Skin deep exposures issue #4
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Transcript of Skin deep exposures issue #4
ISSUE [4]: AUGUST 2013
SKIN DEEP EXPOSURESEXPOSING BEAUTIFUL FROM THE INSIDE, OUT 2013 © NAOMI MAUTZ PHOTOGRAPHY
Exposing BeautifulFROM THE INSIDE, OUT
Photos by Naomi Mautz
SKIN DEEP EXPOSURES MAGAZINE
website I facebook I advertise I contribute I get published I sunscribe
____________________________________________________________________________________
Naomi MautzFounder, Editor, Designer, Writer
Michael MautzCreative Director, Ads Manager, Writer
Joe & Wendy CarnsSenior Editors
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2013
FEA
TURE
CO
NTR
IBU
TORS
EDITORIALS WOMEN’S INTERESTS FITNESS AND NUTRITION PHOTOGRAPHY
Katy MarturanoFreelance Writer
Christa WolfeFreelance Writer
Michael MautzWriter
Melinda ThompsonFreelance Writer,
Wendy CarnsFreelance Writer
MeLinda StruskaPersonal Trainer
Naomi MautzPhotographer
____________________________________________________________________________________
SPECIAL CON
TRIBUTIO
NS
Stephen CarnsFreelance Writer
EDITORIAL PHOTOGRAPHY
Heather LathamPhotographer
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Photo by Naomi Mautz
my strength, but have always encouraged me to #ght against the limitations that HSP presents in my life. A"er being dragged to the gym a year ago by one such dear friend, I am now a much healthier person. I am so grateful for her belief in me and her refusal to watch me feel sorry for myself. Because she forced me to realize the strength she saw in me, I now strive to live that testimony for others. Yes, I have a disease and I am limited but I can and I will put up a #ght against those limitations and live the life I have been given to the fullest. !ese three last three years have taught me to #nd strength in my darkest days. !e times I think I can’t possibly survive one more day are the times when God shows me what I am really made of and that all things are possible through a God who strengthens me, on whose wings I can rise up and face tomorrow.I strive to live each day in such a way as to inspire others to stand strong against their limitations; to learn to love and take care of themselves and to adopt an attitude of gratefulness in their circum-stances no matter what they are. Nothing is prom-ised to us in this life. We don’t get to choose the circumstances we will face, but it is our choice what we do in the face of those circumstances.
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To learn more about HSP or to support
the search for a cure
visit: www.sp-foundation.org
FarewellSUMMER
Photos by Naomi Mautz
Photos by Naomi Mautz
Photo By Heather Latham
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26 SKIN DEEP EXPOSURES MAGAZINE
YOUR
ART
HERE
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Photo by Naomi Mautz
Living With My Disability: DAPHNE HEGRENESS continued.
“Life is about making a conscious decision to live and to love
and to never give up.” Daphne decided early on that she did not want to let being an am-putee keep her from living her life to the fullest. It took her a while to #gure out what her new limitations were. But even as she discovered hurdles, she quickly found ways to overcome them. She discribed how every day she was faced with new obstacles to overcome. It was always the things others take for granted that felt like the biggest challenge. !ings like walking, running, biking, skiing and working. Every new accomplishment was a victory no matter how small or insigni#cant it may have seemed.Since having her leg amputated, a whole new world has opened up to Daphne. She has been given so many amazing oportunities she never would have had otherwise.“When I got cancer and then when I lost my leg I felt like God did not just give me a new chapter in life, he gave me a new book! A whole new world was opened up to me, di!cult at times, but always incredible.” Never having been much of a runner, Daphne became passion-ate about learning to run on her new prosthetic. A"er struggling through several issues, including not having the right leg, Daphne met her hus-band, Je$, a Physical !erapist, who has acquired an internship work-ing with amputees. Je$ began work-ing with Daphne, and a"er a year of training, he taught her to run again. Daphne soon learned that she loved to sprint. She began training at the Olympic Training Center in Califor-nia and competed at the Paralympic trials last summer.
“I am continually being given new oportunities to share my faith and what God has done in my life with others. I have
spoken at camps, youth groups and public schools about being
an amputee. Having a disability comes with many unique trials, struggles and hardships. But I
believe it is in those times we have the greatest oportunity to grow. I have seen "rst hand how God uses our weaknesses to show us His strength. He o#en turns the struggles in our lives into some-
thing beautiful to be used for His glory.”
Daphne admits to still struggling with her disability on a daily basis, but in the midst of her struggles she tries to always remind herself that God has gotten her this far and he isn’t going to leave her now. A lot of doors have been opened to Daphne since she lost her leg and she has been able to meet many inspirational people who have taught her strength and endur-ance. She has witnessed so many oth-ers who have to face each day with unique burdens of sickness and an ar-ray of disabilities but they do it with a smile on their face, praising God for what they have been given despite the things that have been taken away. See-ing such amazing faith is a constant reminder that she serves a huge and faithful God.
“Life is about making a conscious decision to live and to love and
to never give up.”
Photos by Naomi Mautz
EXPOSEDkaty
ON THE COVER
“I have learned that I am a whole lot stronger than I ever gave myself credit for.”
When I fell, there was a guy who took the opportunity, with the guise of helping me up, to attempt to sexually assault me, thinking that I was inebriated. I was so an-gry, at the guy of course, but also at being in a situation of such vulnerability. I went home that night and fell on my knees. I couldn’t live like this anymore. I needed a purpose, something to #ght for. I would not allow myself to be a victim anymore. I started pouring myself into researching HSP, getting involved in support groups and fundraising. I sought out others with HSP who
My experience with HSP has been a lot like the ex-perience most people have to acquiring a disease that alters their lives. I de#nitely went through a period of de-nial, telling myself it would go away and then absolute anger that this was happen-ing to me. I had my time of depression and feeling sorry for myself and that maybe lasted a little longer than I am proud to admit. !at all changed though one night while I was out with friends. We were hanging out and I fell near the bar. Because of the way I walk people o"en assume that I am drunk.
SDE: How would you describe yourself?
KATY: Hmmm. !at is hard. I’d normally say that I’m an average girl but that is boring and not quite the truth. I am someone who strives to be unique. Recently, I think a lot of that comes from living with HSP. Anytime I walk anywhere my strut gets attention. I o"en get stared at, which bothers me, but somewhere along the way I realized that I am di$erent. !ere is no point in #ghting it so I might as well celebrate it. Instead of being embarrassed about the things that make me di$erent, I bring at-tention to them. !is gets things out in the open and relieves the awkward discomfort that people tend to have around me. I try to make my disease and the struggles that come with it my biggest tri-umphs and I have found strength in the process.
SDE: What inspires you?
KATY: Music has always been a huge inspiration to me. Lyrics are just poetry put to a melody and I have a deep love of poetry. I listen to di$erent types of music depending on my mood and circumstanc-es. Sometimes when I am listening to the lyrics of a song, hearing someone express feelings that I can relate to in that moment in such a poetic way is somehow cathartic.
SDE: Can you tell me a little bit about your experi-ence with HSP? What has it been like for you?
KATY: HSP is a family of neurological disorders that can manifest in a number of di$erent ways. For me, the myelin sheath around the nerves in my legs is thinning and so there is a communication glitch between my brain and the nerves in my legs . So when my brain sends the signal to walk, for instance, sometimes the message is interpreted as spasms and violent twitches and other times my legs will just lock up completely. So the simple act of walking, in my case can become a sticky situ-ation and when I am able to propel myself from point A to point B it is a very twitchy process.
were strong and brave and I found that I could draw an enormous amount of strength from them. I wanted to be an encouragement and support for others as well. Even-tually I became the Colorado ambassador for the HSP Foundation. I am involved in research projects and in facilitating HSP awareness.
SDE: What do you wish more people understood about your disease?
KATY: Honestly, I think the biggest frustration comes, not from people’s ignorance of HSP, but from a lack of common manners more o"en than not. As ridiculous as it sounds, I wish more people understood the a$ect that their reactions have. I know that people are going to be curious and that is okay. I don’t have a problem explain-ing my disease to other people; I have made it my life’s goal to educate people about HSP. My legs don’t work the way I would like them to and I might walk a little funny, but my ears and my eyes work just #ne and I can see you staring at me and hear you talking about me and making jokes at my expense. Attracting attention because I am di$erent is something I have really struggled with since acquiring this disease. Instead of allowing that to take a part of me away and make me a victim, insecure and
looking for ways to hide, I have learned to embrace it by looking for ways to intentionally draw attention to my-self. Now when people are curious about me my purple hair or my tattoos are safe topics with which to start up a conversation with me. !ese things help me to give the message that I am strong and unapologetic about whom I am, I am not a victim. And I can always tell myself that people are staring at me because my hair is awesome!
SDE: As women, we are so o!en misunderstood, especially by other women. What is something about you that seems to be taken the wrong way or misunderstood?
KATY: I am a very guarded person but at the same time I am very loud and extroverted. I don’t have a problem talking to strangers but I also wall myself o$ from oth-ers so I can come across as shallow and self absorbed. I know it is a defense mechanism that I have developed. I require others to prove to me that they are someone I can trust before I let my guard down. You and I have talked in the past about how it is the nor-mal chain of events to go through a certain process when getting to know someone. Naturally, we put our best foot forward upon meeting someone new. !ere are steps to go through in order to build di$erent levels of trust in re-lationships. Usually we are given the opportunity to keep those things that we are most insecure about in our lives locked away to a degree only to be entrusted to those of our choosing. Having HSP, has in many ways, taken that process away from me. I am immediately on display. !ere is no option of going into a new situation with someone, testing the waters and then having the gradual leading up to revealing the things about myself that I am insecure about. It is kind of like the dream where you are in a room full of people and you are naked. Learning how to live in that nakedness and own it is a tough thing to do.
SDE: "rough everything, you have managed to accom-plish so much and become such a light for others. What is the accomplishment you are the most proud of?
KATY: A"er becoming the Colorado Ambassador for HSP, I decided it was time to get o$ my butt and #ght this disease instead of sitting back and letting it have control of me. About a year ago I joined Curves and got involved in Yoga. I have since dropped 70 pounds. I am stronger, more con#dent and I no longer feel like a victim.
CONTINUED ON PAGE 44
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“I want to be someone that emanates strength and defiance in the face of the limitations.”
CONTINUED FROM PAGE 43
SDE: I know it is hard to go through something like this so suddenly. Sometimes the hardest thing is just making sense of why. O!en the answer to that never comes. What have you been able to take from this circumstance in your life? How have you grown from it and what perspective have you gained?
KATY: More than anything, I think I have come to a point where I’m not sure I will ever know why. I hate not knowing why, but if I have to live with this disease, I want it to mean something. I want to be some-one that emanates strength and de#ance in the face of the limita-tions. Sometimes circumstances are put into our lives that don’t make any sense to us, but I strongly believe that God takes our crap circumstances and uses them to make something beau-tiful if we will let him. I know I have learned that I am a whole lot stronger than I ever gave my-self credit for and I want to show others that they are too.
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Photography by Naomi Mautz
“It is kind of like the dream where you are in a room full of
people and you are naked.”
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