Lymphedema and Lipedema Networks in Europe

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North Europe

The edema forum (as well as the lymphnetzwerk site) is now multilingual. All users from abroad can then have all texts translated into their respective languages. You can choose the desired language on the upper right-hand corner of the site.  EdemaForum   doctors lymph network  Edema Clinics  Lipedema Clinics           more (edema) clinics in europe and worldwide 


Sweden  SÖF is the National support Organization for patients and advocates for Lymphoedema, lipoedema, Dercum´s Disease and venous oedema which develop inte Lymphoedema. SÖF takes the lead role in educating and supporting patients by providing a high standard of information and promoting self-care. SÖF was established 1999 and has evolved into an independent and influential Organization. We collaborate with academics, clinicians, researchers, educators and other national organizations to improve the conditions för patients.. www.svenskaodemforbundet.se/   Styrelsen   

www.facebook.com/Svenska Ödemförbundet   www.youtube.com/Svenska  Ödemförbundet 


Denmark  DALYFO blev etableret i foråret 1992 af lymfødempatiener på Skodsborg Kurcenter. Baggunden var den enkle, at lymfødempatienter ikke kunne få behandling i det offentlige sygehusvæsen. Det eneste sted, man kunne få behandling, var på Skodsborg Kurcenter, hvor de havde en uddannet fysioterapeut med speciale i lymfedrænage. Et fåtal fik kaution fra deres amt og dermed betalt behandlingen, mens alle andre selv måtte betale for behandlingen.http://www.dalyfo.dk/  | bestyrelse


Norway " Norsk Lymfødemforening ble stiftet 28. oktober 1986 som en landsomfattende interesseorganisasjon.I april 2017 ble det vedtatt å inkludere lipødem og skifte navn til Norsk lymfødem- og lipødemforbund (NLLF). NLLF har som målsetting å utøve rådgivende, opplysende og hjelpende virksomhet overfor alle med lymfødem, lipødem og deres familier. Foreningen arbeider for at personer med lymfødem/liødem skal få best mulig livskvalitet. Foreningen ønsker å spre kunnskap om begge lidelser og konsekvensene av dette til politikere, helsemyndigheter og i samfunnet generelt, for derved å bidra til best mulig behandling og økt satsing på http://www.nllf.no/  sentralstyret                                                                    


England  The Lymphoedema Support Network is a registered charity and the UK's national patient support organisation for lymphoedema. The Lymphoedema Support Network (LSN) takes the lead role in educating and supporting other patients with this condition by providing a high standard of information and promoting self-help. Since its inception in 1991, when there was very little information or help available for patients, the LSN has evolved into an independent and influential charity. It is the only national patient-led organisation offering information and support to people with this condition and has a unique understanding of the patients' experience   www.lymphoedema.org   Team |  www.mlduk.org.uk/ |  www.lympho.org  Team

The International Lymphoedema Framework (ILF) unites national frameworks around the world and works together to raise awareness of lymphedema through research and knowledge. Only a collaborative and multidisciplinary partnership between all lymphedema communities and the recognized expert groups can improve the treatment of lymphedema. https://www.lympho.org 


England, Wales, Northern Ireland and Scotland  Talk Lipoedema was founded by three women, Isobel MacEwan, Cara Jones and Joanne Bird. All three women have Lipoedema and are dedicated to making Talk Lipoedema the  leading patient    organisation in the UK for Lipoedema . They all come with a wealth of knowledge and experience in running support groups in the Lipoedema community.  Talk Lipoedema is a UK-based charitable organisation that is active across the UK. It provides support to people with lipoedema, their families and carers. Talk Lipoedema initiates and participates in various projects to increase awareness of the disease, and improve research evidence.www.talklipoedema.org/new-paTeam  


Irland   Lymphoedema Ireland (formerly Irish   Lymphoedema Support Network) was founded in 1995. Our volunteer network offers support, help and information to anyone in Ireland affected with lymphoedema. Membership is open to anyone who suffers from lymphoedema, their family and friends and those with an interest in furthering the aims of the network. All members will be circulated regarding the activities of the group.    Lymphoedema Ireland  Team

We welcome you to the website of Manual Lymph Drainage Ireland (MLD Ireland Ltd). MLD Ireland Limited is the professional Organisation of Health Care Practitioners who have obtained additional and specialised training to provide treatment in the management of lymphoedema and other lymph-related disorders. This website is designed to inform and raise awareness of the effectiveness of Manual Lymph Drainage (MLD) and Combined Decongestive Therapy (CDT). MLD Ireland   Massage Clinic Caherdaniel   Facebook