Finding “the Wiggles Project” on “RUclips” was the first thing I found after I was Diagnosed in 2021. Loved it from the start. You both bring such insights that reminds me to not loose who I am, and to try to keep things in perspective, keep our sense of humor, and to being new things into our lives…thanks. Debby, San Leandro, CA
Great 👍🏽 talk Jennifer & Jeremy! You guys are so open and real... inspiring. And BTW, 45 degrees and sunny after a winter in Montana is definitely shorts weather!
Great talk, Jennifer and Jeremy! I go out of my way to look like a tourist. 😂 it’s my camouflage as a street photographer in Miami. Thanks so much to both of you for all you do. ❤
I love your spirit and your videos, Jeremy! Those are great interview questions. The one that scares me the most is 'what about if/when I can no longer support myself?" I'm 73 and been living alone for 20 years - not looking to be adopted by anyone. Just trying to store up what I can for those 'what if' days that may lie ahead. Anyway, thank you so much for your videos. It was great watching you interview Jennifer!
Thank you, Molly! Parkinson’s is indeed a frightening disease with no real end in sight. You are stronger than you know.And yes Jennifer is truly fantastic!
Nice visit. I had to laugh out loud at the men in loafers with no socks comment. I live close to Hilton Head Island. Loafers, no socks, khaki shorts, and long sleeve shirts with rolled up sleeves- residents and visitors. So unoriginal.
Hey Jeremy, question for you. Has anyone you know stopped or lowered their levodopa and their dyskinesia went away? Or got better? I’m just preparing when mine get bad. Thanks!
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Awe thank you Jeremy, for so much fun yesterday and talking with me!! ❤
Good stuff!
Any time!
⭐️ ⭐️ ⭐️ ⭐️ ⭐️
Thanks guys, always good for a laugh!
Our pleasure!
Finding “the Wiggles Project” on “RUclips” was the first thing I found after I was Diagnosed in 2021. Loved it from the start. You both bring such insights that reminds me to not loose who I am, and to try to keep things in perspective, keep our sense of humor, and to being new things into our lives…thanks. Debby, San Leandro, CA
That is awesome, Debby! I will pass it along to Jennifer.😎
My two favorite people with Parkinson's.....Dyskinetic Storm & Jay Mac! lol Good to see you guys chatting it up.
Right back at ya!
People like you and Jmac are the sunny side for so many
Wow, thank you, David!
Great 👍🏽 talk Jennifer & Jeremy! You guys are so open and real... inspiring. And BTW, 45 degrees and sunny after a winter in Montana is definitely shorts weather!
Love that!
Great talk, Jennifer and Jeremy! I go out of my way to look like a tourist. 😂 it’s my camouflage as a street photographer in Miami. Thanks so much to both of you for all you do. ❤
Love that!
You are such a good advocate and cool with it. I really enjoyed the interview
You were my inspiration to start this channel!
I love your spirit and your videos, Jeremy! Those are great interview questions. The one that scares me the most is 'what about if/when I can no longer support myself?" I'm 73 and been living alone for 20 years - not looking to be adopted by anyone. Just trying to store up what I can for those 'what if' days that may lie ahead. Anyway, thank you so much for your videos. It was great watching you interview Jennifer!
Thank you, Molly! Parkinson’s is indeed a frightening disease with no real end in sight. You are stronger than you know.And yes Jennifer is truly fantastic!
Well done guys!! ZzTop baby ❤❤👌🏽🇨🇦
Sharp dressed man!
I’ve learned, and continue to learn, a lot about the many dimensions of this disease from you both! Meeting Mick Fleetwood - wow!
Jennifer is truly amazing!
Very entertaining podcast.
Jennifer is the best!
Nice visit. I had to laugh out loud at the men in loafers with no socks comment. I live close to Hilton Head Island. Loafers, no socks, khaki shorts, and long sleeve shirts with rolled up sleeves- residents and visitors. So unoriginal.
Jennifer would love this!
Hey Jeremy, question for you. Has anyone you know stopped or lowered their levodopa and their dyskinesia went away? Or got better? I’m just preparing when mine get bad. Thanks!
Lowering your dose can help, but with some people like me dyskinesia is unavoidable.