show video detail
Girl, 17, battling rare disease that transforms her muscle into a second skeleton
- Published_at:2013-07-29
- Category:News & Politics
- Channel:iknewitb4u
- tags:
- description: Seanie Nammock has FOP - an incredibly rare genetic condition Her muscle and tendons are slowly turning to bone The slightest knock can cause painful flare-ups and lock up her body Just 600 people in the world have FOP, which receives little funding With her painstakingly-applied make up and fashionable clothes, Seanie Nammock is like any other teenager. But behind her stylish looks, the teenager is battling a devastating genetic condition that is slowly paralysing her. The 17-year-old, from West London, is suffering from fibrodysplasia ossificans progressiva (FOP), a disorder that is turning her muscle and tendon into bone.
| ranked in date | views | likes | Comments | ranked in country (#position) |
|---|---|---|---|---|
| 2013-07-31 | 5,763 | 5 | 0 |
( ,#98)
|
