Living with limb girdle muscular dystrophy: Cerys

In September Cerys shared her unique and inspirational story, living with limb girdle muscular dystrophy in her twenties.
Now she's back to answer your questions!
#limbgirdlemusculardystrophy #musculardystrophyuk #musclewastingconditions #LgmdAwareness #lgmdawareness #musclesmatter

[@DragonRiderElf]

thank you for making this! I am 15 and we recently discovered I have LGMD due to genetics (I’ve had it for a while but we didn’t know until it started affecting my hips as well). I genuinely appreciate you making this video!

[@Speakmymind08]

Hello Karen my name is Danny, I’m a 43 year old with lgmd I have 3 kids 2 boys and 1 girl Brad Shane and Zoe. I live with lgmg for a long time since I was born but I have to say you are a great person doing this.

[@michaelhodson3055]

Hi 👋 how long did it take for you to get a diagnosis on what you had? I had a muscle biopsy done last January and I'm still waiting for the results but I think I could have LGMD

[@Speakmymind08]

Please remember no one is perfect I use this method for my whole life

[@deepakaswal2000]

do you need graphic designer