A community of people with lived experience
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LAA eNewsletter – September 2023 |
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YOU HEARD IT HERE! |
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Dear Members and Friends, Welcome to the latest edition of our e-Newsletter. There are some key dates coming up, so be sure to save them in your calendars!
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REGISTRATION IS NOW OPEN - INFORMATION DAY 4 NOVEMBER |
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The LAA is in the process of organising its next Information Day! Hold onto your hats QLD, we’re coming your way. When: Saturday 4 November 2023 Where: Brisbane North – Kedron-Wavell Club Speakers: Prof Sandi Hayes, Dr Amanda Pigott, Dr Jen Sanderson….and more! Pop it in your diary. Can’t be there in person? Not to worry, this is a hybrid event. You can watch from anywhere in Australia!
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LYMPHOEDEMA STAKEHOLDER WORKSHOP - ADELAIDE |
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The LAA was delighted to participate in the recent Lymphoedema Stakeholder Workshop on the 5th of July, run by Flinders University. The goal was to discuss key priorities for improving lymphoedema care in Australia. They were interested in learning about the barriers to care delivery and how they could support people at risk of, or living with lymphoedema. A particular focus was also placed on improving care for those who may have difficulties accessing health services because of rural or remote residence or other access barriers. We were fortunate enough to have 2 of our board members attend and represent the LAA voice. Thank you, Kellie Thomas and Lyn Balfour, for your involvement in the project at both a South Australian and National level.
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ANNUAL GENERAL MEETING - SAVE THE DATE |
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The LAA board would like to announce the date of the Annual General Meeting. When: Thursday 26 October 2023 Time: 7.00pm AEDT Venue: via Zoom with a guest speaker to follow As always, the LAA invites nominations to the board, or volunteers for subcommittees. Please reach out and initiate a conversation if you are interested in a role. We would be happy to schedule a time to discuss in more detail and answer any questions that you might have about board opportunities, or volunteering in general.
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NODE NEWSLETTER COMING SOON |
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The Newsletter Subcommittee is currently working on the Spring edition of Node News. Read articles like Jenny Gilbert’s Lymphoedema Management Part 2, the AIHW Report and Tips and Tricks. We are always looking for ways to involve our members and stakeholders in Node News. Perhaps you might like to share your story or tell us about your local support group? click here
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RITCHIES IGA CARD PROGRAM |
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Do you or your family and friends shop at a Ritchies IGA? We have joined their Community Benefit Program. Nominate the LAA as your chosen charity and start shopping! Step 1: Download or update the Ritchies Card App. Download Ritchies flyer here Step 2: Search and select the Lymphoedema Association Australia when prompted to nominate a club, school or charity. Step 3: Every time you shop at any Ritchies IGA, scan your app or card, and Ritchies will contribute 0.5% of your total spend to us. All you Ritchies IGA customers…..let’s go shopping!
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LAA ONLINE SHOP |
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SUPPORT LYMPHOEDEMA ASSOCIATION AUSTRALIA |
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The LAA relies on the generosity and support of our community to continue our work. While there are numerous worthy causes to consider, lymphoedema often remains less recognised compared to other conditions, We invite you to make a tax-deductible donation to support our efforts in advocating for the lymphoedema community. Every contribution helps us make a difference. To donate, please click here
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UPCOMING SUPPORT GROUP MEETINGS |
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Here are a few upcoming support group meetings. These can be found on our website under events. The LAA is currently working on some guidleines and resources to help emerging support groups. We are keen to see new groups form, especially in states where there aren't any yet! Stay tuned for more information.
To find out more about the Support Group Meetings Click here
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RENEW YOUR MEMBERSHIP FOR 2023-2024 |
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We'd love for you to renew your membership with LAA! We wanted to remind you that your membership with us is up for renewal. Your continued support as a member is vital to our organisation and the services we provide. By renewing your membership with LAA, you demonstrate your commitment to being an active participant in the lymphoedema community. Your membership not only allows us to count you as an important member of our community but also enables us to continue fulfilling our mission of advocacy, education and support. We value your commitment and look forward to having you as a member for another year. Thank you for being part of our community, and we eagerly anticipate your continued involvement. If you haven't joined the Lymphoedema Association Australia yet, we invite you to seize this opportunity and become a member. - JOIN NOW!
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Sponsor: Thank you to Haddenham Healthcare, our Foundational Partner, for their generous support in helping us further our mission and serve the lymphoedema community.
Disclaimer: This e-newsletter is intended for informational purposes only and does not constitute medical advice. Please consult with your healthcare professional for personalised advice and treatment options related to lymphoedema or any other medical condition. The LAA is a non-profit organisation that relies on the support of donations, sponsorships and grants. We may occasionally feature sponsored content or include promotional messages in our communications, but we remain committed to providing impartial and reliable information to our members and stakeholders. Copyright 2023 Lymphoedema Association Australia. All rights reserved. To visit the Lymphoedema Association Australia website, Please follow the link hereo To unsubscribe from our newsletter. click hereisit
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These cooling towels are really helpful for people with lymphoedema to help battle the Australian heat. They can
