Hier finden Sie Adressen von Hämophiliezentren in Ihrer Nähe

Mit diesem Ortsverzeichnis von Hämophiliezentren und Hämophiliebehandlungsmöglichkeiten möchte die DHG ihre Patienten informieren und auf das Behandlungsangebot in den verschiedenen Regionen hinweisen. 

Behandlungszentren auf www.haemophilie-therapie.de

www.haemophilie-therapie.de/haemophilie/zentren

www.haemophilie-therapie.de

Experteninformationen für Ihren Weg zur individuellen Hämophilietherapie

www.dhg.de/haemophiliezentren

Behandlungszentren auf www.dhg.de

www.immundefekte.info ist eine Initiative der Octapharma GmbH. 

www.immundefekte.info ist eine Initiative der Octapharma GmbH. Die Website will einen Beitrag zu einem leichteren Umgang mit der Herausforderung Immundefekt im Alltag leisten. Auf der Internetseite finden Sie neben zahlreichen interessanten Informationen zu Immundefekten auch Adressen und Internetlinks von Behandlungszentren in Ihrer Nähe. Hier finden Sie erfahrene Ärzte, die sich speziell auf die Diagnose und Therapie von Immundefekten spezialisiert haben.

www.immundefekte.info

Hier finden Sie Adressen und Internetlinks von Behandlungszentren in Ihrer Nähe

Die Website will einen Beitrag zu einem leichteren Umgang mit der Herausforderung Immundefekt im Alltag leisten. Auf der Internetseite finden Sie neben zahlreichen interessanten Informationen zu Immundefekten auch Adressen und Internetlinks von Behandlungszentren in Ihrer Nähe. Hier finden Sie erfahrene Ärzte, die sich speziell auf die Diagnose und Therapie von Immundefekten spezialisiert haben.

Behandlungszentren auf www.immundefekte.info

https://www.immundefekte.info/immundefekt/behandlungszentren/

 www.info-itp.de  richtet sich an Patienten, die an der Immunthrombozytopenie (ITP) erkrankt sind.

www.info-itp.de  richtet sich an Patienten, die an der Immunthrombozytopenie (ITP) erkrankt sind. Bei dieser Erkrankung werden körpereigene Blutplättchen (=Thrombozyten) durch das eigene Abwehrsystem zerstört. Blutplättchen spielen eine wichtige Rolle bei der Blutgerinnung. Fehlen sie oder sind zu wenige von ihnen im Blut, kann es vermehrt zu Blutungen kommen.    Hier finden Sie viele hilfreiche und aktuelle Informationen rund um diese Erkrankung. 

www.info-itp.de

Das Infoportal zum Thema Von-Willebrand-Syndrom

Viele Menschen, die vom Von-Willebrand-Syndrom betroffen sind, wünschen sich einen regen Austausch und aktuelle Informationen rund um Therapie, Diagnostik und das Leben mit der Erkrankung.  Die Website unterstützt Sie dabei. 

www.info-von-willebrand.de

The decision to create the International Patient Organisation for ...

The decision to create the International Patient Organisation for Primary Immunodeficiencies (IPOPI) emanates from an interim organising committee that met in Oxford, UK, in 1990. Two years later, IPOPI was formally established in Lugano, Switzerland. The small group of representatives from the primary immunodeficiency community (PID) who met in 1990 identified the need to start an organisation that provides international representation and support to national PID patient groups around the world. IPOPI’s mission is to improve awareness and access to early diagnosis and optimal treatments for PID patients worldwide.

IPOPI

International Patient Organization for Primary Immunodeficiency's

The mission of the Foundation for Primary Immune Deficiency Diseases is to support education ...

The mission of the Foundation for Primary Immune Deficiency Diseases is to support education about, diagnosis and treatment of, and research into primary immunodeficiency diseases in India and the USA. 

Foundation for Primary Immune Deficiency Diseases

The Immune Deficiency Foundation is a national patient organisation dedicated to improving ...

The Immune Deficiency Foundation is a national patient organisation dedicated to improving the diagnosis, treatment and quality of life of people with primary immunodeficiency diseases through advocacy, education and research.

Immune Deficiency Foundation

The Jeffrey Modell Foundation was established in memory of its namesake, who died of ...

The Jeffrey Modell Foundation was established in memory of its namesake, who died of pneumonia at the age of 15 due to an underlying primary immunodeficiency disease (PID). The Foundation is dedicated to early and precise diagnosis, meaningful treatments, and ultimately cures for the ever-increasing number of known PIDs. The Foundation works for clinical and basic research to better understand and treat PIDs; serves as a national and international information and education resource regarding the diagnosis and treatment of genetic immunodeficiency; advocates on behalf of patients and families to ensure their access to comprehensive care; and promotes public awareness of PIDs.

Jeffrey Modell Foundation

Save One Life was founded in 2000. It supports people with bleeding disorders living in ...

Save One Life was founded in 2000. It supports people with bleeding disorders living in developing countries to live independent and productive lives by having vital access to medical and economic resources. 

Save One Life

Hemophilia Federation of America, Inc. (HFA) is a patient education, services and advocacy ...

Hemophilia Federation of America, Inc. (HFA) is a patient education, services and advocacy organisation serving the rare bleeding disorders community. HFA is exclusively focused on the bleeding disorders patient and caregiver community.Based in Washington, D.C., HFA works in conjunction with other national and state organisations on behalf of families living with bleeding disorders.  

Hemophilia Federation of America

The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and ...

The National Hemophilia Foundation (NHF) is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. Established in 1948, NHF has chapters throughout the USA. Its programmes and initiatives are made possible through the generosity of individuals, corporations and foundations as well as through a cooperative agreement with the Centers for Disease Control and Prevention. 

National Hemophilia Foundation

Primary Immunodeficiency UK (PID UK works with healthcare professionals and others to improve ...

Primary Immunodeficiency UK (PID UK works with healthcare professionals and others to improve the care and life of people affected by primary immunodeficiencies (PID).  The charity provides educational information, and raises awareness and understanding of PID to facilitate earlier and accurate diagnosis, better monitoring and improved care.  The charity supports patients in many ways including helping them establish their own support groups.  PID UK’s website features a growing library of patient resources, including clinical information, practical guidance on living with a PID and patient stories to help people gain a better understanding of PID. 

Primary Immunodeficiency UK (PID UK)

Octapharma’s help enabled PIPO to organise the first primary immunodeficiency symposium held ...

Octapharma’s help enabled PIPO to organise the first primary immunodeficiency (PID) symposium held in Uganda. The goal was to build connections between PIPO, doctors and the health authority in order to raise the awareness of PIDs among both the public and the medical profession.

Primary Immunodeficiencies Patient Organization 

Primary Immunodeficiencies Patient Organization (PIPO) Limited

PIO is an organisation for those with congenital immune deficiency, their families, healthcare ...

PIO is an organisation for those with congenital immune deficiency, their families, healthcare professionals and all other interested parties.

Primär Immunbrist Organisationen – PIO

FBIS is an organisation for people with haemophilia.

FBIS is an organisation for people with haemophilia, their families and all other interested parties.

Förbundet Blödarsjuka i Sverige (FBIS)

AFNP works in the field of acquired dysimmune and inflammatory peripheral neuropathies ...

AFNP works in the field of acquired dysimmune and inflammatory peripheral neuropathies. The organisation helps people with such diseases, supports their families and works to promote better knowledge of, and research into, such conditions. Octapharma worked with AFNP to help people use the FLEXIG following their immunoglobulin treatment.

AFNP

Formed in 1998 by the families of children with primary immunodeficiency disorders (PID), IRIS ...

Formed in 1998 by the families of children with primary immunodeficiency disorders (PID), IRIS has nearly 500 members. IRIS disseminates information to health professionals and the public, supports the families of patients and research for new treatments, optimises access to care and works to improve the diagnosis rates of PID. Octapharma has helped IRIS create resources to help children understand how the immune system works  and helped with the FLEXIG app which enables people to better monitor their immunoglobulin treatment.

IRIS

AFH is the French national association for people with rare bleeding disorders. Founded in ...

AFH is the French national association for people with rare bleeding disorders. Founded in 1955, AFH promotes the rights of people with haemophilia, von Willebrand disease and other genetically influenced bleeding disorders. Octapharma supports AFH in its advocacy for continuous improvement of knowledge, treatment and management of rare bleeding disorders. 

The association represents people with primary immune deficiency (PID) and their families ...

The association represents people with primary immune deficiency (PID) and their families in Brazil. It works to improve the quality of life of carriers of congenital PID by fighting for their rights and understanding their strengths and potential.

National association of PID patients

FBH represents more than 26,000 patients and their families. The organisation campaigns for ...

FBH represents more than 26,000 patients and their families. The organisation campaigns for better treatment and quality of life for all people with haemophilia, von Willebrand disease and other hereditary bleeding disorders in Brazil.

Brazilian Federation of Haemophilia 

Nützliche Links

Haematology

Immunotherapy

Critical care

Australia

Belgium

Brazil

Denmark

Date of Revision

Germany

The Bahamas

Ecuador

France

French Polynesia

French Guiana

Gabon

Gambia

Georgia

Ghana

Gibraltar

Grenada

Greece

Greenland

Guadeloupe

Guam

Guatemala

Guernsey

Guinea

Guinea-Bissau

Guyana

Haiti

Heard Island and McDonald Islands

Honduras

Hybrid

India

Indonesia

Iraq

Iran

Ireland

Iceland

Isle of Man

Israel

Italy

Jamaica

Japan

Yemen

Jersey

Jordan

Canada

Kazakhstan

Qatar

Kenya

Kyrgyzstan

Kiribati

Kuwait

Laos

Lesotho

Latvia

Lebanon

Liberia

Libya

Liechtenstein

Lithuania

Luxembourg

Madagascar

Malawi

Malaysia

Maldives

Mali

Malta

Morocco

Marshall Islands

Martinique

Mauritania

Mauritius

Mayotte

Macedonia

Mexico

Micronesia

Moldova

Monaco

Mongolia

Montenegro

Montserrat

Mozambique

Myanmar

Namibia

Nauru

Nepal

New Caledonia

New Zealand

Nicaragua

Netherlands

Niger

Nigeria

Niue

North Korea

Northern Marianas

Norfolk Island

Norway

Oman

Austria

Pakistan

Palestine

Octapharma takes an active role in our community

Octapharma sponsort und unterstützt Organisationen weltweit. Hier bieten sich weitere Informationsmöglichkeiten.

Verschiedene Organisationen bieten zahlreiche Informationen und Hilfestellungen an.

[YOUR MESSAGE]%0D%0A%0D%0A%0D%0ALocation: ${location}%0D%0A%0D%0AReport:%0D%0A${report}

Nützliche Links

Über uns

Plasma

Produkte

Karriere

Service