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HAVAS Life London

We specialise in rare disease and global health across brand, corporate and cause communications.​

Creating bold ideas from powerful insights that deliver measurable, meaningful advantage.​​​
 

Thought leadership

January 10, 2025
Published by Jeffrey Anderson on January 10, 2025
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Launch excellence in rare disease

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January 10, 2025
Published by Jeffrey Anderson on January 10, 2025
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Spotting creative opportunities is like spotting yellow cars

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January 8, 2025
Published by Jeffrey Anderson on January 8, 2025
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Rare, but out there

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We were very happy to share the experience of Eid We were very happy to share the experience of Eid this month at our office, and enjoy a moment of connection and reflection with our colleagues. Thank you to everyone who took part!
Game, set, match! Last week we held our first Game Game, set, match!
Last week we held our first Games ‘n’ sip,  where we indulged in the age-old tradition of teaching each other how to play our most beloved games whilst staying refreshed with pizza and drinks. We laughed, we cried, we got held up on the definition of a round object. 

Many thanks to everyone who attended, watch this space for the next one (did somebody say monopoly?) #CreativeAgency #VibrantCollaboration #SocialClub #GamesNight
🧧 We were delighted to celebrate Lunar New Year in 🧧 We were delighted to celebrate Lunar New Year in the office this year, with lucky red envelopes and fortunes! Wishing everyone prosperity, joy, and plenty of good vibes for the year ahead!✨ 新年快乐 / Happy Lunar New Year!
#LunarNewYear #TeamCelebration
36% of people with rare disease say they have been 36% of people with rare disease say they have been teased or called names because of their condition.

We listened to over 250 people who either live with, or care for someone who lives, with a rare condition - to understand the systemic experience of stigma and the emotional manifestations across global rare communities.

Read our *Rare Next Futures Report* where we explore these rare experiences and how we can take collective action to reduce the burden of stigma in #Rare. Link in bio.

#RareDiseaseDay #RDD2026
#MakeStigmaRare #RareNext #HavasHealthNetwork

@havashealthnetwork
Imagine being labelled everywhere you go. This is Imagine being labelled everywhere you go.

This is the reality for hundreds of thousands of people living with rare disease, and suffering harmful stigmas born of ignorance.
 
Join @havashealthnetwork to take collective action this #RareDiseaseDay.

Find out how in our new Futures Report, "Stigma: The Invisible Multiplier of Burden in Rare Disease". Link in bio.

#MakeStigmaRare #RareNext #HavasHealth #RareDiseaseDay2026 #RDD
36% of people with rare disease have been challeng 36% of people with rare disease have been challenged over their disability.

We listened to over 250 people who either live with, or care for someone who lives with, a rare condition - to understand the systemic experience of stigma and the emotional manifestations across global rare communities.

The @havashealthnetwork *Rare Next Futures Report* is out now - exploring these rare experiences and the burden of stigma in #Rare. 

Collective action starts now.

Read the report at the link in our bio.

#RareDiseaseDay #RDD2026
#MakeStigmaRare #RareNext #HavasHealthNetwork
42% of people with rare disease feel their healthc 42% of people with rare disease feel their healthcare professional doesn’t take their condition seriously.

We listened to over 250 people who either live with, or care for someone who lives, with a rare condition - to understand the systemic experience of stigma and the emotional manifestations across global rare communities.

Our Rare Next Futures Report is out now - exploring the rare experience and how we can take collective action to reduce the burden of stigma in #Rare.

Read the report at the link in our bio.

#RareDiseaseDay #RDD2026
#MakeStigmaRare #RareNext #HavasHealthNetwork
@havashealthnetwork
89% of people have been treated unfairly because o 89% of people have been treated unfairly because of their rare condition.  This is 100% unacceptable.

Progress in #RareDisease is moving at a remarkable pace, yet one barrier continues to limit the benefits for those who need it most: STIGMA. As with many aspects of rare, stigma is under researched and the impact underestimated. 

This #RareDiseaseDay, @havashealthnetwork is proud to publish our 2026 Rare Next Futures Report, examining the systemic experience of stigma and the emotional manifestations across global rare communities. 

We listened to over 250 people who either live with, or care for someone who lives with, a rare condition to understand their rare reality and amplify the global community’s voice. Read the Rare Next Futures Report, link in our bio.

This year, we also build on our support of the rare community by shining a light on @raregivers – a vital organisation that honours caregivers in rare.

We invite you to collaborate with us to shape the future of #Rare. Collective action starts now.
#RareNext #RDD #MakeStigmaRare #HavasHealthNetwork

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    Paul Kinsella
    Chief Creative Officer, Havas Health & You, Europe

    Fusing insights and data with bold creative ideas

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    RAiRE
    Havas Life London Large Language Model (LLM)

    Our innovative AI tool delivering powerful insights for rare disease

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    Dirk Poschenrieder
    Managing Director, Havas Health, Germany

    One of our key superpowers at HAVAS is collaboration

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    Our new strategic operating system approach

    Making modern marketing easier

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