We're here with Chip Wilson today, the founder of Lulu Lemon. Thank you very much for joining us today, Chip.

So my pleasure, Jemima.

So most people probably know you as, you know, the founder of Lulu Lemon, one of the most successful apparel brands of our day.

But we're here today to talk about something different, which is the organization that you've launched last year,

so FHD.

And you launched it because you were diagnosed

with this rare form of muscular dystrophy

a few decades ago.

I think a lot of people don't really know much about

FSHD so I thought it could be useful to kind of start with your story of

getting diagnosed and how the disease has impacted you?

I mean, thanks for having me first off.

This is, I mean, whatever you, I can do to get the story out there in order for more people

to be recognized, especially when they're young

with the muscular dystrophy that would be great.

It is a different there's different forms of muscular dystrophy I mean there's the shens or even ALS

is another one. I have FSHHD vascular scapular muscular. So a lot of people that have

mine have no muscles in their face so they have no expression so it makes it very

difficult but mostly it hits the scap or

muscles in the upper body. When I was young I was a swimmer like a probably a

world-class swimmer and in butterfly and batsjoke but I could not swim

freestyle because I couldn't get my arm out of the water every time I would do it my

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