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The Lymphedema Association of Nova Scotia (LANS) is pleased to offer a Compression Garment Funding Pilot Program to help improve access to medically necessary compression garments for people living with lymphedema or chronic edema in Nova Scotia. The goal of this Pilot is to reduce the financial burden of the cost of compression and to collect information to support change to the current Nova Scotia Provincial Health Insurance Program (MSI)
June 6 2pm via Zoom link
Saturday July 25 9am-1pm
445 Sackville Dr
(Rain Date July 26)

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
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.