
Senator John R.
Warner (R-VA) sent Michael John Coleman, Executive Director and Founder
of MAGNUM, the National Migraine Association, to London to attend
the Symposium representing the United States. Mr. Coleman hand-delivered
powerful bipartisan letters showing support for this major headache
and Migraine health event from Senator Warner and Congressman James
P. Moran (D-8th District, VA) to Ms. Ann Rush, Director of The Migraine
Trust. Part of Senator Warner's letter reads:
"The
Symposium's slogan, "RESEARCH Is the Key" is most fitting
for this important international gathering. The ongoing research
and recent experimental treatment regimens suggest new hope for
the millions who suffer from serious head pain problems. Yet this
is just the beginning and efforts like yours must continue if we
are to build the public awareness and support needed to achieve
our goal of relief for head pain sufferers."
Part
of Congressman Moran's letter reads:
"In
today's world it is more important than ever to see international
cooperation in medical research. The slogan for your symposium,
"Research is Key," is extremely appropriate as you gather
with other nations to discuss the best ways to treat Migraines.
It is my hope that with a more multi-cultural look at head pain,
we will be able to forge new ideas and help ease suffering for all."
Mr.
Coleman had an opportunity to speak with Dr. Stephen Silberstein as
he was
going to be interviewed by ABC-TV news. Dr. Silberstein said he was
"very happy that our government gave official messages of policy
to be issued and to show how seriously our government takes head pain
issues."
Coleman
also spoke with Dr. Jes Olesen of Denmark, who wears many hats in
the European and international medical community. He recently attended
a pain conference in Brussels with ministers from eight major
European governments to discuss head pain and other brain and neurology issues.
Regarding the letters, he told Coleman, "This is exactly the
kind of thing we need from more governments to get head pain and other
pain issues on radar screen. I'm pleased that MAGNUM is present to
report back and advise the US government." Ann Rush, director
of the Migraine trust said she was "pleasantly surprised that
the conference was acknowledged by the American government at such
a prestigious level. Coleman was "quite impressed with the Migraine
Trust and the quality of the symposium Ms. Rush has organized."
He added that "It's exciting and gratifying to have the support
of our government and to be present here to see the true progress
that is finally being made in the treatment of Migraine disease. It
is significant that research on Migraine prevention is increasing."1
|

Professor
Peter J Goadsby, Symposium Chairman
Opening remarks at the Migraine Trust
International Research Symposium
Photo © MAGNUM, 2002
All rights reserved.
Used with permission of MAGNUM.
|
More about WHAM
Kary Shannon, Chief Operating officer of the WHA, commented:
"World
Headache Awareness month 2002 represents 37 organizations in 26
countries working to get the attention not only of public and press,
but also of interested healthcare providers, primary care physicians,
and other professionals it to understand and raise awareness about
headache and headache disorders. To support that was presentation
of the prestigious Elizabeth Garret Anderson (EGA) Award to Dr.
Anne MacGregor at the Migraine Trust Symposium. Anne was recognized
for her tireless commitment to research, specifically that focused
on women and menstrual headache disorders and the effects of hormones
on these disorders and for her and public education. Because of
that, her ability to under the full dynamics of headache disorder
sufferers is profound. Continued research and public education are
vital, and the WHA is honored to present this award to Anne. 'I
look forward to a time when there is no need for a World Headache
Awareness Month.'2
Preparations for WHAM 2003 are in progress, and the WHA is developing
a comprehensive media and awareness platform for use by non-medical
organizations.
Valerie
South, Chief Operating Officer of the International Headache Society
commented about "exciting things" going on in the field,
saying about Migraine prevention that there is, "more interest
now. It's exciting that prevention is finally being looked at in tandem
with acute treatment."3
Dr.
Jean Claude Krusz, a headache/Migraine and pain specialist from Dallas,
Texas, offered a doctor's point of view on treating head pain disorders
today, saying:
"There
are so many newer treatments/tools - acute and preventive biochemical
tools. Take advantage of what's out there with guidance of a headache
and Migraine specialist. New categories of meds will hopefully treat
acute Migraine, offering better quality of life. If there is enough
frequency, it warrants daily treatment - newer categories of meds
with lifestyle changes in sleep, exercise, other environmental factors.
This can make a huge difference in how you control head pain rather
than head pain controlling you. Treatment is best when the patient
becomes major player, part of team, not walking into the doctor's
office to be fixed like changing light bulb. Team effort, meds are
one aspect. It's important to understand that these family disorders,
affecting everyone in family. Not only are they familial disorders,
sometimes with multiple family members affected, but they do affect
everyone, so it's important to draw everybody in as part of the
treatment algorithm to learn about awareness. Organizations are
important, and support groups need to bring in family members, children,
so everyone has as much information as possible. Expose everybody
to information or you won't get as good results. It's the 'Absent-spouse
syndrome.' The person who is absent never hears what transpires
in terms of education and awareness and feels the person is making
up their symptoms. This is how things go on too often. I tend to
try to bring family units in and make sure everybody hears what
we have to say."
Dr.
Krusz was also impressed with the letters from Senator Warner and
Congressman Moran, saying:
'...
incredible reading because they're not something canned. They were
put together by their own staff and show an incredible amount of
awareness. There are 100 million headachers in the country. It's
one of the largest medical clubs around other than perhaps chronic
pain. Because of groups like MAGNUM, we're seeing more awareness.
The Joint Commission (JCAHO) rules stop discharging patients in
pain. It's incredible that Congress is so aware. We need a major
initiative in the head pain field to raise public awareness, with
concerted awareness, with patients standing up and fighting for
the right to be treated and recognized as a legitimate group of
patients. Certainly cancer, blindness, deafness, and other chronic
disabilities are. Head pain and other pain need to be in that kind
of grouping so that 10 to 15 years from now treatment isn't so elementary
as it is now.'4

More
about the WHA
The World Headache Alliance was incorporated in 1997 and has offices
in London, England, and Ontario, Canada. There are currently 38 member
head pain organizations in 26 countries around the world. To assist
in reducing the burden of headache disorders, the WHA has two main
goals:
-
To
lobby governments and other agencies on the unmitigated burdens
of headache and the cost-effectiveness of their alleviation
-
To
raise awareness of headache as a public health concern.
As stated on their web
site, "The World Headache Alliance (WHA) exists to relieve
the suffering of people affected by headache throughout the world,
in particular, by sharing information among headache organisations
and by increasing the awareness and understanding of headache
as a public health concern with profound social and economic impact."

More
about the IHS
The
International Headache Society (IHS), a professional scientific
group, has a mission very similar to that of the WHA. The two organizations
have a very close working relationship, with the WHA working through
lay organizations and the IHS working through professional groups
and individuals.
The IHS was founded in
1981. As stated in their Articles of Association their objectives
are "to relieve sickness and to protect and preserve health in
the United Kingdom and elsewhere in the world, including in any one
or more of the individual countries of the world, in particular by
promoting research into the causes, mechanisms, diagnosis, treatment
and other aspects of headache..."
developed head pain disorder
classification and diagnostic criteria that are internationally accepted
as the standards in treating diagnosing, classifying, and treating
these disorders. Director Val South reports that the IHS is in the
process of updating these documents and invites those interested to
review the proposed updates and post their comments to the IHS web
site at www.i-h-s.org.
Summary
Without awareness of head pain disorders, we will make little or no
progress toward timely and quick diagnosis, prevention and treatment
of these disorders and their symptoms or toward a better quality of
life for all those afflicted by them. It's WHAM - World Headache Awareness
Month! Let's each of us do our part by educating ourselves and those
around us.
Resources & References
1
From a telephone interview
conducted by Teri Robert with Mr. Coleman from the
International Research Symposium
on September 24, 2002.
2 From a telephone interview conducted by Teri Robert
with Ms. Shannon from the International
Research Symposium on
September 24, 2002.
3 From
a telephone interview conducted by Teri Robert with Ms. South from
the International
Research Symposium on
September 24, 2002.
4 From
a telephone interview conducted by Teri Robert with Krusz from the
International
Research Symposium on
September 24, 2002.