m Wednesday in the Holmes Building at Bethune-Cookman
College.
· A lunch at noon Thursday (cost $20) at LPGA Clubhouse, Daytona Beach,
featuring Kevin McCarty
director of Florida's Office of Insurance Regulation and a panel on employee
health insurance. (386)
255-0981, Ext. 222 for reservations.
· A Health Expo from 10 a.m.to 1 p.m. Friday at the Volusia Mall.

Heart drugs hope for MS

2006-12-24 11:14:28

Heart drugs hope for MS
Statins prevent damaging cells getting into the brain
Cholesterol-lowering drugs could tackle the development of multiple sclerosis at
a very early stage,
scientists have found.
Statins, usually given to patients with heart disease, could one day be given to
MS patients - if
the findings of laboratory and animal tests are confirmed in human trials.
MS is caused by the immune system turning in on itself and attacking the body's
own central nervous
system.
This happens because immune cells called T lymphocytes produce too many
cytokines, chemicals which
inflame the nervous system.
This triggers the activation of other immune cells, called macrophages, which
leads to the
progressive destruction of myelin - the tissue that sheathes and protects the
nerves.
Without myelin, the nerves cease to function properly, and patients gradually
lose the ability to
move normally. Eventually they become paralysed.
This latest research, by scientists at the Institute of Ophthalmology and
University College London
found that statins prevent the damaging lymphocytes accumulating in the brain in
the first place by
blocking their pathway in.
'Passive'
Their research focussed on the blood-brain barrier and a signalling molecule
called Rho GTPase.
The lymphocytes, or white blood cells, have to cross the barrier to get into the
brain.
In order for them to get through, Rho GTPase, which is present in the cells of
the brain's blood
vessels, has to be switched on.
The research team found statins blocked the molecules from doing their job.
This prevents the lymphocytes accumulating in the brain and therefore damaging
the myelin sheath and
the nerves.
It was already known that statins could alter the state of the cytokines, making
them "passive"
instead of "aggressive".
Crucial stage
Professor John Greenwood, one of the scientists leading the research, told BBC
News Online: "It's
fair to say this could alleviate and attenuate disease progression."
He added: "More than 85,000 people in the UK suffer from MS and at present there
is no effective
treatment or cure.
"These new results provide direct evidence that statins, which are a well
tolerated and widely used
class of drug, may inhibit a crucial stage in the development of inflammatory
lesions in the brain.
"They could thus be of significant benefit in the treatment of patients
suffering from MS."
But he was reluctant to say statins could be a cure for MS.
"I think the only true cure will be when we discover what causes MS," he said.
Further studies will now take place.
'Encouraging'
Mike O'Donovan, chief executive of the MS Society, which partly funded the
research, told BBC News
Online: "These encouraging results in a model of MS show that statins might play
an important role
in the control and treatment of the disease.
"We hope it will not be too long before trials involving patients can be
conducted."
The research is published in the FASEB (Federation of American Societies for
Experimental Biology)
journal.

Infection with Common Bug May Raise MS Risk

2006-12-24 07:55:45

Infection with Common Bug May Raise MS Risk

March MS Dialogue Teleconference and (New in 2003) Expert Chat!

2006-12-24 05:49:35

Message:
March MS Dialogue Teleconference and (New in 2003) Expert Chat!
Topic: Overcoming Obstacles and Erasing the Myths of Multiple Sclerosis
Discover helpful ways for accepting and living with a diagnosis of MS, including
the importance of empowering yourself. You'll see how and where to find credible
and current information to help dispel the "myths" surrounding MS and help
you better manage the disease.
Speakers:
* Dr. Ben Thrower, Director of the MS Center at Shepherd Center in Atlanta.
* Wendy B., MS Advocate
Dates:
* Teleconference 1: March 11 - 8:00 PM EST
* Teleconference 2: March 12 - 8:00 PM EST
* Online Chat: March 18 - 8:00 PM EST
Call 1-800-938-1912 to register for one of the teleconferences then go to
www.copaxone.com and join to participate in the interactive chat session
on the 18th!
Teleconferences and chat are FREE and open to everyone!

MS Watch Gathering

2006-12-23 13:45:06

Subject: MSWatch Gathering â April 2003
Message:
MSWatch Gathering â April 2003
Dates: April 24-26, 2003 Location: Branson, Missouri
Join your MSWatch friends for a fun weekend in Branson Missouri! This gathering
is being organized by âHelalaâ, âMakadoâ, âWheelinâ and other
members here at MSWatch!
Weekend Agenda:
Thursday, April 24 â arrivals
* 8:00pm â meet in lounge, get to know each other!
Friday, April 25
* Day â Free time to enjoy Branson
* Evening â 6:00pm - Dinner at Lake Chateau Restaurant with guest MS speaker
who bicycled across America. Branson 2003 T-shirts will be provided to all
attendees. (Location: Lake Chateau Hotel, 415 N State Hwy 265. About 5 miles
from the Quality Inn.)
Saturday, April 26
* Morning â Free time
* Afternoon:
1:00-4:00: Teva Neuroscience Special Presentation
***Heavy appetizers and door prizes available***
1:00 â Registration
1:30 â Presentations begin -
Presentation 1: âSO MANY QUESTIONS, SO MANY CHOICES, SO MANY DECISIONSâ
presented by John L. Kareus, DO from Cooper Clinic, Fort Smith Arkansas.
Presentation 2: âGETTING PAST THE âWHY ME?â AND ON WITH THE WHATâS NEXT?
Presented by Linda Crossett, Advanced Nurse Practitioner living with MS.
Presentation Location: Radisson Hotel â Tablerock Ballroom A
120 S. Wildwood Drive, Branson, MO 65616 (417) 335-5767
(About 2 miles from the Quality Inn.)
* Evening â Free time to enjoy Branson
Sunday, April 27
* Morning - Meet for breakfast and say goodbye
Main hotel for MSWatch members April 24-27th:
QUALITY INN
3269 Shepherd of the Hills Expressway
Branson, Mo. 66516
Call: 800-254-3308 or 417-335-6776
HOTEL HAS FREE BREAKFAST W/ROOMS
Rates: $49.95 Single or Double, $54.95 Triple or Quadruple
* Ask for the MSWatch rooms and rate. There are 6 handicapped rooms in the
hotel.
Other hotels are available in the area. Go to www.branson.com/branson or
www.bransonchamber.com for more information on the Branson Missouri area.
**RSVP to: bob13345@....
Official web site at: http://concept21.homestead.com/bransonchat.html
Branson, Mo., is about 250 miles southwest of St. Louis Missouri and 35 miles
south of the Springfield Missouri airport.
Sponsored in part by Teva Neuroscience
           Â
COPAXONE® (glatiramer acetate injection) Product Information
© 2002, Teva Neuroscience, Inc.
Powered by SoftWatch Relationship Serverâ¢

MS Dialogue

2006-12-23 11:07:11

March MSDialogue Teleconference and Chat Series
03/07/2003
March MS Dialogue Teleconference and (New in 2003) Expert Chat!
Topic: Overcoming Obstacles and Erasing the Myths of Multiple Sclerosis Discover
helpful ways for accepting and living with a diagnosis of MS, including the
importance of empowering yourself. You'll see how and where to find credible and
current information to help dispel the "myths" surrounding MS and help you
better manage the disease.
Speakers:
* Dr. Ben Thrower, Director of the MS Center at Shepherd Center in Atlanta.
* Wendy B., MS Advocate
Dates:
* Teleconference 1: March 11 - 8:00 PM EST
* Teleconference 2: March 12 - 8:00 PM EST
* Online Chat: March 18 - 8:00 PM EST
Call 1-800-938-1912 to register for one of the teleconferences then go to
www.msdialogue.com and join to participate in the interactive chat session on
the 18th! Teleconferences and chat are FREE and open to everyone!
Note: 8:00 PM EST = 7:00 PM Central, 6:00 PM Mountain, 5:00 PM Pacific Time
COPAXONE® (glatiramer acetate injection) Product Information
© 2002, Teva Neuroscience, Inc.

from MS_Watch Clay Walker

2006-12-23 05:11:52

New spokesman for Teva Neuroscience will offer hope to MS patients
03/07/2003
Country music singer Clay Walker will be a spokesman for the company that makes
Copaxone (glatiramer acetate injection), which he uses to treat his
relapsing-remitting multiple sclerosis,
âI would like to provide hope for others that there are treatments available
that can help and that research promises an even brighter future,â Walker said
in a Teva Neuroscience press release.
According to Teva Neuroscience Inc., Walker will educate other patients about
treatment options based on his own experience and will offer encouragement for
patients managing the disease.
âPatient outreach has always been an important part of our vision at Teva
Neuroscience, and we believe Clayâs positive outlook and passion for life will
raise the spirits of the MS community and give people living with MS the courage
to explore new options,â Teva Neuroscience Chief Executive Officer Larry
Downey said.
In February, Walker formed a not-for-profit organization called the Band Against
MS Foundation to provide support and education for MS patients as well as to
raise funds for research programs seeking a cure and organizations that provide
assistance for people living with MS.
Despite battling MS since 1996, Clay is about to complete his first album for
RCA Records, which will be released in the summer of 2003.
COPAXONE® (glatiramer acetate injection) Product Information

Will GLAXO Halt Drugs From Canada?

2006-12-22 19:49:55

Will GLAXO Halt Drugs From Canada?
NOT IF AMERICANS ARE ASKED
By Patricia Barry
As more and more Americans turn to Canada to buy prescription drugs â at
prices up to half those at home â one drugmaker is trying to halt the
cross-border trade.
Pharmaceutical giant Glaxo-SmithKline has taken steps to cut off supplies
to Canadian licensed pharmacies that continue to sell its medicines to
Americans.
âIf Glaxo gets away with this, other big drug manufacturers will follow
their lead,â says Billy Shawn, owner of an Ontario Internet pharmacy.
About 1 million Americans, mostly age 65 and older, now fill prescriptions
by mail order from Canada, according to the Canadian International Pharmacy
Association, (CIPA), a group that represents licensed pharmacies selling
drugs to the United States via the Internet.
âWeâve created an option for American seniors to afford their
medications,â
says pharmacist Andy Tros-zok, CIPAâs spokesman. âNow Glaxo is going to rip
that out of their hands.â
American-made prescription drugs mostly cost less in Canada, where the
government regulates prices. U.S. law does not permit reimportation, but
the rule is not enforced for individual consumers.
Glaxo says it is acting âin the interests of patient safety.â CIPA counters
that the exported drugs are the same quality and sent through the U.S. mail
in the same way as American mail order drugs. Hitting back, CIPA is asking
U.S. customers to protest and consider switching from Glaxoâs nonmedical
products like Aquafresh toothpaste and antacid Tums
--
Shirley B.
#6 ASMS Lists
To reply by email, remove 'nick'.

Cowboys retirement

2006-12-22 17:47:59

I hope u enjoy your retirement!! I hope your ms improves a bit with less
stress & more rest,
Thank u for all u have done for this group, carol
Thank you jayne for sharing this goood news with this group,

VS: Christopher Reeve Paralysis Foundation: Legislative Update

2006-12-22 14:03:50

This issue is rather interesting for us with MS and there is a suggestion for all you americans

have a nice day

Annette
-----Oprindelig meddelelse-----
Fra: Hope Network [mailto:hope@...]
Sendt: 9. marts 2003 19:33
Til: avv@...
Emne: Christopher Reeve Paralysis Foundation: Legislative Update
The Hope Network
[INLINE]

They Heard Your Voice
Legislative Update from CRPF Senior VP and Director of
Government Relations, Michael Manganiello

Two weeks ago the House of Representatives exhaustively debated H.R. 534 (the Weldon Bill banning all forms of cloning) and its alternative H.R. 801 (the Greenwood Bill which allowed for therapeutic cloning). After a lengthy discussion, which included scientific, ethical, and social issues, H.R. 534 passed-banning all types of cloning.

While this is an initial blow to the possibility for therapeutic cloning treatments, this is not a defeat for the Hope Network. Your voices were heard and you made a difference in the votes of many Representatives. Because of your involvement and your enthusiasm, we had more champions of therapeutic cloning on Capitol Hill than ever before!

We now move to the Senate debate. Thousands of Hope Network members sent emails and letters to their Representatives. We want to double those numbers. We want to flood the Senate with your opinions on medical progress. If each of you sent this email to one friend, our voice would be that much louder and our presence that much more influential.

Simply tell your friend to click here, sign up and send the prewritten email/letter.

We promise to keep educating, keep informing, and keep working towards medical progress.

You can easily see your effect in the most recent Hope Network victory-President Bushs signing of the 2003 spending package, which includes the final stage of doubling the National Institutes of Healths (NIH) budget from $13.6 billion in 1998 to $27.1 billion in 2003. Your emails, letters, and phone calls made a difference that will impact hundreds of thousands of Americans affected by disability. For more on this issue and others, click here for the Hope Network Headquarters.

The Hope Network has proven itself to be an effective voice for the medical research and disability community. We are gaining ground and going strong. However, we will need your continued support throughout the year as the therapeutic cloning debate resumes, the Christopher Reeve Paralysis Act is reintroduced, and other challenges arise.

Thank you for your enthusiasm and dedication!
Michael Manganiello
Director of Government Relations
The Hope Network

We Must. We Can. We Will.
Take Action Now!

Christopher Reeve Paralysis Foundation
500 Morris Ave Springfield, NJ 07081
(800) 225-0292
Donate Now!

lines

:) OT: I seem to have a roommate]

2006-12-22 07:15:36

Warning!!!

OT: :) Bless Your Little Pea Pickin Heart--Southern speak

2006-12-22 01:48:48

Another choice one from Richard. I'm from up Nawth, but still enjoyed it.
Irene
Southern lingo
Bless Your Heart!
Someone once noted that a Southerner can get away with the most awful
kind of insult just as long
as it's prefaced with the words, Bless their heart". As in, "Bless his
heart, if they put his brain
on the head of a pin, it'd roll around like a BB on a six lane highway."
Or, "Bless her heart,
she's so bucktoothed, she could eat an apple through a picket fence."
There are also the sneakier ones:
"You know, it's amazing that even though she had that baby 7 months
after they were married, bless her heart,
it weighed 10 pounds."
As long as the heart is sufficiently blessed, the insult can't be all
that bad.
I was thinking about this the other day when a friend was telling about
her new Northern friend who was upset
because her toddler is just beginning to talk and he has a Southern
accent. My friend, who is very kind and,
bless her heart, cannot do a thing about those thighs of hers, was
justifiably miffed about this. After all,
this woman had CHOSEN to move to the South a couple of years ago. "Can
you believe it?" said her friend.
"A child of mine is going to be taalllkkin liike thiiss."
Now, don't get me wrong. Some of my dearest friends are from the North,
bless their hearts. I welcome
their perspective, their friendships and their recipes for authentic
Northern Italian food. I've even gotten
past their endless complaints that you can't find good bread down here.
And the heathens, bless their hearts, don't like cornbread!
The ones that really gore my ox are the native Southerners who have
begun to act almost embarrassed about their speech.
We've already lost too much.
I was raised to swanee, not swear, but you hardly ever hear anyone say
that anymore, I swanee you don't.
And I've caught myself thinking twice before saying something is "right
much " "right close" or "right good" because
non-natives think this is right funny indeed. Bless their hearts!
I have a friend from Bawston who thinks its hilarious when I say I've
got to "carry" my daughter to the doctor,
or "cut off the light". She also gets a giggle every time Im "a-fixin"
to do something. And, bless their heart,
they don't know where "over yonder" is, or what "I reckon" means.
My personal favorite was my aunt saying, "Bless her heart, she can't
help being ugly, but she could've stayed home."
To those of you who're still a little embarrassed by your Southerness:
Take two tent revivals and a dose
of sausage gravy and call me in the morning. Bless your heart!
And to those of you who are still having a hard time understanding all
this Suthen stuff, bless your hearts,
I heah theyre a-fixin to have classes on Suthenese as a second language!
--
Richard Lee Holbert '85 North Richland Hills, Texas
oldag85tx@... ICQ # 288109551

OT: :) How to bathe a cat

2006-12-21 18:18:53

Some people say cats never have to be bathed. They say cats lick
themselves clean. They say cats have a special enzyme of some sort in
their saliva that works like new, improved Wisk - dislodging the dirt
where it hides and whisking it away.
I've spent most of my life believing this folklore. Like most blind
believers, I've been able to discount all the facts to the contrary, the
kitty odors that lurk in the corners of the garage and dirt smudges that
cling to the throw rug by the fireplace.
The time comes, however, when a man must face reality: when he must look
squarely in the face of massive public sentiment to the contrary and
announce: "This cat smells like a port-a-potty on a hot day in Juarez."
When that day arrives at your house, as it has in mine, I have some advice
you might consider as you place your feline friend under your arm and head
for the bathtub:
-- Know that although the cat has the advantage of quickness and lack of
concern for human life, you have the advantage of strength. Capitalize on
that advantage by selecting the battlefield. Don't try to bathe him in an
open area where he can force you to chase him. Pick a very small bathroom.
If your bathroom is more than four feet square, I recommend that you get
in the tub with the cat and close the sliding-glass doors as if you were
about to take a shower. (A simple shower curtain will not do. A berserk
cat can shred a three-ply rubber shower curtain quicker than a politician
can shift positions.)
-- Know that a cat has claws and will not hesitate to remove all the skin
from your body. Your advantage here is that you are smart and know how to
dress to protect yourself. I recommend canvas overalls tucked into
high-top construction boots, a pair of steel-mesh gloves, an army helmet,
a hockey face mask, and a long-sleeved flak jacket.
-- Prepare everything in advance. There is no time to go out for a towel
when you have a cat digging a hole in your flak jacket. Draw the water.
Make sure the bottle of kitty shampoo is inside the glass enclosure. Make
sure the towel can be reached, even if you are lying on your back in the
water.
-- Use the element of surprise. Pick up your cat nonchalantly, as if to
simply carry him to his supper dish. (Cats will not usually notice your
strange attire. They have little or no interest in fashion as a rule. If
he does notice your garb, calmly explain that you are taking part in a
product testing experiment for J.C. Penney.)
-- Once you are inside the bathroom, speed is essential to survival. In a
single liquid motion, shut the bathroom door, step into the tub enclosure,
slide the glass door shut, dip the cat in the water and squirt him with
shampoo. You have begun one of the wildest 45 seconds of your life.
Cats have no handles. Add the fact that he now has soapy fur, and the
problem is radically compounded. Do not expect to hold on to him for more
than two or three seconds at a time. When you have him, however, you must
remember to give him another squirt of shampoo and rub like crazy. He'll
then spring free and fall back into the water, thereby rinsing himself
off. (The national record for cats is three latherings, so don't expect
too much.)
-- Next, the cat must be dried. Novice cat bathers always assume this part
will be the most difficult, for humans generally are worn out at this
point and the cat is just getting really determined. In fact, the drying
is simple compared to what you have just been through. That's because by
now the cat is semipermanently affixed to your right leg. You simply pop
the drain plug with you foot, reach for your towel and wait.
(Occasionally, however, the cat will end up clinging to the top of your
army helmet. If this happens, the best thing you can do is to shake him
loose and to encourage him toward your leg.) After all the water is
drained from the tub, it is a simple matter to just reach down and dry the
cat.
In a few days the cat will relax enough to be removed from your leg. He
will usually have nothing to say for about three weeks and will spend a
lot of time sitting with his back to you. He might even become
psychoceramic and develop the fixed stare of a plaster figurine.
You will be tempted to assume he is angry. This isn't usually the case. As
a rule he is simply plotting ways to get through your defenses and injure
you for life the next time you decide to give him a bath.
But at least now he smells a lot better.

Reminder - Steve's birthday!

2006-12-21 06:09:18

We would like to remind you of this upcoming event.
Steve's birthday!
Date: Friday, March 7, 2003
Time: All Day
Steve Able's birthday!e is detectorist@...

Reminder - Rosie's birthday!

2006-12-21 03:12:47

We would like to remind you of this upcoming event.
Rosie's birthday!
Date: Friday, March 7, 2003
Time: All Day
Her email addy is ROlipant@...
She lived in CO for years but returned east to be near
daughter's family in Vermont last year.

UNICEF link added

2006-12-20 20:47:07

I've added Unicef card link to our links.
Jayne

People Helper: 'I Do Not Have A Bad Day in My Life'

2006-12-20 15:43:49

People Helper: 'I Do Not Have A Bad Day in My Life'
March 4, 2003
By John Sharify
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Email This Story
Printer-friendly Version
TACOMA - When I first met Bob Torres, I knew this guy was something else. He
looked me in the eye
and told me flat out:
"I'll put it to you this way. I do not have a bad day in my life," says Torres.
Not one bad day in his life! If I should be so lucky.
"I'm always positive. I never have a negative bone in my body," says Torres.
And yet, this 60-year-old Tacoma man has had two heart attacks, chronic back
pain, diabetes, and for
the past 17 years, he's had Multiple Sclerosis.
But you don't hear this man complaining.
"LIke I say, my life is really good. It really is," says Torres. His life might
be good, but his van
is breaking down. The Dodge minivan has more than 160,000 miles on the odometer,
and a constant gas
smell.
I thought People Helper viewers might want to help this man with the gentle
soul. So I'm asking you:
Will you help Bob get a new van? Help this man who doesn't have an extra dime to
call his own.
"If a trip around the world cost a quarter, hell I couldn't get out of Tacoma,"
says Torres.
Bob never complains, so let me do it for him: His van is a mess. It's seen its
last days. So with
your generosity, we can get Bob Torres a van he so desperately needs. And for
that, you know Bob
will be forever grateful.
"I'm rich. I'm the richest man in the world. Blessed by God in more ways than
you believe. Now
financially I'm the poorest dude around," says Torres with a smile.
I told you was something else. Something special.
How To Help
If you're interested in making a donation, you can call the People Helper at
(206) 441-HELP, or you
can email John Sharify at peoplehelper at komo4news dor com
Or better yet, checks can be made out to:
People Helper
P.O. Box 19087
Seattle, WA 98109
On the bottom of the check, be sure to include to whom you would like the funds
to go. In this case,
it's Bob Torres's new van.
Your donations are tax deductible and you will receive a receipt by mail with
our thanks. Any extra
funds will go to the general People Helper fund to help others in need.

Reminder - Kathi's birthday!

2006-12-20 11:10:07

We would like to remind you of this upcoming event.
Kathi's birthday!
Date: Thursday, March 6, 2003
Time: All Day
Kathi's email addy is
Kathi1960@...

new MS Watch survey on Cognition

2006-12-20 09:44:02

MS Watch March survey in on cognitive problems in MS.
Remember you don't have to be on Copaxone to use the
site.
Jayne

MS Research Participants Requested

2006-12-20 01:51:59

Note - sorry if this message is appearing twice - had problems posting it.
Hi,
I hope it's ok to post the following message on your board:
I am looking for a few people (approx 30-40) with MS, in CANADA, who
might be interested in taking part in a MS research study we may be
conducting in the next few months. This would be in the form of a
telephone conversation of about 30 minutes and will concentrate on the
various existing/future medical treatments for MS and the various
problems encountered by MS sufferers.
Many such research surveys are done via physicians, but this time we
need the first-hand experience of the people directly affected by this
condition.
As a sign of appreciation for the help provided, we will send every
participant a voucher or gift.
We conducted another study last year about pain, (in the UK, France
and Germany)in relation to MS and 2 other conditions, and had a lot of
help from people on that occasion - and I'm very grateful to everyone
who took part!!
As mentioned, this time we need participants from Canada (and possibly
a few more UK participants)
If you are interested in participating/helping out, or if you would
like further details, please email me on
sophiew@...
You can also call me on our toll-free number :
1-866-235-9358 (please bear in mind the time difference with Europe
and leave a message if our office is closed)
UK freephone 0800 279 2178 (we do need a few more participants in the
UK as well)
Thank you very much in advance
Sophie Wintrich
Patient Studies Manager
Fieldwork International
London, England
+44 208 246 4650
sophiew@...
www.fieldworkinternational.com

NYTimes.com Article: A Prescription Plan Hailed as a Model Is a Budget Casualty

2006-12-19 19:39:42

This article from NYTimes.com
has been sent to you by jayneadler@....
Thought this'd be of interest.
Jayne
jayneadler@...
A Prescription Plan Hailed as a Model Is a Budget Casualty
March 5, 2003
By TIMOTHY EGAN
PORTLAND, Ore., March 3 - In a state that says it is
already so short of public money it does not have enough to
keep all the schools open and prosecute many criminals,
Oregon took another drastic step this week to cover budget
shortfalls: it cut off medications to thousands of
schizophrenics, manic-depressives, drug addicts and others
who are poor and have no health care.
A decade ago, Oregon was widely hailed as a pioneer in
providing health insurance, including prescription drug
coverage, not only to the poor but also to people who make
just enough money that they do not qualify for most federal
Medicaid programs.
Now, in a reversal that has stripped a once ambitious
program to its core, Oregon has pared back the insurance,
and removed prescription drug coverage for things like
mental illness and drug addiction. Most of the cuts went
into effect March 1, but others started Feb. 1, just days
after Oregonians voted in a referendum against a tax
increase to balance their budget.
And while state officials are looking for some way to
restore some of the health program, they admit that they
will not be able to offer anything like the expansive
benefits of the past.
So throughout Oregon this week, about 100,000 poor people
are suddenly scrambling for the basic medications that
allow them to function.
For Dave Cesario, 45, who is H.I.V. positive, diabetic and
on methadone to stave off addiction to heroin, it meant
going cold turkey Saturday.
"I'm just numb; I don't know what to do," said Mr. Cesario,
who lives with his disabled wife and 12-year-old son. "My
only hope is that the drug companies will have mercy and
I'll be able to get some free samples."
For Karen Hansen, 50, who has prescriptions for everything
from anxiety disorder to high blood pressure, the cutoff
means taking only the few drugs that will keep her alive.
She lives on $689 a month in Social Security disability
payments, and her monthly prescription bill, without
assistance, is $615.
"I don't buy the newspaper, I eat hot dogs that they give
out free and get other meals from the food bank," Ms.
Hansen said. "But that only saves about $200."
The step is the latest response to a budget crisis that led
state officials to make nearly $600 million in cuts in the
last two years, and will require another $2 billion in
reductions, according to projections, in the new budget
cycle that begins this June.
Hit by a harsh recession after a series of tax-cutting
measures pared the budget to the bone, Oregon, which has no
statewide sales tax, now lacks enough money for health
care, schools, prisons and criminal prosecution.
Portland schools had planned to cut nearly five weeks off
the school calendar this year. But teachers agreed on
Monday to work two weeks without pay, and that offer -
together with a plan for a temporary business tax - looks
as if it will now save the school year. But the state has
announced plans to close a number of schools.
Prisons have let out some criminals early. And starting
today, prosecutions of people arrested for theft and drug
crimes are being delayed because there is not enough money
for prosecution or legal defense. Officials say those
arrested are being released and may be tried later, in the
summer, if the legislature can come up with new funds.
The latest round of cuts came after Oregonians considered a
referendum in January on whether to raise taxes
temporarily. The measure was narrowly defeated, after
opponents of the tax increase said the state could find
ways to cut without major consequences.
Unable to raise taxes, and having cut financing for police,
prosecutors and schools, state officials turned to the
Oregon Health Plan. They ordered the board that governs the
plan to decide how and where to cut. It chose to revert to
more basic coverage, stop paying for many prescription
drugs and charge higher premiums and co-payments.
Dr. Patricia Kullberg, medical director of the health
department of Multnomah County, which covers Portland, said
she just did something she had never done in 21 years as a
family physician: she advised a patient which medications
he could stop taking and suffer the least. The patient lost
his prescription drug benefit for arthritis, depression,
high cholesterol and hypertension.
"I feel like I'm living in some foreign country where
suffering is routine," she said. "It's scary. What we're
doing is condemning people to the long-term consequences of
their diseases."
The hardest hit, say state officials, are the mentally ill.
Jim Underwood, a mental health specialist with Cascadia
Behavioral Healthcare in Portland, said his patient Robert
Seaman, 47, a paranoid schizophrenic, was likely to become
delusional again without his medications.
Mr. Seaman had trouble responding to questions in an
interview. "Without his meds, he has trouble with getting
food, shopping, all the basic survival things," Mr.
Underwood said.
The legislature is working this week on a temporary patch.
The proposal would take video poker and cigarette tax money
and drain a reserve fund to make up an immediate shortfall
of $250 million. If this passes, and it appears it will, it
would restore medications for only about two months.
Mary Ellen Glynn, a spokeswoman for Gov. Ted Kulongoski, a
Democrat, said the next two-year budget could be even
worse, because voters refuse to raise taxes. "We're in real
double-bind," she said.
Advocates for the mentally ill put the issue more starkly.
David Eisen, clinical director for Central City Concern, a
private nonprofit agency that provides care for drug
addicts and the mentally ill, said people whose basic
medical needs were met by prescription drugs costing the
state about $90 a month per person, were now going to start
showing up in hospital emergency rooms, or jail, where they
will cost the state far more.
"The people who made this decision thought they could save
a few million dollars," Mr. Eisen said. "But the crime rate
will rise, emergency rooms will be flooded with people, and
in the end, the state is going to pay five to eight times
more than they would have saved."
In most states, the federal Medicaid program covers the
basic medical needs of the poor. Oregon was given a waiver
to shape its own program because it promised to provide
near-universal coverage for the poor, something only a
handful of states have tried to do. In good times, the plan
worked, and it was widely praised as a resourceful use of
limited public funds for health care.
One measure of its success was that Oregon has one of the
lowest percentages of mentally ill people in institutions.
Prescriptions and mental health clinics have allowed people
to work, or live in community settings, without presenting
a danger to themselves or others, state health officials
say.
Critics of the plan, however, said it was allowed to grow
too fast, and even though Oregon rationed out services -
drawing up a list of what would be covered and what would
not - it still proved too generous. State Representative
Jackie Winters, a Republican, said that over the last 20
years, social services in the state have quadrupled, far in
excess of population growth.
"We expanded beyond the basics, and now we realize you
can't cover everything you want," Ms. Winters said.
Now a number of legislative committees are studying ways to
redo the Oregon Health Plan. Even if state revenues become
less anemic, the plan is unlikely ever to be as ambitious
or far-reaching as it was, supporters and opponents say.
And for now, the cutbacks mean that most people who were
given coverage have lost their prescription drugs. Some are
now wandering the streets or screaming in public squares.
About one-fourth of the 400,000 people covered by the
Oregon Health Plan lost prescription coverage in two rounds
of cuts over the last month and half.
Tony Tescara, 66, who lives on $630 in Social Security,
relies on heart medication from the state. When he heard we
was cut off - after his pharmacists refused to fill a
prescription - he says he panicked.
"It was a big shock," Mr. Tescara said. "I took extra nitro
pills, just worrying about this medical thing. I called my
caseworker and said, `What am I supposed to do now?' She
said call the doctor and ask for samples."
Mr. Tescara said he was ashamed to beg for medicine. "I
feel like I'm a lowlife looking for handouts," he said.
"I'm not. It's the first time in my life I have to ask for
help."
State officials say relying on free samples, which
thousands of Oregonians are doing this week to get their
medications, will help only the luckiest.
http://www.nytimes.com/2003/03/05/national/05OREG.html?ex=1047904010&ei=1&en=d59\
0057f45bf4c1c
HOW TO ADVERTISE

:) OT: Burma Shave

2006-12-19 08:34:47

I enjoyed these. I barely remember these signs since they were mostly gone by the time I was born in 1950, but every once in a while we'd spy some. I think there are a number of highways in the Dakotas, Montana, or Wyoming that would benefit from these again! They are so boring!! Thanks to Richard for these.
Irene

BURMA SHAVE
For those of you who never saw the Burma Shave signs, here is a quick lesson in our history of the 1930's and '40's. Before the Interstate, when everyone drove the old 2 lane roads, Burma Shave signs would be posted all over the countryside in farmers' fields. They were small red signs with white letters. Five signs, about 100 feet apart, each containing 1 line of a 4 line couplet......and the obligatory 5th sign advertising Burma Shave, a popular shaving cream.
DON'T LOOSE YOUR HEAD
TO GAIN A MINUTE
YOU NEED YOUR HEAD
YOUR BRAINS ARE IN IT
*** Burma Shave***
DROVE TOO LONG
DRIVER SNOOZING
WHAT HAPPENED NEXT
IS NOT AMUSING
***Burma Shave***
BROTHER SPEEDER
LET'S REHEARSE
ALL TOGETHER
GOOD MORNING NURSE
***Burma Shave***
CAUTIOUS RIDER
TO HER RECKLESS DEAR
LET'S HAVE LESS BULL
AND MORE STEER
***Burma Shave***
SPEED WAS HIGH
WEATHER WAS NOT
TIRES WERE THIN
X MARKS THE SPOT
***Burma Shave***
THE MIDNIGHT RIDE
OF PAUL FOR BEER
LED TO A WARMER
HEMISPHERE
***Burma Shave***
AROUND THE CURVE
LICKETY-SPLIT
ITS A BEAUTIFUL CAR
WASN'T IT?
***Burma shave***
NO MATTER THE PRICE
NO MATTER HOW NEW
THE BEST SAFETY DEVICE
IN THE CAR IS YOU
*** Burma Shave***
A GUY WHO DRIVES
A CAR WIDE OPEN
IS NOT THINKIN'
HE'S JUST HOPIN'
***Burma Shave***
AT INTERSECTIONS
LOOK EACH WAY
A HARP SOUNDS NICE
BUT ITS HARD TO PLAY
***Burma Shave***
BOTH HANDS ON THE WHEEL
EYES ON THE ROAD
THAT'S THE SKILLFUL
DRIVER'S CODE
***Burma Shave***
THE ONE WHO DRIVES WHEN
HE'S BEEN DRINKING
DEPENDS ON YOU
TO DO HIS THINKING
***Burma Shave***
CAR IN DITCH
DRIVER IN TREE
THE MOON WAS FULL
AND SO WAS HE.
***Burma Shave***
DRUNKEN DRIVERS
HERE'S YOUR CHANCE
TO HOBBLE HOME
IN AN AMBULANCE
***Burma Shave***
And my all time favorite:

PASSING SCHOOL ZONE
TAKE IT SLOW
LET OUR LITTLE
SHAVERS GROW
***Burma Shave***
Now, do those bring back memories??!!!

Reminder - "Challengers' MS Support Group Mtg

2006-12-19 02:49:43

We would like to remind you of this upcoming event.
"Challengers' MS Support Group Mtg
Date: Wednesday, March 5, 2003
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

from MS Watch inludes tax info

2006-12-18 19:37:32

elcome to MSXPRESS - the biweekly newsletter for