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Showing posts with label treacher collins. Show all posts
Showing posts with label treacher collins. Show all posts

Wednesday, December 20, 2017

Media News: The Love Story Behind Assuaged


The Assuaged​ owners Thane Murphy (Disabled USMC Veteran) and Cynthia Murphy (Treacher Collins Syndrome) have a unique 'rags-to-riches' love story that made its way across the media news!

Follow the link to watch the video by Barcroft Media! http://bit.ly/2Ba9zUC

Daily Mail Reports: Woman told she was too ugly to #love and spent her childhood being beaten and #bullied has finally accepted her severe facial deformity because to her husband she is ‘the most #beautiful woman in the world.’





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Saturday, December 9, 2017

Craniofacial Doctor Andrew Wexler Retirement Gathering


The farewell gathering for Dr. Andrew Wexler was an amazing turnout. They even pulled my patient chart and had it out on the table. It was funny but so meaningful! ðŸ’–


Dr. Wexler has treated children with craniofacial disorders for over 35 years. He is famous for his silly bowties and genuinely caring for his patients. Those born with these conditions often undergo surgery as young as two years old. Surgery is a daunting and complex process, but he’s always ensured to bring humor just before going under the knife. He has changed many lives, including mine.

 

Not only has Dr. Wexler helped bring immense inner joy to many, but he’s given us the realization that surgeries are only surface level. Plastic surgery does not bring harmony to the heart or fix what's missing inside. He’s always advocated that fact. 


Many patients didn't show because of the wildfires in Los Angeles, but several of his colleagues attended, I lost count! I'm so thankful for Dr. Francis helping me to arrange the occasion. 

I met some incredible people on The Kaiser West LA #craniofacial team. These are amazing people who truly care to make a difference in our lives. Without their delicate care all these years, I wouldn't be here today. I'm forever grateful. 

Dr. Wexler thank you for making such a positive impact on my life! You will be deeply missed by all!



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Saturday, November 25, 2017

Dear Special-Needs Parents: We're Being Duped by a Faulty Healthcare System

Cynthia Murphy | Craniofacial-Vegan Activist |

Cynthia Murphy (Treacher Collins) and Sophie (Pfeiffer Syndrome)

Have you noticed the increase of chronic illness among children and adults with disabilities? I’ve seen countless families torn apart and derailed after being left on the trail of devastation. Sadly, many of these grief-stricken people have been affected to such a degree, all ties have been broken, and now their children are no longer with us.

It’s heartbreaking to bear witness to these parents trying to cope with the death of a child while longing for what should have been. A parent’s worst fear is outliving their children. It’s even especially painful for these families living with immense regret and guilt that they didn’t do enough.
We are often left to suffer health disparities due to craniofacial anomalies, a rare genetic disease that causes severe internal and external bodily malformations. Chronic illnesses are inevitable.
The reality is that we’ve been deceived and failed by many of our own specialist doctors within a misleading healthcare system.
I first noticed the staggering increase of child craniofacial-related deaths last year while assisting Dr. Justine Lee of UCLA to gather participants for a study involving a rare genetic craniofacial condition known as Saethre-Chotzen Syndrome.

I increased my networking efforts by joining hundreds of groups and amassed my friends list to nearly three thousand. I’ve had personal conversations with almost everyone, and I don’t add friends I can’t verify. However, I’ve learned the tragic challenges that many of these shattered families face.

R.I.P. Kip Ryder (Saethre-Chotzen Syndrome

Every day when I open my Facebook, generally the first thing I see is a child suffering from chronic disease attributed to their craniofacial disorder. In moments of apprehension and fear, parents often post their experiences, including graphic images. They reach out in hopes of securing guidance from other parents who’ve endured the same experience.

Many parents are aware of the hundreds of craniofacial support groups available, and so they utilize them to help answer questions that their doctors won’t.

Mother Beverley Harry admits that a nutritional diet led the way to excellent health for her nine-year-old daughter, Becca, who was born with a rare form of Crouzon’s Syndrome. “It’s been a journey fighting doctors for information about nutrition because it goes against their practice and they aren’t knowledgeable on the subject,” she says. “I chose to take control of my child’s health and ditched doctor care, and I only utilize our medical doctor when needed for surgeries, etc.”

Beverley affirms that it’s our responsibility to look after our children’s health. She’s had numerous doctors misinform her and prescribe ineffective and even harmful medications. Things have dramatically improved since changing her daughter’s diet including the use of pure colloidal silver, a miraculous naturopathic mineral healing agent.
Becca now no longer needs physio or occupational therapy as she’s gained tremendous strength, and all development delays have significantly improved.
I was born with Treacher Collins Syndrome, and I’ve also been a victim of this flawed healthcare system. October 2015, I nearly died in the Utah Mountains landing myself in the Salt Lake City Hospital for a week. I was found blue and foaming at the mouth, and after the incident, my oxygen levels dropped to the low sixties during my sleep. Doctors couldn’t figure out what was wrong, so I was discharged with a severe sleep apnea diagnosis.

I’m awaiting a second major jaw reconstruction surgery due to severely restricted airways and because the first one was unsuccessful. I was informed that the first jaw surgery failed because I was too young and undeveloped at age nineteen.


One year following my near-death experience I became plagued with several chronic illnesses including eye infections, acute infectious sinusitis, digestive issues, enlarged spleen, oozing Baha infections, headaches, constipation, hemorrhoids, chronic fatigue, and progressive periodontal disease. Also, I have four braces, for my wrists and knees due to advanced arthritis and problematic muscle and ligament pain involving cracking and popping joints.

One of the most significant challenges I’ve overcome is suffering from four to six monthly chronic bladder and yeast infections. At one point, I was on my menstrual period for nearly two months.
That is when I discovered that prescription drugs are incredibly detrimental to the body.
These pills are not natural earth substances. They are harmful man-made compounds that are far from curing illness. The acclaimed documentaries American Addict reveal the pharmaceutical trade and how many Americans are being affected today.

Last year I made a choice to walk away from all prescription drugs, and my husband and I decided to adopt herbalism and organic vegan diets. Both of us endured different illnesses. My husband, a disabled USMC veteran and PTSD sufferer, was diagnosed obese and pre-diabetic, and I was taking more than fourteen prescription drugs for numerous ailments including depression. Nothing worked, and I felt so sick that I couldn’t function. I relied on narcotics for pain and anxiety. For years, I had been questioning why every prescription gave me more problems. One medication regularly led to three more.

I’ve accumulated so many pills over the years that I could submerge my entire body with them, literally.

I felt my body failing and my mentality slipping while being trapped in a clout of destructive thoughts. I was even headed towards a hysterectomy at age thirty-one, because of birth control pills I’d taken for over fifteen years.

The quality of my life has vastly improved since I’ve discontinued taking medication.
I’m here to tell you that we live in a sick care system that is devised as a complex maze that has us clambering out to referred specialists who can’t answer our questions. They deny nutrition and instead use the power of their pen.
This process leaves us feeling exhausted, especially when the costs associated with taking time off work and traveling far distances drain our bank accounts.

Many of us are startlingly aware of the health epidemic taking over our country, and it’s not just the craniofacial community either. It’s America. Our country is ranked as having the lowest food qualities in the world. There are toxic chemicals and GMOs allowed in our foods that other countries don’t allow.

This particularly affects us in the craniofacial realm because naturally our bodies are more sensitive. However, make no mistake, the ongoing sick-care epidemic is affecting everyone everywhere.
Evidence of this has been documented in the groundbreaking films What the Health, Forks Over Knives, and Hungry for Change, all available on Netflix.

Please take some time to educate yourself on holistic health practices and organic veganism for the sake of discovering complete wellness for you and your children. We deserve better than this, and it’s during these times we need to support each other the most.

In addition to my advocacy for craniofacial differences, my husband, Thane, and I built a charitable reference and recipe app named Assuaged to help guide families find safe foods and products to buy. We founded Assuaged on the concept of the Blue Zone movement and in the region of Loma Linda, California—one of only five geographical areas in the world and the only one in the United States.
Research studies and several news reports have established that blue zone residents maintain supreme health and live past the age of one hundred.
We are passionately seeking to bridge the gap between healthcare and self-care to meet the needs of healthy living as a method for longevity. We’re going beyond charity and unifying people through love and compassion.
Assuaged is now available to download for FREE via iOS.
Cynthia Today at Optimal Health | The Murphys Happily Married 11+ Yrs | Thane, USMC 2004

Thursday, November 2, 2017

Craniofacial Conditions and Chronic Illness


Wow, we've been receiving many applications for the Cochlear Baha hearing aid giveaway. Please apply if you have a #craniofacial condition and are in need! You can submit an entry following the link at the end of my new article. 💜
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If you have a chance, please do read it. I've included significant health information backed by personal experiences, interviews, medical studies and movie documentaries.



Monday, October 16, 2017

What the Controversial 'Wonder' Publicity Campaign Demonstrates About Craniofacial Equality

I understand why many are offended by the “Real-life Auggie” campaign being promoted by the film “Wonder,” adapted from R.J. Palacio’s New York Times bestseller of the same title. People feel as if they are being presented as a circus animal or behind a glass cage. When I first heard this metaphor, it sent razor-sharp shivers down my spine. We are people, not commodities.

While I firmly believe there is no ill-will intended by this campaign, it does not send the appropriate message. And it’s painfully excruciating to hear how this affects others. My friend and advocate Ann Piesen, born with Treacher Collins Syndrome states, “I’m concerned as it creates the impression that I’m being observed. We are not a novelty because of a movie.”

Initially, all I could think was, what is happening to our society and why haven’t we reached a level of mainstream equality yet?

I believe that this film has a powerful opportunity to raise much-needed awareness, and I’ve become grateful for its existence through the many relationships I’ve formed during its promotion. It’s natural for viewers to want to meet real people, because that’s how we can watch and authentically relate to the truths portrayed on screen. Personal experience is reality, and we can’t lose sight of that.

I’ve been advocating for awareness for over two years now, and I regularly speak with several families online who are hesitant for any craniofacial organizational involvement due to several different factors including fear of exploitation, further stigmatization, and money. I’ve retained the “Erin Brockovich” label in the craniofacial community as I work to provide valuable information, connections, and resources while maintaining confidentiality with these families, many of whom I carry meaningful relationships with. Most are aware that I work strictly as an awareness advocate and I do not promote fundraising or self-gratifying surgeries.

My goal is to foster community collaboration and awareness efforts so we can enact the real change needed.

I support many organizations for their awareness efforts, because without them we wouldn’t be here today. I am especially supportive of the annual retreats and events provided by the Children's Craniofacial Association. I have close friends now that I wouldn’t have had before.

While I don’t see any intentional acts of degradation in the campaign for of this movie, I understand why some find it offensive. Many seek to protect their children and to feel equal to everyone else. The craniofacial community is often sensitive, and rightfully so. We must collaboratively affirm our awareness actions and seek to protect each other in a compassionately equal and logical manner.

Our faces may reveal a physicality some can’t understand or relate to, but we mustn’t forget to express that we are people too. Like anyone else, we have thoughts and feelings deeply connected to the roots of our souls. We’re unique and competent individuals seeking to passionately experience our lives. Many of us have impressive educational skills and qualities that are missed because we’re often taken at face value.

Several medical research studies document that children born with craniofacial abnormalities typically have average intelligence. However, due to widespread stigma, too many people assume otherwise. There is so much value, worthiness, and beauty beneath the surface of our faces.

I can easily name dozens of individuals born with mild to severe craniofacial anomalies and their success stories. These individuals are government employees, writers, doctors, models, therapists, actors, educators, artists, singers, mechanics, nurses and more. We’re here to show everyone that we are not the stigma of our disability or defined by incapabilities.

We have exceptional talents within us all, but we must fight to find them together. We must supersede our fears and act bravely to accomplish what we desire in our lives. No fictional movie or book can achieve what we can together in the form of our collective voices!
I hope you can resonate with my words because we're all in this together.

For more information on our collaborative efforts in raising further craniofacial awareness, please join us on Facebook at Craniofacial Support and Resources.


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READ: A recent medical study 'Children with craniofacial conditions face most difficult social pressures in elementary school' research by specialist Dr. Justine Lee of UCLA Mattel Children’s Hospital
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Published via The Mighty
Read More Articles written by Cynthia Murphy
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Article references 'Wonder' the book written by R. J. Palacio and Lionsgate upcoming film starring Julia Roberts, Jacob Tremblay and Owen Wilson

Monday, September 11, 2017

Craniofacial Differences or not - Make a Moral Choice and use your Voice

Do you believe in energy? I do. I believe that everything we surround ourselves with including music and people imparts within us. Do you believe in signs? I do, they’re everywhere. We’re surrounded by a loving light, my friends.

I’m not really into being a celebrity fan unless there’s meaning. I’ve met countless celebrities growing up in Big Bear while working the luxury hotels and ski resorts as a teenager into adulthood. Personally, I think celebrities are overrated, but not the inspiring ones. You know the influential people who are trying to do something about the ugliness out there in the world? Stuff is happening right in front of our eyes, but we’ve been blinded, my friends.

Look beyond the news, and you will find what I’m talking about. Nothing is being hidden from us; the deception is in plain sight. We're seeing more cases where causes of immorality and #charity are being combined and defined together - I'll get to that later on.

A few weeks ago I learned of the harsh publicity Taylor Swift endured. Terrible things were said about her. One thing that gravitated me towards her is how she took a stand for our rights, as women and many other things. Abuse is #abuse, and it should never be tolerated. If you don’t recognize by now that we the people are responsible for standing up for ourselves and our American rights - you need to take a minute please because we can lose them. We need to keep this world in balance and harmony with what’s morally right. Take a stand for what's right, even if you're terrified. The escape from your fears will be far much easier than what's to come.

We all have a story and different traumas - some in more severity than others. I know I’ve gotten abused in more ways than I can count. I was born with a physical deformity, my step-father did terrible physical and sexual things to me starting at a young age, and my mother abandoned me altogether. I could go on, but I'll spare you the details... I thought about suicide for years, and I hated myself internally, though I showed others a more confident side.

For years I blamed God. I engaged in secretive, emotional self-harm, and I acted out, but I stayed passionate in my career ambitions. I never stopped working and going to school, and I've never quit pursuing my rights for #equality.

I may have failed standing up for my rights as a child, but that all changed when I became an adult. I've filed several cases against employers and every time I was asked 'what financial incentive I wanted' when all I was seeking was EQUALITY. We are all worthy of that and more. Sadly, I see that it’s starting to slowly diminish in today's society.

A few days ago I heard Taylor’s Swift new song, and now it’s stuck on loop in my head LOL. That’s where energy comes in. You may not realize that what you listen to does, in fact, affect you. And with that said my friends, you can, and you will feel the energy coming from it. I felt genuineness from Taylor's song, and I’m grateful she took a stand for all of us. I hope you'll continue to do the same, if not make the change.

Saturday, September 2, 2017

Updated List of 2017 Craniofacial Events

Happy Saturday & Craniofacial Acceptance Month!

I'm still working on my challenge video nomination. Also, the events page is currently being updated. If you're hosting or know of any upcoming craniofacial events - please let me know. I am happy to share any cranio related events. You should be able to post any events to the group yourself directly.

I've been dealing with some medical issues and working to launch our charitable project. But I'll always be dedicated to sharing these cranio events. Meeting others in your realm of experience is remarkable and life-changing. I hope this helps you connect. You can view the List of updated events at: Craniofacial Events and Connection<3 br="">

Monday, March 27, 2017

Treacher Collins Syndrome Weight Loss

I couldn't sleep so here goes another video on the subject of weight loss from me to you.



Craniofacial Diaries Deep Thoughts

Making the switch to an all vegan diet has dramatically changed my life for the better... I wish I knew the importance of health 30 years ago. I've never felt so spirituality connected and healthy in my life. Things I failed to see before, I see now. I'm not as emotionally fragile. I used to need people who never needed me to begin with. I feel emotions much more intensely unlike before, but I like it better this way. I'm not blind to any negative energies that try evading my space. I only care to know moralistic and loving people. Today I'm happy and I feel content with being me.

Overall, I feel progress, but I must admit that I'm still frustrated. I'm not quite there and I do fear that it will worsen, especially if I don't gain some weight soon. I'm 95 pounds at 5'5. I know I'm not alone, there's more of us out there who are enduring the same symptoms. Fear not judgement. Share your experiences. Knowledge is power.

I need strength in my bones. I feel very weak. This is so not me... The bones in my legs, arms and feet regularly pop, and it's not comforting either. I regularly use various heating pads (praying they don't catch fire) and KT tape which both help me tremendously. A nice bath in Epsom Salts is comforting at times too. I have two knee braces and two wrist guards for each wrist that I often wear. My right hand moreso than the left. My tailbone is very bony and uncomfortable to sit on for long periods of time, especially during driving.

You can ask anyone who really knows me that home is not where you'll always find me. I love going out and experiencing life, even if I'm a lone ranger when doing so. I miss nature. This just isn't me.. I'm confident I'll find some answers soon. Meanwhile, I'll be sure to share everything with you too. ❤

Thursday, August 11, 2016

Craniofacial Events Connection- Online Schedule of upcoming events within the United States


https://www.facebook.com/groups/CraniofacialEventsConnection/


Virtual schedule of upcoming events for individuals and families of Craniofacial Differences throughout the United States.


CRANIOFACIAL INVOLVEMENT: If you or a family member has a craniofacial abnormality and if you would like to take part in upcoming events involving craniofacial differences, please come join our new group that is exclusively for events all throughout the U.S. There are a variety of annual children camp events, picnics, family events, support groups, you name it! 

The experience of meeting others with craniofacial differences is a remarkable one, but even more so - the building of close relationships is without a doubt - a precious life treasure. Please come stand with us.


To find an upcoming event nearest you please 
https://www.facebook.com/groups/170897816665027/

Tuesday, May 10, 2016

How This Upcoming Film Proves Hollywood Still Doesn't Understand Disability


https://themighty.com/2016/05/wonder-disability-and-diversity-in-the-entertainment-industry/

The furor over the 2016 Oscars didn’t get my attention at the time. Then I started noticing what those protesting the awards had pointed out. People of color really were being excluded, even for roles that should have automatically gone to them. In fact, according to the University of Southern California, although an average of 75.2 percent of speaking roles already go to white actors, some of those parts are actually characters of color. Why does Hollywood ignore the real thing when casting? And it’s not limited to race and ethnicity.

There is currently a film in the making that should have brought joy to the craniofacial community. Adapted from R.J. Palacio’s New York Times bestseller, “Wonder,” the film will star Oscar and Academy-Award winning actress Julia Roberts as the mother of a boy with a severe facial abnormality. But wait. The boy will be played by Jacob Tremblay, who doesn’t have a craniofacial disorder. To top it off, Julia Roberts was given the starring role of a Latina, when she is a Caucasian actress with no cultural or blood ties to Latin America.

Tremblay will have to be “disfigured” with realistic and prosthetic makeup. Also, he’s going to have to fake a speech impediment. Acting out any behavioral and physical disability is challenging, because there’s a fine line dividing authenticity from misrepresentation. Some films are so tainted by inaccuracy that the acting obviously does not represent the real-life person portrayed, which can be perceived as insulting.

It’s not an isolated incident, either. “Grey’s Anatomy” was touted for including an episode on Treacher Collins syndrome (TCS). When I first saw that episode and the grotesque makeup comparable to Frankenstein on the actress, Amanda Leighton, I immediately felt betrayed. I was disappointed that a woman who doesn’t have the disorder was selected to begin with. I felt that my self-image and the image of TCS was vastly misrepresented. She had a small part, with only a few lines to perform in one episode. Why couldn’t they have sought someone more fitting for that role? Especially considering that five years prior, “Nip/Tuck,” another American television drama series, featured TCS and a very similar acting role, but cast a man who actually had the disorder.

Many of us find it very disappointing that the casting director chose an actor who doesn’t have a craniofacial disorder to play Auggie. We feel that the message behind this choice is contrary to the book “Wonder.” Many of us, including myself, have dealt with the insults of our faces being called a mask on all days but Halloween.

There is irony in the fact that the actor will be altered with makeup, changing his appearance to ours. There is no denying that Jacob Tremblay is an incredibly talented actor and has the capability to perform the role for the film adaptation of “Wonder,” and the same goes for Julia Roberts. However, we must seek to protect what we represent, and we must do so with realism and authenticity.

One of my all-time favorite movies is the heartbreaking 1985 film, “Mask.” The film starred Cher as the mother to a young boy who had a facial disfigurement known as “lionitis.” The movie takes you through his journey in seeking public acceptance and finding love; all the while, he had already outlived his life expectancy. Rocky Dennis was played by actor Eric Stoltz, who does not have a facial disfigurement himself, but he exceeded all of our expectations in playing this role, which also won an Oscar for best makeup. I have a full understanding that this film was made 30 years ago, when there were not many options in diversity. However, we are now in the 21st century, in a world of 7.4 billion people. Special effects and makeup are detailed, expensive and time-consuming. During filming, cast members often spend five to 12 hours a day in makeup. So why not cast a boy who actually has a craniofacial disorder?

It doesn’t have to be this way. It shouldn’t be this way. Stacy Keach, now honorary head of the Cleft Palate Foundation, was one of the first to prove that an actor born with a cleft lip and a partial cleft of the hard palate could be powerful, sexy and anything he aspires to be. Cheech Marin is Latino and born with a cleft lip, and proved that a comedian with a disability can be successful. Believe me, there is a man, woman or child with a craniofacial difference right now who has aspirations to pursue a career in the entertainment industry. We should encourage individuals from all walks of life, regardless of race, gender, sexual orientation, religion or disability to become actors and models.

Most people want to watch movies that are not based on stereotypes. We are the audience who contributes to the success of films. We are inspired by seeing real minorities on the screen, not Caucasian actors cast as ethnic characters, and not actors pretending to have a disability or physical difference. We want to feel as if we are living there in the moment and part of the film. We want to watch movies that resonate with our experiences. We are the real individuals actually living the truth behind the movies. We are just asking for an accurate picture of how we live on a daily basis, and to see and feel the real deal.

Article originally appeared on The Mighty, a website where people with disabilities, diseases and mental illness share their stories.

Join our online community to find upcoming Craniofacial Events and Gatherings nearest you

Sunday, May 8, 2016

How I Found My Voice as an Advocate for Treacher Collins Syndrome


https://themighty.com/2016/04/treacher-collins-syndrome-self-advocacy-with-a-rare-disease/


I wasn’t born an advocate for Treacher Collins syndrome (TCS), and if anyone had asked me what I wanted to be when I grew up (which few people did), it would have been the last thing to cross my mind. Like others with disabilities, I was just trying to survive and lead a normal life by pursuing my educational studies and working full time.

Later, I advocated for my friends and family because I had a law background and they didn’t. I did legal paperwork, helped get financial aid for students and wrote any number of letters to help any number of people. Yet I still didn’t consider myself an advocate, especially since a lot of what I did was an attempt to buy friendships.

Someone told me recently that she could not connect with others who had Treacher Collins. I think I might have been the same way when I was younger. I didn’t want to be in the Treacher Collins world. I wanted to be in the “normal” one. Unfortunately, the people in that world, most of them anyway, were the ones who judged. They couldn’t understand our differences; and in all honesty, we couldn’t fully relate to them either.

This year, I met two people older than I who have established careers and who are comfortable with who they are. They don’t care if other people are looking at them, and they made me question why I still do sometimes. Although our stories are different, they inspired me. About the same time I met them, I started posting articles and videos on social media. Immediately I heard from hundreds of people saying that I am an inspiration to them. Now, I get it. Advocacy is about awareness. It’s the bigger picture. It’s about relating to others in more ways than one.

There weren’t any books on craniofacial differences when I was growing up. I had no advocates. Thus, I was essentially alone in a sad, depressing world. I wanted to be part of so many things, and I couldn’t. Getting picked last for baseball or group projects in art, history, or drama is a horrible feeling. It happened to me all the time, and I hated it.  

When I advocate for Treacher Collins, I’m doing it for everyone who has ever suffered those feelings of inadequacy and exclusion. And I’m doing it for me.

Yes, I’m afraid sometimes. And no, I can’t always separate myself from the criticism I receive. When you’ve experienced ridicule, the last thing you want to do is speak out publicly and leave yourself vulnerable to criticism. Still, I feel I have a voice that stems from my experience, and I am committed to making it heard.

No one “kind of” has Treacher Collins — just as no one “kind of” gets bullied, “kind of” gets discriminated against, or “kind of” suffers from insecurities and depression as a result of all those. No one is “kind of” an outcast.

I’m advocating for the person who maybe only has the distinctive eye shape. I’m advocating for the young person facing his or her 30th surgery. I’m advocating for the people who, like me, have to function simultaneously between a sound and silent world.

I’m advocating for myself, and I’m advocating for you.

Article originally appeared on The Mighty, a website where people with disabilities, diseases and mental illness share their stories

Article republished on CCA Kids Blog "Growing Into Advocacy" and also republished on the Megan Meier Foundation Blog 

Join our online community to find upcoming Craniofacial Events and Gatherings nearest you