The Susan Skinner Memorial Fund Scholarship (SSMF) provides a unique opportunity for recipients to network and develop skills that can be used to empower themselves and others to advocate for the improved care of women with bleeding disorders in their communities and worldwide.
The mission of the SSMF scholarship program is to cultivate leadership and promote the engagement of women of all ages in the global bleeding disorders community through education, training, and networking.
SSMF scholarship program recipients are offered the opportunity to attend major WFH events.
Questions? Please contact us at firstname.lastname@example.org.
The Susan Skinner Memorial Fund endowment supports the training and education of women with bleeding disorders. Scholarships are awarded every two years to US and international recipients and cover their participation in the WFH World Congress, Global National Member Organization Training and Annual General Assembly.
NMO/Chapters should answer all questions below:
A personal letter of recommendation is required from a mentor or somebody who has had an influence in your life: work supervisor/volunteering supervisor/a teacher/etc. The individual providing this recommendation should include their name, email address and telephone number. The relationship type should also be clearly stated in the letter.
The fund commemorates the late Susan Skinner, an American woman determined to ensure the availability of safe and effective treatment for her two sons. The WFH USA is deeply grateful to Thomas Skinner who created the fund, family members and friends, as well as organizations in the bleeding disorder community who continue to support the fund.
Support the Susan Skinner Memorial Fund Scholarship by donating today.
The WFH USA believes deeply in the value of educations and exchange. We offer U.S.-based healthcare professionals the opportunity to attend WFH international meetings and conferences. We can do so thanks to generous support of The Hemophilia Alliance.
You can read more about past recipients here.
With twenty-seven years of experience working with the bleeding disorder community, World Federation of Hemophilia (WFH) Psychosocial Committee Chair and 2019 Hemophilia Alliance Travel Grant recipient Ed Kuebler continues to be delighted at the commitment the community displays in pursuit of the WFH vision of Treatment for All.
Recognizing that training women leaders ensures the diversity our community need to thrive; the Hemophilia Alliance has been a longtime supporter of the Susan Skinner Memorial Fund. They deepened their engagement with the global community through the establishment of the Travel Grant Program, which allows US-based multidisciplinary healthcare professionals the opportunity to attend WFH global training workshops. The wealth of experience and perspective attendees bring back home to their communities helps patients across the country. Their patience and support as we grappled with changing norms in these challenging times gave us the flexibility to meet our community’s needs with revamped programming.
Angelo Bianchi Bonomi Hemophilia and Thrombosis Centre
Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico
International Hemophilia Training Center – Bangkok
Malmö Centre for Thrombosis and Haemostasis
Department for Hematology and Coagulation Disorders, Skåne University Hospital
Skåne University Hospital
Hospital Universitario La Paz
Haemostasis and Thrombosis Unit
Haematology Service, University and Polytechnic Hospital
Haemophilia Comprehensive Care Centre
Charlotte Maxeke Johannesburg Academic Hospital
Singapore General Hospital Haemophilia Treatment Clinic
Centre International de Traitement de l’Hémophilie (CITH) de Dakar
Centre National de Transfusion Sanguin (CNTS)
National Medical Research Center of Hematology of the Russian Academy of Medical Sciences
University Medical Centre Utrecht
Nara Hemophilia Centre
Nara Medical University
National Hemophilia Center, Tel Hashomer
Sheba Medical Center
University of North Carolina Hemophilia & Thrombosis Center
Nationwide Children’s Hospital
Gulf States Hemophilia and Thrombophilia Center
University of Texas Health Science Center at Houston
Orthopaedic Hemophilia Treatment Center
Mount Sinai School of Medicine
Mount Sinai Medical Center
Mayo (Rochester) Comprehensive Hemophilia Center, and International Hemophilia Training Center (WFH)
Mayo Clinic/Foundation and Mayo Medical School
Hemophilia & Thrombosis Treatment Center
University of California San Diego
National Institute of Immunohaematology (ICMR) and KEM Hospital
Christian Medical College, Vellore
Paris Haemophilia Centre (Necker (N) and Kremlin Bicetre (KB) Hospitals)
Shabrawishi Hospital, Egyptian Society of Hemophilia, and Cairo University
University of Toronto Hemophilia Centres
St. Michael’s Hospital
Hemocentro – “Unidade de Hemofilia Cláudio Luiz Pizzigatti Corrêa”
Hemocentro Unicamp, University of Campinas
Haemostasis and Thrombosis Unit
Division of Haematology
Cliniques universitaires Saint-Luc
Hemofiliecentrum Leuven, University of Leuven
Medical University of Vienna
Department of Medicine I
Clinical Division of Hematology and Hemostaseology
Ronald Sawers Haemophilia Centre
Instituto Asistencial “Dr. Alfredo Pavlovsky”
(Fundación de la Hemofilia)
Instituto De Investigaciones Hematológicas “Dr. Mariano R. Castex” (IIHEMA
(Academia Nacional de Medicina)
The WFH was established in 1963 by Frank Schnabel, a Canadian businessman born with severe hemophilia A. He believed that patient organizations could be much more effective—and do more to represent the interests of people living with bleeding disorders—if they worked together. The first WFH Congress was held in Copenhagen, Denmark, on June 25, 1963, and was attended by representatives from 12 countries. Now, the WFH and our global network of national member organizations (NMOs) represent the interests of people with hemophilia and other inherited bleeding disorders in 147 nations.
Katharine Dormandy Haemophilia Centre and Thrombosis Unit
Royal Free Hospital
Manchester Haemophilia Comprehensive Care Centre (Children’s and Adult’s)
Manchester Royal Infirmary and Manchester Children’s Hospital
Oxford Haemophilia Centre and Thrombosis Centre
Sheffield Haemophilia and Thrombosis Centre
Royal Hallamshire Hospital
The WBDR Minimal Data Set (MDS) is a set of data on demographics, diagnosis, symptoms and treatment which are collected on patients participating in the WBDR.
The WBDR Extended Data Set (EDS) is a larger set of data, with more details than the MDS, which includes questions on patient demographics, diagnosis, symptoms, treatment and burden of disease. The EDS can be used by hemophilia treatment centers to collect data on patients participating in the WBDR. The WBDR Extended Data Set (EDS), was added to the database in March 2019.
Hemophilia of Georgia has stood with us for over three decades, playing an early role in distributing donated factor via the WFH Humanitarian Aid program. Our relationship has deepened over the years as they continued to support this program and came on board as a founding Chapter Challenge champion in 2016. Their belief in educating future leaders is clear in their investment in the Youth Leadership Workshops, which has led to the training of over 50 young adults. They also support workshops devoted to educating providers and patient leaders on how to collect and use data to advocate for better patient care. Their staff generously volunteer their time as trainers and as well as serving on various committees.
|2012||Piet de Kleijn
|2010||Dr. Mammen Chandy
|2008||Dr. Man-Chiu Poon
|2006||Dr. Norma de Bosch
|2004||Dr. Parttraporn Insarangkura
Dr. Carol K. Kasper
The National Hemophilia Foundation helps advance our mission on several fronts. They inspire others to follow their lead as a founding champion of the NHF Chapter Challenge. Their commitment to equality of access is demonstrated in their support of the Cornerstone Initiative, which lays the foundation for care in the world's most underserved regions, as well as programs that aim to raise awareness and improve care of women with bleeding disorders and those with von Willebrand disease. We also benefit from their steadfast engagement with various programs including the WFH Twinning Program and their individual leaders’ contribution to our leadership and committees.
Do you sometimes wish you could do more? A bequest is a simple way for you to make a significant gift without changing anything about your financial security and lifestyle today. Your legacy will sustain care for the generations to come.
Download these sample clauses to give to your legal advisor.
We understand if you prefer to remain anonymous, but we would be very honoured if you would let us know of your intentions so that we may thank you personally. We would also be happy to answer any questions you may have or give you additional information. Please contact Jennifer Laliberté at 514‑875‑7944 ext.2822 or email@example.com.
The information on the WFH USA website is provided for general information purposes only. The WFH USA does not engage in the practice of medicine and under no circumstances recommends particular treatment for specific individuals. For diagnosis or consultation on a specific medical problem, the WFH USA recommends that you contact your physician or local treatment centre. Before administering any products, the WFH USA urges patients to check dosages with a physician or hemophilia centre staff, and to consult the pharmaceutical company’s printed instructions.
While every effort has been made to ensure the accuracy of the information on this site, the WFH USA does not guarantee the information is accurate, and is not responsible in any way whatsoever for damages arising out of the use of this website or any of the information contained herein.
Messages posted to WFH USA discussion forums, Facebook, Twitter, and other social media platforms do not represent the opinions of the World Federation of Hemophilia, its staff, or Board of Directors. The author of a message is solely responsibility for its content. Information posted on WFH USA social networks and platforms should never be a substitute for individualized professional medical advice, even when the author has medical qualifications or is considered an authority. Information posted to a discussion group should not be used to diagnose or treat a specific health problem without consulting a qualified healthcare professional. The WFH USA recommends that you contact your physician or local treatment centre if you have any individual questions or concerns.
References and links to other websites or references to other organizations, products, services, or publications do not constitute endorsement or approval by the WFH USA. The WFH USA is not responsible and assumes no liability for the content of any linked websites.
The WFH USA does not collect personally identifying information about you when you visit our site, unless you choose to provide such information to us. Providing such information is strictly voluntary. This policy is your guide to how we will handle information we learn about you from your visit to our website.
Throughout our website, we provide links to other servers which may contain information of interest to our readers. We take no responsibility for, and exercise no control over, the organizations, views, or accuracy of the information contained on other servers. When linking to the WFH USA, we request that you ensure that there are no associated connections for commercial purposes. Any official use of the name WFH USA or the use of its logo needs to be approved by the WFH USA. If you have a link you’d like us to consider adding to our website, please send an email to firstname.lastname@example.org with the subject “Link request.”
All information, photographs, graphics, and other material on this website are protected by copyright. While users of this website may use the content for personal, non-commercial use, none of the content of this website can be modified, translated, transferred or sold, copied, reproduced, published, or distributed, in whole or in part, without the prior written consent of the WFH USA. To view a copy of the WFH USA’s permissions guidelines, click here.
The WFH USA encourages the dissemination of its information and welcomes proposals on the reprinting, redistribution, and translation of its materials. If you would like to publish information that you find on our website, please send your request to email@example.com.
If you have suggestions on how to make the site more accessible, please contact us at firstname.lastname@example.org.
Our website provides users the opportunity to opt-out of receiving communications from us through a special online form or via the communication they have received. You may, at all times, choose to receive which communications within the organization you can receive or none at all. You may also update your contact information previously provided to us via another online form.
If you have any questions about this privacy statement, the practices of this site, or your dealings with this website, you can contact us at email@example.com.
The WFH USA has been made aware of various correspondences—circulated via e-mail and telephone—coming from individuals impersonating WFH USA staff or falsely stating that they are associated with the WFH USA. These correspondences, which may seek to obtain money using the name of someone affiliated with the WFH USA, are fraudulent and come from outside of our organization.
If you receive a suspicious solicitation, exercise extreme caution. In the case of an email, look at the email address to see if it looks suspicious (for example, all WFH USA emails come from @wfhusa.org or @wfh.org).
We are asking you to remain vigilant, and if you have any doubts about the correspondence, please forward the email to the WFH USA at firstname.lastname@example.org or call 1-877-417-7944.
|Buenos Aires, Argentina||Planetario|
|La Torre Monumental|
|Monumento Plaza Congreso|
If you’re aware of a landmark that is lighting up red for World Hemophilia Day 2022 that is not on this list, please forward the official confirmation from the landmark to email@example.com to have it added to the list.
|2006||Dr. Bruce Evatt|
|2019||Yogyakarta / Solo (Indonesia) – Utrecht (Netherlands)|
|2018||Abidjan (Ivory Coast) – Brussels (Belgium)|
|2017||Santa Cruz de la Sierra (Bolivia) – Buenos Aires (Argentina)|
|2016||Kampala (Uganda) – London (UK)|
|2015||Varna (Bulgaria) – Bonn (Germany)|
|2014||Arequipa (Peru) – Los Angeles (USA)|
|2013||Davangere (India) – Liverpool (UK)
Ludhiana (India) – Detroit (USA)
|2012||Hanoi (Vietnam) – Melbourne (Australia)|
|2011||Manado (Indonesia) – Utrecht (Netherlands)|
|2010||Delhi (India) – Winnipeg (Canada)
Yaoundé (Cameroon) – Geneva (Switzerland)
|2009||Chisinau (Moldova) – Warsaw (Poland)
Colombo (Sri Lanka) – Vellore (India)
|2008||Gaborone (Botswana) – Philadelphia (USA)|
|2007||Vientiane (Laos) – Brest (France)
Damascus (Syria) – Montpellier (France)
|2006||Lima (Peru) – Fort Worth (USA)|
|2005||Yerevan (Armenia) – Minneapolis (USA)
Casablanca (Morocco) – Caen (France)
|2004||Beirut (Lebanon) – Geneva (Switzerland)
Santo Domingo (Dominican Republic) – Caracas (Venezuela)
|2003||Cairo (Egypt) – Knoxville (USA)|
|2002||Moscow (Russia) – Liverpool (UK)
Panama – Valencia (Spain)
|2001||Bangalore (India) – St. Louis (USA)|
|2000||Pune (India) – Bradford (UK)|
|1999||Montevideo (Uruguay) – Buenos Aires (Argentina)
Tianjin (China) – Calgary (Canada)
|1998||Plovdiv (Bulgaria) – Bonn (Germany)|
|1997||Bogota (Colombia) – Los Angeles (USA)
Tartu (Estonia) – Stockholm (Sweden)
|1996||Timisoara (Romania) – Munich (Germany)
Riga (Latvia) – Munster (Germany)
|1995||Klaipeda (Lithuania) – Malmo (Sweden)|
|1994||Bratislava (Slovakia) – Tel Hashomer (Israel)|
The outcomes of interest collected by the WBDR include demographic characteristics, clinical and treatment-related outcomes, burden of disease outcomes, and patient-reported outcomes.
The WBDR includes five functional scales as part of its extended data set:
|2019||Dr. Adolfo Llinás
|2012||Piet de Kleijn
|2011||Dr. Lily Heijnen
|2010||Dr. Horacio Caviglia
|2009||Jerome D. Wiedel
|2008||Dr. Federico Fernández-Palazzi
|2005||Dr. Marvin Gilbert
Yangzhou College, Xuzhou Medical University
|The effects of intra-articular injection of TNF-alpha Antagonists in treatment of haemophilic synovitis|
|Association between multi-segment foot kinetics and blood induced joint damage in adult patients with hemophilic ankle arthropathy|
|Decrease in joint inflammation, swelling and pain after a swimming protocol in animal model of experimental-induced hemarthrosis|
|2015||SM Javd Mortazavi
|Bilateral total knee arthroplasty in patients with hemophilia: A safe and cost-effective procedure|
|2013||Lize F.D. van Vulpen
|A fusion protein of IL4 and IL10, is equally effective in protecting cartilage from blood-induced damage compared to the individual components|
|Pseudotumor Surgery in Haemophilia A patients: Comparitive results between inhibitor and non-inhibitor patients|
United Kingdom and
Monique van Meegeren
|Early onset administration of IL-4 and IL-10 prevents blood-induced cartilage damage in vitro|
|Influence of an Aquatic Training Protocol on the Reduced Risk of Cardiovascular Morbidity and Mortality in a Hemophiliac|
|Impact of Hemophilia Ankle Arthropathy on Gait Disability: Analysis of Energetic and Mechanical Variables|
|2008||Jose Alberto Tlacuilo-Parra
|Bone Turnover Markers and Bone Mineral Density in Children with Hemophilia|
|Protective Abilities of Interleukin-10 in Blood-induced Cartilage Damage|
|2006||Axel Seuser and E. Kusch
|Multi-Center Study of Orthopedic Outcome of the Lower Extremities in 249 Children with Hemophilia|
|2005||Frank van Genderen, Nico van Meeteren, Lily Heijnen, Piet de Kleijn, Marijke van den Berg, Paul Helders
|The Hemophilia Activities List: Final development and validation of a hemophilic-specific self-assessment questionnaire on functional abilities|
|2004||Goris Roosendaal, Zalima N Jahangier, Kim MG Jacobs, Johannes WJ Bijlsma, Floris PJG Lafeber
|Radiosynoviorthesis using YTTRIUM-90 results in adverse direct effects on cartilage: a human in vitro study|
|2003||Axel Seuser, Thomas Wallny, Günter Schumpe, Elmar Trunz, Hans-Hermann Brackman
|How to advise young haemophiliacs to find the right sport? A new and safe algorithm|
|2002||James Luck, Jr. and Mauricio Silva
|Long-Term Review of Total Knee Arthroplasty|
|Oxytetracycline Chlorohydrate: A new material for chemical synovial orthoses|
|1999||William J. Ribbans and J.L. Hicks
|Communication and Co-operation for the New Millennium – The Future of the Musculoskeletal Committee in the 21st Century|
|1998||Adolfo Llinas, Mauricio Silva, Monica Duarte, Gonzalo Ucros, Graciela Perini, Angela Maria Cerquera, Andres Forero
|Chromic phosphate synoviorthesis without age restriction should be the first treatment option for chronic active hemophilic synovitis|
|2020||Dr. Ozlem Turan
|2017||Dr. Heike Singer
University Hospital Bonn
|The Christine Lee Young Researcher Award for best free paper presentation:
“Detection and localization of intracellular FVIII in IPS derived endothelial cells from three Hemophilia A (HA)-patients with null mutations”.
|2017||Dr. Badle Saket
Clinical Research Fellow Barts and the London School of Medicine and Dentistry
The Royal London Hospital Haemophilia Centre London, United Kingdom
|The Christine Lee Young Researcher Award for best moderated poster presentation:
“Pharmacokinetic intervention to optimise FVIII prophylaxis: UKPK trial interim analysis”.
The Netherlands (2014 winner)
Sweden (2013 winner)
|2014||Dr. Magdy El Ekiaby|
|2012||Dr. Alok Srivastava|
|2008||Dr. Steve Kitchen|
|2004||Dr. Angus McCraw|
Dr. Brian Luke and Dr. Man-Chiu Poon
|2000||Dr. Alok Srivastava|
Dr. Carol K. Kasper
|2016||Professor Thierry Vandendroessche|
Professor Marinee Chuah
|2016||Doctor Midori Shima|
|2012||Martha Patricia Monteros Rincon|
Antonia Luque de Garrido
Jean Michel Bouchez
The outcomes of interest collected in the WBDR include demographic characteristics, clinical and treatment-related outcomes, burden of disease outcomes, and quality of life. The quality of life scale, EQ-5D-5L, is part of the WBDR extended data set. It is available in more than 130 languages and in different modes of administration.
If you would like a different language, please email us at firstname.lastname@example.org.
Arabic (Algeria, Morocco, UAE)
English (Ghana, India, Jamaica, Kenya, Nigeria, and the Philippines)
French (Algeria, Belgium, and Morocco)
Spanish (Argentina, Panama, Spain, and the U.S.A)
For more information, please visit: euroqol.org/eq-5d-instruments/eq-5d-5l-about.
Our vision of Treatment for All is for a world where all people with inherited bleeding disorders have access to care, regardless of their type of bleeding disorder, gender, or where they live. Our mission is to improve and sustain care for people with inherited bleeding disorders around the world.