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September 2011 :
A day with Fabienne Larouche to visit the recording studios of "30 vies"

 

2011 :
Part of the profits will be given to the foundation. Come get ready for fall with our advices and to drink a good glass of wine. Price and sample will be given away.

 

7 April 2011


A BREATH OF HOPE formed to children with opsoclonus myoclonus-SYNDROME WITH RARE DISEASE IN A CHILD TEN MILLION IS REACHED.

Blainville, April 7, 2011 - Laurie-Ann Foundation Duchaine is a nonprofit organization whose primary mission is to improve the quality of life for people with opsoclonus myoclonus syndrome, as well as their families.

It is named after a daughter Laurie-Ann who was diagnosed three weeks after his first anniversary in 2002 with this syndrome.

That in order to consolidate other families with the same neurological problem that the idea came to create this foundation.

The story of Laurie-Ann has appeared in various newspapers and even made about television and radio. Laurie-Ann Foundation Duchaine has set four main goals: provide financial support to families regarding the costs incurred by the disease, opsoclonus myoclonus promote the disease worldwide, improve the quality of life for families whose child has of the disease and opsoclonus myoclonus and actively participate in medical research on the syndrome of opsoclonus myoclonus.

She self-financing through contributions of its members, individual and corporate donations and various campaigns and fundraising events. The Laurie-Ann Duchaîne Foundation invites you to his press conference to be held April 14 at 10:00 Bleu, Blanc, red for the unveiling of the outline of his first campaign fundraiser whose goal is to raise $ 20 $ 000.00.

In order to achieve this, a dinner show hosted by Claudia Marques and guest artists will be held on May 10 from 18:00 to 22:00 at the restaurant Blue, White, Red. Tickets go on sale at a cost of $ 99.00 per person.

An auction hosted by Yvon Lambert, former hockey player of the Montreal Canadiens, will also visit the site. More details on the mission of the Foundation and opsoclonus myoclonus syndrome, will be given at holding the press conference. Please help us to make the life of a sick child and his parents better.

A sick child is already asking so much energy that her parents should not have to do all this research, namely that can help and how. That is why the Foundation Laurie-Ann Duchaine was created, more than a month.

WHAT?

  • Unveiling the outline of the mission given that the Foundation
  • Unveiling of the first campaign fundraising goal $ 20,000,00
WHO?
  • Presentation by Laurie-Ann Duchaine, aged 9 years, reaching the opsoclonus myoclonus syndrome, official spokesperson of the Foundation of the same name.
  • Marie-Eve Lanthier, Foundation President Laurie-Ann Duchaîne.
  • Claudia Marques, master of ceremonies.

WHEN?

  • Thursday, April 14 at 10:00

WHERE?

  • Restaurant Blue, White, Red 399, boul. Labelle Rosemere
  • You must RSVP no later than Monday, April 11, 2011 from PB Communications 514-567-6534 or email p.beland@communicationspb.com