My name is Luiza Simon ,my mother and I are symptomatic carriers of haemophilia A(mild) , and my brother has severe haemophilia A and this year ,on the International Haemophilia Day ,I’m looking forward to raise money for the Haemophilia Foundation Australia to support all the programs and research’s that they do to help all the families and people in need , and to bring awareness about what it is haemophilia. I hope you can join this cause with me =) and thank you in advance for being part of this.
Haemophilia Foundation Australia (HFA) is the national peak body that represents people with haemophilia, von Willebrand disease and other bleeding disorders, and their families.
Haemophilia Foundation Australia (HFA) is the national peak body that represents people with haemophilia, von Willebrand disease and other bleeding disorders, and their families.
Lu, we’re proud of you! Keep up the good work.