Archive for June, 2016

LGBT Pride Tribute.

49 Statements of Gratitude.

For my dear friends in the LGBT community,  for friends I’ve yet to meet, and for those I no longer have the chance to meet…..

I Thank you.
Thank you for being proud.
Thank you for sacrificing your dignity and your lives to stand up for who you are.
Thank you for being brave even when you’re afraid.
Thank you for your friendship.
Thank you for your creativity.
Thank you for your vibrancy.
Thank you for your strength.
Thank you for your wisdom.
Thank you for your leadership.
Thank you for your frustration.
Thank you for your vulnerability.
Thank you for your courage.
Thank you for your sensitivity.
Thank you for your children.
Thank you for supporting marriage when marriage didn’t support you.
Thank you for staying focused.
Thank you for speaking out.
Thank you for not giving up.
Thank you for believing me when I say I don’t ever want you to give up.
Thank you for being powerful against hatred.
Thank you for dancing.
Thank you for singing.
Thank you for your music.
Thank you for not accepting less than equal.
Thank you for staying strong when others try to weaken you.
Thank you for fighting for love.
Thank you for accepting others who don’t accept you.
Thank you for that example.
Thank you for growing stronger than your bullies.
Thank you for finding your confidence against all odds.
Thank you for your joy.
Thank you for showing respect to those who are disrespectful to you.
Thank you for your self love.
Thank you for your honesty.
Thank you for your transformation.
Thank you for your authenticity.
Thank you for making a difference by being true to yourself.
Thank you for your emotions.
Thank you for your grace.
Thank you for facing your fears.
Thank you for listening.
Thank you for teaching past generations, and future generations, unconditional love.
Thank you for raising the bar.
Thank you for your intimacy.
Thank you for protecting your loved ones.
Thank you for knowing your worth.
Thank you for your inclusion.
Thank you for your persistence in making the world a better place.
Thank you for being YOU!
I love you. We love you. You ARE loved.
©Suzanne Fiore Photography
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Photojournalism in the Home

I am so honored and excited to share this visual story with you today. The two moms that I worked with recently are celebrating their anniversary this weekend and I couldn’t imagine a better time to celebrate their love, commitment and their family!

About a month ago, I went to their home, for an entire day, and captured what a day in their life looks like. They were so open and vulnerable, allowing me to take photos of them from morning ’til night, without hesitation. I couldn’t have been more grateful to work with them as I begin this new way of photographing the lives of my clients.

I am introducing Day in the Life sessions into my work. These sessions can be a half day or a full day. My approach is photojournalistic in style, meaning I will photograph what I see exactly as it is. No direction and no moving things around. My goal is to capture and communicate an honest visual interpretation of what your day entails.

If you would like to learn more and would like to see what a day in YOUR life looks like in photographs, contact me here.

Part of this package includes a slideshow of your day. You can see a Day in the Life of these 2 moms, and their vivacious daughter, by viewing the video below.

©Suzanne Fiore Photography
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Music Credit:
Time on my Hands
Song by: Vincent Youmans
Pianist: Teddy Wilson
Available on iTunes
Lucy in the Sky with Diamonds
Song by: The Beatles
from: John Bucchino’s Beatles Reimagined
Available at and on iTunes

Rett Syndrome, Lily, and Christine.


Newsworthy: Everyday Acts of Kindness. (2)

A blog series highlighting the art of caregiving.

Photo narrative by: Christine Salerno

©Suzanne Fiore Photography

At the end of May I followed these two incredibly strong ladies for part of their day. I wanted to put a face to a rare disease, that Lily was diagnosed with, called Rett Syndrome. The photos here, along with the story accompanying the photos, were posted at that time.  Her mother, Christine, informed me yesterday that Lily had a setback with her breathing. Some nights it takes her 5 hours to fall asleep because she is either holding her breath or hyperventilating for hours at a time. When she does finally begin to fall asleep, she forgets to breathe and wakes up again gasping for air.

(Christine has written a more detailed description of their journey. Learn more by clicking on this link.)

Lily’s 6th birthday is in a few weeks. You can join me to give her the most meaningful gift by donating to the Rett Syndrome Research Trust here.

I will be following these two courageous girls again in March to continue to bring awareness to the daily obstacles that a Rett syndrome diagnosis brings. Please consider sharing this story so that others can get to know & support Lily & Christine.

These ladies are such an inspiration to me. Why they aren’t on the front page of every newspaper as an example of strength, courage, success, love, and perseverance is a mystery to me. Let’s show Lily and Christine that we support their strength and bravery by sharing their story.


Every morning, I tell Lily that she is the sweetest, smartest, hardest working, bravest 5 year old I know.  

And once you hear a bit about her story, you’ll see why this is true.



You see, Lily has Rett Syndrome.  Likely you’ve never heard of it.  This is how it’s sometimes described: ‘imagine a girl with the symptoms of Parkinsons, Crohns Disease, Epilepsy, Severe Anxiety and Cerebral Palsy all in one little girl’.  It’s pretty devastating.  Most girls that have Rett never walk, never talk, need feeding tubes, have limited to no hand function and are on multiple medications to ease symptoms.



Lily is described as being on the high functioning side of Rett Syndrome.  Lily walks (somewhat unsteadily, but independently for the most part), has some words that come and go, has some hand function and can eat normally.  She’s unable to learn sign language because her hands don’t function well, but thanks to technology, I’m able to communicate with this kiddo.  


Though Rett Syndrome impacts almost EVERY aspect of her body, it hasn’t impacted her intellect.  Up until recently it was believed that girls with Rett Syndrome were cognitively impaired, but – because of amazing technology – researchers, teachers and parents (though most parents already knew this) realized that these girls are smart. During the week, Lily goes to a special needs preschool where she has upwards of 4 therapy sessions a day.  Once she gets home, she has another 2-4 sessions throughout the evening. I tell people that she’s busier than the CEO of the company I work for.  This kid works hard.  And she has to.  If we don’t constantly keep at the skills she has, she will lose them.  



Lily needs 24/7 constant care and supervision.  She can’t walk up and down stairs independently.  Opening and closing doors isn’t possible.









On the weekends, I like to let Lily choose what to do, and I don’t push her too hard.  Usually it means waking up early, having her morning smoothie, listening to music, going for a walk, and picking out flowers for our apartment.






Lily communicates with her eyes.  It’s amazing how much she can get across with one glance.


Even though Lily has Rett Syndrome, she is still a kid, a 5 year old kid.  And she’s constantly pushing boundaries, seeing what she can get away with – like walking into the street.



SFiore_LilyChrisDocumentary72BWBlog  Untitled-1

SFiore_LilyChrisDocumentary12BWBlog Usually, I’ll make her lunch at home.  She’s on a restrictive diet as girls with Rett have mal-absorbtion issues on top of GI issues so I do a LOT of cooking and prepping.  Sometimes in the evening, I’ll take her out to dinner.  She’s extremely social and likes to make her way around the restaurant, and introduce herself in her Lily way (which usually means walking up to the person, smiling into their face and then looking at the food on their plate). SFiore_LilyChrisDocumentary57Blog


She needs help feeding herself.  She can no longer hold a cup to drink from. 




Music is really important to Lily.  One of her occupational therapists (she has 4) described that as Lily doesn’t have an internal equilibrium, music acts as that equilibrium which soothes and centers her.







We have a lot of fun throughout the day.


SFiore_LilyChrisDocumentary6BlogHaving a child with special needs opens up a whole new world to a parent.  Some of it is devastating.  But some of it is magical.  For me, and for Lily, we try to focus on the magical.


If you’d like to learn more about Rett Syndrome, click here.