Hong Kong Star Stephanie Ho Reveals Son's Angelman Syndrome Diagnosis to Raise Awareness

Hong Kong Cantopop star Stephanie Ho and her husband, actor Frederick Cheng, have publicly revealed that their 2-year-old son, Asher, has been diagnosed with Angelman Syndrome, a rare genetic disorder. The couple shared this personal news on Instagram and during a public appearance on Lawrence Cheng's show 'HiEggo' on June 1, 2024, to raise awareness about the condition.

Raising awareness about Angelman Syndrome can lead to increased research and funding for the rare genetic disorder, leading to significant improvements in the lives of affected individuals and their families. By sharing their personal story, Stephanie Ho and her husband can help reduce stigma and encourage others to seek support, potentially leading to earlier diagnoses and better outcomes.

Angelman Syndrome is a neurodevelopmental disorder caused by the absence of a functional UBE3A gene on chromosome 15. It affects approximately 1 in 10,000 to 20,000 individuals and results in developmental, behavioral, and medical challenges. People with Angelman Syndrome often have happy demeanors but face significant difficulties, including being non-verbal and prone to seizures.

Ho and Cheng initially thought Asher's development was slower because of a delay, but further testing revealed the rare genetic disorder. The diagnosis was made last year, and the couple decided to share their story to support other families facing similar challenges. Ho expressed their emotional experience, saying, *"Finding out about his disorder broke our hearts and we grieved for the healthy child we once imagined, running, playing music, going to college, but it also gave us a clearer direction in ways to support him in the future."*

Despite the initial shock, the couple has united in their determination to support their son. They have sought information about Angelman Syndrome, reached out to support groups, and connected with other families facing similar challenges. Frederick Cheng initially struggled to accept the diagnosis, feeling responsible for his child's suffering, but has since become an active advocate for raising awareness.

Ho emphasized the importance of understanding their son's unique needs and adjusting their expectations. She said, 'I had to adjust my mindset and gain a clear understanding of our child's actual situation and needs.' She also expressed concerns about Asher's future, which motivates her to work harder and prepare to be his pillar of support. Despite the challenges, Ho finds inspiration in Asher's resilience and joy.

The couple is organizing a charity concert to provide assistance and support to patients and their families affected by Angelman Syndrome. They aim to raise awareness about the condition by sharing their story and encouraging other caregivers to seek support. Ho wrote on Instagram, *"We understand that caregiving for a special-needs child can be isolating, and we want other carers to know that they are not alone in this experience."*

Currently, there is no specific therapy or medication for Angelman Syndrome, but clinical trials are in progress. Treatment focuses on managing symptoms, including medication to control seizures. Ho remains hopeful for a cure, stating, 'We are positive and hopeful that in the near future there will be a cure for this rare disease.'

According to the Hong Kong Angelman Syndrome Foundation, there are approximately 60 confirmed cases of the condition in the region, with potentially more undiagnosed individuals. The disorder is usually diagnosed between the ages of 2 and 5 years when characteristic behaviors and features become more evident.

Ho and Cheng's decision to share their son's diagnosis aims to cultivate a supportive community for families affected by Angelman Syndrome. As Ho stated, *'We'll be forever by your side. We love you so much, baby Asher.'*

Key Takeaways

• Hong Kong celebrity couple Stephanie Ho and Frederick Cheng reveal their 2-year-old son Asher has Angelman Syndrome.
• Angelman Syndrome is a rare genetic disorder affecting 1 in 10,000-20,000 individuals, causing developmental and behavioral challenges.
• The couple aims to raise awareness and support for affected families, reducing stigma and encouraging earlier diagnoses.
• There is currently no cure, but treatment focuses on managing symptoms, and clinical trials are in progress.
• The couple is organizing a charity concert to support patients and families affected by Angelman Syndrome.