Pages
- “Invisible Heroes” Campaign
- 404
- About us
- Advocacy
- Become a member
- Become a volunteer
- Consultations and support
- Contact us
- Cookie Policy
- Data Protection Policy
- diploméierte Psycholog/ Psychotherapeut (m/w)
- Donations
- Events
- Gallery
- 20th anniversary
- 25th anniversary
- Assistance Dog Workshops
- Christmas Party 2022
- Christmas Party 2023
- Educational farm
- Familljefest 2019
- Family Day 2021
- Family Day 2022
- Family Day 2023
- Horse Therapy
- Inauguration Kockelscheuer
- Inauguration of the North site
- Prof Tebani Conference
- Quiz night 2020
- Rare Disease Day 2021 – Light It Up
- Rare Disease Day 2022 – Global Chain of Lights
- RaReflections Exhibition Opening
- RaReflections finissage
- Legal notices
- Living with a rare disease
- Membership
- My profile
- National Plan
- National Rare Disease Alliance
- News
- Newsletter Archives
- Rare Disease Day 2024
- Rare diseases Luxembourg
- Rare Rewind
- RaReflections
- Recreational activities
- Refund and Returns Policy
- Resources
- Sitemap
- Support us
- Testimonials
- The “30 000 hopes – 1 plan” campaign
- The “Talk TO me, not ABOUT me” campaign
- What is a rare disease ?
Posts by category
- Category: ALAN activities
- The “Rare Rewind” awareness campaign
- Recruitment : psychologist
- Recruitment : coordinator of the national alliance
- Annual Report 2023
- ALAN’s psycho-social consultation service is recognized by the European Commission
- Rare Disease Day 2024
- Recruitment : psychologist
- Offices closed during christmas holidays
- ALAN’s 25th anniversary: academic session, children’s book & advocacy campaign
- Results from the Rare Barometer survey on the diagnostic odyssey
- General Assembly: annual report & new president
- Rare diseases in Luxembourg: a crucial public health issue and a pressing socio-political decision
- The “Talk TO me, not ABOUT me” awareness campaign
- Annual Report 2021
- Rare Disease Day 2022 : photo exhibit & building illumination
- Inauguration of ALAN’s new offices
- Campaign to raise awareness for rare, invisible diseases
- Annual Report 2020
- Rare Disease Day 2021 – Light It Up for Rare Diseases
- New location & new website
- Annual Report 2019
- ALAN receives European award for its commitment
- Launch of the “Infoline Maladies Rares Luxembourg”
- Category: Covid-19
- Open letter regarding the COVID-19 pandemic – December 2021
- Survey results: COVID-19 vaccination of people with rare diseases
- Cancellation of recreational activities and courses due to the COVID-19 pandemic
- New open letter to the government regarding the health crisis
- Government’s response to our open letter
- Open letter to the government regarding the health crisis
- COVID-19 and rare diseases – Message from Dr Michel Hoffmann
- Category: Rare Disease Day