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General…

Welcome to a supportive space for your real alopecia journey — beyond the highlight reel.

Let’s be honest: social media is filled with stunning bald influencers living their best lives. They glow. They pose. They boldly declare "Bald is Beautiful." And it is. But if you're quietly wondering, “Why…

Whole in the Mirror

From Fractured Identity to Fierce Self-Acceptance

What happens when the mirror no longer reflects who you thought you were?

In RJ Jones’ novella, Whole in the Mirror, meet Talia Rivers—a gifted photographer whose life is upended by a diagnosis of alopecia. As Talia confronts fear, loss, and…

Turning Alopecia Into Empowerment

Chloe Bean has done something truly remarkable. She’s taken what many of us with alopecia feel…

SATURDAY, AUGUST 3, 2024

15th ANNUAL INTERNATIONAL ALOPECIA DAY!

Every year on the first Saturday of August, people from around the world come together to celebrate…

It is essential to recognize that you are not alone in this, as there are 6.5 million people in the US affected by Alopecia. Embrace your new bald appearance and find happiness within yourself, appreciating the journey you have undertaken. Allow Alopecia to be your beautiful cure

30 Days, 30 Facts: A Social Media Initiative

One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. 

Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness about alopecia, a condition that affects millions of people worldwide.…

BE PROUD AND BE VISIBLE by flooding social media

with your International Alopecia Day photos and greetings!

IAD is a way to raise public awareness, AND to…

I don’t have Alopecia, anxiety or depression. I haven’t had suicidal thoughts roam the sacred space of my mind, nor have I been bullied for my appearance. I am not familiar with the feeling of a panic attack or crippling social anxiety and, I have never felt so deeply overcome with mental pain that I couldn’t breathe. But - I was there for Leon through all of the above and this absolutely devastated me.

When you love someone, everything becomes a simultaneous…

SATURDAY, AUGUST 1 will be the 11th annual International Alopecia Day (IAD) - the day to celebrate worldwide who we are.

This year, due to the pandemic, International Alopecia Day organizers request that we all will need to follow CDC and your local health department guidelines about social distancing and safety.

But, even if you can't have the…

Hello

Has anyone seen the #alopeciaisfashion Hashtag?

We are doing a campaign to talk about issues in the fashion industry with Alopecia and also to say yes we can be whatever we want to be in the fashion industry with Hair Loss. Please hashtag #alopeciaisfashion in all your Instagram posts, twitter, facebook. The campaign is a brainstorm of hair Heals Organisation who support all affected by Hair Loss with buying wigs, beauty…

Hi everyone, 

I found out three months ago that I have female pattern hair loss. My hair had been disintegrating for over a year but I didn't know what was causing it. I'm in my mid twenties and have a brother a year younger who's losing his hair too. I knew my dad went bald at a young age, but never in a million years would have guessed I could inherit the hair loss as a girl. 

My dermatologist has me taking 200mg spironolactone and using the 5% minoxidil foam. I'm still…

Hi everybody!

Here you are my Youtube channel in case you are interested on videos related with alopecia.

https://www.youtube.com/channel/UCwSIVpu2jMWFBzU-t_69ldA

See you there!

Hola, hola!

Aquí os dejo el enlace a mi canal de Youtube donde iré subiendo vídeos relacionados con la alopecia. Si os interesa, ahí va:…

KATELYN Payne, 13, lives in County Durham with her dad Darren, 44, mum Ann-Marie, 37, and twin brother Hayden. She says:

“As my classmates and I ran inside after a rainy PE lesson, I could only watch as they wrung out their wet…

Hi fellow alopecia and hairloss knowers

I am so happy to be who I am.

This year I started my university days at Stellenbosch University in South Africa, studying my passion. At this time I was still uncomfortable to be seen without my wig (I have Alopecia Universalis)- with only close friends and family having ever seen me with my untanned head.

I wanted to be brave, to shake off the cloak that societal beauty standards insisted on wrapping around my adolescent body, but…

Early on when I was first impacted by Alopecia and I wanted to explain it to the few people I told.  I would say that I had an auto-immune disease called Alopecia.

One day someone stopped be as I verbalized this and told me not to ever profess/claim a disease with my mouth or in my mental thoughts.

His position was that are words and powerful, almost as powerful as our thoughts.  And that we should all be particular of the language we use to edify our lives.

I…

Hi Everyone,

First and Foremost im kind of glad(and sad in another way) to have found and be a part of platform full of Humans who think,feel,behave and have suffered the same way as i did..

Im Santhosh a 25 Year Old Graduate from India and I've been Suffering from Alopecia for Nearly 15 Years now,Ive lost my Eye Brows & Eye Lashes(Albeit not Completely but there are Circular Patches plenty of them infact) and Has Started to Lose Hair in Patches on My Scalp off…

Sasha mother wrote me and said:

"This is my gorgeous girl sasha aged 4, the way she handles her alopecia is inspiring and brave and makes me so proud to be her mummy.

My wee girlie is currently in a competition to be Once Upon a Tutu calendar girl on Facebook I am hoping people could please vote for my gorgeous girl.

To vote go to…