
Swiss Lymph Kids

The meeting day
The Swiss Lymph Kids Day is a day specially designed for children living with lymphedema or a vascular malformation, as well as for their brothers, sisters and parents.
Inspired by the spirit of the Swiss Lymph Kids Camp, this day offers a friendly moment to meet, exchange and move together, in a caring environment adapted to all.
On the agenda
Welcome and aperitif/snack at noon
Group games and movement activities
Large-scale treasure hunt in teams (children and parents)
Fun and cooperative challenges
Time for families to exchange ideas
Barbecue / Canadian meal in the late afternoon
For whom?
Children and adolescents affected by lymphedema or vascular malformation
Siblings
Parents and relatives
Objectives of the day
To allow children to meet other young people living the same reality
Promote movement in a fun and appropriate way
Creating connections between families
To offer a positive, inclusive and supportive moment
Practical information
Schedule: Meeting at 11:00 AM
Meeting place: KVM clubhouse, Chemin Fin du Mossard in Morat (next to Lidl)
What to bring: swimsuit (weather permitting), barbecue/potluck lunch for the late afternoon, and good cheer
Register via our website; on the LymphoSuisse event page, select the date!
The Camp
We are delighted to present the second camp by LymphoSuisse for pediatric patients. Families from French-speaking Switzerland, Ticino, and German-speaking Switzerland are invited to participate in an extraordinary camp focused on lymphedema and vascular malformation.
The aim of this second edition is to gather and connect in an inclusive and supportive environment where each participant feels encouraged in managing their condition. A team of healthcare professionals will help you better understand the disease and provide insights into its impact on the entire family, both during the camp and beyond.
The Reka Holiday Village in Hasliberg, in the Bernese Oberland, offers a natural and peaceful setting for a 4-day camp. Each family will have private accommodations and access to the camp's programs and facilities.
This second Swiss edition draws inspiration from the “International Children's Camp” organized every five years by the University Hospital of Montpellier, and the first Swiss Camp which have been highly successful. The outcomes of such camps are evident in the following areas:
For Patients:
- Understanding the disease
- Improved disease management and access to treatment
- Strengthened self-management skills
- Exchange of tips and tricks among families
- Combating isolation
- Building a supportive community
For Professionals:
- Promoting research and proximity to patients
- Raising awareness about lymphedema
- Improving access to treatment and understanding patient needs
- Contributing to better management of lymphatic diseases
Practical Information
poster coming soon
Location and Date
The camp will take place from Friday, May 14 to Monday, May 17, 2027 (Pentecost weekend) at the Reka Holiday Village in Montfaucon, Canton Jura. You will stay in your own appartement (various sizes available) and enjoy access to the holiday village facilities, including an indoor pool, wellness area, gym, playground, picnic area, and more.
Reka Holiday Village
Dorf 372H
6084 Hasliberg
Costs
A flat fee of 200 CHF per family is required, regardless of the number of family members. This symbolic amount ensures that all families, regardless of financial circumstances, can attend the camp. (Registration fees should not be a barrier; LymphoSuisse is available to provide solutions.)
Costs for accommodation, evening meals, brunch, and activities will be covered for all participants (patients and families).
Breakfast and lunch must be arranged by participants. Each appartement has a kitchen, and food baskets will be offered for convenience.
By registering for the camp, you automatically become a member of LymphoSuisse (free of charge).
Who Can Participate?
All young individuals aged 2 to 18 years with primary lymphedema from French-speaking Switzerland, Ticino, and German-speaking Switzerland are invited, along with their parents (or guardians) and siblings, subject to availability.
How to Register?
Complete the following online registration form: https://forms.gle/BezT8mo6i8bNz57h6
Registration Deadline: 31 January, 2027.
Registrations will be confirmed after the deadline. The organizers will review applications and select families based on the following criteria:
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Type of lymphedema
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Representation from each canton
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Order of registration
The camp is limited to 10-12 families. However, if demand is high and funding allows, this limit may be increased.
Program
This is a preliminary program subject to change. We guarantee time for meetings, therapy sessions, exchanges with healthcare teams, discussion groups, and excursions.
Friday, May 14,.2027
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From 5:00 PM
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Welcome
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6:30 PM
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Aperitif and get-to-know-you entertainment
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Workshop: Lymphedema: understanding it better, what's new?
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Saturday, May 15, 2027
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Individual breakfast
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9:15 – 10:00 AM
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Physiotherapy session in the pool
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9:15 – 10:00 AM
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Entertainment program for siblings
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10:30 AM – 12:00 PM
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Workshop:
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Workshop: Lymphatic drainage
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Workshop: Bandaging
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Workshop: Appropriate footwear
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Custom measurements and personal advice
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10:30 AM - 12:00 PM
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Entertainment program for siblings
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12:00 – 13:30 PM
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Meal and free time
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From 13:30 PM
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Outdoor activity
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From 7:00 PM
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Dinner and entertainment
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Sunday, May 16, 2027
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Individual breakfast
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9:15 – 10:00 AM
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Physiotherapy session in the pool
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9:15 – 10:00 AM
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Entertainment program for siblings
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10:30 AM - 12:00 PM
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Workshop:
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Custom measurements and personal advice
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Compression tools
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Aids for donning stockings
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12:30 PM
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BBQ and games in the Rekavillage
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From 2:30 PM
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Workshops in the Rekavillage:
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Parent, child, and sibling discussion groups;
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free time
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From 7:00 PM
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Dinner and party
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Monday, May 17, 2027
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Individual breakfast
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9:15 – 10:00 AM
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Physiotherapy session in the pool
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9:15 – 10:00 AM
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Entertainment program for siblings
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10:30 AM - 2:00 PM
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Health brunch: for all LymphoSuisse members
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Organizing Committee
Claudia Lessert, Physiotherapist, President of LymphoSuisse, Department of Angiology, CHUV
Gilles Le Borgne, our head chef
Adeline Lienhard, our entertainment fairy
Magali Ackermann, Mother of a child with lymphedema
Veronica Matti, Mother of a child with lymphedema
Partners

Hasliberg
Financial Support
With your help, you contribute to the success of Switzerland’s first camp. If successful, we plan a second edition in another canton.
Donations:
LymphoSuisse c/o Service d’angiologie
Ch. de Mont-Paisible 18
CH-1011 Lausanne
Bank details:
N° IBAN : CH95 0076 7000R 5388 6206
Code BIC de la BCV : BCVL CH2LX XX





