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AIDEZ-NOUS DEFEAT MSA MAINTENANT

Defeat MSA Canada est une organisation enregistrée au Canada qui aspire à équilibrer les efforts pour soutenir les patients, éduquer les professionnels de la santé, sensibiliser le public et encourager la recherche prometteuse.

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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

Representing Defeat MSA Alliance & Advocating for People with MSA @American Academy of Neurology (AAN) Annual Meeting www.aan.com/conferences/annual-meeting/- Dr Pratik Bhattacharya, Philip M Fortier & Sandra Bettenhausen & Defeat MSA Awareness Shoe Phil MsaShoe Fortier, Where is the MSA Shoe? in attendance....#aan #AANAM #msa #msaawareness #WeRememberMSA #neurology #defeatmsa #kickmsa ...
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Thank you to our Multiple System Atrophy friends and family for helping us raise awareness during our #Move4MSA and #MoveForThoseWhoCant March campaign. .We asked you to move daily to help bring awareness to MSA and you didn't disappoint! 31 days of moving and encouraging #MSAawareness. Thank you to each and everyone of you who moved for our MSA warriors and MSA angels and thank you for sharing our awareness posts. The work doesn't stop at the end of the month, please donate or continue to spread awareness..With awareness comes funding, with funding comes treatment and a cure! Keep sharing and keep believing. 💜.To our #MSAwarriors: This is for you, keep fighting, keep moving and keep hope!.To our #MSAAngels: We love you, we miss you and we move in your memory..www.MSACanada.ca www.defeatMSA.org.#Move4MSA #MoveForThoseWhoCant #MSAsucks #MSAawareness #DefeatMSA #KickMSA #MSAawarenessmonth #campaign #March #Donate #jerusalema #jerusalemachallengeI do not own the rights to this music ...
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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

MSA AWARENESS WARRIORS ZOOM BACKGROUND

MSA AWARENESS WARRIORS ZOOM BACKGROUND

USE ZOOM? DOWNLOAD A BACKGROUND WHICH HONORS ALL THOSE BATTLING MSA - FOR MSA AWARENESS MONTH! #defeatmsa #kickmsa #msawarriors #zoomlife #zoombackground #msaawarenessmonth #msaawareness #MultipleSystemAtrophy #msaheroes #msahero

“Are we there yet?..No”- Anne Kastelic (Caregiver, Ohio)

"Anne Kastelic (Aide-soignante, Ohio)

Caregiver Blog Post #2 La voie du diagnostic... Sommes-nous déjà arrivés ?...Non Maintenant ?...Non Quand allons-nous y arriver ? Dit toute personne qui a fait un voyage en voiture. Notre voyage a pris 3 ans et demi pour qu'un médecin accepte un diagnostic de "MSA possible/probable" et nous avons vu ...

Blog des chercheurs

POSSIBLE NEW DRUG

POSSIBLE NEW DRUG

Curious about the possible new drug being studied that might slow MSA? See this graphic for information about the mechanism of action (MOA). For Research Updates & More, Register on the Hub: https://defeatmsa.org/research-registry/ #defeatmsa #kickmsa...

“ANNOUNCING NEW MSA GENETIC STUDY IN CANADA”

“ANNOUNCING NEW MSA GENETIC STUDY IN CANADA”

November 23, 2020 WINDSOR, ON - Defeat MSA Canada/Vaincre L’AMS Canada, Defeat MSA Alliance: Defeat Multiple System Atrophy and MSA United International enthusiastically announce a new genetic study in partnership with the Canadian Open Parkinson's Network (C-OPN)....

Blog de l'avocat

GET SOME GEAR & RAISE AWARENESS ALL YEAR LONG!

GET SOME GEAR & RAISE AWARENESS ALL YEAR LONG!

Defeat MSA Canada/Vaincre L’AMS Canada Board Member & MSA Patient Advocate Kelly Murphy tests out the new mug! Maybe a 'wee nip of something strong?  Order One Now! www.MSAcanada.ca There are also online stores for some of our affiliated MSA United charites:...

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

New MSA/AMS Patient Advocate On National Canadian TV !!!

New MSA/AMS Patient Advocate On National Canadian TV !!!

We are grateful to MSA/AMS Patient Advocate Valerie Garneau. Valerie is the new Patient Advocate & Board Member for Defeat MSA/Vaincre AMS Canada. She spoke on national French Canadian TV about Multiple System Atrophy to raise awareness! Thank you Valerie for your...

“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

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Vaincre L'AMS CANADA - une organisation à but non lucratif | PRIVACY POLICY

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