The North Wiltshire Group of the Motor Neurone Disease Association is run by volunteers and aims to support to local people with MND, their families & carers.
Volunteers needed!
Have you got strong admin skills? Are you a social/digital media whiz? Are you great with people? Or are you more of a creative? You might even want to develop your skills in any of these areas? Whatever your interest, get in touch.
https://t.co/rx1RH9NsGl
A plea: this account is run by frontline NHS staff. After the scenes today in Trafalgar Square our inbox is distressing. You don’t know how much it meant to all of us to see the tidal wave of support on the hashtag #gotyourbackNHS. If you support us please follow and RT 💙💙💙
Have you been recently diagnosed with #MND? Alex from the Bristol & Bath group will be running a support meeting next Monday 12th July at 10am via Zoom. To join pls contact Alex - https://t.co/pf9nv7JOIt @MNDNorthWilts@MNDA_Glos
And now it is today… Important messages in this tweet. Great to know trustee @hjls73 from our group will be supporting today by discussing more plans for volunteers with @mndassoc
Our first Psychological Care Masterclass, hosted by presented by @ejmayberry and @hocking_sian, is taking place on Monday. This is a great opportunity to gain confidence in supporting the psychological needs of people with #MND.
Book your place at https://t.co/NurfNAnjU1
At #Mobiloo, our mission is to make the world more #inclusive by bringing our #ChangingPlaces wherever you want to go with the best team of drivers/attendants that help make it all possible. Whether you are a user or event organiser, pls get in touch if we can help at all 😃
John, who is living with motor neurone disease, started an incredible challenge encouraging people to do 1000 repetitive exercises.
The awesome #MND1000 has now raised over £13,000.
Find out more about the challenge here 👇
https://t.co/QpWlQBIA47
Well 2020 didn't quite go to plan did it?
Last year was a challenging for everyone. We fear that 2021 could be just as challenging for charities. That's why we need your support to help those affected by motor neurone disease. Visit 🧡https://t.co/NvW2WGmyff
👊 #TakeOverMND
2,500 people with #MND have died while waiting for the @DWP review into benefits for terminally ill people to be published.
People affected by #MND urge you to publish the review now @JustinTomlinson ⏰
#Scrap6Months#ImStillWaiting
If you're an @mndassoc volunteer we're running a webinar on Thursday evening at 18:00 talking about our new act to adapt campaign and how you can get involved. If you would like to attend email [email protected]
.@JustinTomlinson It’s a year since the @DWP announced its terminal illness review and people with #MND are still waiting. Please publish the findings urgently, #Scrap6Months and create a lifetime award
.@JustinTomlinson It’s a year since the @DWP announced its terminal illness review and people with #MND are still waiting. Please publish the findings urgently, #Scrap6Months and create a lifetime award
Today is #GlobalMNDAwarenessDay and I am extending a #HandOf solidarity to everyone affected by this disease. We will all keep fighting for better support, awareness, and action.
"I feel like I don't count, that I belong to a group that's not worth bothering about because we'll be dead soon anyway." Phil Rossall who is living with MND
@DHSCgovuk must add #MND to the extremely vulnerable from #Covid19 list now.
#GetMNDonTheList
https://t.co/SATZn5tsTF
This Saturday at 7PM the @mndassoc & I will host a live pub quiz @Facebook to keep you entertained during the #coronavirus#lockdown
All welcome. Details here: https://t.co/vBpu9FJJog #TeamMND
I want 10,000 people taking part so all RTs are hugely appreciated.
@JustinTomlinson I hope you can help to sort this out, given how much time you have spent getting to understand #MND and its impact on ability to breathe, and the support you have given to @MNDNorthWilts Please add people with MND to the list @mndassoc@mndcampaigns