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All proceeds from sales go towards MWT projects, for more details please contact us directly.

"Creativity is contagious, pass it on"

Albert Einstein

Molly Watt Trust T-shirts for Sale

High quality cotton t-shirts with embroidered Molly Watt Trust logo.

Available in small, medium, large and x-large.

Price is £10 plus £2.50 P&P

t shirt

Wristbands for Sale

Show your support by wearing our unique wristbands.

Price includes P&P

wristbands

Pins for Sale

Show your support wearing one of our unique pins showing the MWT logo, designed by Molly.

Price includes P&P

pins

Prints for Sale

We are delighted to be able to not only exhibit but also to offer prints of all pictures for sale at £15 including postage and packaging.

We would like to invite others with Usher Syndrome to donate their work to the gallery.

Donate

To support the work of MWT please click on any of the Donate buttons below or alternately you may send a cheque made payable to Molly Watt Trust and sent to Queen Anne House, 25-27 Broadway, Maidenhead,Berkshire, SL6 1LY.

All donations and support are gratefully received.

Please complete this form if applicable so that we may claim an additional 25% in gift aid.

Recent Blogs

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A Decade of Progress

Well it’s the year of 2020 everyone! It certainly has been a time of reflection for me, as a result I wanted to share my last decade in a blog that...

Ultimately we can all be winners

This year saw me nominated for three awards, Young Digital Leader for Digital Leaders for the second time (Too old for that one again) Positive Role Model for Disability, National...

Virgin Train #Fail

We were truly horrified to hear of Molly's recent expereince at London's Euston Station and it must never happen again: I travelled from Maidenhead to London Euston to catch a train...

Helen diagnosis 'I felt my world fel…

My name is Helen Colson. I’m 29 years old & live in Southport, Merseyside. I was diagnosed with Retinitis Pigmentosa and as I am moderate-severely deaf, Ushers Syndrome last year. It...

Olivia's Usher Life - Last few month…

Hello Everyone! Would like to wish you all happy deaf blindness week! I’m so sorry that I haven’t posted in it feels like ages! But I’ve got soooo much to...

Where did our journey with Usher Syn…

Where does our story begin..... Alice (now 16) was born profoundly deaf. In Oct 17 at a routine eye test (Alice has always worn glasses) they picked up an issue...

The evolution changing Usher Syndrom…

Usher Syndrome is a strange thing, strangely it is evolving even though it hasn’t changed. It remains a condition without a cure. There are variations in level of deafness, in level of...

Whispers in the Dark

It’s never been easy. Having to scan the floor in front of you when walking down the street. Having to pre-plan the route to the nearest toilet in a restaurant...

GAAD - Not if but how!

Indeed back in the 19th Century it was Helen Keller who stated “DEAFNESS SEPERATES US FROM PEOPLE AND BLINDNESS SEPERATES US FROM THINGS”. Back then she was right, she lived...

Equal access to sound for all

Today is ‘Rare Disease Day -2019’ So I decided on a blog about hearing aid technology that can and does enhance lives. This http://www.nciua.org.uk/latest-new/ was brought to my attention several weeks ago. ...