Advocate • Educate • Empower

Be the Change

Lipedema Canada Director Crystal Ellingsen at the World Lipedema Congress in Germany 2023

Lipedema Canada is the leading national organization that provides support and advocacy for those living with lipedema, their families, and healthcare professionals who support them.

We help transform the lives of people facing the condition by fostering a sense of community, increasing awareness among medical professionals, and advocating for government acknowledgment and support. 

We represent those with lipedema in a way no other organization can: because we are living with it too.

what makes us different

Dedicated to Lipedema

Our Vision
Equitable access to healthcare across Canada, ensuring every individual affected by lipedema receives the care and support they need.
Our Mission
To advance equitable healthcare for all Canadians affected by lipedema, through advocacy, education, and compassionate support.
Previous slide
Next slide

Our Values

Empowering awareness, education, and advocacy to ignite transformative change for the lipedema community nationwide.

We are Change Driven

We are passionate and perseverant in our actions to ensure that change happens for those with lipedema in Canada.

We are Comprehensive 

We have a forward thinking mindset, considering all aspects of education and support.

We are Community Minded 

We foster an inclusive, relatable, accessible community by offering a strong network of support.

Our Goals

Lipedema Canada / Lipœdème Canada has four main pillars guiding our not-for-profit organization

01

Fostering Community

Engagement:  Actively maintain in-person and online communities, including Facebook pages and support groups, to provide forums for community connection, information exchange, and peer support.

Community Feedback: Regularly engage with our community to understand and address their needs, incorporating their lived experiences and suggestions into our resources and advocacy efforts.

Events Participation: Attend conferences, wellness events, and other events to directly interact with the lipedema community and the professionals who support them.

Volunteer Opportunities: Welcome volunteers to join committees and special projects, ensuring everyone has a chance to participate in Lipedema Canada’s efforts.

02

Increasing Awareness of Lipedema

Educational Materials: Provide free brochures and educational resources available for order through our website.

Comprehensive Website: Maintain a website that is comprehensive, accessible, scholarly, and regularly updated with the latest information and resources on lipedema.

Targeted Awareness: Address topics like managing lipedema through conservative and surgical methods; and highlight limitations in access to resources, care, and funding.

Physician Engagement: Distribute resource materials to physicians across Canada to raise awareness and help them support patients with lipedema. Offer scholarly information for clinicians to enhance their knowledge.

Canadian Standard of Care: Assemble a working committee of Canadian clinicians to review current research and publish the first Canadian Standard of Care for lipedema.

Educational Curriculum: Advocate for the inclusion of lipedema education in medical, nursing, and physiotherapy programs across Canada.

03

Advocating for Government Acknowledgment and Healthcare Coverage

Awareness Month: Advocate for a national month of awareness for lipedema, with individual provinces also requesting specific days of recognition.

Diagnosis Code: Request the inclusion of a specific lipedema diagnostic code (EF02. 2 Lipedema – ICD-11) in provincial billing systems to accurately count and support those affected.

Insurance Coverage: Lobby provincial governments to provide insured benefits for compression therapy, manual lymphatic drainage, mental health services, medication support, and lipedema reduction surgery as medically necessary services.

Government Collaboration: Form working groups with provincial governments to enhance diagnosis, treatment, and access to medically necessary care.

04

Organizational Management

Professional Standards: Operate under the Canadian Not-for-Profit Act (NFP Act), ensuring the highest standards of ethics and professionalism. We are supported by legal counsel to maintain our organizational integrity.

Skill Set Recruiting: Seek dedicated and skilled individuals for our board of directors through a thorough interview process, focusing on those who can commit time and expertise to advance our mission.

Bilingual Accessibility: Ensure all resources, website content, and social media posts are available in both official languages.

Charitable Status: Register as a charitable organization with the Canada Revenue Agency to receive government and grant funding to better support the lipedema community.

Sponsorship Engagement: Collaborate with reputable companies that serve the lipedema community to develop products that meet their needs. Our sponsors are trusted partners who share our goal of improving the lives of those with lipedema.

Collaboration: Work with provincial groups, societies, associations, and advocacy groups, wherever possible, to support our shared goals of improving the lives of Canadians with lipedema.

Global Engagement: Stay informed on the latest lipedema research and engage with the international medical and research community to adopt best practices for managing and supporting lipedema.

faces of change

Board of Directors

Angel Anderson

President

Emma Cloney Vice President and founding member of Lipedema Canada.

Emma Cloney

Vice President

Emma Cloney

Vice President

Holly Hedd Director of Communications and founding member of Lipedema Canada

Holly Hedd

Director of Communications

Holly Hedd

Director of Communications

Crystal Ellingsen

Director

Michelle Finley

Secretary

be the change

Want to Join the Board?

Join us in making a real difference in the lives of people living with lipedema in Canada. We are seeking a few passionate and motivated individuals who are dedicated to advocacy and want to inspire change as part of our Board of Directors.

Supported by Professionals

Medical Advisory Board

We are currently accepting applications for professionals to join the Lipedema Canada Medical Advisory Board. This dedicated and educated team of diverse professionals will be the pioneering team behind creating a Canadian Standard of Care for Lipedema.

If you are a clinician (doctor, nurse practitioner, nurse, surgeon, physiotherapist, occupational therapist, social worker, nutritionist, certified lymphedema therapist, garment fitter) or other relevant specialist working with lipedema patients, we would like to hear from you.

If you are interested in being considered for the Medical Advisory Board, please fill out the form below and submit your CV to the Executive for consideration.

Dr. Miriam Berchuk - medical advisor to Lipedema Canada

Dr. Miriam Berchuk

Medical Advisor

Dr. Miriam Berchuk

MD, FRCPC (Anaesthesia) 

Diplomate American Board of Obesity Medicine

Kelsi Abbott

Medical Advisor

Kelsi Abbott

Physiotherapist CLT

Megan Diamond_Medical Advisor

Megan Diamond

Medical Advisor

Megan Diamond

Custom Compression Fitter

Diamond Athletics