“Megan is an awesome girl, she’s outgoing, smart, and above her years in age,” is how her mom, Paige, describes her. She’s bubbly, artistic, and learning to be a photographer. She loves to paint fingernails and she’s quite good at it, even better than some manicurists. Megan is 16-years-old and just finished her freshman year of high school. The year has provided some new challenges to a girl that looks different from most of the other kids.
Megan has alopecia areata. She has no hair on her head or body. It is not known what triggers this condition, but it is due to inflammation around the hair follicle that prevents the hair from growing. It’s often patchy on the scalp, but can involve any area with hair. There are treatments available, but they are limited and there are no cures.
Losing her hair when she was 12 was difficult, but it grew back with treatment; although she lost it again. When she was 15, her dad told her it was time to shave her head and she broke down in tears. She has learned the blessings and challenges of alopecia.
Megan looks different from other kids and moving to a new school in a small town last year was challenging. She is the only one with alopecia areata. She wears a wig to school, but it’s too hot to wear for most of the Texas summer. “Everyone knows, and she doesn’t care,” said her mom, “but she does have challenges making friends in a new school.”
A Children’s House for the Soul offers a safe, loving place to share stories and find other kids who are unique too. Megan attended the “Love the Skin You’re In” conference and loved meeting other young people with her condition. When Megan was out of the conference room during a break, another younger girl without hair came into the room for the first time. When Megan returned, the younger girl looked at her with the biggest grin on her face. She looks like me. She felt accepted. She fit in.
Paige also enjoyed the conference. “I loved the Christian speakers with scripture, bringing God into it,” said Paige. She appreciated that everyone saw each other for who they are, not just what their outward appearance may show.
Paige and Megan wish more people with alopecia, often mistaken for cancer treatment, would come out and share their condition. Megan is happy to share her story, if only people would ask.
SHARE IT!
Related Posts
How to Distract your Kid During Wet Wraps: A Battle Strategy
Getting your child to comply with wet wraps can feel like can be a battle! Which if you think about it, is a little ironic, because by administering wet wraps you are helping your child’s suit of armor, their skin defends itself against the outside world! So let us talk strategy, determine some “weapons” for your arsenal, and let’s realign so that you and your child can go from enemies to allies.
Acne Positivity – Coping Toolkit!
When we feel overwhelmed or stressed, it can be tempting to tell ourselves (or each other!) Just relax, calm down! When we are stressed or freaking out, that is easier said than done. That’s why preparing a “coping tool kit,” a set of strategies for dealing with stress can be really powerful.
Acne Positivity – Stop that stinkin’ thinking with empowering and encouraging thoughts!
Do you freak out when you break out? I know I have! It is natural when we have a break-out to look in the mirror and think things like “These pimples are gross!” “I hate my skin!” “Things are never going to get any better!” Even though it is natural we think this way, it is harmful too.
Acne Positivity – don’t pop those pimples!
Stop picking, popping, poking your pimples!
I know, it’s sort of like eating the whole bag of potato chips…we all know we aren’t supposed to do it, and yet, the temptation is SO STRONG! So…how do you stop?
Start with choosing an alternative activity!
Heart + Sole Walk and Family Festival Recap
We had so much fun at our first annual Heart + Sole Walk and Back To School Family festival! We want to thank all of our sponsors and everyone who came out to support our mission to make the world a more kind and understanding place for those with skin conditions.
Acne Positivity – Parental validation
As a Child Life Specialist working with teens and kids who have special skin, there is one question I get A LOT. “How do I talk to my teenager, when they tell me they don’t like how they look?” Parents are so worried that they will say the “wrong thing.” And truthfully, I have spent …
Skin Discovery Box – Film Premiere
We had an amazing time celebrating the launch of our brand new SKIN DISCOVERY BOXES, a very special collaboration with our friends at CeraVe! CeraVe’s tireless pursuit of therapeutic skincare for all is truly more than skin deep and we couldn’t be more thankful. We celebrated in style thanks to our friends at Star Cinema …
Texas Children’s Vascular Anomalies Program
A Children’s House for the Soul believes that it takes a village to support a child and family impacted by skin disease and birthmarks and that we are all better together.
Open House – Ribbon cutting to bring a children’s house home
Open House and Ribbon Cutting/Bring A Children’s House Home: On June 5th we began a very exciting new chapter of our A Children’s House story in the form of opening up our new beautiful space to serve children and teenagers with skin conditions and birthmarks and their families. This space includes a salon, a library & craft space, a teen room, and more! We also debuted our incredible new custom mural from up and coming local artist Eli Pallaert.
Trivia Night – Event Recap
Our Family Trivia night was oh so much fun, and a huge success! We had so much fun getting to reconnect with all our friends and enjoy some laughs while snacking out on pizza and snowcones!
growing up with a vascular birthmark
In honor of Vascular Birthmark Awareness Month, our childlife specialist Lindsay O’Sullivan had a great conversation with Jose about growing up with his special masterpiece skin!
Ichthyosis Awareness month with Ally
In this interview, Ally shares about her experiences growing up with Ichthyosis. Ally shares how: Meeting other kids with special skin can help kids to feel less isolated and give them a very special sense of comradery and understanding. Parents don’t have to do everything perfectly to be the perfect parent for their child and …
Mother’s Tea – Event recap
What a wonderful time to relax, enjoy friendly company, and share their hearts on being a mama to a kiddo or teen with special skin. It was truly so special! These mamas were made a masterpiece!
A Message about Vascular Birthmarks
Vascular birthmarks are very common in children. These birthmarks are made of blood vessels in the skin and can occur anywhere on the body. They may be pink or red in color, blue or purplish, flat or raised. Since they are vascular, sometimes they will feel warm to touch and may change in color with …
2021 Capital Campaign Update
We have some exciting updates about our Capital Campaign! Learn about our short and long term plans for our own space.
You Can’t Teach What has no history
You Can’t Teach What Has No History “This is how much God loved the world: He gave his Son, his one and only Son. And this is why: so that no one need be destroyed; by believing in him, anyone can have a whole and lasting life. God didn’t go to all the trouble of …
Ectodermal Dysplasia Awareness
In honor of Ectodermal Dysplasia Awareness month in February, we sat down with two of our dearest friends Zach and his mama Susan! Zach is an avid golfer, an Aggie, and is affected by Ectodermal Dysplasia. Susan and Zach teach us about ED and the importance of finding community. They also had helpful tips and …
How to Conquer Alopecia Universalis
Join us for a fun and inspiring interview with this incredible lady Ana Maria! Ana Maria Triana is 15 years old and the author of How to Conquer Alopecia Universalis. Ana Maria gives heartfelt advice, shares wisdom beyond her years, and will leave you feeling full of compassion and confidence. A Children’s House for the …
THANK YOU, MOM! By Rachael Wrobel
In honor of the upcoming National Epidermolysis Bullosa (EB) Awareness week, we wanted to share this great piece from our friend, Rachael Wrobel about how her mama mothered her well, even despite the challenges of EB.
Alopecia Areata – A Mother’s Journey
I am fortunate enough to be Mama to three little girls. Shortly after my eldest daughter’s first birthday (about 4 years ago) I noticed her hair was thinning. I was told by many it was just typical baby hair loss until it just couldn’t be described at “typical” any longer.