Adah’s page

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Thank you for visiting my fundraising page..


Adah is a beautiful, smart and sweet girl. She was diagnosed with Rett Syndrome when she was almost 3 yrs old. Adah is much aware of her limitations and she wishes to be like any other child that speaks, plays, runs and have a normal life.


Donating through this website is simple, fast and secure.


What is Rett Syndrome?

Rett Syndrome is serious lifelong neurological disorder that is caused by random mutations in a gene called MECP2. Diagnosed almost exclusively in girls, symptoms typically appear in toddlerhood. Many children with Rett are unable to speak, walk or use their hands. Breathing problems, feeding tubes, seizures, anxiety, gastrointestinal and orthopedic issues are common.

Despite the debilitating nature of the disorder our girls are so much more than a laundry list of symptoms. Their beauty and their strength inspire and motivate us.

Rett Syndrome stands apart from other neurological disorders due to the dramatic reversibility of symptoms in animal models. Our confidence that Rett Syndrome is curable guides our every decision.

Learn more about Rett here.

Who is RSRT?

The Rett Syndrome Research Trust (RSRT) was launched in 2008 with a singular goal: to drive the development of treatments and cures for Rett Syndrome and related MECP2 disorders. As one of the few neurological disorders to demonstrate dramatic symptom reversal in the lab, Rett Syndrome has captured the attention of the world’s premiere university and pharmaceutical industry scientists. RSRT is operating at the nexus of this activity, leading and advancing the research agenda.

By funding the most Rett research worldwide, $35 million since 2008, we strive to put ourselves out of business as soon as possible.

Learn more about RSRT here.

Supporters (4)

  1. Patricia Daniels 
    11 months ago
    $50
  2. BRUCE COHN 
    11 months ago
    $25
  3. Graziella Cohn 
    11 months ago
    $25
  4. Graziella Cohn 
    11 months ago
    $25

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