Doddie Aid is back!!! Do it for you, do it your way, and help fund crucial MND research ππ
And for researchers, join our amazing community! Sign up for our new β¨researcher leagueβ¨ and show your colleagues how it's done (it's all friendly competition... isn't it?) πͺ
02.12.2025 15:29
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Nikky, Federica and I certainly were the dream team π
23.10.2025 17:34
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JCI Insight -
Prenatal SMN-dependent defects in translation uncover reversible primary cilia phenotypes in spinal muscular atrophy
New paper from @tomgillingwater.bsky.social: Federica Genovese's fantastic PhD, showing reversible prenatal primary cilia defects in the Taiwanese mouse model of SMA. Lots of work still to be done to understand how low levels of SMN lead to the cellular defects we know; this project is part of itπ
23.10.2025 14:17
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Amazing π how I wish I could have been there!! Congrats Tom - I do intend to celebrate with both of them tonight at least π
29.08.2025 15:20
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Very proud to be a part of this community ππ
One that brings together people affected by MND, their friends and families, our supporters and fundraisers, and also our researchers ~ thank you!
04.07.2025 08:43
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Front cover of Science Signaling journal with a micrograph of fluorescently labelled neuromuscular junctions (NMJs)
There are still few better feelings as an academic than when your paperβs image is chosen for the front cover of a journal #ProudPI #NMJ Confocal micrograph taken by the amazing @drchayts.bsky.social
15.04.2025 18:11
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Thereβs only a few days to go until our webinar focusing on the Discovery Network and Advancing Treatments Award:
ποΈ 15 April
β° 12pm
Researchers, if youβre thinking of applying, the webinar is a great chance to have questions answered and gain insights.
Join here π
us06web.zoom.us/webinar/regi...
11.04.2025 09:08
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π©βπ¬ Join Dr Olivia Bird and me on the 15th of April at 12pm and ask us all your questions about our grant calls!
π£ Please share with researchers in your network who may be interested in applying, early career researchers included π
07.04.2025 09:41
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Our Discovery Network Award is open for applications again: join a highly collaborative network of fantastic researchers and receive up to Β£1 million over 3 years!
Please share - and get in touch if you have any questions/would like to discuss a project proposal #MND #ALS #AcademicSky
24.03.2025 11:16
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β οΈβ οΈβ οΈ Our Advancing Treatments Award is open for expressions of interest again! Get in touch with the research team at the Foundation if you have a project in mind/questions! ππ #MND #ALS #AcademicSky more announcements soon π€«
18.03.2025 22:30
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We need new science stories
I am midway through writing my 8th book. Please send help.
We need new science stories. New substack post, drunken cameo from @profaliceroberts.bsky.social
open.substack.com/pub/arutherf...
16.03.2025 08:38
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What good are remarkable scientific innovations and groundbreaking new treatments if policymakers don't follow suit, in the face of all the indisputable evidence in front of them?
05.03.2025 10:16
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We know from many studies and peer-reviewed publications that doing so alleviates financial costs for health organisations. We know it saves lives and can massively improve quality of life.
05.03.2025 10:16
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Spinal muscular atrophy in the UK: the human toll of slow decisions
Spinal muscular atrophy (SMA) is a recessive condition that affects globally one in
14β800 newborns.1 Infants with SMA type 1 do not acquire motor milestones and rarely
survive beyond the first year o...
The fact that the UK still doesn't do newborn screening for SMA is nothing short of scandal. We have treatments we've known for years need to be administered as soon as possible.
Spinal muscular atrophy in the UK: the human toll of slow decisions - The Lancet www.thelancet.com/journals/lan...
05.03.2025 10:16
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Legends! β€οΈβπ₯
04.03.2025 16:25
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What is the most exciting ALS/MND discovery research you've read recently/you're working on that is *not* focused on TDP43 or RNP biology? Please share some suggestions and papers!! #ALS #MND #AcademicSky
06.02.2025 14:52
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Gold.
24.01.2025 12:05
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My Name'5 Doddie is on Bluesky! ππ Give us a follow β¬οΈ
12.01.2025 21:48
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Lovely winter day to get started with #DoddieAid2025 - get moving this January, and join our challenge while supporting crucial research into Motor Neuron Disease #WeirInThisTogether
doddieaid.com/how-to-join
02.01.2025 15:55
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Super useful! Could you please add me too? :) MND researcher now working at My Name'5 Doddie Foundation, a research-funding charity in the UK (with international collaborations!)
04.12.2024 10:44
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Great that you like the Nation Leagues! Thanks so much for your support π€
03.12.2024 12:29
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In case anyone on BlueSky hasn't seen it, this may be the funniest scientific study ever published. Bringing it up now as the amazing @scotsfriction.bsky.social has just issued a "teaspoon amnesty" for our common room www.bmj.com/content/331/...
28.11.2024 11:18
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I could definitely see that play a role in your love for EM!
27.11.2024 21:16
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Ooo, I'd love to take a peek at this one!
27.11.2024 09:24
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Doddie Aid 2025
Doddie Aid is a mass participation event, encouraging you to get active in January and raise funds to help find a cure to Motor Neuron Disease.
If you're a researcher working on MND, we created a Researcher League in the app - join it here directly for some healthy competition and to get involved with the community who raises the funds for your research
Please share! ππ
@ukmndri.bsky.social
app.doddieaid.com/dashboard/le...
26.11.2024 17:10
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MNDF announces milestone Β£18 million of funding for MND research as Doddie Aid 2025 launches on second anniversary of Doddie's death
There is much still to do, but with your support, we will continue to fund research and work towards finding a cure.
Letβs make 2025 the biggest Doddie Aid yet - Weir in this together.
Read the full announcement here:
www.myname5doddie.co.uk/whats-on/art...
26.11.2024 17:10
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Every single one of the 100,000 people who has joined us to jog, cycle or stroll over the past four years of Doddie Aid has played a role in this milestone.
Two years on from Doddieβs death, we are as focused as ever on reaching his goal of a world free of MND.
26.11.2024 17:10
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Weβre officially launching Doddie Aid 2025, with the announcement that My Nameβ5 Doddie Foundation has so far committed Β£18 million to vital motor neuron disease research π¬
Sign ups are now live, click below to get involved and download the new app π
doddieaid.com
#DoddieAid25 #DoddieAid #MND #ALS
26.11.2024 17:10
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