“Ataxia sucks. Weed makes it suck less.” I once read that on a Support Group page and still think about it far more than I should. Can’t recall who said it, but I love the simplistic accuracy of it. Thanks, friend.
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…Because I Did (I mean, I do?)
Today is our 7th Wedding Anniversary! So, take a trip with me down memory lane…
#AnswersAboutAtaxia
Last week I had asked for anonymous questions about Ataxia from my blog readers in hope of fueling awareness and understanding for #IAAD22… and y’all did not disappoint!
Hopefully, my honest answers don’t either.
#AskMeAboutAtaxia
In light of International Ataxia Awareness Day (9/25/22), the National Ataxia Foundation created a campaign called #AskMeAboutAtaxia –
“A great way to spread awareness is to encourage people to learn about Ataxia. The best way to help others understand something that they are unfamiliar with is to allow them to ask questions… Our goal is to get a conversation started. If you give your friends and followers the opportunity to ask questions – you never know how many people you might reach! Share what you know about Ataxia and your experiences…”
So, ask me ANYTHING about living with Ataxia, from now until 9/26. It’s anonymous – I won’t know who asks what. And I’ll answer them all in my next new blog post!
Need inspiration? I did this same activity with my high school students a few years ago!
Read all about it here: SCA Q&A