Lymphoedema Association of South Africa

JOIN OUR 2024 CONFERENCE:

when

11 & 12 October 2024 Registration starts at 7h30

Where

Century City Conference Centre, Cape Town

Who

Lymphoedema Therapists / registered with A/HPCSA

PRICE

R2250 - R3050

CAN I JOIN AS A PATIENT?

Yes at our Patient meet and greet on 11th October at 17h30. See below.

Hello Lymphies!

We’re thrilled to invite you to our upcoming Patient Mingle and Meet.

 

What’s a mingle and meet you ask? We’ve got two incredible speakers lined up for you, both Lymphies who took a while to be diagnosied and now devoted patient advocates. This is also your chance to chat with doctors and lymphedema therapists, explore and try various Lymphoedema products, meet fellow Lymphies, and connect with others who truly understand. Don’t miss out—this event only happens once every two years!

Details:

  • Date: 11th October
  • Time: 17:30 – 19:30
  • Venue: CC Conference Centre
  • Price: Free
  • Who’s Welcome: Anyone with lymphedema, and those affected by it—family and friends are all invited!
  • And yes, there will be snacks and drinks 

Contact us

Fill out the form below, and we will be in touch.

OR email us info@laosa.co.za

LAOSA'S MINGLE AND MEET

Hello Lymphies!

We’re thrilled to invite you to our upcoming Patient Mingle and Meet. We’ve got two incredible speakers lined up:

  • Amy Rivera: Born with primary lymphedema and facing years of misdiagnosis, she is now  a powerhouse advocate for the lymphedema community.
  • Lindy Kruuse: After nearly two years of searching for answers, Lindy finally received a diagnosis of lymphedema in her left leg. She’s passionate about sharing her journey to help others find answers.

But that’s not all! This is your chance to chat with doctors and lymphedema therapists, explore various Lymphoedema products AND meet fellow Lymphies. 

LAOSA'S MINGLE AND MEET

Hello Lymphies!

We’re thrilled to invite you to our upcoming Patient Mingle and Meet. We’ve got two incredible speakers lined up:

  • Amy Rivera: Born with primary lymphedema and facing years of misdiagnosis, she is now  a powerhouse advocate for the lymphedema community.
  • Lindy Kruuse: After nearly two years of searching for answers, Lindy finally received a diagnosis of lymphedema in her left leg. She’s passionate about sharing her journey to help others find answers.

But that’s not all! This is your chance to chat with doctors and lymphedema therapists, explore various Lymphoedema products AND meet fellow Lymphies.