Bringing real people's stories to light... documentary film and photography that changes lives. Working with health, research, communities and charities.
Clean air is a human right. Last night, hundreds gathered on the South Bank to see the unveiling of Dryden Goodwin’s #BreatheforElla, honour Ella’s memory @EllaRobertaFdn & galvanise support for #EllasLaw. Incredibly moving evening. On for 2 more nights @Rambertdance
We are currently making a short film to promote 'Gastrostomy tube - Is it for me?' If you have MND, have used the decision aid and might be interested in taking part, please get in touch asap. We would come to you to film @mndassoc
Excited to announce the launch of the 'Gastrostomy tube - Is it for me?' decision aid on the MND Association website. This decision aid was developed as part of the DiAMoND study.
mndassociation.org/diamond-p….
Our @starworks_cp child prosthetics programme have produced a wonderful video, highlighting the approach taken, showcasing the individual projects and spotlighting our children and young people ambassadors that make the whole programme come together - devicesfordignity.org.uk/202…
Our @starworks_cp child prosthetics programme have produced a wonderful video, highlighting the approach taken, showcasing the individual projects and spotlighting our children and young people ambassadors that make the whole programme come together - devicesfordignity.org.uk/202…
We have co-created Neurocare Knowhow for #careworkers👋 to help support the care of people living with neurological conditions in the community and in care homes. Please help us make it better. Find out more in our film youtu.be/6d56_aPn-60@NeuroAlliance
We’re looking for care workers and PAs working with people living with neurological conditions to be part of our co-design team in Oct. if you’re interested in taking part please email us info@neurocareknowhow.co.uk
We are calling on the Government to define people with #MND as being extremely vulnerable as a matter of urgency.
If you have MND, we recommend that you register as extremely vulnerable at gov.uk/coronavirus-extremely….
This may help you get the best possible support! #Coronavirus
Have you seen the #myBreathing website? It's brand new.
It aims to support people living with motor neurone disease on choices they can make about their breathing support. The project was part funded by our @SYMNDA and @MNDManchester Branches.
Visit > mybreathing.mymnd.org.uk!
A fantastic addition to the ‘myMND’ information resources. Developed in collaboration with people living with MND, helping inform about the option to start non-invasive ventilation (NIV). Check it out and share far and wide @mndassoc@SYMNDAmybreathing.mymnd.org.uk
If you missed this great news last Friday, check it out!
We were very proud to help fund some of this work, and also have our branch play a part in the feedback to inform the final version!
Thanks to @profcjmcdermott and @cathy_soreny for their engagement with us all.
Delighted to see this launched today, really pleased our @MNDManchester branch helped a little towards its funding.
Was a pleasure to meet with @cathy_soreny and thanks to her and @profcjmcdermott who engaged our branch during the process.
Some great work, with our local touch!