TreatmentWho Are We?
The Lymphedema Association of Saskatchewan Inc. (LAS) is a non- profit organization founded in 2004 by a group of people who recognized the need to help those who have or are at risk of developing lymphedema and related lymphatic disorders. We strive to be a learning association, committed to ongoing education. LAS works to empower affected individuals and their families to successfully manage these conditions.
LAS Goals
- Educate and inform the public regarding the causes and management of lymphedema and other lymphovenous disorders.
- Educate and inform Saskatchewan Health of the needs and costs involved in managing these conditions.
- Empower affected individuals and their families to successfully manage these conditions.
- Support and encourage the advancement of lymphovenous research.
- Raise funds to achieve the goals of LAS .
- Assist individuals looking for information support on lymphedema and other lymphovenous disorders.
LYMPHEDEMA SUPPORT GROUP ~PRIVATE FOR PATIENTS~
This group is through Facebook, meet people from all around the world with lymphedema! Share your story, read others stories, get and give advice, learn tips and connect with others who are struggling with lymphedema. Extremely supportive and loving group!!!
If you are interested in joining this group please add Angela Connell-Furi to your friends list on Facebook and leave a message that you want to be added to the group! Please note that this group is private for lymphedema patients and their caregivers and can not be seen by others who are not in the group. Hope to see you in the group soon!
New Facebook Group
We now have a Facebook group for the Association and all members and potential members are welcome.
Association events will be posted on there. Join and meet other members, ask questions, etc.
You must ask to join. Go to Facebook