• Skip to main navigation
  • Skip to main content
  • Skip to footer

T – Page 3 – The Norrie Disease Foundation

The Norrie Disease Foundation logoThe Norrie Disease Foundation
The Norrie Disease Foundation

Primary Menu

  • About Norrie Disease
  • Research
    • Research Projects
    • Research Resources
    • Frequently Asked Questions
  • Living with Norrie Disease
    • How we can help
    • Norrie Disease Conferences and Family Days
    • Diagnosis and Management
    • Genetics and Inheritance
    • Gosh Developmental Vision Clinic
    • Educational Needs
    • Community Stories
    • Useful links
  • News
  • About Us
    • Contact Us
    • Our Team
    • Annual Reports
    • Accessibility
    • Privacy Policy
  • Get Involved
    • Fundraising
    • How your money is spent
    • Inspiring Stories
  • Skip to menu toggle button

Header info sidebar

Find us on social networks

  • NDF on Facebook
  • NDF on Twitter
  • NDF on Instagram

Cookies law

Browsing the website you agree to use cookies »

Search the site

Author: T (page 3)

Author: T (page 3)

Slovakia Bound

By David Wilkins It’s a time old cliché that a letter or an email can change your life.…
Continue reading “Slovakia Bound”…
Posted on: 25 Sep 2019Written by: T

Norrie Family meet

zander enjoying softplay
Fifteen families met in London and enjoyed soft play; mingling; bouncy castle; trampolining and meeting new and old friends.
Continue reading “Norrie Family meet”…
Posted on: 08 Jul 2019Written by: T

New Research Partnership

The Norrie Disease Foundation are very excited to announce their new research partnership with Sparks and Great Ormond…
Continue reading “New Research Partnership”…
Posted on: 28 Jun 2019Written by: T

Cameron’s SmileMy New Bed

I came home from school to find my new bed has been delivered. I used to have a…
Continue reading “Cameron’s SmileMy New Bed”…
Posted on: 01 Jun 2019Written by: T

Strictly come Fundraising

NDF trustee, Theresa Peacock, turned the big Four-O earlier this year and to celebrate she held a Strictly…
Continue reading “Strictly come Fundraising”…
Posted on: 29 May 2019Written by: TComments: Comments: 0

Well Done Oliver

The Norrie Disease Foundation had their first ever runner in the London Marathon this year. Oliver Stowe was…
Continue reading “Well Done Oliver”…
Posted on: 01 May 2019Written by: TComments: Comments: 0

Cameron’s Smile – don’t be sad

I was born without it and I will never know any different. You don’t need eyes to see…
Continue reading “Cameron’s Smile – don’t be sad”…
Posted on: 01 May 2019Written by: T

Posts Navigation

« Previous page 1 2 3 4 Next page »

Sidebar

Latest News

22 Jul

Join the National Norrie 25km fundraising walk weekender 5th & 6th September

Come walk with lovely friendly people – make new friends or reconnect with old ones whilst raising vital…
Continue reading “Join the National Norrie 25km fundraising walk weekender 5th & 6th September”…
04 Jul

James Arwyn-Jones receives prize for best Otology oral presentation at BACO 2026

We are so proud of James Arwyn-Jones, Norrie disease Surgeon Scientist PhD for receiving the prize for best…
Continue reading “James Arwyn-Jones receives prize for best Otology oral presentation at BACO 2026”…
23 Jun

Helpful feedback from the London NDF Family Day

Some more helpful feedback from the London NDF Family Day from Rob Edge, Grandad to 2 year old…
Continue reading “Helpful feedback from the London NDF Family Day”…

Socialize with us

  • NDF on Facebook
  • NDF on Twitter
  • NDF on Instagram

Donate or Fundraise

Imagine a world without sight. Now imagine it without sound too.

Footer sidebar

Charity Registration Number: 1171274

Fundraising Regulator logo

Contact Us

The Norrie Disease Foundation
PO Box 12476
Colchester
CO1 9RB

Donate

Copyright The Norrie Disease Foundation 2025. Website development: T Waldock
  • NDF on Facebook
  • NDF on Twitter
  • NDF on Instagram
  • Back to top ↑