Lymphoedema Association of South Africa

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Be Counted

So little is known of the chronic condition – Lymphoedema.

 

LAOSA is on a mission to categorize, catalog and champion change for all our Lymphy family members.

 

Help us by being counted. 

Are you ready to contribute to Change?

  • Have you been diagnosed with Lymphoedema?
  • Are you looking for answers to your swollen limbs?
  • Has your doctor or therapist registered with LAOSA?
CONTACT US NOW
Thenjiwe Healthcare

in proud partnership with:

Thenjiwe Healthcare

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. 

ITS FREE TO JOIN > SIGN UP NOW