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OUR MISSION
 
The BC Lymphedema Association promotes
 healthy and hopeful living with lymphedema.

2010 BOARD OF DIRECTORS




CATHERINE DICECCA - President

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Catherine DiCecca is a Registered Massage Therapist (RMT) with over 13 years in this field.  She trained at the West Coast College of Massage Therapy in Vancouver.  In 1994, she trained with the Dr. Vodder School for Manual Lymph Drainage and Combined Decongestive Therapy and has been using this technique for people with lymphedema.  Catherine is also an instructor for the basic level of the Manual Lymph Drainage for health care professionals.


She has served as an investigator and the Chair of the Inquiry Committee for the College of Massage Therapists in BC.  She was on the board of the non-profit Society NAVALT® (North American Association of Lymphatic Therapists) and was their newsletter editor for a number of years.


In treating people who have lymphedema and knowing the lack of information that is available to them, Catherine’s interest in seeing this association created has been foremost.  When the opportunity arose, she eagerly participated and made herself available in whatever way that she was needed.



LUCETTE WESLEY – Vice-President

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Lucette has over 30 years experience working in the field of group insurance, including 15 years of senior leadership positions with several major Canadian insurance companies.  She has volunteered her time as an executive of the South Burnaby Garden Club for many years and is an avid gardener.  She has now joined the board of the BC Lymphedema Association as Vice-President and Privacy Officer.  She has friends who are cancer survivors and lymphedema patients.  She advocates a healthy lifestyle and a positive attitude as the best tools for those living a full life with lymphedema.



PATRICIA MONTAGANO - Secretary

Patricia is a Registered Nurse (RN, BSN) with over 15 years of experience in this field. She graduated with honours from the University of British Columbia, School of Nursing in Vancouver.  She is a certified expert garment fitter for all types of compression garments and is trained by the Boston School of Advanced Compression.  Her passion is helping those with breast cancer or lymphedema navigate through the health care system.  In meeting and treating people with lymphedema and breast cancer, she is well aware of the lack of information about lymphedema.


Patricia developed and implemented various types of patient centered teaching clinics, ranging from diabetes, wound care, lymphedema treatment, and compression therapy.


Recently Patricia and her husband of 15 years celebrated the birth of their third child.  She currently works with her husband at BC MedEquip Home Health Care, where she can focus on providing her expertise and experience to the public.  Patricia looks forward to helping the BCLA achieve their goals.



LYNN (WARNOCK) HOLLOWAY – Treasurer


Lynn is a founding member of the BCLA and was the secretary for over 3 years. She has recently returned to the Board in the capacity of Treasurer, as well as maintaining the positions of Newsletter Editor and Membership Coordinator. Since the onset of lymphedema in her left leg as a result of cancer treatment in 2003, she has been committed to the creation of this organization as a vehicle to advance awareness and services for this disorder.


In her professional life, Lynn was a bookkeeper/office manager in a variety of settings for over 25 years. She currently resides in Parksville on Vancouver Island with her husband, Michael.  He is great moral support and is instrumental in assisting her control her lymphedema by wrapping her leg and helping her don her compression garment daily.



MICHAEL DEL BALSO - Director

Michael has a business and marketing background with an MBA and B.Comm.  He has worked in both the public sector and private sector and has developed award-winning best practices.  Michael has been involved in the community for many years coaching championship sports teams.  Over the years, he has gained valuable experience in fundraising and organizing events, having been actively involved with United Way campaigns. Michael's goals are to create awareness about lymphedema, educate those with the condition that treatment options are available, and motivate them to get expert medical advice regarding their condition.  Michael offers his knowledge and experience to the Board of the BC Lymphedema Association so that those with lymphedema can lead healthy and hopeful lives.



FATIMA INGLIS – Director

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Fatima is a Physiotherapist working at Holy Family Hospital in Outpatient Services.  She specializes in treating musculo-skeletal conditions, which includes lymphedema.  She became interested in the current treatment of lymphedema in 2002 following information she received at a course she attended in Seattle, WA.



CHRISTINE PEARSON - Director

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Christine joined the Board Sep/09.  She brings with her a wealth of knowledge as a wound clinician with the Vancouver Coastal Health Authority (VCHA), where she sees a number of patients with lymphedema.  She is aware of the lack of knowledge in the medical community about lymphedema and is interested in making changes through education in that arena.  She also recognizes that obtaining appropriate treatment for lymphedema can be very costly and out of reach for some.  Christine looks forward to lymphedema treatment becoming more accessible and covered by BC Medical.


She currently serves on the Board of Directors of the Canadian Association of Wound Care, a national association based in Toronto, as well as on other local and regional health committees through her job with VCHA.



LENE TONNISEN - Director

As a Registered Massage Therapist since 1997, Lene started her training in the Dr. Vodder Method of Manual Lymph Drainage & Combined Decongestive Therapy (MLD/CDT) in 1996 and was certified in 1998. She has been using it to treat various injuries and conditions, including lymphedema, since then. She joined the BCLA and became a board member in the spring of 2010.


She has worked and/or volunteered in a variety of settings, including sport massage at 2 different international events; massage therapy at the World Burn Congress in 2007;  doing combination treatments with a Psychologist; worked at a disability rehab centre in Burkina Faso, Africa; presentations given to wound care clinicians/nurses about  lymphedema & wound care management using MLD/CDT; has become a certified fitter for JoViPak night-time compression garments; and trained some ladies in Cambodia in how to do Massage.


Lene desires to see the treatment of lymphedema progress & become more standardized so that many more people can benefit from it. A big part of this is to make people aware that there ARE treatment options and she hopes that the BCLA will be a key resource towards that end!



LEONA TOWERS – Director

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Leona Towers joined the board in May/09.  As a retired teacher, she brings with her organizational and writing skills that she will use to help advocate for lymphedema awareness, education, and research.  Leona developed secondary lymphedema in both legs many years after surgery and radiation treatment for cancer.  She is a retired teacher who enjoys physical activity, travelling, gardening, and learning.



DR ELLIOTT WEISS - Director

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Elliott has been a Medical Advisor to the BCLA since its inception.  He is a Medical Specialist with a title of Division Head, Physical Medicine and Rehabilitation (PMR).  In his work at UBC, he is involved in teaching medical students and residents, and is also a Clinical Instructor.  He acts as a Medical Consultant for one of Canada’s largest disability insurers.  His clinical practice includes all subspecialties of PMR.  He became interested in primary and secondary lymphedema many years ago and his clinical practice involves the diagnosis and management of lymphedematous conditions, both from a medical and a disability perspective.


 
 

BC LYMPHEDEMA ASSOCIATION (BCLA)

#215 - 5589 Byrne Rd, Burnaby, BC  V5J 3J1

1-866-991-BCLA (2252)

info@bclymph.org

Disclaimer: This site is for information and community support only, and should not be used as a substitute for professional medical care. Always 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, but the BCLA cannot be responsible for the content of those sites.