Have you been watching @ITVCorrie?

It's been 4 months since viewers saw character, Paul Foreman, diagnosed with #MND . Viewers are now watching Paul's symptoms worsen.

The #Corrie story has been amazing in raising awareness of MND.

Read more below via @MENNewsDesk.

Rob Burrow has inspired the nation; let’s support the legend in bringing home a National Television Award🎬❤️
You can vote here: nationaltvawards.com/vote

Another chance to watch ‘Rob Burrow: Living with MND’.

It’s on BBC Two at 7pm on Friday 25th August and on BBC iPlayer now.

Plus you can vote for the documentary in the National TV Awards here nationaltvawards.com/vote

Make sure you vote NOW for free at nationaltvawards.com to help the Burrow family win at National TV Awards so they can keep banging the drum for the whole MND community, spread the word but don't just Like and Repost, make sure you vote too

We are at an unprecedented time in MND research with more positivity around trials than ever before and a number of potential medicines now moving along the pipeline.

Read our latest Access to Emerging Treatments update below.

Claiming benefits may appear daunting and difficult but can make a significant difference to your financial position.

The MND Association benefits advice service provides advice by phone and email.

Visit 💬 mndassociation.org/benefitsadvice

#MND #Corrie

⬇️ Please vote for our wonderful patron Rob Burrow MBE and his incredible family to win at this year’s NTAs. Thank you 🙏 💙 #TeamMND

#LUFC fans, do your thing and please vote to raise as much awareness for MND Association as possible 💙💛

The bravest man and his amazing family deserve this award Rob Burrow MBE Please vote for them ❤️🙏🏻
nationaltvawards.com/vote
This is the link to vote

🤍 Rob Burrow MBE and his family joined us at Elland Road last night, asking #LUFC fans to vote for their documentary at this year's NTA Awards. Vote now at bit.ly/44bsevS

Have you watched ‘Rob Burrow: Living with MND’?

It’s on BBC iPlayer now and will run again on BBC Two at 7pm on Friday 25th August.

It’s been nominated for a National TV Award where you can vote in Authored Documentary - all the details are here - nationaltvawards.com/vote

In case you missed it: In our latest access to treatments update, we have encouraging news about the NHS Drug Repurposing Scheme.

We're also continuing to investigate multiple paths for early access for low-dose IL-2, in addition to looking at compassionate use.

Click below.

In our latest access to treatments update, we have encouraging news about the NHS Drug Repurposing Scheme.

We're also continuing to investigate multiple paths for early access for low-dose IL-2, in addition to looking at compassionate use.

Read our full update below.

🤍 'Rob Burrow: Living with MND', a documentary about the Leeds Rhinos legend and his family's courageous journey, is up for an NTA award! Vote now!

The ‘Rob Burrow: Living with #MND ' documentary has made the final shortlist at this year's National Television Awards.

You can vote for it to win below.

Huge congrats to BBC Breakfast team and thank you to our patron, Rob Burrow MBE and his family for helping to raise awareness!

❤️ “He always had that nurturing part of him. It made him a good teammate, good teacher, brilliant dad”

It's a year since former footballer & BBC Sport Lancashire summariser Len Johnrose died

Len was diagnosed with motor neurone disease in 2017

Family & friends share their memories

Please vote for our truly inspirational patron Rob Burrow MBE and the whole incredible Burrow family. We are so grateful for all they do for the #mnd community. With thanks too to the brilliant Claire Ryan Sally Nugent Richard Frediani. Vote here - nationaltvawards.com💙🙏

Everyone at the MND Association would like to wish our Royal Patron, HRH The Princess Royal, a very happy birthday.

The Princess continues to support the work of the MND Association and has attended three events this year, the latest being our MND Think Tank summit.

We'd like…

Please vote for Rob Burrow Living with MND in the National TV Awards for the Burrow Family who keep banging the drum for the #MND community and all people living with this cruel disease 🥁

Get voting here: nationaltvawards.com

Today we remember our Ambassador Len Johnrose who died from MND a year ago today. Len dedicated huge amounts of time to raising awareness and funds for @MNDAssoc including his Project 92 & #IceFoot92 campaigns. We miss Len's kindness & humour & we are thinking of his loved ones💙