IMP Launches New TK2d Video
To mark TK2d Awareness Day 2025, we’ve released a new video that amplifyies the voices of those living with and affected by TK2d, a rare mitochondrial disease.
We’re honoured to share a powerful video featuring three members of the TK2d community:
- Lisa speaks with courage and love about the early signs of TK2d and the heartbreaking loss of her daughter, Lacey.
- Aneesa reflects on her son Jeremiah’s diagnosis and the hope sparked by a clinical trial.
- Viviane, an adult living with TK2d, shares the long journey to diagnosis and the strength she’s found in connecting with others who understand.
Their stories are deeply personal, but they also speak to a collective need for greater awareness, more research, and stronger support systems for everyone affected by TK2d.
Please take a moment to watch, share, and help us spread the word. Every view, every share, every conversation helps increase awareness.
This video is also available with subtitles in the following languages: