A cozy virtual space to connect with other lymphies—hosted by lymphies.
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.
Not just to share some of my own 40+ years of lived experience…but to create space for your wisdom too.
Because your 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.
Summer can bring a whole new layer of challenges with lymphedema.
Together, we’ll share some of our favourite ways to cope with the heat and still enjoy the season. We’ll begin with one simple question:
What is ONE thing you wish you knew earlier about having lymphedema in the summer?
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.
For this Founder Event, 50% of ticket sales 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 open until June 5th
A recording will be available for registrants
Come with tea, comfy clothes, and exactly as you are
A cozy virtual space to connect with other lymphies—hosted by lymphies.
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.
Not just to share some of my own 40+ years of lived experience…but to create space for your wisdom too.
Because your 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.
Summer can bring a whole new layer of challenges with lymphedema.
Together, we’ll share some of our favourite ways to cope with the heat and still enjoy the season. We’ll begin with one simple question:
What is ONE thing you wish you knew earlier about having lymphedema in the summer?
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.
For this Founder Event, 50% of ticket sales 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 open until June 5th
A recording will be available for registrants
Come with tea, comfy clothes, and exactly as you are
