Stacy Deanne: The Little Girl Whose Life Inspired a Lifetime of Advocacy
4.2 out of 5
Language | : | English |
File size | : | 352 KB |
Text-to-Speech | : | Enabled |
Screen Reader | : | Supported |
Enhanced typesetting | : | Enabled |
Print length | : | 216 pages |
Lending | : | Enabled |
Stacy Deanne was born in 1985 with a rare genetic disorder called Angelman syndrome. This disorder affects the nervous system and causes severe intellectual and physical disabilities. Stacy was unable to walk, talk, or feed herself. She also had seizures and other health problems.
Despite her challenges, Stacy was a happy and loving child. She loved to be around people and would often smile and laugh. She brought joy to everyone who knew her.
Stacy's parents, Debbie and Dave, were determined to give their daughter the best life possible. They worked tirelessly to find the best medical care for her and to provide her with a loving and supportive home. They also became advocates for other families with children with disabilities.
In 1995, Debbie and Dave founded the Stacy Deanne Foundation. The foundation's mission is to provide support and resources to families with children with disabilities. The foundation also works to raise awareness of Angelman syndrome and other rare genetic disorders.
Stacy Deanne passed away in 2001 at the age of 16. Her legacy continues to live on through the foundation that bears her name. The Stacy Deanne Foundation has helped thousands of families with children with disabilities. It has also raised awareness of Angelman syndrome and other rare genetic disorders.
Stacy Deanne's life was a testament to the power of love and advocacy. She showed the world that everyone, regardless of their abilities, deserves to be loved and valued. Her story is an inspiration to us all.
Here are some ways that you can support the Stacy Deanne Foundation:
- Donate to the foundation
- Volunteer your time
- Raise awareness of Angelman syndrome and other rare genetic disorders
- Support families with children with disabilities
Together, we can make a difference in the lives of children with disabilities.
4.2 out of 5
Language | : | English |
File size | : | 352 KB |
Text-to-Speech | : | Enabled |
Screen Reader | : | Supported |
Enhanced typesetting | : | Enabled |
Print length | : | 216 pages |
Lending | : | Enabled |
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4.2 out of 5
Language | : | English |
File size | : | 352 KB |
Text-to-Speech | : | Enabled |
Screen Reader | : | Supported |
Enhanced typesetting | : | Enabled |
Print length | : | 216 pages |
Lending | : | Enabled |