Marla Fauchier: 5 Minutes For Special Needs

Thursday, July 10, 2008

5 Minutes For Special Needs

Ashley's mom Deborah at Pipecleaner Dreams interviewed me for the new site 5 Minutes For Special Needs that has just opened. My interview is set to post on July 13th. Please stop by for my interview and leave a sweet comment.

You can also visit Michelle at In the Life of A Child for the 5 Minutes For Special Needs button to put on your blog.

6 comments:

kristina said...: Superb! Great to find a new site and community.; July 11, 2008 at 1:07 AM
Bonnie said...: Thanks for sharing Marla, it looks like a great site and I look forward to reading your interview!; July 11, 2008 at 8:24 AM
Ashley's Mom said...: Thanks Marla!; July 11, 2008 at 8:36 AM
Maddy said...: Well that's no good! How am I supposed to remember two days from now!
Best wishes dearie; July 11, 2008 at 11:15 AM
Maddy said...: So does that mean that 'Trish' will be gone and you'll be there instead?

Sidebar comes to the rescue.
Cheers; July 11, 2008 at 11:17 AM
Drama Mama said...: Oooh. I like the link - it's on my blog. Looking forward to seeing you there!; July 12, 2008 at 11:02 PM

Why Do I Blog?

All That is Dazlious is a place for me to share my photography, insights, joys and struggles. In everyone's life there are challenges and joys. I want to capture these moments and share them with other parents who are going through similar experiences. Blogging has opened a new world of support for me.

My daughter was born with a rare chromosome disorder, is Autistic and struggles with Cyclical Vomiting Syndrome. Reaching a diagnosis took years and yet I celebrate my daughter for exactly who she is.

It is my belief that Autism is a genetic disorder and that there is no cure. My goal is to help my daughter be the person God has called her to be.

I may share what I have learned or find valuable in regards to my daughter’s diagnosis.

I do not claim to have the answers in regards to Autism, chromosome disorders or CVS. How I choose to help my daughter progress is a personal and difficult decision. I respect that others may choose different paths for progress.

Our journey has only just begun and it is my hope that in sharing bits and pieces of it with you that I will see the goodness and progress within my life and Maizie's.

I enjoy reading the blogs of other parents raising children with special needs. Reading blogs written by individuals with Autism and/or chromosome disorders is another way I gain insight, education and ideas for caring for my daughter.

I hope you enjoy reading about our dazlious and not so dazlious moments.

Enjoy!