#easyfundraising

Please sign up to #easyfundraising and help us raise FREE funds for the Nystagmus Network whenever you’re shopping online.

THIS IS FREE MONEY FOR US!

Our supporters have already raised over £1,000 and it hasn’t cost them a penny!

Plus, when you raise your first £5, easyfundraising will match it!

Please sign-up using our unique link and search for The Nystagmus Network.

 Sign up here – thank you!

A postcard advertising the Nystagmus Network weather lottery.

Join our Weather Lottery

It may not stop the wind and rain, but, if you play the Nystagmus Network Weather Lottery, you will feel a little bit warmer inside.

For £1 per week you will be in with the chance to win up to £25,000 AND every penny of profit, after prize money has been paid out, comes directly to the Nystagmus Network.

Please support us and sign up to the Nystagmus Network Weather Lottery today.

SIGN UP HERE

Thank you.

A box of knitted mascots.

Thank you, Lynda

Our lovely knitting volunteer, Lynda has just delivered a new supply of Nystagmus Network mascots for our online shop.

Each mascot represents a child who has nystagmus and wears a warm woolly hat and scarf against the stormy weather. Every mascot is individual, just like real children.

All profits from the sales of the mascots go directly to the Nystagmus Network and every mascot sold helps us raise awareness of the condition and gives a child (or an adult!) a woolly friend just like them.

You can order your mascot from our online shop, here.

Thank you, Lynda!

Mike wears his Nystagmus Network T short and smiles for the camera

Mike’s a Nystagmus Super Hero

In case you haven’t heard yet, Southampton born, Mike Larcombe, who has CN, set off on his Walk for Wiggly Eyes on 16 December.

Mike is walking the entire length of both islands of New Zealand to raise awareness of nystagmus and funding for nystagmus research.

The Nystagmus Network is one of Mike’s 3 chosen beneficiary charities. The others are Gift of Sight in Southampton and Blind and Low Vision NZ.

The ‘wiggly walk’ is going to take around 3.5 months in all. It’s an incredible undertaking.

Please watch his progress and send Mike your support along the way, if you can, via Facebook or Instagram. The views are amazing!

To donate to Mike’s fundraising page, please click here.

THANK YOU

Thomas and Ben are #NystagmusStars

Today we have 2 #NystagmusStars for the price of 1! Their Mum says: “These are my two nystagmus stars, Thomas and Ben, who are confident, happy and loving boys.” 

To nominate your #NystagmusStar or to make a donation to help the Nystagmus Network support lots more people to reach their potential, please click here.

Thank you

Phoenix is a #NystagmusStar

Phoenix is 12. He has nystagmus and albinism. At a recent parents’ evening his teachers said he is exceeding most of his targets and they had nothing but praise for him. His Mum is very proud of him, too.

To nominate your #NystagmusStar or to make a donation to help the Nystagmus Network support lots more people to reach their potential, please click here.

Thank you

Ryan is a #NystagmusStar

Following a difficult birth, Ryan has nystagmus and is severely partially sighted. According to his Mum, he’s the funniest, most sensitive little man ever and whoever meets Ryan falls instantly in love with him, because he smiles from the start of the day to the end. She calls him “my number one star, my boy, my fighter and my son … Ryan.” 

To nominate your #NystagmusStar or to make a donation to help the Nystagmus Network support lots more people to reach their potential, please click here.

Thank you