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AIDEZ-NOUS DEFEAT MSA MAINTENANT

Defeat Multiple System Atrophy (MSA) Canada/Vaincre L’atrophie Multisystématisée (AMS) Canada is a Canadian registered organization that aspires to balance efforts to support patients, educate medical professionals, raise public awareness, nurture promising research and advocate for the MSA community.

 

GIVE HELP, GIVE HOPE

  • Help Us Support MSA Research in Canada!
  • Help Us Support MSA Patients in Canada!
  • Help Us Support MSA Awareness in Canada!
  • Help Us Educate Medical Professionals in Canada!

4 Ways to Support Our Efforts:

1) Create a Facebook Fundraiser: https://www.facebook.com/fund/defeatmsacanada/

2) Create a Canada Helps Fundraiser (dedications to a loved one are possible too): https://www.canadahelps.org/en/charities/defeat-msa-multiple-system-atrophy-canada/

2) Donate Directly to Our Secure Website (dedications to a loved one are possible too): www.msacanada.ca/donate-to-us/

4) Via Cheque, Send to:  Defeat MSA Canada/Vaincre AMS Canada,  3041 Dougall Avenue, Suite 208, Windsor, Ontario N9E 1S3

HELP US GIVE HOPE.  CLICK OUR LINKTREE TO CHOOSE ONE A FUNDRAISER:  https://linktr.ee/defeatmsacanada

NO AMOUNT IS TOO SMALL – BECAUSE EVERY AMOUNT GIVES HOPE TO THOSE THAT NEED IT! 

Help Put Canada on the MSA Map! Help All Those Affected By MSA in Canada!

NOUVELLES MÉDIAS SOCIAUX

Cover for Defeat MSA Canada/Vaincre l’AMS Canada
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Defeat MSA Canada/Vaincre l’AMS Canada

Defeat MSA Canada/Vaincre l’AMS Canada

Defeat Multiple System Atrophy (MSA) Canada/Vaincre Atrophie Multisystématisée (AMS) Canada aspires to balance support, education, awareness and research. Help Us Speak for Those That Cannot!

TERRIFIC TURNOUT FOR THE FIRST ANNUAL JERRY CARROLL MSA AWARENESS 5K IN DAWSONVILLE, GA (USA)! Thank you to the Carroll Family and Friends! #inmemorial #jerrycarroll #defeatmsa #KickMSA #MSAresearchWant to organise a run in your town for Defeat MSA Canada/Vaincre l’AMS Canada ?Email us: defeatmsa@gmail.com ... See MoreSee Less
Voir sur Facebook
Voir sur Facebook
The team at Fluidic Analytics helped #KickMSA @Synuclein Meeting in Leuven,Belgium (April 12-15,2022). Fluidic Analytics was top commercial sponsor of the MSA related research meeting and Defeat MSA Alliance, our US partner was the top charity sponsor. #defeatmsa #MSAresearch #Synuclein #leuven #kuleuven #belgium #science Monika Piziorska Alex Spice ... See MoreSee Less
Voir sur Facebook

#Pyramidal sign is a motor feature in @GreenJournal & @MDJ_Journal criteria for #MSA dx. Why is it important to look for? 🧐

🧠Could it be explained by #GCI severity?
🗣️Is it related to stridor, autonomic, and subtypes?

Pls see our article @ANA_journals http://doi.org/10.1002/acn3.51576

The team @fluidicanalytic helped #KickMSA @Synuclein Meeting in Belgium,April 12-15,2022. Fluidic, a top commercial sponsor & Defeat MSA Alliance (our US partner) was the top charity sponsor.
#defeatmsa #MSAresearch #synuclein #leuven #kuleuven #belgium

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À LA RECHERCHE D'AUTRES MOYENS DE PARTICIPEZ ?

À LA RECHERCHE D'AUTRES MOYENS DE PARTICIPEZ ?

EXPERT MSA
SPOTLIGHT

Wouter Peelaerts, PhD

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 from KU Leuven 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 Parkinson’s and Multiple System Atrophy. He has received numerous accolades for his research, including the 2020 JiePie award for MSA research, a prestigious 2017–2019 Fulbright Fellowship and the ATCG and ID&T postdoctoral award. In 2017, he joined the lab of Dr. Patrik Brundin 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 Alliance’s Scientific Research Section.

Liste des publications

Christopher T. Tulisiak, Mercado G, Peelaerts W, Brundin L, Brundin P. 2019. Chapter Seventeen – Can infections trigger alpha-synucleinopathies? Progress in molecular biology and translational science. Vol 168. 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. ɑ-Synuclein strains and the variable pathologies of synucleinopathies. J Neurochem 139(Suppl 1):256–274.

 

Liens utiles

“Sticking With MSA” -Dr. Wouter Peelearts (Defeat MSA Alliance Blog Launch, April 2019)

Fulbright grantee (2017–2018)

Integrated DNA Technologies and Advanced Technologies and Community Giving Foundation award (2017)

FWO postdoctoral fellowship (2017 – 2020)

Annual Award for Movement Disorders, best scientific article published by a young investigator (2015)

sur la

Vaincre la chaussure de sensibilisation de la MSA - #KickMSA

La chaussure de sensibilisation Defeat MSA ™ a voyagé dans de nombreux pays, a côtoyé quelques personnalités et a visité de nombreux sites célèbres. The Shoe est un outil de sensibilisation à la MSA, qui permet d'accroître le soutien aux patients atteints de MSA et à leurs soignants et de lutter contre la MSA en recueillant des fonds essentiels pour la recherche. Son voyage est entrepris en mémoire de tous ceux qui sont morts de la MSA et en soutien à tous ceux qui luttent actuellement contre l'atrophie multisystémique !

Jusqu'à présent, la chaussure a "donné un coup de pied à la MSA" dans de nombreux pays du monde. Pour en savoir plus sur l'histoire et le voyage du MSA Awareness Shoe, cliquez sur l'onglet MSA Awareness ou visitez son site web : www.MSAshoe.org

#DefeatMSACanada #KickMSA #MSAcanada #DefeatMSA

sur la

Vaincre la chaussure de sensibilisation de la MSA - #KickMSA

La chaussure de sensibilisation Defeat MSA ™ a voyagé dans de nombreux pays, a côtoyé quelques personnalités et a visité de nombreux sites célèbres. The Shoe est un outil de sensibilisation à la MSA, qui permet d'accroître le soutien aux patients atteints de MSA et à leurs soignants et de lutter contre la MSA en recueillant des fonds essentiels pour la recherche. Son voyage est entrepris en mémoire de tous ceux qui sont morts de la MSA et en soutien à tous ceux qui luttent actuellement contre l'atrophie multisystémique !

Jusqu'à présent, la chaussure a "donné un coup de pied à la MSA" dans de nombreux pays du monde. Pour en savoir plus sur l'histoire et le voyage autour du monde de la chaussure de sensibilisation à la MSA, cliquez sur l'onglet "sensibilisation" ou visitez son site web : www.MSAshoe.org

#DefeatMSA #MSACanada #KickMSA #DeFeetMSA

Rejoignez le réseau mondial MSA Sensibilisation initiative

BESOINS DES BREVETÉS NOTRE AIDE

Defeat MSA Canada invite tous nos amis et alliés, partout dans le monde, à se joindre à nous dans ce noble combat, à parler au nom de ceux qui ne peuvent pas, avec un seul esprit, un seul cœur et une seule voix : vaincre MSA pour toujours !

Rejoignez le réseau mondial MSA Sensibilisation initiative

NOTRE HÉRITAGE SUBVENTIONS

NOS

HÉRITAGE

SUBVENTIONS

Le Vaincre la MSA Canada personne spéciale nommée Subventions d'héritage permet aux donateurs de financer une bourse de recherche scientifique, d'éducation médicale, de soutien aux patients ou de sensibilisation du public et de la nommer en leur nom propre, en hommage à une personne ou en mémoire d'un être cher. Le programme Subventions d'héritage désigne quatre niveaux de subventions : $10.000 (Platine), $8.000 (Or), $5.000 (Argent) et $2.000 (Bronze) en plus de Subventions d'héritage des collectes de fonds de départ à $1000 chacune. Veuillez nous envoyer un courriel : legacyfunds@MSAcanada.casi vous souhaitez en savoir plus sur ce cadeau durable.

MSA BLOGUE 

Blog des aidants

Blog des chercheurs

Alterity reports additional support for ATH 434

Alterity reports additional support for ATH 434

ALTERITY PRESS RELEASE: MELBOURNE, AUSTRALIA AND SAN FRANCISCO, USA – 4 November 2021: Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) (“Alterity” or “the Company”), a biotechnology company dedicated to developing disease modifying treatments for neurodegenerative...

MODAG Collaboration Update – MSA Drug

MODAG Collaboration Update – MSA Drug

Congratulations to MODAG! On behalf of MSA/AMS patients around the world, we are thankful for your efforts! 💜. https://www.tevapharm.com/news-and-media/latest-news/teva-and-modag-announce-licensing-collaboration-for-neurodegenerative-disease-drug-candidate/

Blog de l'avocat

MSA AWARENESS ANGELS ZOOM BACKGROUND

MSA AWARENESS ANGELS ZOOM BACKGROUND

USE ZOOM? DOWNLOAD A BACKGROUND WHICH HONORS THOSE LOST TO MSA, ALL OUR ANGELS - FOR MSA AWARENESS MONTH! #defeatmsa #kickmsa #msaangels #zoomlife #zoombackground #msaawarenessmonth #msaawareness #MultipleSystemAtrophy

Patient’s Blog

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“Defeat MSA Canada is an amazing organization, giving voice to those affected by this little known, devastating disease. This grass roots effort grew as a work of love and devotion by its founders. Indescribable grief and suffering has been channeled into positive action to help fund vital research and provide support for others dealing with MSA. It is an important and worthwhile organization and I hope to see it continue to serve more and more Canadians in need.”

Elena Fracassa, MS

“The charity remains true to its objective of supporting patients and families living with this dreadful disease, through supporting vital research and helping to network to connect families affected by MSA. This disease does not have a marathon or a 5k run in its name; the charity uses an intriguing device: a traveling shoe as a symbolic marathon to spread awareness among lay public about this devastating disease. “

Dr. Pratik Bhattacharya, MD, MPH

Copyright 2021 | Defeat MSA CaNADA -  a REGISTERED CHARITABLE Organization | PRIVACY POLICY

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