Our International Rare Disease Day event is back!
Save the date and come see us on Saturday the 24th February for a fun afternoon filled with science and cake 🙂
To book your FREE place, click here
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Our International Rare Disease Day event is back!
Save the date and come see us on Saturday the 24th February for a fun afternoon filled with science and cake 🙂
To book your FREE place, click here
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With hands on activities, chatty scientists and lots of interesting presentations about genetics, this event attracts over 100 participants every year.
Come join us for a Free afternoon of informal chatting about science, and find out about state of the art research at Newcastle University. Oh, and cake!
Booking is essential, please book your place here: http://tinyurl.com/h3bfqno
The Theme of this year’s International Rare Disease Day is Research (see here for details)
The Insitute of genetic Medicine would like to invite members of the public and patient organisations to participate in a week long programme of hands on research, meet the scientist sessions and informal workshops that will take place at the Discovery Museum 20-16th of February 2017. Come meet us and find out about rare disease research and genomic medicine in the North East!
Cartilage growth plate in an adolescent lion at the Animals Inside Out exhibition at Centre for Life in Newcastle
Institute of Genetic Medicine in Newcastle are hosting their popular Ooen Day for A-level students on the 13th of July 2016.
To book a place, please contact: IGMEngagement@ncl.ac.uk
We are pleased to announce we’ll be hosting our popular Genetics Matters event again on the 27th of February 2016 as part of the International Rare Disease Day. Come meet the scientists, touch real specimens, chat about rare diseases and hear about the exciting state of the art research at Newcastle University.

“Genetics Matters” annual event serves to showcase genetic research and to give the patient and charity organisations a voice and a platform to interact with the members of general public. The theme of the Rare Disease Day in 2016 is “Patient Voice”, recognising the crucial role that patients play in research by voicing their needs and instigating change.
We would like patients or members of patient families to be present on the day and actively participate, sharing the presenting with our scientists. We believe that the patients’ voice is important in directing the course of scientific research and that it is important to remember that behind the tubes and microscope slides there is also a human story, and that we are all working towards a common goal.
This event is FREE to attend, but we have limited places available, so if you would like to attend, please book your place here: