tattoo Brown Rahman Syndrome, DMNT3A, TBR

My name is Janice Hill from the Midwest. The reason to raise as much money as possible is to help with research. All money received will go To support research and education efforts for this newly identified, rare syndrome. To educate the greater community and raise awareness. To provide support for families in need of assistance. As the research is ongoing there is no time limit to receive funds. Please donate as much as you would like. My grandson, Ayden Isaacs was diagnosed with this rare mutation and I would love for him to get all the help possible. TBR Syndrome was just discovered in 2014 and is so new that there are only about 20 children who have been diagnosed with this rare condition.