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About the Lymphedema Association of Ontario 


Your trusted resource for lymphedema support, education, and advocacy. At LAO, we are dedicated to empowering individuals affected by lymphedema and promoting awareness within the community.


Our website serves as a gateway to a wealth of valuable resources and programs. Through our commitment to excellence, we strive to fulfill the needs of our members and the general public alike. Here's how LAO can make a difference in your journey:

  • Knowledge and Support: Access expertly curated information on lymphedema, its latest developments, and treatment options.
  • Engaging Webinars and Events: Exclusive webinars by leading experts and community events to stay informed and connected.
  • Virtual Support groups every month with varying topics lead by a speaker for advice, information and community. 
  • Pathways Magazine: Receive our inspiring magazine with practical advice, uplifting stories and local resources.
  • Connecting with Professionals: Find local therapists and clinics with our LAO Directory.


Join our vibrant community today by becoming a member of LAO. By doing so, you not only unlock a wealth of exclusive resources but also contribute to our mission of making a meaningful difference in the lives of individuals with lymphedema.


Together, let's navigate the journey of lymphedema, empower each other, and inspire hope. Donate or become a member now and be a part of the positive change.

LYMPHEDEMA AWARENESS MONTH

MARCH 2024

EVENTS:

Managing Your Lymphedema: An Online Patient Education Event

When: Tuesday, March 26, 2024 5:30 p.m. - 7:00 p.m.

Where: Zoom - Online


Join us for an online patient education event on Managing Your Lymphedema as part of our Florence Winberg Education Series. 

This event will give you information about: * Subject to change

  • Support and Resources from Lymphedema Association of Ontario
    (Dolores Steinwall, President of Lymphedema Association of Ontario)
  • Tips and Strategies to Manage Your Lymphedema
    (Ann DiMenna, Physiotherapist, Markham Lymphatic Centre)
  • A patient to share their story

Patients, caregivers and families are welcome to attend online.

REGISTER HERE

WORLD LYMPHEDEMA DAY NEWS --

The following cities have proclaimed March 6th as Lymphedema Day!

Please feel free to read the proclamation letters by clicking on each city.

Toronto Brantford Markham Peterborough

Barrie Kitchener Pickering Ottawa

Milton Waterloo Township of Scugog Clarington


Upcoming LAO Events

Upcoming events

    • 10 Apr 2024
    • 5:00 PM - 6:00 PM
    • Zoom
    Register


    Virtual Support Group 

    April 10th, 5:00 pm (EST) on ZOOM

    Please join us for our monthly virtual support group consisting of lymphedema patients and LAO volunteers. Our support groups are a great opportunity for you to share and discuss your personal lymphedema management skills, information, hopes, fears, successes and hardships, all in a safe space to facilitate support and growth. 

    Join us on the second Wednesday of every month!

    __________________


    Basic Housekeeping:

    • Please keep yourself on mute to reduce background noise
    • There is typically a Q&A period at the end, so please save your questions for then
    • Feel free to use the chat feature to ask questions or raise your hand to talk
    • Please do not take screenshots, photographs or videos. If the webinar is being recorded, it will be uploaded to the LAO website for you to access after the meeting.

    Disclaimer:
    The content of this presentation is confidential and property of the presenters. It is not intended to be distributed to any third party without their consent. As such, please do not screenshot, record, or tape the contents of this meeting or the individuals in attendance.

    The opinions expressed in the presentation are those of the presenter and not necessarily those of the LAO. Therefore, the LAO is not responsible for any content or information in the webinar. The LAO does not endorse any particular vendor product, company or personnel, and our webinars are for educational purposes only.

    Please note that if a webinar is being recorded you are providing consent to be recorded. You may keep your camera off if you wish to do so.

    Moreover, Information collected through polls or surveys may be addressed in future meetings and in meeting notes, that are available for other patients access. Through your attendance, you have consented for The Lymphedema Association of Ontario to use your first name only, for confidentiality purposes in note taking.

    • 08 May 2024
    • 5:00 PM - 6:00 PM
    • Zoom
    Register


    Virtual Support Group 

    May 8th, 5:00 pm (EST) on ZOOM

    Please join us for our monthly virtual support group consisting of lymphedema patients and LAO volunteers. Our support groups are a great opportunity for you to share and discuss your personal lymphedema management skills, information, hopes, fears, successes and hardships, all in a safe space to facilitate support and growth. 

    Join us on the second Wednesday of every month!

    __________________


    Basic Housekeeping:

    • Please keep yourself on mute to reduce background noise
    • There is typically a Q&A period at the end, so please save your questions for then
    • Feel free to use the chat feature to ask questions or raise your hand to talk
    • Please do not take screenshots, photographs or videos. If the webinar is being recorded, it will be uploaded to the LAO website for you to access after the meeting.

    Disclaimer:
    The content of this presentation is confidential and property of the presenters. It is not intended to be distributed to any third party without their consent. As such, please do not screenshot, record, or tape the contents of this meeting or the individuals in attendance.

    The opinions expressed in the presentation are those of the presenter and not necessarily those of the LAO. Therefore, the LAO is not responsible for any content or information in the webinar. The LAO does not endorse any particular vendor product, company or personnel, and our webinars are for educational purposes only.

    Please note that if a webinar is being recorded you are providing consent to be recorded. You may keep your camera off if you wish to do so.

    Moreover, Information collected through polls or surveys may be addressed in future meetings and in meeting notes, that are available for other patients access. Through your attendance, you have consented for The Lymphedema Association of Ontario to use your first name only, for confidentiality purposes in note taking.


To keep up to date with community Lymphedema news, events from other organizations, and resources, please click here for our page "Other Lymphedema News"






Our Generous Sponsors:











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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