MNDAChiltern (@MNDA_Chiltern) profile picture

Chiltern branch of the Motor Neurone Disease Association. Supporting people living with MND locally

Buckinghamshire
Joined July 2012
Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)Photo by MNDAChiltern (@MNDA_Chiltern)
Huge thank you to all of our MND Connect Helpline volunteers for the incredible support they offer those living with and affected by #MND. Contact our helpline via: πŸ“ž 0808 802 6262 πŸ“§ [email protected] We're proud members of @HelplinesUK #HelplinesAwarenessDay24

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You can make a huge difference to the MND community. Find out more below πŸ‘‡
We're 86 away from our target of 800 letters to MPs. Urge your MP to become a member of the #MND group in Parliament and attend the next meeting in March. It is vital people with #MND continue to have a voice in Parliament. Write today πŸ‘‡ ecampaigns.mndassociation.or…
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Are you interested in sharing your experience of MND to help identify which research should be prioritised? If so, @Lifearc1 would like to hear from you. Together with @MNDScotland & @MNDoddie5, we're excited to support LifeArc's MND Insights Group!

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Support care grants can make a huge difference, offering essentials like: β€’ Riser recliner armchair β€’ Adaptations to property β€’ Stairlifts β€’ Washer dryer toilet β€’ Respite care costs "I'm now able to sit in the living room with my family, not stay in bed all day" πŸ‘¨β€πŸ‘©β€πŸ‘§β€πŸ‘§

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We’ve launched our latest campaigning action for the new #SupportMNDCarers campaign❗️ We need you to write to your MP, urging them to back our call for a government review of carer's assessments. Take a minute and email them today πŸ‘‡ ecampaigns.mndassociation.or…
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MNDAChiltern retweeted
I’ve released a book about my Dads battle with the disease. He was 11 months from diagnosis to death. All profits are being split between @mndassoc & @MNDoddie5 DM me to buy one #MND
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MNDAChiltern retweeted
What a moment. @Rob7Burrow and his family are truly incredible and I don’t think it’s possible for me to love Sir Kevin Sinfield anymore than I currently do
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Today Chair of the APPG on MND @ALewerMBE raised the challenges unpaid MND carers face around accessing respite services. Good to hear @Helen_Whately commit to reviewing specialist training for MND for the social care workforce in upcoming social care reforms.
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Best of luck to supporters Kate and Dan who will be taking on the epic Three Peaks Challenge on the 5-6 Aug to raise money for the association in honour of Kate's Dad Chris who has the disease. You can show your support by donating here justgiving.com/fundraising/k…
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It's #GlobalMNDAwarenessDay - a day to raise awareness of motor neurone disease around the world. β€’ 6 people will be diagnosed today β€’ 6 people will die today β€’ It has NO cure Please retweet our graphic highlighting the key facts. More people need to know πŸ’™ thank you! #MND
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We're delighted to announce and be part of a new MND Collaborative Partnership that has committed Β£4.25 million to MND research. This investment seeks to make MND treatable within years, not decades. #GlobalMNDAwarenessDay #DrivingMNDResearch

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MNDAChiltern retweeted
Today I have started my Campaign to become a Trustee for the MND Association! Please read my post on Facebook - Ian Lev featuring my new poem β€œTime With MND” Please vote for me when the Ballot opens from the 30th May - cheers! Keep Strong πŸ’ͺ Keep Positive!😎
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MNDAChiltern retweeted
Newly diagnosed with #MND? It's obviously a hugely difficult time for you and your family. If you are looking for support please join this friendly online group - next meeting April 22. @1stchatter @sarahjebson @MNDsouthlondon @MNDwestsussex @westsurreymnda
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Who likes a nice gin? πŸ™‹ Well now you can enjoy one knowing you've contributed to the fight against MND thanks to Paul Jameson's @50MillionGin. Paul, who has #MND, created the gin to celebrate #United2EndMND. Β£8 of every bottle sold, will be donated to the Association!

Nominations to become an MND Association Trustee are now open. Our Trustees are a group of volunteers who take overall responsibility and act collectively to govern the organisation, ensuring our long-term aims are met. Closing date πŸ—“οΈ πŸπŸ— 𝐀𝐩𝐫𝐒π₯ 𝟐𝟎𝟐𝟐. Click below.

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MND Matters Episode 13 πŒππƒ 𝐓𝐑𝐒𝐧𝐀 π“πšπ§π€ 𝐚𝐧𝐝 𝐒𝐭𝐨𝐫𝐲𝐛𝐨𝐨𝐀 Learn more about how technology can help those with #MND and hear from Mike and Diana, both living with the disease, who have used the new #IWillAlwaysBeMe voice banking book. Click below to listen now!

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MNDAChiltern retweeted
Fancy your chance of winning: β€’ A coffee with Eddie Redmayne OBE β€’ Tickets to the sell-out Cabaret show β€’ Overnight stay at the Corinthia Hotel, London Help us raise money for the MND Association 🀞 click below to enter our prize draw closing a week today!

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Hold us to our five promises... 🀝 mndassociation.org/mndpromis… #MNDPromises
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MNDAChiltern retweeted
This is a brilliant project which I have been honoured to be part of, well done to the team who had the creativity and innovation to make this happen !! @mndassoc
β€œVoice is a huge part of our identity” New software is helping those living with motor neurone disease to preserve their voices. Richard Cave from the MND Association explains to #BBCBreakfast how this technology is changing lives ‡️
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MNDAChiltern retweeted
Want to get involved in an event where you're in control? Why not try your own virtual event! Whether it’s a 10km run or a 20km Cycle, sign up now - because people with MND have no time to wait πŸ’™ mndassociation.org/takeover-…. #TakeOverMND
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