We hope you will become a member of the Association. The membership fee is only $25 per year. The Alberta Lymphedema Association relies upon your support to continue its work to promote awareness and education of Lymphedema within the medical community and the general public in Alberta.
On March 6, 2019, the Alberta Lymphedema Association presented a check for more than $29,000 to the Calgary Health Trust to help ensure patients who use Calgary Ambulatory Lymphedema Services (CALS) will have access to care that will improve their quality of life.
The Alberta Lymphedema Association is a charitable organization that aims to aid and support those impacted by lymphedema of all kinds.Working from a patient perspective, together we support, empower and advocate for those impacted by this disease in order to promote optimal health. We invite you to learn more about us:
Want to know more about lymphedema? Visit our resources section to learn about lymphedema and the lymphatic system, view web resources & presentations, and more.
Membership in ALA is $25/yr and includes a subscription to Pathways magazine, a Log Book to track appointments, measurements and more, and news of upcoming events.
Alberta Lymphedema Association maintains a list of medical professionals who work with patients to diagnose and treat lymphedema. See our current list of therapists.
Happy new year, everyone! We appreciate you sticking around as…
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Have you heard of “Social Prescribing”? The United Way of…
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