Description

This month, we have the opportunity to break the silence around a subject still largely unknown : alopecia.

This condition, although affecting 20% of women, is often overlooked.

It’s time to talk openly about female hair loss, which is why we are calling for testimonies.

If you would like to share your experience with alopecia, please send us a voice message on WhatsApp at +33 6 95 28 78 85. With one or more vocals, tell us your story : how and when did you discover your hair loss ? What type of alopecia is this ? (Pelade, androgenetic alopecia, etc.) How do you live with your hair loss ? Which solution do you use to deal with it ?

Speak up ! The goal is to make women’s voices heard more widely 💪

Your testimony could become a podcast episode on the channel Comme un diadème.

We are waiting for you on WhatsApp ! 😉

Join the community Comme un diadème on social networks !

Instagram :  https://www.instagram.com/comme.un.diademe/?hl=fr 

Facebook : https://www.facebook.com/Commeundiademe/ 

Tik Tok : https://www.tiktok.com/@comme.un.diademe 

Contact us : contact@commeundiademe.com    

See you soon for a next podcast ! 😊  

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Transcription

• Speaker #0

  This is my fake hair journey, the podcast that tells you about alopecia but also all the solutions that we have to deal with it. The goal here will not be to feel sorry for our bad scalps but to learn to live with this pathology and even maybe to laugh about it. And if you really like fun and informative content about alopecia, don't hesitate to follow ComardiaDem on YouTube, Facebook and Instagram.

• Speaker #1

  Hi girls, September is the month of alopecia awareness. And as you maybe know, if you already follow me, I have androgenetic alopecia. So it's the equivalent of formal pattern baldness. So this is a wig, okay? But under the wig, I don't have a lot of hair. And as you can see, my scalp becomes really, really visible. It's something really difficult to handle psychologically. And I think it's really important to talk about this subject because... There are not a lot of people discussing about that on social media. There are some women, but I think we all need to share more about more information about this subject because it's really, really important. Because a lot of women feel really alone and insecure about this problem. But we are a lot to face this pathology. So with Comandia DEM, you can see on my YouTube channel that I share a lot of videos in English, but also in French, because I'm French, as you can maybe hear, about alopecia in general, androgenetic alopecia, but also about wigs and hair topper and other solutions that you can use when you have alopecia, for instance, hair fiber. powder and also sometimes I discuss about the treatments like minoxidil, rogaine, etc. But we also need to hear your voice because I'm not the only one to have androgenetic alopecia and I think it's really important that people understand that there are a lot of women facing this pathology. So this is why I am asking you if you could send us your Testimony, your story, your pathway with alopecia. It can be androgenetic alopecia, but also effluxium, telogen, alopecia areata, fibrosing alopecia. You can discuss about everything that you want about your alopecia, about how you feel with this pathology. In English, on vocals with WhatsApp. And we will share your story. On the podcast of Common Diadem, I will write you the name. I have a loss of memory. Because it's important that we all share our story because people need to know what is alopecia, what is also androgenetic alopecia, because we are maybe 20% of women facing this. And it's not fair that most of people don't know what this is. We need to inform. We need to share information to share our story because alopecia needs to be more visible on social media because when it will be more visible, people around us will be able to support us better. So don't hesitate to send our vocals message. on messages on WhatsApp. I will be really, really happy to hear them and to share them to our community. So see you soon.