Lymphedema Association Of Nova Scotia
Lymphedema Association Of Nova Scotia
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Lymphedema Association Of Nova Scotia (LANS)

Lymphedema Association Of Nova Scotia (LANS)Lymphedema Association Of Nova Scotia (LANS)Lymphedema Association Of Nova Scotia (LANS)

lymphedemanovascotia@yahoo.com

(902) 401-3683

We are a not for profit organization that focuses on promoting Lymphedema Education and Awareness and offering support to people with Lymphedema in Nova Scotia, New Brunswick and Prince Edward Island.

LANS 2026 Compression Garment Pilot Program

Round 2 applications are now open. The application deadline for Round 2 will be December 1, 2026. Pilot Program Round 2


 Thank you for your interest in the program and for helping support improved access to compression garments in Nova Scotia.

Upcoming Events

LANS Lymphedema Education and Resource Day

September 19 


Free registration for In Person Attendance 

Zoom Registration Link available soon

ABOUT US

Did You Know?

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Did You Know?

Lymphedema is 

- a chronic health condition with many faces

-  it can be congenital and present itself at different times

- it can be because of Cancer treatment or other surgeries

- it can show up for many reasons more
- it is estimated that over 1,000,000 children and adults live with lymphedema 

- up to one in four Breast Cancer survivors will develop lymphedema at some point in their lifetime

- more people live with lymphedema in their legs than arms


 

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Who We Are

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Become a Member

Become a Member

Become a Member

Become a member of the Lymphedema Association of Nova Scotia  (LANS).

It’s one of the most important ways to keep supporting the LANS. Membership fees help to fund our activities – members help us to spread the word and raise awareness about lymphedema.


To become a member or to find out more about our Individual, Professional, or Corporate Memberships, please contact us.

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