Taya-Velocardiofacial Syndrome (VCFS) or 22q11.2 deletion syndrome

Taya-Velocardiofacial Syndrome (VCFS) or 22q11.2 deletion syndrome

Child Entry for Website

We wish we could personally invite each and every family to take part in the Aware of Angels organization. Do not be shy about contacting us or sending us your stories! We want this to benefit as many as we can.

(Note, your child does not have to be part of the Photography Project to be featured on website.)

Include 1-4 digital photograph(s) Please email story and photos to  childgenetics@gmail.com

If you do not want a photo included please make note of that-we still want to share your story.

If your photograph(s) does not have a “watermark” or “logo” already on the image, awareofangels.org will be placed to help with privacy issues.

Please use the following questions as a guideline only, they may give you a start if you aren’t sure what to write. Answers can be as long or short as you would like.  We really want yours and your child’s story. We are looking for ways that researchers, teachers, doctors and therapists can better improve the quality of life for these children and the future of others. If you need something that doesn’t currently exist to treat your child, put it in your story. Some questions may not apply to you. We want to know what can help you as well as getting to know your Angel.

*If you are willing, please list a contact email in your answers to be shared on site (for other’s to connect with you) It is important for those families searching for answers to find someone in a similar situation. Feel free to mention any blogs, or websites you manage for your child as well.*

~By submitting photos and text you allow Aware of Angels to share that information on awareofangels.org and other social media outlets~
Please keep us updated on your child.  We really look forward to meeting so many amazing families. Thank you!