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Lymphœdema in India

Posted on 2025-03-18 by cricpadmin
Posted in Activities, Filariasis | Leave a comment |

Lymphœdema in Uganda

Posted on 2024-04-10 by cricpadmin

At the Makerere University Environmental Health Students’ Association 19th Scientific Conference in April 2024 Dr Arthur Bagonza presented qualitative results from a study funded by the ILF into the burden and prevalence of lymphatic filariasis in Uganda.

Posted in Activities, Filariasis | Leave a comment |

Demographic data

Posted on 2024-02-08 by cricpadmin

The availability of demographic data is an important factor when considering the allocation of limited resources to meet an urgent or critical need in a society. The lack of such data can lead to a waste of resources in an area where there is a low prevalence of the condition being addressed. An understanding of how the condition is already being addressed in different areas is also important, for where the response is already good, then resources may be better directed elsewhere.

We therefore need tools to measure both the prevalence of the condition and the quality of the response to that condition in the community.

One such tool was used in the Autumn of 2023 in two areas in Uganda. Being community focussed and taking into account cultural sensitivity the approach was through the elders of the communities to obtain their support and then through the heads of the households. Only with their consent could we approach individuals within the community. Given the burden of the condition upon the community the response was for the most part positive and the team was given access to the best part of the communities.

The Demographic data and screening questionnaire collected data enabling the team to asses the extent of the problem, the communities’ response and provide indicators for the way forward in the allocation of resources to assist the communities and the sufferers in the treatment of the condition.

Posted in Research | Leave a comment |

The second question is

Posted on 2024-02-01 by cricpadmin

Did you read about South Africa, Switzerland, the Netherlands or India today? You can find more information about all the ILF national frameworks and learn more about the ILF here

So today’s question is:

What is the main cause of lymphœdema worldwide?

Answers please in the comments box below. If you wish to remain anonymous please say so otherwise we shall publish, subject to editorial discretion, what you have to say.

Posted in Questions | Leave a comment |

The first question is

Posted on 2024-02-01 by cricpadmin

What do we do and why?

All the national lymphœdema frameworks work hard in researching, accessing, educating, and above all hearing and treating patients – the patients are why we do what we do.

The next two questions are for you today:

What is the biggest challenge for you with lymphœdema?
What is your greatest wish long-term for living with lymphœdema?

Answers please in the comments box below. If you wish to remain anonymous please say so otherwise we shall publish, subject to editorial discretion, what you have to say.

Posted in Questions | Leave a comment |

IAD dispelling myths

Posted on 2024-01-02 by cricpadmin

Please have a look at the link regarding NTD day work:


NTD day work.

Thank you

Posted in Filariasis | Leave a comment |

IAD Integrative Medicine Treatment

Posted on 2023-12-29 by cricpadmin


Integrative medicine treatment

Posted in Filariasis | Leave a comment |

Camp 2024

Posted on 2023-12-16 by cricpadmin

Our sister website lymph4kids and lymph4parents are pleased to announce an international camp for children and young people to be held at a venue in France, 3rd-7th July 2024.

Further details to follow… watch this space!

The video above is from a previous camp held in Italy

Posted in Activities | Leave a comment |

IAD salutes its Mentor

Posted on 2023-10-31 by cricpadmin

Prof Ryan, Oxford UK:


Terence Ryan

Posted in Activities, Research | Leave a comment |

Good morning!

Posted on 2022-05-24 by admin

Welcome to Lymph4U!

This site is for those who suffer from lymphœdema in low resource settings. We are here to serve each other, let us do so as each one struggles in a different way with the complexities of this condition which we call lymphœdema.

The administrators hope that your visit to today will help you, as you consider our ideas, leave your own and participate in what we are trying to do.

Please contribute, please comment, please add material.

Comments are moderated before being published, so please also be patient with our administrators!

Posted in Uncategorized | 1 Comment |
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