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Wednesday, November 14, 2018

My Wheelchairs' Egos

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For this set of prints, I used images from my original paintings and drawings to combine in photoshop to create new works. I do not really keep a sketch book, so I use the work that I already done as the sept for the next piece. Once that I was satisfied with the new image, I printed them on overhead projector film. Then that was exposed in a light until to burn/etch the image into the photo-lithograph plate. After that you are all set to roll as with any other plate.
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Thursday, November 8, 2018

Tiny Houses For PWDs

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I remember when I was young my mom would often ask where I want to when I get older. I would always reply a motor home, so I could keep moving around the country, once again it seems I was ahead of my time. In a new trend people are building tiny houses that are accessible for People With disabilities, this is a better alternative then renting a subsidized housing that one will never own and is out dated.

Back in the late 90’s people invested in building community living places for the elderly, I would do the same for PWDs. Buy property and run water and electric hook ups for tiny house.  That way PWDs have option of place to live in their own houses.  I would also build places so there could be PCAs on call 24 hours a day, but they would have their own spaces.   I am just an old soul hippy at heart, because you know what this sounds like!


Wednesday, October 17, 2018

Some Fun and Crazy Stuff

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July 10,
A new water park in San Antonio is making sure kids with disabilities don't miss out on the splashing fun this summer.

June 29
The first black Barbie to use a wheelchair is here, and people are loving the message it sends to kids
I like how she comes with her own ramp, as she can tackle anything that gets in her way! I always thought that it would be cool to have a ramp the rotated around my electric chair, it would rest in back of me and when needed, it could rotate from back to forward, over my head. It could also double as a roof in bad weather.
June 29,
50 States. 50 labels. One way to score $100* - MTN DEW®
I wonder if anyone has done the math to see how much it cost to collect of 50 bottles in order to win the $100? Maybe MTN DEW figured people are traveling anyway for festivals so they could use some extra cash.I can see, if they come in 6 packs, people trading them as they do with Olympic pins.
June 13,
This reminds me when I used to go to Skate Land, I would get go on the rink once an hour with three guards. One would push me while one skate in front and the other would protect our 6.

Jun 13,
I really do not know how much work would get done during those late nights during finals? This is the type of thing people wanted to design to get me of my knees when I do my art.

May 2,
Special Needs Drum Corps To Make History By Competing At World Championships

Sunday, September 16, 2018

If PWDs is the largest minority, than we should become the majority vote!


America will always be a work in progress, because that is what it is to  be human. just because someone is voted to be our leader does not mean they have the perfect answer and no law is without it's flaws.  That is why I  voted since the age of 18, so I could be part of the debate and hopefully shape the world into a better place.  I might not see the effect in my life time, our jub is to give guidance for future generations.

Tuesday, July 10, 2018

Starbucks to Stop Using Disposable Plastic Straws by 2020

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My hippy side says alright, alright, alright, but as a Person With a Disability this might lead to frustration.  I have never used a paper straw myself, I do wonder how long they hold up from the biting that I do.  I did hear that Starbucks might offer metal straws, I wonder if they will be available for an extra cost?  Before Brooke gave me a metal straw I really did not like frozen drinks, because I could not suck them up due to my biting. By this time I started to have missing teeth, so the straw had a slot to fit through. Other wise this type of straw would be too hard on teeth, talk about a
Gimp Dilemma!

Saturday, July 7, 2018

The Phyllis Kind Collection

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Art is Like Playing Monopoly As some of you remember I was represented by the Phyllis Kind Gallery for many years, this was a good time in my life. The Oscars just fell into tour laps and HBO wanted to connect me to a gallery, that is how Phyllis I crossed path. From the moment we met, she referred to my work as my children. Really, each art piece is a child, the seed is the idea and they bloom into their own identity as we work on them. Phyllis had the philosophy of finding the right buyer for each piece. I was off to a good run; my first solo show was a huge success. Then 9/11 occurred and understandable other things took precedence to art. I always knew art is more of luxury in life, face it I never did art for the money that is more of a bonus. Over the next few years I had two more solo shows at the Kind Gallery.

Then in 2006, I got a call no Artist would ever what to receive. Time to come pick up your work because the gallery is moving to a smaller place. To me this is mix emotions since my work is going into storage, but at least I have the opportunity to get my kids back. Whoever has taken an Art history class, has heard many stories about galleries closing and the Artist can’t find their work. Interesting enough when Dena and I went to pick up the kids, Phyllis kept a hand full of my work. To be honest, I was frustrated that they kept the prints that I worked on in the summer of 2002. That summer I basically took over the print shop at Towson University and hired Dawn, Jessica and Brian to run edition for me, thanks to Tonia Mathews. All of women/men power and supplies were out of pocket, I think you would see why I would be worried about what happened to the editions. For the next dozen years, I had no idea of what happen to Phyllis, or my work. Even the producers of King Gimp could not get through to the gallery.

Two weeks ago, an email popped up in my inbox from Phyllis’ daughter, saying the gallery is finally closed and would I like to come get the rest of my work? Right away; I’m reply yes and I am thinking self, the flipping prints! I wanted to ask about how Phyllis is doing in person. Last Saturday Dena, Daisy and I packed into our van and set out for NYC. When Dena and Rachel put the first load into the van, I did tear up. This is not only the end of a chapter in my life, but an end of an era in the Art world. As they finished loading the work, Rachel says it must feel good getting your children back. I know that is something her Mom would say, I hope she is having a relaxing retirement living on the West coast. Before we headed back home, I asked Rachel to please kiss her mom for me. As we were heading home, I asked Dena; honey do you know what we have here? This was Phyllis’ private collection of my work. You know she handpicked what she wanted to keep, because she knew it’s value. Rachel said as she was moving my work to lobby, people ask if it was for sell. The thing about art, the Artist know it’s value, people like Phyllis tell you it’s value but there is no proof unless people see the dollars flowing.
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Thursday, July 5, 2018

C.P. Wisdom

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This is one of many emails I receive from students and educators to share my view  about living as a person with a disability.

What do you talk about in your motivational speeches?

I mostly tell stories from my life, a lot of is related to living as a person with a disability but really they can relate to everyone. We all have challenges in life, but I want to show people there is always a way to get over them. If one way is not work try another, it is okay to ask for help. I also talk about find your passion in life, because they become asks of kindness that can change our world for the better. Even the smallest can change a life for the good.

How do you communicate in different ways?

The biggest one is my art, I do a lot of social media to keep up with disability topics and to put my thoughts out for people to think about. I really am not one to talk about my daily life on it, but put out a lot of my art and things that I feel passionate about. I feel like social media has open a new world of communication for the disabled community.

How has cerebral palsy affected your life? How do you express yourself?

Having CP is just about doing things differently, I can do what ever I want just with twist. It is a life style that chose me, it might take longer to do things but I get them done. If might take me twice as long to have a conversation in the end my thoughts may be valuable then others.

What is your belief about cerebral palsy?

I still feel that I do have CP, but it does not control me. It does present more challenges in life, but CP is just part of my personality and help lead me down the path I am taking in life. I have never asked why I have CP, or if there was a way to fixed it. Once I was visiting a school and a student asked me the magic pill question to take away my CP. I replied, I would not take it because having CP is only way of life I know. To take away my CP would be like dropping off to live on another planet

Friday, June 29, 2018

Just Another Thought


It seems as respect and working together are vanishing terms in today's society.  Another reason to move to Europe, Pets are welcome at a lot of places. That was the best chilling out at Cafe's with dogs being lazy under the tables. The time we where in Chile, we sat at a picnic table all day and our neighbor's dog would come for morning coffee and beacon and check on us through out the day. Our Country just needs to chill out, maybe that is why more States are legalizing pot.

Thursday, June 7, 2018

Wheelchair-Friendly Tiny Houses Could be a “Big” Option for People With Disabilities

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If I had the money, I would invest in property to run water and electric hook ups all through out the place. I have been seeing a lot of these types of blogs.

It is a great idea for many reasons, consider the amount of money PWDs throw away on just renting. Also the fact that we live in one place for most of our lives due to affordability. Would buying tiny houses also save tax payers money, if programs were setup to buy, rather then live 40-60 year in subsidized housing?

I am sure people still have to rent the land to park just as a trailer park. The tiny option may be the way for PWDs to be included in the latest housing trend. I think it would cool to start a Gimp commune.