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LAO Board of Directors


Dolores Steinwall • Pickering

President


Dolores had a long and successful career with Bell Canada and was a Senior Project Manager, PMP at the time of her retirement. In August 2014 she was diagnosed with stage 3 cancer in her breast and lymph nodes. Although she is now cancer-free, she has lymphedema in her right arm and side. She is very passionate about helping others with this condition. Since 2015 she has been a volunteer on the Sunnybrook Patient Family Advisory Council, and in 2016 she began to volunteer at Wellspring. While doing this work, she has raised awareness and advocated on behalf of patients.

Dolores joined the LAO as a Director in April 2019, and was appointed president in August 2019. 


1st 3-year term as of April 20, 2019






Rob Caparelli • Toronto

Treasurer


Rob Caparelli currently works with one of Canada's largest private mortgage services companies (CMLS Financial) as an Assistant Vice President focusing on commercial mortgage lending. His firsthand experience in dealing with this terrible disease (his father had severe secondary lymphedema in both legs and his abdomen) has motivated him to do anything he can to help spread awareness and more importantly, to help find a cure for it. He believes his current position at CMLS, and degree in Economics, while also playing Junior A/NCAA hockey, has provided him the opportunity to learn how to effectively & efficiently use his time and more importantly how to allocate resources in order to see that they are utilized to their fullest potential in ultimately finding a cure for this disease.



1st 3-year term as of April 20, 2019






Ana Stosic • Oakville

Director - Events Committee


Ana is currently working on completing her Master in Science, specifically in the field of cancer genetics, at Sick Kids Hospital with the Faculty of Medical Science at the University of Toronto. Her exposure to various medical conditions for which there is a lack of awareness and recognition drove her to join the LAO in hopes of bringing change in the field of lymphedema. Her background in research, science, and medicine, as well as her skills attained in numerous volunteer positions, will cater and assist the work of the LAO, bringing awareness to the condition through fundraising and events.


1st 3-year term as of June 19, 2018














Tony Wight • Toronto

 Secretary, Director - Awareness Committee


Retired after a lengthy career with an IT multinational, and having acted as the principal caregiver for a close family member suffering from secondary arm lymphedema, Tony wants to help the LAO achieve its important goals of early lymphedema awareness and treatment services guidance. Based on his proximity to the relative suffering from this debilitating condition, he recognizes there is an urgent need in Ontario for further patient, caregiver and health care provider education as to what to watch for, where to seek immediate help and the availability of required financial assistance. He believes that his service as Charter President of a Rotary Club and his many years of service in that organization will also help prepare him to assist the LAO in its critical work.


1st 3-year term as of June 19, 2018









Jaclyn Jones • Burlington

Director 


Jaclyn is the Co-Owner & President of a Marketing & Advertising agency and has over twenty years’ experience in developing strategic plans, conducting market research, community engagement initiatives, as well as collateral material development for print, broadcast and online applications for not-for-profit, services-based and manufacturing clients.  Jaclyn lives with secondary lymphedema (arm) as a result of axillary lymph node dissection and cancer treatment.  She joined the LAO to help improve access and delivery of resources, education and continued support to the existing community who lives with or may be at risk of developing lymphedema. 


1st 3-year term as of September 11, 2018



   



Charlotte Schultz • Markham

Director - Advocacy Committee


Charlotte is a retired RN and a three time cancer survivor. Living with lymphedema since 2010, she is concerned and upset about the lack of medical care and research funding for post-cancer treatment and in particular issues related to lymphedema. In her experience she feels that most MD's are not knowledgeable about lymphedema diagnosis and treatment. She looks forward to supporting the LAO to act as both a resource for lymphedema sufferers and as an advocacy group to raise awareness of lymphedema among the public, medical and political communities.


Returned to complete 1st 3-year term August 2019







Board of Director Opportunities

Are you interested in serving as Volunteer Board Member of the Lymphedema Association of Ontario (LAO)?  The Board of Directors acts in a position of trust for the lymphedema community and is responsible for the effective governance of the organization. The Board guides the development of services and programs in response to community need and sets the tone of responsible stewardship to ensure policies, procedures and performance are upheld. 

We are actively in searching for new Directors to help govern our Association as we begin a period of transformation. 

We are particularly interested in receiving applications from those living with primary lymphedema.  As well as from individuals living in Northern Ontario, London/Sarnia and the Ottawa region.  Our hope is to work alongside individuals that have a strong desire to help promote the awareness and education of lymphedema for residents of Ontario

The details:

  1. The Board of Directors for the LAO is comprised of a minimum of 3 and a maximum of 10 Directors. Directors serve as volunteers with remuneration for expenses related to long distance telephone calls or travel for required board meetings.  Applications are being accepted from interested members of the lymphedema community to fill vacancies as they arise.

  2. All Board Members must be members in good standing of the Lymphedema Association of Ontario.

  3. Directorship is available to those living with primary or secondary lymphedema, family members and their caregivers.

  4. Health professionals who are NOT in private practise are also eligible and very welcome. As an alternative, if you can give us some of your time, we are forming an Advisory Board.

  5. Regular meetings of the Board are held six to eight times per year, via teleconference. In addition, there is an annual full day planning meeting usually planned in the Spring (at the beginning of our fiscal year). We may also require in person meetings as required.

  6. Each Director is expected to participate in at least one other committee of the Board (e.g. Advocacy, Awareness, Events & Communications, Finance, Governance (Secretary) ) and is also required to attend the National Conference organized by the CLF when held in Ontario. The annual conference, to answer questions to interested people about our membership, programs and services.

  7. A Board term is three years, renewable for one consecutive term.

  8. Previous Board experience is not a requirement but would be beneficial.

  9. Time commitment is approximately 10 hours a month, varying on activity.

Please contact us at info@lymphontario.ca to request more information or to receive a Board of Directors application.  The successful candidate will gain valuable board experience and an opportunity to build their network, competencies and skills in a not-for-profit organization.







Lymphedema Association of Ontario
Mailing Address: 262-2869 Bloor St. W., Toronto, ON M8X 1B3 Canada
1-877-723-0033 | 416-410-2250 | info@lymphontario.ca

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