This was meant to have been resolved but sadly still accessing Riluzole is still a big problem Alex’s Dad David Setters Katy Styles

Our first meeting for 2024 - come along & join us for a chat

Carer‘s Support East Kent, provide vital support and information to all unpaid Carers in East Kent. Get in touch to see how WE can support YOU on your caring Journey.
0300 302 0061 [email protected]

We are still looking for healthcare professionals in the UK who care for people with #MND who have #cough and secretion issues?

Please fill in this survey to share your views via link or QR code.

shef.qualtrics.com/jfe/form/SV_eD…

Your right to a Carers Assessment 👇🏼 Local councils can help!

How about a lovely walk from Chilham to Canterbury?

This special walk will raise vital funds for MNDA-EastKent

🗓️28th May starting at Chilham and heading to Canterbury to support families living with MND.

📧[email protected]
#bankholidayweekend #KentAONB

Annual Christmas lunch for our patient ‘get together’; as always lovely food, service & atmosphere TheYarrowHotel

Huge thanks to Associate Sponsor Flackley Ash Hotel & Match Supporters Chequers on the Green and Jackie's News Please come along to support MND West Kent MNDA North West Kent Mid Kent Branch MNDA MNDA-EastKent MNDA East Sussex West Sussex North Just pop in to watch or book lunch ticket by Tuesday July 19.

Book your tickets now!

Come to sunny My Tenterden on July 26th to enjoy cricket Tenterden CC Annual Festival Week & help raise funds MNDA-EastKent to support people living with motor neurone disease & to find a cure for this cruel disease. To book your place at #Batting2EndMND see details on below.

Save the date! Delighted that refugee campaigner Lord Alf Dubs will give Alex Ward Memorial Lecture at St Mildred’s Tenterden 3pm on Saturday 23rd July. Alex was a member ashfordcouncil lost to motor neurone disease in 2020 aged 31. Free entry. Donations encouraged MNDA-EastKent

Very interesting & thought provoking reading MND Association MNDA-EastKent

Need a break? A little me time?
Good news! We have some funding available for you to take a break while the person you care for is looked after by a care agency. If you would like to take up this offer please email us at [email protected]

Please share & encourage people to take part in this study

Thank you to everyone who has taken part so far. If you haven't yet, please consider taking a few minutes of your day to do so. #ALS #MND MND Association My Name'5 Doddie Foundation MND Scotland

Join me & invite your MP to the next APPG on Motor Neurone Disease meeting on #MND Research here 👇🏽

By increasing MP support for #United2EndMND , we can pressure the Govt to properly fund #MND research into effective treatments & a cure to give people with MND hope bit.ly/3o1yQdj

'We are so disappointed on behalf of everyone in the MND community. Our researchers are on the cusp of a breakthrough in discovering treatments for MND. But they need a meaningful injection of funding.' - Sally Light.

Reaction to the #Budget2021 here
👉 mndassociation.org/united-to-end-…

After a very long time, today was our first face to face ‘get together’ for patients & families - thank you to all who joined us plus Ali, Jon & all the staff @thedrilhallsandwich for looking after us; as always amazing hospitality

Come & join us for our first face to face meeting in a long time at The Drill Hall Sandwich MNDA-EastKent MND Association @AhmedA_MND

Six free apps AHPs should know to help clients with MND: Tues 14th Sep 1-2:30pm UK. Free, online and interactive. Live demo & content added for a client. Try yourself through the session if you have an Android phone/tablet: email [email protected] to register
Pls Share :)