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Galerie

Des moments forts

Fête d'hiver 2024

320 photos

Conférence Prof. Tebani

40 photos

Fête de Noël 2023

31 photos

25e anniversaire

284 photos

Fête familiale 2023

31 photos

Finissage RaReflections

31 photos

Fête de Noël 2022

22 photos

Fête familiale 2022

33 photos

Rare Disease Day 2022 - Global Chain of Lights

41 photos

RaReflections Vernissage

40 photos

Inauguration Kockelscheuer

32 photos

Fête familiale 2021

32 photos

Ateliers Chiens

11 photos

Rare Disease Day 2021 - Light It Up

34 photos

Ateliers ferme pédagogique

71 photos

Soirée quizz 2020

40 photos

Inauguration du nouveau site à Erpeldange

24 photos

Thérapie équestre

18 photos

Fête familiale 2019

37 photos

20eme anniversaire

38 photos

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À propos d’ALAN

ALAN – Maladies Rares Luxembourg est une association sans but lucratif (a.s.b.l.) fondée en 1998 et reconnue d’utilité publique depuis 2000. 

La mission d’ALAN consiste à améliorer la qualité de vie des personnes et des familles touchées par une maladie rare.

ALAN est soutenu par le ministère de la Santé et de la Sécurité, AFM-Téléthon et des généreux donateurs.

Reconnue d’utilité publique par arrêté grand-ducal du 29 avril 2000Registre de commerce : F 22 42Agréments : SANTE 2021/19 et 2020/02

(+352) 266 112 - 1info@alan.lu


Parc Luxite
13, rue de l'Innovation
L-1896 Kockelscheuer


CCPL LU95 1111 0004 2638 0000
BCEE LU89 0019 1300 5184 5000
BLUX LU30 0080 3239 1490 2001

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Suivez nous

Dear friends, As this year draws to an end, the Dear friends,
 
As this year draws to an end, the Board of Directors and the team of ALAN wishes you happy and serene holidays among your loved ones, as well as a Happy New Year.
 
Please note that our offices will be closed between the 23rd of December and the 1st of January.
 
Thank you for your support and trust throughout the year, and we look forward to seeing you again in 2025.
Combining the magic of Christmas with the magic of Combining the magic of Christmas with the magic of horses, makes kids’ eyes sparkle extra bright🌟 

A huge THANK YOU to our friends at the @ate_lux for hosting an amazing show and to Kartesia Philanthropy for sponsoring and supporting the Winter Festival 

Special thanks also go to our photographer Henri Goergen who captured these special moments

You can view the rest of the photos on our website : https://alan.lu/gallery/winter-festival-2024/
You don’t know how strong you truly are until yo You don’t know how strong you truly are until you’re put to the test. Through her journey with her chronic and rare disease, Stephanie has learned to be even more open and direct, to push her limits and to be 100% herself.
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by Coma-Media (Pixabay)
 
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion #addisondisease
At 19 years old, no one thinks about being confron At 19 years old, no one thinks about being confronted with a chronic, incurable disease… Cassandra’s life was turned upside down by her rare disease when she had just started university.
Over the years Cassandra has had to pivot many times. Today, she is graphic designer @lecachougraphic and the proud owner of a jewellery business @absynthiacreations 
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by RomanSenykMusic (Pixabay)
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion
#eds
#edsawareness
Most people know what a stroke is. But few people Most people know what a stroke is. But few people know that children can have strokes too. It is indeed rare, but not impossible. As illustrated by Leo.  However, because it is so rare, there are unfortunately many hurdles associated with it, as Leo’s parents, Manon and Natascha know all too well.
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by prazkhanal (Pixabay)
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion
#stroke
#strokeawareness
In her teenage years, Lara noticed that something In her teenage years, Lara noticed that something was not quite right with her body. But it was a very long way until she was finally diagnosed with a rare disease.
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by Olexy (Pixabay)
 
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion
Jean-Francis’s daughter was born with Rett syndr Jean-Francis’s daughter was born with Rett syndrome, a rare genetic disease that mainly affects girls and leads to intellectual disability and severe motor impairments.
Jean-Francis is also president of the Association luxembourgeoise du Syndrome de Rett (@alsr.lu ) which advocates for the affected girls and their families here in Luxembourg.
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by Coma-Media (Pixabay)
 
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion
#rettsydrome
#sydromederett
Abby lives with a disease so rare that no other pe Abby lives with a disease so rare that no other person in the world is known to have the same genetic change.
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by SoulProdMusic (Pixabay)
 
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion
Vicky’s son, Matteo, lives with Pitt-Hopkins syn Vicky’s son, Matteo, lives with Pitt-Hopkins syndrome, a rare neurological disease.
Life with a rare disease is often marked by many ups and downs. It is a complicated journey that highlights all the more how resilient, strong, courageous and full of joy of life the affected boys, girls, women and men are.
For the Rare Rewind campaign, we asked people affected by a rare disease what they would say to themselves if they could travel back in time to the moment when it all started.
For more details about the campaign visit our website:  www.alan.lu/rare-rewind
——————————————
Music by Gentle (Pixabay)
 
#Luxembourg
#Letzebuerg
#Luxemburg
#raredisease
#raresdiseases
#maladierare
#seltenekrankheit
#lebenmitbehinderung
#patientempowerment
#patientadvocacy
#spooniecommunity
#spoonie
#specialneeds
#chronicillness
#chronicillnesswarrior
#disabilityadvocate
#disabilityawareness
#invisibledisability
#handicapinvisible
#maladiechronique
#chronischkrank
#inclusion
#pitthopkins
© 2021 ALAN. Mentions légales

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