Be you Be bald
Welcome 💙
This is a inclusive environment for all my baldies especially those of color with Alopecia My name is Cheyenne. Any phase really, you name it.
Hey there,
I would love to know more about you, so I'll start first...
Hi! A little bit about me: I was born and raised in Southern California, spent most of my undergrad years in Washington, DC and then New Orleans, LA. I have Alopecia universalis and was diagnosed at the age of 6. I have been through every phase of my Alopecia journey, the embarrassment, the sadness, the anger and the loving it.
for all those who tuned in…thank you 💙
COME TAP IN ON INSTAGRAM TONIGHT! 💙
How is everyone?! 🫶🏽
checking in…how are you feeling today?
Y’all the bald queen herself is applying for the sephora squad 💕 Leave her testimonial at: https://www.sephorasquad.com/leave_testimonial/107814
So excited to partner with Tallon. Check out our IG PAGE 💙 7pm ET on April 28th!
OUR GROUP PAGE: https://www.facebook.com/groups/6221636814563264
Hey y'all... I am working on creating a group so we can all post!
INSTAGRAM LIVE 💕
SO EXCITED TO COLLAB! 💙💙💙
Change calling… For a long time they said being bald was not feminine. They said it wasn’t attractive or beautiful. Then we all saw a shift it became a trend to be bald and folks by the masses shaved their head. Change is beautiful. It’s exciting. We should all lean into change and into inclusivity. I’m excited for what’s to come 💙
I’m working on still growing this community. Help me by tagging your favorite Alopecians in the comment and sharing this post 💙
My goal today is to drink a lot of water 😅 What’s yours?
HAPPY SUNDAY 💕
CHECK OUT OUR INSTAGRAM PAGE 💙
How’s your day? 💙
CONFESSION:
- My head is either too hot or too cold… anyone else relate? 🤨😂
THE DIAGNOSIS:
I remember feeling frustrated at how many doctors it took to get a solidified diagnosis. I also remember being presented with options like needles in my head or some scalp oils, shampoos that would burn, etc. None of those options seemed fit for a 6 year old, so my mom did what any parent would do. She created her own solutions: wigs, hats, scarves. My support system was my light at the end of the tunnel. How was your diagnosis?
September…whose ready?! 💙💙💙
Make up has always been a huge outlet for me throughout my journey with Alopecia…I’m curious, what’s your outlet? 👀💕
Any fun Saturday plans? 👀💙
💙💙💙💙
HAPPY FRIDAY! 🫶🏽
VULNERABLE POST:
- When I first got diagnosed with Alopecia I was 6, so my hair didn’t matter much. Once I went to middle school and bullying began. I became very insecure and felt very out of place. I felt alone. In high school my biggest insecurity wasn’t my bald head but my eyebrows! Seems so silly now but up until 2 years ago I would spend hours in the mirror trying to draw on the most perfect eyebrows. I made the decision to get micro bladed eyebrows in 2021 and my life has changed ever since. I love my eyebrows and have grown to love my Alopecia even more now. It’s a journey and these things take time, everyone has their own journey and timeline and that’s okay. Take your time. Go at your own pace and whatever makes you feel most comfortable is what matters. Be you 💙
WHO CAN RELATE?! 👀
CHECKING IN…family, how are we feeling? How’s your mental health? 💙
Business:
I am creating this so that all of you business owners/ entrepreneurs can share what you do/ wish to promote with the group 💙
I am so excited our group is growing! The little girl in me dreamed of a community like this. Check our the instagram page I have also created