Questions & answers on aniridia

Posted on June 7, 2014 by Aniridia Network

Session at Aniridia Network UK Conference 2014

By: Panel of experts and individuals affected by aniridia

A chance to ask that question that you always remember on the way home from your appointment or that there never seems to be the right time to ask?

The panel comprised:

The Q&A panel seated at a table

Mary, Amanda, Veda, Victoria and Jenny

  • Mary Cox
    Person with aniridia and parent of someone with aniridia
  • Amanda Churchill
    Consultant Senior Lecturer in Ophthalmology
  • Veda-Jayne Petre
    Disability Rights Adviser
  • Dr Victoria Towell
    Research Associate, UCL Institute of Ophthalmology
  • Jenny Langley
    Person with WAGR and ANUK Trustee

About Aniridia Network

A charity support group for people with the genetic visual impairment aniridia and their families in the UK and Ireland. Our vision is that people with/associated with aniridia are hopeful, confident, supported and well informed regarding aniridia. Founded in 2000. First registered as a charity in 2011 and fully in 2018.
This entry was posted in Medical staff talking, Parents' accounts, Patients' tales, Welfare experts advising and tagged , . Bookmark the permalink.

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