Someone on your team is quietly managing lymphoedema.
Most workplaces never find out.

I'm Marece Wenhold — PhD in public policy, lived experience of lymphoedema, and a community of 24,000 people who know exactly what it's like to stay silent at work rather than explain.

Built in New Zealand. Designed for every workplace.

"Lymphoedema at Work exists so that no one has to manage an invisible chronic condition in silence at work — in any workplace, anywhere in the world."

A social enterprise · Built on lived experience · Grounded in public policy · Powered by a community of 24,000

The gap

It's not just swelling. It's the weight of carrying it quietly.

Lymphoedema is long-term swelling, most often after cancer treatment. But living with it means constant invisible management — the compression garments, the flights planned around elevation, the hot days managed in silence. None of it shows. So people say nothing at work. They push through and hope to be met with understanding.

That silence is the gap we close. Not the medicine, not the law — the human, everyday part in between: how a workplace actually responds when someone finally speaks up.

We do

Manager conversations, practical adjustments, return-to-work process, and a culture where people feel safe to speak up.

We don't

Medical or legal advice. For anything clinical, we point to the employee's therapist or GP. For legal questions, to HR or an employment lawyer. We signpost clearly to both.

Free guide

"Working Well With Lymphoedema" — five things every workplace should know. One page, instant download.

Download free →

The Workplace Toolkit

Scripts, templates, and a clear process for managers and HR. $495 per organisation, licensed for any workplace worldwide.

See what's inside →

Talks & workshops

The lived-experience perspective brought into your organisation — for managers, teams, or your wider community.

Enquire →
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Free resource, always

The one-pager is free for every individual, everywhere — regardless of whether their employer is ready to listen yet.

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Quarterly donation

One free toolkit donated to a community or not-for-profit organisation every quarter.

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Community contribution

Anonymised insights shared to advance understanding of lymphoedema in workplace settings.

The product

The Lymphoedema-Aware Workplace Toolkit

Everything a manager or HR team needs to support a staff member with lymphoedema — clearly, confidently, and without overstepping into medical or legal territory. Practical, non-clinical, grounded in lived experience. Designed for any workplace, anywhere in the world.

  • Manager & Employer Guide — understanding the condition's impact at work and how to respond well.
  • Manager Quick-Reference — the essentials and the scripts, on two pages.
  • Adjustment Conversation Template — a fillable structure for agreeing what helps.
  • Return-to-Work Process Checklist — for supporting someone back after treatment.
  • Team Awareness One-Pager — a gentle explainer to share with colleagues.
  • Signposting Appendix — exactly where to go for the clinical and legal answers we don't provide.
Licensed per organisation
$495 NZD / one-off

Applies to any workplace, anywhere in the world. Free updates for 12 months from purchase.

Buy the toolkit Request a demo

General workplace guidance only — not medical or legal advice. Terms of use included with purchase.

A social enterprise. A portion of every sale supports lymphoedema awareness and community resources.

Why trust this

Built on two decades of public policy, data, and governance.

Marece Wenhold brings a rare combination: deep public sector expertise, rigorous data science, and nine years of lived experience. This isn't generic wellbeing content.

Kāpiti Coast District Council
Senior Advisor, Performance, Planning & Reporting · 4 years
Victoria University of Wellington
Senior Researcher, School of Government · 3+ years
ANZSOG
Australia & New Zealand School of Government · Researcher
Volunteer Kāpiti
Board Trustee · Current
University of the Witwatersrand
PhD, Public Policy Analysis
University of Canterbury
Postgraduate Diploma, Applied Data Science

Also worked with or for

Idasa Dept of Rural Development · SA Office of the Premier · SA NZ Electoral Commission PRINCE2 Certified IBM SPSS Certified
From the community

People can tell when something's built for them.

The following are from members of The Lymphie Sanctuary community — people living with lymphoedema every day.

Testimonial coming soon — permission requested.
Testimonial coming soon — permission requested.
Testimonial coming soon — permission requested.
For organisations

Bring lymphoedema awareness into your workplace.

Beyond the toolkit, we work directly with organisations and the networks that serve them. Built in New Zealand, designed for every workplace worldwide.

Talks & workshops

For managers, HR, or whole teams. The lived-experience perspective that turns abstract policy into real understanding and real change. Online or in-person.

Enquire →

Partnerships

For EAPs, occupational health providers, and cancer support organisations who want this resource available across their client or member base. Annual licensing available.

Start a conversation →

Global reach

No jurisdiction-specific legal guidance — just the human, practical response that works anywhere in the world. Clients in NZ, Australia, the UK, and beyond.

Get in touch →
Warm pilot offer

Are you a good first fit?

We're looking for a small number of founding organisations to pilot the toolkit at a reduced rate — in exchange for feedback and a case study. If you're a NZ employer, EAP, or occupational health provider, get in touch.

Express interest
The origin

The Lymphie Sanctuary

Lymphoedema at Work grew out of The Lymphie Sanctuary — a private symptom-tracking app built from lived experience, and a community of over 24,000 people that formed around it. People from New Zealand, Australia, South Africa, the UK, the US — all managing the same daily reality.

Everything in the toolkit comes from what that community has taught me: where workplaces get it wrong, what actually helps, and the difference a single understanding manager can make.

Visit thelymphiesanctuary.com
What the app does

A private daily journal for people living with lymphoedema.

  • Two-minute daily check-in — heaviness, pain, compression, triggers, sleep, stress
  • Tracks patterns over time — so you arrive at appointments with real data, not vague memories
  • Self-compassion tracker built in — no streaks, no pressure, no leaderboards
  • Beautiful Excel export formatted for clinic appointments
  • Your data never leaves your device — architecturally enforced, not just policy
  • NZ$19.99 once. Lifetime access. No subscription. Ever.
Endorsed by lymphoedema therapists in New Zealand, Australia, South Africa, and the United Kingdom.
As heard on Access Media NZ · June 2026.
The connection

Two halves of the same promise.

The toolkit helps the employer respond well. The Sanctuary helps the individual employee manage day to day. Together they're a complete offer — an organisation that truly supports its people, and a private tool that empowers the person living with the condition.

"People can tell when something is built by someone who understands. That creates a different kind of trust."

For organisations purchasing the toolkit, employee licences for The Lymphie Sanctuary app are available as a staff benefit. Ask us about bundled pricing.

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Privacy-first, by architecture.

Your health data never leaves your device — not even for a millisecond. This isn't a policy choice; it's how the app is built. The server stores only your email and licence key. Nothing else. Ever. Read the full privacy policy →

Marece Wenhold, PhD Public Policy · Applied Data Science
Kāpiti Coast, New Zealand
Living with lymphoedema · 9 years
Get the free guide
About

Why this, why me.

I'm Marece Wenhold. I hold a PhD in public policy and a postgraduate diploma in applied data science — I've spent my career helping organisations make sense of complex information. But the most personal challenge I've ever faced has been my own health.

About nine years ago, lymphoedema appeared in my left leg, unexplained. I manage it daily — the compression, the heaviness, the constant negotiation between a body that works differently and a life that doesn't pause for it. Like so many people in our community, I've had to figure out a lot of it myself.

What I also know is that the hardest part isn't always physical. It's arriving at a clinic appointment and genuinely not being able to remember your week. It's the invisible cognitive load of managing something that never switches off. And it's sitting at work wondering whether today is the day you say something — and deciding, again, that it's safer not to.

Living with a chronic invisible illness means constantly translating your reality for other people — doctors, family, and employers. I built Lymphoedema at Work to close the gap between that lived reality and what workplaces actually know how to do. Not medical advice. Not legal advice. Just the human part done properly.

— Marece

Free resource

Working Well With Lymphoedema

Five things every workplace should know — on a single page. Free. Instant download. Share it with your HR team or manager today.

Download the free guide

No email required. No signup. Just download and share.

Get in touch

Whether you're an employer, HR team, EAP, or organisation supporting people with lymphoedema — I read every email personally.

Email Marece directly

info@thelymphiesanctuary.com

Pilot & partnership enquiries

Interested in piloting the toolkit at a reduced rate, or exploring an intermediary partnership for your organisation or network?

Start the conversation