WEGO Health Activist Awards

The Chronic-ills of Rach has been
nominated for “Rookie of the Year” in
WEGO’s annual Health Activist Awards.

I am really chuffed!

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Especially because I was nominated by my blogging hero, Michelle from Living With Bob.  That’s like a kid who loves to play footie being nominated for a rookie award in their local club by David Beckham.  She’s a huge voice in the world of Dysautonomia Awareness.  It’s a big privilege for me to join my voice with hers in making some noise.  I might live in a small country down here at the bottom of the world, but antipodean voices are just as loud when we get them out onto the web. Blogging is a pretty amazing thing, don’t you think?
Want to be a part of the decision about the awards?

You can endorse my nomination: here.

And whether you do or whether you don’t, thank you.  For being here and reading my blog.  The community of people that is forming around the Chronic-ills of Rach, and Dysautonomia awareness in general, makes my heart sing. Michelle, thanks for the nomination. You are such an encouragement. Mwah! X

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Doing My Bit…

Fundraising for a rare illness is a tough gig.  We don’t have marketing teams or big business sponsorship. There isn’t a Dysautonomia Awareness holiday, although October is unofficially our awareness month.  Down here in Australia and New Zealand, our numbers are quite small.  There are around 400 of us across Australia and New Zealand, that we know of. We do our bit any way we can.  For some of us that means raising awareness by typing our stories out onto the web.  Maybe we host cupcakes-for-a-cure sales or write letters or lobby government with regards to medications access and other related issues. 

My friend Michelle over at the hilarious Living With Bob blog has started up an online donation page to help raise funds for the Baker IDI institute in Australia.  They are conducting research specifically into disorders related to syncope (fainting).  Every Dysautonomiac has had to deal with that scary side of things at some time in our illness. The things they may find in their research are the closest thing to dysautonomia research in this part of the world.  It’s important that we help in any way we can.  But we are a small group of people and most of us are too sick to do fundraising runs, awareness feats worthy of media attention, or much of anything that is going to inspire people to reach into their pockets to raise money for research.  It’s a frustration that perpetuates the invisibility of illnesses like ours in the wider community.  We aren’t well enough to push for attention, but we need it.  So today, I’m letting my fingers do the talking.

Because Michelle has so valiantly taken on the task to raise money for research, and perhaps because she has been feeling too crap lately to get vertical, I felt like it was time we all pull together and lend some support to her fundraising efforts.  Here is a link to her fundraising page.  I will be coming up with some other ways to help Michelle raise money for Dysautonomia Awareness as we draw closer to Dysautonomia Awareness Month.  But for now, I thought I’d introduce you to her efforts.  Maybe you can help.  Maybe you know someone who could help?

Here she is, clicking her Dorothy heels for Dysautonomia.
https://give.everydayhero.com/au/clicking-my-heels-for-dysautonomia

Fall Seven, Get up Eight(7)