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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
 

Crazy Busy

Yesterday I was supposed to fly back to New York from Detroit - how the hell did I end up in South Carolina?  Spirit Airlines, that's how. 

I think this is the busiest I've ever been in my life - even moreso than finals in college, because I wasn't travelling the country.  When was my last blog post... before NYCC Special Edition?  That convention went pretty well, albeit surprisingly slow at times, with it being at Javits.  But met some nice peeps and I even got to see Maki from the Penny Arcade "Strip Search" reality show. 

The day after that 2-day convention, I flew to Michigan to be in a friend's wedding.  Weddings are always fun, especially when you're in the bridal party :)  It was fun to reconnect with friends and dance, and visit Ann Arbor again.  Got to spend some time with family, but I still have that Power Rangers coloring work amidst everything, so it wasn't a true "vacation" to relax.

Right now I'm en route to Baltimore for the Graphic Medicine Conference.  I'm giving a 15-minute presentation with David Brenner of the Familial Dysautonomia Foundation for our work on the comic strip "No Tears:  Life With FD."  You can see the whole program of awesome stuff here and our presentation is called "Comic Strip as Connection, Identification and Education for Rare Disease."  At first we were part of the shorter "lightning round" talks, but someone cancelled and we were upgraded to a longer talk at 1pm Friday.

Oh yeah, and the reason I'm in South Carolina now is because my flight back to NYC was cancelled yesterday.  I was supposed to fly back to NYC, unpack stuff, pack stuff I needed for the convention (besides the talk, there's a small convention for the conference on Saturday), and take Bolt Bus to Baltimore today.  Since all the flights were booked until Saturday, the best Spirit could do was fly me to Myrtle Beach, then Baltimore today.  I won't have all the things that are usually at my table for the mini convention, but I'll make it work with what I do have.

It's now cheaper to check bags than have a carry-on.  I'll need to look more closely at all the extra fees when getting flights next time.  After I got my new flight settled, when I saw it had a connection, I was expecting them to lose my luggage, after the run-around I got yesterday.  Luckily I was able to get them to upgrade my little luggage as a carry-on, so no way I'm losing anything.  Although the part in The Daily Misfortune about losing luggage and it being sent to the wrong address actually happened with Delta a few years ago.  It got sent to my friend's address - the same one who got married this past weekend.  Everything comes full-circle! 

tags: Spirit Airlines, Delta Airlines, The Daily Misfortune, mindy indy, graphic medicine conference, Familial Dysautonomia Foundation, No Tears: Life With FD, penny arcade, strip search penny arcade, maki naro
Thursday 06.26.14
Posted by Mindy Steffen
 

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
 

Carmine Street Comics Studio

Mindy Indy at the Carmine Street Comics studio space. Hey peeps!  Tuesday was super nice at Carmine Street Comics.  The picture above shows more of what their little studio set up is like.  The artist sits on that elevated platform in the front window of the store.  I was actually successful at luring some curious new people into the store!  (well, "luring" may not be the best word, but you know what I mean).  The desk space is just big enough for me to work on my comic pages.  That day I worked on drawing and inking the weekly comic I do for the Dysautonomia Foundation - No Tears:  Life With FD.  It was super great and super chill drawing at that space.  I had a nice big window, the door was open and let in the fresh spring air, but best of all - I got to talk with comic peeps every so often!  Saw some friends, met some new people, talked about comic stuff.  MUCH better than just working on stuff alone at home and going stir crazy (and more productive too, since it's not easy to climb up and down from there all the time, I'm not distracted).  And hey, I even sold a book, so that was a nice extra bonus!

Each day Carmine St. Comics has rotating artists drawing in the window.  Today (Thursday) is Ellen Stedfeld's turn.  Friday is Sean Von Gorman's turn, and he's having a special party event.  He has a book out:  The Secret Adventures of Houdini.  Sean usually does an escape act of some kind during his events.  In his own words: "When I crash a party ANYTHING CAN AND WILL HAPPEN!"  So stop by Carmine St. Comics this Friday May 10th anytime from 2pm to 10pm to witness the insanity.  I may or may not be there (gotta prep for Kids Comic Con THIS WEEKEND).

Also, Carmine St. Comics Community Showcase is going on next Wednesday May 15th 11am-10pm!  ALL of the daily window artists will be there at some point of the day sketching, signing, partying, having an all-around good time!  Special prizes available to customers of the store!

All this awesome stuff going on at 34 Carmine St. in Manhattan off the West 4th stop.  Look for the big green awning that says Imperialist Bookstore, and the Carmine St. Comics sign will be underneath it.  GOOD TIMES!

tags: artist's studio, Carmine St- Comics, Carmine Street Comics, comic, Ellen Stedfeld, Familial Dysautonomia Foundation, mindy indy, Mindy Steffen, No Tears: Life With FD, Sean Von Gorman, The Daily Misfortune, The Misfortune Cookie, The Secret Adventures of Houdini
categories: Comic Events, Uncategorized
Wednesday 05.08.13
Posted by Mindy Steffen
 

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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