Awareness Heroes
By the time they get to Phoenix
Often, after one of my more energetic blogs, people write to me and say “You’re amazing, Ali!” I thank you for the compliment. It gives me a warm glow, but trust me, I’m only bite-size amazing.
Often, after one of my more energetic blogs, people write to me and say “You’re amazing, Ali!” I thank you for the compliment. It gives me a warm glow, but trust me, I’m only bite-size amazing.
A breakthrough in early detection of Parkinson’s could diagnose the condition years before we notice any visible symptoms. But would you want/have wanted to know sooner? I’m not sure.
“How long have you had Parkinson’s?” It’s a question I’m often asked, and there is always more than one answer.
I’m shamelessly recycling and repurposing my blog content to meet the needs of a new cohort of people with Parkinson’s, and their supporters.
If I had to deliver an Oscar acceptance speech for all the people who have supported me over the last six years, we’d all be here till next Tuesday fortnight and miss the Vanity Fair party.
How stealing a couple of spare days from December has helped me prevent January brain fog
Today I mark five years since my GP first mentioned Parkinson’s. I’ve come a long way since then, and it’s time for an update.
People new to Parkinson’s need support from the minute the tornado hits Kansas. By the time we reach the Emerald City, it’s too late.
When we moved house at the end of April, switching utilities was relatively smooth. Building a new health care team is going to take considerably longer
I’ve found Parkinson’s is just about manageable with the right resources. But what about people who don’t have the money, the connections, the information they need to move forward with confidence?