Welcome to Aaron's Tracheostomy Page
This site is dedicated to my son Aaron who had a tracheostomy for the first 4 years of his life. I hope that Aaron's Page will be helpful to others caring for a child with a tracheostomy, or to anyone seeking to learn more about tracheostomies.
MissionTo help assure the highest quality home care for children with tracheostomies.To provide needed tracheostomy information in order to ease some of the anxiety related to caring for a child with a trach. A well-informed family will usually experience less anxiety. To facilitate parent-to-parent networking and support. Information is necessary for parents of medically challenged children, however what often helps parents most is knowing that they are not alone. |
Announcements:
- The 3rd annual Trach Fair will be held July 9th@ 10am at Phoenix Children’s Hospital Cohen Center. Download Flyer
- Save the Date: Second Tracheostomy Fair and Conference for Caregivers. Saturday, Oct. 15, 2011 at The Children's Hospital of Philadelphia. Brochure will be available soon. Questions, contact Cindy M. Perr.
What's New?
- The Quality of Life of Young Children and Infants with Chronic Medical Problems: Review of the Literature, Antoine Payot, MD, PhD and Keith J. Barrington, MB, ChB, April 2011.
- Trache Tite Tracheostomy tube holder
- Famous People with Tracheostomies updated January 29, 2011
- Follow us on Twitter.
- New tracheostomy video forum added to the message boards: Video Forum
- On Facebook? Come joins us at the new tracheostomy.com social network group. Instructions here.
- More...