Her name means "big swallow," but sporadic ALS has momentarily "frozen" her wings. Ming Dayan was diagnosed in 2021, and she’s now in her fourth year of living with the disease. By her side is husband Peng Chao – "super" is right – whose unwavering support 💖 helps them face each day.
To keep things on track, they set alarms every 15 minutes. Whether it’s a quick breathing exercise, a sip of water, or a moment to laugh together, these gentle reminders bring structure and hope 🕒✨.
They’ve even pledged their legacy to science, planning to donate to ALS research 🔬, so future patients might have stronger wings to fly. It’s their way of turning hardship into purpose.
Despite the disease’s cruelty, Ming and Peng refuse to focus on the negatives. Their story reminds us that love, routine, and a dash of bravery can light up the darkest days. Here’s to more frozen wings taking flight again 🦋.
Reference(s):
How a Chinese couple navigates the challenges of ALS together
cgtn.com
