Ben is a Postdoctoral Research Associate at SITraN examining changes in metabolism for those living with MND/ALS in an attempt to discover treatments for the condition.
📺 He talks us through his day in our latest Lab Lives story at https://t.co/fzPubTS6Uz
Great to see @drbenpchall talking about his research!
Earlier this year he also wrote a guest blog discussing the importance of using models of #MND#ALS to help find out what goes wrong in the disease. 🧫
Read his blog to find out more ⬇️
https://t.co/zX5iGAHYW6
Well, I won’t be expecting the call from @bbcstrictly any time soon! 😂
But I somehow got through it and it was all for a wonderful person and a vital cause: the Rob Burrow Centre for MND @LeedsHospitals.
Any final donations very gratefully received 🙏🏻👇🏻
https://t.co/RKRhfEG9u7
#Researcherspotlight 💡
Dr Tobias Moll from @neuroshef is investigating how communication breaks down between motor neurons.
He aims to test a new potential treatment strategy and hopefully reduce damage to nerve cells.
More info: https://t.co/p49fuZLXLW
To find out what goes wrong in #MND#ALS researchers will often use models of the disease.
One way to do this is to grow cells in a dish. 🧫
@Drbenpchall discusses how researchers are now able to create 3D models in our new blog ⬇️
https://t.co/ahvFJvne0z
📢 The International Symposium on #ALS#MND is back for its 35th year! 📢
📆 6 – 8 December 2024
📍 Montreal, Canada
✍️ Abstract submission opens 7 May
💻 Virtual option (incl. selected live-streamed sessions)
More info ⬇️ #alsmndsymp
https://t.co/G3fnZYaWHi
Janette Allen has started her 1 in 300 challenge to raise money for MND Research at SITraN. You can find the details below. Please share!
@neuroshef@mndresearch@sheffielduni
https://t.co/lU7CaMJdzr
Really enjoyed hosting @Fred_Steyn@AmberGreen67157@JerynChang and Sally Neville in Sheffield! Great to discuss research ideas and exciting opportunities for future collaborations!
Thanks @FoH_RSA for awarding me and @drbenpchall a Career Development Award to host this event!
Had such an amazing time at #alsmndsymp hearing about the most exciting ALS/MND research and meeting fellow researchers.
Was a really great experience for my first international conference, and I was so grateful to be able to present a poster of my research!
Over the past 3 days over 1600 people from the #MND#ALS community came together to share the most exciting and promising research.
We heard over 100 talks and saw almost 400 posters.
Thank you for participating.
Together we can create a world free of MND. 💚
#alsmndsymp
It’s the final day of #alsmndsymp!
In the last two days we’ve heard over 85 presentations from researchers around the world and there’s still more to come! 🌍
Today we’ll hear more about models used to study #MND in the lab and ways to improve clinical trial design. 🔬
We heard from @LauraFerraiuolo how star shaped brain cells, called astrocytes ⭐, might not work properly in #MND.
She shared how restoring the function of astrocytes may help protect motor neurons.
This could be a potential target for future therapy development.
#alsmndsymp
As Kev starts his final day of the #7in7in7 challenge, the latest and exciting research is being presented at #alsmndsymp.
The scale and momentum of #MND#ALS research is greater than ever!
The money raised by Kev will help continue this momentum. We can’t thank Kev enough 💚