About This Site

Originally this site was created to help me (Sarah's Husband Dave) communicate to everyone how Sarah was doing.

When Sarah was first diagnosed, we did what I expect anyone else would, research it on the internet! And I have to say it wasn’t our best move. Everything I read nearly had me in tears and nearly crushed all our hope, so much so, at the time I banned Sarah from reading such stuff (she ssssssssoooooooo ignored me I know, but she handled it well)

This made me wanted to create a site that would inspire hope and have a unique positive angle in contrast to all the other sites out there, and to share her experiences and all the funny times that other sites forget to mention.

Not only that but to also tell everyone what an amazingly brave girl Sarah was - tougher than nails this girl with an amazing determination.

So for any other FHC sufferer that stumbles across this site, I hope this site can make you smile, give you strength through tough times, give you something to relate to and know you’re not alone.

To everyone else, friends, family, friends of friends, family of friends of friends (!) I hope you enjoy this site as much as I enjoy not having to repeat myself 55000 times with the same story and updates….my phone bill dropped considerably after creating this site!

Thanks

Dave