Last April, I threw an art show featuring artists living with Parkinson’s. I had people from CT, MA, and RI show, and one artist from Germany! I organized it all, down to every detail. I had a merry band of volunteers helping artists hang their collections.
It was far more successful than I had anticipated! But, SO MUCH WORK. I wavered for months wether I would do it again.
Then, an artist contacted me. She thanked me for the exposure my show gave her art. She sold quite a few pieces, and although she has been creating her entire life, finally feels like a legitimate artist.
I feel the power in bringing her, (us) out into the light. To highlight, not hide. We get told to take it easy, to rest, to let go, we lose so much control and often feel powerless. I want these artists to stand up boldly and tell the world “I have value. I still can, I still do.”
As long as I’m able, the show will go on.
Hi, that’s really great that you could promote another artist with Parkinson’s pain. I have a good friend that paints with MS. And she’s been getting hers recognized through the Minneapolis, Art, so good for you. I know it’s a lot of work, but schuur paid off for that one lady it’s hard to do things with Parkinson and get noticed sometimes but it’s good to just keep on going.
That’s fantastic that you have decided to do it again! I’ll be there, and if there is anything I can help with, please let me know.
I will! Thanks for your support, Mike.
That is fantastic! Did you sell any pieces? Your energy reminds me of the one dance teacher on Fame (bet ya no one saw that reference coming 
) She had the tall walking stick that she would use to keep the beat. But she had a fire in her that kept her moving forward.
Would an online exhibit be less draining? I am sure Mike has a ton of extra time! LOL! Each piece could have a 3 minute video explaining the piece by the artist or something.
Yes, I sent an email to the 11 artists who participated last year, and the few who have responded have told me it impacted them similarly. The facility that we used is still getting positive feedback back, 6 months later.
Hi Jenn- this makes me so happy to read the positive impact the show had- which is why it is so important to do again. APDA CT is happy to support it for April 2024 <3
Art is such a wonderful salve!
When I lost my sense of smell I decided to devote more energy to photography. Around that time I read about brain plasticity and was hoping to repurpose the neural ‘real estate’ from smell to visual. Can’t tell if it worked but it has given me great pleasure see the world as a place full of possible photographs.
I’m sure your show inspired and encouraged. What a great idea!
I absolutely love this and would like to participate as an artist next time.
Let’s talk about it! I’ll have dates available soon.