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MLD News Australasia & SE Asia 
In this issue

Image from the British Lymphology Society #SockIt to Lymphoedema campaign
March is Lymphoedema Awareness Month 
What will you do to raise lymphoedema awareness this month?
  • Hold a morning tea to raise money for lymphoedema research?
  • Sign a petition to lobby the WHO to recognise lymphedema as a global health challenge?
  • Talk to someone about living with lymphoedema?
  • Attend one of the many support group events n offer?
    Read more at Talking Lymph....
Lymphoedema in Regional Australia
Training opportunities and the Moving Lymph Scholarship


Moving Lymph is dedicated to bringing training in lymphatic therapies to Regional Australia. if you would like to see with the Dr Vodder courses or the MTC Lymph Taping courses offered in your area please use our online survey to let us know you are interested.

If you live in Regional Australia and would like to apply for the Moving Lymph Scholarship to attend the Certificate in MLD & CDT on the Gold Coast in August please complete the Moving Lymph Scholarship application here.
Graduates are eligible for listing on the NLPR.
Lymphoedema Awareness activities around the world
The Lymphoedema Support Group of NSW is taking their annual conference to regional NSW. If you are in the Tamworth area please support this event. They also have a breakfast for health professionals.
In the UK the British Lymphology Society encourages you to wear odd socks and take photos of yourself doing something active as part of their #SockIt campaign.
Use the hashtag #EveryBodyCan when you post your odd socks shots.
 
The Lymphoedema Support Group of South Australia are focusing their lymphoedema awareness efforts on helping people to understand what it is like to live with lymphoedema. Post a comment to their Facebook page to share your story.
 

Every year Niagara Falls is lit with teal blue for #WorldLymphedemaDay View it live tonight.
The Lymphatic Education & Research Network have a petition to ask the WHO to recognise lymphoedema as a global health challenge. Sign the petition here. LE&RN also host lymphedema walks all around the country and have great resources for patients and practitioners on their website.
Paediatric Lymphoedema Service Provision (PLOS) Survey

Jane Phillips is a Melbourne based lymphoedem therapist and part of a team who will present on paedatirc lymphoedema at the ALA conference in May.

To address awareness of lymphoedema in children, the team has put together a survey to gather information about how many therapists are treating children with lymphoedema and what need exists for paediatric lymphoedema treatment.

If you treat anyone under 18 for lymphoedema, please xomplete the survey. Paediatric Lymphoedema Service provision (PLOS) Survey
Do you have lymphoedema yourself?
Register your details on the the International Lymphatic Disease and Lymphedema Patient Registry. This comprehensive registry will serve as a repository of information that will enhance the future ability of health care professionals to accurately identify, categorize, treat, and prevent these diseases. Register here.
MTC Lymph Taping
 
Find Out More
Email Jan
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Our mailing address is:
jan@movinglymph.com.au

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Moving Lymph Pty Ltd · Eastwood · Adelaide, SA 5063 · Australia

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