In 2007 a team of photographers went across Canada to document the health care delivery experience of marginalized, remote and vulnerable populations.

Their cameras uncovered the stories of “invisible minorities” – people who have barriers to health care either due to where they live or how they live. They are found on the fringes of civilization. They are living among us in the inner city. They suffer from unseen illness or systemic social barriers. These photo essays give us all an exclusive look into an experience that is very Canadian, but foreign to most of us.

The Frontline Health collection is presented in collaboration with the Canadian Public Health Association. See the first 7 photo essays from the selections below. New stories will be released every month over the next year.

Subscribe here to receive instant notification when a new story is posted http://eepurl.com/rGwyr

• More Frontline Health Stories

This past week, the audio recording of Tig Notaro’s comedy stand-up routine about her breast cancer diagnosis last summer turned up on Louis CK’s site for a $5 download. Here’s an excerpt of Louis’ reaction:

The show was an amazing example of what comedy can be. A way to visit your worst fears and laugh at them. Tig took us to a scary place and made us laugh there. Not by distracting us from the terror but by looking right at it and just turning to us and saying “wow. Right?”. She proved that everything is funny. And has to be. And she could only do this by giving us her own death as an example. So generous.

Now New York City is about to turn Cancer into the funniest joke in town. First off-Broadway and then Columbia University will celebrate the art of laughing at cancer.

On October 19, the 2011 Canadian Comedy Award winner for Best One Person Show headlines the prestigious United Solo Theatre Festival just off-Broadway. Daniel Stolfi turns his tussle with non-Hodgkins Lymphoma at the age of 25 into a tour de force of dramatizations, characterizations, humiliations and exhilarations. He takes on stigma, icons like Lance Armstrong, and confronts the assault on his hair, his sex drive and his machismo with flair and flamboyance that leaves you belly aching and heart aching. Then he dances, like no Cancer can dance at all.

At Columbia University on November 7, Will Reiser of last year’s feature film “50/50” delivers a speech at the prestigious Narrative Medicine program. Doctors studying the art of narrative competency will be listening to this career funny man describe how he turned his personal cancer journey into one laugh track after another in the hit film starring Joseph Gordon Levitt and Seth Rogen.

Imagine. A roomful of doctors, who are studying serious literature to learn how to better understand patient stories to improve their practice, are going to be listening a young hellcat storyteller. Now this is progress! Its recognition that valid story comes in many forms and that comedy holds equal weight in the battle of creative expression.

It’s also recognition that comedy makes a seemingly tough subject like cancer digestible by the public. The TV series “The Big C” starring Laura Linney, is about a suburban mother, diagnosed with melanoma cancer, who tries to find the humour in the disease. According to WashingtonPost critic Hank Stuever: “It’s for people who are repelled by the warm-fuzzy, disease-o’-the-week dramas of cable television.” And the darkside series “Breaking Bad” turns a high school teacher’s cancer diagnosis into a life of crime that takes many funny and bizarre twists.

Laughing at cancer is no longer taboo. If you’re in New York City this week, take in “Cancer Can’t Dance Like This” and get your belly aching.

• More Stories That Can Make You Laugh, and maybe cry a little too

I watched the tears drop from my nurses’ eyes as they gently took my blood and when they hugged me goodbye at the end of their shifts. My sweet curly red-haired son died and was born still after his cord knotted when I was 37 and a half weeks pregnant – he was nearly 6 pounds. My nurses and family remained by my side, the specialist who induced me followed up on his day off and my family doctors cried with me at home.

I was deeply moved and comforted by my caregivers’ expressions of grief. While I was living my worst nightmare I could not help but wonder what it was like for my healthcare colleagues to grieve and bear witness to our devastating loss. As a nurse I experienced grief of my own patients as well as identified with their families’ losses – these moments transformed me.

When my son died in 2001, I could not find research on nurses’ experiences of grieving when a baby dies and how this changed them. Healthcare professional grief was and continues to be hidden and not often discussed. Given I was a nurse and a researcher, I decided to invite my colleagues to explore nurses’ experiences of grieving with me through the use of digital video in order to create a research-based documentary. I chose this medium to conduct my research so I could share my research to a broad audience.

I also wondered how mothers lived and transformed with the loss of their babies. Again, little was known of mothers’ experiences when a baby dies and so I decided to do my own research using the arts and film. Today I am working on a fourth documentary exploring children’s experiences when a baby sibling dies; another hidden and often unrecognized grief. Fathers, who are also often overlooked, are included in this children’s documentary.

It is my hope that these documentaries of grief, loss, resilience and transformation open up spaces for sharing experiences with one another and that we as a society will embrace grieving and loss as a natural human experience so we can feel less isolated and alone. These films are my son, Ethan’s, living legacy and reflect the love and continuing connection my family and I have with him.

• More by Christine Jonas-Simpson

In November 2010, two disabled guys from London, on a roadtrip in California, dreamt up a huge project they wanted to bring to the world. Imagine two lifelong friends, two electric wheelchairs, two Personal Care Assistants, a hoist and an accessible car stirring up a big cocktail of imagination and innovation, during a dream adventure.

This idea was to start an online disability lifestyle magazine like no other…

After months of working hard to turn the vision into a reality; Martyn Sibley and Srin Madipalli launched www.disabilityhorizons.com. Disability Horizons pioneers an innovative 21st century approach to disability by empowering an aspirational community to provide and share content that informs, inspires and entertains.

The Disability Horizons community is already 20,000 strong. Their readers write the articles, share their wealth of disability knowledge and progress towards their individual dreams together. Articles include personal stories on employment, sport, travel and relationships. The guys share many of their own daring escapades and have regular article contributions from high profile organisations, service providers, politicians, celebrities, entrepreneurs and various opinion formers that have the power to shape and change lives.

There is a page for readers to pose their own questions, an area to post unwanted disability items (the classifieds section), a resources profile page for disability companies to share useful products/services, and the Disability Horizons ‘Travel Zone’.

In honour of the Paralympic Games, Disability Horizons has graciously agreed to share some of their stories with us. The insights continue to grow our understanding of how people around the world have common and uncommon experiences in managing life limiting conditions.  The Dynamic Duo at Disability Horizons are breaking new ground and give new meaning to the old phrase “walk the walk”.

• Stories from Disability Horizons

Relevant Hashtags: #FringeTT, #TentTalk #FringeClub

♦♦♦ Pre Event ♦♦♦

13:00 via @PatientCommando: Join us Today for our @Toronto_Fringe tent talk with @CancerCantDance details on FB http://t.co/9Sba9WPu

13:05 via @PatientCommando: PM Tent Talk at 581 Bloor Street for @Toronto_Fringe – Come one, Come all.

(RT via @mhoul3)

13:12 via @Colleen_Young: @PatientCommando see you at the #FringeTT at 5pm for your show. Can’t wait http://t.co/vPGmEfJk

13:39 via @PatientCommando: Everything you need to know about today’s Tent Talk event – http://t.co/0sIdoxca

(RT via @Toronto_Fringe, @rosabourin, @BeeRaskob)

16:00 via @PatientCommando: 1 Hour to show time @Toronto_Fringe “Healing Through Theatre” #FringeTT http://t.co/0sIdoxca

(RT via @EatPooLove)

16:41 via @PatientCommando: Getting our team sorted, the camera primed and twitter feed at the ready

♦♦♦ Event Start ♦♦♦

17:00 via @verbitty: Taking in a @Toronto_Fringe #TentTalk at Artist Alley about theatre’s power to heal, follow me for all the live action!

17:01 via @PatientCommando: Tent talk starting and its a packed house

17:02 via @PatientCommando: Clare from @Toronto_Fringe kicks us off

17:04 via @PatientCommando: Intros with Brian G Smith, Dan Stolfi, Zal, and Dr. Jeremy  Photo: http://t.co/4Uw41jZK

17:06 via @PatientCommando: Zal talking about what we do http://t.co/fIZCl19c 

17:08 via @verbitty: Patients like to tell their story, empowers them to engage their providers for better care

17:08 via @PatientCommando: Dr. Jeremy talking about how telling a story “works”

17:10 via @PatientCommando: Improv creates an authentic story – Brian G Smith Photo: http://t.co/G7K5egPI

17:12 via @verbitty: Arts Health Initiative uses humour with retirement residents, reduces agitation and increases sociability

17:13 via @PatientCommando: Improv and humorous patient storytelling shows a 20% decrease in agitation in patients

(RT @IHaveIIH)

17:13 via @verbitty: Not just using humour, but empathy and emotion to connect with patients

17:14 via @verbitty: Patch Adams: Treat the disease you win or lose; treat the patient, you win everytime

17:14 via @PatientCommando: You treat the patient you win everytime. #PatchAdams

17:16 via @PatientCommando: Zal demonstrates theatre and connection Photo: http://t.co/boaXjWrk

17:18 via @PatientCommando: Zal demonstrating the power of impressions Photo: http://t.co/ATD8cExA

17:19 via @verbitty: Theatre is about illusion and perspective, applying to healing changes views on illness and response

17:20 via @PatientCommando: Dan Stolfi shares his story Photo: http://t.co/ILFyTmTP

17:24 via @verbitty: Cancer Can’t Dance Like This: from Fringe to national, giving cancer sufferes a voice via awareness and education

17:25 via @PatientCommando:@CancerCantDance shares benefits of telling an award winning show and now working with Brian Photo: http://t.co/JMI0bKU3

17:33 via @PatientCommando: @CancerCantDance and @Toronto_Fringe 100 play “Dr. Know it all”. Hilarity ensues Photo: http://t.co/Z2IakYAV

17:33 via @verbitty: From Giraffe Elboowtology to Elephant Testicles (Period): Three-Headed Doctor and other improv games

17:35 via @PatientCommando: Dr. Jeremy discusses med school, humour, and narrative.

17:37 via @PatientCommando: Questions from the audience. I think I know this guy…

17:39 via @verbitty: Acceptance of hardships, sickness or otherwise, gives you power over it to use for humour and theatre

17:39 via @PatientCommando: @CancerCantDance shares insights from his journey – when to introduce story to a patient and share

17:42 via @verbitty: Theatre liberates you from the downs of sickness active listening creates doctor-patient empathy

17:42 via @PatienCommando: “Theatre can build #empathy” – Zal Press

17:43 via @verbitty: Using humour and more accessible patient language to help patients laugh sooner and cope better

17:44 via @PatientCommando: No one wants to hear “knock knock, it’s cancer.” – Dr. Jeremy Photo: http://t.co/kzjjC6QZ

17:47 via @PatientCommando: A patient story can provide the reframing necessary for a posititve patient-doctor relationship.

17:49 via @verbitty: Medicine is a blend of art and science

17:51 via @PatientCommando: Zal – talking about patient commando. Come visit us. (shameless plug)

17:52 via @verbitty: Patient Commando amplifies patient voice empowers, engages, teaches narrative skills to play own role in healing

17:55 via @PatientCommando: How to balance humour and mockery in patient relationships. @CancerCantDance shares his experience. Photo: http://t.co/kuzIjYJO

17:56 via @verbitty: Line between using vs imposing humour, coping vs mockery; know audience, turn topic on self so others relate

18:00 via @PatientCommando: One more improve/creative exercise with @CancerCantDance Photo: http://t.co/m7HJ8oqx

(RT @thisisjboogie)

18:06 via @PatientCommando: Questions from the audience turn this activity into a terrifically funny activity

18:08 via @PatientCommando: Thank you to all who attended. Now to @EatPooLove’s show at the Randolph theatre at 9PM. Thx @Toronto_Fringe

18:10 via @verbitty: Hilarious #TentTalk on theatre and healing! Talks every day at 5, visit Artist Alley at @Toronto_Fringe for a talk or come see a show!

21:40 via @Toronto_Fringe: @PatientCommando Read the live tweets that The 100 made at the #TentTalk Great talk today!

♦♦♦ End of Event ♦♦♦

For more photos on our Fringe Festival event visit us on Facebook.

Thanks to all who helped support this event via Twitter.

@MargaretAtwood @Toronto_Fringe @EatPooLove @pipbradford @Vnusinbluejeans @BeeRaskob @sarahmagni @OffTheTwuff @AijaGreen @MarryMeOwen @verbitty @mhoul3 @kathykastner @colleen_young @StampedAStory @thisisjboogie @danielstolfi @cancercantdance @harriseve @med_writer @rosabourin @IHaveIIH

Our Executive Director Zal Press, will be joined by speakers Daniel Stolfi, of the Award Winning Theatre Production, Cancer Can’t Dance Like This, and Dr. Jeremy Rezmovits, from Toronto’s Sunnybrook Hospital.  Brian G. Smith, Creative Director for Patient Commando and The Second-City Alumni will facilitate this humorous one-hour event.

During a kick-off event at the CBC’s Glenn Gould Theatre last year, Brian orchestrated a brilliant performance that demonstrated the power of theatre and humour. While today’s event will be a slightly different program it will undoubtably build upon the efficacy of performance.  Join us.

If you can’t make it we’ll be on Twitter the entire time tweeting #FringeTT

The morning after my first bowel resection over 21 years ago, I was lying in bed still woozy from anesthetic. A troop of white coated doctors entered the room and surrounded my bed. It was my surgical team.

The lead resident was filling me in on how successful the operation was, how much bowel was removed, when he added, “Oh, by the way, while we were in there we removed your appendix too.”

He was much too casual about taking one of my body parts. I panicked momentarily, groping myself between my legs to make sure the surgeons hadn’t got carried away “while they were in there”!

I’ve learned to live with the consequences of those missing lengths for a couple of decades. I know I’ve been lucky. There are people in far worse condition than me. Then 5 days ago I came across Michael Seres online.

Michael didn’t just have a bowel resection. After years of chronic Crohn’s disease his bowel completely collapsed. A resection wasn’t going to do the trick. He needed a whole new bowel and was slated to be one of the very first people in the UK to undergo a bowel transplant.

The transplant took place in October, 2011. It hasn’t been an easy journey. But on Sunday, June 8, 2012, Michael sets a new standard in guts and glory by being an Olympic Torchbearer for the 2012 London Olympics.

You can watch him walk streamed live online here at approximately 9 a.m. EDT. If you miss it, we’ll be featuring it next week on our site.

We’re also going to be featuring Michael’s writings which are honest, enlightening, and visceral. With all that he’s undergone, he continues to understand the inherent connection between his reality and that of his wife and children. Through his constant blogging, and that of his wife Justine and young son Nathan, we will share all the intimate details of this unique story.

Even as one who has lost parts of my gut, I have difficulty relating to losing it all, then getting someone else’s to replace it. Michael Seres is my new hero. Aside from offering himself up as a guinea pig for this procedure, he’s taking us all along for the ride.

Thanks Michael. It’ll be exciting to see your walk on Sunday. Be careful playing with torches.

Here’s a couple of Michael’s blog posts to get you started.

The Toronto Fringe Festival is arguably the city’s largest theatre event.  This summer from July 4-15, over 150 performances will be presented to an expected audience of 100,000. That’s a whopping 4% of Toronto’s population.

What makes the Fringe exciting is the process in how acts are selected for the festival.  Each year hundreds of creative applicants send in their ballot to have a show slotted for a Fringe playbill. With no judge or jury, the shows are picked at random, making for a wildly organic and impressive lineup.

Fringe audiences are accustomed to alternative theatre.  Which is why it’s the perfect environment to showcase the new, truthful, gritty, and sometimes slightly less glamourous stories.  In our minds The Fringe is also the ideal arena for patient storytelling.

Last year proved this with the highly acclaimed performance of Daniel Stolfi’s “Cancer Can’t Dance Like This”. Daniel’s show has since gone on to win the Canadian Comedy Award for Best One Person Show, and garner national attention.

This year will be no different. In fact this year’s program offers at least two patient story events for public consumption. Details of these shows below.

Healing Through Theatre

Host: Brian G. Smith (Second City Alumni) Panel: Zal Press (Patient Commando),  Dr. Jeremy Rezmovitz (Sunnybrook Hospital), Daniel Stolfi (Cancer Can’t Dance Like This)

Eat Poo Love 

By: Paul Clement, Evan Mackay, Dan Mackay Cast: Dan Mackay, Evan Mackay, Paul Clement

Paul Clement survived Stage 2 Colon Cancer and went on to blog about it (selected blogs available here), and eventually co-wrote a stage version of the blog which will be performed at the 2012 Toronto Fringe Festival as “Eat, Poo, Love”.  He recently appeared on the RogersTV program ‘daytime Peel’ to discuss his journey through the illness, and his fundraising work with Colon Cancer Canada.

We’re exceptionally pleased that The Toronto Fringe Theatre Festival and its patrons continue to support patient storytelling.  Our thanks.

I’m reminded of the time my father came to visit me in the hospital after my second bowel resection.

He entered the room in earlier afternoon, walking at a measured pace with his cane, neatly dressed in a suit, winter overcoat and fedora. Ignoring my mother’s exhortations that a man of 91 and such short stature shouldn’t be travelling by public transit on a wintery day, he navigated the system to come and sit by my side.

He related in extreme detail, and with great pride I might add, how he walked to the bus stop, got on the bus and leisurely rode the 35 minutes to the subway. He described all of the new buildings he had noticed along the way and admired the courage of the developers and the creativity of the architects. Getting off the bus, he transferred to the subway, agilely maneuvering down the long escalators leading to the cavernous stations. “I took my time” he cautioned, when my eyes opened wide with the image of his aching, arthritic knees adjusting to the many steps. Once off the subway his chest puffed up as he was able to breathe the cold fresh March air and coast the rest of the way by foot to the hospital.

That was pretty much the dialogue that day. I was 2 days out of surgery, still deeply under morphine influence, aching gut, and not up for company. It didn’t matter to him that I wasn’t very hospitable or communicative. He wanted to be there with his son. That was all that mattered and the conversation wasn’t that important.

For the next 3 days he repeated the trip, same suit, same hat. Same conversation.

My father’s sense of duty is an example of how the illness experience can be interpreted by a parent witnessing the illness of a child, regardless of their age (I was 49 at the time). It starts with the first sniffle as a baby.

This weekend we celebrate Father’s Day and the relationship of parents and children challenged with an illness. There’s Aza Raskin’s lyrical memory of his late father Jef Raskin, inventor of the Mac, and Pulitzer Prize winner Buzz Bissinger’s brutally honest memoir of his road trip with brain damaged son Zach. Unlike the conversations I had with my dad that week over 12 years ago, not one of these stories is the same.

Feel free to add your story to theirs.

I’m biased, of course. I’ve been living with Crohn’s disease for over 31 years. It’s one of the family of nasty Inflammatory Bowel Diseases, (yes, Bowel diseases) that includes Ulcerative Colitis, but does not include IBS, or Irritable Bowel Syndrome (more on that in another post).

Since its such a gross topic (bowel disease, you can only imagine) I’ll skip the details of my experience and go straight to highlighting those individuals who have shared with us some remarkable stories. You’ll see the index below to get you started and every day this week you’ll see some of these stories and individuals highlighted on our home page.

Trust me. It takes a little bit of courage to talk about your toilet habits in public. It can be funny, but these folks aren’t getting paid to entertain a crowd at a comedy club. What they are doing is breaking down the stigma attached to these illnesses, and in so doing, are changing the world one story at a time.

Bravo to these articulate souls. We’ve got award winning author Jon Reiner, mountain climber Rob Hill, prominent advocate Michele Hepburn, Ben from across the pond in the UK, and many others in writing and video. Feel free to add your story to theirs.