Alex Ward MND Angel 💙🧡 (@alexwardfund) 's Twitter Profile
Alex Ward MND Angel 💙🧡

@alexwardfund

Celebrates Alex Ward & supports #United2EndMND @MNDAEastKent. Alex aged 31 Councillor & road safety advocate lost to MND 22/7/20. alexwardfund.org

ID: 1331566209687498752

calendar_today25-11-2020 11:52:08

3,3K Tweet

530 Followers

897 Following

Lynn Pritchatt (@lynnpritchatt) 's Twitter Profile Photo

I am one of the proud Ambassadors for the incredible MND777 Challenge ❤ Former ITV Coronation Street actor and Mel Evans MBE Foundation Patron Peter Ash sends his good wishes to everyone involved 🥁👏❤. One week today Day 1 will be underway 🏃🏃🥁🥁

MND Research (@mndresearch) 's Twitter Profile Photo

Members of the team are at #BNA2025 🧠 MND Association have partnered with MND Scotland and My Name'5 Doddie Foundation to support a session highlighting UK MND translational research. The session will showcase the cutting-edge work happening across the UK to better understand, diagnose, and

Members of the team are at #BNA2025 🧠

<a href="/mndassoc/">MND Association</a> have partnered with <a href="/MNDScotland/">MND Scotland</a> and <a href="/MNDoddie5/">My Name'5 Doddie Foundation</a> to support a session highlighting UK MND translational research.

The session will showcase the cutting-edge work happening across the UK to better understand, diagnose, and
MND Campaigns (@mndcampaigns) 's Twitter Profile Photo

📢 This June, Parliament will spotlight 'The Hidden Realities of MND' for #GlobalMNDAwarenessDay. Invite your MP to attend: act.mndassociation.org/invite-your-mp…

📢 This June, Parliament will spotlight 'The Hidden Realities of MND' for #GlobalMNDAwarenessDay.

Invite your MP to attend: act.mndassociation.org/invite-your-mp…
Anthony Carbajal (@carbajalphoto) 's Twitter Profile Photo

I can’t walk, but I can still lead. I can’t speak, but my words still echo. I may be dying, but damn it, I’m still alive.

Marie Holmes (@marie_mndani) 's Twitter Profile Photo

Have you lost someone to MND in NI? Join us on Friday 23rd May at 2.00pm in Hillsborough Castle Cafe for MNDA Northern Ireland Past Carers Afternoon Tea. Email [email protected] to book you place. MND Association #mndani

Have you lost someone to MND in NI? Join us on Friday 23rd May at 2.00pm in Hillsborough Castle Cafe for <a href="/MNDA_NI/">MNDA Northern Ireland</a> Past Carers Afternoon Tea.
Email marie@mndani.com to book you place. <a href="/mndassoc/">MND Association</a> #mndani
MND Association (@mndassoc) 's Twitter Profile Photo

James cycled 100-miles over the mountains of Scotland raising £6,000 for the MND Association in honour of his friend, Paul. derbyshiretimes.co.uk/news/people/fr…

MND Association (@mndassoc) 's Twitter Profile Photo

Have you been inspired to get into running? 🫵 We'd love you to join #TeamMND for a running event near you. From 5k run runs to marathons, there is something for you. Check out our regional running hub to find events near you. 👟#MND

Johnny Timpson (@johnnytimpson1) 's Twitter Profile Photo

🧵 As Patron of the Vocational Rehabilitation Association UK 🇬🇧 ⁦VRA UK⁩ vraassociationuk.com and a GAIN (Group for Autism, Insurance, Investment & Neurodiversity) ⁦GAIN:Autism, Insurance, Investment, Neurodiversity⁩ gaintogether.org founder and board member I welcome… gov.uk/government/pub…

Chatham House (@chathamhouse) 's Twitter Profile Photo

The defining contribution of Donald Trump’s first 100 days has been the injection of uncertainty: into international relations, into trade – and at home in the United States. chathamhouse.org/2025/04/trumps…

David Ward (@daviddjward) 's Twitter Profile Photo

Privileged to attend HM King Charles’ garden party at Buckingham Palace today with Emma_MacLennan. Amused to chat with late John Smith’s 1992 Commons sparring partner ex Chancellor Lord Lamont. Great to meet also with fellow Tenterden residents Tim & Mary Monckton.

Privileged to attend HM King Charles’ garden party at Buckingham Palace today with <a href="/Emma_MacLennan/">Emma_MacLennan</a>. Amused to chat with late John Smith’s 1992 Commons sparring partner ex Chancellor Lord Lamont. Great to meet also with fellow Tenterden residents Tim &amp; Mary Monckton.
Liz Groundland (@lizgroundland) 's Twitter Profile Photo

This will be such a fab night with great raffle prizes & auction to be announced soon. Don't miss out £75 ticket for drinks reception & 3 course meal or get a table of 10 for £700. This will be such a great event which raise funds for people living with #MND and their families

This will be such a fab night with great raffle prizes &amp; auction to be announced soon. Don't miss out 
£75 ticket for drinks reception &amp; 3 course meal or get a table of 10 for £700. This will be such a great event which raise funds for people living with #MND and their families
Team Catton (@g_catton) 's Twitter Profile Photo

Celebrating day 500 of my #SockItToMND mission with some biccies! 🥳🧦🍪Fundraising for MND Scotland in memory and celebration of my amazing Mum 💙

Celebrating day 500 of my #SockItToMND mission with some biccies! 🥳🧦🍪Fundraising for <a href="/MNDScotland/">MND Scotland</a> in memory and celebration of my amazing Mum 💙
Leeds Rhinos (@leedsrhinos) 's Twitter Profile Photo

One week after the 2025 #RobBurrowLeedsMarathon, you can still support the cause. The Leeds Rhinos Marathon range is still available to purchase online and in-store. A 20% donation will be made to the MND Association from every sale to continue to help fund vital research and support.

One week after the 2025 #RobBurrowLeedsMarathon, you can still support the cause.

The Leeds Rhinos Marathon range is still available to purchase online and in-store. A 20% donation will be made to the <a href="/mndassoc/">MND Association</a> from every sale to continue to help fund vital research and support.
ALS Advocacy (@alsadvocacy) 's Twitter Profile Photo

Harvard University research into ALS, Tuberculosis and more in jeopardy over Trump administration's grant cuts theweek.in/news/health/20…

Greg Broadhurst (@gregbroadhurst) 's Twitter Profile Photo

This year our MND Association - Manchester & District Branch branch has our winter ball! It’ll raise funds for MND Association in Greater Manchester and tickets are selling well. Grab yours soon! To sponsor a table as a business is £100, and contact Liz Groundland if you are interested. Prizes are welcome as well.

This year our <a href="/MNDManchester/">MND Association - Manchester & District Branch</a> branch has our winter ball!

It’ll raise funds for <a href="/mndassoc/">MND Association</a> in Greater Manchester and tickets are selling well. Grab yours soon!

To sponsor a table as a business is £100, and contact <a href="/LizGroundland/">Liz Groundland</a> if you are interested. Prizes are welcome as well.
MND Campaigns (@mndcampaigns) 's Twitter Profile Photo

Huge thanks to Jo Platt for sponsoring our upcoming parliamentary event for #GlobalMNDAwarenessDay. Having seen the impact of #MND first-hand, Jo met us today to discuss how we can amplify the voices of the MND community in Parliament. There's still time to invite your MP

Huge thanks to <a href="/JoPlattLeigh/">Jo Platt</a> for sponsoring our upcoming parliamentary event for #GlobalMNDAwarenessDay.

Having seen the impact of #MND first-hand, Jo met us today to discuss how we can amplify the voices of the MND community in Parliament.

There's still time to invite your MP
ALS/MND Alliance (@alsmndalliance) 's Twitter Profile Photo

Applications now open! The Patient Fellows Program is back for the 36th International Symposium on ALS/MND. 🌐 Apply by June 30: ow.ly/1HIG50W2Fjp

Applications now open! The Patient Fellows Program is back for the 36th International Symposium on ALS/MND. 🌐 Apply by June 30: ow.ly/1HIG50W2Fjp
ALS Canada (@alscanada) 's Twitter Profile Photo

Each year, 1,000 Canadians are diagnosed with amyotrophic lateral sclerosis (ALS), a disease that progressively paralyzes people with limited treatments and no cure. In honour of #LouGehrigDay, learn more about ALS, share what you know, and unite in raising awareness to create

Each year, 1,000 Canadians are diagnosed with amyotrophic lateral sclerosis (ALS), a disease that progressively paralyzes people with limited treatments and no cure. In honour of #LouGehrigDay, learn more about ALS, share what you know, and unite in raising awareness to create