Wig Recipients

Respectfully, please do not take photos of the children from this web-page or share their stories to protect their privacy.

Chloe shares her story...

Maggie's Wigs 4 Kids of Michigan - Child Ambassadors - chloe

Making this decision to share a photo of myself without hair was the hardest thing so far in my life. When I was about 8 years old I started losing my hair and my parents didn't know what was happening. Then I was diagnosed with Alopecia. Of course there is no cure for it so you can only imagine what I was going through at such a young age. I was lost and confused; I thought I would never be able to be like all the other girls who had long, beautiful hair.

When I was 10 I lost the majority of my hair and that's when I started going through treatment. This involved getting steroid shots in my head which wasn't fun at all. Through having hope and praying, my hair grew back during Middle School. This was a dream come true to me. It's all I ever wanted...My hair was so thick I honestly thought I outgrew my autoimmune disease....little did I know, God had a different plan for me.

At the end of sophomore year I noticed I had one little bald spot and that turned into two, three, four and kept increasing.... Eventually, my hair got so bad again during the summer that I started junior year with a wig. Living in a society where people base everything off appearances, I was so embarrassed and felt like the world turned against me. I was about to take all online classes so I could isolate myself from everyone, but I decided to be strong and have faith.

Until this day I still question "why me?" Why does God put you through such hard times? Maybe he is helping me become an empowered woman. Whatever the reason is, I now have accepted the fact I have alopecia and instead of it controlling my life, I am now in control. I don't care if people point or stare; just don’t judge somebody until you have walked in their shoes. Maybe one day my hair will grow back again and until that day happens...I’m happy being me.

Interview with Colleen, Mother of Wig Recipient Reece

Maggie's Wigs 4 Kids of Michigan - Child Ambassadors - reece

Colleen, as a parent, what has this program meant to you? 

It’s given me my son back! It’s meant a LOT to me!  Reece is joking, laughing, having fun and being himself again. When he was first diagnosed with alopecia, he became self-conscious and nervous as he had to style his hair to cover the spots of missing hair every morning. It was really hard to watch him go through this. He would worry if he was at school that if the wind blew or something else caused his hair to move, that the other students would realize he was different. He endured a lot of stress and anxiety during that time prior to learning about Maggie's Wigs 4 Kids of Michigan and receiving a wig. 

Reece, how did you feel once you received a wig for the first time?

I wasn’t used to it at first and I thought everyone was going to be weirded out by sudden change, but they weren’t and that was awesome.

Colleen, can you please comment on the change you noticed in Reece at that time?

He was very grateful; as we all were, that he can go out and not worry about his spots. He was more confident and less worried…he started to regain his sense of self-esteem. The teachers even commented on him returning to school – that he was being like a kid and seemed more like himself again. 

When he got his yearbook and saw the photos of himself before he received his wig, which he has now nicknamed George, he didn’t like the photos without his wig! What an amazing gift the wig is and what a difference it makes! Reece has his life back and it’s wonderful. It would be such a different life if we didn’t have access to a resource like Maggie's Wigs 4 Kids of Michigan – I am so grateful every day. Reece is already so loving, gentle and kind – I feel his true spirit shows through again now that he has his wig.

Reece, what words of encouragement would you offer other children who are experiencing hair loss and thinking of getting a wig from Maggie's Wigs 4 Kids of Michigan?

It’s worth it. Don’t be scared of getting a wig and looking different the next day, when you didn’t have hair before  – your friends will be there no matter what for you. 

Friendship is very important, isn’t it? Isn’t it nice to come to a place like Maggie's Wigs 4 Kids of Michigan where you can be with other children who have gone through this and enjoy social activities as well?  

I am looking forward to the field trips and activities.  It’s a really good program. 

Colleen, do you have any further thoughts you would like to share? 

First off, we want to volunteer any time for Maggie – just keep us informed so we can help out for fundraisers, events, etc! If anyone would like to talk to Reece about what it’s like to have hair loss – feel free to call and let us know. He would be happy to speak with other kids!

We are extremely grateful for everything Maggie's Wigs 4 Kids of Michigan has done and for doing it in such a wonderful, positive way. Mr. Corey, the organization's social worker is amazing and Maggie, the Founder & CEO, is too! Everyone is so caring… and the wig makes the biggest difference! 

There is nothing that compares to seeing your kid normal and the wig is quite normal-looking with real hair. Reece feels like everyone else now. Normalcy is awesome! 

Meet more of our wig recipients!

With the permission of the children and their families, they have chosen to share their photos.

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