
Rick asked me the other day if we are going to have a honeymoon and I realized that if we take one the week after the wedding, it will be a last minute road trip that we plan the day after the wedding!
Spontaneous getaways are always the most fun anyway...
Meanwhile, we are combining business with pleasure since we already had this trip booked before planning the wedding.
One month after the wedding, we will be attending the Myelin Project Annual Meeting being held in Toronto this year. Through our foundation, Cure ALD, we sponsored a table at the fundraising gala. We have eight seats open if anyone wants to join us!
SCIENCE AND SOCIETY GALA
Hosted by the Canadian Myelin Project
Four Seasons Hotel - Toronto
Friday October 23, 2009
7:00 PM
This inaugural event is part of The Myelin Project Annual Meeting being held in Toronto this year and hosted by the Canadian Myelin Project. This is the annual meeting of The Myelin Project Scientific Advisory Panel and scientific researchers from all over the world that are invited to come and present their research findings. This meeting will host approximately 15 world-renown researchers. This event will give partrons the opportunity to sit with a scientist for the duration of the dinner during the gala.
Tickets to the gala and table sponsorships are still available
regular table $250 individual or $2500 for the table
scientist table $350 individual or $3500 for the table
the scientist table is for 11 people, the 11th person is the scientist...
nice option...you get to sit with a scientist!!
Funds raised will go towards the Augusto Odone Young Investigator Award for Adrenomyeloneuropathy (AMN) research and Sick Kids Hospital that has performed successful Bone Marrow Transplant (BMT) procedures on boys with Adrenoleukodystrophy (ALD).
For more information, please contact Helen Hatzis at the
Canadian Myelin Project Helen.hatzis@myelin.org
On line registration for this event is available at http://www.myelin.org/en/cev/22
Diane joined the Myelin Project Board of Directors when her son, Wyatt, was diagnosed with ALD in 2002. If you decide to make a contribution to them directly, please name Wyatt Zmrzel or Diane Suchomel in the "Dedicated on behalf of" section. You may also donate to Cure ALD Foundation: www.cureald.org