Welcome To
MSA
Down Under
Help us Defeat MSA Now
Defeat MSA Down Under is a registered charity serving the needs of those affected by Multiple System Atrophy in Australia and New Zealand. It aspires to balance patient support, medical education, public awareness and promising research.
News From Social Media
*NEW* IMPORTANT UPDATE - INFORMATION FROM BIOHAVEN | Defeat MSA Alliance
defeatmsa.org
JUNE 1, 2021 DEFEAT MSA ALLIANCE RESEARCH PROGRAM ADVISORS: IMPORTANT QUESTIONS & INFORMATION FROM BIOHAVEN Ā Can I still join the trial? Answer: Enrollment for the phase 3 study closed in July of 20...
Research, Support, Education and Awareness - MSA Down Under
www.msadownunder.org.au
Welcome To MSA Down Under What is Multiple System Atrophy?Learn About MSA and Symptoms, See Known Treatments Learn More Raise AwarenessRaise MSA Awareness, Volunteer to Help, Host MSA Shoe! Learn More...
Just posted a photo https://www.instagram.com/p/CO1OViRHyYl/?igshid=1q4iqvbuliqdl
Off to DENMARK -The MSA Awareness Shoe leaves Greece & heads to the Danish Kingdom!
#KickMSA #DefeatMSA #msaawareness @ Copenhagen, Dennmark https://www.instagram.com/p/COwuDjjHzwl/?igshid=5r062qy45uaf
APRIL - MAY 2021 - VISIT PROFILE URL FOR NEWSLETTER https://www.instagram.com/p/COZb1DQnOUj/?igshid=6rf04gbkjezo
MSA Research
Patient Programs
MSA Education
Public Awareness
Giving Programs
LOOKING FOR OTHER WAYS TO GET INVOLVED?
LOOKING FOR OTHER WAYS TO GET INVOLVED?
MSA Expert
Spotlight
Wouter Peelaerts, PhD
KU Leuven, Belgium
Dr. Wouter Peelaerts is an experienced neuroscientist with special expertise in degenerative brain diseases. He earned his Ph.D. in biomedical sciences fromĀ KU LeuvenĀ and subsequently completed a postdoctoral fellowship there focused on neurobiology and gene therapy under the mentorship of Prof. Veerle Baekelandt. His efforts helped uncover new insights that further link the abnormal protein alpha-synuclein to neurodegenerative diseases, in particular Parkinsonās and Multiple System Atrophy. He has received numerous accolades for his research, including the 2020 JiePie award for MSA research, a prestigious 2017ā2019 Fulbright Fellowship and the ATCG and ID&T postdoctoral award. In 2017, he joined the lab ofĀ Dr. Patrik BrundinĀ at Van Andel Institute, MI, USA. His current research focuses on drug repurposing and how infections can trigger Multiple System Atrophy. Dr. Peelaerts serves on the Scientific and Medical Research Advisory Committee for the six charities that make up MSA United International Consortium, which includes Defeat MSA Alliance (USA). He is Chair of the Allianceās Scientific Research Section.
List of Publications
Christopher T. Tulisiak, Mercado G, Peelaerts W, Brundin L, Brundin P. 2019. Chapter Seventeen ā Can infections trigger alpha-synucleinopathies? Progress in molecular biology and translational science.Ā Vol 168.Ā Pages 299-322.
Quansah E*, Peelaerts W*, Langston JW, Simon DK, Colca J, Brundin P. 2018. Targeting energy metabolism via the mitochondrial pyruvate carrier as a novel approach to attenuate neurodegeneration. Mol Neurodegener 13:28.
*Contributed equally
Peelaerts W, Outeiro TF. 2017. Synuclein misfolding as a therapeutic target. Disease-modifying therapies and targets in neurodegenerative disorders. Academic Press.
Peelaerts W, Baekelandt V. 2016. É-Synuclein strains and the variable pathologies of synucleinopathies. J Neurochem 139(Suppl 1):256ā274.
Spotlight Links
āSticking With MSAā -Dr. Wouter Peelearts (Defeat MSA Alliance Blog Launch, April 2019)
Fulbright grantee (2017ā2018)
Integrated DNA Technologies and Advanced Technologies and Community Giving Foundation award (2017)
FWO postdoctoral fellowship (2017 ā 2020)
Annual Award for Movement Disorders, best scientific article published by a young investigator (2015)
about the
Defeat MSA Awareness Shoe – #KickMSA
The Defeat MSA Awareness Shoe ā¢ has traveled to dozens of countries, rubbed shoulders with some notable people and visited many famous landmarks. The Shoe is a tool for spreading MSA awareness, increasing support for MSA patients and their caregivers and fighting MSA by raising vital research dollars. It’s journey is undertaken in memory of all those that have died due to MSA and in support of all those presently fighting Multiple System Atrophy!
To date, the Shoe has “Kicked MSA” in a dozen countries across the world.
As of 2020, our beloved Shoe is kicking MSA down under. If you are in Australia or New Zealand and you interested in having the Shoe stop by, send us an email: themsashoe@gmail.com
We will do our best to include in the schedule!Ā
#DefeatMSA #KickMSA #DefeetMSA #MSAdownunder
about the
Defeat MSA Awareness Shoe – #KickMSA
The Defeat MSA Awareness Shoe ā¢ has traveled to dozens of countries, rubbed shoulders with some notable people and visited many famous landmarks. The Shoe is a tool for spreading MSA awareness, increasing support for MSA patients and their caregivers and fighting MSA by raising vital research dollars. It’s journey is undertaken in memory of all those that have died due to MSA and in support of all those presently fighting Multiple System Atrophy!
To date, the Shoe has “Kicked MSA” in a dozen countries across the world. Learn more about the story and the globetrotting journey of the MSA Awareness Shoe. #DefeatMSA #KickMSA
Join the world-wide MSA AwarenessĀ initiative
Join the world-wide MSA AwarenessĀ initiative
Patients Need Our Help
Defeat MSA Down Under invites all our friends and allies, around the world, to join us in this noble fight, to speak for those who cannot, with one mind, one heart and one voice: to Defeat MSA forever!
Join the world-wide MSA AwarenessĀ initiative
Our Legacy Grants
Our Legacy Grants
The Defeat MSA Down Under special Individual Named Legacy Grants program enables donors to fund a scientific research, medical education, patient support or public awareness grant and name it in their own name, in tribute to someone or in memory of a loved one. The Legacy Grants program designates four levels of grants: $15,000 (Platinum), $10,000 (Gold), $5,000 (Silver) and $2,500 (Bronze). MSA research grants begin at the $10,000 level. Please email us: director@msadownunder.org.au
MSAĀ BlogsĀ
Caregiver’s Blog
No Results Found
The page you requested could not be found. Try refining your search, or use the navigation above to locate the post.
Researcher’s Blog
āANNOUNCING NEW MSA GENETIC STUDY IN CANADAā
November 23, 2020 WINDSOR, ON ā Defeat MSA Down Under sister charities, Defeat MSA Canada/Vaincre LāAMS Canada, Defeat MSA Alliance: Defeat Multiple System Atrophy and MSA United International consortium enthusiastically announce a new genetic study in partnership...
āREM Sleep Behavior Disorder, Genetics and MSAā By Lynne Krohn (McGill, MontrĆ©al)
Lynne Krohn, PhD student, McGill University (MontrƩal) A major goal in MSA research is to develop successful clinical interventions which can stop or slow the disease progression. Currently, there are options available for symptomatic treatment of MSA, but no...
Advocate’s Blog
CAMPAIGN TO INCLUDE ALL NEW ZEALANDERS IN HEALTHCARE REFORM
ATTENTION WORLDWIDE MSA COMMUNITY: In support of our MSA community in NZ, we need your support for a campaign in Parliament to include all New Zealanders living with a Rare Disorder in healthcare reform. No matter where you are in the world, please consider adding...
Defeat MSA USA, MSA Down Under & MSA United Announce Research Congress
ST. CLAIR SHORES, MI, February 10, 2021 - DEFEAT MSA ALLIANCE is pleased to announce its sponsorship of the 7th International Congress of Multiple System Atrophy: Toward a Cure for Multiple System Atrophy. In 2020, Defeat MSA Alliance, along with 6 other partnering...
GIVE HELP, GIVE HOPE – RAYS OF HOPE HOLIDAY FUNDRAISER!
GIVE HELP, GIVE HOPE - ANNOUNCING THE 2020 RAYS OF HOPE HOLIDAY FUNDRAISER! Help Us Support MSA Research in Australia and New Zealand! Help Us Support MSA Patients and Carers in Australia and New Zealand! Help Us Support MSA Awareness in Australia and New Zealand!...
Patient’s Blog
No Results Found
The page you requested could not be found. Try refining your search, or use the navigation above to locate the post.
“Defeat MSA allied charities were formed to give voice to those affected by this little known, devastating disease. Indescribable grief and suffering has been channeled into positive action to help fund crucial research and provide ongoing support for those dealing with MSA. Each one of the Defeat MSA charities are worthwhile organizations. I hope to see each of them continue to grow and reach more and more people in need.”
Elena Fracassa, MS
“All the charities associated with Defeat MSA are committed to the funding of clinical research, that kind which is most valuable to patients living with MSA today. Defeat MSA is also dedicated to supporting patients, educating medical professionals and raising public awareness. This disease does not have a marathon or a 5k run; instead they use an intriguing device: a traveling shoe in a symbolic marathon to spread awareness within the medical community and among the general public about this devastating disease.”
Dr. Pratik Bhattacharya, MD, MPH
LOOKING FOR OTHER WAYS TO GET INVOLVED?
JOIN THE MOVEMENT TOĀ #DEFEATMSA
Follow us on Twitter
Follow us on Facebook
Follow us on Instagram
Follow us on YouTube
Follow us on LinkedIn
Follow us on Twitter
Follow us on Facebook
Follow us on Instagram
Follow us on LinkedIn
Follow us on YouTube
Get Involved
