Ellen Wille
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Adore Mono Part
- Vendor
- EllenWille
- Regular price
- $1,316.33
- Sale price
- $1,316.33
- Regular price
-
$1,548.62 - Unit price
- per
Sold out -
Advance
- Vendor
- EllenWille
- Regular price
- $1,825.88
- Sale price
- $1,825.88
- Regular price
-
$2,148.09 - Unit price
- per
Sold out -
Affair Hi
- Vendor
- EllenWille
- Regular price
- $632.69
- Sale price
- $632.69
- Regular price
-
$744.34 - Unit price
- per
Sold out -
Air
- Vendor
- EllenWille
- Regular price
- $617.95
- Sale price
- $617.95
- Regular price
-
$729.35 - Unit price
- per
Sold out -
Aletta Mono Part
- Vendor
- EllenWille
- Regular price
- $399.15
- Sale price
- $399.15
- Regular price
-
$469.58 - Unit price
- per
Sold out

I Am Perfect!
Hair loss is a personal and, at times, painful journey for those experiencing hair loss due to certain illnesses or diseases.
The "I Am Perfect" campaign, sponsored by TressAllure and collaborators, is designed to help you learn more about the world of wig-wearing and how wearing wigs can help you regain confidence.
Alopecia and Hairloss Awareness
Meet Andrew
My thoughts on my progress:
Alopecia was present in my life much earlier than I could have realized. There were signs, but no pathological cause was ever detected in my body. I have always been vigorous and energetic, and I am still today, I never feel agonizing fatigue. I also tolerate stressful tasks well. Then, almost overnight, I lost all my hair. This happened to me in 1995. I was very terrified, I thought that some serious disease that claimed my life had attacked my body. The world has ended from my point of view! I went to doctors, I was in a terrible state mentally, my zest for life and energy disappeared together with my hair in an instant. I turned into a sick, pathetic person. As I mentioned, no organic reasons were found to explain this. At that time, there were no groups where similar people could meet, I didn't know anyone who was going through what I was going through. I knew there were bald people, but I never had the chance to talk to them. I didn't know their stories. I didn't know the autoimmune disorder existed, I had never heard of Alopecia. I completely closed myself off from the eyes of the outside world, I didn't dare to show my bald appearance openly. I covered my head with caps and scarves, and for a short time I also wore wigs, but I hated them. I avoided company, became almost a recluse. I spent all my time feeling sorry for myself and hating the world for it all. A fog of dark ignorance settled over me. I lived like this for a long time, I wanted my hair back. I thought that you could only succeed in life with hair. When social networking sites appeared, I kept in touch with the outside world through them. Then the light slowly appeared forever. Support groups were created and through them I was able to meet people like myself. I read their stories, I got a glimpse into their lives, their everyday life, I saw their wonderful experiences, which they live with bald, yet liberated joy. I envied them for this freedom. Then I started to think that I could do this myself. My inhibitions are what hold me back from the free, joyful world. I started to show my real self, which of course was not so easy right away. I often encountered situations that knocked my self-confidence back. It took me many years to develop into who I am today. I owe this development to the Alopecia communities and Alopecia support groups.Today I am a happy person, grateful to all my alopecia friends who helped me in my development. I drew the conclusion that we need each other's experience and support. I also try to help everyone affected by Alopecia. I'm a bald person, so you can stare at me, it doesn't bother me because I've become happy and free.
