Рет қаралды 18
Sarah Noble lives with a rare genetic disease Mucolipidosis! alpha/beta. Mucolipidosis is considered part of the Ultra-orphans of the Lysosomal Storage Disease family of which there are over 60 known different disorders. There is no cure or treatment for this disease ML. This short is about my week in style. What I got up to heading towards my holiday.
Thank YOU for supporting me, it means the world to me!
It would really help support my channel if you could LIKE my video, SUBSCRIBE to my channel and press the BELL button so you never miss a video! which are just about my life and how I deal with day-to-day things.
LET'S CONNECT!
Facebook - @rarelifestories
Instagram - @rarelifestories
Until them I wish you peace, happiness and lots of love. Sarah Noble