00  BC Lymphedema Association

OUR HISTORY


The inaugural meeting of the 'soon-to-be' BC Lymphedema Association was held on March 21, 2006 in a Vancouver restaurant.  Catherine DiCecca, a Registered Massage Therapist with a practice in Vancouver, had brought together three of her patients to meet - Rayma Hagan, Lynn Holloway, and Deanna Trewin.  She had already spoken to them individually about their various issues they were dealing with and thought that by forming some sort of group, perhaps more could be done to help each other.


Everyone had woes to tell of compression garment issues - poor fit and long wait times between ordering and receiving.  They all wanted to be able to learn more by trading information about limb care (what's worked and what hasn't) and to educate the public, medical community, and insurers about the issues lymphedema sufferers have to deal with.  Catherine advised what other provinces and organizations were doing and suggested we could learn from them given they were already established.  They left that evening feeling empowered and excited that perhaps together they could create positive change to meet their needs!  


They continued to meet and gather information about how to become a registered BC Society and get their charity status.  Along the way, more people joined in their quest and began to build the association we have today.  We are indebted to the Alberta Lymphedema Association for the many phone calls and emails helping us step-by-step.


In the Fall of '07, we had done an extended planning session and come up with our Mission Statement, Goals, and Objectives with the help of a professional business coach.   Another friend developed the logo for us, and many of the board members loaned money to the Association to begin the work.


We had also started to communicate on a national level with other Canadian lymphedema associations.  (Currently, we have monthly conference calls to share information and learn how we can have a stronger voice together to make an impact.)


After much organizing, we finally were ready to 'launch' and had our 'coming out party' at the North Vancouver Lymphedema Awareness & Networking Day on June 20th at the Delbrook Recreation Centre.  


We look forward to our growth and ability to advocate for and support the many people in BC now and in the future that are living with this condition.  We trust that there are many other people living in BC that will want to get behind our work and join us through membership, volunteering, and donating.  Until there is a cure, we will continue to promote living healthy and hopeful lives with lymphedema!

BC LYMPHEDEMA ASSOCIATION (BCLA)

1-866-991-BCLA (2252)  |  info@bclymph.org


MAIL:  PO Box 34527, Pemberton Plaza PO, North Vancouver, BC  V7P1T0

Disclaimer: 


This site is for information and community support and is not be used as a substitute for professional medical care. Seek the advice of your physician with any question about a health problem or medical condition. 


This site also includes links to websites providing information about lymphedema.  BCLA is not responsible for the content of those sites.


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