A cozy virtual space to connect with other lymphies—hosted by my self, Amy - a fellow lymphie - that’s me in the second photo.
No pressure.
No expectations.
Just real conversation with people who understand what it’s like to live with lymphedema.
Over the years, I’ve learned so much from other people living with lymphedema.
Little life hacks.
Encouragement on hard days.
Ways to make everyday life feel a little easier.
Sometimes just hearing “me too” from someone who truly gets it can feel like a lifeline.
That’s why I wanted to create this gathering. To create space for our shared lived experience wisdom
Because lived experience matters.
Your story, your routines, your resilience, your humour, and your creativity may be exactly what another lymphie needs to hear.
A gentle welcome from me, along with a chance to settle in with your tea and get comfortable.
Members will have the opportunity to briefly share a little about their lymphie story, journey, or what brought them to the gathering.
Sharing is completely optional.
You are welcome to simply listen and take it all in too.
Living your life should be your choice - not something you have to give up because of your Lymphedema - chatting with others can help you find ways to adapt so you don’t have to give up on your dreams!
Together, we’ll share some of our favourite ways to cope with Lymphedema around a them like clothes, travel, sleep, etc. Check the sign up list for topics.
What is ONE thing you wish you knew earlier about having lymphedema?
Something you discovered through trial and error…
something that became a saving grace…
or wisdom you wish someone had shared with you sooner.
Because that kind of shared knowledge is powerful!!
you’ve been craving connection with people who truly understand
you’re tired of feeling like you’re doing this alone
you want to learn new lymphie life skills and share your own wisdom too
or you simply want a soft, supportive space to be yourself
This gathering is about meeting you exactly where you are on your lymphie journey.
50% of ticket sales will support an organization in need.
2026 spring/summer gatherings will support:
Lymphedema Warriors of Uganda Association — Wheels of Hope Campaign, helping them provide transportation so lymphedema patients can access care.
Because access to care shouldn’t depend on where you live in the world.
Lymphedema is a world-wide condition, lymphies everywhere need & deserve support and access to care.
Sales are open until 1 day before the event date at which time they will close.
A cozy virtual space to connect with other lymphies—hosted by my self, Amy - a fellow lymphie - that’s me in the second photo.
No pressure.
No expectations.
Just real conversation with people who understand what it’s like to live with lymphedema.
Over the years, I’ve learned so much from other people living with lymphedema.
Little life hacks.
Encouragement on hard days.
Ways to make everyday life feel a little easier.
Sometimes just hearing “me too” from someone who truly gets it can feel like a lifeline.
That’s why I wanted to create this gathering. To create space for our shared lived experience wisdom
Because lived experience matters.
Your story, your routines, your resilience, your humour, and your creativity may be exactly what another lymphie needs to hear.
A gentle welcome from me, along with a chance to settle in with your tea and get comfortable.
Members will have the opportunity to briefly share a little about their lymphie story, journey, or what brought them to the gathering.
Sharing is completely optional.
You are welcome to simply listen and take it all in too.
Living your life should be your choice - not something you have to give up because of your Lymphedema - chatting with others can help you find ways to adapt so you don’t have to give up on your dreams!
Together, we’ll share some of our favourite ways to cope with Lymphedema around a them like clothes, travel, sleep, etc. Check the sign up list for topics.
What is ONE thing you wish you knew earlier about having lymphedema?
Something you discovered through trial and error…
something that became a saving grace…
or wisdom you wish someone had shared with you sooner.
Because that kind of shared knowledge is powerful!!
you’ve been craving connection with people who truly understand
you’re tired of feeling like you’re doing this alone
you want to learn new lymphie life skills and share your own wisdom too
or you simply want a soft, supportive space to be yourself
This gathering is about meeting you exactly where you are on your lymphie journey.
50% of ticket sales will support an organization in need.
2026 spring/summer gatherings will support:
Lymphedema Warriors of Uganda Association — Wheels of Hope Campaign, helping them provide transportation so lymphedema patients can access care.
Because access to care shouldn’t depend on where you live in the world.
Lymphedema is a world-wide condition, lymphies everywhere need & deserve support and access to care.
Sales are open until 1 day before the event date at which time they will close.