Our Reader’s Special Needs Blogs

Writing and parenting beyond the norm. You can read more at Mother of Confusion.

Read our Exclusive Interview with Genevieve Hinson from “Writing and Parenting Beyond the Norm”.

Married for over 16 years and mom of a 6 year old son who has autism, I spend most of my time as my Little Guy’s case manager/advocate/cheerleader/ everything else.

I blog about making sense out of life with autism, and I also contribute to 5 Minutes for Special Needs and Created and Called.

Read our Exclusive Interview with Trish from “Another Piece of the Puzzle”.

Autism Assistance Resources and Information
is designed to help parents of children who have autism and other disabilities find resources to help their children thrive. The blog provides information about grants, financial assistance, funding strategies and other helpful resources for families coping with autism and other disabilities.

Read our Exclusive Interview with Michelle McFarland-McDaniels from “Autism Assistance Resources and Information”.

The joys and challenges of raising three boys on the autism spectrum, twins plus their younger brother.

Read our Exclusive Interview with lonestar818 from “Everyday Adventures & Random Thoughts”.

I am a mother of two austitic teens and my blog: Fearless Females is for fearless women (and men too) who desire inspiration, a kindred connection, fearless bonding and some soul searching. Here, I share my personal experiences, stories and helpful information about raising children with autism…with a healthful blend of some humor–and encourage other fearless topics too!

http://fearlessfemales.blogspot.com/

Read our Exclusive Interview with Holly Collins from “Fearless Females”.

All That is Dazlious is a place for me to share my photography, insights, joys and struggles. I am an artist and currently homeschool my daughter Maizie who is ten years old.

We adopted our daughter at birth. She was thought to be a healthy baby. Our daughter was born with a rare chromosome disorder, is Autistic and struggles with Cyclical Vomiting Syndrome. Reaching a diagnosis took years and yet we celebrate our daughter for exactly who she is.

Read our Exclusive Interview with Marla Baltes from “Marla Baltes on all that is Dazlious”.

Hi, I am a stay at home mother of 3 kids. Corianne, Wesley and our newest Melissa. My middle child, Wesley is the reason I started the blog. He was born, a titch preemie, but reasonably healthy but at 6 months of age, started having breathing problems and was put on oxygen. At around a year old he was diagnosed with NEHI, Neuroendocrine Cell Hyperplasia of Infancy, a rare interstial lung disease. Interstial lung disease, means his lungs are permantley scarred. Our blog is about the joys and trials of having a son with ILD, on oxygen. So check us out at “Tales of NEHI Mom http://coriwes.wordpress.com/

Read our Exclusive Interview with Wesley, Corianne, Melissa, Mom and Dad from “Tales From a Nehi Mom”.

Little Hand Big Heart is a site about children and adults with upper limb deformation due to Amnionic Band Syndrome. We are Moms that have been in that same situation as you. We have wondered those same thoughts. We are here to support you and tell you that everything will be just fine. Your child is going to grow up and have a normal life.

Little Hand Big Heart is here to support Mothers who have children born with a deformation due to ABS. We tell stories, Give tips, and Share our life experiences with you so that you know you are not alone.

Read our Exclusive Interview with Tricia from “Little Hand Big Heart”.

I am a stay at home mom who is never at home. I blog about life with a 4 1/2 year active son and a 22 month old daughter who has Down syndrome.

Read our Exclusive Interview with mommyto2 from “God’s Handiwork”.

Special Needs is an understatement when it’s your first child. We brought our baby home for the first time at 6 1/2 months old expecting to be a stay at home mom, but in actuality I became a stay at home nurse to my baby. Our daughter Caleigh was born at 28wks with Gastroschisis. She spent the first 6 1/2 months of her life in the NICU. After 9 bowel surgeries she has intestinal failure, short bowel syndrome. Caleigh also has PVL resulting in Cerebral Palsy & complex partial seizures. Caleigh’s Corner is a place that I journal Caleigh’s progress and setbacks. I journal my thoughts and feelings as a special needs mother and at the same time I hope that I can help another family through their similar situation.

Read our Exclusive Interview with Holly from “Caleigh’s Corner”.

I’m a first-time Mom to my gorgeous baby boy, Christian. Christian was born profoundly Deaf due to the Connexin 26 gene mutation. He was implanted with his CI in his right ear on April 21st, 2008, and activated on May 27th, 2008. I started this blog to chronicle our journey with Christian’s hearing loss, and to connect with our parents of Deaf and Hard of Hearing Children.

Read our Exclusive Interview with Christian’s Mommy from “Live Laugh Love Family”.

I started our blog Myah’s Page in hopes of connecting with other families and mothers who are raising children with Special Needs.
Myah is our sweet daughter born with a rare chromosome deletion; she teaches us many lessons on a daily basis. I also blog about every day mother woes, and share my opinion about other “mommy things.”

Read our Exclusive Interview with Lori from “Myah’s Page”.

I am a mom of three girls (weddings) ages 12, 6 and 4. My youngest daughter has Down syndrome. In addition to writing about the joys and challenges of everyday life, I write a weekly post on Tuesdays about Down syndrome awareness. I ran an in-home daycare for 5 years and recently closed it to go back to work part-time outside the home. I have a love for writing and continue to explore a career in freelance writing.

Read our Exclusive Interview with Debbie Yost from “Three Weddings”.

I’m an autistic college student and I blog about life on the autism spectrum and tips for parents raising autistic children.

Read our Exclusive Interview with Cale from “Spectrum Siblings”.

I am an American Mom living in Tuscany and the co-author of the book RALLY CAPS My daughter Sofia is a six year old drama queen and Jordan is a twelve year old Deaf Italian Stallion who wears a cochlear implant. I write a daily blog that focuses on how to be a strong parent advocate for a child with a disability without losing one’s identity as a woman.

Read our Exclusive Interview with Jodi Cutler Del Dottore from “An American Mom in Tuscany: Jordan’s Cochlear Implant Story and Raising Their Voices: Inspirational Stories in Deafness”.

A blog where you can find several news about the new trends of the market, regarding industrial goods and services, business, equipment, economy from each part of the world. An open window on what can be useful for your knowledge.

Read our Exclusive Interview with “News on Web”.

I am a working, stay at home mommy and I blog aboutmy youngest son who was born with Hydrocephalus.

Read our Exclusive Interview with Carla from “So This Is Holland?”.

I’m a SAHM/PT college-level writing instructor/freelance editor/faithful believer in Jesus Christ. The purpose of my blog is to have a place to write about the http://www2.rmcil.edu/eagle/Archives/April2008/rmcnews05.html

Read our Exclusive Interview with Jeannie from “The Adventures of Mr. Busypants”.

I’m a single mommy to a 6 year old with special needs and a 3 year old with a “princess” complex. I work at Juvenile Hall with a unit full of teenage criminals. This is my blog that chronicles our chaotic lives, and has become my own little form of therapy.

Read our Exclusive Interview with Kristen from “Adventures in Bipolar Land”.