LYMPHEDEMA CONFERENCE / THE UNIVERSITY CLINICAL HOSPITAL OF SANTIAGO DE COMPOSTELA – GALICIA - (SPAIN) / THE LYMPHEDEMA, LIPEDEMA AND CHRONIC VENOUS INSUFFICIENCY ASSOCIATION OF GALICIA

Continuing with the Cycle of Conferences on Lymphedema/Lymphoedema, which are being organized in different hospitals of the Galician Autonomous Region, and focused on spreading information on the disease both to health professionals and the general public, the Galician Association of Lymphedema, Lipedema and Chronic Venous Insufficiency (AGL) has organized a new event that will take place on Friday, November 30, 2018, at 6.30 pm, in the ASSEMBLY HALL Nº1 of THE UNIVERSITY CLINICAL HOSPITAL OF SANTIAGO DE COMPOSTELA.

SPEAKERS:

Bibiana Villamayor Blanco (Physical Medicine & Rehabilitation Specialist)

Carlos Manero García (Lymphedema Physiotherapist)

Nerea Camellas Melero (Plastic Surgery Specialist)

Manuela López de Vicuña (Lymphedema Garment Technician)

CHAIRPERSON:

Juan Manuel Lameiro (Presidente of AGL)

OBJECTIVES OF THE CONFERENCE:

Bringing updated information about this disease to health professionals.

Facilitating a meeting place between professionals, those affected by lymphedema, and the general public interested in this disease.

Seeking starting points to try improving health care for this illness.

DIRECTED TO:

Health professionals

People affected and their family

General public

Associations

AGL OBJECTIVES:

The Galician Association of Lymphedema, Lipedema and Chronic Venous Insufficiency (AGL) , intends to direct its actions towards social awareness, including offering individual patient advice and promoting specialized training.

Because the disease is poorly understood, despite the large numbers of existing cases, most diagnoses are late or delayed.

We would like to raise awareness towards the medical professionals, to promote research and improved treatments; and provide a minimum knowledge to those affected and their family, so they can collaborate in the maintenance of the improvements obtained, through professional health treatment.

FOR MORE INFORMATION:

Email: aflinfedema@yahoo.es

Phone: 986 505 443 / 630 024 428

Articles which may also interest you: 
(Click on the texts)

• WHY IS ELEPHANTIASIS A FORGOTTEN AND NEGLECTED DISEASE

• IS THERE DISTRESS ASSOCIATED TO UNDER-TREATMENT OF LYMPHEDEMA - PSYCHOLOGICAL CONSEQUENCES OF LYMPHEDEMA

• WHY IS THE WORLD NOT TREATING A TREATABLE DISEASE LIKE LYMPHEDEMA. TURNING A BLIND EYE TO ELEPHANTIASIS

• WHAT IS THE BEST TREATMENT FOR LYMPHEDEMA

• IS LYMPHEDEMA DISABLING - INABILITY TO WORK AND DISABILITY RECOGNITION 

• INTERNATIONAL AWARENESS CAMPAIGN TO PROMOTE CORRECT TREATMENT FOR LYMPHEDEMA

• ELEPHANTIASIS IS NOT ONLY LYMPHATIC FILARIASIS 

• CAMPAIGN TO PREVENT CHILD ELEPHANTIASIS DUE TO PRIMARY AND SECONDRY LYMPHEDEMA 

• BEWARE WITH NEW TERMINOLOGY DISCRIBING LYMPHEDEMA TREATMENT

• WHAT KIND OF DOCTOR TREATS LYMPHEDEMA/LYMPHOEDEMA - WHAT TYPE OF DOCTOR IS SPECIALIZED IN LYMPHATIC DYSFUNCTION - WHICH MEDICAL SPECIALITIES ARE RELATED TO LYMPHEDEMA

• FAST TRACK SOCIAL SECURITY DISABILITY RECOGNITION FOR CHILDREN WITH LYMPHEDEMA

• INTERMITTENT PNEUMATIC COMPRESSION (IPC) PUMP DEVICES. SERIOUS SIDE EFFECTS POR LYMPHEDEMA

• BEST PRACTICE PROTOCOL GUIDE FOR LYMPHOEDEMA (in Galician)

• A LYMPHEDEMA STORY - DOCTOR KENNETH GERSHENGORN AND THE MAUREEN DIGAN CLINICAL CASE

• WHY IS A BUTTERFLY THE SYMBOL FOR LYMPHEDEMA

• LYMPHEDEMA - INTERNATIONAL DISEASE CODING AND CLASSIFICATION

• WHAT DOES INTERMITTENT PNEUMATIC COMPRESSION PUMP THERAPY (IPC) DO, AND DOES NOT DO FOR LYMPHEDEMA. 

• WHAT IS PHLEBOLYMPHEDEMA.

• SPANISH LYMPHEDEMA ASSOCIATIONS – UPDATED LIST – PATIENT LYMPHEDEMA ASSOCIATIONS OF SPAIN – SPANISH NATIONAL FEDERATION OF LYMPHEDEMA ASSOCIATIONS

CLICK ON THE TEXTS 
TO SEE  LYHMPHEDEMA INCIDENCE 
AND PREVALENCE

CAMPAIGN 

For global awareness it is being asked that the 

WHO - WORLD HEALTH ORGANIZATION, 

name: 

"LYMPHEDEMA - AWARENESS & CURES"

as the World Health Day campaign 

  

  KATHY BATES

LYMPHEDEMA EMBASSADOR

SIGN THE PETITION HERE