Earlier this year, we shared with you the news that an individual who had been one of the founding families of the National Foundation for Ectodermal Dysplasias (NFED) had passed from cancer. Remembering JoAnna Daniel Nix was our loving tribute to her beautiful spirit.

Note from JoAnna’s mom, Sandy

JoAnna’s generosity and big heart continue. Her mother, Sandy Daniel, donated 32 of JoAnna’s wigs to the NFED. They are brand new or very lightly worn. It was JoAnna’s wish that other girls/women affected by ectodermal dysplasia could benefit from them.

It’s our honor to grant her wish!

How to Apply for a Wig

To be eligible to receive a wig, you must be a female who is affected by ectodermal dysplasia and registered with the NFED.

If you find a wig below that you like, click on the “Apply for a Wig” button. You will be taken to a Sign-up Genius form. Enter the access code – wigs. You will see that each wig is listed by the number and title as shown on each picture below.

Click on the wig of your choice and enter the information requested. Kayla Hollenkamp from our staff will follow-up with you.

Wigs are given out “as is”. We don’t have any other information on the wigs other than its name below.

We will send them out first come, first serve basis. Only one wig per family. If you have any questions, please contact Kayla at 618-566-2020.

Apply for a Wig Apply for a Wig

We thank the Daniel family for all of their support through the years and for honoring JoAnna’s wishes. We hope many of you will enjoy and wear these wigs!

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