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Visit our booth in the Registration Hall & test your skills in our daily Pipetting Game 🧪
Beat our board member Prof. Anja Ehrhardt!

Our game ist open:
📅 Every day
⏰ 10:30 AM – 05:30 PM

Each day’s top pipetter will get a prize at the end of the day from our Microbes plushies🦠
#ESGCT2025 #DGGZTeV

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E: More than you can imagine.
Ava from Australia with her mother Tammie. Ava has a rare metabolic disease.
Create awareness and inspire change for people with rare diseases, their families, loved ones and care takers.

More on rarediseaseday.org or scan the QR code

E: More than you can imagine. Ava from Australia with her mother Tammie. Ava has a rare metabolic disease. Create awareness and inspire change for people with rare diseases, their families, loved ones and care takers. More on rarediseaseday.org or scan the QR code

#RareStories and #RarePersons :

Each Person is rare and valuable - regardless if the disease is rare

#Rarediseaseday
#GeneTherapy
#DGGZTeV

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E: More than you can imagine.
Algas from Ruanda has a rare neurological disorder due to a genetic cause.
Create awareness and inspire change for people with rare diseases, their families, loved ones and care takers.

More on rarediseaseday.org or scan the QR code

E: More than you can imagine. Algas from Ruanda has a rare neurological disorder due to a genetic cause. Create awareness and inspire change for people with rare diseases, their families, loved ones and care takers. More on rarediseaseday.org or scan the QR code

#RareStories and #RarePersons :

Each Person is rare and valuable - regardless if the disease is rare

#Rarediseaseday
#GeneTherapy
#DGGZTeV

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E: More than you can imagine.
Charo from Argentina has a rare neurological disorder.
Create awareness and inspire change for people with rare diseases, their families, loved ones and care takers.

More on rarediseaseday.org or scan the QR code

E: More than you can imagine. Charo from Argentina has a rare neurological disorder. Create awareness and inspire change for people with rare diseases, their families, loved ones and care takers. More on rarediseaseday.org or scan the QR code

#RareStories and #RarePersons :

Each Person is rare and valuable - regardless if the disease is rare

#Rarediseaseday
#GeneTherapy
#DGGZTeV

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E: More than you can imagine.
RRadost from Bulgaria has a rare form of cancer.
Creating awareness and inspire change for people with rare diseases, their families, loved ones and care takers.

E: More than you can imagine. RRadost from Bulgaria has a rare form of cancer. Creating awareness and inspire change for people with rare diseases, their families, loved ones and care takers.

#RareStories and #RarePersons :

Each Person is rare and valuable - regardless if the disease is rare too

#Rarediseaseday
#GeneTherapy
#DGGZTeV

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Patients with #rare cancers have a suboptimal survival compared to patients with more common cancer types

Patients with #rare cancers have a suboptimal survival compared to patients with more common cancer types

#RareFact 9

Patients with #rare cancers have a suboptimal 5-year survival, partially because they need #rare individual treatments.

#Rarediseaseday
#GeneTherapy
#DGGZTeV

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1 in 5 cancers is a rare form

1 in 5 cancers is a rare form

#RareFact 8

Even generally common diseases like cancer can be highly specific in individual form and treatment.

#GeneTherapy
#Rarediseaseday
#DGGZTeV

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Equity means accessibility and a fair chance for a good life

Equity means accessibility and a fair chance for a good life

#RareFact 7

Place of birth, gender and skin color should not decide the availability of treatment options.
We are working towards research and treatment being equally accessible to everyone.

#GeneTherapy
#Rarediseaseday
#DGGZTeV

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70 percent of genetic disorders start during childhood

70 percent of genetic disorders start during childhood

#RareFact 6

Many #rarediseases start during childhood - the younger the patient the more time to gain

#GeneTherapy
#Rarediseaseday
#DGGZTeV

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72 percent of rare disease have a genetic cause

72 percent of rare disease have a genetic cause

#Rarefact 5

Most rare diseases have a genetic cause - brilliant #scientists around the world and in #Germany are developing #GeneTherapy approaches to treat or cure them.

#Rarediseaseday
#DGGZTeV

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There are more than 6000 rare diseases described

There are more than 6000 rare diseases described

#RareFact 4

There are many #rarediseases . There is a lot to do.

#rarediseaseday #GeneTherapy
#DGGZTeV

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Taken together the number of patients affected by rare diseases is comparable to the population of the 3rd largest country on earth

Taken together the number of patients affected by rare diseases is comparable to the population of the 3rd largest country on earth

#RareFact 3
#Rarediseaseday

An entire country full of patients affected by rare diseases surely would try to build a medical system and the necessary research to accommodate their needs - we should aim to do the same

#GeneTherapy
#DGGZTeV

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5 percent of the global population are affected by rare diseases

5 percent of the global population are affected by rare diseases

#RareFact 2

Because it is #rarediseaseday, today we are sharing facts and information on rare diseases

On all other days we #research ways to treat patients with #rarediseases
#communicate our findings and build networks for #cooperation and the future of #GeneTherapy

#Aware for #rare
#DGGZTeV

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Welcome to the bluesky account of the German Society for Gene and Cell Therapy #DGGZTeV

Just in time for the #rarediseaseday the DGGZT is finally part of the bluesky family.
We are here to #connect #communicate and spread #awareness

Follow us for more
#Rare #GeneTherapy #Germany #Science

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