This June, we're holding an event in Parliament for #GlobalMNDAwarenessDay with the theme: 'The Hidden Realities of MND'. 📅
Invite your MP to attend using our email template below: https://t.co/VOXf7yclfn
Thanks to your support, we are close to reaching 20,000 signatures! #PrescribeLife#tofersen
Sign our petition to help people living with SOD1 #MND access a life-changing treatment 👇
https://t.co/IiCfNq25MM
It’s absolutely vital we get proven treatments to those with motor neurone disease as soon as possible.
To do this, today alongside @MNDScotland and @MNDoddie5, we've written letters to both regulators and ILTOO Pharma regarding the MIROCALS trial.
Read more information below.
Do you live in #Wales? 🏴
Invite your Senedd Members to join @mndassocWALES as they discuss research & potential #MND treatments at the Senedd next month.
It's vital we have as many MSs attend as possible.
https://t.co/mwtovqIYJ5
People living with MND don't have time to wait.
Today, alongside @mndassoc & @MNDScotland, we have written joint letters to both regulators and ILTOO pharma regarding the MIROCALS trial.
Full update 👇
https://t.co/hhlQsvr0Yr
Thousands of families like Tom's need support that's right for them to navigate the challenges of MND.
This Christmas, the kindness of supporters like you will mean we can give more families the support they need through their MND journey.
Read more about our latest appeal.
The MND Association is extremely concerned that the Department of Health and Social Care has halved its £500m investment into social care, which it committed to provide in 2021, to just £250m.
Read our response below.
Fantastic to be part of the first executive meeting of the UK #MND Research Institute.
Our Director of Research, Dr Jane Haley, is working alongside others to take further steps towards accelerating #MND research across the country.
We are #United2EndMND 💙