It is with deep regret that we have had to make the decision to postpone our Open Day due to...
15 hours ago
RT @TheLymphieLife: Christine Chandler is president of BC Lymphedema Association, one chapter of a natn'l volunteer-run group. Her experien…
15 hours ago
RT @mediUKLtd: And finally, here's Nina! Nina heads up the 8-strong Clinical Team at medi. Between video calls, Nina likes to do a bit of d…
16 hours ago
RT @mayordcsdc: This week is Lymphoedema Awareness Week & the Guildhall, Strand Road Council offices, & Alley Theatre will be lit up blue e…
Welcome to Lymphoedema Ireland
This website provides information, news and other resources for Irish people with lymphoedema and also to family members, medical professionals and others who wish to know more about the condition.
World Lymphoedema Day: March 6th
The 6th is World Lymphoedema Day. You can help raise awareness by: sharing the video printing out the fact sheet...
Tina from Dublin
I have Lymphoedema in my torso which I have since breast cancer surgery and now have been diagnosed with it...
Norma from Cork
My name is Norma. I am 57 years old and I live in Dunmanway West Cork. My Lymphoedema story started...
Sharon from Mayo
My name is Sharon. My Lymphoedema is Secondary post cancer, it is Breast Cancer’s ugly reminder each and every day. ...
Andrea from Donegal
Hi my name is Andrea. I live in Dunkineely, Co. Donegal. I have Primary and Secondary Lymphoedema. When I found...
Dorothée from France
I am French and came to Ireland in 2008. Since then I lived in Dublin. I got primary lymphoedema on...
Tracey
My name is Tracey. I am 43 years old. I developed Secondary Lymphoedema following a hysterectomy in 2001 for the...