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More Amelia's

Charities, what would we do without them? In all honesty, I never really payed much attention to charities before I got poorly and that sounds absolutely awful but I think most people have this perception; that charities don't do what they say they do and actually the money doesn't go where you're told it does..I was one of those people. 

When you're chucked into a situation that you weren't expecting you feel totally alone and you really don't understand until you're in it. Charities are one of the most incredible things to ever exist. They have the ability to help people that need it and provide support as well as hope. Unfortunately a lot of charities don't get the recognition they deserve and I've only had the pleasure of working with a few charities that really do deserve a lot of recognition; Rainbow Trust, Molly Olly's Wishes, The Family Fund and Make A Wish Foundation. I've written about my experiences and wishes with all of these charities on a previous blog post Make A Wish. 

I've currently been working on a project with the Rainbow Trust to get them more recognition by creating short films with other families. My support worker Amelia is absolutely incredible and before Amelia joined, I had a lady called Oonagh. Both incredible women. Unfortunately Oonagh left and Amelia took over, and I don't take to new people very well when it comes to my illness but Amelia honestly is just amazing and we just clicked. 

The thing with Amelia for me is that she's not a friend, she's not family, she cares, but in a different way so you're not afraid to tell her how you're feeling because the connection is different. When you speak with family and friends, you're worried. You're scared because you don't want them to be sad because of what you've spoken to them about and you don't want them to get hurt or be reminded that you are ill. You live with your family every single day, you see your friends every single week, you want yourself and them to be happy and to be honest all you want is to have a nice day so you don't really want to talk about. I really don't know if I'm explaining this very well at all, and I know what I'm trying to say but I just can't put it into words so I'm just praying you all read this and understand what I mean.

Without Amelia, I'm not really sure where I'd be. It's not just the emotional support, it's about having someone that's there and you're not afraid to let them in. Thanks to Amelia, I'm able to enjoy myself more because I have her to talk to. We laugh 90% of the time, we smile a lot, and we talk often, and that's the best way to be. She can't take my disease away, but she can be there for the bad days and the good days, to make everything a little easier and a lot more enjoyable. 

A lot of what I'm saying will probably be spoken about it the videos too, from not just me, others. There are so many families that Amelia supports. And I'm so glad that I could take part in this video as well as writing this post, to help raise awareness; because without the sponsors, we have no Amelia, and without Amelia we have no support.

Below is the link to one of our short films for Rainbow. Please feel free to check it out and pass the link on.

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Love, Erika