Great Taichung TV series

Great Taichung TV Series, with great enthusiasm, which social enterprise concerns about public welfare groups, produced 6 episodes of programs, starting with the understanding of rare diseases, and cooperating with the documentary film created by Jingyi University and rare disease families in 2017 to discuss the impact of different diseases on life and how to bring in various resources to help the rare disease families to hope that the public can comprehend the real world of the rare disease families with videos.

People can watch the series by Youtube. URL:
https://www.youtube.com/watch?v=Slb-2rZr97k&list=PLVNFy-oJNjk53Q6N6gAagfBsHRRbHq-oO&index=4 

EP1: Williams syndrome
Tung-yun, a multiply handicapped, owns her family’s endless love and grows up gradually in her life. We should both help her on the long road ahead.

EP2: chromosome abnormality
Wei-chia, unable to communicate with the world in any language, uses his eyes to observe the world. His parents construct a bridge with love and patience between him and the outside.

EP3: Marfan Syndrome
Chien-Feng, a shy young man, is extremely talent in his inner world. Inspired by his congenial mom, he can create his own work in confident and comfortable environment, guadually be more independent. 

EP4: Marfan Syndrome
Boring life day to day is daily roitine of many rare disease families. Although this kind of life is really ordinary, it is what the caregivers yearn extremely for.

EP5: Multiple Sclerosis
The conversation with the doll is the most sincere frankness of Hsin-chieh. Only finding the expression of suffering from rare disease can she enhance with motion.

EP6: mitochondrial defect
A girl expects that she can fulfill her dream on her own. Hsin-chiao always smiles with sweet, going ahead to her dream step by step. Although her steps move slowly, the dream never ends.

Translator: Flora (Treacher Collins syndrome), Reviewer: Sandy