2020 The Year Of The Alopecians
Guys the last couple weeks have been amazing for the alopecia community. First Ricki Lake went public with her struggles with hair loss. Then Representative Ayanna Pressley shared that she lost all of her hair to alopecia this past year. I’m not going to lie, Rep. Pressley’s candid conversation about her alopecia gave me alllllll of the feels. It is emotional seeing women with such large platforms coming forward with their stories of hair loss. When I first lost my hair in 2015, I remember scouring the internet looking for female “celebrities” who were also dealing with hair loss. With close to 7 million people in the U.S. who have been affected by alopecia, I assumed there had to be a few ladies in the public eye who were dealing with it too. My searches hit dead end after dead end. I don’t know why, but it felt heart breaking not to find anyone. All I wanted was a “Celebrities, they are just like us!” moment so I could feel a tiny sense of normalcy. Which I know is ridiculous because celebs are nothing like us, but I yearned for a to connect with someone who was traveling in my same shoes. I was desperate to find a woman who had bald forced upon them, but was still out there killing the game in life. I wanted to find anybody who could help me see that it was going to be okay.
When Rep. Pressley’s video and article started making the rounds, I felt this overwhelming sense of oh hellllllll yes! This is exactly what the alopecia community needs! 2015 Supriya would have done anything to see a video like this in my first months as a bald woman. The emotions and experiences she describes are so on point that it gives me goosebumps. It feels like she read my mind and was sharing my thoughts with the world.
Some of my favorite quotes:
“I did not want to go to sleep because I did not want the morning to come, where I would remove this bonnet and my wrap and be met with more hair in the sink and an image in the mirror, in the mirror of a person who increasingly felt like a stranger to me.”
“I was wearing this wig, fully clothed. But in that moment, I couldn’t recall the last time I’d ever felt more naked.”
“I didn’t have the luxury of mourning what felt like the loss of a limb. It was a moment of transformation, not of my choosing”
“I felt naked, exposed, vulnerable. I felt embarrassed. I felt ashamed. I felt betrayed.”
I felt these quotes in my SOUL! I will never forget the days where sleep was my biggest fear. Every night I prayed that I would wake up and the hair loss would be done. Yet every morning I would wake up to find more piles of hair on my pillow case. And when I purchased my first wig, I thought I would finally feel normal. Instead, I felt like the elephant in the room. I felt vulnerable, scared, and shameful of my secret. I felt like my wig was actually a light up sign on my head that read, “Look at her! It’s sideshow Sup! She is bald! That is a wig!” Like Rep. Pressley, I didn’t have the luxury of mourning what felt like the loss of a limb. Say it again with me, I didn’t have the luxury of mourning what felt like the loss of a limb. My God, truer words have never been spoken! There is no mourning time with alopecia. It is a loss that is felt daily, but society expects you to function as if nothing has changed. I couldn’t call off of work every time alopecia sent my mind into a state of disarray. If I had, I would have called off every single day for 2 and a half years. Life must go on no matter how badly you miss your hair. No matter how devastated you are that your hair is now gone and there is a chance you will never see it again for the rest of your life. After all, to society, “At least it's just hair”. Words that are so easy to say until you become the person whose hair was lost in a matter of months.
This is why stories like Rep. Pressely and Ricki Lake are just SO IMPORTANT. There is comfort and solace in knowing the emotions you are feeling are shared by other women in all walks of life. From a bad ass congresswoman, to an iconic talk show host and actress. It fills my cup knowing these stories are out there inspiring others on their hair loss journeys. It is further proof that you can have success, you can have happiness, and you can have love regardless of if you have hair or not!!!
If you haven’t seen the article from The Root yet, here is the link. You will not be disappointed. Thank your Representative Pressley for being so raw and inspiring. You are truly out here changing lives!
THE Representative Ayanna Pressley


2. I got to see my most favorite kids from Akron (Lebron James obvi..no offense if you are one of my friends from Akron, I still love you just as much) playing in Denver. At the time I was hoping, wishing, praying, it wouldn’t be my last time getting to see him play in CAVS wine and gold, but alas it was. I hate to break it to you Bron, but purple and yellow will never look as good as wine and gold. Just sayin! PS I miss you and please come back!!
3. OMG I went on my first dates since losing my hair and my first dates using a dating app. This will for sure be its own blog entry at another time. Yes, it was awkward, hilarious, fun, and wayyyy outside of my comfort bubble as expected. I went on two dates with two different dudes and didn’t go on a single other date after that. Baby steps people, baby steps.
4. This is a sad one. I had to say goodbye to my little kitty Jasper. I got him in 2009, and he traveled with me from Ohio to Denver. He was my #1 sidekick through all of the rough times, the good times, and everything in between. Saying goodbye to him was one of THE HARSDEST things I ever had to do. I miss you every single day my little buddy.
5. Got my first Shuly wig!! This is my 3rd human hair wig since losing all of my hair, and it is hands down my most favorite. The hair quality is amazing and it is everything I’ve wanted in a wig and more. If I was a baller shot caller, you better believe I’d fly my butt to NYC to get a dozen more. But one will have to do for now 😊
6. Took my first trip to NASHVegas to celebrate my BFF Heather’s Bachelorette weekend!! The trip was a total blast!! I literally don’t understand how college kids in Nashville can graduate. How can you choose studying over all of the other fun things to do out there?! Props to you if you’ve done it. This trip was interesting because it was my first time having girlfriends see me first thing in the morning…no hair…no makeup….full bald…eyebrowless Supriya. Straight up ET phone home alien mode. I had MAJOR anxiety about it the entire trip, but everyone there made it so easy me. Pro tip--if you want to know how to make peace with alopecia, find yourself a strong AF girl squad who will give you all of the confidence in the world!
7. TAYLOR SWIFT. Yes, I am a 35 year old Swifty. Yes, I jumped all of these verified fan hoops to secure my place in the ticket line. Let me tell you, it was all WORTH it. I don’t know about you, but I was feeling 22 that night!
8. Had another family reunion in Siesta Key. 900000% humidity is worth it for fun vacations with the fam!
9. I moved on up! Literally. I moved up one floor into a new renovated apartment that I LOVE LOVE LOOOOOVE! Thank you renovations, target, and hobby lobby for making my girlie decorating dreams come true.
10. After 6 months of being pet free, I adopted a tiny little kitten and named him Neville Longbottom! He is the cutest, funniest, craziest wild man of a cat. Everyday he makes me laugh and he is currently curled up next to me while I type this blog. I may suck at relationships, but man am I great at being a cat mom.
11. Last, but not least, I started this BLOG!!! After months and months of feeling unfilled with life, of feeling like the world was going to shit and I was doing nothing to contribute to society, I decided to get off my overly anxious butt and do something about it. Here I am sharing my story with family, friends, and strangers, all while making new alopecia friends every single day. I cant wait to see what this blog will bring me in the New Year!
HAPPY NEW YEAR everyone!! Hope you all are safe, have fun, and drink lots of Pedialyte. Nobody wants to start a new year with a new hangover. Am I right? Talk to you in 2019 boos!!
Now let’s fast forward to today. I was brunching (PS brunch is a VERY regular occurrence in my life #BasicAF) with my friends Kera, Rachel, and Mattie. Rachel asked me what my long-term goal is with this blog. I think its just this. To share these raw emotions and stories. To be able to connect with people who are going through this and help them feel less alone. To help people going through alopecia know that their emotions are valid, that their feelings are real, that its okay to feel sad no matter how many times people tell you “at least its just hair”. If I can help one person struggling, then I know I am doing the right thing. 😊 That’s all for now friends. Hope you have a fabulous week my sweet boos!! Byeeeee.
I've been going back and forth about posting these for some time now, but since you're reading this it means I finally grew a pair and posted 😳. Don't worry I do not have cancer. I do have an autoimmune disease called alopecia, and two years ago my body thought it would be super fun to start attacking my hair until I had none left. Pretty rude if you ask me. May of 2015 I was doing my hair and noticed a pile of hair in my hands. For the next 4 months my hair fell out by the handful. Finally I caved and shaved the last few strands off and started living the wig life. (I was doing it before Kylie Jenner made it trendy). The summer of 2016 alopecia decided to take my eyebrows. So now they are a combination of tattoos and makeup. Yes that means my first and only tattoo was a face tat. 😧 Finally this year I lost my lashes. I'm now officially hair free. Best disease ever neck down (free laser..am I right?!), not so fun lashes up.As someone who has been battling depression, anxiety, and body image issues the bulk of her adult life, alopecia was a crushing blow. It's not all that surprising to me that my biggest medical hurdle to date was caused by my own body attacking itself. Being my own worst enemy tends to be the story of my life.Losing your hair is a weird thing. Everyone tells you "at least you're not dying"...which is true and something I'm beyond thankful and grateful for. But losing my identity strand by strand was not exactly the best feeling in the world either. Maybe it sounds vain, but I've spent many many tearful days consumed with sadness, missing the person I used to be..physically at least. I was already getting myself out of a rock bottom part of my life when this disease entered my world, and it definitely slammed me right back down to rock bottom in a hot second.Im not sure why I'm making this part of my life Facebook official now. Maybe it means I'm finally making peace with things? Maybe it's because through this process I've cut out the most toxic people I've ever had in my life and replaced them with some of the most amazing humans on the planet who have accepted me, loved me (hair or no hair), and supported me every second of this nightmare. Or maybe it's just so someone else who may be going through a shitty shitty time can see that things can get better. Because it does get better. Even when it feels physically and mentally impossible. It gets better. Somehow some way.Either way that's my story. If you've read this far into my novel of a post, thank you for reading. Also I may or may not be throwing up after hitting post. Not nervous about this at all. 😰😰😰😬😬😬😱PS if you have any alopecia questions, please don't hesitate to ask!📷cred: the AMAZING Green Chair Stories