Join me in making a difference! This October as your probably know is Rett Syndrome Awareness Month and for the month of October I will be walking 5kms everyday, maybe dying my hair purple and once again I will be going Speechless for 24 hours. 100% of all funds raised will go to the RSAA who fund all aspects of research, enable drug trials, support families to attend such trials, sponsor family gatherings, spread awareness and host the 9th Rett world congress just to name a few. Her Fight is My Fight.
Formed in Melbourne in July 1989, the Rett Syndrome Association of Australia Inc. (RSAA) is a not-for-profit organisation which is managed by a Committee of volunteers, most of whom are parents of Rett syndrome children. RSAA is currently working on running clinical trials in Australia.
Formed in Melbourne in July 1989, the Rett Syndrome Association of Australia Inc. (RSAA) is a not-for-profit organisation which is managed by a Committee of volunteers, most of whom are parents of Rett syndrome children. RSAA is currently working on running clinical trials in Australia.
Love Tabitha RS