- New Global Headquarters Dedicated to
This year's global theme, "Patient Voice," highlights the need for
greater understanding of the experiences of rare disease patients and
calls attention to the unique challenges faced by this community.
"Today serves as a special milestone for
Alexion's Rare Disease Day 2016 activities include:
-
Today,
Alexion will dedicate its new global headquarters inNew Haven, CT , to rare disease patients worldwide in an official ribbon-cutting ceremony with government officials, community partners, and patients and their families. -
Alexion is a sponsor and participant in the Rare Disease Legislative Advocates (RDLA) 5th Annual Rare Disease Week onCapitol Hill inWashington, D.C. , and will participate in briefing legislators on rare diseases in multiple states. -
Alexion will attend MASSBIO Rare Disease Day at the State House inBoston, MA , coordinated by theNational Organization for Rare Disorders (NORD), which includes patient organizations, professional societies, government agencies, medical researchers, life sciences companies, and patients. -
Alexion is a sponsor of NORD's National Rare Disease Day Activities, which include local State House events, such as medical grand rounds, university and medical school events, and K-12 school events throughoutConnecticut . -
Alexion is a Platinum sponsor of the 2nd Annual Utah Rare Disease Day Symposium (February 27 ) and the Utah World Rare Disease Day State House Event, "Utah Rare Dinner" (February 29 ). -
Alexion is a sponsor of theCanadian Organization for Rare Disorders (CORD)'s 2016 Rare Disease Day activities (March 9-10 ), which include the launch of the Rare Disease Strategy, updates on rare disease research, and training for rare disease patient groups.Alexion is the ActionHero Sponsor of CORD's Rare DiseaseDay Gala , the Leadership Sponsor of itsRare Disease Day Conference , and a Founding Partner and Premier Sponsor of "Rare Alliance Canada," which launched today in Ottawa.
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Alexion will attend the Rare DiseaseUK (RDUK) Parliamentary reception at the House of Commons inLondon, England (March 3 ). -
The Company is a corporate sponsor of the
Genetic and Rare Disease Organization (GRDO)'s 2016Rare Disease Day Conference , held today atDublin Castle inIreland . The event will bring together representatives from patient organizations, politicians, caretakers, medical professionals, researchers, and members of the industry. -
In
Spain ,Alexion is supporting the Federación Española De Enfermedades Raras (FEDER)'s "Creating Networks of Hope," a national event held at theSuperior Council for Scientific Research in Madrid (March 4 ). In addition,Alexion is supporting the Plataforma Malalties Minoritaries' "All Together for Rare Diseases" meeting at the Hospital Clínic deBarcelona to support rare disease patient associations in Catalonia. -
Alexion will support initiatives driven by Denmark's rare disease organization, Sjældne Diagnoser. -
In
Sweden ,Alexion will join members of Parliament, county councils, and administrators in support of Sweden's rare disease organization, Sällsynta Diagnoser.
-
In
Colombia ,Alexion will participate in events organized by Asociación Colombiana de Pacientes con Enfermedades de Depósito Lisosomal (ACOPEL) and Fundación de Apoyo Solidario a Pacientes con Enfermedades Raras (FUNDAPER) that will bring together artists and government officials to support rare disease patients in the country.
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Alexion will participate in rare disease awareness events at local hospitals throughoutAustralia and distribute educational resources to further spread awareness about rare diseases.
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In
China ,Alexion is a sponsor of theChinese Organization for Rare Disorder's Patient Care Video Release Ceremony being held inBeijing (February 29 ) as well as the Shanghai Rare Disease Medical Association's 2016 Rare Disease Day.
Today,
For more information about Rare Disease Day in the
About Rare and Ultra-Rare Disorders
In
Despite the very small numbers of patients they affect, the impact of rare and ultra-rare diseases on patients, their families, and society is profound, as many of these conditions are severe, chronic and progressive, with significant premature mortality. Patients with severe and life-threatening ultra-rare diseases often live without hope and have no effective treatments.
About
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References:
1.
2. REGULATION (EC) No 141/2000 OF THE EUROPEAN PARLIAMENT AND OF THE
COUNCIL of
3. REGULATION (EU) No 536/2014 OF THE EUROPEAN PARLIAMENT AND OF THE
COUNCIL of
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