Visiting children with rare diseases and listening to their dreams
2022-09-07
Bauer Equipment supports Lifewire’s charity drive, visits rare disease families, and learns about their dreams and reflections.
Supply donations to patients to welcome Mid-Autumn Festival
2022-09-03
Lifewire shares Mid‑Autumn joy with rare disease patients, thanks to donations of chicken essence, mooncakes, masks and daily supplies.
Charity Screening Addresses Sick Children
2022-08-19
Thanks to 一杯涼水, nearly 100 Lifewire families enjoyed two touching charity film screenings.
Master 7 loves sick children, even Master 7 can sing and laugh
2022-08-16
Master 7 invited Lifewire’s rare disease children to her concert, spreading joy and positive energy amid the pandemic.
Lifewire becomes a recipient of the "Green Health Association"
2022-08-10
Lifewire joins Green Health Association, thanks members for supporting rare disease children and promoting green living.
Support The [童你補身] Project
2022-08-10
Tsz Kin and other rare disease kids suffer muscle degeneration. Mothers strive to care for them, and [童你補身] needs your support for their health supplements.
A Letter from Kwan Yi, a girl with spinal muscular atrophy to chase her dreams
2022-07-26
Despite SMA, Kwan Yi creates vivid art with strong will and shares gratitude through her works and thank-you letters.
Next Stop, Master's Degree
2022-07-12
Despite SMA, Pei Shan graduated from HKU with a full scholarship. Lifewire’s "童你追夢" helps with her transport costs for master’s study.
Victor Golf Charity Tournament⛳
2022-07-11
Victor hosted a charity golf tournament, raising HK$150,000 to support rare disease children’s treatment.
A 60-year-old "girlish mind" mother chases her dreams with children with a rare disease
2022-07-08
60-year-old June donates all pole dance birthday party proceeds to Lifewire’s Children Chasing Dreams, inspiring rare disease kids to pursue dreams.
Lifewire X Lions Club 【Children's Dreams】 Painted Wall At Sai Wan
2022-06-23
Colorful mural at Kennedy Town’s Pui Fai Road Rest Area, created by rare disease kids, families & volunteers to raise awareness and promote inclusion.