Port-Wine Stain Birthmark

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    Community Voices
    Community Voices

    how did you guys embrace your birthmark? I can't seem to do mine. I am 13

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    Community Voices

    Are there phrases or terms you wish people wouldn't use when it comes to your illness or condition?

    ...What do you wish people would say instead?

    People often call me "disfigured" because of my facial birthmark. But instead of saying I have a facial "disfigurement," I'd rather people say I have a "facial difference." My face is just a little different than the norm, and that's OK. I'm not disfigured, which has such a negative feeling and connotation behind it.

    #RareDisease #ChronicIllness #FacialDifference #MentalHealth #Anxiety #Depression #Education #Birthmark #PortWineStainBirthmark

    9 people are talking about this
    Crystal Hodges

    When a Stranger Yelled at Me in San Francisco Because of My Birthmark

    Yesterday, I felt beautiful. With my favorite glittery eye shadow on my eye lids and eye liner that made my eyes pop, my makeup for the evening was on point. As my fiancé, Richard, and I stood outside of the Museum of Ice Cream in San Francisco, waiting for our turn, we spoke of our wedding and upcoming marriage. “Excuse me, ma’am!” I heard someone yell, distracting me from our conversation. Looking to my left, there was a person standing over their bike about 15-20 feet from where he and I stood, looking at me. I was the “ma’am” I had heard this person call for. Dramatically touching their face, they rudely yelled a loud response to my facial birthmark, “You have lipstick ALL OVER your face!!” Looking back at Richard, wanting to finish my train of thought, I found myself stuttering, “Um…umm…ummm…I honestly have no idea what I was saying. I need a minute.” And in that moment, I think he could see my heart being shaken as he looked into my eyes, watching me stumble for my words. Once I finished what I had to tell him, I asked him, “Did you hear what was said?” And he had. The exact phrase wasn’t the worst I have ever heard. But being yelled at in a large city, in a rude and dramatic way? That was a first. My heart stung a bit, making me lose my mental footing for a few minutes. Often when I share hard stories, like this one, I people tell me, “Don’t let other people bring you down,” or, “You should ignore people” – and I get that. To an extent, I believe and preach that. But I also know my feelings are valid, and it’s OK to feel what I felt in that moment – and what I feel the next day. It’s OK to process and honor those feelings however I feel the need to. And some days I hear people’s comments and laugh them off with joy, other days some comments are just plain hard. Tomorrow morning I’m speaking to 150 kiddos in their school cafeteria. As their new school year starts, I hope to remind them to be kind to one another – no matter what their peers look like or don’t look like, whether they’re online or off. Maybe, just maybe…if they get in a good habit of that this year, in seventh grade, they won’t yell at a stranger in a busy city. Maybe they won’t steal other people’s images, or tell strangers they need plastic surgery. Maybe they’ll get to know people first, seeing them as a human being with feelings before they see their condition or what makes them “different.”

    Crystal Hodges

    The Other Side of Carrie Underwood's Comment About Her Facial Scars

    In January, Carrie Underwood publicly shared that during a fall a few months prior, not only had she broken her arm, she also injured her face. Not knowing how her face would look in the months to come, she shared with her fans, “When I am ready to get in front of a camera, I want you all to understand why I might look a bit different. I’m hoping that, by then, the differences are minimal, but, again, I just don’t know how it’s all going to end up.” On Thursday, Redbook shared an interview with Underwood in which they talked about her facial injury. When asked if having a facial injury shook her confidence, Underwood replied: It was also a perception thing, because I look at myself [now] and I see it quite a bit, but other people are like, ‘I wouldn’t have even noticed.’ Nobody else looks at you as much as you think they do. Nobody notices as much as you think they will, so that’s been nice to learn. As I read that last line, and as I read the interview, I realized how different Underwood’s experience is from my own and from most people with facial differences. As someone with a unique facial feature, and as a fan of Underwood’s, I’ve paid close attention to her story. I’ve been waiting to see how Underwood would handle her situation and how people would react. Would she cover her scars with makeup? Would she stare a body positive movement while inspiring women around the world? Would she make her goal and mission to change Hollywood’s beauty expectations for women, and its perception of facial differences and scars? While I’m glad that Underwood’s experience has been positive when it comes to people’s reactions, her experience has been quite different than mine. People ask: “How’d you burn yourself?” “What’s wrong with your face?” “You’d be more beautiful if that birthmark weren’t so prominently placed.” “You know there’s makeup that can cover that, right?” I hear questions and statements like these both in the real world and in the digital. It isn’t uncommon for me to leave the house and hear someone say something about the purple hue on my face, or to stare at it. My face is “different.” It’s not what people expect to see when they look my direction. More often than not, people notice my difference – they always have. For people living with a facial difference, what Underwood said, “Nobody else looks at you as much as you think they do,” couldn’t be further from the truth. People stare. Strangers ask questions – sometimes kind, but more often with an unkind and harsh tone. Trolls write hateful comments online. People without medical degrees offer unsolicited health advice. People give unwanted makeup advice. People notice. Underwood’s injuries and scars happened to her later in life. She has had to adapt to the changes her face had undergone. I was born with a facial difference and don’t know life without it. Underwood’s facial injuries have injured her confidence. My facial difference made mine stronger. Her scars can easily be hidden by expensive makeup she can easily afford. I can buy the makeup, but I can still see the outlining of my birthmark, and nothing can touch the symmetry issues my birthmark has caused to my lip, nose, and cheek. My port wine stain birthmark has given my left eye glaucoma, causes migraines, affects my teeth and so much more. From what has been made public so far, her scars are just appearance-based. Underwood and I? Our stories and situations are different. Our experiences are different, as are the reactions we’ve received. Yet, if and when she chooses to share more of her experience around her facial injury and scars – I plan to follow her story. Because even in the midst of our different experiences, both of our experiences are real. They’re both valid. They both matter. Image Courtesy of Carrie Underwood’s Facebook page

    Crystal Hodges

    How to Respond to Stares at Birthmark – According to GIFs

    If you live with a physical difference, you know the stares. Go into store? Someone’s staring. Go into a restaurant? There’s someone watching your every move. Visit a new church? You likely won’t leave the parking lot without another glance lingering a little too long. Living with a facial difference my whole life, I’ve come to realize there are a few specific types of stares: 1. The curious stare. 2. “Ew, what am I seeing right now?” 3. “Ahhh!” 4. “I have the same condition, and I can’t believe you do too!” 5. “I know someone else with the same kind of birthmark you have, and I think you’re so beautiful.” 6. “Look at her face” mockery stare, with a side of laughter to go along with it. 7. The accidental  “I don’t realize I’m staring at you” stare, which may be them just gazing your way – without even noticing the physical difference. 8. “I know you just caught me staring at you, but I’m gonna keep staring at you anyway.” With this stare, they may not of realized they were doing it initially – although some are intentional from the get-go. But eventually they get the “Oh, oops!” look after they realize they’re caught, or they realize what they were doing. But even though they now know what they’re doing, they keep staring anyway and become intentional with the act. 9. “I’m trying to understand what I’m seeing right now”  – which is more common from children, with a dash of the curious stare. They’re curious, they may just not realize just yet that staring isn’t a kind way to go about their curiosity, because someone just hasn’t taught them that just yet. 10. “You poor thing.” 11. The “motion detector” stare – when the person’s stare follows your every move. 12. When people invade your personal space, while staring at you – following you like a shadow, taking every step you take, staying a little too close too long. 13. The never-ending stare. I’m sure there are many types of stares I’m not listing, but those are the main 13. And because there are several types of stares, there are several ways I can choose to respond. Depending on the kind of stare I’m receiving, depends on which one I pick. 1. Make funny faces at them. 2. Ask, “I noticed you looking at me today. I’m terrible with faces sometimes – do I know you from somewhere?” 3. As a child, my mom gave me some the best advice that I carry with me to this day. At the age of 5 or 6, she couldn’t prevent me from seeing a man stare at me. Whatever the situation was, she couldn’t stand in front of them to block my view, nor distract me. (And she always tried her best, and still does…Even though I’m taller than her, and can see stares above her head.) Quick witted infused with wisdom, she told me, “I know what they’re doing is uncomfortable and unkind, but what if you smile at them? What if they’re having the worst day of their life today, and you’re the only one to smile at them? What if you end up making a friend?” 4. Unleash all the swag. 5. Wave at them if they’re in another car next to you at a red light, or if they’re several feet away from you. 6. Do a stare down. Depending on my mood and energy level, the type of stares I’m receiving, or if I’ve had a lot of comments and stares that day – this one can be more common than I care to admit. 7. Introduce yourself. 8. Walk away from the situation, if possible. 9. Go for a shock factor. 10. Act like a princess. You can do a nice hair flip, or wave like a royal – like Anne Hathaway in “Princess Diaries.” 11. Make more funny faces. 12. If someone’s staring is making you super uncomfortable, write them a note. While eating lunch, I once had a man stare at me for a solid 30 minutes, and I almost asked to be moved to another table…And I’ve never felt the need to ask that before. At one point he even did the, “Oh shoot, I just got caught” face, and he’d look away – just to start at me again. But instead, I borrowed a pen and pieces of paper from the waitress and wrote the man a note. I kept it kind and simple, and introduced myself in the note. I even explained it was OK for him to be curious, but not OK for him to stare at me, and that he needed to see me as a person – not a birthmark. This is probably the boldest response I’ve ever given, and the most controversial. But, the people who disapproved weren’t there, and I probably could have done better with some of the details before hitting the “post button.” I also shared the note with people close to me, and explained the situation to them before asking the waitress to give the note to the man. Had they told me it wouldn’t be a good move, these are the people I trust to call me out on it and who have a right to say so…But given what was happening, all agreed it was appropriate. Some people asked, “What if he thought you were beautiful?” 1. He didn’t have the “Oh wow, look at her” stare. 2. He was sitting by his parents…and his wife. 3. And if he did think I was beautiful, no man should stare at a beautiful woman so long that it makes her uncomfortable and makes he feel as though she needs to switch seats. 13. Ask them if they have any questions. 14. Tell them they should see the other guy. 15. Ask, “You keep staring – is there something on my face?” This is especially relevant if you have a facial difference, and it adds more humor to the situation. 16. Ignore them. 17. Sing a song. My stanza option? The song that reads: “I was looking back to see if you were looking back to seeIf I was looking back to see if you were looking back at me” 19. Do a little dance. 20. Bluntly tell them they’re being awkward. 21. Tell them to stop staring. And depending on the situation, you can either ask kindly or be firm. 22. Make a joke – but don’t make it self-depreciating. I usually have birthmark jokes ready to go for a variety of situations. 23. Tell them to take a picture because it lasts longer. 24. Hold a sign up to your face with information about your illness, or follow these celebrity’s lead and hold up a sign about organizations people should pay more attention to. 25. Often when people stare, they forget about boundaries and personal space. If that becomes an issue, just do this… However you choose to respond, know that it’s OK. If you share about these experiences (whether it be about stares or comments people make about you) on social media or publicly, and you share your response, it’s possible people will try and tell you that you were in the wrong for how you handled the situation. The more I share about these experiences, and the bolder I become in how I stand up for myself, the more “you were wrong to do that” feedback I get…But that feedback is 99.9 percent from people who don’t have a physical difference, who don’t know me very well. And here’s the thing – you have the right to stand up for yourself however you deem necessary. You know the full experience in a way others don’t, especially if they weren’t there. You have the right to be as bold as you decide is appropriate. It’s OK to tell people, “This isn’t OK” – whether you say it with humor, boldness, or bluntness. If you live with a physical difference, how do you respond when people stare at you?

    Crystal Hodges

    What You Should Know About Online Health Advocates

    This year has been a really hard advocacy year. Actually, it probably has been the hardest one yet. Because there’s so much positive to share in my journey (speaking opportunities, articles, media interviews, etc.) I think that it’s equally as important to be open about the hard, vulnerable, and raw stuff too. This year I’ve had people tell me I was in the wrong for standing up for myself in a way I felt was necessary – even though they weren’t in my shoes, or experiencing the situation personally. They weren’t even in the room. Last month I had a video a company made about my story. While they did a great job with the video and I was proud of the outcome, it still resulted in some cruel comments… many of which resulting in my hitting the “report” button. Strangers telling me to “F-off” and that my medical condition isn’t valid and is “insignificant” because they were going off what they can see – not realizing there may be more to my condition than what meets the eye. A parent of a kid with similar condition accusing me of having a “false” and “hypocritical” public image – all because I didn’t respond to their email fast enough. (While also guilting me to be friends with her daughter.) …and that’s only four issues I’ve run into in the last three months alone. In all my years of an advocate, I’ve never felt so drained. Never felt so tempted to quit. Just the other day, due to another hard situation not mentioned, I even found myself saying words I never thought I’d say to my fiancé, “One day I may just stop.” And the thing is, I can quit anytime I want. I can delete my blog, I can speak and write about other topics I’m passionate about — human trafficking, travel, or even photography. I can be known as someone other than “the girl who blogs about life with a birthmark.” But then I remember why I do what I do. I’m an advocate for myself, because I believe we should all advocate for ourselves to the best of our abilities. No one knows our bodies like we do, and no one can get the care for their own body’s need like we can. I’m a storyteller so others can realize they’re not alone in their journey. Maybe our stories are different, but there is someone who can relate – and who looks like them. I’m an educator so when someone is unkind to me because of my facial difference, maybe they’ll be kinder to the next person they meet in similar shoes. Maybe the next generation of people with facial differences will be seen as people with a name and story, instead of made to stand out through harsh comments and uncomfortable stares. I’ve thought about quitting more times this year than I care to admit. But I do this because it’s what I feel called to do – even on the hard days. God’s not done with my story yet, and He’s not done with my storytelling. Sometimes I wonder why my skin isn’t “thicker by now.” But then I’m thankful that it’s not, because I’m afraid “thick skin” for me would equate to a “hard heart” — and I so desperately want to keep that tender. I also remind myself that my feelings are real, and they’re valid. It’s OK to feel them, process them, and honor them. Maybe one day I will “quit,” and hopefully someone else will be ready to carry the advocacy baton when and if that time comes. But until then, I remember the beautiful moments — like surprising a sweet kiddo with the same facial birthmark in the hallways of her school. I remember the emails of people who write me and say, “I thought I was the only one — but then I stumbled on your blog!” I remember the good moment that have passed and that have yet to come. I remember self-care, that it’s OK to take breaks and/or sabbaticals, and I’ll remember why I do what I do. I remember that advocacy work isn’t always easy, but it’s not always this hard either. All that being said, as you follow and connect with health advocates online, here are a few things that I think are important to remember as you follow and connect with me, and other health advocates and role models: 1. We are so thankful you’re willing to be a part of our journey with us on our blogs and social media. Oh boy, are we thankful for you! Whether you found us through media interviews and have no direct experience with our condition, a parent of a child with the condition, or you live with it firsthand – thank you for sharing our blog entries, social media posts, and for being a friend on the journey. 2. We’re likely not doctors. I constantly get emails asking for medical advice, including what treatments I think people should do and asking what their medical options are. Some people have even asked me to diagnose them. While I have a lot of medical knowledge, if we have the same conditions, our conditions may affect us differently. I don’t have a medical degree, and I can’t give you a medical opinion. All I can do is share my patient experience – what treatments work for my specific case, how the treatments affect my body and my mental health. If you ask me for medical advice for port wine stain birthmarks or Sturge-Weber syndrome, I’ll probably just send you to The Vascular Birthmarks Foundation where they can then connect you with doctors where you can find the advice you’re looking for. I’d love to hear your story, share more details about mine, and encourage you, but please don’t ask me for medical advice. 3. Most of us wish we had time to reply to every email, social media comment, message on Facebook, message on Instagram, and every Snap sent to us on Snapchat. But often we don’t. Or, at least not within an immediate timeframe. Hearing from you is one of my favorite things about my job! But, unless we have a note pinned to the top of our page, “I promise to respond to every message within 24 hours,” please don’t expect us to write back within a day, or even a week. We’re not on-call, nor are we a like a “one hour film development” center. While we’re seen posting a lot online, we also live a life away from the computer – much of which isn’t published online for the world to see. Personally, I have a job, a fiancé I’m planning a wedding with and building a future with, family obligations, and friendships that I need to tend to face-to-face and way from the screen.Also, it’s important to remember that not only do I write about my conditions, but I live with them as well. Sometimes I have to take care of myself before I can help take care of others. I have doctor’s appointments, laser surgeries, speaking engagements, and sometimes I travel. I also usually have a thousand ideas in my head at any given time, and I’m trying to manage them so I can best serve the health community I’m in. To navigate my advocacy work and every day life, I do my best to reply to messages when I can. But I also have a habit of going through all my inboxes at least once month in effort to reply to people – but even then, sometimes I accidentally miss a few people. Sorry about that. 4. It’s OK to message us again if we don’t reply to your first email. But please be kind. It’s possible we didn’t see your message, even if Facebook said we did. It’s possible that your email never reached our Yahoo or Google accounts. Please don’t assume we don’t want to talk to you, or that we have set up a “contradictory image” in the public eye. We’re doing our best, really, we are. 5. Even if we don’t reply, we soak in your encouragement. Encouragement from others is so vital to what we do. Sometimes I even print people’s emails or messages to help me on the days that are hard health days, or even hard advocacy days. Your encouragement serves as a reminder that we are impacting the world for the better, that we are making a difference – even if it feels like we’re not. 6. When we tell about an experience we’ve had, remember you weren’t there – which means you don’t get to see the full picture, regardless of how well we’ve written the story. Sometimes the hardest part about sharing stories online is that, often, I was the only one there. I write stories sharing about times when people stare at me, or make a comment about my facial difference, and I share them to the best of my ability with full honesty. Yet, sometimes that’s not enough. An experience has many elements, including things such as emotions, smells, tastes, body language, and tone – and they’re 3D, layered with details. They’re constricted between black and white letters on your screens, or the within the pixels of videos we may share. But because I was the only one there, there are several elements that readers will miss – so therefore wrong assumptions are made, and fair questions aren’t asked. In the past, people have responded in anger and judgement, telling me I was in the wrong by choosing how I responded to someone saying something unkind about my facial difference, or how I responded to someone who spent several seconds – if not minutes – staring at me. Instead of hoping for the best and assuming I have a level head on my shoulders, I get criticized for standing up for myself in a hard moment… and in a way I deem necessary. 7. You may not agree with how we choose to advocate for ourselves, but it may be just right for us in that particular moment. Like I mentioned above, I’ve had people tell me I was in the wrong for advocating for myself in certain situations. For example, during my online dating experiment one man wrote to me and said, “Oh, what happened to that beautiful face?” I replied with wit and humor, “Oh my gosh…What do you mean? Is something wrong with my face?” People instantly started writing comments on my Facebook post about the experience. Most were supportive and understood my humor, especially when people who were following the online dating fiasco knew I was open and blunt about my birthmark in my pictures and my profile. But one woman told me I went about my response in the wrong way. Once again, while most people were supportive, there were a few people who weren’t – and who let it be known. In the end, I can only make the best decisions I can with the knowledge I have in the moment. And that’s just what I’m doing. 7. I believe in the form of accountability, but there’s a time and place. I’m only human.I won’t always get it right when I advocate publicly and privately. But while I share stories online, if you have feedback – stop and think before you hit the “post” button. Is your comment better shared publicly, or would it be kinder to show a little grace and message me privately so we can have a constructive conversation? Are you leaving the comment to be “right,” or because you genuinely want to give feedback to help me grow and learn as an advocate? Before you message me, it may be a good idea to write your email, sit on it, reread it the next day, and then send it. But also, remember I do have people in my life holding me accountable. I rely on my mentors, my parents, my best friend, and fiancé for guidance. They’re honest and blunt opinions are the ones I trust the most, and the ones I constantly seek in hard situations. 8. We don’t always have to be nice when we advocate for ourselves. While I try to stay kind in my responses to people’s comments and stares, there’s nothing that says I have to respond in a kind way. Some situations do call for a little bit of sarcasm and sass, and while I rarely ever tap into them and can only count on one hand the amount of times I’ve used this method, I have the right to implement those tactics when I deem necessary. My heart and feelings come first, and sometimes responding to unkindness with a sarcastic joke is more necessary than a smile. 9. Please don’t guilt us into being friends with your children. Are you trying to find a mentor and friend for your kiddo with a medical condition? Someone who’s been through the hardships first hand? That’s amazing! I wish I had that as a child and teenager and I totally see the value and beauty in that. While I love befriending others with the same conditions, and helping kids on their journey, I can’t always be everyone’s “go-to.” If I end up being great friends with your child one day, yay! I’m so glad. But please don’t force it, try to guilt me into it, or get angry if my life doesn’t allow it at that time. 10. Sometimes we have to put up boundaries. Did you know that Facebook only allows people to have 5,000 friends? Because of this reason alone, sometimes we won’t add people with the same condition as friends. Many of us also have public pages people can “like,” and you can see the same content you’re looking for on that corner on the web. (You can find my Facebook page here.) We also want to have a safe space online, where we can talk about random life events we may not want the public to see or know about. We may want to post pictures of children in our lives, while wanting to remain confident that we haven’t added any unsafe strangers to our friend list. In many of my talks, I discuss internet safety after having my image stolen – and I believe in practicing what I preach. 11. We’re not your only option. Did you know that there are likely Facebook support groups for your condition that you can join? Depending on your condition, there may even be support groups in your hometown. Sometimes nonprofits even host events once or twice a year in different cities so you can connect with people in similar health conditions, and to learn about your conditions. I know the Vascular Birthmarks Foundation alternates between the general LA area and New York area every year, and they even have top specialists in the field for port wine stain birthmarks, hemangioma, and Sturge-Weber syndrome, surgeons, and dentists that you can make free appointments with during the events. Usually this event takes place every October. 12. We’re only human. If you think about it, this generation of social media has redefined what it means to be a health advocate. Not only are we advocating in doctor’s offices or giving speeches, but we’re advocating online and in a digital permanent marker. In a way, we’re the first of our kind as we manage our own health, situations that may arise in the doctor’s office or when we go out in public, and also online. Many of us are learning as we go, and we’re doing our best. 13. It’s OK if we decide to “quit,” and even we I don’t, you’re welcome to join us in the advocacy world! If you want to share your story and join me, your perspective and story is welcome! There’s always room at the table for you. Your story is yours, and you can share it or keep it private. That decision is all yours, and both choices are perfectly OK! The same goes for me. Occasionally, I may be on the quiet side and take a sabbatical. One day I may even decide to switch gears and talk about other important life topics. I’m a woman of many talents and interests. From baking to human trafficking, from photography to travel, who knows if one day I may choose a different focus. For now, though, I’m continuing the journey as a health advocate. I love what I do and I’ve enjoyed the journey as an advocate for people with port wine stain birthmarks, Sturge-Weber syndrome, and facial differences. I’m not perfect at my job or in my work, but I promise you that I’m doing my best as I spread awareness about these conditions, and as I teach about kindness. Thank you for being a part of my journey, and thank you for showing me kindness I spread awareness and advocates – both when I get it right, and even when I get it wrong.

    Crystal Hodges

    How My Fiancé Supports Me, My Birthmark and Laser Treatments

    It was obvious on my dating profile. It was shown in all my pictures, it was written within my “about me” section. I was intentional about it being obvious. Granted, I was doing an online dating experiment to see how people react to those with facial differences, like mine – a port wine stain birthmark that dwells on my left side of my face. I remember one of our first phone calls, just a few days before our first date and he bluntly said, “I don’t want to waste my time, and I don’t want to waste yours – but I need to let you know I’m looking for something that could lead to something serious. I don’t want to just date for fun.” I knew this was my opportunity to throw in my “I don’t want to waste anyone’s time” line. Responding, I told him, “That’s what I’m looking for too, so we’re on the same page. But since I don’t want to wast my time either, nor yours – so I need to make sure you’re OK with my birthmark.” I can’t remember exactly what I said after that. I’m pretty sure I threw in a blunt, “If you’re not OK with it, that’s OK. You’re just not the guy for me – because I don’t feel the need to hide it, or hide who I am. And I won’t change who I am for a guy’s preferences or expectations.” But maybe I just thought that, maybe I didn’t say it. I was nervous to be so bold, but it was important. Did I warn him of the comments that could come? Did I warn him about the treatments I have to undergo to make my birthmark stay healthy? Or did that come later? I can’t remember all that I said, but I do remember ending it with something like, “Are you OK with it? Do you have any questions about the birthmark, or about life with it?” He didn’t understand why anyone would see it as an issue, or as a valid reason to not date a girl. Our first date lasted over eight hours. And since that call, we’ve spent hours on the phone. We’ve seen each other every two weeks since our first date – and we’ve gotten engaged. He’s even gone with me to two of my laser treatments – one where I stayed awake, the other where I went under. Growing up, we took friends with us to almost every treatments. It always made it more fun, more of an adventure. As an adult, I’ve gotten pickier on who I want to go with me. Letting someone see me get lasered (which can be quite painful) and then to let them see the initial affects of the treatment can be such a vulnerable thing – especially since I don’t usually leave my house for nearly a week after undergoing one of them, depending on the swelling and discomfort I’m experiencing. I remember him asking to go to one for the first time. At the time, he was my boyfriend, but I knew that was a whole level of new level of vulnerability for our relationship – and it was up to me and if I was ready for that. To an extent, I was. I wanted him to go and experience “real life with Crystal Hodges,” but I was afraid of also letting him go to a treatment – letting him see the process and the pain, to let him smell the burning flesh and hair. What it it was too much for him? What if he’d go, and realize this wasn’t a life he wanted? Sometimes it does feel like a lot to ask of him. The stares. The comments. The migraines caused by the effects the birthmark has on my brain. The treatments. The occasional smells of burnt flesh and hair. The swelling. The risk of growth. The risk of him being accused of abuse – both potentially serious accusations, or flippant. How is it not a lot? But he knew from the get-go. He chose to jump in, he has chosen to stay. In the midst of my fears, he’s gone above and beyond. Knowing my tradition that started as a child where I take a stuffed animal for every treatment, for his treatment experience, he brought me a handmade bear he commissioned someone to make me. He took selfies with my mom as they wore the “Willie Wonka” glasses they had to wear to protect their eyes – because that’s what we do every time. And even though he lives three hours away from me, he came home with us that weekend and just held me as we binged my favorite movies and TV shows. He didn’t even care that I fell asleep on and off throughout our viewing experiences. Yesterday was my second treatment since our treatment began, but this time I was being put under. Knowing I was feeling anxious and nervous, he put his own nerves to the side and rubbed my feet as I waited. He even made my stuffed animal dance to the music I was playing, knowing he’d get laughter out of me. He started showing “in sickness and in health” at the first treatment I invited him to, months before he asked me to marry him – and he continues to do so every day since, with every treatments since. He embraces who I am, as I am – lasered or not lasered. He loves that I love the color purple, and sometimes he’ll even wear the color purple to color coordinate with my natural look. He laughs with me as I make new birthmark jokes. He sees me as beautiful when the world tells me I’m not, and when I don’t feel so beautiful after a treatment – and he makes sure to tell me so on a regular basis. He partakes in the traditions I started as a child without even being asked. And when people stare or make comments? Per my request, he lets me handle it depending on how I see fit – but is ready to jump in if I need or want him to. I don’t have to ask him to stay through it all, because for him, it’s not even a question. And when I walk down the aisle in the coming months? By desires of my own and also by his request, I’ll be wearing white, but with a splash of natural color – keeping my birthmark untouched and unchanged.

    Crystal Hodges

    Ways People React to My Facial Difference - as Told by GIFs

    When you live with a facial difference, life is never boring. People are constantly in awe when I share stories about how people react to my face. From harsh comments to staring, I do my best to not only describe the stranger’s words but their tone and body reaction. But in a world where GIFs are growing in popularity, I’ve created a list of the most popular responses I get from strangers when I’m out in the public, as told by GIFs – whether I’m on a date with my boyfriend or if I’m shopping in Target with my mom. (Also, please note that most of these statements and experiences were simplified to one sentence from the interaction.) 1. “Is that contagious?” 2. “Is that a tattoo?!” (Mostly asked by children but not uncommon among adults either.) 3. “How do you shower?” 4. “I’m so jealous, I wish I had one too.” 5. “You’re ugly.” 6. A common question often asked is, “What’s wrong with your face?” Walking into a church a few years ago, a woman I’ve known my whole life even greeted me with, “Oh, I thought you were the girl who has something wrong with your face.” 7. “Hey – you have the same birthmark as me!” 8. “You know doctors can fix that, right?” 9. “You’re so brave. If I were you, I wouldn’t even leave my house.” 10. “Oh my gosh, are you OK?!” 11. *Stares* 12. *Staring, while awkwardly looking away when caught, occasionally sneaking a peak* 13. *The horror stare* 14. *When people follow my every movement with their stares* 15. “If you had enough faith, you’d be healed.” 16. “Why does your face look like that?” 17. “Oh my gosh… Your face looks really bad.” 18. “What is on your face?” 19. “Oh, is that a Halloween costume? Who are you dressed up as?” 20. “You poor thing.” 21. “You’re so beautiful.” 22. Once I went to the mall to try on makeup that hides my birthmark – which would be used for a very special occasion. (I rarely choose to hide the birthmark.) Once I was in the chair, I was invisible. Only my birthmark and my mother remained in makeup artist’s company. Instead of asking me what I thought about the makeup, she kept referring to my mother with statements such as, “Doesn’t that look better now?” She even slipped out a casual, “See? With her hair down, you can’t even see it anymore.” While this is one example alone, this GIF represents when people don’t see beyond my birthmark, when I as a human… a person… becomes invisible. 23. “What do you use to cover your birthmark? You should try this makeup brand. It hides things like that better.” 24. That one time my picture was stolen, and I was turned into a meme that went viral to over 30 million people… and cyberbullied in the process. 25. “Ew, gross.” 26. “Can I touch it?” (And let me point out that not everyone will ask, some people will just reach up and touch my cheek – especially children.) 27. ER Doctor: “I know you’re here for an allergic reaction, but did you know that you can get that birthmark treated?” 29. *More staring* 28. “You’re wrong. That’s not a birthmark – you have cancer.” 29. When people won’t believe it’s a birthmark and insist there is something doctors can do about my face. 30. When people take one look at me and their gut reaction is a swear word. 31. “Do you have purple boogers?” (Usually asked by children. But just in case you’re wondering – no, I do not.) If you also live with a facial difference or body difference, what GIFs describe the reactions you’ve gotten from strangers?  

    Rhonda Hodges

    Lessons From My Daughter With a Facial Port-Wine Stain Birthmark

    The first time I can recall seeing someone with a facial port-wine stain birthmark was when I was pregnant with my daughter, Crystal. I was in a department store shopping for baby supplies for this new little one who was going to be entering our world soon. When I saw the lady with the birthmark, I remember thinking, “I’m so thankful my 6-year-old daughter, Amanda, is healthy and doesn’t’ have anything like that.” Little did I know the little baby I was carrying would have the exact same birthmark. Now, I am so ashamed that I could not look past the birthmark to see the beautiful woman in the baby aisle. I’m certain she is loved and respected by many people and is making a difference in her circle of friends and family. When Crystal was born, we noticed a little bit of additional pinkness on the left side of her face. We didn’t think anything about it at first, but within a few hours, it became increasingly darker. The pediatrician who did her first baby check while in the hospital came in to see me when I was alone. His words were curt, sharp and his bedside manner was extremely in need of improvement. He only offered medical terminology to explain the birthmark and was not patient when I asked for further information. He said something to the affect of, “She has a birthmark, there’s nothing that can be done about it and you’ll have to deal with it.” He left the room and I never saw him again. It should go without saying that I looked for a different pediatrician for Crystal. Once I found a new pediatrician, we began talking about options to lighten her birthmark. Since this was over two decades ago, the information about port-wine stains was limited. The technology to treat these birthmarks was being developed, the specialists that we saw made it sound as though with just a few pulsed-dye laser treatments, her birthmark would barely be visible. In my excitement to see what she may look like without it, I asked a co-worker who worked with computers if he could digitally remove her birthmark, so I could see what she’d look like. Computer technology was quite different 26 years ago, so it took him a while to do it. He removed her birthmark, but she didn’t look like my baby. My initial request seemed harmless, but as I think about it today, I wonder, did I want her to look “normal” for me or for her? I am now ashamed I ever asked him to digitally remove the mark. As she grew, my husband and I had many conversations about how she would adapt to the world. Would she be able to “fit in?” Would she be accepted by her peers? Would she be withdrawn and anti-social? How are we going to manage her growing up “different” from other kids? I am now ashamed that we ever questioned her ability to fit into the world. If you know Crystal, she is loved by so many people and her social life is much better than mine! Our concerns and thoughts limited our own ability to see her full potential. I am so thankful we never expressed those thoughts to her. As parents, it was (and still is) our job to encourage our kids to dream and see their dreams come true. Today, Crystal’s motto is, “Making a difference with my difference.” And making a difference, she is! When Crystal was about 12 years old, someone told us about some makeup that a lot of burn patients and other port-wine stain bearers wear. It does a wonderful job to hide flaws and scars. I told her about it and she was excited to try it. I was too. Maybe a part of me wanted her to like it so I wouldn’t have to watch others stare at her when we went to the store or out in public (I am known to stare people down as they stare at her. Notice, that’s not in past tense. Crystal still catches me doing that today, even though she’s taller than me). She tried the makeup and was excited to show her “new look” to our extended family. On this day in the public, I was not looking to stare people down. I was more interested in how Crystal felt. She looked so different and I wasn’t sure I liked it. I was ashamed that I’d encouraged her to try it. She was comfortable in her skin, why couldn’t I be? I’m so glad she decided it was too much work, the makeup was too heavy, and she liked the way she looked without it. I wish my shame over how I felt melted away like the makeup did when she washed it off. But it didn’t. She was and is still today very comfortable in her own skin — her face is not flawed. Even through my thoughts and actions, Crystal has become a self-confident woman. She can do anything she sets her mind to accomplish. She is considerate, loves others and shows compassion in more ways than I can count. I believe God made her different so she can reach people and show them love when perhaps no one else does. She can show them that they, too, are beautifully made. She confidently tells people that we are all different. Some people just wear their difference on the outside for everyone to see. She is using her difference to make a difference in so many lives. I am blessed to be her mother and would not change her for the world. I was entrusted with this beautiful baby and have had the privileged to watch her grow into a beautiful woman. If you want to read more about Crystal’s story, visit her website:  www.crystalhodges.com. You’ll be able to read her blog and get to know her humor, fears, heartaches and dreams. You, too, will be encouraged by her difference. We want to hear your story. Become a Mighty contributor here .