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Why give to the National Trichotillomania Learning Center?

December 16, 2010

Happy Holidays Everyone!

I hope this season finds you & your family well & happy.  For those of you living with Trichotillomania the stress of the holidays can be challenging for both you and your support network of family & friends.  

The good news is; you don't have to go through this alone!  The National Trichotillomania Learning Center provides treatment option information, support group contact information and a WEALTH of other resources to help.   I urge those of you who can give to donate what you can to this wonderful organization so they can expand their reach to help even more people in the coming year.

Below is some general information from their website with links to the highlighted information - if you have not yet taken a look at their website - CHECK IT OUT!   It's awesome! 

As always I welcome your comments and questions.

Warmly,

Judi Wygant-Collier

 

If you are looking for information, support, and resources for trichotillomania (TTM), skin picking and other body-focused behaviors, you have come to the right place. TLC is a non-profit organization working with the world's leading clinicians and researchers to provide the most accurate and up-to-date information possible.

You will find a wealth of resources on this website, including treatment overviews,books and videos, online discussion groups, and helpful advice about finding a therapist or starting a support group. We hope you will join us at one of the local events we hold all across the country - they are a great way to meet other families coping with these problems.

If you can't find what you need on this website, please contact us. We also urge you to become a Member of TLC. As a member, you will receive a comprehensive information packet, including complete local treatment contacts. Your support enables us to provide critical services, including this website, to the millions of adults and children suffering with these disorders

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