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Mindy Indy

Independent Cartoonist

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Saying Goodbye to A 7 Year Web Comic - No Tears: Life With FD / FD Heroes IRL

FDman-girl-anyone-web.jpg

The only thing you can count on is change! I’ve really been blessed to work with the Dysautonomia Foundation on a very niche and meaningful web comic for the past 7 years, but now the foundation is going in a new direction. In 2012, I met David Brenner and his son Michael at a small comic con in Jersey (Toys on the Hudson in the fall). David (then director of the foundation) had been thinking of a FD comic for awhile since his son loved comics. He loved how my Misfortune Cookie mini comics featured unfortunate subjects in a lighthearted manner, and knew I was the right fit to make his ideas a reality.

The very first No Tears: Life With FD comic! Created in January 2013

The very first No Tears: Life With FD comic! Created in January 2013

Backing up a bit, FD stands for Familial Dysautonomia, a rare Jewish genetic neurological disorder that effects the sensory and autonomic nervous systems. For example people with FD may have trouble swallowing so they need a feeding tube, as in the comic above. I’ve also done a few comics featuring the BiPap machine, because sometimes people with FD have trouble breathing while sleeping. The comic’s title has a double meaning - one of the symptoms of FD is the absence of overflow tears / corneal drying. The title also encourages FD patients and their families to have hope through their daily struggles. Topics in the comic series range from dealing with specific FD situations, like Crisis, to social scenarios of persons with disabilities, and more. The comic has always had a light-hearted and touching theme focusing on the closeness of families.

uncertainty.jpg

In the beginning, David wrote the scripts and I hand drew (and even hand-lettered) the comic, coloring it on the computer. It would be posted each week on the foundation’s Facebook Page.

MissSchool-web.jpg

In 2016, sadly David Brenner passed away from cancer and was dearly missed by all. I wondered if the comic would continue, since it had personal ties to David himself. But the interim director, Paul Schack, was happy to continue the comic. It became more of a collaborative endeavor, as I suggested more script ideas and eventually wrote the scripts all by myself, with some edits by Paul. This is the first comic script that was all my own. I also switched to creating the whole comic digitally using my wacom tablet, and turning my handwriting into a font for digital lettering.

Dating-web.jpg

Previously the comic had different characters for each strip, with a few recurring characters like a family with a newborn baby with FD. But when I wrote the script, (and also thinking of fresh subjects for the strip) I had lots of creative freedom to explore subjects like special needs dating with recurring characters Adam and Ariel. And I also loved featuring FD Man and FD Girl (top comic) for positive messages! David originally came up with the idea for FD Man, but FD Girl was one of my additions to the comic, and they made a great team!

AndrewS-web.jpg

In late 2018, the Dysautonomia Foundation hired a permanent new director, Lanie Etkind. Again, I wondered if the comic would continue. In 2019, Lanie and others at the foundation suggested focusing on real people who had FD for the comic, like a spotlight. Thus, “FD Heroes IRL” was born! People with FD who were interested in being featured reached out to me and I asked them some questions. I then created a script from their responses (this is much like how I work with people to create custom comics). The FD community loved the new comic too! Andrew S’s comic, above, was personally very inspiring to me because he didn’t let FD stop him from going on an awesome road trip!

And well, since the community is small (it’s a rare disease affecting only 200 people on Earth), the comic has seemed to run its course. I’m so happy to have been involved with the FD community and have contributed to making their days a bit brighter through the comic. Really, it’s amazing the comic has ran for 7 years! I’ve learned so much about FD and always tell new people I meet about the disease and the comic when they ask about what I do as an artist. Spreading awareness!

Comic in memory of Scott Fass, who passed away from FD.

Comic in memory of Scott Fass, who passed away from FD.

I found the comic work I’ve done for the FD Foundation to be incredibly rewarding and I feel like the comic touched people’s lives, even if in a small way. I like working with non-profits because of the meaningful impact. For a few years I also did a comic for the RLS Foundation called “Night Walkers.” When one door closes, another one opens. I’m definitely open to continuing my comics journey with other non-profits! Please forward this blog post or tag someone on social media who you think would be interested in working with me to create comics that have a positive impact on people who may be going through struggles of any kind.

tags: No Tears: Life With FD, FD Foundation, Familial Dysautonomia, Familial Dysautonomia Foundation, FD Heroes IRL, web comic, freelancing, comic art
Wednesday 11.20.19
Posted by Mindy Steffen
 

Honorary Custom Comic!

Some of you may have seen the weekly No Tears:  Life With FD comics I create and share on Facebook.  FD stands for Familial Dysautonomia, a very rare disease.  The guy who writes the scripts for the comics, David Brenner, the FD Foundation's executive director, has worked there for a whole decade!  Some people from the foundation reached out to me and we came up with the idea to make him a custom comic as a special honorary gift!  They wanted to depict David as a Navy Seal, the most specially trained, technology savvy, and elite fighters of the USA.  I definitely listened to the In the Navy song a lot while working on this :)  (Can anyone find the Beatles Yellow Submarine "Easter Egg" I placed in there?)  I made the comic in a record time of 8 days, along with my teaching job and other duties.  I presented the comic at last Sunday's FD Day, their annual conference.  Everyone loved it!

Usually I draw custom comics for couples, as you can see from the custom comics section on my site.  It's a great way to tell the story of how the couple met, got engaged, and so on!  But I think the honorary custom comics are extra special.  Sometimes the couples comics are just for 2 people, unless they're displayed at a wedding reception.  But the honorary comics can be displayed in the office and seen by everyone!  It's kind of like a visual resume - if you're new to the company, or not as familiar with the honoree's day-to-day work, you can tell what a hard worker and amazing role model the person is in the comic! 

tags: Familial Dysautonomia, FD Foundation, FD Day, No Tears: Life With FD, honorary custom comics, custom comics, navy, visual resume, The Daily Misfortune, mindy indy
Friday 06.10.16
Posted by Mindy Steffen
 

"The Forward" spotlights my work on "No Tears: Life With FD"

"The Forward," a Jewish American online magazine focusing on politics, arts, and culture, recently highlighted my work on the weekly comic "No Tears:  Life With FD."  There's a video of me creating the comic strip.  The video also shows David Brenner, executive director of the FD Foundation, talking about Familial Dysautonomia and how this comic has helped connect patients, families, and others beyond.

Read the corresponding article here:  http://forward.com/culture/318404/sketching-life-with-a-rare-disease/  It came out wonderfully!  I also love how I'm referred to as "Indy," like how reporters refer to interviewees by their last name.  The only thing is that I don't live in Manhattan anymore, haha!  Thea interviewed me in the midst of all my moving boxes!  I made sure to warn her that she'd be walking into the middle of a tornado, but she was cool with it.  You have to be prepared for some things, y'know?

All in all, it's been great to be involved with the FD community for so long, and to touch people with the comics I create.  Hopefully this article and video will spread more awareness of Familial Dysautonomia.

And Boston Comic Con was a great success!  Special thanks again to my friend Jennie Wood for sharing her table space!  I got lucky and was on the corner of an aisle - more visibility!  Also the AirBnB was AWESOME!!!  I stayed with an older couple in what was practically a mansion.  The bathroom alone was bigger than my room in Harlem.  It was a whirlwind trip though, taking Megabus at 6AM going there, and this Daily Misfortune happened on the midnight bus back.  I switched seats with the guy so he could lean on the window instead of me :P 

tags: The Forward, No Tears: Life With FD, Familial Dysautonomia, Boston Comic Con, Jennie Wood, AirBnB, Megabus
Thursday 08.06.15
Posted by Mindy Steffen
 

This and That

So back when I was in Motor City Comic Con, a guy came up to my table and was like "I'll write an article about you if you draw me with a penguin."  Here's the drawing, which he absolutely adored, and here's the article!  http://annecarlini.com/ex_interviews.php?id=1309  Sometimes the bartering system DOES work!  Interview by Russell Trunk of Exclusive Magazine.

Ah last time I blogged it was about Special Edition, which was great!  My friend and fellow cartoonist Warner helped man my table when I couldn't be there on Sunday.  I took a bus, then cab across town (cabs were hard to catch at the west end... maybe this is a sign I should get Uber) to draw at the annual FD Day for a few hours.  FD is short for Familial Dysautonomia, and I draw a weekly comic strip for their organization.  I was even drawing and eating on the cab on the way back to Pier 94 - a super busy day!  But I like the excitement.

Haven't posted in awhile because the current apartment hunt has been such a time sucker!  Literally every single night this month, Molly and I have been going to Brooklyn for hours.  The sequel is practically writing itself.  I think the end is in sight though.

tags: motor city comic con, Exclusive Magazine, Special Edition NYC, Familial Dysautonomia, Apartment Hunt, The Daily Misfortune
Tuesday 06.16.15
Posted by Mindy Steffen
Comments: 2
 

FD Day

So I've been creating a weekly comic for the Familial Dysautonomia Foundation (which I haven't posted in awhile here, but they always post it on their facebook).  This Sunday is FD Day, a conference for people and families affected by the condition, but it's also open to the public if you're curious!  They'll have a lot of NYU doctors talking about new research, treatments, and other stuff.  I'll be there sketching for the kids in a room with other fun stuff like a magician and balloon animals.

Here are some FD comics to catch up on - No Tears:  Life With FD.

On this comic, the Foundation and I were trying to come up with good places for the group of people to be in - what if the grumpy old man was a bus driver?  No, some FD people have difficulty getting on buses.  What if he was a barber, or at a movie ticket counter?  Those were ok, but I came up with something I encounter regularly:  grumpy people at the checkout lane :)

This was one of my personal favorites :)  Although the FD community online prefers the really sweet ones vs the LOL ones (this one got only like 2,000 "views" as opposed to the usual over 10,000).

Like this is a really sweet one.  People went NUTS over this one!

And people really responded to this one well.  Lots of good comments flying around on the web.

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, FD Day, mindy indy, Mindy Steffen, No Tears: Life With FD, The Daily Misfortune, The Misfortune Cookie
categories: Familial Dysautonomia, The Daily Misfortune
Thursday 05.30.13
Posted by Mindy Steffen
Comments: 1
 

FD catch up

It's hard to find veins in people with FD.  Although I'm sure many people can relate to this strip!  Below is last week's strip too - I was so busy with GNM stuff, no time to post everything:

Usually people with FD may faint if suddenly standing up from laying down and vice-versa. Patients go on a "Tilt Table" - a table that slowly tilts from vertical to horizontal - to measure changes in their system.

Unlike suburbia, bushes are rare in the city.  There are some trees here and there, but unless you're Bugs Bunny, not able to hide behind.

 

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, The Daily Misfortune
categories: Familial Dysautonomia, The Daily Misfortune
Tuesday 03.19.13
Posted by Mindy Steffen
 

Crisis

When a person with FD is in "crisis," their body loses control of blood pressure, heart rate, and body temperature, among other things.  When talking about drawing this comic with people at the Dysautonomia Foundation, they emphasized the green face because FD people in crisis feel very nauseous.  I suggested also drawing a garbage can next to the bed (like if they needed to throw up).  I learned that people with FD cannot actually vomit because of an operation they all have.  Basically, because they can't swallow normally  (they eat via stomach tube) if they threw up it could get into their lungs be a serious problem, so the operation makes some kind of knot in their intestines (if I'm remembering correctly).  Meeting with the Foundation and asking questions leads to very educational conversations for me and prevents me from making slightly "incorrect" drawings.

Pretty much all of my Daily Misfortunes are like the "crisis" in the first panel of this week's FD comic.  But that's one reason the Foundation wanted me to draw their comics - I can create a somewhat lighter tone to bad situations.

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, The Daily Misfortune, The Misfortune Cookie
categories: Familial Dysautonomia, The Daily Misfortune, Uncategorized
Wednesday 03.06.13
Posted by Mindy Steffen
 

Two comics... nothing to do with each other.

No Tears:  Life With FD

This "No Tears" is a more melancholy one.

This practically happened to my sister yesterday.

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, The Daily Misfortune
categories: The Daily Misfortune, Uncategorized
Wednesday 02.27.13
Posted by Mindy Steffen
 

No TV

People with FD have a lot of treatments, exercises, medications, etc added to their daily routines.

This is what a friend posted on facebook.  You can't make this shit up.

tags: Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, The Daily Misfortune
categories: The Daily Misfortune
Tuesday 02.19.13
Posted by Mindy Steffen
 

Packing

And you thought YOU had a lot to pack!  People and families living with FD have a gazillion other medical things to bring.

This is true in my case. I graduated from the University of Michigan and in NYC, people haven't heard of it and think it's some podunk school (even though it's one of the "Big 10"). If I had gone to SVA on the other hand, that would matter more.  Just gotta keep learning throughout life.

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, The Daily Misfortune, The Misfortune Cookie
categories: The Daily Misfortune
Wednesday 02.13.13
Posted by Mindy Steffen
 

FD Comics Success

I'm happy to say that "No Tears" is approaching virality on Facebook!  Almost every person that "liked" the comic also "shared" it!  People really related to this particular comic.

tags: comic, custom comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, No Tears: Life With FD, The Daily Misfortune
categories: The Daily Misfortune
Wednesday 02.06.13
Posted by Mindy Steffen
 

How do you pronounce that?

"Dysautonomia" is a really long word, sounds similar to other things, and is hard to remember for those unfamiliar with it.  Even when I'm talking with people about this strip, some of them have trouble with the word, so imagine the frustrations people living with FD have to go through communication-wise, on top of the condition itself.

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, No Tears: Life With FD, The Daily Misfortune, The Misfortune Cookie
categories: The Daily Misfortune
Tuesday 01.29.13
Posted by Mindy Steffen
 

Hakuna Matata

Did you know that people with FD can eat and talk perfectly at the same time?  The "secret power" of a feeding tube.  People on facebook really liked that the kid with FD is happy here.

tags: comic, custom comic, Familial Dysautonomia, Familial Dysautonomia Foundation, feeding tube, mindy indy, Mindy Steffen, No Tears: Life With FD, The Daily Misfortune, The Misfortune Cookie
categories: The Daily Misfortune
Tuesday 01.22.13
Posted by Mindy Steffen
 

No Tears: Life With FD goes to Disney World

This is the next in the series of comics I'm making for the Familial Dysautonomia Foundation.  People really liked this one on facebook!  One person commented "we say FD sucks but in Disney World it sucks a little less :)".  I'm glad people are relating to the comics.  I'm also happy to announce that the Foundation has decided to keep doing these weekly comics for 6 months!  YAY ongoing gig!

tags: comic, Familial Dysautonomia, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, The Daily Misfortune, The Misfortune Cookie
categories: The Daily Misfortune
Wednesday 01.16.13
Posted by Mindy Steffen
 

Comics for the Dysautonomia Foundation

First off, Happy New Year!  Mindy indy is back to blogging after a break for the holidays.  I've been making a lot of custom comics lately!  This one is for the Familial Dysautonomia Foundation.  Familial Dysautonomia (FD) is a rare genetic neurological condition that affects the sensory and autonomic nervous systems, causing severe gastrointestinal, cardiac, pulmonary, orthopedic, renal and ophthalmologic problems.  The Dysautonomia Foundation is a 501(c)(3) nonprofit public charity that supports medical treatment, research, public awareness and social services for the benefit of people afflicted with FD. The Foundation has established the world's only two FD treatment centers and is the largest single source of funding for research and treatment specifically for the benefit of people with FD.

The FD Foundation contacted me after meeting me at the Toys on the Hudson convention.  They wanted a comic to brighten up their Facebook Page.  The comic is educational for people not familiar with the condition, and is also something that families and people with FD can relate to.  I did 3 comics so far for them, and they'll want me to do more if it gets good responses on Facebook, so please "share" and "like" the comic on their page!  Thanks a bunch!

tags: comic, custom comic, Familial Dysautonomia, Familial Dysautonomia Foundation, FD, FD Foundation, mindy indy, Mindy Steffen, No Tears: Life With FD, The Daily Misfortune, The Misfortune Cookie, Toys on the Hudson
categories: Custom Comics, The Daily Misfortune
Friday 01.04.13
Posted by Mindy Steffen
 

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