Blogs and REsources

Rare Disease Day 2016

Dr. Bree was happy to have the opportunity to represent the National Foundation for Ectodermal Dysplasias (NFED) with Susan Hamm, who is also a Board member of A Children’s House for the Soul, at tonight’s Rare Disease Day event at The Health Museum hosted by Texas Children’s Hospital and Baylor College of Medicine. We were …

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February is Ectodermal Dysplasias Awareness Month

February is Ectodermal Dysplasias Awareness Month. As a member of the National Foundation for Ectodermal Dysplasias (NFED) Scientific Advisory Council, Dr. Bree is proud to raise awareness for this wonderful organization and the amazing families it serves! BE HEARD. INSPIRE OTHERS. BE YOURSELF.

Happy New Year 2016!

Praying God gives you a year of favor full of His unending love. “May the favor of the Lord our God rest on us” Psalm 90:17

Merry Christmas!

Merriest of Christmases to you and your family! May we all be blessed beyond measure as we remember the true reason for the season: https://www.youtube.com/watch?v=7vJPAQJAyjg

Thank you for your generosity!

It has been two weeks since Giving Tuesday and we are still overwhelmed by your generosity! We are grateful for each and every one of your donations and your prayers for A Children’s House for the Soul! We look forward to making a difference in this world by helping children and teens with skin conditions …

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You are invited!

You are invited to celebrate The Reason for the Season! at Trinity Lutheran Church, 800 Houston Avenue, Houston TX 77007. We hope to see you there!

Camp Dermadillo reunion

Calling all Camp Dermadillo campers and volunteers! We hope you can join us for our Camp Dermadillo reunion!!!

Giving Tuesday

If you would like to help improve the life of a child or teen with a skin condition or birthmark, please consider donating to A Children’s House for the Soul this Giving Tuesday! You donation is tax-deductible and is a great way to make a difference! https://achildrenshouse.org/donate/ “How wonderful it is that nobody need wait …

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Hello world!

Welcome to our brand new website!  We are glad you are here!

Join our community

Do you or someone in your family have a skin disease or birthmark? Join us at an event, engage with us online, or learn about the many others ways to get involved in ACHFTS.

Make a donation

Please consider a one-time or monthly donation to help support future projects that will help even more children and teens love the skin they are in.