Jamie

from Eibhlín Mulroe Plus

00:00
472

Jamie O'Brein describes life with a Rare Disease where there is no cure called Ehlers-Danlos syndrome type III

# vimeo.com/16998980 Uploaded 474 Plays / / 0 Comments

  1. 4

    Jamie

    by Eibhlín Mulroe

    Uploaded

    Jamie O'Brein describes life with a Rare Disease where there is no cure called Ehlers-Danlos syndrome type III

    # vimeo.com/16998980 474 Plays / / 0 Comments
  2. 4

    Caroline

    by Eibhlín Mulroe

    Uploaded

    Caroline Heffernan speaks about living with Cystic Fibrosis

    # vimeo.com/17003349 109 Plays / / 0 Comments
  3. 4

    Liz and Claudia

    by Eibhlín Mulroe

    Uploaded

    Liz Scanlon speaks as a mother of a child with a Rare Disease

    # vimeo.com/17074544 386 Plays / / 0 Comments
  4. 4

    Joe

    by Eibhlín Mulroe

    Uploaded

    Joe Mooney, CEO of MDI

    # vimeo.com/17077285 117 Plays / / 0 Comments
  5. 4

    Margaret

    by Eibhlín Mulroe

    Uploaded

    Margaret Whelan, Pompe Disease Patient

    # vimeo.com/17079476 290 Plays / / 0 Comments

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IPPOSI Patient Video Diaries

Created by Eibhlín Mulroe Plus

The Irish Platform for Patients' Organisations, Science and Industry (IPPOSI) have asked people to describe to the public what life is like living with a rare disease in Ireland.

IPPOSI is a patient-led group and has been involved in Rare Disease policy development for many years and felt it important for the patient to tell and control their own story. All of these videos have been approved by the patient participants


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The Irish Platform for Patients' Organisations, Science and Industry (IPPOSI) have asked people to describe to the public what life is like living with a rare disease in Ireland.

IPPOSI is a patient-led group and has been involved in Rare Disease policy development for many years and felt it important for the patient to tell and control their own story. All of these videos have been approved by the patient participants and they have consented to telling their story to the world online. It is hoped that the public will better understand the issues for people living with Rare Diseases after watching these videos. Also, there maybe other patients with similar conditions in the world who would just like to know someone else has the rare diseases they have.

Individual Rare Diseases are Rare but it is not Rare to have a Rare Disease. There are 6-7000 Rare Diseases, it is estimated that 6-8% of EU citizens have or have yet to be diagnosed with a Rare Disease. 157,000 people in Ireland have a Rare Disease.
For further information on IPPOSI or the patient's profiled in these videos contact info@ipposi.ie
ipposi.ie

Credits:
Produced and Directed: Eibhlin Mulroe, IPPOSI

Camera: Joe Hoey

Post Production: Cathy Grieve and Diarmaid Keane
Red Diamond Media

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