BENEFITING: ANGIOMA ALLIANCE
EVENT DATE: May 01, 2017
In 2002, Angioma Alliance began with a mother, an infant, and a need. Connie Lee, President and Founder of Angioma Alliance and parent of a child with CCM states,”Fifteen years have allowed us to create a national and international community where there was none, to drive research to the cusp of better treatments, and to provide real hope to the thousands of families living with cavernous angioma. I am profoundly grateful.”
WE HAVE COME A LONG WAY, BUT WE HOPE YOU WILL JOIN US IN SUPPORTING OUR MISSION FOR THE NEXT 15 YEARS.
$15 FUNDS THE COSTS ASSOCIATED WITH PROVIDING FIVE PATIENT BOOKLETS TO PEOPLE WITH CCM AND THEIR LOVED ONES.
$150 FUNDS ATTENDANCE OF ONE YOUNG RESEARCHER INTERESTED IN FINDING A TREATMENT OF CCM TO THE SCIENTIFIC MEETING.
$1,500 FUNDS GENETIC TESTING AND COUNSELING FOR ONE INDIVIDUAL.
$15,000 FUNDS 3 REGIONAL PATIENT MEETINGS.
PLEASE DONATE here.
You can also donate by mail to: Angioma Alliance, 520 W 21st St Ste. G2-411, Norfolk, VA 23517
IF THE ANGIOMA ALLIANCE COMMUNITY HAS HELPED YOU, PLEASE SHARE WITH US ON FACEBOOK. Angioma Alliance is a national 501c3 nonprofit patient advocacy and research organization whose mission is to inform, support and empower individuals affected by cavernous angioma and drive research for better treatments and a cure. because brains shouldn’t bleed.® For more info go to www.angioma.org