Our Special Child


A ring created to connect all of the stories of our special children so that they are easy to access and so that children can know there are others going through similar experiences. If you have a special needs child with a story page this is the ring to join.




A FREE central web site bringing national resources for people with disabilities in one convenient location.
Plus stories, help and a way to connect with others.

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An interactive support site for those who will be having ileostomy, colostomy, j pouch or urostomy surgery. For new and experienced ostomates.

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A site dedicated to my dauaghter, Leah Rose, born on 9/19/03, and diagnosed with Freeman Sheldon Syndrome and a midline cleft in the soft palate.

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Bring More Visitors To Your Site! Want to be at the top of the ring's hub at all times? For less than $1.00 per month (that's 3 cents a day) you can feature your site to increase not only visitors, but it can help those who are charitable organizations in need of funds and more. If you are interested in participating then go to 'Site Promotion & Extra' and enter in the 'Featured Sites Fee' box the maximum you would be willing to pay to have your Site included in the featured Sites area. If the RingMaster has previously entered a fee amount you will be shown that amount with a message indicating the RingMaster is willing to feature your site. If you enter a lower amount, the RingMaster may NOT feature your site. The Ringmasters can feature up to 3 sites. For more info, go to: http://dir.webring.com/help?nextpg=MgmtNav15;usernum=;next


As of November 1, the ring will give a time frame of 2 WEEKS (instead of 1 week) for pending and suspended members to upload the ring's navigation code. Suspended members may find that either they have no navigation code or the wrong code installed. Other reasons is your site has been deleted/not responding and you may need to contact your server. If you have changed your URL, please edit your site ASAP before the navigation checker suspends your site. Please also note that a new navigation code (SSNB) will need to be uploaded on to your new URL, otherwise the old one is treated as 'FAIL'.




Support for preemies.NICU through school age.Special needs,disability,cerebral palsey,autistic,developmental delays,sensory integration disorder,oral aversion,ADD/ADHD,progress,anything and everything about your preemie.Pregnant after a preemie?

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Just to let all the members in the ring 'Our Special Child Webring' that the forum is up and running. The forum is open to families of children with special needs. I also wish to open the forum to individuals to discuss information to help the families who have a child with a disorder/disease in any way. I'd also like to 'Thank You' to the many people have come forth with sites that are valuable to helping children with disabilities.

God Bless

Julie
Forum Owner




CJ has a deletion of chromosome 6q (6q- 25.3-qter), cerebral palsy, hydrocephalus and epilepsy. He was also born with a tethered spinal cord, which has been operated on. All things considered, he is doing remarkably well.

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In thirty-five years of parenting, our family has grown through adoption to twenty-six children. Ten of these children have profound mental retardation. Each child has their own personality, strengths, and special qualities. This site is built around these ten of my children, with love and appreciation. It also includes stories of some of my other children with disabilities.

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My daughter successfully used the ketogenic diet and her story is on the web site. As we have very little support in Australia, I have provided information and links to support networks, especially for Australian parents of children with uncontrolled epilepsy. It provides information on alternative treatments including the ketogenic diet and also how to use the ketogenic diet when your chi

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The purpose of this site is to increase awareness of cerebral palsy and to share with you how I am dealing with it, the treatment I am receiving, and other possible alternatives available.

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15 years as a counselor at a camp for children with special needs

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Camping for children with special needs

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A support site for families and people dealing with down syndrome and other disablities.

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This site is about Kalib who was born 4 months premature, survived all the problems of premature birth (including a spinal cord injury) and then survived a Wilm's Tumor (cancer). He is an inspiration to many. His site contains lots of pictures, his story, a glossary page, a links page and various other info.

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