Tag Archives: disabled artist

My book has a title!

I had a lovely conversation with the amazing performer and liberatory educator Crocodile Lightning yesterday.

Me: Hey my dear, I am making this book of my art. It will be a small print run, but a beautiful book, and full of beautiful folks.

I would love to include you, if you give enthusiastic consent.

And of course you are also welcome to say no!

Sun 8:22 PM

Crocodile Lightning ✨
Crocodile Lightning ✨

Can you tell me a bit more about the book please? Your intention, vision, where it’s sold? Thank you for thinking of me.

❤️

Me: It is a book of my drawings, half San Francisco (2005-2015) and half Berlin (2015-2024).

It will be drawings from dungeons, play parties, burlesque shows, drag shows, street events like Folsom and Folsom Europe. Some nudity but no actual sex.

My intention and vision is to honor the people I have known and drawn in queer and kinky community, to show their courage, gender affirmation, passion and creativity. My idea is that since my documentary drawing has only ever been online, as online spaces become more censored, it will be disappeared, and so will these records of intimate human beauty and strength and tenderness.

I believe my work has value and my seeing of all these beautiful folx has value, and I want to know a little bit of it will survive in some places.

It will be called “Demimonde: the live drawing of Suzanne Forbes“.

it will be sold almost entirely on through the kickstarter, unless a few queer bookstores order a few. I don’t expect to sell or print more than 100 copies, if I am very lucky.

No publisher is interested in me and I am much too sick to pursue sending it out to publishers, so it is an entirely self published book.

The Kickstarter is to fund the printing and to pay the book designer/layout person, and my editor, Anuradha Vikram.

I’m not going to be paid or make any money from the book, I will actually lose a lot of money, but it’s really important to me.

This drawing of two butches at Midori‘s AIDS LifeCycle fundraiser at a SF dungeon in 2007 is a typical drawing I’m including.

Open photo

I am so blessed to have known and drawn such incredible people. I am working hard and we are hoping to launch the kickstarter in September.

If you subscribe to the substack below, I’ll keep you posted on the book! So grateful to the 100+ folks who are following this newsletter and here for this message.

Thanks for reading Suzanne’s Substack! Subscribe for free to receive new posts and follow the progress of my memorial art book.

Go Blue for MECFS and the Millions Missing!

goblueformecfs May 12Today is May 12, International MECFS Awareness Day.

I’m already wiped out from all the online awareness stuff I’ve been doing all day. But I wanted to share some of it here, on my online homebase.

goblueformecfs May 12I made lots of graphics!

There’s a social campaign called #goblueformecfs I really like. The idea to use the hashtag on a post of yourself wearing or with something blue. The blue ribbon for ME dates back to 1995.

It wasn’t hard for me to wear blue!

It was a nice chance to show all my blue textile arts projects.

photo by ZIlle Defeu of Midori performing at Feminas Potens in 2010. Suzanne Forbes is drawing in the background.I shared a little about what having MECFS has cost me.

Here’s a photo taken at Femina Potens in 2010, by Zille Defeu. Midori performing and me drawing in the background.

Victoria Copeland with Millions Missing pillowcase 2023

Victoria Copeland with Millions Missing pillowcase 2023.

MECFS affects millions of people of the Global Majority.

This is policy analyst, researcher, abolitionist praxis MSW and MECFS patient, Victoria Copeland. Vee is wearing her MEAction Still Sick Still Fighting shirt and lying on the Millions Missing pillowcase she made for the 2023 action in Washington DC. I asked her if I could share her picture with her info, because she deserves a treatment for this terrible disease.

GoBlueForMECFS art by Victoria Aronoff aka Stupid Sloth Cards May 12 2023

GoBlueForMECFS art by Victoria Aronoff aka Stupid Sloth Cards May 12 2023

This isn’t about me.

Personally. I’ve had a lot of life, a lot of lovers, and lots of my dreams came true. I’m one of the lucky ones… and one of the privileged ones. But #mecfs is a disease that strikes traumatized bodies, that strikes mostly AFAB people, including trans guys, that you have to convince your doctor you have. It’s a disease that invisibly disables and kills BIPOC people, and they almost never get help or justice. The #medicalracism is enormous. Vee deserves the life she wants and to do the work she wants to do in the world. The world needs her.

So please @goblueformecfs for young people, for aunties, for moms, for trans guys, who have never gotten any help.

Here are some resources:

MEAction’s Resource list.

Mepedia

Health Rising is our favorite site for ME research news

Deutsche Gesellschaft für ME/CFS (German Association for ME/CFS) Run by volunteers, that’s how fucking underfunded this disease is!

And there’s so much more to say, but I am exhausted.