Sarah (@tiny_milton) profile picture

Mum to Emily, Eve & Benjamin x

burgess hill
Joined August 2010
Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)Photo by Sarah (@tiny_milton)
What is motor neurone disease (#MND)? A third of people die within a year, and more than half within two years of diagnosis. Six people die of MND each day. It has ๐ง๐จ cure. Our vision is a world free from MND. You can help. ๐Ÿ’™ #LivingWithMND
50
64
7,427
We can offer support to children and young people who have a loved one who is living with motor neurone disease (#MND). Our online hub has lots of information that you may find useful. Click below to find out more. ๐Ÿ’ฌ #ChildrensMentalHealthWeek

7
1
13
3,145
Tis the season of Hats again. Let the shannigans begin. ๐Ÿ˜‚ Hope ye are all ticking along out there. Grab a cuppa. Also on Afternoon Delight I will be playing here on MSR for the first time. Local girl. Emily Milton's song, Believe all in aid of MND. mndassociation.org/ โ€“ at Burgess Hill, England
2
2
so wonderful to hear that @Rob7Burrow is reading the CBeebies Bedtime Story this weekend ๐Ÿ“– sending love to all the MND family โ™ฅ๏ธ 6:50pm Saturdayโ€ฆ on @CBeebiesHQ ๐ŸŽ‰
27
161
10
2,872
Former Leeds Rhinos player Rob Burrow is to read a CBeebies Bedtime Story using ground-breaking technology, the first time a bedtime story has been read this way. bbc.com/mediacentre/2022/rugโ€ฆ
61
468
138
4,443
Iโ€™m backing the #SupportMNDCarers campaign which launches today. People with #MND are so reliant on carers, often unpaid family & friends. @mndassocโ€™s report shows only 25% of carers have been assessed to check if they need extra support. Please ask your MP to back a review ๐Ÿ‘‡
Unpaid carers are at breaking point. Today, we launched our #SupportMNDCarers campaign calling on @SteveBarclay to launch an urgent government review into carer's assessments @mndcampaigns

2
20
91
Weโ€™re sorry to hear that Doddie Weir OBE has died. Since sharing his MND diagnosis in 2017, Doddie became an inspiration to many, raising awareness and campaigning tirelessly on behalf of those with MND. Our thoughts are with Doddieโ€™s wife Kathy, his 3 sons, family and friends.
212
855
302
10,930
ยฃ 1 , 0 0 0 , 0 0 0 ๐Ÿฅน Heโ€™s done it again. Kevin Sinfield has raised over one million pounds for those living with and affected by motor neurone disease. Heroic ๐Ÿ’™ This is going to make such a massive difference: donate.giveasyoulive.com/funโ€ฆ Thank you all ๐Ÿงก #Ultra7in7
80
432
130
2,957
Please watch โ€œLiving with MNDโ€ tonight on BBC2 ๐Ÿ™ People with MND (and their family) have to get on with life - AND WE DO. But the promised ยฃ50 million towards finding a Cure needs to be given NOW ๐Ÿ™๐ŸฅฒDO NOT DO A U TURN ON THIS FUNDING ๐Ÿ™
69
437
12
2,885
It's #GlobalMNDAwarenessDay - a day to raise awareness of motor neurone disease around the world. โ€ข 6 people will be diagnosed today โ€ข 6 people will die today โ€ข It has NO cure Please retweet our graphic highlighting the key facts. More people need to know ๐Ÿ’™ thank you! #MND
6
231
28
227
Our five promises are for those living with and affected by motor neurone disease. They will power everything we do. Hold us to our promises. Please retweet this to spread the word ready for #GlobalMNDAwarenessDay tomorrow. ๐Ÿค #MNDPromises

I am absolutely disgusted that NO MONEY has been received of the ยฃ50 million over 5 years for MND !!! Government and Health Minister should hang their heads in shame. Was the โ€œpromiseโ€ just a cruel sick lie ? Give us the money PLEASE ๐Ÿ™
395
38
1,669
On #InternationalNursesDay we'd like to give thanks to the countless nurses up and down the country caring for those living with motor neurone disease. The work they do, especially in the last two years, is incredible. We're proud to work alongside @theRCN. ๐Ÿ‘ฉโ€โš•๏ธ #NursesDay #MND
9
1
44
๐Ž๐ฎ๐ซ ๐Ÿ๐ข๐ฏ๐ž ๐ฉ๐ซ๐จ๐ฆ๐ข๐ฌ๐ž๐ฌ ๐ญ๐จ ๐ฒ๐จ๐ฎ... 1: MND is treatable and ultimately curable 2: Everyone gets the care they need when they need it 3: Every day with MND counts 4: You are heard 5: No one faces MND alone We won't rest until they're kept! #MNDPromises

2
16
2
63
Motor neurone disease (MND). It kills a third of people within one year, and more than half within two years of diagnosis. Six people will be diagnosed today. ๐ˆ๐ญ ๐ก๐š๐ฌ ๐ง๐จ ๐œ๐ฎ๐ซ๐ž. More people need to know this. ๐๐ฅ๐ž๐š๐ฌ๐ž ๐ฌ๐ก๐š๐ซ๐ž.
3
189
7
244
I am absolutely disgusted in this government. They will too busy having parties!
MND Association patron, @Rob7Burrow, shares his thoughts on the #United2EndMND research funding. Tomorrow, together with the coalition, we meet @GillianKeegan to discuss the ยฃ50 million promised by @GOVUK!
87
488
45
2,429
MISSING: Owen is missing from his home in Saltdean in Brighton, East Sussex. He was last seen leaving home at around 7pm on the 26 March. He is 16 years old, 5โ€™11/6ft and of medium build with dark hair. Last seen wearing a black hoody, grey tracksuit trousers and white trainers.
11
1,275
37
1,027
This is the face of someone who just spent 9 hours in personal protective equipment moving critically ill Covid19 patients around London. I feel broken - and we are only at the start. I am begging people, please please do social distancing and self isolation #covid19
10,826
90,485
5,360
333,733