Lymphoedema Association of South Africa

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Get in touch:

Contact Us for Membership Inquiries, Event Updates, Educational Opportunities, or Donations.

OR

Whether you’re a Lymphie seeking support, searching for a therapist, or interested in collaboration, we’re here to connect and engage with you. Reach out today

Email us:

info@laosa.co.za

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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.