Symposium Blogathon: Focus on… Fabiola De Marchi

Symposium Blogathon: Focus on… Fabiola De Marchi

Reading Time: 2 minutes

This blog is part of our Symposium Blogathon series – where we are counting down to the 33rd International Symposium. Numbers in bold blue type correspond to the code in the abstract book. Click on the number to be redirected to the full abstract. 

As a new feature of the Symposium Blogathon, we got in touch with a variety of international researchers who will be presenting at the 33rd International Symposium on ALS/MND. We chatted about what they will be presenting and what they are most looking forward to at the Symposium this year.

Today, we hear from Dr Fabiola De Marchi, from University of Eastern Piedmont, Italy. Stem Cells are cells which have the potential to grow into any cell type, including motor neurones. Fabiola’s research looks at testing the use of mesenchymal (muscle) stem cells as a treatment for ALS/MND.

Information Sheet | Research Team
Information Sheet F – Stem Cells

Listen below to find out more. You can also read Fabiola’s poster abstract for the Symposium here.

Fabiola is also a volunteer with Associazione conSLAncio Onlus, which is an all-volunteer, multidisciplinary Italian ALS Association. conSLAncio develops new initiatives to not only help the Italian community but adds a new dynamic to the global effort to end ALS.

The team from conSLAncio are regulars at the Symposium and have written several guest blogs over the years discussing what it is like to present their work at the Symposium.

Blog | 8 June 2022 | Research Team
Symposium Spotlight: Experience of a Researcher

Make sure you come back after the Symposium to hear more from Fabiola including some of the results of her work and what it means for people living with MND.

Fabiola’s sessions to look out for:

Session 2 – Clinical Trials

Session 9 – Trial Design and Clinical Endpoints

Stay Informed

If you have come across this blog through the Symposium website, or a general search please subscribe (see top right-hand corner of page) and you’ll be notified every time we upload a new article.

You can follow our research account on Twitter. We tweet about up to the minute research and will be tweeting throughout the Symposium using the hashtag #alsmndsymp.

Take a look at the schedule of blogs for November as we continue counting down to the 33rd International Symposium on ALS/MND with our Symposium Blogathon.

To listen to talks live, take part in the Q&As and visit the live poster sessions, register for the International Symposium now.

The MND Association’s vision is a world free from MND. Realising this vision means investing more in research, further developing partnerships with the research community, funding bodies and industry, while ensuring that advances in understanding and treating MND are communicated as quickly and effectively as possible. Our Research Development team, composed of 11 members, work hard to achieve this. Principally, the Research Information team within this are involved in communication activities including this MND Research blog.